Ahmedabad Healthcare Jobs

Roles & Responsibilities:• Regulatory query management and responses• Scientific and technical justification preparation• Compliance and regulatory documentation• Cross-functional coordination with internal teams• CAPA handling and continuous improvement activities• Maintaining confidentiality and ethical standardsQualification:• M.Pharm in Regulatory AffairsExperience:• 3 to 5 years in Regulatory Affairs (Pharma)Skills:• Expertise in regulatory query management• Strong scientific and technical writing skills• Familiarity with compliance and regulatory documentation• Ability to work cross-functionally• Strong attention to detail and confidentialityAbout the Company:Accuprec Research Labs Pvt. Ltd. is a leading contract research organization (CRO) dedicated to providing regulatory, clinical research, and pharmaceutical solutions to the global healthcare market. Based in Ahmedabad, Gujarat, the company specializes in regulatory affairs and aims to ensure compliance with all relevant standards and regulations.

Roles & Responsibilities:• eCRF development, testing, and maintenance• Clinical data validation and query management• Preparation of CDM documentation (DMP, DVP, eCCG)• Data reconciliation activities and user training• Medical coding using standard dictionaries• Handling EDC systems and related tools (IWRS, ePRO)• Supporting end-to-end clinical data management activitiesQualification:• M.Pharm (Pharmacology / Quality Assurance)• BDS / BAMS / BHMSExperience:• Site-level experience as a Clinical Research Coordinator (CRC)• Hands-on experience in late-phase clinical trials• Working knowledge of EDC systems and CDM processes• Exposure to IWRS, ePRO, and clinical data toolsSkills:• Strong knowledge of clinical data management processes• Proficiency in handling eCRFs, IWRS, and ePRO systems• Expertise in medical coding using standard dictionaries• Strong analytical and problem-solving skills• Excellent communication and training skillsAbout The Company:Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad. Lambda operates across India, USA, Canada, UK, Spain, and Poland, offering clinical research services with a focus on late-phase clinical trials. With competitive compensation and global exposure, Lambda provides a structured career growth path in the clinical research industry.

Roles & Responsibilities:• Perform dental examinations and diagnose dental conditions• Develop treatment plans and provide appropriate dental care• Conduct dental procedures including fillings, crowns, bridges, root canals, and extractions• Educate patients on oral health, hygiene, and preventative care• Maintain detailed and accurate patient records• Work closely with other dental professionals to ensure high-quality patient care• Follow patient hygiene and safety protocolsQualifications:• Bachelor’s degree in Dentistry (BDS) or equivalent qualification; MDS is a plus• Valid dental license to practice in India• Experience in dental examinations, diagnostics, and treatment planning• Proficiency in using modern dental instruments and technology• Strong communication skills and ability to collaborate with dental professionalsExperience:• Not specifiedSkills:• Clinical expertise in performing a variety of dental procedures• Patient education and communication• Treatment planning and diagnostics• Teamwork and collaboration• Commitment to hygiene and safety standardsAbout the Company:Smile Care Dental Studio is one of the country’s most advanced dental clinics, offering top-notch treatment with state-of-the-art instruments while prioritizing patient hygiene and safety. The clinic provides consultations and treatments for a wide range of dental issues, including cosmetic dentistry, ensuring a comfortable and pleasant patient experience.

