Pune Healthcare Jobs

Why This Role MattersDental Surgeons play a vital role in diagnosing oral health conditions, performing advanced dental treatments, and ensuring patients receive high-quality dental care. Their expertise helps maintain oral health, prevent dental diseases, and provide specialized treatments that improve patients’ overall well-being.Job DescriptionHealth Chakra Pvt Ltd is seeking a Dental Surgeon to join the hospital-based dental OPD at Hinjewadi Superspecialty Hospital in Pune, Maharashtra. The role involves performing a wide range of modern dental procedures, managing patient diagnosis and treatment planning, and maintaining strict clinical protocols within a hospital environment.Key Features of the Role• Position: Dental Surgeon / Associate Dentist• Company: Health Chakra Pvt Ltd• Location: Pune, Maharashtra, India• Employment Type: Full-Time• Salary: ₹20,000 – ₹30,000 per month• Working Hours: 9:00 AM – 6:00 PMResponsibilities• Perform contemporary dental procedures while maintaining high standards of patient care• Conduct patient diagnosis, treatment planning, and follow-up consultations• Perform procedures such as rotary endodontics, pulpectomy, and tooth preparation for zirconia crowns• Manage pediatric dentistry procedures and assist in treatment planning for implants and aligners• Maintain accurate patient records and follow clinic documentation protocols• Adhere strictly to clinical guidelines and healthcare protocols established by the organization• Ensure patient comfort, safety, and satisfaction during treatmentsRequired Qualification• Bachelor of Dental Surgery (BDS)Important Requirements• Minimum 3 years of clinical experience in dentistry• Strong knowledge of contemporary dental procedures and technologies• Fluency in English for effective patient communication• Willingness to travel up to 25% if required• Ability to work in a hospital-based dental OPD environmentWhat We Offer• Competitive monthly salary package• Opportunity to work in a hospital-based dental OPD• Exposure to advanced dental procedures and modern dental technologies• Professional clinical environment for skill developmentExperience and Skills• Rotary endodontics and root canal treatments• Pediatric dentistry procedures such as pulpectomy• Tooth preparation for zirconia crowns• Implant and aligner treatment planning• Patient diagnosis, treatment planning, and follow-up care• Clinical documentation and healthcare protocol complianceSalary Insights• Monthly salary range: ₹20,000 – ₹30,000• Compensation may vary depending on experience and clinical expertiseCompany OverviewHealth Chakra Pvt Ltd is a healthcare organization focused on delivering professional medical and dental services. The organization collaborates with hospital-based OPDs to provide modern healthcare solutions and maintain high standards of patient care.FAQsWhat qualification is required for this role?A Bachelor of Dental Surgery (BDS) degree is required.Is prior experience necessary?Yes, a minimum of 3 years of experience in dentistry is required.What type of dental procedures are expected in this role?The role involves procedures such as rotary endodontics, zirconia crown preparation, pulpectomy, and treatment planning for implants and aligners.Where is the job located?The position is based in Pune, Maharashtra, India.Application Tips• Highlight your BDS qualification and clinical experience in your resume• Mention experience in rotary endodontics, implants, or pediatric dentistry if applicable• Include details of dental procedures you have independently performed• Emphasize patient communication and treatment planning skills• Prepare to discuss clinical cases and treatment approaches during interviews

Why This Role MattersPhysiotherapists play an essential role in helping individuals recover from injuries, manage physical impairments, and improve mobility. Through therapeutic exercises, manual therapy, and rehabilitation programs, physiotherapists support patients in regaining independence, reducing pain, and achieving better long-term health outcomes.Job DescriptionPhysiocures Home Care Physiotherapy Services is seeking a dedicated Physiotherapist to join its team in Pune, Maharashtra. This full-time role offers an opportunity to work closely with patients requiring rehabilitation and mobility support. The position is suitable for fresh graduates who are passionate about patient care and eager to develop their clinical skills in a supportive healthcare environment.Key Features of the Role• Position: Physiotherapist• Company: Physiocures Home Care Physiotherapy Services• Location: Pune, Maharashtra, India• Employment Type: Full-Time, Permanent• Salary: ₹3,50,000 – ₹4,50,000 per year• Experience Level: FresherResponsibilities• Assess patients with physical impairments, injuries, or disabilities• Develop individualized physiotherapy treatment plans• Deliver rehabilitation therapies including exercise therapy, massage, and manual therapy• Monitor patient progress and adjust treatment programs accordingly• Educate patients and families about injury prevention and long-term health management• Maintain accurate patient records and treatment documentation• Support patients in achieving mobility, strength, and recovery goalsRequired Qualification• Bachelor of Physiotherapy (BPT) or equivalent qualificationImportant Requirements• Valid driving licence (required)• Strong communication and patient care skills• Ability to work independently and manage patient treatments• Commitment to patient rehabilitation and recoveryWhat We Offer• Competitive annual salary between ₹3,50,000 and ₹4,50,000• Flexible working schedule• Leave encashment benefits• Opportunity to gain hands-on experience in physiotherapy practice• Supportive working environment focused on patient careExperience and Skills• Basic physiotherapy assessment and rehabilitation skills• Exercise therapy and manual therapy techniques• Patient education and rehabilitation planning• Communication and interpersonal skills• Ability to monitor treatment progress and patient outcomesSalary Insights• Annual salary range: ₹3,50,000 – ₹4,50,000 depending on experience• Additional benefits including flexible scheduling and leave encashmentCompany OverviewPhysiocures Home Care Physiotherapy Services provides physiotherapy and rehabilitation services to patients requiring mobility support and recovery from injuries or disabilities. The organization focuses on delivering patient-centered care through personalized treatment plans and professional physiotherapy support.FAQsAre fresh graduates eligible for this role?Yes, the position is open to fresher physiotherapists who want to begin their professional careers.Is a driving licence required?Yes, candidates must have a valid driving licence.What type of treatments will physiotherapists provide?Treatments include exercise therapy, manual therapy, massage therapy, and rehabilitation guidance.Is the role full-time?Yes, the position is a full-time permanent role.Application Tips• Clearly mention your BPT qualification in your resume• Highlight internships, clinical postings, or physiotherapy training experience• Demonstrate strong communication and patient interaction skills• Emphasize interest in rehabilitation and patient care• Mention your valid driving licence in the application

Why This Role MattersThe Dental Surgeon plays a key role in delivering comprehensive dental care within a hospital-based dental OPD. By diagnosing dental conditions, performing advanced procedures, and ensuring proper treatment planning, dental surgeons help improve patient outcomes while maintaining high standards of clinical care and safety.Job DescriptionHealth Chakra Pvt Ltd is hiring a Dental Surgeon for a full-time position in Pune. The role is based at Hinjewadi Superspecialty Hospital and involves performing contemporary dental procedures, diagnosing patients, creating treatment plans, and ensuring follow-up care while maintaining strict adherence to clinical protocols and documentation standards.Key Features of the Role• Position: Dental Surgeon / Associate Dentist• Company: Health Chakra Pvt Ltd• Location: Pune, Maharashtra, India• Employment Type: Full-Time• Workplace Type: On-site (Hospital-based Dental OPD)• Salary: ₹20,000 – ₹30,000 per month• Working Hours: 9:00 AM – 6:00 PM• Experience: Minimum 3 years requiredResponsibilities• Perform a wide range of modern dental procedures while ensuring high standards of patient care• Diagnose dental conditions and develop effective treatment plans• Carry out procedures such as rotary endodontics, pulpectomy, crown preparation, and pediatric dental treatments• Assist in treatment planning for implants and aligner therapies• Monitor patient progress and conduct follow-up consultations• Maintain accurate patient records and clinical documentation• Follow Health Chakra protocols and hospital clinical guidelines• Coordinate with healthcare teams to ensure comprehensive patient careRequired Qualification• Bachelor of Dental Surgery (BDS) from a recognized institutionImportant Requirements• Minimum 3 years of clinical dental experience• Strong knowledge of rotary endodontics and restorative dental procedures• Experience in pediatric dental treatments such as pulpectomy• Knowledge of crown preparation including Zirconia crowns• Basic understanding of implant and aligner treatment planning• Proficiency in English communication• Willingness to travel up to 25% if requiredEmployment Options• Full-time position• On-site hospital-based dental roleWhat We Offer• Opportunity to work in a hospital-based dental OPD environment• Exposure to contemporary dental procedures and advanced treatment planning• Structured clinical protocols and professional practice standards• Opportunity to collaborate with multidisciplinary healthcare teams• Clinical experience in implants, aligners, and pediatric dentistryExperience and Skills• Rotary endodontics and root canal treatments• Crown preparation including Zirconia crowns• Pediatric dentistry procedures such as pulpectomy• Implant and aligner treatment planning• Patient diagnosis and treatment planning• Clinical documentation and patient record management• Communication and patient consultation skillsSalary Insights• Monthly Salary: ₹20,000 – ₹30,000• Salary may vary depending on clinical experience and expertiseCompany OverviewHealth Chakra Pvt Ltd is a healthcare organization that provides medical and dental services through hospital-based facilities. The company focuses on delivering patient-centered care with modern clinical practices and standardized healthcare protocols.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) degree.How much experience is required?A minimum of 3 years of clinical dental experience is required.What procedures will the Dental Surgeon perform?The role involves procedures such as rotary endodontics, crown preparation, pulpectomy, and treatment planning for implants and aligners.Where is the job located?The role is based in Pune, Maharashtra at Hinjewadi Superspecialty Hospital.Application Tips• Highlight experience in rotary endodontics and crown preparation• Mention clinical experience in pediatric dental procedures such as pulpectomy• Include experience with implant or aligner treatment planning• Emphasize patient consultation and treatment planning skills• Showcase knowledge of clinical documentation and hospital protocols

