Pharmacy Jobs

Roles & Responsibilities • Author, review, and finalize aggregate safety reports including PSUR, PBRER, DSUR, and RMP • Perform signal detection, signal validation, and signal management activities • Ensure compliance with global regulatory requirements (ICH, GVP, FDA, EMA) • Collaborate with global safety, medical, and cross-functional teams • Maintain high-quality regulatory documentation within defined timelines • Support responses to health authority queries related to aggregate safety reports • Ensure consistency, accuracy, and scientific integrity of safety data Qualification • Graduate or Postgraduate in Life Sciences • B.Pharm / M.Pharm / PharmD / M.Sc or equivalent qualification Experience • Minimum 4+ years of hands-on experience in Pharmacovigilance • Strong experience in aggregate report authoring OR signal management activities • Experience working on global regulatory submissions preferred Skills • In-depth knowledge of pharmacovigilance regulations and guidelines • Expertise in aggregate safety reporting and signal management • Familiarity with global safety databases (preferred) • Strong medical writing, analytical, and documentation skills • Excellent communication and coordination abilities • Ability to work independently in a remote environment About the Organisation IQVIA is a global leader in Human Data Science, providing advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a strong global presence and focus on innovation, IQVIA supports pharmaceutical and biotech companies in improving healthcare outcomes worldwide.

Roles & Responsibilities • Coordinate and manage day-to-day clinical trial activities • Assist investigators during subject screening, enrollment, and follow-up visits • Maintain essential trial documentation in compliance with ICH-GCP guidelines • Ensure protocol adherence and accurate, timely data collection • Liaise with sponsors, CROs, ethics committees, and study stakeholders • Support monitoring visits, audits, and regulatory inspections • Ensure subject safety, data integrity, and ethical conduct of studies Qualification • M.Sc in Life Sciences • B.Pharm / M.Pharm • Nursing or other related healthcare disciplines Experience • Prior experience in clinical research or clinical trials preferred • Freshers with strong interest in clinical research are encouraged to apply Skills • Working knowledge of ICH-GCP and clinical trial regulations • Strong documentation and coordination skills • Good communication and organizational abilities • Attention to detail and ability to manage multiple tasks About the Organisation Siaram Research is a growing clinical research organization committed to ethical research practices, regulatory compliance, and scientific excellence. The organization provides a supportive and growth-oriented environment for professionals aiming to build a long-term career in clinical research and healthcare research coordination.Send your CV to: Shekhar@siaramresearch.com

Roles & Responsibilities • Coordinate day-to-day clinical operations activities • Support clinical research documentation and data handling • Assist in study coordination and internal team communication • Maintain accurate records and regulatory compliance documents • Collaborate with cross-functional clinical and operational teams • Track timelines and ensure operational processes are followed • Support ongoing clinical projects and reporting activities Qualification • Graduate or Postgraduate in Life Sciences or Pharmacy • PG Diploma / Certification in Clinical Research (preferred) Experience • 6 months to 1 year of experience in clinical operations or research • Freshers with relevant clinical research training or internship can apply • Immediate joiners will be preferred Skills • Strong communication and coordination abilities • Good documentation and MS Office skills • Attention to detail and organizational capability • Basic understanding of clinical research processes • Ability to work collaboratively in a team environment About the Organisation DPHS India is a growing healthcare and clinical research organization focused on delivering quality clinical operations and research support services. The organization provides hands-on exposure to real-world clinical projects and offers strong learning opportunities for professionals at the early stages of their clinical research careers.

Roles & Responsibilities • Ensure compliance with cGMP, GxP, EH&S, and regulatory guidelines • Complete SOP training and perform activities only after proper authorization • Manufacture and process batches as per BMR under supervision • Handle and transfer raw materials, semi-finished, bulk, and finished goods • Operate, clean, and maintain production equipment as per SOPs • Maintain GMP, hygiene, and cleanliness in production areas • Perform in-process checks and ensure accurate online documentation • Report deviations, incidents, and improvement suggestions through QMS • Conduct line clearance during product or batch changeovers • Monitor environmental conditions as per BMR and SOP requirements • Ensure calibration and preventive maintenance of equipment • Troubleshoot machine and process-related issues • Manage issuance, retrieval, and destruction of dies, punches, sieves, and bags • Attend cGMP, safety, hygiene, and on-the-job training programs • Support yield improvement, cost control, and efficient production operations • Carry out additional tasks assigned by the Production Head Qualification • Diploma in Pharmacy or B.Sc. (Science) Experience • 2–5 years of experience in pharmaceutical production • Hands-on exposure to Granulation, Compression, Coating, and Encapsulation Skills • Strong knowledge of GMP and regulatory compliance • Experience in solid oral dosage manufacturing operations • Equipment handling, documentation, and troubleshooting skills • Attention to hygiene, safety, and quality standards • Team collaboration and effective communication • Process improvement and problem-solving ability About the Organisation Lupin Limited is a leading global pharmaceutical company with a strong presence in branded and generic medicines. With manufacturing facilities that meet international regulatory standards, Lupin is committed to delivering high-quality, affordable healthcare solutions worldwide.

