Ahmedabad Healthcare Jobs

Roles & Responsibilities • Prepare Clinical Study Reports (CSR) for BA/BE studies and patient-based clinical trials (PK, PD, and clinical endpoint studies) based on clinical data received after study completion, in compliance with regulatory requirements, SOPs, client standards, and approved templates • Draft and finalize project reports with all required appendices in eCTD format, including: – Module 2: Clinical Summary – Module 5: Study reports, literature, appendices, and Bioanalytical Reports (BR) • Ensure reports meet applicable regulatory guidelines and submission requirements • Submit final compiled, signed clinical study reports (eCTD-compliant) to clients • Coordinate with Project Managers regarding report requirements, sponsor comments, and responses • Draft final reports and submit to sponsors through the Project Manager • Liaise with Bioanalytical (BR) and Statistics teams to integrate bioanalytical and statistical reports into the final submission • Address sponsor queries and incorporate feedback within agreed timelines • Ensure documentation quality, accuracy, and regulatory compliance throughout the reporting process Qualification • B.Pharm, M.Pharm Experience • Experience in clinical study report writing, BA/BE studies, or clinical research documentation preferred • Exposure to eCTD submissions and regulatory reporting is an advantage Skills • Strong understanding of BA/BE and patient-based clinical trials • Knowledge of PK, PD, and clinical endpoint studies • Familiarity with regulatory guidelines and SOP-driven environments • Experience with eCTD Modules 2 and 5 • Excellent medical/scientific writing skills • Strong coordination and communication skills • High attention to detail and compliance focus About the Organisation Veeda Clinical Research (Veeda CR) is a globally reputed Contract Research Organization providing end-to-end clinical research, bioanalytical, and regulatory services. Veeda is known for its regulatory compliance, scientific excellence, and high-quality clinical documentation supporting global submissions.

Roles & Responsibilities • Review and provide comments on draft clinical protocols, Informed Consent Documents (English ICD), Case Report Forms (CRF), and related documents as per SOPs and applicable regulatory guidelines • Review and comment on draft clinical reports, including clinic-related sections and appendices, in compliance with SOPs, regulatory guidelines, and sponsor requirements • Review final eCTD reports received from report writers to ensure regulatory and submission readiness • Ensure document reviews are completed within defined timelines and priority requirements • Review updated documents incorporating sponsor comments and regulatory observations to ensure compliance • Review sponsor comments and regulatory queries and provide appropriate responses within stipulated timelines • Participate in the review and maintenance of departmental SOPs • Coordinate with internal teams for implementation of new or revised SOPs • Ensure corrective and preventive actions (CAPA) are implemented for identified findings, comments, or gaps • Perform any additional responsibilities assigned by the reporting authority Qualification • B.Pharm (Any Specialization) • M.Pharm / MS / M.Sc (Science – Any Specialization) Experience • Experience in clinical research documentation, regulatory review, or clinical operations is preferred • Exposure to SOP-driven environments and regulatory guidelines is an advantage Skills • Strong knowledge of clinical research documentation and regulatory requirements • Attention to detail and compliance-focused mindset • Ability to manage timelines and work on priority-based tasks • Good written communication and document review skills • Ability to coordinate with cross-functional teams • Understanding of SOPs, eCTD structure, and sponsor/regulatory interactions About the Organisation Veeda Clinical Research (Veeda CR) is a globally recognized clinical research organization providing integrated solutions across clinical development, bioanalytical services, and regulatory support. Veeda is known for its strong compliance culture, scientific expertise, and commitment to delivering high-quality, regulatory-compliant clinical research services.