Why This Role MattersThe Dentist (Mobile Polyclinic Van) role plays a vital part in improving access to essential dental care for underserved communities. By delivering dental services through mobile healthcare infrastructure, dentists help bridge healthcare gaps for individuals who may otherwise lack access to quality oral health services, particularly in rural and resource-limited settings.Job DescriptionHealth Within Reach Foundation is hiring a Dentist for a full-time on-site role in the Pune Division. The position involves providing dental services through a Mobile Polyclinic Van based in Koregaon Park and covering areas within approximately 30 km around Pune. The dentist will conduct examinations, perform dental procedures, administer anesthetics, and educate patients on oral health practices while working with other healthcare professionals to deliver coordinated patient care.Key Features of the Role• Position: Dentist (Mobile Polyclinic Van)• Company: Health Within Reach Foundation• Location: Pune Division, Maharashtra, India• Base Location: Koregaon Park, Pune• Employment Type: Full-Time• Workplace Type: On-site (Mobile clinic services)• Experience: 3+ years preferredResponsibilities• Conduct dental examinations and diagnose oral health conditions• Provide dental treatments and procedures in a mobile clinic setup• Administer anesthetics when required during dental treatments• Educate patients on oral hygiene and preventive dental care• Maintain accurate patient records and treatment documentation• Collaborate with other healthcare professionals for integrated care• Deliver dental services to underserved populations in rural and urban communities• Ensure safe and hygienic dental practices within the mobile clinic environmentRequired Qualification• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid license and certifications to practice dentistry in Pune or MaharashtraImportant Requirements• Minimum 3 years of clinical experience in dentistry• Strong knowledge of dental procedures and treatments• Ability to work independently as well as in team-based healthcare settings• Compassionate and patient-centered approach to care• Excellent communication and interpersonal skills• Fluency in Hindi and preferably Marathi• Experience working with underserved or resource-limited populations is an advantageWhat We Offer• Opportunity to contribute to a meaningful social healthcare mission• Exposure to community-based and mobile healthcare delivery• Collaborative work environment with multidisciplinary healthcare professionals• Experience working with underserved populations• Opportunity to create social impact through accessible dental careExperience and Skills• Dental diagnosis and treatment planning• Mobile healthcare or community dentistry experience• Patient counseling and oral health education• Preventive and restorative dental treatments• Clinical documentation and patient record management• Communication and teamwork in healthcare settingsSalary Insights• Salary: Not disclosed in the job postingCompany OverviewHealth Within Reach Foundation is a non-profit organization and Section 8 company under the Companies Act 2013. Based in Pune, the foundation focuses on delivering quality healthcare services to underserved populations using mobile healthcare infrastructure and digital technologies. Its mission is to overcome barriers such as distance, poverty, and limited healthcare availability by bringing medical and dental services directly to communities in need.FAQsWhat qualification is required for this role?Candidates must have a BDS degree from a recognized institution with valid dental practice certification.How much experience is required?The role typically requires at least 3 years of clinical dental experience.What type of work environment is involved?The dentist will work in a Mobile Polyclinic Van providing services within approximately 30 km around Pune.Is knowledge of local languages required?Fluency in Hindi is required, and knowledge of Marathi is desirable.Application Tips• Highlight experience in community dentistry or mobile healthcare services• Emphasize patient counseling and preventive dental care experience• Mention experience working with diverse or underserved patient populations• Include language skills such as Marathi and Hindi• Showcase adaptability and ability to work in mobile or outreach healthcare environments

Why This Role MattersThe Scanning Dentist role is important in modern digital dentistry, where advanced technology is used to improve treatment accuracy and patient experience. By using intraoral scanners and digital treatment planning tools, dentists help create precise dental impressions and support efficient treatment planning while maintaining high standards of patient care.Job DescriptionClove Dental is hiring a BDS Dentist for a Non-Clinical Intra Oral Scanning role in Pune, Maharashtra. The position focuses on digital dentistry, including intraoral scanning, patient consultations, and treatment planning using advanced dental technology. This role is suitable for dentists interested in digital workflows and patient consultation rather than traditional clinical procedures.Key Features of the Role• Position: Scanning Dentist (Non-Clinical Role)• Company: Clove Dental• Location: Pune, Maharashtra, India (also opportunities in Hyderabad)• Employment Type: Full-TimeResponsibilities• Perform digital impressions using advanced 3D intraoral scanners• Support digital treatment planning using specialized dental software• Conduct patient consultations and explain treatment procedures and outcomes• Maintain patient records and clinical documentation• Coordinate appointments and manage patient communication through calls and emails• Provide follow-up support and maintain patient relationships• Stay updated with advancements in digital dentistryRequired Qualification• Bachelor of Dental Surgery (BDS)• Registration with the Dental CouncilImportant Requirements• Strong communication and interpersonal skills• Ability to explain treatment procedures and costs to patients• Basic knowledge of digital dentistry technologies• Willingness to commute within designated clinic zones• Prior dental clinic or patient management experience preferredEmployment Options• Full-time positionWhat We Offer• Opportunity to work with advanced digital dentistry technology• Exposure to modern dental treatment planning systems• Professional environment in a leading dental chain• Career growth in digital dentistry and patient consultation rolesEmployee Benefits• Health insurance• Provident Fund (PF)• Professional development opportunitiesExperience and Skills• Digital dental scanning and imaging• Patient consultation and communication• Dental treatment planning support• Patient record management and documentation• Knowledge of digital dentistry workflowsSalary Insights• Salary: ₹25,000 – ₹35,000 per monthCompany OverviewClove Dental is one of India’s leading dental care networks with clinics across multiple cities. The organization focuses on delivering high-quality dental care through modern technology, digital dentistry solutions, and experienced dental professionals.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) and Dental Council registration.Is this a clinical treatment role?No, this is a non-clinical role focused on intraoral scanning and digital treatment planning.Are benefits provided?Yes, employees receive health insurance and Provident Fund benefits.Where is the job located?The role is based in Pune, with opportunities also available in Hyderabad.Application Tips• Highlight your BDS qualification and Dental Council registration• Mention experience with patient consultations and communication• Include knowledge of digital dentistry or dental imaging tools if available• Demonstrate strong interpersonal and patient management skills

Why This Role MattersThe Physiotherapist plays an important role in helping patients recover from injuries, manage physical conditions, and improve their mobility and quality of life. By providing targeted physiotherapy treatments, rehabilitation programs, and preventive guidance, physiotherapists support patients in reducing pain, restoring movement, and maintaining long-term physical health. This role contributes to delivering patient-centered care through evidence-based treatment methods and collaborative healthcare practices.Job DescriptionPhysiocures is hiring a Physiotherapist for a full-time on-site role in the Pune/Pimpri-Chinchwad Area. The physiotherapist will assess and diagnose patients with various physical conditions, develop personalized treatment plans, and deliver physiotherapy interventions aimed at improving mobility and recovery. The role also includes educating patients on exercises and preventive care, monitoring patient progress, maintaining clinical records, and collaborating with healthcare professionals to ensure effective rehabilitation outcomes.Job DetailsJob Title: PhysiotherapistCompany Name: PhysiocuresLocation: Pune / Pimpri-Chinchwad Area, Maharashtra, IndiaEmployment Type: Full-TimeWorkplace Type: On-siteSalary: Not disclosedRoles and Responsibilities• Assess and diagnose patients with physical injuries, conditions, or mobility limitations• Develop and implement personalized physiotherapy treatment plans• Perform physiotherapy interventions including manual therapy and therapeutic exercises• Design rehabilitation programs to improve patient mobility and physical function• Educate patients on injury prevention, self-care, and home exercise programs• Monitor patient progress and adjust treatment plans as required• Maintain accurate patient records and clinical documentation• Collaborate with healthcare professionals to ensure comprehensive patient careQualification• Bachelor’s or Master’s degree in Physiotherapy from a recognized institution• Valid physiotherapy license or certification as requiredExperience• Prior experience in physiotherapy practice or rehabilitation services is preferred• Experience in physical rehabilitation or sports physiotherapy is an advantageSkills• Expertise in patient assessment and clinical diagnosis• Proficiency in manual therapy techniques and therapeutic exercises• Knowledge of anatomy, biomechanics, and evidence-based physiotherapy practices• Strong communication and interpersonal skills• Ability to educate patients about preventive care and rehabilitation exercises• Organizational and documentation skills• Ability to work collaboratively within a multidisciplinary healthcare teamImportant Requirements• Valid driver’s license• Strong commitment to patient-centered care and rehabilitation outcomes• Ability to adapt treatment plans to diverse patient needs• Attention to detail in clinical evaluation and documentation• Ability to work effectively in a team-oriented healthcare environmentAbout the CompanyPhysiocures is a patient-focused organization that provides personalized physiotherapy and rehabilitation services. The organization focuses on improving mobility, reducing pain, and enhancing the quality of life for patients through evidence-based treatment methods. With a strong emphasis on compassionate care, professionalism, and innovative therapies, Physiocures aims to deliver effective rehabilitation solutions tailored to each patient’s individual needs.FAQsWhat qualification is required for this role?Candidates must have a Bachelor’s or Master’s degree in Physiotherapy from a recognized institution along with the required professional licensure.Where is the job located?The position is based in the Pune/Pimpri-Chinchwad Area in Maharashtra, India.Is prior experience required for this role?While experience in physiotherapy or rehabilitation services is preferred, experience in sports physiotherapy or physical rehabilitation is considered an advantage.What type of treatments will the physiotherapist provide?The physiotherapist will provide patient assessments, manual therapy, therapeutic exercises, rehabilitation programs, and preventive care guidance.Application Tips• Highlight your experience in patient assessment and rehabilitation planning• Mention proficiency in manual therapy techniques and therapeutic exercise programs• Emphasize knowledge of anatomy, biomechanics, and physiotherapy practices• Showcase communication skills and ability to educate patients on preventive care• Include examples of teamwork in multidisciplinary healthcare environments

