Pharmacy Jobs

Role & Responsibilities: • Prepare, review, and finalize regulatory strategies for complex dosage forms including injectables, peptides, microspheres, liposomes, nano-suspensions, ophthalmic, otic, topical, and DDCP products for US and EU markets • Lead regulatory strategy and execution for 505(b)(2) products across US and EU regions • Draft, review, and finalize Pre-ANDA, Pre-IND, and Scientific Advice meeting packages for regulatory agency interactions • Prepare and manage controlled correspondences on complex regulatory issues • Draft, review, and finalize deficiency responses for complex and 505(b)(2) products • Review API and finished product in-vitro characterization and sameness reports • Perform DMF reviews for complex APIs as per established workflows • Collaborate closely with cross-functional teams to support development, filing, and approval activities • Ensure timely delivery and high-quality regulatory outputs aligned with management expectations • Provide regulatory guidance and training to team members on evolving requirements for complex products Qualification: • Master of Pharmacy (M.Pharm) or PhD in Pharmacy with specialization in Regulatory Affairs or Pharmaceutics preferred Experience: • Minimum 8-10 years of experience in Regulatory Affairs for injectable dosage forms • Overall professional experience of 12+ years in pharmaceutical regulatory functions Skills: • In-depth understanding of complex product regulatory strategies for US and EU markets • Strong experience in end-to-end regulatory activities including strategy, filing, and deficiency responses • Expertise in drafting controlled correspondences and regulatory meeting packages • Strong critical thinking, decision-making, and compliance judgment abilities • High level of ownership, accountability, and quality mindset • Ability to work effectively in cross-functional and matrix organizations • Collaborative, solution-oriented, and team-focused approach About the Company: Amneal Pharmaceuticals is a global pharmaceutical company committed to expanding access to affordable, high-quality medicines across a broad range of therapeutic areas. As an equal opportunity employer, Amneal values diversity, inclusion, and integrity, fostering a workplace culture that encourages collaboration, innovation, and regulatory excellence while upholding the highest standards of quality and compliance.

Role & Responsibilities: • Support and manage regulatory activities related to Chemistry, Manufacturing, and Controls (CMC) for licensed and clinical biologic products • Provide regulatory strategy input to product development teams and offer guidance to commercial and clinical stakeholders • Ensure regulatory strategies are aligned with global Health Authority requirements and submissions are completed on time with high quality • Coordinate with global manufacturing sites to align regulatory strategies and communicate key updates to senior management • Provide regulatory support for additional CMC-related projects as required • Prepare agency consultation packages, briefing documents, and presentations for regulatory interactions • Engage with regulatory agencies for consultations, responses, and clarifications • Manage regulatory filing activities including query responses, variations, and post-approval changes for global products • Conduct regulatory reviews as per US and EU requirements and communicate additional data requirements to cross-functional teams Qualification: • Master of Pharmacy (M.Pharm) from a recognized institution Experience: • 2-4 years of experience  Skills: • Strong knowledge of CMC regulatory requirements and global regulatory frameworks • Experience with regulatory submissions, agency interactions, and post-approval changes • Understanding of US FDA and European Medicines Agency requirements • Strong coordination and stakeholder management skills • Excellent written and verbal communication abilities • Ability to work in a cross-functional and global environment About the Company: Sun Pharma is a leading global pharmaceutical company committed to helping employees “Create their own sunshine” by fostering a culture of continuous growth, self-driven leadership, and collaboration. With a focus on innovation, quality, and global healthcare impact, Sun Pharma provides an empowering environment where individuals grow stronger every day, take charge of their careers, and thrive together as a community.