Roles & Responsibilities:• Lead integrated, multi-modality drug discovery programs across chemistry disciplines• Solve complex synthesis and route-design challenges using advanced analytical approaches• Apply modern discovery platforms including ELNs, cheminformatics, and digital workflows• Collaborate closely with Biology, ADME/DMPK, and platform science teams for integrated delivery• Mentor and guide scientists to global standards of quality and scientific rigor• Build, manage, and represent o2h Discovery partnerships with global biotech and pharma clientsQualification:• Ph.D. / Postdoctoral training from a leading international university (US / UK / EU preferred)Experience:• 5–20 years of industrial experience in small-molecule drug discoverySkills:• Strong expertise in medicinal and synthetic chemistry with advanced problem-solving skills• Experience with advanced modalities (ADCs, peptides, covalent inhibitors, TPD)• Hands-on knowledge of modern productivity tools (HTE, flow chemistry)• Proficiency in digital chemistry platforms and data-driven discovery• Excellent scientific communication, leadership, and mentoring abilitiesAbout the Organization:o2h Discovery is a global co-discovery partner with integrated discovery platforms in the UK and India, enabling biotech and pharma clients to accelerate pre-clinical drug discovery through innovation and scientific excellence.

Roles and responsibilities:• Design and implement personalized rehabilitation programs for patients• Conduct biomechanics and functional assessments for neurological and orthopedic conditions• Monitor patient progress and modify treatments as needed• Educate patients and caregivers on exercises, injury prevention, and rehabilitation strategies• Collaborate with multidisciplinary healthcare team members• Maintain accurate patient records and documentation• Conduct comprehensive assessments of patients’ biomechanics, gait, and human performance• Use advanced assessment tools and motion analysis systems to evaluate patient conditions• Perform muscle assessments to identify weaknesses or imbalances• Stay updated with the latest physiotherapy practices and techniques• Apply AI/ML and data-driven approaches to optimize rehabilitation outcomesQualification:• Bachelor’s or Master’s degree in Physiotherapy or relevant field• Valid physiotherapy license/certification• Proficiency in neuro and orthopedic rehabilitation or sports physiotherapy• Familiarity with biomechanics, gait analysis, and human performance assessmentExperience:• Experience in neuro and orthopedic rehab or sports physiotherapy preferred• Freshers with strong clinical training may also be consideredSkills:• Strong communication and interpersonal skills for patient interaction and collaboration• Ability to work independently in a part-time consulting role• Competence in advanced technologies for motion capture and analysis• Analytical skills for interpreting gait and biomechanics data• Commitment to continuous learning and staying updated with industry trendsBenefits:• Flexible part-time work schedule• Opportunity to work with cutting-edge technology in motion analysis and rehabilitation• Exposure to a deep-tech, data-driven healthcare environmentWorking hours:• Part-time; 3–5 hours daily (flexible), may require on-site visits to clinics or rehab centersAbout the company:SynerSense® integrates sports, health & wellness, biomechanics, AI/ML, and data science to deliver advanced, data-driven human performance and rehabilitation solutions. The company leverages motion capture technology, digital human movement analysis, and edge computing platforms to provide precise assessment and rehabilitation services anywhere, across clinical, sports, and industrial settings.

Roles & Responsibilities:• Diagnose and treat dental conditions using appropriate treatment plans• Conduct routine dental checkups and provide preventive care• Perform preventive, restorative, and cosmetic dental procedures• Advise patients on oral hygiene and overall dental health• Collaborate with the dental team to deliver high-quality patient care• Utilize modern dental equipment and techniques effectively• Maintain accurate and updated patient recordsQualifications:• Bachelor of Dental Surgery (BDS), DDS, or equivalent dental degree• Valid dental license to practiceExperience:• Relevant clinical experience in general dentistry preferredSkills:• Proficiency in general dentistry techniques, diagnosis, and treatment planning• Strong communication and interpersonal skills• Good organizational and time-management abilities• Knowledge of dental technology and equipment• Patient-focused approach with high professional standards• Commitment to continuous learning and professional developmentAbout the Company:All Smiles Dental Club (ASDC) is a modern dental practice committed to delivering high-quality oral healthcare services. The clinic focuses on advanced treatment techniques, state-of-the-art equipment, and a collaborative environment to ensure excellent patient outcomes.