Why This Role MattersThe Clinical Physiotherapist plays a crucial role in supporting the physical development and rehabilitation of children with developmental or mobility challenges. By providing specialized pediatric physiotherapy treatments and collaborating with multidisciplinary teams, the physiotherapist helps improve motor skills, mobility, and overall functional independence in children.Job DescriptionWalnut Child Development Clinic is hiring a Clinical Physiotherapist for a full-time permanent position in Pune, Maharashtra. The role involves providing pediatric physiotherapy treatments, assessing developmental conditions, and working with a multidisciplinary rehabilitation team to support children’s physical development and recovery.Key Features of the Role• Position: Clinical Physiotherapist• Company: Walnut Child Development Clinic• Location: Pune, Maharashtra, India• Employment Type: Full-Time, Permanent• Workplace Type: On-site• Salary: ₹30,000 – ₹35,000 per month• Work Location: Lohegaon, Tingre Nagar (Pune)Responsibilities• Assess children’s physical development, mobility, and motor function• Develop individualized pediatric physiotherapy treatment plans• Provide therapeutic exercises and rehabilitation interventions for children• Monitor patient progress and modify therapy programs when necessary• Work collaboratively with multidisciplinary healthcare teams• Educate parents and caregivers on exercises and developmental support techniques• Maintain accurate clinical documentation and treatment records• Support children in improving mobility, coordination, and functional abilitiesRequired Qualification• Master of Physiotherapy (MPT) – MandatoryImportant Requirements• 1–2 years of pediatric physiotherapy experience preferred• Strong knowledge of pediatric rehabilitation and physiotherapy techniques• Good communication and patient interaction skills• Willingness to learn and grow within a clinical rehabilitation environment• Ability to join immediately if selected• Willingness to commit to a minimum one-year employment periodEmployment Options• Full-time permanent roleWhat We Offer• Paid time off and paid sick leave• Annual bonus and performance-based incentives• Continuing education programs for professional development• Opportunity to work in a multidisciplinary pediatric rehabilitation teamExperience and Skills• Pediatric physiotherapy assessment and treatment• Child development and motor skill rehabilitation• Therapeutic exercise and rehabilitation planning• Patient and caregiver counseling• Clinical documentation and patient record management• Multidisciplinary healthcare collaborationSalary Insights• Monthly salary range: ₹30,000 – ₹35,000• Additional benefits include paid leave, incentives, and professional development programsCompany OverviewWalnut Child Development Clinic is a pediatric rehabilitation chain based in Pune that focuses on supporting children with developmental and physical challenges. The clinic provides multidisciplinary therapies and rehabilitation services designed to improve mobility, functional abilities, and overall developmental outcomes for children.FAQsWhat qualification is required for this role?Candidates must have a Master of Physiotherapy (MPT).What experience is preferred for this position?Candidates with 1–2 years of pediatric physiotherapy experience are preferred.What is the salary range for this role?The salary ranges from ₹30,000 to ₹35,000 per month.Where is the job located?The job is located in Lohegaon, Tingre Nagar, Pune, Maharashtra.Application Tips• Highlight your MPT qualification and pediatric physiotherapy experience• Mention experience in child rehabilitation and developmental therapy• Include clinical assessment and treatment planning skills• Demonstrate ability to work with multidisciplinary teams• Emphasize patient and caregiver counseling skills

Why This Role MattersThe Safety Science Analyst plays an important role in monitoring and managing drug safety data in clinical research and post-marketing environments. By handling adverse event reports, documenting safety information, and ensuring timely regulatory submissions, the analyst helps protect patient safety and supports compliance with global pharmacovigilance standards.Job DescriptionFortrea is hiring a Safety Science Analyst for a 6-month contract position in Pune. The role involves supporting pharmacovigilance operations by processing adverse event reports, maintaining safety databases, preparing safety documentation, and assisting with regulatory submissions while ensuring compliance with quality and safety standards.Key Features of the Role• Position: Safety Science Analyst• Company: Fortrea• Location: Pune, Maharashtra, India• Employment Type: Contract (6 Months)• Workplace Type: Office-based• Experience: 0–1 year of pharmacovigilance or relevant experience• Category: Clinical / PharmacovigilanceResponsibilities• Perform case intake and triage of incoming safety reports from clinical trials or spontaneous sources• Enter safety data into adverse event tracking and safety database systems• Write patient safety narratives and code adverse events using MedDRA terminology• Assist in listedness assessment against appropriate product labels when applicable• Generate queries and obtain missing or inconsistent information in coordination with medical teams• Submit expedited serious adverse event (SAE) reports to clients, regulatory authorities, and investigators within timelines• Assist in preparing and submitting periodic and expedited safety reports to global regulatory agencies• Support reconciliation of safety databases when required• Maintain documentation related to adverse event reporting requirements across regions• Upload and archive safety case documentation and study records• Follow company SOPs, quality systems, and pharmacovigilance regulations• Collaborate with cross-functional teams to maintain effective safety operationsRequired Qualification• B.Pharm, M.Pharm, Pharm D, BAMS, BDS, BHMS, or Nursing degreeImportant Requirements• 0–1 year of pharmacovigilance, clinical safety, or relevant healthcare experience• Strong attention to detail and accuracy in data handling• Good written and verbal communication skills• Basic knowledge of MS Office applications• Ability to work effectively in a team environment• Understanding of clinical safety processes is preferredWhat We Offer• Opportunity to work in a global clinical research organization• Exposure to pharmacovigilance and clinical safety operations• Experience with safety databases and regulatory reporting processes• Professional work environment with industry-standard safety practices• Opportunity to develop skills in drug safety and regulatory complianceExperience and Skills• Adverse event case processing and safety data entry• Medical narrative writing and MedDRA coding• Pharmacovigilance documentation and regulatory reporting• Safety database management and reconciliation support• Attention to detail and data accuracy• Communication and teamwork in clinical research settingsSalary Insights• Salary details not specified in the job listing• Compensation may vary depending on qualifications and experienceCompany OverviewFortrea is a global clinical research organization that supports pharmaceutical, biotechnology, and medical device companies in developing life-changing treatments. The company specializes in clinical trials, pharmacovigilance, regulatory services, and drug development solutions while maintaining high standards of patient safety and data integrity.FAQsWhat qualifications are required for this role?Candidates must hold a B.Pharm, M.Pharm, Pharm D, BAMS, BDS, BHMS, or Nursing degree.Is prior experience required?0–1 year of pharmacovigilance or related healthcare experience is preferred.What does the Safety Science Analyst do?The analyst processes adverse event reports, manages safety data, writes narratives, and supports regulatory submissions.Where is the job located?The position is office-based in Pune, Maharashtra.Application Tips• Highlight your pharmacovigilance or clinical safety knowledge• Mention experience with adverse event processing or safety databases• Include details of your healthcare qualification (B.Pharm, BDS, Nursing, etc.)• Demonstrate attention to detail and data management skills• Emphasize teamwork and communication abilities

Why This Role MattersThe Scanning Dentist plays an important role in modern digital dentistry by using advanced scanning technology to capture precise dental impressions and assist in treatment planning. By utilizing 3D intraoral scanners and digital tools, this role improves diagnostic accuracy, enhances patient comfort, and supports efficient treatment workflows. The position also contributes to patient education and ensures high standards of digital dental care.Job DescriptionClove Dental is hiring a Scanning Dentist for a full-time permanent position in Pune, Maharashtra. The role focuses on digital treatment planning using advanced intraoral scanning technology, conducting patient consultations, and maintaining accurate clinical records. The dentist will also manage patient interactions and administrative tasks while delivering high-quality digital dental care.Key Features of the Role• Position: Scanning Dentist• Company: Clove Dental• Location: Pune, Maharashtra, India• Employment Type: Full-Time, Permanent• Workplace Type: On-site• Experience: Freshers or candidates with 1 year of experience• Salary Range: ₹20,000 – ₹25,000 per monthResponsibilities• Use advanced 3D intraoral scanners and digital software to capture accurate dental impressions• Support digital treatment planning for customized dental procedures• Conduct patient consultations and explain treatment options, benefits, and expected outcomes• Maintain high standards of patient care throughout the treatment process• Provide follow-up support and aftercare guidance to patients• Manage patient records, appointment scheduling, and communication through calls and emails• Stay updated with advancements in digital dentistry and integrate new technologies into clinical practiceRequired Qualification• Bachelor of Dental Surgery (BDS)Important Requirements• Freshers or candidates with up to 1 year of experience can apply• Basic understanding of digital dentistry and dental scanning technology• Good communication and patient consultation skills• Ability to manage patient records and clinic administration tasks• Willingness to learn and adapt to new digital dental technologiesWhat We Offer• Opportunity to work with advanced digital dental technology• Professional growth in digital dentistry and treatment planning• Collaborative work environment with experienced dental professionals• Health insurance benefits• Provident Fund benefitsExperience and Skills• Digital dental scanning and intraoral imaging• Patient consultations and treatment explanations• Digital treatment planning tools and software• Clinical documentation and patient record management• Communication and patient relationship management• Basic administrative and scheduling tasks in clinicsSalary Insights• Salary Range: ₹20,000 – ₹25,000 per monthCompany OverviewClove Dental is one of the largest dental clinic networks in India, established in 2011. With more than 700 clinics nationwide, the organization provides modern dental treatments using advanced technology and strict sterilization protocols. Clove Dental focuses on delivering global standards of dentistry with strong emphasis on patient safety, hygiene, transparency, and high-quality clinical care.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) degree.Can freshers apply for this position?Yes, freshers and candidates with up to 1 year of experience are eligible to apply.What does a scanning dentist do?The role involves using digital intraoral scanners for dental impressions, assisting in digital treatment planning, and conducting patient consultations.Where is the job located?The position is based in Pune, Maharashtra, India.Application Tips• Highlight knowledge of digital dentistry and intraoral scanning technology• Mention clinical internship experience or exposure to dental imaging tools• Emphasize communication and patient consultation skills• Include experience with dental software or digital treatment planning if applicable• Clearly mention BDS qualification and clinical training in your resume