Roles & Responsibilities • Ensure compliance with global pharmacovigilance regulations (EMA, EU GVP, ICH E2A/E2B, FDA, local guidelines) • Maintain and update pharmacovigilance documentation including SOPs and PV Master File (PSMF) • Assist during regulatory inspections, audits, and CAPA implementation • Support preparation, review, and submission of safety documents:  ICSRs, PSURs / PBRERs, DSURs, Risk Management Plans (RMPs) • Submit safety reports to EudraVigilance and other global safety databases • Perform literature screening and safety data evaluation • Assist in signal detection, risk minimization activities, and safety review meetings • Support preparation of SmPC, PIL, and package leaflets • Code and review adverse events using MedDRA and WHO-DD • Maintain accurate safety databases, trackers, and compliance logs • Complete mandatory PV trainings and stay updated with evolving regulations Qualification • B.PharmExperience • 0–1 year of experience in Pharmacovigilance • Freshers with PV training are eligible Skills • Basic understanding of pharmacovigilance regulations (EMA, EU GVP, ICH, FDA) • Knowledge of ICSR processing and safety reporting • Familiarity with MedDRA and WHO-DD coding • Strong attention to detail and documentation accuracy • Good written and verbal communication skills • Compliance-oriented and proactive learning mindset About the Organisation Lincoln Pharmaceuticals is a well-established Indian pharmaceutical company with a strong presence in domestic and international markets. The company is committed to quality, patient safety, and regulatory excellence, offering strong career growth opportunities in pharmacovigilance, regulatory affairs, and drug safety operations.

Roles & Responsibilities • Prepare and review CTD and ACTD dossiers for OSD products • Compile and maintain Process Validation (PV) documentation • Prepare and review stability study documentation • Develop Product Development Reports (PDR) • Perform artwork checking and regulatory compliance review • Prepare SmPC, package inserts, and leaflets • Ensure AMV and CDP matching and regulatory accuracy • Prepare and review specifications, COA, and MOA documents • Handle finished product specifications and DMF documentation support • Draft and submit product permissions, COPP, and FSC dossiers • Independently prepare, review, and manage regulatory documentation Qualification • B.Pharm / M.Pharm / M.Sc (Pharmacy background preferred) Experience • 1–4 years of experience in Pharmaceutical Regulatory Affairs • Hands-on exposure to OSD regulatory submissions • Strong knowledge of CTD and ACTD formats • Familiarity with Indian and export regulatory requirements Skills • Strong regulatory documentation and dossier compilation skills • High attention to detail and compliance accuracy • Good written and verbal communication skills • Ability to work independently and manage multiple submissions • Strong understanding of pharmaceutical lifecycle management About the Organisation Noronic Pharmaceutical Private Limited is a growing Indian pharmaceutical company focused on delivering high-quality pharmaceutical products across domestic and international markets. The organization offers a stable work environment, hands-on regulatory exposure, and long-term career growth opportunities for Regulatory Affairs professionals.

Roles & Responsibilities:• Assess patients and evaluate physical and functional conditions• Provide physiotherapy treatment for pain relief and rehabilitation• Design and implement individualized treatment and exercise programs• Monitor patient progress and update therapy plans as required• Educate patients on posture correction, exercises, and injury prevention• Maintain accurate patient records and treatment documentation• Ensure patient safety, hygiene, and a supportive clinical environmentQualifications:• Bachelor’s Degree in Physiotherapy (BPT) or equivalent qualificationExperience:• Freshers and experienced candidates can applySkills Required:• Strong clinical assessment and rehabilitation skills• Good communication and patient-handling abilities• Professional, ethical, and patient-centric approach• Ability to work independently and manage casesWork Timings:• Morning: 9:00 AM – 1:00 PM• Evening: 4:00 PM – 8:00 PMAbout the Company: Samarpan Physiotherapy Clinic is a patient-focused physiotherapy center providing comprehensive care for pain management, rehabilitation, and long-term physical wellness in a professional and caring environment.