Roles & Responsibilities• Prepare, review, and coordinate regulatory documentation and artwork components• Ensure artwork and labeling compliance with EU, US, and ROW regulatory requirements• Support regulatory submissions in line with applicable guidelines and standards• Collaborate with cross-functional teams to meet project timelines and deliverables• Maintain accurate regulatory records, version control, and documentation archives• Provide regulatory support for pharmaceutical and healthcare productsQualification• Bachelor’s degree in Pharmacy / Life Sciences or related disciplineExperience• Experience in regulatory documentation and submissions preferredSkills• Knowledge of global regulatory compliance requirements (EU / US / ROW)• Strong analytical and organizational skills• Excellent written and verbal communication skills in English• High attention to detail and ability to manage multiple projects• Ability to work effectively in a team-oriented environmentAbout the OrganizationNeocubes Pharma LLP (Neoplus Translation & Neocubes Pharma) – A regulatory-focused organization delivering high-quality regulatory affairs, pharmacovigilance, and safety monitoring services for EU, US, and ROW markets, offering strong learning and growth opportunities in regulatory documentation and artwork compliance.

Roles & Responsibilities:• Assess, plan, and implement physiotherapy treatment programs for patients• Assist in rehabilitation and recovery of patients with physical difficulties caused by illness, injury, or disability• Educate patients and caregivers on exercises, posture correction, and lifestyle modifications• Collaborate with doctors and the healthcare team for effective patient care• Maintain accurate records of patient assessments, progress, and outcomes• Ensure a safe, hygienic, and professional treatment environmentNumber of Vacancies: 3Qualifications:• Bachelor of Physiotherapy (BPT) or Master of Physiotherapy (MPT)Experience:• Fresher to 1 year of clinical experienceSkills Required:• Strong knowledge of physiotherapy techniques and treatment modalities• Good communication and interpersonal skills• Empathy with a patient-focused approach• Ability to work independently and within a healthcare team• Willingness to learn and adapt to clinical requirementsAbout the Company:Eraya Healthcare is a patient-focused healthcare provider committed to delivering quality physiotherapy and rehabilitation services. The organization emphasizes professional care, collaborative treatment approaches, and positive patient outcomes within a supportive clinical environment.

Roles & Responsibilities:• Assess clients and guide them through safe and effective wellness programs• Design basic exercise plans, mobility drills, and posture routines• Work closely with senior physiotherapists, nutritionists, and fitness coaches• Track client progress and maintain motivation throughout rehabilitation• Support preventive care and lifestyle transformation initiativesQualifications:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT)Experience:• Freshers welcome• Candidates with less than 2 years of experience may applySkills Required:• Good communication and interpersonal skills• Strong interest in fitness, rehabilitation, and preventive care• Ability to work collaboratively in a multidisciplinary team• Patient-focused and motivational approachBenefits:• Health insurance• Paid time off• Paid sick time• Full clinical and wellness training• Strong career growth opportunitiesAbout the Company:ReLiva Physiotherapy and Rehab is one of India’s leading physiotherapy and wellness providers, focused on rehabilitation, preventive care, and lifestyle transformation. The organization offers structured training, modern clinical exposure, and excellent growth opportunities for early-career physiotherapists.

Roles & Responsibilities:• Ensure implementation and compliance with cGMP, SOPs, and quality systems.• Review and approve batch manufacturing records, SOPs, and quality documents.• Handle deviations, change controls, OOS, and CAPA activities.• Support internal, external, and regulatory audits and inspections.• Monitor in-process activities and ensure adherence to quality standards.• Maintain QA documentation and ensure data integrity practices are followed.Qualification:• B. Pharm / M. PharmExperience:• 2 to 6 years of experience in Quality Assurance• Experience in regulated pharmaceutical manufacturing environment preferredSkills:• Strong knowledge of cGMP, QMS, and regulatory guidelines• Documentation, investigation, and compliance skills• Attention to detail and problem-solving ability• Good communication and coordination skillsAbout the Organization:BioMatrix Healthcare Private Limited, established in 2007 and headquartered in Ahmedabad, Gujarat, is a leading export-oriented pharmaceutical company engaged in the research, development, and manufacturing of oral solid dosages, liquids, and dry syrups, with global certifications including WHO-GMP, EU-GMP, and Health Canada, and a strong presence in over 30 international markets with more than 1000 product registrations worldwide.