Roles & Responsibilities • Design and optimize bioconjugation strategies for Antibody-Drug Conjugates (ADCs) • Develop and evaluate linkers, payloads, and conjugation processes • Perform in-process analytical characterization including DAR, purity, and stability analysis • Handle purification and downstream processing using chromatography and filtration techniques • Conduct in-vitro biology work such as potency assays and mechanism-of-action studies • Collaborate closely across chemistry and biology teams for end-to-end ADC development • Maintain accurate documentation and support data interpretation and reporting Qualification • Master’s or PhD in Pharmacy, Biotechnology, Biology, Chemistry, or related disciplines Experience • 0–10 years of experience • Freshers with strong academic or research background are welcome • Industry or academic experience in ADCs, biologics, or oncology research is an advantage Skills • Knowledge of bioconjugation, ADC chemistry, or synthetic organic chemistry • Experience with monoclonal antibodies, protein handling, or cell culture techniques • Understanding of analytical characterization methods (DAR, purity, stability) • Familiarity with purification and downstream processing techniques • Ability to work at the chemistry–biology interface • Strong teamwork, problem-solving, and scientific communication skills About the Organisation Laurus Labs is a leading Indian pharmaceutical company with strong expertise in APIs, formulations, and advanced R&D, now expanding into Antibody-Drug Conjugates (ADCs) to deliver next-generation oncology therapies for patients in India and worldwide.

Role & Responsibilities • Develop, implement, and manage the Project Quality Plan from start to closeout • Plan and lead internal and external audits; track Non-Conformance Reports (NCRs) and close-out actions • Coordinate material testing, inspections, and submittals in line with project timelines • Oversee subcontractor prequalification, surveillance, and quality performance tracking • Ensure timely submission of test reports, Operations & Maintenance (O&M) manuals, and closeout documentation • Support commissioning and snagging processes to ensure quality at handover • Mentor and develop QA/QC team members, fostering a culture of quality excellence Qualification • QA/QC certification from a recognized body (preferred) Experience • 10+ years of quality assurance and control experience in construction or fit-out environments, including a senior role managing QA/QC systems on complex projects Skills • In-depth understanding of quality management systems, ISO standards, material specifications, and inspection/testing protocols relevant to interior fit-out works • Proven ability to implement and monitor project-specific quality plans, lead audits, manage NCRs, and ensure compliance with project and contractual requirements • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) • Familiarity with digital QA/QC platforms and reporting tools is a plus • Strong leadership, documentation, and stakeholder coordination skills • Experience with close-out documentation, T&C inspections, and consultant/subcontractor quality coordination • Ability to thrive under pressure and drive a culture of quality excellence across multi-disciplinary teams • Benefits: Medical insurance, perks & benefits as per labor law, annual air ticket About The Company • Confidential Company – A prominent player in the construction and interior fit-out industry, specializing in delivering high-quality projects. The company is committed to excellence in project execution, ensuring the highest standards of quality, safety, and compliance across its operations.

Role & Responsibilities • Check machine/line clearance and cleaning as per written approved procedures before the start of batch manufacturing/packaging processes • Ensure correct status labeling and identity labeling of production rooms, materials, and machines • Provide startup release for machine/line to begin manufacturing/packaging after ensuring all procedures are followed and there are no deviations from cGMP rules or written procedures • Collect samples of bulk, intermediate, or finished products and validation samples • Report any problem, deviation, or non-compliance that arises during work and before progression of the concerned issue Qualification • Bachelor’s degree in Pharmaceutical Science (preferred) or Science Experience • 2 - 4 years of experience in a similar position Skills • Very good understanding of cGMP rules and guidelines • Proficiency in the English language • Good computer skills • Strong interpersonal and communication skills About The Company • APEX Pharma – A renowned pharmaceutical company based in Egypt, specializing in the development, manufacturing, and distribution of pharmaceutical products.

Role & Responsibilities • Assist in developing brand plans aligned with the marketing strategy • Support promotional campaigns across digital, field, and events • Coordinate compliant marketing materials for promotional activities • Monitor brand performance, sales trends, and market data • Ensure brand consistency across all marketing channels • Collaborate with cross-functional teams to execute brand strategy Qualification • Bachelor of Business Administration (BBA) in Management Experience • 5 - 8 years of experience in brand management, preferably in the pharmaceutical or healthcare industry Skills • Strong knowledge of marketing strategies and brand management techniques • Experience with digital marketing and promotional campaigns • Ability to analyze sales trends, market data, and brand performance • Excellent communication and organizational skills • Proficiency in marketing tools and software About The Company • Oman Pharmaceutical Products (OPP) – A leading pharmaceutical company in Oman, specializing in the development, manufacturing, and marketing of pharmaceutical products.

Roles & Responsibilities • Operate and monitor plant equipment for solvent reaction and recovery processes • Execute production activities as per safety, quality, and GMP guidelines • Assist in day-to-day plant operations, routine maintenance, and troubleshooting • Maintain accurate documentation, batch records, and SOP compliance • Work in shift-based operations to meet production targets • Support team activities to ensure smooth and efficient manufacturing processes Qualification • B.Sc. (Chemistry), Diploma in Chemical Engineering / Diploma in Pharmacy • M.Sc. (relevant chemistry or pharma background) Experience • 0–2 years of experience in pharmaceutical production or plant operations • Freshers are encouraged to apply for Apprentice positions Skills • Basic knowledge of plant operations and manufacturing processes • Understanding of solvent handling, reactions, and recovery systems • Familiarity with GMP, safety standards, and SOPs • Good teamwork, documentation, and shift-working capability Walk-in Interview Details • Date: 2nd February 2026 • Time: 10:00 AM to 3:00 PM • Venue: Sun Pharmaceutical Industries Ltd, Plot No. 24/2 & 25, Phase IV, G.I.D.C., Panoli - 394116, Dist. Bharuch, Gujarat Documents to Carry • Recent passport-size photograph • PAN card copy and Aadhaar card • Educational mark sheets and certificates • Experience letter (if applicable) • Current CTC details, last 3 months’ salary slips, appointment letter About the Organisation Sun Pharmaceutical Industries Ltd is India’s No. 1 pharmaceutical company and a global leader, committed to delivering high-quality, affordable medicines through innovation, excellence, and world-class manufacturing practices.

Role & Responsibilities • Provide medical review, analysis, and guidance during the case handling and reporting cycle of Adverse Event (AE) and Adverse Reaction reports for investigational and marketed products • Conduct signal detection, analysis, evaluation, and ongoing safety surveillance activities • Provide medical guidance and input to Drug Safety Associates (DSAs) and specialists in the medical aspects of drug safety • Act as a pharmacovigilance representative and safety scientist • Maintain a good working knowledge of the Adverse Event profile of assigned products, labeling documents, data handling conventions, client’s guidelines, and international drug safety regulations • Ensure compliance with internal and regulatory timelines for adverse event reporting • Communicate and discuss issues related to the review process with the Project Manager • Interact with internal and external contacts to resolve issues • Attend and present client/cross-functional meetings with other stakeholders Case Report Medical Review • Perform medical review of cases according to client Standard Operating Procedures (SOPs) • Write Pharmacovigilance/Marketing Authorization Holder (MAH) comments and assess company causality • Assess seriousness and expectedness of reported events • Provide medical advice to the case processing team Qualification • MBBS or MD (Medical Doctor) Experience • Fresher or relevant experience in pharmacovigilance/Drug Safety is preferred Skills • Excellent interpersonal, verbal, and written communication skills • Client-focused approach to work • Flexible attitude with respect to work assignments and new learnings • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail • Strong knowledge of international drug regulations, including GCP (Good Clinical Practice) and GVP (Good Pharmacovigilance Practice) • Ability to assess the clinical relevance of medical data and interpret its clinical meaning About The Company • Parexel – A leading global provider of biopharmaceutical services, Parexel specializes in drug development and regulatory consulting. With a focus on high-quality services and innovative healthcare solutions, Parexel works with clients to ensure the safety and efficacy of drugs across the clinical development lifecycle.

Role & Responsibilities • Perform medical review and assessment of individual case reports of adverse events (AEs) and other safety information related to Sanofi products • Review and evaluate medical information from case reports, determining the causality assessment • Prepare detailed and thorough safety narratives • Participate in the medical evaluation of safety signals, risk management planning, and benefit-risk assessment • Respond to medical information requests from healthcare providers, patients, and regulatory authorities • Provide medical expertise and input to cross-functional teams, including regulatory affairs and clinical teams Qualification • Medical degree (MBBS, MD, or equivalent) • 3+ years of experience in pharmacovigilance, drug safety, or a related field Experience • Proven experience in reviewing adverse events, causality assessment, and preparing safety narratives • Familiarity with safety signal management and risk management strategies • Experience working with cross-functional teams in a pharmaceutical or biopharmaceutical company Skills • Medical review and evaluation of adverse events • Causality assessment and benefit-risk assessment • Strong understanding of safety information processing and reporting • Ability to respond to medical information requests and provide expertise to healthcare providers • Excellent communication and collaboration skills About The Company • Sanofi – A global biopharmaceutical company focused on human health. Sanofi is dedicated to discovering, developing, and distributing therapeutic solutions to improve the lives of people facing serious illnesses.

Role & Responsibilities • Prepare and quality-check aggregate reports such as Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Safety Update Reports (PSURs), and US Periodic Adverse Drug Experience Reports (PADERs) from aggregate data • Conduct signal detection-related analyses, including cumulative analyses, issue event analyses, and Signal Evaluation Reports • Review published literature and case listings, ensuring vigilance over important/designated medical events • Interact with client personnel to discuss potential signals and issues detected with products • Support the preparation and maintenance of Risk Management Plans (RMPs) • Follow-up with clients to obtain missing or incomplete information to resolve and clarify issues • Perform medical review of individual case safety reports (ICSRs) and narratives for Clinical Study Reports (CSRs) • Provide medical advice to drug safety scientists on the processing of ICSRs and CSR narratives • Maintain knowledge of the adverse event safety profile of assigned drugs, labelling documents, and client guidelines • Ensure compliance with global regulatory reporting obligations and internal timelines for report submissions • Maintain records in compliance with guidelines and Standard Operating Procedures (SOPs) Qualification • A degree in Medicine (MBBS) or a post-graduation qualification (MD), preferably in a clinical branch • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) • Strong ability to evaluate and interpret data, synthesize scientific information, and write concise and accurate medical text Experience • Experience in drug safety, pharmacovigilance, or regulatory reporting is preferred • Fluency in written and spoken English • Ability to work with web-based applications and proficiency in computer skills in Windows 10/Windows 7 Skills • Ability to make concise, accurate, and relevant synopses of medical text and data • Attention to detail and strong analytical skills • Typing and transcription accuracyAbout The Company • Continuum India – A leading contract research organization (CRO) trusted by global leaders in the pharmaceutical and healthcare industries. Continuum India specializes in providing comprehensive services in the domains of pharmacovigilance, regulatory affairs, evidence evaluation, and technology solutions.

Roles & Responsibilities • Dispense medications accurately in compliance with DHA regulations • Provide patient counseling on medication usage, dosage, and side effects • Ensure safe, effective, and patient-centered pharmaceutical care • Maintain prescription records and proper pharmacy documentation • Manage inventory, stock levels, and expiry control • Ensure adherence to pharmacy SOPs and quality standards • Deliver excellent customer service and professional support Qualification • B.Pharm / M.Pharm • Valid DHA License or DHA Eligibility Skills • Strong knowledge of medications and pharmacy practice • Good communication and patient-counseling skills • High level of accuracy, professionalism, and attention to detail • Customer-focused mindset About the Organisation Gaelan Pharmacy is a patient-focused healthcare provider committed to delivering high-quality pharmaceutical services, fostering professional growth, and maintaining excellence in pharmacy operations. 📩 Email your CV to: careers@gaelanmedical.com 📌 Subject: Application for Pharmacist

Roles & Responsibilities • Dispense medications accurately as per DOH guidelines • Counsel patients on proper medication usage and side effects • Ensure compliance with DOH regulations and pharmacy SOPs • Maintain prescription records and proper documentation • Manage inventory, stock control, and expiry monitoring • Coordinate with doctors and healthcare staff as required Qualification • B.Pharm / M.Pharm • Valid DOH License or Eligibility Skills • Good knowledge of pharmacy practice and medications • Strong communication and patient-handling skills • Attention to detail and accuracy • Willingness to work in Mussafah, UAE About the Organisation Confidential Company a reputed healthcare organization in Mussafah offering professional growth opportunities for licensed pharmacists. Interested candidates can send their CV via WhatsApp: 📞 +971543811998

Roles & Responsibilities • Dispense medicines as per prescriptions and ECHS guidelines • Maintain pharmacy stock, inventory records, and expiry control • Ensure compliance with Pharmacy Act and ECHS SOPs • Support medical officers and paramedical staff in polyclinic operations • Maintain proper documentation and patient records • Perform duties assigned by Officer-in-Charge, ECHS Polyclinic Qualifications • B.Pharm from a recognized institute OR • 10+2 (Science stream) from a recognized board and • Approved Diploma in Pharmacy recognized by Pharmacy Council of India • Registered as Pharmacist under the Pharmacy Act, 1948 • Minimum 3 years of relevant experience (for Diploma holders) Contract Period • 11 months for Civil candidates • 1 year for Ex-Servicemen (ESM) • Contract renewable for additional period based on performance, age limit, and ECHS norms Application Process • Submit application in prescribed format (available on official website) • Attach self-attested copies of educational qualifications, experience certificates, and medical fitness certificate (countersigned by SEMO/CMO) • Applications to be submitted in duplicate Last Date to Apply16-02-2026 Important Instructions • Candidates must bring original certificates, mark sheets, experience documents, discharge book (for ESM), PPO, service records, and 2 passport-size colour photographs at the time of interview • No TA/DA will be provided About the Organisation Ex-Servicemen Contributory Health Scheme (ECHS) provides comprehensive healthcare services to ex-servicemen and their dependents through a network of polyclinics across India.

Roles & Responsibilities • Support clinical research activities as per assigned role • Assist in data collection, documentation, and compliance activities • Follow SOPs, GCP guidelines, and regulatory requirements • Coordinate with internal teams for smooth study execution • Ensure accurate reporting and timely completion of assigned tasks Qualifications • Relevant degree in Pharmacy / Life Sciences / Clinical Research or related field Experience • 0 to 5 years of relevant experience • Freshers with strong interest in clinical research can apply Skills • Good communication and documentation skills • Basic knowledge of clinical research processes and guidelines • Attention to detail and ability to work in a team • Willingness to work full-time in an on-premise setup About the Organisation ADVITY Research is a clinical research organization focused on delivering high-quality research services, fostering talent, and building careers in the clinical research domain.

Roles & Responsibilities • Dispense medications accurately as per DHA guidelines • Counsel patients on proper use of medicines and possible side effects • Ensure compliance with pharmacy laws, regulations, and SOPs • Maintain proper documentation and prescription records • Manage inventory, stock control, and expiry tracking • Coordinate with doctors and healthcare staff when required Qualifications • B.Pharm / M.Pharm • DHA License or Eligibility (mandatory) Experience • Freshers or experienced candidates can apply Skills • Good knowledge of pharmacy practice and medications • Strong communication and patient-handling skills • Attention to detail and accuracy • Willingness to work in Dubai About the Organisation Confidential Company a reputed healthcare organization in Dubai offering professional growth opportunities for licensed pharmacists. Interested candidates can send their CV via WhatsApp: 📞 +971509590699

Roles & Responsibilities • Assist in regulatory documentation and compliance-related activities • Support preparation, review, and maintenance of regulatory submissions • Gain hands-on exposure to regulatory processes under expert guidance • Coordinate with internal teams for data collection and documentation • Support ongoing regulatory projects and new initiatives • Follow company SOPs and regulatory guidelines Qualifications • B.Pharm / M.Pharm / MD / BDS / BAMS / BHMS Skills • Strong interest in Regulatory Affairs • Good communication and documentation skills • Fluency in English, Hindi, and Marathi • Willingness to learn and adapt in a professional environment Additional Details • Working Days: Monday to Friday • Travel Allowance provided • Opportunity for payroll absorption for high-performing interns About the Organisation Agenome Research is a research-driven organization offering practical, real-world exposure in regulatory affairs, focused on developing skilled professionals through hands-on training and expert mentorship.

Role & Responsibilities • Lead and manage pharmacovigilance activities for drug safety • Evaluate and process adverse event reports to ensure regulatory compliance • Review and analyze safety data from clinical trials and post-marketing surveillance • Prepare and submit pharmacovigilance reports, including PSURs and DSURs • Provide safety expertise in interactions with regulatory authorities and health professionals • Collaborate with cross-functional teams to ensure compliance with global safety regulations • Mentor junior team members and contribute to continuous process improvements Qualification • MBBS/MD or equivalent medical degree Experience • 2-4 years of experience in Pharmacovigilance or Drug Safety • Hands-on experience with safety databases and ICSR processing Skills • Strong understanding of global pharmacovigilance regulations • Excellent communication and interpersonal skills • Ability to analyze and interpret clinical data • Detail-oriented with strong problem-solving skills • Ability to work collaboratively in a team-oriented environment About The Company • APCERLS – A global provider of pharmacovigilance and regulatory affairs services, dedicated to supporting the healthcare industry with innovative safety solutions and regulatory compliance across various therapeutic areas.