Ahmedabad Healthcare Jobs

Role & Responsibilities • Lead regulatory submissions and ensure compliance with local and international regulations • Prepare and review regulatory dossiers and submissions for product approvals • Communicate with regulatory agencies to resolve issues related to product submissions • Support the regulatory strategy for new product development • Monitor changes in regulations and provide guidance to internal teams Qualification: Degree in Life Sciences / PharmacyExperience: 2-3 years Skills • Strong knowledge of regulatory affairs and submission processes • Experience in product registrations and renewals • Proficient in using regulatory tools and software • Strong communication skills in English & Hindi • Ability to manage multiple projects and priorities About The Company • The company is expanding its regulatory affairs team to support business growth. The company provides a collaborative environment and opportunities for career advancement. With a focus on compliance and business development, the company serves clients across various sectors.

Role & Responsibilities • Assist in the preparation and submission of regulatory documents • Monitor and ensure compliance with regulatory requirements • Support the regulatory team in product registrations and renewals • Maintain communication with regulatory agencies and stakeholders • Assist in compiling and reviewing technical documentation Qualification: Relevant degree in Life Sciences / PharmacyExperience: Freshers Skills • Basic computer skills • Strong communication skills in English & Hindi • Attention to detail and organizational skills • Willingness to learn and adapt to regulatory practices About The Company • A growing team dedicated to regulatory affairs and business development. A dynamic environment focused on delivering quality services and ensuring compliance. The company values innovation, collaboration, and growth within the life sciences industry.

Roles & Responsibilities:• Diagnose and treat a variety of dental conditions• Perform preventive and restorative dental procedures• Educate patients on proper oral hygiene and care practices• Maintain accurate patient records and treatment documentation• Manage dental emergencies efficiently and professionally• Collaborate with the dental team to ensure high-quality patient care• Stay updated with advancements in dental treatments, techniques, and technologies• Adhere to hygiene, safety, and clinic protocols consistentlyQualification:• Bachelor’s degree in Dental Surgery (BDS) or equivalent dental qualification• Valid license to practice dentistryExperience:• Relevant clinical experience as a General Dentist preferredSkills:• Preventive and restorative dentistry procedures• Diagnostic and treatment planning skills• Patient communication and interpersonal skills• Knowledge of dental instruments, tools, and modern techniques• Attention to detail and hygiene standards• Teamwork, time management, and problem-solving skills• Professional and patient-focused approachAbout the Company:Smile Return Dental Clinic in Ahmedabad, Gujarat, is a patient-centered dental practice committed to delivering high-quality dental care. The clinic emphasizes modern dental technologies, professional ethics, and comprehensive treatment approaches to ensure optimal oral health and patient satisfaction.

Roles & Responsibilities• Assess patients with physical challenges and plan appropriate physiotherapy treatment programs• Facilitate and deliver physiotherapy treatments to support patient recovery and rehabilitation• Monitor patient progress and modify therapy plans as required• Maintain accurate patient records and treatment documentation• Build and maintain strong rapport with patients and caregivers• Work collaboratively with doctors, nurses, and healthcare staff• Ensure quality patient care through adherence to clinical protocols• Support administrative and reporting requirements related to patient careQualifications• Master’s degree in Physiotherapy (MPT – Cardio) from a recognized institution• Strong knowledge of physiotherapy, anatomy, physiology, and medical terminologyExperience• 1 – 5 years of experience as a Physiotherapist in a hospital or clinical settingSkills• Excellent interpersonal and communication skills• Ability to build trust and rapport with patients• Strong teamwork and collaboration skills• Good administrative and documentation abilities• Patience, tolerance, and a compassionate approach to patient care• Good physical health and fitnessAbout the CompanyPhysiocares – RRT, located in Nikol, Ahmedabad, Gujarat, is a healthcare facility providing comprehensive physiotherapy and rehabilitation services. The organization is committed to high-quality patient care, professional standards, and effective rehabilitation outcomes through skilled clinical practice.