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: • Prepare, compile, and submit regulatory dossiers for pharmaceutical export registrations to global regulatory authorities • Maintain CTD/eCTD documentation for product registrations, renewals, variations, and post-approval changes • Ensure compliance with international regulatory requirements and current guidelines across export markets • Act as a liaison with regulatory agencies, export authorities, and external consultants for submission queries and follow-ups • Coordinate with internal teams including QA, QC, Production, R&D, and Supply Chain to collect required technical documentation • Track submission timelines, monitor status, and respond to deficiency letters within defined timelines • Maintain organized regulatory databases, files, and documentation as per regulatory and company standards • Provide regulatory intelligence on evolving global regulations impacting pharmaceutical exports • Support labeling, packaging, and artwork compliance as per importing country requirements Qualification: • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, or a related discipline Experience: • 1-4+ years of experience in pharmaceutical regulatory affairs • Preferable exposure to export regulatory submissions and international markets Skills: • Strong knowledge of global regulatory frameworks and export documentation requirements • Hands-on experience with CTD/eCTD dossier preparation and submission tracking • Familiarity with electronic submission systems and regulatory agency portals • Excellent communication, coordination, and stakeholder management skills • Strong organizational ability and attention to detail • Good command of written and spoken English About the Company: The organization operates within the pharmaceutical sector, supporting global product registrations and export compliance across multiple international markets. It emphasizes regulatory excellence, cross-functional collaboration, and adherence to global quality and compliance standards to ensure timely product approvals and sustainable business growth.

Role & Responsibilities: • Assist Clinical Project Managers with day-to-day project administration including preparation of project documents, review of presentations, and participation in internal and client meetings and calls • Act as a liaison between cross-functional teams to ensure timely completion of study milestones and deliverables • Support project start-up, execution, and close-out activities, including finance-related tasks such as invoice reconciliation, budget tracking, and forecasting support • Monitor project progress, track outstanding action items, and respond to internal and client inquiries • Communicate project updates to stakeholders and support issue resolution to maintain project timelines • Serve as acting Project Manager when required under supervision • Verify imaging protocol requirements and ensure queries are reviewed, addressed, and resolved appropriately • Support logistics coordination including materials distribution and tracking • Ensure compliance with SOPs, GCP, ICH, FDA regulations, and quality standards • Contribute to process improvement initiatives and maintain project documentation accuracy • Participate in trainings, team meetings, and perform additional duties as assigned Qualification: • Associate’s degree from a recognized institution • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or related field- preferred Experience: • Minimum 1 year of experience in pharmaceutical drug development, clinical trials, clinical research, or clinical imaging studies • Experience supporting project management activities in a clinical research environment is an advantage Skills: • Strong working knowledge of Microsoft Office tools • Understanding of clinical research, healthcare, or medical imaging processes • Experience with imaging protocols, data verification, and query resolution is desirable • Excellent organizational, interpersonal, and communication skills • Strong attention to detail with the ability to manage multiple tasks • Ability to work independently as well as collaboratively in a team environment • Adaptable, proactive, goal-oriented, and responsive to changing priorities • Professional and positive attitude in all interactions About the Company: Clario is a global leader in medical imaging and clinical trial endpoint technologies with over 30 years of expertise in delivering secure, compliant, and innovative solutions that enhance clinical research. The company partners with pharmaceutical and biotechnology organizations worldwide to unlock better evidence and accelerate the development of life-changing therapies, empowering teams to make a meaningful impact on patient lives every day.

Role & Responsibilities: • Dispense prescription medications accurately and efficiently in accordance with prescriptions and standard operating procedures • Review prescriptions for appropriateness, dosage accuracy, and potential drug interactions • Maintain accurate and up-to-date patient medication profiles and pharmacy records • Oversee inventory management including stock monitoring, ordering, storage, and expiry control • Ensure compliance with applicable pharmacy laws, regulations, quality standards, and company policies • Maintain statistical, operational, and financial pharmacy records • Support safe medication practices and ensure patient safety at all times • Provide clear medication counseling and respond to patient queries professionally • Coordinate with internal teams to ensure smooth pharmacy operations • Work effectively in a fast-paced environment while managing multiple tasks • Be flexible to work in shifts as per business requirements Qualification: • Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) / Pharm.D from a recognized institution • Active and valid Pharmacy license in Telangana – mandatory Experience: • Freshers or candidates with relevant pharmacy experience are welcome • Experience in hospital, retail, or healthcare service environments is an advantage Skills: • Strong knowledge of pharmaceuticals, pharmacology, and pharmacy operations • Excellent attention to detail and accuracy • Good communication and interpersonal skills • Ability to multitask and work efficiently under pressure • Customer-focused approach with commitment to quality service • Basic computer and record-keeping skills About the Company: Saince HealthTech (SHT) is the India subsidiary of Saince Inc., USA, an award-winning healthcare solutions provider with a 95% customer satisfaction rating among hospitals and physicians. Headquartered in Hyderabad, SHT supports healthcare organizations across the United States and has been recognized as one of the fastest-growing private companies in the nation. The company is committed to innovation, quality, and excellence in healthcare delivery while offering a supportive and growth-oriented work environment.