Role & Responsibilities • Execute medicinal chemistry research for hit-to-lead optimization • Design, synthesize, and characterize adamantane–quinoxalone hybrid compounds • Perform multi-step organic synthesis and heterocyclic chemistry • Analyze compounds using spectroscopic and analytical techniques • Support drug discovery efforts for precision chemotherapy in AML • Maintain proper laboratory records and documentation • Assist in data analysis, report preparation, and research publications • Collaborate with project team and Principal Investigator • Ensure compliance with institutional and ICMR research guidelinesQualification • PhD in Organic / Medicinal / Pharmaceutical Chemistry • OR PG degree with relevant research experience • Strong background in organic synthesis, heterocycles, and drug discoveryExperience • Hands-on research experience in medicinal or organic chemistry • Experience in drug discovery projects preferred Skills • Expertise in organic synthesis and medicinal chemistry • Strong knowledge of heterocyclic chemistry • Experience with analytical and spectroscopic techniques • Scientific writing and data interpretation skills • Ability to work independently and in a research teamAbout Company • NIPER Ahmedabad is a premier national institute under the Government of India , Focused on advanced pharmaceutical education and researchProject Funding: ICMR Department: Medicinal Chemistry Positions: 02 Salary: ₹78,000 + HRA (Approx. ₹1.01 Lakh/month) Tenure: 1 Year (Extendable up to 3 Years) Last Date to Apply: 05 February 2026

Key Responsibilities Act as scientific liaison with healthcare professionals and KOLs Support medico-marketing activities, CMEs, and scientific content development Deliver clinical training and scientific presentations Collect and manage clinical/real-world data Support channel partner onboarding and post-sales medical supportQualifications Degree in Medical/Life Sciences (MBBS, BDS, BPharm, MPharm, MSc, Biomedical, etc.)Experience 2–3 years of experience in Medical Affairs/MSL or medical device industry (preferred)Skills Strong scientific communication and presentation skills KOL engagement and stakeholder management Clinical data interpretation and problem-solvingAbout Company Bioscan Research, based in Ahmedabad, is an innovative healthcare technology company focused on improving outcomes for traumatic brain injury patients.

Roles & Responsibility • Perform bioanalytical sample analysis using LC-MS/MS instrumentation • Execute method development, method validation, and routine analysis of study samples • Ensure accurate documentation, data review, and compliance with regulatory requirements • Handle instruments including operation, troubleshooting, calibration, and routine maintenance • Maintain data integrity and follow laboratory SOPs and quality standards • Support BA/BE studies and bioanalytical activities as per project timelines • Collaborate with cross-functional teams to ensure timely and high-quality deliverables Qualification • B.Sc / M.Sc / B.Pharm / M.Pharm or equivalent relevant qualification Experience • Freshers can apply for Analyst role • Up to 5 years of relevant bioanalytical laboratory experience preferred for Senior Analyst role Skills • Strong knowledge of bioanalytical workflows and BA/BE studies • Hands-on experience or understanding of LC-MS/MS operations • Good understanding of data integrity and regulatory compliance • High attention to detail and analytical thinking • Ability to work effectively in a team-oriented environment About the company Sycon Clinical Research Private Limited is a growing full-service Clinical Research Organization based in Gujarat, specializing in bioavailability and bioequivalence studies, clinical operations, and advanced bioanalytical services; the company operates state-of-the-art facilities, follows high ethical and quality standards, and is committed to delivering precise, reliable, and regulatory-compliant research outcomes that support global drug development programs.

Roles & Responsibilities • Respond to medical and product-related inquiries from healthcare professionals, consumers, and internal teams • Document medical inquiries and responses accurately in approved databases and formats • Support development and updating of standard response letters, FAQs, and reference materials • Collect, document, and route adverse event (AE) information in compliance with drug safety SOPs • Perform medical literature searches using databases such as PubMed, OVID, and EMBASE • Maintain and update product and medical information databases • Assist in creation, review, and maintenance of SOPs and procedural documents • Prepare weekly and monthly reconciliation and activity reports • Ensure compliance with project guidelines, SOPs, and regulatory requirements • Coordinate with internal stakeholders and clients for timely and accurate medical responses Qualification • B.Pharm or M.Pharm (any specialization) • PhD (Pharmacy) – optional Skills • Medical information services and scientific communication • Medical literature review and data interpretation • Basic understanding of pharmacovigilance and adverse event intake • Familiarity with PubMed, OVID, and EMBASE databases • Strong written and verbal communication skills • Attention to detail and compliance-oriented mindset About the Company Apcer Life Sciences is a global provider of pharmacovigilance, regulatory, medical information, and clinical research services, supporting pharmaceutical, biotechnology, and medical device companies with compliant, technology-driven solutions across the product lifecycle.

Role & Responsibilities • Review patient adverse events and medical data in pharmacovigilance databases. • Assess drug safety, causality, and potential risks. • Perform medical review of ICSRs and support safety evaluations. Qualifications • MBBS or MD only. Experience • 1–6 years of experience as a Medical Reviewer in Pharmacovigilance. Skills • Strong understanding of drug safety and adverse event assessment. • Attention to detail and regulatory compliance knowledge. About the Company • India’s 2nd largest KPO in the Life Sciences & Healthcare domain.

Roles & Responsibilities • Prepare, review, and support development of high-quality clinical and regulatory documents • Assist in creation and review of CTD modules, Investigator’s Brochure (IB), protocols, ICFs, eCRF/CRFs, and safety reports • Ensure documents comply with SOPs, regulatory guidelines, and approved plans • Conduct literature searches and organize scientific data for clinical documentation • Perform quality control (QC) checks on clinical and regulatory documents • Support regulatory submission documentation activities • Ensure timely delivery of assigned documentation tasks Qualification • B.Pharm or M.Pharm from a recognized university Experience • 2-3 years of experience in clinical research documentation • Experience in a CRO or pharmaceutical industry preferred Skills • Knowledge of clinical trial documentation and regulatory requirements • Strong scientific writing, review, and QC skills • Ability to interpret clinical data and literature • Good attention to detail and time management • Strong communication and documentation skills About the Company Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations across India, USA, Canada, UK, Spain, and Poland. The company provides end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide, offering strong global exposure and long-term career growth opportunities in clinical research.

Roles & Responsibilities • Conduct in-process, on-site, and off-site audits to ensure trial activities are performed, recorded, analyzed, and reported in compliance with regulatory, organizational, and client requirements • Perform system audits as per the annual audit calendar to ensure compliance with Lambda SOPs, quality systems, protocols, and applicable regulations • Carry out retrospective audits of study raw data including ICFs, protocols, project management plans, IMP plans and release checklists, SMPs, CSRs, and medical imaging documents • Support completion of assigned system audits and preparation of detailed audit reports • Review and contribute to SOPs related to Clinical Data Management and Quality Assurance • Audit clinical databases and CDM documents prior to database lock • Calculate clinical database error rates and communicate findings to CDM; prepare CDM audit status for audit certificates and QA statements • Review Data Management Plans, SAPs (CDM aspects), and CRF/eCRF designs for assigned projects • Conduct system audits of Clinical Data Management functions and report outcomes • Review TMF, SMF, site selection visit reports, and IMP release documentation Qualification • M.Pharm Experience • 2-3 years of experience in late-phase Quality Assurance within clinical research Skills • Strong knowledge of ICH-GCP, regulatory guidelines, and clinical trial quality systems • Experience in CDM audits, database reviews, and SOP compliance • High attention to detail with strong analytical and reporting skills • Effective communication and documentation abilities About the Company Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization headquartered in Ahmedabad, India, with operations across India, the USA, Canada, Europe, and the UK, delivering end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide.

Roles & Responsibilities • Execute manufacturing activities for transdermal patches, semi-solids (cream, ointment, lotion), ODF, and MDI as per GMP guidelines • Perform equipment qualification, calibration, and routine maintenance • Operate and monitor production machines for coating, blending, filling, and solid oral dosage forms • Carry out in-process checks and maintain batch manufacturing and packing records • Conduct analytical testing using HPLC, GC, KF titration, and related instruments (QC roles) • Maintain accurate documentation in LIMS and ensure GLP compliance • Support shift-based operations and coordinate with cross-functional teams • Follow safety, quality, and regulatory standards at all times Qualification • ITI / Diploma / B.Sc / BE / B.Tech / B.Pharm / M.Sc (relevant disciplines) Experience • 1-7 years for Officer / Executive / Analyst roles • Freshers or up to 1 year experience eligible for FTE / FTA / Apprentice roles Skills • Knowledge of GMP, GLP, and pharmaceutical manufacturing practices • Hands-on exposure to semi-solid preparations, transdermal systems, or QC instruments preferred • Ability to operate and troubleshoot production equipment • Good documentation, communication, and teamwork skills • Willingness to work in shifts About the Company Zydus Lifesciences Limited is a leading Indian pharmaceutical company with a strong global presence, known for innovation, high-quality manufacturing, and specialized dosage forms, offering stable careers and long-term growth opportunities.

Role & Responsibilities • Conduct medical review and approval of selected scientific and literature articles • Review Individual Case Safety Reports (ICSRs) in the safety database • Perform medical labeling, causality assessment, and seriousness evaluation • Follow up with reporters to obtain missing or additional safety information • Review aggregate safety reports, including Periodic Safety Update Reports (PSURs) and Periodic Adverse Drug Experience Reports (PADERs) • Provide medical and scientific conclusions for benefit–risk assessments • Review and support Risk Management Plans (RMPs) • Contribute to signal detection and signal management activities • Ensure compliance with global pharmacovigilance regulations Qualification • MBBS or MD in Pharmacology Experience • 0–1 year of experience in pharmacovigilance or drug safety Skills • Strong understanding of ICSR processing and safety databases • Knowledge of global PV regulations (ICH, GVP, FDA, EMA) is an advantage • Prior experience in a regulated pharmaceutical company is a plus About the Company • Emcure Pharmaceuticals is a leading Indian pharmaceutical company, offering expertise in pharmacovigilance and drug safety operations globally.

Roles & Responsibilities • Lead and execute analytical development activities using LC, LC-MS, HPLC, GC, and GC-MS as per departmental role • Perform method development, validation, and troubleshooting for pharmaceutical and related products • Handle analytical testing, data interpretation, documentation, and regulatory-compliant reporting • Support R&D activities including synthesis, formulation development, nano-material characterization, and technology evaluation • Operate and maintain advanced analytical instruments such as HPLC, LC-MS, GC-MS, NMR, XRD, AFM, and related systems • Conduct patent and market searches and contribute to selection of niche APIs and KSMs • Ensure compliance with GLP, NABL, and regulatory guidelines • Mentor junior team members and support laboratory setup, process improvement, and cross-functional collaboration Qualification • M.Sc / M.Pharm or equivalent • Ph.D in Nanotechnology preferred for R&D Manager role Open Positions & Requiremnets • Manager (LC, LC-MS - AD Department): 10-15 years • Research Associate - HPLC (AD&QC Department): 3-7 years • Manager - (R&D Department): 10-15 years • Research Associate / Sr. Research Associate (Method Development & Validation – HPLC, Analytical Dept.): 3-6 years • Research Associate / Sr. Research Associate (GC, GC-MS – AD&QC Dept.): 3-6 years Skills • Strong hands-on expertise in analytical techniques and instrumentation • In-depth knowledge of method development, validation, and regulatory documentation • Experience in pharmaceutical, CRO, or regulated laboratory environments • Analytical thinking, problem-solving, and attention to detail • Ability to work independently and lead teams where applicable About the Company Accuprec Research Labs Pvt Ltd is a NABL-accredited and GLP-certified Contract Research Organisation based in Ahmedabad, Gujarat, offering advanced regulatory testing and research services for pharmaceuticals, medical devices, herbal products, and allied industries, with a strong focus on quality, innovation, and scientific excellence.