Roles & Responsibilities• Oversee and manage day-to-day clinic operations• Examine patients to diagnose oral health conditions and treatment needs• Perform preventive, restorative, and specialized dental procedures as per expertise• Discuss dental concerns with patients and educate them on oral hygiene practices• Order and interpret diagnostic measures such as X-rays, models, and reports• Use dental instruments and equipment to examine, diagnose, and treat patients• Maintain accurate patient records, treatment plans, and clinical documentation• Ensure adherence to clinical protocols, hygiene, and safety standards• Coordinate and communicate effectively with other dentists, assistants, and staff• Supervise junior dentists and support team performance and quality care deliveryQualifications• BDS / MDS from a recognized dental institution• Valid State Dental Council registrationExperience• BDS with minimum 4+ years of clinical experience• MDS with minimum 1+ year of clinical experienceSkills Required• Strong knowledge of dental procedures, tools, and diagnostics• Excellent patient communication and interpersonal skills• Good computer skills with experience in healthcare databases and applications• Ability to maintain detailed clinical records and documentation• Strong leadership and clinic management skills• Commitment to ethical dental practice and quality patient careAbout the CompanyClove Dental is India’s largest network of dental clinics, established in 2011 with a mission to deliver global standards of dentistry across every neighborhood. With 650+ clinics, 1500+ dentists, and over 1 million patients served every month, Clove Dental is known for its state-of-the-art technology, strict hygiene and safety protocols, transparency, and ethical practices. Built on core values of trust, respect, and integrity, Clove Dental continues to set benchmarks in clinical excellence and patient-centric care across India.

Roles & Responsibilities• Oversee daily clinical operations and ensure smooth functioning of the dental clinic• Examine patients to assess oral health conditions and diagnose dental issues• Discuss treatment plans with patients and provide preventive, restorative, and corrective dental care• Perform dental procedures such as cleanings, fillings, root canals, extractions, and other specialty treatments as per expertise• Order and interpret diagnostic tests including X-rays, scans, and dental models• Maintain accurate and detailed patient medical and treatment records• Ensure adherence to hygiene, sterilization, and safety protocols• Supervise, guide, and coordinate with junior dentists and clinical staff• Deliver high standards of patient care, ethics, and professionalismQualifications• BDS or MDS from a recognized institution• Valid State Dental Council registrationExperience• BDS: Minimum 4+ years of clinical experience• MDS: Minimum 1+ year of clinical experienceSkills Required• Strong clinical knowledge of dental procedures, tools, and diagnostics• Proficiency in computer systems and healthcare databases• Excellent written and verbal communication skills• Good patient-handling and interpersonal skills• Strong management and leadership abilities• Ability to maintain detailed clinical documentationAbout the CompanyClove Dental is India’s largest network of dental clinics, established in 2011 with a mission to deliver global standards of dentistry across every neighborhood in the country. With 650+ clinics and a team of over 1500 dentists, Clove Dental treats more than 1 million patients every month and has completed over 15 lakh treatments in the last decade.

Role & Responsibilities • Serve as a key representative of the Medical Affairs function, providing scientific and clinical expertise on Bioscan Research's technologies and innovations • Communicate complex medical and scientific information to healthcare professionals (HCPs) in a clear, accurate, and compliant manner • Establish and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the field of traumatic brain injury • Collaborate with cross-functional teams to support clinical development, regulatory activities, and marketing efforts • Provide training and support to internal teams on the scientific and clinical aspects of the company's products • Monitor and report on trends in the field of traumatic brain injury and related medical advancements Qualification • Advanced degree in a relevant scientific or medical field (MD, PhD, or equivalent) Experience • Prior experience as a Medical Science Liaison or similar role in the pharmaceutical, biotechnology, or medical device industry • Experience in communicating scientific data to healthcare professionals • Knowledge in the area of traumatic brain injury or related fields Skills • Strong scientific and clinical knowledge, particularly in traumatic brain injury and neurotechnology • Excellent communication and interpersonal skills to engage with HCPs and KOLs • Ability to present complex scientific concepts in a clear and compliant manner • Strong problem-solving and critical thinking skills • Ability to work independently and collaboratively in a cross-functional environment About The Company • Bioscan Research – A company dedicated to improving traumatic brain injury patient outcomes through innovative technologies, including the machine learning-powered NIRS device, CEREBO, which aims to advance clinical understanding and treatment strategies for brain injury.

Roles & Responsibilities: • Perform medical assessments of client’s product ranges and evaluate adverse events • Conduct medical reviews of aggregate reports and prepare clinical expert statements • Detect signals for client’s medicinal products and manage risk management plans • Provide guidance and participate in follow-up of adverse events, offering backup medical support • Interact with staff at various levels to resolve issues during reviews • Contribute to enhancing pharmacovigilance processes and writing SOPs • Ensure compliance with local regulations and global pharmacovigilance requirements • Assist in developing SOPs for the department and clients, and communicate with clients and regulatory agencies if needed Qualifications: • Relevant degree in Life Sciences, Pharmacy, or related field Experience: • 0–1 year in pharmacovigilance or related field Skills: • Knowledge of local and national pharmacovigilance requirements • Strong communication and client interaction skills • Ability to work effectively with staff at various levels and functional areas • Marketing, business generation, direct sales, and client servicing skills About the Organization: This organization is a dynamic employment and recruitment services firm providing specialized healthcare and pharmacovigilance staffing solutions. They focus on regulatory compliance, quality processes, and client satisfaction while fostering a collaborative environment for professional growth.

Roles & Responsibilities: • Perform routine and advanced quality control analysis of raw materials, in-process samples, and finished products. • Conduct stability studies in accordance with ICH guidelines. • Ensure strict compliance with GLP, GMP, and data integrity requirements. • Maintain accurate analytical documentation, laboratory records, and reports. • Support internal and external regulatory audits and inspections. • Operate and handle QC laboratory instruments and analytical techniques. Qualification: • B.Sc / M.Sc / B.Pharm / M.Pharm Experience: • 1–3 years of Quality Control experience in a regulated pharmaceutical industry. Skills: • Hands-on exposure to QC analysis and stability testing. • Strong understanding of GLP practices and GMP compliance. • Knowledge of regulatory guidelines (USFDA / WHO-GMP preferred). • Good documentation and data integrity awareness. • Ability to work in a regulated, audit-driven environment. About the Organisation: Emcure Pharmaceuticals Ltd. is a leading Indian pharmaceutical company with a strong presence in regulated markets, known for its focus on quality, compliance, and innovation, offering stable career growth and exposure to global regulatory standards. Email your application to:bhavik.parekh@emcure.com

Roles & Responsibilities: Quality Control: • Perform routine QC testing of raw materials, in-process samples, and finished products. • Conduct analytical testing as per approved specifications and SOPs. • Maintain accurate documentation, test records, and data integrity. • Support stability studies and sample management activities. • Follow GMP, GLP, and safety guidelines strictly. • Assist during audits, inspections, and compliance activities. Formulation Production: • Assist in formulation manufacturing operations as per Batch Manufacturing Records (BMR). • Support granulation, blending, compression, coating, and packing activities. • Ensure adherence to GMP guidelines and production SOPs. • Maintain production records, logbooks, and documentation accurately. • Follow safety procedures and work in shift-based operations. • Support equipment cleaning, area maintenance, and production readiness. Qualification: • Quality Control: M.Sc. (Analytical Chemistry) / B.Pharm / M.Pharm • Formulation Production: D.Pharm / ITI / Diploma (relevant discipline) Experience: • Fresher only (Pass-out candidates).Walk-in Interview Details: • Date: 31-01-2026 (Saturday) • Venue: Ahmedabad Management Association (AMA), ATIRA Campus, Dr. Vikram Sarabhai Marg, Near Panjrapol Cross Roads, Ahmedabad – 401506 • Candidates should carry updated CV, relevant education documents, Aadhaar card, and recent photographs. • Smart phone required for online registration and assessment.About the Organisation: Macleods Pharmaceuticals is one of India’s fastest-growing pharmaceutical companies with a strong presence across multiple therapeutic segments, ranked among the top pharma companies, and committed to excellence in quality, innovation, and manufacturing through its world-class facilities and Centre of Excellence training programs.