Role & Responsibilities: • Attend doctor’s prescriptions at the sales counter and advise patients on the correct dosage and usage of medicines • Dispense medicines accurately as per prescriptions and arrange unavailable medicines from in-house pharmacies to ensure complete prescription fulfillment • Consult doctors before substituting any prescribed medicines • Cross-check medicines with billing details including patient name, medicine name, quantity, batch number, expiry date, and MRP • Counsel patients and customers on medication usage, possible reactions, and general health guidance • Maintain strong professional relationships with customers and doctors • Maintain records for free home delivery and ensure timely follow-up and execution • Handle inbound calls related to drug information, patient counseling, education, and home delivery orders • Address patient queries and concerns related to drug therapy and medication information • Handle cash transactions at the billing counter when required • Ensure proper storage of drugs under recommended refrigeration and security conditions (cold chain management) • Enter stock details into the system and reconcile with issued stock from stores • Maintain out-of-stock records and coordinate timely replenishment • Perform physical stock verification by category twice weekly and daily rack-wise checks for fast-moving items • Ensure proper shift handover and takeover procedures • Focus on sales generation and achievement of pharmacy targets • Manage billing activities and perform additional tasks as assigned by the in-chargeQualification: • D.Pharm / B.Pharm / M.Pharm from a recognized institution • Registered with the Pharmacy Council of India (PCI)- mandatoryExperience: • Freshers or candidates with relevant retail pharmacy experience up to Supervisor levelSkills: • Strong knowledge of commercial and prescription drugs • Excellent prescription interpretation and dispensing skills • Patient counseling and drug information skills • Good interpersonal and communication abilities • Basic computer and billing system knowledge • Customer-focused approach and attention to detailAbout the Company: Apollo Pharmacy is one of India’s largest and most trusted pharmacy retail chains, committed to delivering high-quality healthcare products and services across the country. The organization places strong emphasis on patient safety, customer satisfaction, and professional excellence while offering on-roll employment, competitive compensation, benefits, and attractive performance-based incentives.

Role & Responsibilities: • Perform end-to-end Pharmacovigilance case processing activities including case identification, data entry, MedDRA coding, case quality review, submission, follow-up, and case closure for Individual Case Safety Reports (ICSRs) • Review and assess adverse event reports from various data sources such as clinical trials, spontaneous reports, literature, and post-marketing surveillance • Ensure accurate and timely processing of safety cases in compliance with client SOPs, global regulatory requirements (ICH, GxP), and timelines • Perform medical review support activities including seriousness, expectedness, causality assessment, and narrative writing as per guidelines • Ensure data quality, consistency, and completeness in the safety database • Support regulatory submissions to health authorities within defined timelines • Collaborate with internal teams, supervisors, and quality teams to resolve routine issues and discrepancies • Follow established processes, work instructions, and quality standards • Manage individual workload efficiently and meet productivity and compliance targets • Participate in training sessions and process improvement initiatives • Work as an individual contributor within a team environment; role may require rotational shiftsQualification: • Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) from a recognized institutionExperience: • 1-3 years of experience in Pharmacovigilance Operations, Drug Safety, or related Life Sciences roles • Experience in ICSR processing and safety database handling preferredSkills: • Pharmacovigilance Operations • Drug Safety Surveillance • ICSR Case Processing • MedDRA Coding • Adverse Event Reporting • Regulatory Compliance (ICH, GxP) • Safety Database Management • Attention to detail and analytical skills • Good written and verbal communication skills • Ability to follow SOPs and work instructionsAbout the Company: Accenture is a global professional services company with leading capabilities in digital, cloud, and security, combining unmatched experience and specialized skills across more than 40 industries. Accenture provides Strategy and Consulting, Technology and Operations services.

Role & Responsibilities • Dispense medications accurately and review prescriptions • Provide patient counselling on medication usage, dosage, and side effects • Ensure compliance with DHA regulations and pharmacy SOPs • Maintain inventory control and proper storage of medicines • Maintain accurate pharmacy records and documentation Qualifications & Experience • Bachelor’s degree in Pharmacy • Valid DHA Pharmacist License • 1–2 years of pharmacy experience Skills • Good knowledge of medicines and pharmacy regulations • Strong communication and customer service skills • Attention to detail and documentation accuracy About the Company • Aston Pharmacy is a community pharmacy in the UAE providing safe and quality pharmaceutical careHow to Apply • WhatsApp your CV to: +971 54 710 4399 • Email: contactus@astonpharmacy.ae

Role & Responsibilities • Dispense medications accurately and provide patient counselling • Ensure compliance with pharmacy regulations and safety standards • Manage inventory and maintain proper documentation • Deliver high-quality customer care and service excellence • Support daily pharmacy operations Qualifications & Experience • DHA / MOH license or eligibility •Bachelor of Pharmacy(B.Pharm) / Master of Pharmacy (M.Pharm) Skills • Strong communication and customer service skills • Multilingual communication abilities • Attention to detail and compliance awareness About the Company • Aster Pharmacy is a leading healthcare retail pharmacy chain delivering quality medicines and patient-centred care across the regionShortlisted candidates will receive venue details via email by 14th January 2026.Interview Details Date: Saturday, 17th January 2026

Key Roles & Responsibilities: • Oversee and coordinate all pharmacy operations, including medication preparation, dispensing, and storage • Ensure compliance with hospital policies, pharmaceutical regulations, and statutory requirements • Supervise, train, and manage pharmacy staff to maintain high operational standards • Maintain accurate prescription records and pharmacy documentation • Monitor and control medicine inventory, including procurement, storage, and stock audits • Ensure proper handling of high-risk and oncology-related medications • Collaborate with doctors, nurses, and healthcare professionals to provide medication-related guidance • Promote patient safety through effective pharmaceutical care and medication management practices • Implement and monitor standard operating procedures (SOPs) within the pharmacy Qualification: • B.Pharm / Pharm.D from a recognized institution • Active pharmacist license (mandatory) Experience: • Prior experience in a supervisory or management role in a hospital or medical setting (preferred) • Strong background in hospital pharmacy operations Skills: • Strong knowledge of pharmacology, drug interactions, and medication safety • Inventory and supply chain management skills • Leadership and staff management abilities • Knowledge of regulatory and compliance standards for hospital pharmacies • Proficiency in pharmacy documentation systems and relevant software tools • Excellent communication, coordination, and decision-making skills About the Company: Kailash Cancer Hospital is a specialized healthcare institution dedicated to providing comprehensive cancer care. The hospital emphasizes patient safety, quality treatment, and professional excellence, supported by a skilled multidisciplinary healthcare team.

Role & Responsibilities: • Deliver undergraduate and postgraduate lectures in Pharmaceutical Sciences • Develop and implement effective teaching plans and academic activities • Guide and mentor students in academic and professional development • Conduct assessments, evaluations, and examinations as per university norms • Participate in curriculum development and academic planning • Engage in research, publications, and academic enhancement activities • Contribute to departmental meetings, accreditation, and institutional initiatives • Adopt modern teaching methodologies and educational technologies Qualification: • B.Pharm and M.Pharm from a recognized institution (mandatory) • Valid Pharmacy Council registration (mandatory) Experience: • 2-3 years of teaching or relevant academic experience in Pharmaceutical Sciences Skills: • Strong command over core pharmaceutical subjects • Effective communication and presentation skills • Student mentoring and academic guidance • Research orientation and academic writing skills • Familiarity with modern teaching tools and methodologies • Commitment to continuous improvement and academic excellence About the University: • Rama University is a reputed institution committed to providing quality education and fostering academic excellence, innovation, and professional development in the field of Pharmaceutical Sciences.

Role & Responsibilities: • Plan, prepare, review, and execute qualification protocols for plant equipment • Coordinate and review all third-party calibration activities across the plant • Review process validation protocols and ensure compliance with regulatory expectations • Prepare and compile process validation reports with accurate data analysis • Prepare qualification and validation protocols and reports for HVAC and Water Systems • Conduct risk assessments for products and equipment • Perform sampling and collection of validation samples • Execute hold time studies including protocol preparation and sample collection • Prepare and review Annual Product Review (APR) documentation • Initiate, evaluate, and close change controls, CAPA, and risk assessments for products and equipment • Handle and oversee cleaning validation activities • Support audits and inspections related to validation and qualification Qualification: • B.Pharm or M.Sc from a recognized institution Experience: • 8-12 years of experience in Quality Assurance, Validation, and Qualification within the pharmaceutical industry Skills: • Equipment Qualification & Validation • Process, Cleaning & Hold Time Validation • HVAC & Water System Qualification • Risk Assessment & CAPA Management • Change Control & GMP Compliance • Documentation & Regulatory Readiness • Strong Analytical & Coordination Skills About the Company:• Sun Pharma Laboratories Ltd is a leading global pharmaceutical company committed to quality, innovation, and compliance, offering a collaborative environment where employees grow, take ownership, and thrive together.

Role & Responsibilities: • Coordinate and respond to analytical queries received from regulatory agencies for US, OAM, and EM markets • Ensure timely inputs from Analytical Development to Regulatory teams for agency responses • Revise specifications and Standard Test Procedures (STP) in line with regulatory query responses • Review pharmacopoeial updates from IP, USP, BP, and EP on a regular basis • Perform gap assessments for pharmacopoeial changes and share impact analysis • Evaluate pharmacopoeial changes and revise related specifications and STPs accordingly • Review and release excipient specifications and STPs for new development, LCM, and market extension projects • Manage excipient reviews for new projects and lifecycle management (LCM) activities • Prepare analytical specifications, Analytical Test Procedures (ATP), and STPs for: – New drug products and APIs – Vendor additions and updates – Pharmacopoeial updates – Lifecycle changes • Provide analytical support to FRD, Regulatory Affairs, AD, and manufacturing plants • Review vendor documentation for outsourced APIs • Track multiple documents under review and approval with cross-functional stakeholders to ensure timely release Qualification: • M.Pharm or M.Sc (Analytical / Pharmaceutical Sciences preferred) Experience: • 3–8 years of relevant experience in Analytical Development within the pharmaceutical industry Skills: • Analytical Development & Documentation • Pharmacopoeial Compliance (IP, USP, BP, EP) • Regulatory Query Management • Specification & STP / ATP Preparation • Lifecycle Management (LCM) Support • Cross-functional Coordination • Attention to Detail & Time Management About the Company: • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company and a leading global specialty generics organization, committed to quality, innovation, and regulatory excellence while fostering a culture of growth, ownership, and collaboration.

Role & Responsibilities: • Perform triage and initial validity assessment of cases including spontaneous, health authority, clinical trial, and literature cases • Enter and process safety data in pharmacovigilance databases • Conduct initial ICSR assessment, where applicable • Evaluate the need for expedited reporting to health authorities and client partners, ensuring adherence to reporting timelines • Prepare standard safety reporting forms such as CIOMS I, MedWatch forms, and XML files • Prepare and send follow-up requests to obtain missing or additional case information • Submit ICSRs to health authorities and client partners • Complete case documentation in line with project and regulatory requirements • Conduct quality checks on ICSRs to ensure accuracy, completeness, and compliance with industry standards • Perform ICSR search and retrieval from EVWEB database and conduct company vs non-company case assessment • Manage case allocation and workload to meet productivity and quality targets • Provide system and process training to team members • Mentor and support new joiners by guiding them on company processes and fostering a collaborative learning environment • Perform additional responsibilities as assigned by the supervisor in line with process requirements Qualification: • Degree in Pharmacy, Life Sciences, Medicine, or related field Experience: • Relevant experience in Pharmacovigilance / Drug Safety preferred Skills: • ICSR Processing & Case Management • Pharmacovigilance Databases (e.g., EVWEB or similar) • Regulatory Reporting & Compliance • Quality Review & Documentation • Attention to Detail & Analytical Skills • Communication & Team Collaboration About the Company: • Cencora is a global healthcare solutions organization committed to creating healthier futures by improving access to medicines, enhancing patient safety, and supporting pharmaceutical innovation worldwide.

Role & Responsibilities: • Dispense prescription and over-the-counter medications accurately • Assist customers with medication-related queries and provide appropriate guidance • Review prescriptions for correctness, dosage, and potential drug interactions • Ensure compliance with all pharmacy laws, regulations, and hospital policies • Maintain accurate records of medications dispensed and prescriptions filled • Manage inventory levels and ensure proper storage of medicines • Support smooth pharmacy operations in a fast-paced environment Qualification: • Graduate or Diploma in Pharmacy from a recognized institution Experience: • 1–2 years of experience as a Pharmacist preferred • Freshers with strong subject knowledge may also be considered Skills: • Strong knowledge of medications, dosages, and drug interactions • Excellent communication and customer service skills • Attention to detail and accuracy • Ability to work efficiently in a fast-paced environment About the Company: • Medizin, Swastha Hospital is a healthcare organization committed to providing reliable medical services and patient-centric care with a focus on quality, safety, and professionalism.

Role & Responsibilities: • Dispense prescription medications accurately in compliance with legal and professional standards • Review prescriptions for correctness, potential drug interactions, allergies, and contraindications • Provide patient counseling on medication usage, dosage, side effects, and storage • Monitor drug therapy and recommend modifications when required • Maintain accurate patient records and pharmacy documentation • Supervise pharmacy technicians and support staff • Ensure compliance with pharmacy laws, regulations, and safety protocols • Manage inventory, storage, and safe handling of medications • Participate in health promotion, disease prevention, and wellness initiatives • Collaborate with physicians, nurses, and other healthcare professionals Qualification: • B.Pharm (Bachelor of Pharmacy) or Pharm.D (Doctor of Pharmacy) from a recognized institution • Valid Pharmacist license/registration with the appropriate regulatory authority Experience: • Freshers or candidates with 1–2 years of relevant experience can apply Skills: • Strong knowledge of pharmacology and therapeutic guidelines • Patient counseling and communication skills • Attention to detail and ethical practice • Pharmacy operations and documentation • Ability to work independently and in a multidisciplinary healthcare team Preferred Skills: • Experience in hospital, retail, or clinical pharmacy settings • Proficiency in pharmacy management systems and electronic health records • Strong organizational and problem-solving abilities • Ability to handle confidential information responsibly About the Company: • Bhagwan Mahaveer Jain Hospital is a reputed healthcare institution committed to delivering high-quality medical services with a strong focus on patient safety, ethical practices, and comprehensive care.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Ensure medical accuracy, completeness, and regulatory compliance of safety cases • Apply clinical judgment for case assessment, seriousness, causality, and expectedness • Support global pharmacovigilance and regulatory reporting activities • Ensure adherence to GVP, ICH guidelines, and internal SOPs Qualifications & Experience • MBBS / MD with valid MCI registration • Minimum 1 year of hands-on experience in ICSR medical review Skills • Strong knowledge of pharmacovigilance and clinical terminology • Understanding of regulatory reporting requirements • Good analytical and documentation skills About the Company • Indegene is a global life sciences solutions provider delivering pharmacovigilance, medical affairs, and regulatory services across worldwide markets

Role & Responsibilities • Perform case intake and processing of Individual Case Safety Reports (ICSRs) • Handle Adverse Event (AE) and Serious Adverse Event (SAE) data • Code medical terms using MedDRA and WHO-DD • Perform quality checks on safety case data • Support global drug safety and compliance activities • Work on post-marketing surveillance and COVID-related safety data • Ensure adherence to ICH-GCP, GVP, and regulatory timelines Qualifications & Experience • B.Pharm, M.Pharm, BSc / MSc Life Sciences • Freshers with internship or project exposure in Pharmacovigilance, Clinical Research, Drug Safety, or COVID safety projects Skills • Basic understanding of pharmacovigilance concepts • Good communication and documentation skills • Willingness to work in rotational shifts About the Company • Accenture supports global pharmaceutical clients through structured pharmacovigilance and drug safety operations, offering corporate exposure and stable career growth