Role & Responsibilities • Provide ongoing medical monitoring for assigned clinical trials • Conduct real-time safety review of AEs and SAEs to ensure participant safety • Evaluate safety signals, trends, laboratory and ECG abnormalities • Contribute to protocol development, amendments and review of IBs, CSRs and SAPs • Support preparation and review of safety narratives, DSURs and periodic safety reports • Collaborate with pharmacovigilance teams for safety data management and regulatory responses • Participate in Steering Committees and Data Safety Monitoring Boards (DSMBs) • Provide medical expertise during site initiation, monitoring visits, audits and inspections • Review inclusion/exclusion criteria for complex cases and manage protocol deviations with CAPA • Ensure compliance with ICH-GCP, regulatory and ethical guidelines • Support regulatory submissions and inspection readiness activities • Deliver medical training to internal teams and site staff • Work cross-functionally with clinical operations, data management, biostatistics and project teams Qualifications  • MD or equivalent medical degree (specialty training preferred)Experience • 3–7 years of clinical research experience in pharma, biotech or CRO • Prior experience as Medical Monitor / Safety Physician preferred • Strong understanding of ICH-GCP, FDA, EMA and CDSCO regulatory requirements • In-depth knowledge of clinical trial methodology and drug development lifecycle Skills • Medical monitoring and safety signal evaluation • Protocol development and regulatory documentation • Pharmacovigilance and safety reporting • Clinical trial compliance and audit readiness • Cross-functional collaboration and stakeholder management • Scientific writing and medical training delivery About the Company • Micro Crispr Pvt. Ltd. is a biotechnology-driven organization focused on innovative research and clinical development solutions, supporting advanced clinical programs through strong scientific, regulatory and ethical standards

Role & Responsibilities:• Assess, diagnose, and treat sports-related and general musculoskeletal conditions• Develop and implement individualized rehabilitation and injury-prevention programs• Provide on-field injury management and emergency care during training sessions or matches when required• Apply manual therapy, exercise therapy, taping, and electrotherapy techniques• Monitor patient and athlete progress and modify treatment plans accordingly• Educate patients and athletes on injury prevention, biomechanics, posture, and recovery protocols• Maintain accurate clinical documentation, treatment records, and progress reports• Communicate effectively with patients, athletes, and team members to ensure quality careQualifications:• BPT (Bachelor of Physiotherapy)• MPT (Master of Physiotherapy)Experience:• Freshers and experienced candidates can apply• General Physiotherapists are also eligibleSkills Required:• Emergency handling and on-field injury management• Strong communication and counseling skills• Clinical assessment and rehabilitation planning• Patient management and documentation skills• Ability to work independently and as part of a teamAbout the Company:Health Plus Physiotherapy and Medical Gym, based in Usmanpura, Ahmedabad, is a specialized rehabilitation and wellness center offering physiotherapy, sports injury management, and medical fitness services. The organization is committed to evidence-based treatment, patient-focused care, and promoting long-term physical health through professional rehabilitation practices.

Role & Responsibilities • Perform analytical method development and validation for pulmonary dosage forms • Conduct routine and stability sample analysis as per regulatory guidelines • Support formulation development through analytical inputs • Prepare and review analytical reports, protocols and validation documents • Ensure compliance with GLP, GMP and regulatory standards • Handle analytical instruments related to pulmonary product analysis • Participate in technology transfer and regulatory submission activities Qualifications & Experience • M.Pharm with GPAT qualification • 2–6 years of experience in Analytical Development – Pulmonary products • Strong knowledge of analytical method development and validation • Experience in pulmonary dosage form analysis is mandatory About the Company • Zydus Lifesciences Ltd is a leading global pharmaceutical company with strong R&D capabilities in specialty and complex formulations

Role & Responsibilities • Provide comprehensive medical care to OPD and IPD patients • Diagnose and manage acute and chronic internal medicine conditions • Manage diabetes, endocrine and metabolic disorders • Conduct patient evaluations, investigations and treatment planning • Monitor patient progress and modify treatment as required • Maintain accurate medical records and clinical documentation • Coordinate with multidisciplinary teams for holistic patient care • Participate in clinical rounds and emergency care services Qualifications & Experience • MD / DNB in Internal Medicine • 1–5 years of post-qualification clinical experience • Strong diagnostic and clinical decision-making skills • Good communication and patient-handling skills About the Company • Zydus Hospitals is a leading multi-specialty healthcare provider known for advanced tertiary care services and patient-centric treatment models