Roles & Responsibilities:• Develop, validate, and transfer analytical methods for finished products and APIs.• Perform method development and validation as per ICH and regulatory guidelines.• Handle analytical instruments such as HPLC, GC, UV, and Dissolution.• Prepare and review method validation protocols, reports, and analytical documentation.• Support stability studies, troubleshooting, and investigation activities.• Coordinate with QA, QC, F&D, and Regulatory teams for analytical support.• Ensure compliance with cGMP, data integrity, and laboratory SOPs.Qualification:• B. Pharm / M. PharmExperience:• 2 to 8 years of experience in Analytical Method Development• Experience level aligned to Officer / Sr. Officer / Team Leader roleNo. of Vacancies: 05Skills:• Strong knowledge of analytical method development and validation• Hands-on experience with chromatographic techniques• Understanding of ICH, GMP, and regulatory requirements• Documentation and data integrity skills• Analytical thinking and problem-solving abilityAbout the Organization:BioMatrix Healthcare Private Limited, established in 2007 and headquartered in Ahmedabad, Gujarat, is a leading export-oriented pharmaceutical company engaged in the research, development, and manufacturing of oral solid dosages, liquids, and dry syrups, with global certifications including WHO-GMP, EU-GMP, and Health Canada, and a strong presence in over 30 international markets with more than 1000 product registrations worldwide.

Roles & Responsibilities:• Develop and optimize formulations for oral solid dosage forms as per project requirements.• Conduct product development, scale-up, and technology transfer activities.• Prepare and review development reports, SOPs, and technical documentation.• Coordinate with QA, QC, Regulatory, and Production teams during development and validation.• Support trial batches, exhibit batches, and stability studies.• Troubleshoot formulation and process-related issues.• Ensure compliance with cGMP and regulatory guidelines during development activities.Qualification:• B. Pharm / M. PharmExperience:• 2 to 8 years of experience in Formulation & Development• Experience level aligned to Officer / Sr. Officer / Team Leader roleNo. of Vacancies: 10Skills:• Strong knowledge of formulation development for oral solid dosage forms• Hands-on experience in scale-up and technology transfer• Documentation and regulatory compliance skills• Problem-solving and analytical abilities• Team coordination and project management skillsAbout the Organization:BioMatrix Healthcare Private Limited, established in 2007 and headquartered in Ahmedabad, Gujarat, is a leading export-oriented pharmaceutical company engaged in the research, development, and manufacturing of oral solid dosages, liquids, and dry syrups, with global certifications including WHO-GMP, EU-GMP, and Health Canada, and a strong presence in over 30 international markets with more than 1000 product registrations worldwide.

Roles & Responsibilities:• Support product planning, launch, and lifecycle management activities for assigned brands.• Prepare and update product literature, promotional inputs, and marketing strategies.• Coordinate with sales, regulatory, and manufacturing teams for product-related activities.• Conduct market research, competitor analysis, and trend tracking.• Assist in forecasting, pricing strategies, and portfolio management.• Monitor product performance and provide analytical insights to the management team.Qualification:• B. Pharm / M. Pharm / MBA in MarketingExperience:• 1 to 3 years of experience in Product Management or related pharmaceutical marketing rolesSkills:• Strong understanding of pharmaceutical products and market dynamics• Analytical and presentation skills• Good communication and coordination abilities• Knowledge of branding, positioning, and promotional planning• Proficiency in MS Office and data analysis toolsAbout the Organization:BioMatrix Healthcare Private Limited, established in 2007 and headquartered in Ahmedabad, Gujarat, is a leading export-oriented pharmaceutical company engaged in the research, development, and manufacturing of oral solid dosages, liquids, and dry syrups, with global certifications including WHO-GMP, EU-GMP, and Health Canada, and a strong presence in over 30 international markets with more than 1000 product registrations worldwide.