Why This Role MattersClinical trials require strict documentation practices to ensure transparency, regulatory compliance, and patient safety. The Clinical Document Specialist plays a crucial role in managing and maintaining the Trial Master File (TMF), which contains essential documents that demonstrate the proper conduct of clinical studies.This role ensures that clinical trial documents are accurately filed, reviewed, and maintained within electronic Trial Master File systems. Proper document management is essential because regulatory authorities rely on these records during inspections to confirm that studies comply with international guidelines.Professionals in this role support clinical research teams by organizing documentation, maintaining inspection readiness, and ensuring that trial records remain accurate and complete throughout the study lifecycle. For life sciences graduates, this position offers a strong entry point into the clinical research and regulatory documentation field.Job DescriptionThe Clinical Document Specialist I is responsible for managing clinical trial documentation and maintaining the electronic Trial Master File (eTMF). The role involves reviewing essential study documents, indexing files, and ensuring that documentation meets regulatory and organizational standards.Working closely with clinical project teams and documentation leads, the specialist ensures that all documents are filed correctly and accessible when needed. This position requires strong attention to detail, excellent organizational skills, and a clear understanding of clinical research documentation practices.The role also involves assisting with system testing, resolving documentation issues, and supporting continuous improvement in document management workflows. By ensuring accurate and compliant documentation, the Clinical Document Specialist contributes significantly to the overall quality and integrity of clinical trials.Key Features of the Role:• Entry-level opportunity in clinical research documentation and TMF management• Hands-on experience with electronic Trial Master File (eTMF) systems• Exposure to global clinical trial regulatory standards and documentation processes• Collaboration with clinical research teams, project managers, and documentation leads• Opportunity to support system improvements and process optimization• Career development opportunities in clinical research operations and documentation managementResponsibilities• Review essential and non-essential Trial Master File (TMF) documents within the eTMF workflow• Perform initial indexing and accurate filing of clinical documents in the eTMF system• Ensure documentation meets company quality thresholds and productivity targets• Verify that documents comply with regulatory standards and sponsor requirements• Maintain updated study trackers and document logs for project management teams• Communicate regularly with Clinical Document Team Leads regarding project queries and documentation updates• Support User Acceptance Testing (UAT) activities during system upgrades or product development• Identify documentation workflow challenges and suggest process improvements• Ensure that documents are correctly classified according to TMF structure and regulatory guidelines• Coordinate with internal teams and stakeholders to resolve documentation issues• Maintain accurate records to ensure inspection readiness for clinical trialsRequired QualificationsEducational Requirements:• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related biomedical field• Degrees such as BSc, MSc, B.Pharm, M.Pharm, or Pharm.D are commonly considered suitable for this roleExperience and Skills:• 0–1 year of experience in the life sciences, clinical research, or healthcare industry• Basic understanding of clinical trial phases and clinical development processes• Knowledge of clinical documentation practices and Trial Master File structure• Familiarity with ICH-GCP guidelines and regulatory compliance requirements• Proficiency in Microsoft Office tools such as Word, Excel, and Outlook• Knowledge of eClinical technologies or eTMF systems is considered an advantage• Strong written and verbal communication skills in English• High attention to detail and strong organizational abilities• Ability to manage documentation accurately and maintain quality standards• Good coordination skills for working with internal teams and project stakeholdersSalary Insights:• Professionals with relevant experience in TMF management or clinical documentation may earn higher compensation• Additional benefits may include training programs, performance bonuses, and career development opportunitiesCompany OverviewClinical Document Specialist roles are commonly available in global Contract Research Organizations (CROs), pharmaceutical companies, and clinical research service providers operating in India. These organizations support the development of new medicines by managing clinical trials, maintaining regulatory documentation, and ensuring compliance with international standards.The clinical documentation function plays a key role in ensuring that all study-related information is organized, traceable, and available for regulatory review. Professionals working in this field contribute directly to maintaining the integrity and transparency of clinical research operations.FAQsWhat does a Clinical Document Specialist do?A Clinical Document Specialist manages and reviews clinical trial documentation, ensuring that files are properly organized within the Trial Master File and comply with regulatory standards.What is a Trial Master File (TMF)?The Trial Master File is a collection of essential documents that demonstrate how a clinical trial was conducted and managed according to regulatory requirements.Is prior clinical research experience required for this role?Many entry-level roles accept candidates with little or no experience, provided they have relevant life sciences education and knowledge of clinical documentation processes.What career opportunities can follow this role?Professionals may progress into roles such as TMF Specialist, Clinical Trial Associate, Clinical Project Coordinator, Clinical Data Specialist, or Clinical Operations Associate.Application Tips• Highlight your knowledge of clinical research documentation and ICH-GCP guidelines• Include any training or coursework related to clinical research or regulatory affairs• Emphasize strong attention to detail and document management skills• Mention familiarity with eClinical systems or electronic document management platforms• Demonstrate good communication skills and ability to coordinate with cross-functional teams.

Why This Role MattersHealthcare organizations rely heavily on accurate data to deliver quality patient care, maintain regulatory compliance, and support efficient medical record management. In the healthcare revenue cycle and information management ecosystem, accurate data entry and validation processes play a crucial role in ensuring reliable healthcare documentation and operational efficiency.The Healthcare Data Analyst – ROI Operations role supports healthcare providers and organizations by ensuring that medical records and healthcare data are processed accurately, securely, and in compliance with regulatory requirements. This role contributes directly to maintaining data integrity, protecting patient information, and enabling healthcare organizations to access critical information efficiently.Working with healthcare data also requires strict adherence to privacy standards such as the Health Insurance Portability and Accountability Act (HIPAA). Professionals in this role help maintain confidentiality while ensuring that healthcare data is processed accurately for operational and compliance purposes. At MRO Corp, the Analyst – ROI Operations position supports healthcare information workflows, improves operational efficiency, and contributes to delivering high-quality services to healthcare clients.Job DescriptionThe Healthcare Data Analyst – ROI Operations is responsible for performing accurate healthcare data entry, validation, and analysis tasks while maintaining strict compliance with healthcare regulations and company standards. The role requires strong attention to detail, data processing accuracy, and the ability to work efficiently within target-driven operational environments.The selected candidate will manage healthcare data entry processes, ensure database accuracy, support operational reporting, and collaborate with internal teams to improve data workflows. The role also involves maintaining internal databases, monitoring key performance indicators (KPIs), and ensuring that data integrity standards are consistently met.Key Features of the Role• Job Title: Healthcare Data Analyst – ROI Operations / Healthcare Data Entry Analyst• Company: MRO Corp• Work Type: Full-Time, Office-Based• Work Schedule: 5 Days per Week• Experience Level: Entry-Level to Early Career• Industry: Healthcare Information Management / Revenue Cycle ManagementResponsibilities• Perform accurate healthcare data entry and validation processes according to healthcare regulations and internal standards.• Maintain data integrity by ensuring that healthcare information is accurate, complete, and consistent.• Update and maintain internal databases to ensure data quality and proper documentation.• Collaborate with team members to achieve operational targets and productivity goals.• Work efficiently in different shifts while managing workload in a fast-paced environment.• Assist in analyzing healthcare data and improving data entry processes to enhance operational efficiency.• Follow data entry best practices to reduce errors and maintain quality standards.• Maintain professionalism and attention to detail while handling healthcare information.• Support operational teams in refining data workflows and improving system performance.Key Performance Indicators (KPIs)• Data Accuracy: Maintain high standards of data entry accuracy and eliminate errors to ensure quality healthcare data management.• Productivity Improvement: Monitor individual productivity and continuously improve efficiency in data processing tasks.• Knowledge Application: Apply job knowledge effectively to meet project objectives and operational targets.• Compliance Adherence: Stay informed about regulatory updates, client expectations, and company policies.Required QualificationsEducational Requirements• B.Sc (Life Sciences or related fields)• B.Pharm (Bachelor of Pharmacy)• BA (Bachelor of Arts)• Nursing• Other Life Science or healthcare-related degreesExperience and Skills• 0–3 years of experience in US healthcare processes such as Release of Information (ROI), medical billing, or revenue cycle management.• Basic understanding of healthcare compliance regulations including the Health Insurance Portability and Accountability Act (HIPAA).• Strong attention to detail and data entry accuracy.• Experience working in fast-paced, target-driven environments.• Proficiency in Microsoft Office tools such as Word, Excel, and Outlook.• Knowledge of data entry best practices and healthcare documentation standards.• Familiarity with healthcare data processing platforms or software tools is an added advantage.Additional Preferred Experience• Experience in healthcare document retrieval processes.• Exposure to Release of Information (ROI) operations.• Understanding of healthcare revenue cycle processes such as claims adjudication, claims adjustment, or medical billing.Salary InsightsThe salary for Healthcare Data Analyst – ROI Operations roles typically depends on experience, organization policies, and location.Estimated Salary Range: • ₹2,50,000 – ₹4,00,000 per yearAdditional benefits may include: • Professional exposure to healthcare information management systems• Experience in US healthcare operations and compliance standards• Opportunities for career growth in healthcare analytics and revenue cycle management• Skill development in healthcare data processing and regulatory complianceCompany OverviewMRO Corp is a leading provider of healthcare information management services that help healthcare organizations securely exchange medical records and patient information. The company specializes in Release of Information (ROI) services, healthcare data management, and compliance-driven data processing solutions.By partnering with healthcare providers, hospitals, and medical institutions, MRO Corp ensures accurate medical record management while maintaining strict regulatory compliance and data security standards. The organization plays a key role in improving healthcare data accessibility, operational efficiency, and patient information management.FAQs1. What does a Healthcare Data Analyst – ROI Operations do?This role involves entering, validating, and managing healthcare data while ensuring compliance with healthcare regulations and maintaining database accuracy.2. Is prior healthcare experience required?Candidates with 0–3 years of experience in US healthcare processes such as ROI, medical billing, or RCM are preferred, but entry-level candidates may also apply.3. What skills are important for this role?Key skills include data entry accuracy, attention to detail, knowledge of healthcare compliance standards, analytical thinking, and proficiency in Microsoft Office tools.4. Is this a remote job?No. This is a full-time office-based role with a five-day work schedule.5. What career growth opportunities are available?Professionals can progress to roles such as Senior Healthcare Data Analyst, Healthcare Operations Specialist, or Revenue Cycle Analyst.Application Tips• Highlight experience in healthcare data entry, medical billing, or ROI processes if applicable.• Demonstrate familiarity with healthcare compliance regulations such as HIPAA.• Showcase proficiency in Microsoft Excel and data processing tools.• Emphasize attention to detail and accuracy in handling healthcare information.• Mention any experience working in target-driven operational environments.

Why This Role MattersIn modern healthcare systems, patients often require prior approval from insurance providers before certain medications or treatments can be dispensed. This process, known as prescription prior authorization, ensures that therapies are medically necessary, safe, and aligned with insurance coverage policies. Without proper authorization, patients may face delays in receiving essential medications or incur higher treatment costs.The role of a Prescription Prior Authorization Specialist is crucial in bridging the gap between healthcare providers, insurance companies, pharmacies, and patients. By coordinating authorization requests and verifying coverage requirements, professionals in this role help ensure that patients receive timely access to prescribed medications.Pharmacy professionals bring valuable knowledge to this position because they understand drug therapy, prescription processes, and healthcare documentation. Their expertise allows them to interpret prescription requirements, communicate effectively with healthcare teams, and navigate authorization systems efficiently. This role supports patient care while improving administrative efficiency within healthcare organizations.Job DescriptionThe Prescription Prior Authorization Specialist is responsible for managing medication authorization requests, verifying insurance requirements, and coordinating with healthcare providers and insurers to obtain approval for treatments. The position involves reviewing prescription information, preparing required documentation, and submitting authorization requests to insurance companies or pharmacy benefit managers.Professionals in this role track authorization statuses, resolve issues related to coverage approvals, and ensure that all documentation complies with healthcare regulations. The specialist also communicates regularly with physicians, clinical staff, and patients to provide updates on authorization progress and requirements.This position is well suited for pharmacy graduates who are interested in healthcare support services, medical billing, pharmacy benefit management, or healthcare administration. It offers a structured career path within healthcare operations and insurance coordination while maintaining a strong connection to pharmacy practice.Key Features of the RoleThe role offers pharmacy professionals an opportunity to work in healthcare support services where they can apply their knowledge of medications, prescriptions, and healthcare documentation. Professionals in this position collaborate with multiple stakeholders, including healthcare providers, insurance companies, and patient support teams, to facilitate medication approvals.The job also involves working with healthcare documentation systems and insurance authorization workflows, helping professionals develop strong administrative, analytical, and communication skills. It provides exposure to pharmacy benefit management and healthcare insurance processes, which are growing sectors within the healthcare industry.Responsibilities• Managing prior authorization requests for medications and treatments.• Coordinating with healthcare providers, insurance companies, and patients.• Verifying insurance coverage and authorization requirements.• Preparing and submitting prior authorization documentation.• Tracking authorization status and ensuring timely approvals.• Communicating updates and requirements with physicians and clinical teams.• Maintaining accurate documentation and compliance with healthcare regulations.• Resolving authorization issues and following up on pending approvals.• Handling multiple authorization cases simultaneously while ensuring accuracy.• Ensuring adherence to organizational procedures and healthcare compliance standards.Required QualificationsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Diploma in Pharmacy (D.Pharm)Experience and Skills• Minimum 1 year of experience in prescription prior authorization or related healthcare support roles.• Knowledge of prior authorization workflows and insurance approval processes.• Strong written and verbal communication skills.• Ability to coordinate with insurers, physicians, and healthcare teams.• Excellent organizational and multitasking abilities.• Familiarity with healthcare documentation and regulatory compliance standards.• Attention to detail in reviewing prescription and authorization documentation.• Ability to track multiple cases and manage deadlines efficiently.• Strong problem-solving skills for resolving authorization issues.Salary InsightsThe salary offered for the Prescription Prior Authorization Specialist role typically depends on the candidate’s experience, skill level, and the hiring organization’s policies.Estimated salary range:• ₹2,80,000 – ₹4,50,000 per yearAdditional benefits may include:• Exposure to healthcare support and insurance coordination processes.• Professional development opportunities in medical billing and healthcare administration.• Stable career growth in pharmacy benefit management and healthcare operations.• Opportunities to work with healthcare providers, insurers, and clinical teams.Company OverviewHealthcare service organizations that hire Prescription Prior Authorization Specialists typically support hospitals, pharmacies, insurance companies, and healthcare providers in managing medication approval processes. These organizations help streamline administrative workflows and ensure patients receive medications without unnecessary delays. Such companies often specialize in medical billing, pharmacy benefit management, healthcare documentation, and insurance coordination services. By managing authorization processes efficiently, they play a critical role in improving healthcare delivery and ensuring regulatory compliance.FAQs1. What does a Prescription Prior Authorization Specialist do?They manage authorization requests for medications and treatments, coordinate with insurers and healthcare providers, and ensure approvals are processed efficiently.2. Who can apply for this role?Candidates with D.Pharm or B.Pharm qualifications and experience in prior authorization processes are eligible.3. Is prior authorization experience mandatory?Yes, most employers prefer candidates with at least one year of experience in prior authorization or related healthcare support roles.4. What career opportunities are available after this role?Professionals can advance to positions such as Senior Authorization Specialist, Healthcare Operations Analyst, Medical Billing Specialist, or Pharmacy Benefit Management Professional.Application Tips• Highlight your knowledge of prescription workflows and healthcare documentation.• Emphasize experience in prior authorization or insurance coordination.• Showcase strong communication skills for interacting with healthcare providers and insurers.• Demonstrate your ability to manage multiple cases while maintaining accuracy.• Mention any experience with healthcare management systems or insurance platforms.

Why This Role MattersThe Manager / Senior Executive – QA Validation plays a critical role in ensuring that biopharmaceutical manufacturing systems, utilities, and aseptic processes operate in full compliance with global regulatory standards. In highly regulated environments such as biologics and aseptic manufacturing, validation is fundamental to product quality, sterility assurance, and patient safety.This role ensures that equipment, instruments, HVAC systems, and critical utilities are properly qualified and maintained throughout their lifecycle. By aligning validation practices with cGMP, regulatory guidelines, and internal Quality Management Systems (QMS), the position strengthens audit readiness and inspection confidence.Through collaboration with Production, Engineering, Quality Control, and Regulatory teams, this role supports seamless technology transfer, process optimisation, and operational excellence. Ultimately, it safeguards compliance while enabling innovation within a biopharmaceutical manufacturing environment.Job DescriptionThe Manager / Senior Executive – QA Validation is responsible for planning, executing, reviewing, and approving validation and qualification activities across biopharmaceutical manufacturing operations. The role ensures that all validation activities follow regulatory expectations and internal quality standards.The candidate will provide QA validation oversight for equipment, instruments, AHUs, HVAC systems, aseptic filling operations, and other critical utilities. The role includes active participation in audits, regulatory inspections, deviation management, CAPA implementation, and continuous improvement initiatives.This position is suited for experienced QA Validation professionals with 6–9 years of experience in the biopharmaceutical industry and strong exposure to global regulatory inspections.Key Features of the Role:• Position: Manager / Senior Executive – QA Validation• Department: Quality Assurance• Industry: Biopharmaceutical Manufacturing• Qualification: M.Sc / M.Pharm• Experience Required: 6–9 years in QA Validation• Strong exposure to aseptic filling and HVAC validation• Hands-on regulatory audit experience (USFDA, EU, TGA, WHO)• Focus on lifecycle validation and compliance excellenceResponsibilitiesValidation & Qualification• Plan, execute, review, and approve equipment and instrument qualification activities (DQ, IQ, OQ, PQ)• Ensure effective execution of AHU qualification and HVAC validation• Prepare, review, and maintain validation documents as per the approved Validation Master Plan (VMP)• Support validation of critical utilities, systems, and manufacturing processes• Maintain validation lifecycle management in line with regulatory expectationsQuality Systems & Compliance• Ensure validation activities align with QMS and regulatory guidelines• Participate in deviation investigations, CAPA management, change controls, and risk assessments• Maintain data integrity and compliance across validation documentation• Ensure ongoing cGMP compliance in all validation processesAudit & Regulatory Support• Support and face regulatory inspections and customer audits (USFDA, EU, TGA, WHO, and other agencies)• Prepare responses to audit observations related to validation and qualification• Maintain audit readiness at all timesManufacturing & Operations Support• Provide QA validation oversight for aseptic filling operations and associated equipment• Collaborate with Production, Engineering, QC, and Regulatory teams• Support technology transfer and process improvement initiativesDocumentation & Continuous Improvement• Review SOPs, validation protocols, and reports• Drive continuous improvement initiatives to enhance validation efficiency• Strengthen compliance systems and process robustnessRequired QualificationsThe ideal candidate is a detail-oriented validation expert with deep technical knowledge of biopharmaceutical manufacturing processes and regulatory compliance frameworks.Educational Requirements:• M.Sc in Life Sciences / Biotechnology / Microbiology or related discipline OR• M.Pharm• Strong academic foundation in pharmaceutical validation and quality systemsExperience and Skills:• 6–9 years of experience in QA Validation within biopharmaceutical manufacturing• Strong experience in equipment qualification (DQ, IQ, OQ, PQ)• Hands-on experience in AHU and HVAC validation• Expertise in aseptic filling validation oversight• In-depth knowledge of cGMP and global regulatory requirements• Experience handling regulatory inspections (USFDA, EU, TGA, WHO)• Strong documentation and validation protocol review skills• Experience managing deviations, CAPA, and change control processes• Strong analytical and problem-solving abilities• Excellent cross-functional collaboration skills• High attention to detail and compliance-focused mindsetSalary InsightsCompensation will be competitive and aligned with industry standards based on experience and expertise in QA Validation within the biopharmaceutical sector. Candidates with regulatory inspection handling experience and aseptic validation exposure typically command strong market packages and growth opportunities within global pharmaceutical organisations.Company OverviewEnzene is an innovation-driven biopharmaceutical organisation committed to advancing healthcare through cutting-edge science and robust quality systems. The company emphasises regulatory excellence, advanced manufacturing technologies, and a culture of continuous improvement.At Enzene, employees are recognised as the organisation’s greatest asset. The company fosters a forward-looking culture powered by pioneers who are dedicated to transforming the pharmaceutical industry through innovation, operational excellence, and uncompromising quality standards.FAQsQ1. Is aseptic filling validation experience mandatory?Yes, hands-on experience in aseptic filling operations validation is strongly preferred.Q2. What regulatory exposure is required?Experience handling inspections from USFDA, EU, TGA, WHO, or other global agencies is expected.Q3. Is this role focused only on documentation?No. The role includes active shop floor validation oversight along with documentation review.Q4. What level of experience is suitable?Candidates with 6–9 years of relevant QA Validation experience in biopharmaceutical manufacturing are ideal.Q5. Does the role involve cross-functional coordination?Yes, close collaboration with Production, Engineering, QC, and Regulatory teams is required.Application Tips• Highlight experience in DQ, IQ, OQ, and PQ qualification activities• Mention AHU, HVAC, and aseptic validation exposure• Provide examples of regulatory inspection handling• Showcase deviation management and CAPA experience• Demonstrate knowledge of lifecycle validation principles• Emphasise cross-functional project coordination skills

Why This Role MattersThe Assistant Manager – Global QMS plays a strategic role in ensuring consistent quality standards across multiple sites within a regulated pharmaceutical or biotechnology organisation. A robust Global Quality Management System (QMS) is the backbone of regulatory compliance, operational excellence, and product reliability. This role ensures that quality frameworks are not only implemented but continuously improved to meet evolving global regulatory expectations.By overseeing document review, regulatory compliance monitoring, audit participation, and quality trend analysis, this position safeguards product integrity and patient safety on a global scale. The role bridges site-level operations with corporate quality objectives, ensuring alignment with GMP, ISO, ICH, FDA, WHO, and other applicable regulatory frameworks.Through strong governance, oversight, and collaboration with cross-functional teams, the Assistant Manager – Global QMS strengthens organisational readiness for inspections and drives a culture of quality excellence across the enterprise.Job DescriptionThe Assistant Manager – Global QMS is responsible for supporting the implementation, maintenance, and continuous improvement of the Global Quality Management System across all company sites. The role ensures alignment with internal standards and international regulatory requirements.The position requires active involvement in reviewing and approving quality documents, tracking regulatory commitments, supporting audits and inspections, and monitoring key quality metrics. The individual will collaborate with site Quality Assurance teams to ensure consistent interpretation and application of global quality standards.This role is ideal for experienced Quality Assurance professionals with strong exposure to global QMS frameworks within pharmaceutical, biotechnology, or other highly regulated industries.Key Features of the Role:• Position: Assistant Manager – Global QMS• Department: Quality Assurance• Qualification: M.Sc or M.Pharm• Experience Required: 9–12 years in QA / Global QMS• Industry: Pharmaceutical / Biotech / Regulated Industry• Exposure to global regulatory authorities (FDA, WHO, ICH, ISO, GMP)• Enterprise-wide quality system oversight• Opportunity to contribute to global compliance strategyResponsibilities• Ensure effective implementation and compliance of the Global Quality Management System across all sites• Review and approve quality documents including SOPs, policies, deviations, CAPAs, change controls, and risk assessments• Monitor adherence to global regulatory guidelines such as GMP, ISO, ICH, FDA, WHO, and local regulations• Track regulatory commitments and ensure timely closure of action items• Support and participate in internal audits, external audits, and regulatory inspections• Perform trend analysis of deviations, complaints, OOS/OOT events, and assess CAPA effectiveness• Coordinate with site QA teams to standardise interpretation and implementation of QMS procedures• Prepare quality metrics, dashboards, and reports for management review meetings• Drive continuous improvement initiatives within the Global QMS framework• Identify gaps in quality systems and recommend corrective and preventive actions• Maintain inspection readiness across all operational sites• Support enterprise-level quality governance and compliance initiativesRequired QualificationsThe ideal candidate is a seasoned Quality Assurance professional with strong exposure to global quality systems and regulatory compliance frameworks.Educational Requirements:• M.Sc in a relevant Life Sciences discipline OR• M.Pharm• Strong foundation in pharmaceutical quality systems and regulatory scienceExperience and Skills:• 9–12 years of relevant experience in Quality Assurance or Global QMS• Strong knowledge of global QMS frameworks and regulatory expectations• In-depth understanding of GMP and pharmaceutical quality systems• Experience handling audits and regulatory inspections• Strong analytical and problem-solving capabilities• Experience in deviation management, CAPA evaluation, and risk assessment• Proficiency in documentation control and quality metrics reporting• Ability to collaborate with cross-functional and multi-site teams• Strong written and verbal communication skills• Capability to drive quality improvements at an organisational levelSalary InsightsCompensation will be aligned with industry benchmarks and commensurate with experience and expertise in Global QMS and regulatory compliance. Senior-level exposure to enterprise-wide quality systems typically commands competitive remuneration packages, along with performance-based growth opportunities.Company OverviewEnzene is an innovation-driven pharmaceutical organisation committed to redefining healthcare solutions through advanced science and technology. The company focuses on regulatory excellence, operational efficiency, and a strong culture of quality.At Enzene, employees are regarded as the organisation’s most valuable asset. The company fosters a forward-thinking environment driven by pioneers who are dedicated to disrupting the pharmaceutical industry through innovation while maintaining stringent global quality and compliance standards.FAQsQ1. Is prior Global QMS experience mandatory?Yes, candidates should have substantial exposure to Global QMS or enterprise-level quality systems.Q2. What regulatory knowledge is expected?Strong understanding of GMP, ISO, ICH, FDA, WHO, and other applicable regulatory guidelines is required.Q3. Does the role involve audit participation?Yes, the role includes participation in internal audits, external audits, and regulatory inspections.Q4. Is this a site-level or global role?This is a global-level role supporting quality system implementation across all sites.Q5. What type of industry experience is preferred?Experience in pharmaceutical, biotechnology, or other regulated industries is preferred.Application Tips• Highlight enterprise-level QMS implementation experience• Mention audit and regulatory inspection exposure• Provide examples of managing deviations, CAPA, and risk assessments• Showcase experience preparing quality dashboards and management reports• Demonstrate cross-functional and multi-site coordination skills• Emphasise continuous improvement initiatives you have led