Roles & Responsibilities:• Assist patients in rehabilitation programs under the guidance of Occupational Therapists• Provide hands-on patient care and support therapeutic exercises and interventions• Aid in developing and implementing individualized therapy plans• Support home care services as part of patient recovery programs• Monitor patient progress and report to the supervising OT• Collaborate with occupational therapists and multidisciplinary healthcare teams• Maintain accurate patient records and documentation• Ensure adherence to clinical protocols, safety, and hygiene standardsQualifications:• Bachelor’s degree or diploma in Occupational Therapy or a related field• Knowledge of occupational therapy techniques and rehabilitation practicesExperience:• Experience in rehabilitation and patient care preferred• Experience in developing therapy programs and providing home care services is an advantageSkills Required:• Strong interpersonal and communication skills for effective collaboration• Ability to assist in implementing therapy programs• Compassionate, patient-centered approach• Professional, proactive, and detail-orientedAbout the Company:Kaizen Hospital, established in Ahmedabad, Gujarat in 2011, is a leading gastroenterology superspecialty hospital in India. The hospital specializes in GI diseases and GI cancers, leveraging advanced medical technology, research, and best practices. With multiple OPD centers and specialty clinics across Gujarat and Rajasthan, Kaizen Hospital is committed to delivering high-quality, patient-centric care led by a multidisciplinary team and state-of-the-art infrastructure.

Roles & Responsibilities: • Compound and dispense medications as prescribed by physicians. • Monitor customers’ drug therapies, advise interventions, and inform about potential side effects. • Instruct customers on proper use and timing of prescribed medications. • Conduct health and wellness screenings. • Provide immunizations and basic medical services (blood pressure, temperature, blood sugar checks). • Maintain accurate customer records. • Ensure a safe, clean, and compliant pharmacy environment. • Complete operational pharmacy requirements, including verifying orders, maintaining controlled substance records, and removing expired/damaged drugs. • Adhere to legal and regulatory requirements governing pharmacy practice. • Perform other administrative tasks as needed. Qualification: • Bachelor’s degree in Pharmacy or Pharmacology. • Valid State Pharmacy Registration License (mandatory). Experience: • Minimum 1 year of work experience as a pharmacist. Skills: • Detailed understanding of dosages, chemical compounds, and pharmaceutical brands. • Proficient in Microsoft Office Suite and pharmacy software (e.g., MEDITECH, Mediware). • Excellent organizational, verbal, and written communication skills. • Ability to work independently and provide patient-centered care. About the Organisation:Indira IVF Hospital Pvt Ltd is committed to delivering high-quality pharmaceutical care and ensuring patient safety. With a focus on compliance, customer service, and professional development, the organisation provides pharmacists a structured environment to grow their skills, serve the community, and advance their careers.

Roles & Responsibilities: • Operate advanced analytical instruments such as HPLC, GC, ICP-MS for testing raw materials, finished products, and dosage forms. • Perform method development, validation, and transfer for assays, related compounds, dissolution, and residual solvents. • Prepare method development reports, study protocols, TT reports, and COA for development samples. • Conduct stability analysis as per protocols and maintain accurate documentation in compliance with GLP and GDP. • Participate in investigations, support continuous lab development through training, and adhere to SOPs. • Manage laboratory inventory, raise procurement requests, and attend technical workshops to explore new techniques. Qualification: • Master’s degree in Science (MS/M.Sc) or M. Pharma preferred. Experience: • 5–7 years of experience in analytical method development, validation, and laboratory operations. Skills: • Good Laboratory Practices (GLP), Data Integrity, and Compliance – Advanced. • Analytical Method Development & Validation – Intermediate. • Documentation & Data Review, Interpretation, and Statistical Analysis – Intermediate. • Stability Study Management – Advanced. • Electronic Lab Notebook (ELN)/LIMS Management – Advanced. • Adapts to organizational growth – Intermediate. About the Organisation: Amneal Pharmaceuticals is a global pharmaceutical company committed to innovation, quality, and compliance, delivering high-quality medicines while fostering a diverse and inclusive workplace.

Roles & Responsibilities: • Deliver high-quality, patient-centric healthcare services in line with Apollo Hospitals’ clinical and ethical standards • Collaborate with multidisciplinary medical teams to ensure effective diagnosis, treatment, and patient care • Utilize advanced medical technologies and hospital infrastructure to support accurate and timely healthcare delivery • Maintain patient safety, confidentiality, and compliance with hospital protocols and regulatory guidelines • Participate in continuous learning, quality improvement, and innovation initiatives • Support preventive healthcare, wellness programs, and community outreach activities Qualification: • Relevant educational qualifications as per the specific clinical or healthcare role • Certification and professional registration as applicable Skills: • Strong patient-care orientation and ethical medical practice • Effective communication and teamwork abilities • Adaptability to advanced healthcare technologies and systems • Commitment to continuous learning and quality improvement • Compassion, integrity, and professionalism About the Organisation: Apollo Hospitals is one of India’s most trusted and established healthcare providers, known for its state-of-the-art medical facilities, advanced technology, and highly skilled healthcare professionals. With a strong focus on patient-centric care, innovation, research, and social responsibility, Apollo Hospitals delivers comprehensive healthcare services across multiple specialties while promoting preventive care, wellness, and community health initiatives.

Roles & Responsibilities: • Manage and develop existing and new key accounts and government business at zonal level for IVD instruments and reagents • Drive sales growth, forecasting monthly and annual targets with profitability accountability • Handle key account management, customer relationship management, satisfaction, and retention • Analyze key account performance and market share, prepare corrective action plans • Align with zonal teams and cascade business strategies for growth • Generate leads, negotiate, and successfully close deals • Coordinate with customers and internal teams for timely delivery and payment collection • Conduct periodic reviews with government and key institutional customers • Execute innovative promotional activities, roadshows, CMEs, and product demonstrations • Monitor market trends, competition, and submit regular reports, DCRs, and MIS on TAB • Ensure compliance with company systems, processes, and ethical sales practices Qualification: • BE / B.Tech / B.Sc / M.Sc / B.Pharm / Diploma Experience Required: • 2–5 years of Key Account and Government Business experience in the IVD industry Skills: • Key account & govt. business handling • Strategic sales planning & forecasting • Negotiation & relationship management • Market analysis & reporting • Strong communication and leadership skills About the Organization: Erba Transasia is a leading in-vitro diagnostics company offering comprehensive diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics, with a strong presence in India and global markets.

Roles & Responsibilities: • Promote assigned IVD (in-vitro diagnostics) products to customers at defined frequencies. • Generate leads and convert opportunities into sales. • Coordinate with customers, credit control, and internal teams for timely and outstanding payment collections. • Build and maintain strong relationships with customers and distributors. • Ensure compliance with company systems, policies, and sales processes. • Negotiate effectively and close sales deals successfully. • Ensure timely and accurate delivery of products to customers. • Monitor market trends, competitor activities, and product performance and report insights to management. • Prepare daily call reports, update attendance, capture product complaints, and record opportunities using the TAB system. • Submit Field Expense Statements (FES) within stipulated timelines. • Support roadshows, CMEs, and product demonstrations. • Continuously update technical knowledge and selling skills. Qualification: • B.Sc / B.Pharm / B.Tech / B.E / Diploma. Experience: • Minimum 2 years of experience in IVD Government Sales. Skills: • Strong sales, negotiation, and relationship-building skills. • Good understanding of IVD products and government sales processes. • Ability to coordinate with multiple stakeholders and internal teams. • Strong communication, reporting, and documentation skills. • Willingness to travel extensively within the assigned territory. About the Organization: Erba Transasia is a leading diagnostics company with a strong presence in India and global markets, offering a comprehensive range of in-vitro diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics. Known for innovation, quality, and customer-centric solutions, Erba Transasia supports healthcare providers with reliable diagnostic technologies.

