Pharmacy Jobs

Role & Responsibilities • Review, evaluate, and verify medication orders for accuracy, appropriateness, interactions, and patient parameters • Prepare, compound, and dispense medications as per hospital standards • Provide patient counselling on medication use, side effects, and interactions • Document clinical interventions in the electronic health information system • Maintain control and security of medications including controlled and narcotic drugs • Provide drug information support to healthcare professionals • Supervise and guide junior pharmacists, trainees, and students • Participate in quality improvement and performance projects • Follow hospital policies, SOPs, and regulatory procedures • Participate in training and professional development activities Qualification • Bachelor’s Degree in Pharmacy / Master’s Degree in Pharmacy / Pharm.D Experience • 2 years with Master’s Degree • 4 years with Bachelor’s Degree / Pharm.D Skills • Clinical pharmacy operations • Prescription validation and medication safety • Patient counselling • Drug interaction assessment • Documentation and HIS handling • Team supervision and coordination About the Company • King Faisal Specialist Hospital & Research Centre (Gen. Org.) • One of Saudi Arabia’s leading tertiary care hospitals • Provides advanced clinical care, research, and academic healthcare services

Role & Responsibilities • Dispense medications as per prescriptions • Provide patient counselling on medicine usage and safety • Ensure compliance with clinic pharmacy standards • Maintain pharmacy records and stock control • Support clinical team with medication-related guidance Qualification •Bachelor of Pharmacy (B.Pharm) / Doctor of Pharmacy (PharmD) / Master of Pharmacy   (M.Pharm) • MOH Oman License (Mandatory) Experience • 3+ Years Clinical pharmacy experience preferred Skills • Patient counselling • Prescription validation • Medication safety practices • Inventory and stock management • Good communication skills About the Company • Hiring through Thashkeel Business Consultancy • Reputed clinic based in Sohar, Oman • Offers competitive salary with accommodation and stable clinical work environment📞 WhatsApp / Call: +91 89212 66205 📧 Email: cv@thashkeelindia.com

Role & Responsibilities Dispense medicines as per prescriptions Maintain drug inventory and stock registers Ensure proper storage of medicines Counsel patients on medication usage Follow government pharmacy SOPs Qualification B.Pharm D.Pharm Experience Freshers and experienced candidates can apply Skills Prescription handling Drug dispensing and storage Inventory management Patient counselling About the Company District Health Society (DHS), Pudukkottai Government public healthcare organization Operates primary and secondary healthcare facilitiesStarting date05-01-2026Closing date18-01-2026Official NotificationClick HereApplication FormClick Here

Role & Responsibilities • Manage and execute ICSR regulatory submissions for clinical and post-marketing products • Perform global safety submissions within regulatory timelines • Handle case processing and submissions in ARGUS Safety database • Review AE data and local labeling for accurate scheduling • Monitor submission workflows and resolve pending or failed submissions • Perform major corrections and case distribution • Ensure compliance with global PV regulations, SOPs, WRKs, MANs, and BEDs • Maintain submission tracking and documentation • Identify data gaps and quality issues Qualification • B.Pharm or M.Pharm Experience • 1–4 years in Pharmacovigilance Submission • Experience with ARGUS, ICSR processing, and global regulatory reporting Skills • ARGUS Safety handling • ICSR submissions and distribution • Medical terminology and clinical interpretation • Quality control in PV • Documentation and workflow monitoring • Strong organizational and communication skills About the Company • A leading ITES organization hiring through Outpace Consulting Services • Focused on global pharmacovigilance and regulatory compliance • Provides exposure to international safety submissions and structured compliance processes

Role & Responsibilities • Assist in daily clinical trial coordination activities • Support patient screening, enrollment, and follow-ups • Maintain trial documentation and source records • Ensure compliance with ICH-GCP guidelines and study protocols • Coordinate with investigators, sponsors, and study teams • Assist in data collection and query resolution • Support monitoring visits and audit preparedness Qualification • Any Life Science Graduate (BSc, MSc, B.Pharm, M.Pharm, Biotechnology, Microbiology, etc.) Experience • Freshers only Skills • Basic understanding of clinical research and GCP • Documentation and record-keeping • Good communication skills • Willingness to work on-site • Interest in clinical trials About the Company • Quinoa Clinical Solutions is an emerging clinical research organization • Provides entry-level exposure to clinical trial coordination • Offers mentorship, hands-on learning, and long-term career growth opportunities

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 safe and effective pharmaceutical care to inpatients and outpatients Dispense, review and verify medication orders in accordance with hospital policies Participate in multidisciplinary healthcare teams to optimise patient therapy Conduct medication reconciliation and clinical screening Support weekend, public holiday and on-call pharmacy rosters as required Rotate across Angliss Hospital, Wantirna Health and Peter James Centre after training Maintain accurate pharmacy documentation and patient records Participate in clinical education, training and practice-based research activities Support quality improvement and medication safety initiatives Qualification Bachelor of Pharmacy / Master of Pharmacy Registered or eligible for registration as a Pharmacist in Australia Experience Freshers and community/private sector pharmacists can apply No prior hospital experience required (onsite training provided) Skills Strong clinical and dispensing knowledge Good communication and multidisciplinary team collaboration skills Commitment to patient safety and clinical excellence Willingness to work rotational shifts including weekends and public holidays About the Company Eastern Health is one of Melbourne’s largest public health services, providing emergency, surgical, medical and general healthcare services across multiple hospital campuses. It is recognised for its strong culture of learning, professional development, and practice-based research, delivering high-quality, patient-centred care to diverse communities under its “Healthier Together” promise.

Role & Responsibilities Dispensing prescribed medicines accurately to patients Charging prescriptions and handling cash collections Maintaining dispensing records and pharmacy documentation Managing day-to-day pharmacy operations Supporting inventory handling and stock maintenance Performing additional duties as assigned by the department Qualification D.Pharm / B.Pharm Must be registered with Tamil Nadu State Pharmacy Council Mandatory completion of 1 year traineeship in Department of Pharmacy Only Regular mode candidates are eligible (Private/Correspondence not accepted) Experience Traineeship completed (mandatory) Age Limit Below 30 years Skills Typing and basic computer operation Good record-keeping and documentation skills Attention to detail and accuracy Basic patient interaction and communication skills

Role & Responsibilities • Maintain accurate, complete and inspection-ready Trial Master Files • Review and approve TMF documents for regulatory compliance • Manage version control and document consistency • Maintain eTMF system structure, folders and system health • Ensure continuous inspection readiness of TMF • Act as TMF point of contact during audits and inspections • Coordinate with CRAs for TMF updates • Perform periodic TMF gap analysis and share findings • Drive continuous improvement of eTMF workflows Qualification • Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Public Health / Related discipline • PG Diploma in Clinical Research (preferred) Experience • 0–2 years in Clinical Research • Freshers are eligible Skills • Knowledge of TMF/eTMF processes • Understanding of ICH-GCP and regulatory documentation • Strong attention to detail • Good communication and coordination skills • Proficiency in MS Office and document management systems About the Company Sun Pharma is India’s largest pharmaceutical company with a strong global presence, known for high-quality medicines and world-class clinical research standards.

Role & Responsibilities • Maintain study documentation including protocols, ICFs, CRFs and clinical reports • Organize and manage electronic and paper study files • Support meeting scheduling, minutes preparation and travel coordination • Assist in preparation and submission of regulatory documents • