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Roles & Responsibilities: • Handle preparation, review, and submission of API Drug Master Files (DMFs) • Ensure compliance with ICH guidelines and global regulatory requirements • Manage regulatory submissions for US FDA and other international markets • Coordinate with cross-functional teams for data collection and documentation • Support responses to regulatory queries, deficiencies, and post-submission activities • Maintain regulatory documentation and ensure timely lifecycle management • Monitor changes in global regulatory guidelines and implement updates Qualification: • Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) Experience: • 2-3 years of experience • Hands-on experience in API regulatory affairs with US FDA exposure preferred Skills: • Strong knowledge of API DMF preparation and submission • Good understanding of ICH and global regulatory guidelines • Experience in US FDA regulatory requirements • Excellent documentation and coordination skills • Ability to work in a fast-paced regulatory environment About the Company: Senores Pharmaceuticals Limited is a fast-growing Indian pharmaceutical company focused on the development and manufacturing of complex generics for regulated and emerging markets, including the US, EU, and ROW, with a strong commitment to global quality and compliance.
Roles & Responsibilities: • Compile and review CTD & ACTD dossiers for product registrations, renewals, and variations • Ensure accuracy, consistency, and completeness of regulatory documents before submission • Coordinate with QA, QC, R&D, Production, and Packaging teams to collect technical data • Prepare and submit responses to regulatory queries and deficiency letters within timelines • Manage version control and lifecycle management of regulatory documents • Support post-approval changes, renewals, amendments, and variations • Assist during audits, inspections, and regulatory assessments Qualification: • Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm) Experience: • 2-4 years of experience in Regulatory Affairs • Dossier compilation experience (CTD / ACTD) mandatory • Candidates from merchant pharmaceutical companies preferred Skills: • Strong knowledge of CTD / ACTD formats and global regulatory guidelines • Excellent documentation, formatting, and proofreading skills • Strong coordination and time management abilities • High attention to detail and compliance-focused mindset About the Company: Infocus Remedies Pvt. Ltd., a group company of Saifen Drugs India Pvt. Ltd., is engaged in pharmaceutical manufacturing and global regulatory operations, offering strong exposure to domestic and international regulatory submissions.
Roles & Responsibilities: • Support Corporate Quality Assurance documentation and record maintenance • Assist in quality systems, SOP management, and compliance activities • Participate in internal audits, reviews, and QA coordination tasks • Ensure accuracy, completeness, and timely maintenance of QA documents • Learn and follow pharmaceutical QA standards and regulatory requirements • Collaborate with cross-functional teams for continuous quality improvement Qualification: • B.Sc / M.Sc • B.Pharm (Bachelor of Pharmacy) • M.Pharm (Master of Pharmacy) • Any relevant science background Experience: • Freshers are welcome to apply Skills: • Strong attention to detail and documentation accuracy • Basic understanding of Quality Assurance processes • Good written and verbal communication skills • Willingness to learn corporate QA operations • Ability to work collaboratively in a team environment About the Company: Amneal Pharmaceuticals is a global pharmaceutical company focused on developing, manufacturing, and distributing high-quality generic and specialty medicines. The company offers strong exposure to global quality systems and excellent long-term career growth in the pharmaceutical quality domain.
Roles & Responsibilities: • End-to-end processing of ICSR cases in compliance with global PV regulations • Perform duplicate checks, case validation, data entry, and drug/MedDRA coding • Conduct listedness, causality, and expediting assessments • Prepare high-quality case narratives and ensure timely submissions • Ensure adherence to SOPs, work instructions, and regulatory requirements • Communicate urgent safety issues to Line Manager/QPPV • Maintain accurate documentation and professional communication • Support SOP, WI, template development, and team training • Provide PV guidance to internal teams and clients • Stay updated with regulatory intelligence and implement changes Qualification: • Bachelor’s degree in Pharmacy (B.Pharm), Life Sciences, Biotechnology, Clinical Research, or related discipline Experience: • Freshers eligible • Basic knowledge of Pharmacovigilance, MedDRA, and ICSR lifecycle is an advantage Skills: • Understanding of PV concepts and global safety regulations • Attention to detail and data accuracy • Good written and verbal communication skills • Ability to meet timelines and work in a regulated environment About the Company: Lambda Therapeutic Research Ltd. is a globally recognized Contract Research Organization (CRO) offering comprehensive clinical research and pharmacovigilance services, providing strong career growth opportunities in drug safety and regulatory compliance.How to Apply?Application Link
Role & Responsibilities: • Dispense medicines accurately as per prescriptions and internal indents • Raise pharmacy requisition slips based on stock and operational requirements • Receive medicines from stores and verify quantity, batch number, and expiry against issue slips • Perform daily physical stock verification and reconcile with system data • Monitor short-expiry medicines on a monthly basis and non-moving stock every six months • Maintain proper storage and handling of medicines as per guidelines • Build strong customer relationships to support effective patient care Qualification: • D.Pharm (Diploma in Pharmacy) / B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy) Experience: • Freshers and experienced pharmacists are welcome Skills: • Strong knowledge of prescription dispensing and pharmacy operations • Attention to detail in inventory management and documentation • Good customer service and communication skills • Basic computer and pharmacy software knowledge About the Company: Apollo Pharmacy is India’s leading pharmacy retail chain, known for its commitment to quality healthcare, patient safety, and professional excellence. Working at Apollo Pharmacy offers exposure to premium locations, attractive compensation, and long-term career growth with a trusted national brand.
Role & Responsibilities: • Dispense medicines accurately as per prescriptions and internal indents • Handle and coordinate home delivery of medicines to ensure timely and correct dispatch • Raise pharmacy requisition slips as per stock and operational requirements • Receive stock from stores and verify quantity, batch number, and expiry against issue slips • Perform daily physical stock verification and reconcile with system data • Identify and review short-expiry medicines on a monthly basis • Monitor and review non-moving medicines once every six months • Build and maintain strong customer relationships to support effective patient care • Ensure proper storage and handling of medicines as per guidelines Qualification: • Pharmacist: D.Pharm / B.Pharm / M.Pharm from a recognized institution • Pharmacy Trainee: 12th Pass / Any Graduate Experience: • Freshers and experienced candidates are welcome for both roles Skills: • Basic knowledge of pharmacy operations and drug dispensing • Attention to detail in stock handling and documentation • Good communication and customer service skills • Basic computer knowledge for stock and billing systems • Willingness to work in shifts as per operational requirements About the Company: Apollo Pharmacy is one of India’s largest and most trusted pharmacy retail chains, committed to providing quality medicines and healthcare services with a strong focus on patient safety and customer satisfaction. With a widespread presence across the country, Apollo Pharmacy offers a professional work environment, structured training, and growth opportunities for individuals seeking a career in retail and hospital pharmacy services.
Role & Responsibilities: • Provide professional advice and guidance to patients on medication usage, dosage, and potential side effects • Collaborate with healthcare providers to optimize medication therapy management • Review prescriptions for accuracy, appropriateness, and potential drug interactions • Oversee the preparation, dispensing, and labeling of pharmaceutical products • Conduct medication reviews and patient consultations to ensure safe and effective therapy • Ensure compliance with all legal, regulatory, and safety requirements related to pharmacy practice • Maintain and manage catalogue operations and pharmacy records • Stay updated on new pharmaceutical products, guidelines, and industry developments • Use pharmacy management software for prescription processing and record maintenance Qualification: • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D) from a recognized institution Experience: • 1-2 years of relevant pharmacy experience required • Total professional experience up to 3 years- preferredSkills: • Strong knowledge of pharmaceuticals and medication therapy management • Excellent communication and interpersonal skills • High attention to detail and accuracy in prescription handling • Ability to work collaboratively with healthcare professionals • Proficiency in pharmacy management software and basic computer applications • Flexibility to work various shifts including evenings and weekendsAbout the Company: Equality Healthcare Pvt Ltd is a healthcare services organization based in Motera, Ahmedabad, Gujarat, focused on delivering high-quality, patient-centered pharmaceutical and healthcare solutions. The company emphasizes ethical practices, medication safety, and collaborative care while fostering a professional environment that supports continuous learning and service excellence.