Roles & Responsibilities: Analytical Development Laboratory (ADL): • Perform routine analysis and analytical method development for solid orals, injectables, semi-solids, liquids, oral liquids, and APIs. • Execute analytical method validation, verification, and transfer including protocol and report preparation. • Independently handle HPLC, UV Spectrophotometer, and dissolution apparatus for assay, content uniformity, blend uniformity, dissolution, and related substances testing. Formulation & Development (F&D): • Develop formulations for solids, semi-solids, injectables, and oral liquids. • Conduct product development, stability studies, and scale-up activities in a GMP environment. • Support technology transfer and process optimization. Packaging Development: • Perform packaging material selection, development, and testing for pharmaceutical products. • Ensure packaging compliance with regulatory requirements for different dosage forms. • Support stability, compatibility, and packaging validation activities. Qualification: • ADL: M.Sc / B.Pharm / M.Pharm • F&D: M.Pharm • Packaging Development: B.Pharm / M.Pharm (Diploma/Certification preferred) Experience: • For ADL: 2–12 years • For F&D: 3–10 years • For Packaging Development: 3–10 years Skills: • Strong knowledge of GMP, analytical techniques, and pharmaceutical development processes. • Hands-on experience in formulation, analytical validation, or packaging development. • Good documentation, compliance, and cross-functional coordination skills.Walk-In Interview Details: Date: 1st February 2026 (Sunday) Time: 9:00 AM – 3:00 PM Venue: LINCOLN HOUSE, Behind Satyam Complex, Science City Road, Sola, Ahmedabad – 380060, Gujarat Documents to Carry: • Updated resume • Educational certificates • Experience letters • Relevant supporting documents About the Organization: Lincoln Pharmaceuticals Ltd is a WHO-GMP and ISO-certified pharmaceutical company based in Ahmedabad, focused on delivering affordable and innovative healthcare solutions with a strong presence across domestic and international markets.

Roles & Responsibilities • Perform wet chemistry sample extraction as per study protocols and SOPs • Handle centrifugation, evaporation, freezing, storage, and aliquoting of biological samples • Prepare reagents, solvents, mobile phases, calibration standards, and QC samples • Support method development and validation of drugs and metabolites using LC/MS/MS • Execute validation parameters including accuracy, precision, recovery, matrix effect, and stability studies • Carry out routine bioanalysis for bioequivalence and subject sample analysis • Operate and maintain LC/MS/MS, HPLC, and ICP-OES instruments • Perform system suitability checks, troubleshooting, and basic instrument maintenance • Complete analytical worksheets, QC sheets, raw data records, and logbooks accurately • Ensure compliance with GLP, SOPs, and regulated bioanalytical guidelines • Support audits, inspections, and mandatory training activities Qualification • M.Pharm / M.Sc / MS (Science) – Any Specialization Experience • Hands-on exposure to LC/MS/MS bioanalysis preferred • Experience with biological matrices such as plasma, serum, and urine is an advantage • Regulated bioanalytical lab exposure is desirable (not mandatory) Skills • LC/MS/MS operation and troubleshooting • Wet chemistry and bioanalytical workflows • Bioanalytical method development and validation • GLP compliance and documentation practices • Data integrity and basic MS Office skills About the Organisation Cliantha Research is a leading global Contract Research Organization (CRO) providing integrated clinical research, bioanalytical, and regulatory services. The organization is known for its strong compliance culture, advanced analytical capabilities, and commitment to quality-driven clinical research.

Roles & Responsibilities • Plan and conduct clinical trial audits in compliance with ICH-GCP, regulatory guidelines, and internal SOPs • Review and maintain Quality Management Systems (QMS) documentation and processes • Lead CSV validation and qualification activities related to clinical systems • Ensure audit and inspection readiness for sponsor, regulatory, and internal audits • Manage sponsor interactions and audit responses effectively • Identify compliance gaps and drive CAPA implementation • Lead and mentor QA audit teams to meet project timelines • Monitor audit timelines and ensure timely closure of audit findings • Support continuous quality improvement initiatives across clinical operations Qualification • M.Sc / B.Pharm / M.Pharm / Other relevant life science qualifications Experience • 10 – 15 years of experience in Clinical QA, auditing, and compliance Skills • Regulatory guidelines and compliance requirements • Clinical QMS and auditing practices • CSV validation and qualification • Audit and inspection readiness • Team leadership and timeline management • Sponsor handling and communication About the Organisation Cliantha Research is a globally recognized clinical research organization providing integrated clinical, bioanalytical, and regulatory services. The company is known for its strong quality culture, regulatory expertise, and commitment to delivering compliant and reliable clinical research solutions.