Pharmacy Jobs

Role & Responsibilities Perform medical review of individual case safety reports (ICSRs) from clinical trials, literature, spontaneous sources and regulatory authorities Ensure correct assessment of adverse events for seriousness, expectedness and listedness Review MedDRA coding for adverse events, medical history and concomitant medications Validate causality assessment and product role classification (suspect, concomitant, interacting) Review case narratives for medical accuracy, clinical coherence and regulatory completeness Draft and medically review aggregate safety reports including PSURs and PADERs Review Risk Management Plans (RMPs) and signal management documentation Support pharmacovigilance medical writing and regulatory submission activities Qualification MBBS or MD (preferably Pharmacology) OR PharmD or M.Pharm with drug safety medical writing experience Experience 2–4 years of experience in pharmacovigilance medical review or drug safety medical writing Hands-on exposure to PSURs, PADERs, DSURs, RMPs and signal management reports Skills Strong knowledge of pharmacovigilance regulations and safety reporting standards Proficiency in ICSR medical review and aggregate report writing Accurate use of MedDRA terminology High attention to clinical detail and documentation quality Strong written and verbal communication skills Good organizational and time management skills Working knowledge of MS Office tools About the Company MSN Group is a vertically integrated pharmaceutical company with strong capabilities across APIs, formulations and drug delivery systems. The company operates structured pharmacovigilance and regulatory compliance frameworks supporting global markets, with a strong R&D-driven focus on documentation quality, lifecycle safety management and regulatory excellence.

Role & Responsibilities • Dispense prescriptions accurately with correct dosage, labeling, and legal compliance • Counsel patients on medication use, side effects, and drug interactions • Coordinate with doctors and healthcare teams to clarify and optimize prescriptions • Manage inventory, ordering, storage, and controlled substance handling • Perform final checks on prepared medications and maintain patient records • Support immunizations and basic health screenings when applicable Qualification • B.Pharm or PharmD from a recognized institution • Valid state pharmacy license/registration Experience • Freshers and experienced pharmacists can apply Skills • Pharmacy dispensing and clinical knowledge • Patient counselling and communication • Inventory and controlled drug management • Documentation and regulatory compliance awareness • Basic computer and pharmacy software proficiency About the Company • Healthcare organization committed to delivering safe, ethical, and patient-centric pharmaceutical services through qualified professionals and standardized clinical practices

Key Responsibilities • Establish strategic growth plans, KPIs and performance roadmaps • Ensure strict compliance to hospital pharmacy policies & NABH standards • Manage high-value medicine consignment systems and vendor coordination • Handle internal & external audits and inventory risk mitigation • Maintain optimal stock levels and reduce wastage • Drive customer retention through superior pharmacy service • Evaluate, register and manage vendors • Streamline pharmacy processes and close operational gaps • Coordinate continuously with Quality department for compliance • Lead clinical pharmacy services and protocol implementation • Review medication therapy and improve patient safety • Provide drug information support to doctors and nursing teams • Supervise dispensing, compounding and documentation processes • Mentor clinical pharmacy team members • Participate in multidisciplinary patient care roundsKey Skills & Expertise • NABH Hospital Pharmacy Operations • Clinical Pharmacy & Medication Therapy Management • Inventory Optimization & Consignment Handling • Vendor Management • Audit & Compliance Management • Leadership & Team DevelopmentBenefits • Paid Time Off • Stable hospital environment • Leadership growth opportunityRole Overview We are hiring a Clinical & Hospital Pharmacy Manager to lead pharmacy operations, clinical pharmacy services, vendor management and inventory control while ensuring 100% NABH & quality compliance. This role combines strategic pharmacy leadership with hands-on clinical expertise and is ideal for experienced hospital pharmacists seeking growth into leadership positions.

Key Responsibilities • Manage daily OP, IP & OT pharmacy operations ensuring accurate, safe dispensing • Ensure complete NABH compliance and regulatory adherence • Conduct routine medication audits and documentation checks • Manage OT implants, surgical consumables and implant traceability • Supervise compounding, dispensing, labeling and packaging activities • Train, mentor and monitor pharmacy staff and interns • Ensure controlled drug storage, handling and disposal • Maintain inventory, stock levels and cost tracking systems • Educate patients and clinical staff on drug usage, interactions and storage • Ensure medication purity, strength and identity through routine checks • Maintain detailed pharmacy records and documentationEducation: B.Pharm (Mandatory) Experience: Minimum 5 years as Hospital Pharmacy Manager / In-charge Orthopaedic OT exposure preferred Skills & Knowledge: • NABH standards and audits • OT implants and surgical consumables • Hospital pharmacy compounding • Inventory & cost control • Leadership & staff supervision • Strong communication & documentation skillsBenefits • Provident Fund • Leave Encashment • Stable hospital environment • Career growth in NABH-accredited setupAbout the Company We are seeking a highly experienced Hospital Pharmacy Manager to lead OP, IP and OT pharmacy operations at Ortho-One. This role is critical in ensuring NABH compliance, medication safety, OT implant management and quality pharmacy service delivery across all patient care areas.

Role & Responsibilities • Dispense prescribed medications accurately to inpatients and outpatients • Ensure safe storage, handling and inventory control of medicines • Review prescriptions for dosage accuracy and drug interactions • Provide medication counselling to patients • Support clinical teams in safe medication use practices • Maintain pharmacy documentation and regulatory compliance • Perform night shift pharmacy operations from 9 PM to 9 AM Qualification • D.Pharm or B.Pharm from a recognized institution • Registered Pharmacist with State Pharmacy Council Experience • Freshers can apply • Prior hospital pharmacy experience preferred Skills • Knowledge of hospital pharmacy operations • Prescription review and dispensing accuracy • Inventory and stock management • Good communication skills • Attention to detail About the Company • Hospital-based pharmacist role focused on safe medication dispensing, night duty operations and direct patient care in a super speciality urology institute

Role & Responsibilities • Assist in laboratory operations related to forensic, scientific, and analytical activities • Support faculty and scientific officers during laboratory experiments and demonstrations • Maintain laboratory equipment, tools, and scientific instruments • Prepare samples, reagents, chemicals, and documentation as per laboratory protocols • Maintain proper records of laboratory usage, inventory, and consumables • Follow safety, hygiene, and compliance standards inside laboratories • Support practical sessions, research work, and forensic investigationsQualification • Bachelor’s Degree in any of the following: Physics, Mathematics, Botany, Zoology, Microbiology, Biotechnology, Physical Anthropology, Genetics, Chemistry, Biochemistry, Pharmacology, Pharmacy, Forensic Science or CriminologyAge Limit • Minimum: 18 Years • Maximum: 27 Years • Age relaxation for Government Servants up to 40 years as per Central Government normsTotal Vacancies • 24 Posts (UR – 12 | EWS – 02 | OBC – 06 | SC – 03 | ST – 01 | PwBD – 01 | Ex-Servicemen – 02)Skills • Basic laboratory handling and documentation • Understanding of scientific procedures and safety protocols • Equipment handling and inventory management • Good coordination and record maintenance skills • Attention to detail and compliance orientationAbout the Organization National Forensic Sciences University (NFSU) is an Institution of National Importance under the Ministry of Home Affairs, Government of India. NFSU plays a vital role in forensic science education, research, and technological development, supporting national security and criminal justice systems.Last Date: 18 January 2026

Role & Responsibilities • Dispense medicines as per prescriptions • Maintain medicine stock and expiry records • Store drugs under proper conditions • Maintain pharmacy registers and documentation • Assist doctors and nursing staff with medication requirements • Ensure proper labeling and patient counseling • Follow government health department guidelinesQualification • B.Pharm or D.PharmExperience • Freshers and experienced candidates can applySkills • Knowledge of medicines and dispensing • Inventory management • Basic computer skills • Attention to detailAbout the Organization District Health Society (DHS) Sivaganga operates public healthcare programs and hospital services to improve community health across Sivaganga district under Tamil Nadu Health Mission.Starting date31-12-2025Closing date19-01-2026Official NotificationClick HereApplication FormClick Here

Role & Responsibilities • Assist departments in technical and administrative functions • Support laboratory, engineering and academic operations • Perform assigned apprentice training activities • Maintain records, files and documentation • Follow institutional policies and safety protocolsQualification • Any Degree • B.Pharm • DiplomaExperience • Freshers are eligible • Training-based apprentice role Skills • Basic technical and analytical skills • Computer literacy • Communication and teamwork skills • Willingness to learn and follow procedureAge Limit • Minimum 21 years • Maximum 45 years • Age relaxation as per Government normsImportant Dates • Application Start – 29 December 2025 • Last Date – 19 January 2026Official NotificationClick Here

Role & Responsibilities Dispense medicines accurately as per physician prescriptions Maintain drug inventory, stock registers and expiry monitoring Ensure proper storage of medicines as per pharmaceutical standards Maintain pharmacy records and documentation Support smooth functioning of pharmacy services at ECHS Polyclinic Assist in medicine procurement and stock reconciliation Follow ECHS medical SOPs and quality standards Qualification B.Pharm OR 10+2 with Diploma in Pharmacy Must be registered as a Pharmacist Experience Minimum 3 years of experience as a PharmacistNumber of Vacancies: 17Tenure: One year (extendable based on performance) Salary: ₹36,500 per month Skills Knowledge of drug dispensing and inventory management Ability to maintain records and documentation Understanding of pharmaceutical storage and safety norms Good coordination and basic computer handling skillsAbout the Organization Ex-Servicemen Contributory Health Scheme (ECHS) functions under the Ministry of Defence, Government of India Provides comprehensive medical care to ex-servicemen and their dependents Operates ECHS Polyclinics across Delhi Cantt, Noida, Gurugram and nearby regions

Role & Responsibilities Perform end-to-end ICSR processing for AE, SAE and SUSAR cases Identify, triage and create cases in global safety databases Review source documents for validity and medical relevance Perform MedDRA and WHO-Drug coding Draft case narratives and E2B sender comments Manage follow-ups, reconciliations and regulatory timelines Support audits, inspections and pharmacovigilance projects Handle literature intake, mailbox monitoring and translations Qualification B.Pharm BSc Nursing Bachelor’s Degree in Life Sciences Experience 0–1 year (Freshers eligible) Skills Basic knowledge of pharmacovigilance and ICSR workflows Familiarity with MedDRA and WHO-Drug Good documentation and MS Office skills Strong English communication skills Ability to work in compliance-driven environmentsAbout the Company Accenture is a global professional services leader operating in over 120 countries Delivers technology-driven healthcare and life sciences solutions Provides structured career growth and global exposure in pharmacovigilance

Role & Responsibilities Perform end-to-end ICSR case processing Triage, prioritize and assess adverse event cases Conduct MedDRA and WHO-Drug coding Assess seriousness, causality and expectedness Draft narratives and sender comments Manage follow-ups, reconciliations and regulatory timelines Support inspections, audits and safety surveillance activities Handle literature review and mailbox management Qualification Bachelor of Ayurvedic Medicine and Surgery (BAMS) Bachelor’s Degree in Life Sciences Master’s Degree in Life Sciences Experience 1–3 years of pharmacovigilance experience Skills Strong knowledge of pharmacovigilance workflows Good command over MedDRA and WHO-Drug coding Medical writing and documentation skills Proficiency in MS Office tools Excellent communication and compliance orientationAbout the Company Accenture is a global professional services organization with large-scale life sciences operations Works with international clients and regulatory frameworks Offers long-term growth in drug safety and pharmacovigilance careers

Role & Responsibilities Coordinate and manage clinical trials at site level Support patient screening, recruitment and follow-up Ensure compliance with protocol, GCP and regulatory guidelines Maintain accurate source documents and trial records Coordinate with investigators, CRAs, sponsors and ethics committees Support site initiation, monitoring visits and audits Manage study data and timely reporting Qualification Bachelor’s degree in Life Sciences, Medical Sciences or related field OR Master’s degree in Life Sciences Experience 2–3 years of experience as a Clinical Research Coordinator Skills Strong knowledge of clinical trial operations Good understanding of GCP and site management Excellent communication and documentation skills Good organizational and coordination abilities Attention to detail and compliance-driven approach About the Company HRAPL is a clinical research organization focused on site management and trial execution Provides structured research support with strong compliance standards Offers long-term career growth in clinical research operation

Role & Responsibilities Prepare and submit new product registrations and post-approval variations Author and review CMC Modules 2 and 3 (eCTD format) Handle EU & CIS regulatory filings and agency queries Manage product lifecycle management (PLCM) activities Support new product launches, extensions, and tenders Ensure compliance with global regulatory guidelines Maintain regulatory tracking tools and documentation Coordinate with internal teams and health authoritiesQualification Bachelor’s degree in Pharmacy, Chemistry, or related disciplineExperience 2+ years of experience in CMC Regulatory Affairs Hands-on experience with EU regulatory submissionsSkills CMC Module 2 & 3 authoring eCTD documentation EU pharmaceutical regulations knowledge Strong documentation and regulatory writing skills Excellent communication and coordination skillsAbout the Company ClinChoice is a global clinical research and regulatory solutions organization Provides end-to-end regulatory, compliance, and clinical support to pharmaceutical and biotech companies Known for international regulatory submissions across EU and CIS regions

Role & Responsibilities Study Planning & Coordination Develop and maintain study trackers, dashboards, timelines and operational tools Coordinate logistics for investigator meetings, site communications and trial-related events Support study start-up activities including system access, document readiness and compliance checks Study Execution & Oversight Monitor global enrollment, data flow and quality metrics using dashboards and reports Support and lead assigned RBQM activities including risk assessment and mitigation planning Track study progress and resolve operational issues with Study Delivery Managers and vendors Support global recruitment and retention strategies Stakeholder & Site Engagement Serve as a key point of contact for routine study updates Collaborate with internal teams, CROs, vendors and investigator sites Identify, prioritize and escalate study risks in a timely manner Data, Systems & TMF Management Maintain accurate data in CTMS, eTMF and other clinical systems Support query resolution, reconciliation and data quality checks Ensure TMF inspection readiness and version-controlled documentation Process Improvement Contribute to process optimization, automation and best-practice sharing Support CAPA activities and implementation of lessons learned across studies Qualification Basic Qualifications Bachelor’s degree OR Associate degree with 4 years of clinical execution experience OR High School Diploma/GED with 6 years of clinical execution experience Preferred Qualifications Minimum 2 years of experience in life sciences or medically related field At least 1 year of biopharmaceutical clinical research experience Experience working on global clinical trials Hands-on knowledge of CTMS, eTMF, EDC and Microsoft Office tools Skills Strong understanding of clinical trial operations and compliance TMF filing and regulatory documentation knowledge Excellent coordination, communication and problem-solving skills High attention to detail and data accuracy Ability to work in global cross-functional teamsAbout the Company Amgen is a global biotechnology leader focused on developing innovative medicines that improve the lives of patients worldwide. With a strong commitment to science, quality, and patient safety, Amgen delivers breakthrough therapies across multiple therapeutic areas and supports world-class global clinical research operations.

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

Role & Responsibilities Assist in research activities related to development of nanostructured MoS₂ based SERS and FET biosensors Support experimental setup, data collection, analysis and documentation Perform laboratory work involving biosensors and nanomaterials Maintain laboratory records, reports and research documentation Assist Principal Investigators in project execution and reporting Follow laboratory safety procedures, SOPs and institutional research guidelines Qualification M.Sc / M.Tech / Master’s Degree in Pharmaceutical Sciences, Pharmacology, Biotechnology, Biosciences, Physics, Chemistry, Life Sciences, Nanoscience and Nanotechnology Candidates must have CSIR-UGC NET / GATE or national level qualifying examination Candidates without NET/GATE may also apply (lower fellowship applicable) Experience Minimum 1 year experience in nanoscience / nanotechnology preferred Skills Basic laboratory and analytical research skills Data documentation and reporting MS Office and scientific documentation Attention to detail and accuracy Ability to work independently and in a team Age Limit Maximum 50 years as on 12 January 2026 Age relaxation as per Government of India rules About the Project This DHR-ICMR funded research project focuses on development of nanostructured MoS₂ based SERS and FET biosensors for ultrasensitive detection of biomarkers for Cerebral Ischemia How to Apply Email the application form in prescribed format with self-attested copies of certificates, mark sheets and age proof to rehankhan@inst.ac.in Application must reach by 11 January 2026 Interview will be conducted online on 12 January 2026 at 02:30 PM

Role & Responsibilities Assist in research activities related to emerging pollutants and fingerprint analysis Support sample collection, preparation, and laboratory experimentation Perform analytical testing and documentation of experimental data Maintain laboratory records, reports, and project documentation Assist the Principal Investigator in research coordination and reporting Support data compilation, analysis, and presentation of project results Follow laboratory safety, SOPs, and institutional research guidelines Qualification Essential and desirable qualifications will be as per the detailed advertisement (Annexure I) Candidates must fulfill eligibility criteria specified by the funding agency (NMCG) Experience Research or laboratory exposure in pharmaceutical / environmental / analytical sciences preferred Skills Basic knowledge of laboratory techniques and analytical instruments Data recording and report preparation MS Office and computer documentation Attention to detail and research accuracy Ability to work in a team and follow SOPs Age Limit Maximum age as mentioned in the detailed advertisement Age relaxation for SC/ST/Physically Handicapped/Female candidates as per GoI rules About the Project This project is sponsored by the National Mission for Clean Ganga (NMCG) and focuses on the characterization of emerging environmental pollutants and fingerprint analysis to support clean water initiatives under Government of India programmes Selection & Preference SC/ST candidates will be preferred as per Government of India rules Appointment is strictly project-based and co-terminus with project duration

Role & Responsibilities Work in morning, evening and night rotational shifts Recruitment of study subjects Obtain written informed consent from parents/guardians Prepare drugs under laminar flow for neonatal clinical research Prepare and manage equipment required for study interventions Collect and maintain clinical and research data Coordinate with paediatric and ICU clinical care teams Support the Principal Investigator in project-related research activities Perform any additional duties assigned by the Principal InvestigatorQualification Graduate in Pharmacy (minimum 3 years) with 3 years of experience OR Postgraduate Degree in Pharmacy / Nursing OR B.Sc Nursing with 3 years of Clinical / ICU experienceExperience Experience in neonatal or paediatric clinical/ICU setup preferSkills Neonatal / paediatric clinical handling skills Drug preparation under laminar flow Working knowledge of data entry and computers Research data collection and documentation Coordination and communication with clinical teams Ability to work in rotational shiftsAbout the Company Guru Gobind Singh Medical College & Hospital, Faridkot is a constituent college of Baba Farid University of Health Sciences, Punjab. The institution is involved in ICMR-funded clinical research projects and provides opportunities to work in neonatal critical care research and evidence-based clinical trialsWalk-in Interview Details Date: 06 January 2026 Reporting Time: Before 10:00 AM Interview Time: 01:00 PM Venue: Principal Office, Guru Gobind Singh Medical College, Faridkot Selection Process: Written Test + Interview