Role & Responsibilities • Conduct off-site monitoring visits during study phases • Perform Site Initiation Visits (SIVs) and ensure study readiness • Review protocol prerequisites and site compliance • Execute routine monitoring as per study monitoring plans • Coordinate with sites for feasibility assessments • Prepare and submit study-related reports (SIV, monitoring, close-out, etc.) • Collect and manage essential trial documents • Review trial documents for SOP, protocol, and regulatory compliance • Train and mentor teams on ICH-GCP and regulatory updates • Support internal and external audits and inspections Qualifications & Experience • Degree in Life Sciences, Pharmacy, or Clinical Research • 1-3 years of experience as a Clinical Research Associate or equivalent • Strong knowledge of ICH-GCP guidelines • Experience in clinical trial monitoring and CRO operations • Excellent documentation, communication, and coordination skillsSkills • Proficient in ICH-GCP and regulatory compliance • Strong organizational and time-management skills • Ability to analyze clinical trial data and resolve issues • Good problem-solving and decision-making skills • Excellent communication skills (verbal and written) • Detail-oriented with strong documentation skills About the Company • Veeda Clinical Research is a well-established CRO in India, supporting global and domestic clinical trials across multiple therapeutic areas, offering strong career-building opportunities for aspiring CRAs.
Role & Responsibilities • Manage end-to-end ICSR lifecycle, including data entry into pharmacovigilance databases • Book and triage ICSRs, ensuring compliance with PV regulations • Perform medical coding (MedDRA, WHO-DD) and narrative writing for safety reports • Generate follow-up letters to reporters and ensure timely case closure • Review scientific and medical literature to identify valid ICSRs • Perform quality checks (QC) on safety cases to ensure data accuracy and completeness • Assist in the preparation of aggregate safety reports (PSUR, PBRER, DSUR, if applicable) • Support signal detection activities and ADR trend analysis • Ensure compliance with SOPs, project guidelines, and global pharmacovigilance regulations • Stay updated with regulatory changes impacting pharmacovigilance activities • Coordinate with cross-functional teams and affiliates to resolve safety queries Qualification • B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences Experience • 2–5 years of experience in Pharmacovigilance, particularly in ICSR processing, safety data entry, and medical coding Skills • Knowledge of global pharmacovigilance guidelines (ICH, GVP, FDA, EMA) • Proficiency in MedDRA and WHO-DD coding systems • Strong experience in narrative writing and case quality review • Excellent written and verbal communication skills • Ability to perform quality checks and ensure regulatory compliance Why Join Apcer Life Sciences? • Work with a globally recognized pharmacovigilance and regulatory services company • Exposure to international pharmacovigilance projects and a strong focus on career development
Role & Responsibilities • Prepare, review, and quality-check clinical trial documents • Develop clinical protocols, Investigator’s Brochure (IB), ICFs, CTD modules, CRFs, and safety reports • Ensure documents comply with SOPs, timelines, and regulatory guidelines • Conduct literature searches and scientific data interpretation • Perform QC reviews for accuracy, consistency, and compliance • Support regulatory submission documentation Qualification • B.Pharm or M.Pharm Experience • 2–3 years in clinical research, medical writing, or regulatory documentation • Experience in CRO or pharmaceutical industry preferred Skills • Clinical documentation and medical writing • Regulatory guideline understanding • Literature review and data interpretation • Quality control and compliance checks • Strong written communication About the Company • Lambda Therapeutic Research Ltd. is a global full-service CRO • Operations across India, USA, Canada, UK, Spain, and Poland • Provides exposure to international clinical trials and regulatory projects
Role & Responsibilities • Provide medical oversight for clinical trials • Review safety data and adverse events • Ensure protocol compliance Qualification • MD Pharmacology Experience • Fresher Skills • Safety evaluation, clinical judgment, documentation About the Company Cliantha Research is a global CRO conducting multinational clinical trials.
Role & Responsibilities • Prepare protocols, CSRs, and regulatory documents • Ensure compliance with ICH-GCP guidelines • Coordinate reviews and submissions Qualification • B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences Experience • 1–2 years in medical writing Skills • Scientific writing, regulatory knowledge, documentation About the Company Cliantha Research is a reputed CRO delivering regulatory and medical writing services.
Role & Responsibilities • Validate and reconcile clinical trial data • Perform data cleaning and query resolution • Support database lock activities • Ensure compliance with CDM SOPs and GCP guidelines • Maintain study documentation Qualification • B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences Experience • 3–5 years in Clinical Data Management Skills • EDC systems, data validation, GCP, attention to detail, MS Excel About the Company Cliantha Research is a global CRO providing end-to-end clinical research services supporting international clinical trials.
Role & Responsibilities Perform routine laboratory investigations Prepare samples and reagents for testing Maintain laboratory equipment and cleanliness Record test results and maintain lab registers Follow biosafety and SOP guidelines Qualification DMLT / B.Sc in Medical Laboratory Technology or equivalent Experience Laboratory experience in hospital or diagnostic centre preferred Skills Lab testing and sample handling Equipment maintenance Data recording and documentation Basic computer skills About the University Gujarat University operates central laboratory facilities to support its healthcare and academic infrastructure.Application Start Date: 29 December 2025 Last Date to Apply: 13 January 2026 (05:00 PM) Application Fee: ₹750 (General), ₹500 (SC/ST/SEBC/EWS), Nil for PwD
Role & Responsibilities Dispense medicines accurately as per prescriptions Maintain pharmacy stock, inventory, and expiry records Ensure compliance with Pharmacy Act and University Health Centre SOPs Provide medication counselling to students, staff, and patients Maintain computerized pharmacy records Monitor storage conditions and drug safety standards Qualification Diploma in Pharmacy / Bachelor of Pharmacy Must be a Registered Pharmacist Experience Relevant experience in hospital/community pharmacy preferred Skills Drug dispensing and inventory management Patient counselling and communication Basic computer knowledge Attention to detail and accuracy About the University Gujarat University is a NAAC A+ accredited state university providing healthcare facilities to students and staff through its dedicated Health Centre.Application Mode: Online Application Start Date: 29 December 2025 Last Date to Apply: 13 January 2026 (05:00 PM) Application Fee: ₹750 (General), ₹500 (SC/ST/SEBC/EWS), Nil for PwD
About the Role The Deputy Manager – Pharmacovigilance Safety System (ARGUS) Administrator is responsible for managing and maintaining the safety database infrastructure to ensure compliant, accurate, and efficient pharmacovigilance operations. Key Responsibilities Manage system configuration, user access, workflow setup and system maintenance Monitor compliance and ensure data integrity within the ARGUS safety system Generate and review safety system reports and dashboards Support system validation activities and documentation Provide troubleshooting, user support and training Maintain system-related SOPs, documentation and audit readiness Ensure accurate safety data entry and adherence to regulatory timelines Collaborate with PV operations teams to optimize safety system performance Required Knowledge and Skills Strong understanding of pharmacovigilance regulations including ICH and GVP Knowledge of safety database administration and PV workflows Strong analytical, documentation and troubleshooting skills High attention to detail and organizational ability Excellent communication and training skills Ability to work in compliance with SOPs and quality standards Educational Qualification Bachelor’s or Master’s degree in Life Sciences, Pharmacy or a related discipline About the Company Amneal is a global pharmaceutical organization committed to quality, patient safety and an inclusive workplace culture.
About the Role The Executive – Pharmacovigilance & Drug Safety is responsible for managing signal detection, evaluation, documentation and communication activities to ensure patient safety and regulatory compliance. Key Responsibilities Prepare and maintain signal schedules as per SOPs Identify, analyze and evaluate safety signals from multiple data sources Assess benefit–risk impact and potential label change requirements Prepare product-specific ADR sheets Author Drug Safety Reports for validated signals Communicate signal findings to internal stakeholders Support cross-functional initiatives to enhance pharmacovigilance capabilities Stay updated with global regulatory guidelines related to signal management Ensure compliance with SOPs, timelines and quality standards Assist in development and revision of SOPs, templates and work instructions Deliver signal management training to internal teams Qualification Pharm D / Doctor of Pharmacy Skills and Knowledge Signal detection and evaluation Pharmacovigilance regulations Drug safety reporting Documentation management Strong analytical and communication skills About the Company Amneal is a global pharmaceutical company committed to patient safety, regulatory excellence, and a diverse and inclusive workplace.
Organization: Dr. Reddy's Laboratories Therapy Area: Gastroenterology Eligibility: MBBS with Medical Affairs experience OR MD (Pharmacology) – freshers welcome Strong interest in Gastroenterology Excellent communication and relationship-building skills Key Responsibilities: Engage with leading Gastroenterologists across India Lead impactful medical and scientific discussions Drive medical education, insights, and collaborations Collaborate with cross-functional teams to support therapy advancement Why Join: Contribute to advancing patient care in Gastroenterology Work in a dynamic, science-driven environment at Dr. Reddy's How to Apply: Connect via email: bushrahasankhan@drreddys.com
About Company • Dr. Reddy’s Laboratories is a global pharmaceutical company committed to affordable and innovative medicines • Science-led, patient-centric organization with strong presence across branded generics, biosimilars, and specialty therapies About Role & Responsibilities • Act as Regional Medical Advisor for Gastroenterology / Hepatology portfolio • Execute medical affairs plans aligned with national and global medical strategy • Engage in high-quality scientific exchange with Gastroenterologists and Hepatologists • Build and maintain strong relationships with Key Opinion Leaders (KOLs) • Deliver unbiased scientific presentations, CMEs, advisory boards, and medical meetings • Provide medical support for marketed and pipeline products • Generate and communicate field medical insights to internal stakeholders • Support evidence generation initiatives including RWE, IIS, and publications • Collaborate cross-functionally with Marketing, Sales, Market Access, and PV teams • Ensure compliance with pharmacovigilance, GxP, and company SOPs Qualification • MBBS with prior Medical Affairs experience • OR MD Pharmacology (freshers welcome) Skills • Strong scientific and clinical acumen in Gastroenterology / Hepatology • Excellent communication, presentation, and interpersonal skills • Ability to engage credibly with senior clinicians and KOLs • Strategic thinking with strong execution capability • Working knowledge of pharmacovigilance and regulatory requirements Experience • Medical Affairs experience preferred for MBBS candidates • Fresh MD Pharmacology candidates may be considered • Exposure to field medical roles, scientific engagement, or clinical research is an advantage Procedure • Interested candidates to share updated CV • Shortlisted profiles will be contacted for further discussions and interviews Benefits • Opportunity to work with a leading global pharmaceutical organization • High-impact medical role in a priority therapy area • Strong learning, development, and career growth opportunities • Collaborative, science-driven work environment Apply / Connect • bushrahasankhan@drreddys.com
Roles & Responsibilities:• Assess and treat patients with neurological (stroke, Parkinson’s, facial palsy) and orthopedic (scoliosis, spinal stenosis, cervical issues) conditions• Develop and implement personalized physiotherapy treatment plans• Conduct hands-on assessments and monitor patient progress• Educate patients on exercises, posture correction, and preventive care• Maintain accurate patient records and follow clinical protocols• Collaborate with the physiotherapy team to ensure consistent, high-quality care• Adapt treatments based on patient needs and response to therapyQualification:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT)• Specialization or experience in neurological or orthopedic rehabilitation preferredExperience:• Relevant clinical experience in neuro or orthopedic physiotherapy preferredSkills:• Neuro and orthopedic assessment and treatment• Patient education and communication• Personalized treatment planning and progress monitoring• Teamwork and collaboration• Attention to detail and patient-focused care• Flexibility to work part-time or full-timeAbout the Company:Neurokine Personalised Physiotherapy Care, based in Ahmedabad, provides specialized physiotherapy services focused on neurological and orthopedic rehabilitation. The clinic emphasizes personalized care, hands-on assessment, and patient education, supporting professional growth and advanced skill development for physiotherapists while improving patients’ quality of life.