Roles & Responsibilities:• Prepare, review, and submit regulatory dossiers for international markets as per country-specific requirements.• Handle CTD/ACTD dossier compilation, variations, renewals, and lifecycle management activities.• Coordinate with internal departments such as QA, QC, R&D, and Production for regulatory data.• Respond to regulatory authority queries, deficiency letters, and follow-ups within timelines.• Track regulatory guidelines and ensure compliance with international regulatory standards.• Maintain and update regulatory documentation, databases, and product registration status.• Support audits, inspections, and regulatory intelligence activities.Qualification:• B. Pharm / M. PharmExperience:• 3 to 6 years of experience in International Regulatory Affairs• Hands-on experience in export market registrations is preferredSkills:• Strong knowledge of international regulatory requirements and dossier submissions• CTD/ACTD documentation and lifecycle management expertise• Good coordination and communication skills• Attention to detail and regulatory compliance mindset• Ability to manage multiple submissions and deadlinesAbout the Organization:BioMatrix Healthcare Private Limited, established in 2007 and headquartered in Ahmedabad, Gujarat, is a leading export-oriented pharmaceutical company engaged in the research, development, and manufacturing of oral solid dosages, liquids, and dry syrups, with global certifications including WHO-GMP, EU-GMP, and Health Canada, and a strong presence in over 30 international markets with more than 1000 product registrations worldwide.

Roles & Responsibilities• Conduct Freedom-to-Operate (FTO), prior-art, and patentability searches for APIs, peptides, intermediates, and KSMs• Analyze global patent databases, patent families, and prosecution histories• Prepare patent landscape, polymorph, and infringement risk analysis reports• Support generic drug entry strategy and Day-1 launch assessments• Assist in patent drafting, filing, and prosecution activities• Track patent publications, litigations, regulatory updates, and drug approvals• Maintain and manage internal IP databases• Provide IPR support to R&D, Regulatory Affairs, Business Development, and Project teamsQualifications• M.Sc in Organic Chemistry OR• M.Pharm (Pharmaceutical / Medicinal Chemistry preferred)Experience• 0–4 years of experience in pharmaceutical IPR (API / generics)Skills• Strong knowledge of Patent Laws and Intellectual Property Rights• Hands-on experience in FTO analysis, patent searches, and landscape studies• Excellent analytical, written, and verbal communication skills• Ability to work effectively with cross-functional teamsAbout the OrganizationSynzeal Research is a leading Indian CRO providing integrated discovery, development, and intellectual property support services to global pharmaceutical and biotech companies.

ROLE & RESPONSIBILITIES:• Assist physiotherapists in providing physical therapy and rehabilitation treatments• Support patients during therapy sessions to ensure comfort and safety• Help in executing treatment plans efficiently to aid patient recovery• Monitor patient progress and report observations to the supervising physiotherapist• Maintain cleanliness, safety, and readiness of therapy equipment• Ensure high standards of patient care and professional conduct• Assist in maintaining basic patient records and session detailsQUALIFICATION:• Diploma or relevant qualification in Physiotherapy or a related fieldEXPERIENCE:• Prior experience in a physiotherapy or healthcare setting is an advantage• Fresh candidates with relevant qualifications may also applySKILLS:• Proficiency in physical therapy assistance and patient care• Knowledge of rehabilitation techniques and orthopedic conditions• Excellent communication and interpersonal skills• Ability to work collaboratively within a healthcare team• Patient-focused approach with attention to quality care• Basic organizational and observation skillsABOUT THE COMPANY:Atri Physiotherapy is committed to delivering effective and compassionate physiotherapy services focused on patient recovery and improved quality of life. The clinic emphasizes teamwork, professional care standards, and personalized rehabilitation support in a supportive clinical environment.