Why This Role MattersThe Executive / Senior Executive – Drug Substance Quality Assurance (DSQA) plays a critical role in ensuring that drug substance manufacturing operations consistently meet current Good Manufacturing Practice (cGMP) standards and global regulatory expectations. In a highly regulated pharmaceutical environment, maintaining quality at the shop floor level is essential to safeguarding product integrity, patient safety, and regulatory compliance.This role directly impacts the reliability of manufacturing processes by overseeing line clearance, reviewing batch documentation, monitoring in-process activities, and ensuring adherence to validated procedures. By actively participating in Quality Management System (QMS) processes such as deviations, change controls, and CAPA, the position supports continuous improvement and strengthens compliance culture.Working within a fast-evolving pharmaceutical organisation focused on innovation, this role contributes to building robust quality systems that support regulatory inspections, international market approvals, and sustainable growth in drug substance manufacturing.Job DescriptionThe Executive / Senior Executive – DSQA will be responsible for ensuring cGMP compliance at the shop floor for Drug Substance (DS) manufacturing operations. The position involves active oversight of manufacturing activities, review of documentation, validation support, and participation in quality systems processes.The candidate will work closely with production, quality control, engineering, and regulatory teams to ensure seamless compliance with established procedures and regulatory guidelines. The role requires strong technical knowledge of DS manufacturing processes, validation activities, and quality documentation systems.This position is based in Pune and is open to candidates with 2–9 years of relevant experience in pharmaceutical Quality Assurance, particularly in Drug Substance or Active Pharmaceutical Ingredient (API) environments.Key Features of the Role:• Position: Executive / Senior Executive – DSQA• Department: Quality Assurance• Location: Pune• Experience Required: 2–9 Years• Qualification: M.Sc / M.Pharm• Exposure to global regulatory standards (USFDA, EMA, WHO preferred)• Direct involvement in shop floor QA and QMS activities• Opportunity to work in an innovation-driven pharmaceutical organisationResponsibilities• Perform manufacturing line clearance activities for Drug Substance operations• Ensure proper execution and compliance of in-process checks during manufacturing• Conduct routine GMP rounds at the DS facility and document observations• Review online Batch Manufacturing Records (BMR) for accuracy, completeness, and compliance• Review and approve process validation and cleaning validation protocols and reports• Review and manage Standard Operating Procedures (SOPs) and related documentation• Coordinate sample collection and submission as per BMR, specifications, and validation protocols• Perform shop floor compliance rounds and track corrective actions• Prepare and support Annual Product Quality Review (APQR/PQR) documentation• Initiate and manage Change Controls, Deviations, Incidents, and CAPA• Participate in investigations, root cause analysis, and QMS improvement initiatives• Ensure regulatory readiness for audits and inspections• Conduct risk assessments for critical manufacturing and quality processes• Maintain continuous oversight to ensure adherence to cGMP standardsRequired QualificationsThe ideal candidate will be a detail-oriented and proactive Quality Assurance professional with strong exposure to Drug Substance manufacturing environments.Educational Requirements:• M.Sc in relevant Life Sciences discipline OR• M.Pharm• Strong academic foundation in pharmaceutical sciences and quality systemsExperience and Skills:• 2–9 years of experience in pharmaceutical Quality Assurance• Hands-on experience in DS or API shop floor QA activities• Strong understanding of cGMP and regulatory compliance requirements• Experience in BMR review and documentation control• Knowledge of process validation and cleaning validation• Familiarity with in-process control systems• Experience handling deviations, change controls, and CAPA• Strong analytical, investigation, and problem-solving abilities• Effective communication and cross-functional coordination skills• Ability to work in a dynamic, fast-paced manufacturing environmentSalary InsightsCompensation will be competitive and aligned with industry standards based on experience and qualifications. The organisation offers growth-oriented career opportunities, exposure to global regulatory environments, and a performance-driven work culture.Company OverviewEnzene is an innovation-driven pharmaceutical organisation committed to disrupting the pharmaceutical industry through cutting-edge solutions and advanced manufacturing capabilities. The company emphasises quality excellence, scientific innovation, and regulatory compliance while fostering a culture powered by pioneers and forward-thinking professionals.At Enzene, employees are regarded as the organisation’s greatest asset. The company promotes collaboration, accountability, and continuous improvement to support global regulatory standards and deliver high-quality pharmaceutical products to international markets.FAQsQ1. Is Drug Substance experience mandatory?Yes, hands-on exposure to DS or API shop floor QA activities is highly preferred.Q2. What regulatory exposure is expected?Experience with USFDA, EMA, WHO, or other global regulatory guidelines is preferred.Q3. Is this role focused on documentation only?No. The role includes active shop floor oversight along with documentation review and QMS activities.Q4. What level of experience is suitable?Candidates with 2 to 9 years of relevant QA experience are eligible.Q5. Is validation experience required?Yes, understanding and review of process validation and cleaning validation documentation is expected.Application Tips• Highlight direct experience in DS/API shop floor QA activities• Mention regulatory audit exposure (USFDA, EMA, WHO)• Provide examples of handling deviations, CAPA, and change control• Showcase validation documentation review experience• Emphasise involvement in risk assessment and QMS investigations• Demonstrate cross-functional collaboration with production and QC teams

Why This Role MattersThe Clinical Physiotherapist at Walnut Child Development Clinic plays a crucial role in improving the lives of children with developmental delays and behavioral disorders. This position contributes to early intervention, rehabilitation, and enhancing children’s overall quality of life through specialized pediatric physiotherapy within a multidisciplinary team.Job DescriptionWalnut Child Development Clinic, a leading pediatric rehabilitation chain in Pune, is hiring a full-time, permanent Clinical Physiotherapist for its Lohegaon center. The role involves working closely with a multidisciplinary team to deliver pediatric physiotherapy services for children with developmental and behavioral challenges. Immediate joiners willing to commit for a minimum of one year are preferred.Key Features of the Role• Position: Clinical Physiotherapist (Pediatric)• Organization: Walnut Child Development Clinic• Location: Lohegaon, Pune, Maharashtra (Tingre Nagar)• Employment Type: Full-Time, Permanent• Salary Range: ₹25,000 – ₹35,000 per month• Benefits: Paid leaves, Paid sick time, Annual bonus & incentives, Continuing education programsResponsibilities• Assess children with developmental delays and behavioral disorders• Develop individualized pediatric physiotherapy treatment plans• Deliver evidence-based physiotherapy interventions• Collaborate with multidisciplinary team members• Monitor progress and modify therapy plans accordingly• Educate parents and caregivers regarding home programs• Maintain clinical documentation and records• Participate in professional development and training programsRequired Qualification• Master’s Degree in Physiotherapy (MPT) – MandatoryEducational Requirement• MPT compulsoryImportant Requirements• Special interest in pediatric physiotherapy• Willingness to learn and grow professionally• Immediate joining preferred• Minimum one-year commitment required• Candidates preferably from Pune and nearby areas (NIBM, Fatima Nagar, Wanowrie, Undri, Pisoli, Mohammedwadi, Kondhwa, Katraj, Bibwewadi)Employment Options• Career growth in pediatric rehabilitation• Continuing education supportWhat We Offer• Competitive salary package• Paid time off and paid sick leave• Annual bonus and performance-based incentives• Continuing education programs• Opportunity to work in a reputed pediatric rehab chainExperience and Skills• Pediatric physiotherapy expertise• Strong assessment and treatment planning skills• Knowledge of developmental delay and behavioral disorders• Communication and caregiver counseling skills• Documentation and teamwork abilitiesSalary Insights• ₹25,000 – ₹35,000 per month• Additional annual bonus and incentives based on performanceCompany OverviewWalnut Child Development Clinic is a leading pediatric rehabilitation clinic chain in Pune specializing in developmental delay and behavioral disorder management. The clinic focuses on early intervention, multidisciplinary collaboration, and professional growth of therapists.FAQsWho can apply for this position?Candidates with a Master’s Degree in Physiotherapy (MPT) are eligible to apply.Is pediatric experience mandatory?While prior pediatric experience is preferred, candidates with strong clinical knowledge and willingness to learn may also apply.Is this a full-time role?Yes, this is a full-time permanent position.Is there any minimum commitment period?Yes, candidates are expected to commit for at least one year.What kind of patients will I be working with?Children with developmental delays and behavioral disorders.Are there any additional benefits?Yes, paid time off, paid sick leave, annual bonuses, incentives, and continuing education programs are provided.Is immediate joining required?Immediate joiners are preferred.Is location preference important?Yes, candidates from Pune and nearby areas are preferred.Application Tips• Highlight your MPT qualification clearly at the top of your resume.• Mention any pediatric internship or clinical exposure specifically.• Showcase experience in handling developmental delay or neuro cases.• Emphasize your communication skills with children and parents.• Include details about multidisciplinary teamwork experience.• Mention your willingness for a minimum one-year commitment.• Clearly state “Available for Immediate Joining” in your resume if applicable.

Why This Role MattersThe Clinical Safety Associate plays a crucial role in protecting patient health by ensuring the accurate collection, processing, and reporting of adverse event data from clinical trials and post-marketing sources. This position directly supports pharmacovigilance and Patient Safety Services (PSS) operations by managing expedited safety reports and maintaining regulatory compliance. Timely and accurate safety reporting is essential to meet global regulatory standards and to ensure that medicinal products remain safe for public use. By contributing to the end-to-end adverse event lifecycle, this role supports quality clinical research and strengthens trust between sponsors, regulatory authorities, and patients.Job DescriptionThe Clinical Safety Associate assists with overall Clinical Safety and PSS operations associated with pharmaceutical products. The role involves managing the entire adverse event process, including safety data collected from clinical trials and unsolicited post-marketing reports. The associate is responsible for processing expedited adverse events according to regulatory standards and submitting them to clients and regulatory authorities within agreed timelines. This position may function as part of a client project support team or operate as a standalone safety service provider. The role requires adherence to health, safety, and quality regulations as outlined in company policies and applicable legal frameworks.Key Features of the Role:• Involvement in clinical trial and post-marketing safety reporting• Hands-on exposure to adverse event lifecycle management• Opportunity to work with global regulatory authorities and ethics committees• Experience in MedDRA coding and narrative writing• Participation in Quality Management System (QMS) processes• Collaborative cross-functional working environment• Compliance-driven and timeline-sensitive operationsResponsibilities• Assist in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)• Maintain adverse event tracking systems and ensure accurate documentation• Set up and maintain project files and central documentation records• Report ESRs and PSRs to clients, regulatory authorities, ethics committees, and investigators within study timelines• Log all incoming Adverse Event (AE) and Serious Adverse Event (SAE) reports into departmental tracking systems• Perform accurate data entry of safety information into safety databases• Write detailed and medically accurate patient narratives• Code adverse events using MedDRA terminology where applicable• Assist in listedness assessment against approved product labeling• Generate follow-up queries for missing or inconsistent safety data in consultation with medical teams• Submit expedited SAE reports to clients, regulatory authorities, ethics committees, vendors, and partners within agreed timelines• Support peer and quality review of processed safety reports• Assist in reconciliation of safety databases• Maintain files related to country-specific adverse event reporting requirements• Work in compliance with Standard Operating Procedures (SOPs) and departmental Work Instructions (WIs)• Prepare safety study documentation for archiving at project completion• Coordinate internal and external meetings or teleconferences• Train and mentor PSS assistants or peers as required• Build and maintain strong professional relationships across functional units• Ensure compliance with regulatory requirements and project-specific safety plans• Take responsibility for data accuracy and quality• Provide administrative and operational support to PSS personnel• Perform additional duties as assignedRequired QualificationsCandidates should have an educational background in Life Sciences, Pharmacy, Nursing, Medical Sciences, or related disciplines. Equivalent industry experience may be considered in lieu of formal qualifications. Strong English communication skills (spoken and written) are mandatory, along with proficiency in the local language where applicable.Educational Requirements:• Non-degree qualification with 1–2 years of Safety or relevant industry experience, OR• Associate Degree with 6 months to 1 year of Safety or relevant experience, OR• Bachelor’s Degree (BS/BA) with 0–1 year of Safety or relevant experience, OR• Master’s Degree (MS/MA) with 0–6 months of Safety or relevant experience, OR• PharmD with 0–6 months of Safety experience• A one-year PharmD residency or fellowship may be considered as relevant experiencePreferred disciplines include Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related areas.Experience and Skills:• Experience in processing AE/SAE reports and working with safety databases is preferred• Familiarity with regulatory submissions and reporting timelines• Background in pharmaceutical, biotechnology, or CRO environments is advantageous• Strong attention to detail and commitment to data accuracy• Ability to prioritize tasks and manage multiple responsibilities simultaneously• Good logical reasoning and proofreading skills, especially for numerical data• Proficiency in MS Office and general computer applications• Strong written and verbal communication skills• Ability to work effectively in a team-oriented environment• Good keyboard and documentation management skills• Capability to operate standard office equipmentSalary InsightsThe compensation package is competitive and aligned with industry standards for entry-level to junior pharmacovigilance professionals. Salary may vary depending on qualifications, prior safety experience, technical expertise, and location. Additional benefits may include health coverage, performance incentives, and professional development opportunities.Company OverviewThe organization is a leading Contract Research Organization (CRO) specializing in clinical development and patient safety services. It provides comprehensive pharmacovigilance solutions, regulatory support, and clinical trial management to global pharmaceutical and biotechnology companies. With a strong commitment to regulatory compliance and quality standards, the company supports safe and efficient drug development across therapeutic areas.FAQsQ1. Is prior pharmacovigilance experience mandatory?Prior safety experience is preferred but not mandatory for candidates with relevant educational qualifications.Q2. What is Safety experience?Safety experience includes processing AE/SAE reports, narrative writing, database handling, and regulatory submission exposure.Q3. Is MedDRA knowledge required?Basic understanding of MedDRA coding is beneficial but may be developed during training.Q4. Is this role suitable for fresh graduates?Yes, candidates with 0–1 year of relevant experience may apply based on qualification criteria.Q5. What are the growth opportunities?Employees may progress to Senior Safety Associate, Drug Safety Officer, or Pharmacovigilance Specialist roles.Application Tips• Highlight experience in AE/SAE processing or clinical data management• Mention familiarity with safety databases and MedDRA terminology• Emphasize attention to detail and compliance awareness• Demonstrate understanding of regulatory timelines during interviews• Keep your resume structured, concise, and focused on relevant safety skills• Prepare examples showcasing teamwork and problem-solving abilities

Why This Role MattersThe Prosthodontist plays a critical role in restoring patients’ oral function, aesthetics, and confidence. At Clove Dental, this position ensures delivery of advanced prosthodontic care while maintaining global standards of hygiene, transparency, and clinical excellence.Job DescriptionClove Dental is hiring a Full-Time Prosthodontist for its clinics in Pune, Maharashtra (Aundh, Hinjewadi, Vishal Nagar zone). The role requires a skilled specialist with strong clinical expertise in prosthodontics and the ability to manage patients independently.Key Features of the Role• Position: Prosthodontist• Company: Clove Dental• Location: Aundh, Hinjewadi, Vishal Nagar – Pune, Maharashtra• Employment Type: Full-Time, Permanent• Salary: ₹40,000 – ₹55,000 per month• Work Setting: In-Clinic (On-site)• Experience: 2–3+ Years (Post-MDS)• Start: ImmediateResponsibilities• Diagnose and treat patients with missing or damaged teeth• Create comprehensive prosthodontic treatment plans• Design and fit crowns, bridges, dentures, and other dental prosthetics• Collaborate with dental technicians for functional and aesthetic outcomes• Educate patients on oral hygiene and maintenance• Maintain detailed patient records and clinical documentation• Stay updated with latest prosthodontic technologies and techniquesRequired Qualification• MDS – Prosthodontics• Valid State Dental LicenseEducational Requirement• Recognised MDS degree in ProsthodonticsImportant Requirements• Minimum 2–3+ years of clinical experience• Strong written and verbal communication skills• Comprehensive knowledge of dental procedures, tools, and diagnostics• Good management and patient-handling skills• Ability to maintain detailed clinical recordsEmployment Options• Full-Time• Permanent Role• In-person clinic-based positionWhat We Offer• Opportunity to work with India’s largest dental network• Structured clinical protocols and advanced equipment• Health insurance benefits• Professional growth and exposure to high patient volumeExperience and Skills• Practical experience in prosthetic restorations• Expertise in crowns, bridges, and dentures• Strong diagnostic capability• Effective communication skills• Clinic and patient management abilitySalary Insights• ₹40,000 – ₹55,000 per month• Salary may vary based on experience and expertiseCompany OverviewClove Dental is India’s largest dental clinic network, established in 2011, with 650+ clinics nationwide. The organization manages over 1 million patients per month and has conducted approximately 15 lakh treatments in the past decade. Equipped with state-of-the-art technology and strict hygiene protocols such as the Four-Step Sterilization Protocol, Clove Dental emphasizes trust, respect, integrity, and global standards of dental care.FAQsWho can apply?MDS Prosthodontics candidates with valid state license and 2–3+ years of experience.Is prior experience mandatory?Yes, a minimum of 2–3+ years post-MDS experience is required.What locations are available?Aundh, Hinjewadi, and Vishal Nagar in Pune, Maharashtra.Is this a full-time role?Yes, it is a full-time permanent in-clinic position.What benefits are provided?Health insurance is included.Application Tips• Highlight your MDS specialization clearly in your CV.• Mention the number and type of prosthetic cases handled.• Include details of advanced technologies or techniques used.• Emphasize patient communication and case documentation skills.• Keep your resume focused on prosthodontic expertise.

Why This Role MattersThe Senior Dentist plays a critical role in overseeing clinic operations while delivering high-quality dental care. This position ensures effective patient management, clinical excellence, and coordination among staff to maintain superior treatment standards.Job DescriptionClove Dental is hiring a Full-Time Senior Dentist for its clinics located in Tingre Bagar and Dhankawadi, Pune, Maharashtra. The role requires an experienced dental professional capable of managing daily operations, performing advanced dental procedures, and leading the clinical team.Key Features of the Role• Position: Senior Dentist• Company: Clove Dental• Location: Tingre Bagar & Dhankawadi, Pune, Maharashtra• Employment Type: Full-Time• Salary Range: ₹30,000 – ₹50,000 per month• Work Setting: Dental ClinicResponsibilities• Oversee daily clinic operations• Consult with patients to diagnose and treat dental concerns• Perform regular cleaning and preventive dental procedures• Develop treatment plans to improve oral hygiene• Order and interpret diagnostic measures such as X-rays and models• Use dental tools including drills, probes, brushes, and mirrors• Maintain detailed patient records and treatment documentation• Manage and coordinate with clinic staff for effective patient careRequired Qualification• BDS with minimum 3–4 years of experience OR• MDS with 1–2 years of experience• Valid State Dental LicenseExperience and Skills• Strong computer skills and experience with healthcare databases• Excellent written and verbal communication skills• Ability to maintain detailed clinical records• Comprehensive knowledge of dental procedures and diagnostics• Good management and leadership skillsImportant Remarks• Full-time position• Experience mandatory as per qualification criteria• Posting locations: Tingre Bagar & Dhankawadi – PuneSalary Insights• ₹30,000 – ₹50,000 per month• Salary based on experience and expertiseBenefits• Health InsuranceCompany OverviewClove Dental is a leading dental healthcare provider in India, known for its standardized clinical protocols, advanced dental technology, and patient-focused services across multiple locations.FAQsWhat is the employment type?• Full-TimeWhat is the salary range?• ₹30,000 – ₹50,000 per monthIs experience required?• Yes, as per qualification criteriaWhat qualification is required?• BDS (3–4 years experience) or MDS (1–2 years experience)Where is the clinic located?• Tingre Bagar & Dhankawadi, Pune, MaharashtraApplication Tips• Highlight clinical leadership or management experience• Mention experience with dental software and databases• Include Dental Council license details• Emphasize diagnostic and treatment planning expertise

Why This Role MattersThe Associate Dentist supports the delivery of quality dental care in a well-established clinical setup. This role contributes to patient treatment, maintains professional standards, and ensures smooth functioning of dental services during assigned slots.Job DescriptionApollo Clinic is hiring a Part-Time Associate Dentist for its reputed and running dental setup in Viman Nagar, Pune, Maharashtra. The role is ideal for a qualified dentist seeking evening clinical practice opportunities in an established clinic environment.Key Features of the Role• Position: Associate Dentist• Company: Apollo Clinic• Location: Viman Nagar, Pune, Maharashtra• Employment Type: Part-Time• Salary Range: ₹11,847.97 – ₹35,663.65 per month• Work Setting: Dental Clinic• Shift Availability: Evening Slot (Two slots available)Responsibilities• Provide general dental consultation and treatment• Diagnose dental conditions and plan appropriate treatments• Perform routine dental procedures• Maintain patient records and documentation• Follow hygiene and sterilization protocols• Ensure smooth functioning of the dental clinic during assigned hoursRequired Qualification• BDS (Bachelor of Dental Surgery)• Valid State Dental Council RegistrationExperience and Skills• Experience preferred• Strong clinical and diagnostic skills• Good patient-handling and communication skills• Ability to work independently in assigned slotsImportant Remarks• Part-time position• Evening slots available (Two openings)• Salary depends on experience• Immediate resume submission requiredSalary Insights• ₹11,847.97 – ₹35,663.65 per month• Final salary based on experience and clinical expertiseCompany OverviewApollo Clinic is a reputed healthcare provider offering comprehensive medical and dental services, known for its established clinical setup and patient-centered care in Pune.FAQsWhat is the employment type?• Part-TimeWhat is the salary range?• ₹11,847.97 – ₹35,663.65 per monthIs experience required?• PreferredWhat qualification is required?• BDS with valid Dental Council RegistrationWhere is the clinic located?• Viman Nagar, Pune, MaharashtraApplication Tips• Highlight clinical experience and independent practice ability• Mention Dental Council registration details• Specify availability for evening slots• Attach updated resume with relevant experience