ROLE & RESPONSIBILITIES:• Oversee daily clinical operations and ensure smooth functioning of the dental clinic• Perform diagnostic evaluations and develop comprehensive treatment plans• Deliver a wide range of dental procedures while maintaining high clinical standards• Mentor and guide junior dentists to enhance team performance• Ensure compliance with sterilization, safety, and quality protocols• Collaborate with clinic staff to create a patient-centered environment• Maintain accurate patient records and documentation• Uphold ethical practices and promote exceptional patient careQUALIFICATION:• Bachelor of Dental Surgery (BDS) or Master of Dental Surgery (MDS)• Valid dental license to practiceEXPERIENCE:• BDS with a minimum of 5 years of clinical experience OR• MDS with at least 2 years of clinical experience• Prior experience as a Lead or Consultant Dentist is advantageousSKILLS:• Expertise in diagnostics, restorative dentistry, oral surgery, and orthodontics• Strong leadership, team management, and mentoring abilities• Excellent communication, interpersonal, and problem-solving skills• Ability to maintain strict sterilization standards and clinical safety• Patient-focused approach with strong decision-making capabilities• Organizational skills with attention to detailABOUT THE COMPANY:Clove Dental is India’s largest dental network, operating 650+ specialized clinics across the country. With a team of over 1,300 skilled professionals, the organization is committed to delivering exceptional oral healthcare while maintaining the highest sterilization standards. Clove Dental offers comprehensive services including orthodontics, dental implants, and oral surgery, and has successfully served more than 2 million patients through an ethical, transparent, and patient-first approach.

Role & Responsibilities• Plan, implement, and monitor public health programs and health initiatives• Supervise disease prevention, health promotion, and sanitation activities• Conduct inspections, surveys, and health assessments in assigned areas• Coordinate with healthcare staff, municipal teams, and government authorities• Ensure compliance with public health laws, regulations, and safety standards• Maintain accurate records, reports, and official documentation• Participate in outbreak control, emergency health responses, and awareness campaignsQualification• MBBS degree from a recognized medical institution• Valid registration with Medical Council of India / State Medical CouncilExperience• Freshers and experienced candidates are eligible• Experience in public health or government health services will be an advantageSkills• Strong knowledge of public health systems and preventive medicine• Good administrative and supervisory skills• Effective communication and coordination abilities• Ability to work in field and office-based environments• Documentation, reporting, and analytical skillsAbout The Company• Ahmedabad Municipal Corporation (AMC) is a major urban local governing body responsible for public health, sanitation, and civic services, AMC plays a critical role in implementing healthcare programs and improving community health standards.Application Closing date - 17-02-2026 Official Notification - Click Here

Roles & Responsibilities• End-to-end dossier compilation from start to finish• Strong working knowledge of CTD Modules 1, 2, 3, 4• Conduct literature searches to support drug product development• Day-to-day coordination with manufacturing, QA, QC, R&D, and external clients/agents• Understanding of global regulatory pathways (EU, Brazil, Australia, South America)• Compilation and submission of eCTD dossiers• Regulatory database management and product lifecycle management• Review of commercial and regulatory documents• Identification of variation categories for post-approval changes• Timely compilation, review, and submission of variationsQualification• B.Pharm / M.Pharm / M.ScExperience• 3–5 years of relevant Regulatory Affairs experience• Hands-on exposure to EU, Brazil, Australia, and South American marketsSkills• Strong knowledge of eCTD, CTD modules, post-approval variations, and lifecycle management• Excellent coordination and communication skillsAbout the OrganizationCORONA Remedies Ltd. is a reputed Indian pharmaceutical company known for its commitment to quality, innovation, and global regulatory compliance. The company offers a collaborative work environment with opportunities to handle international regulatory submissions and complete product lifecycle management.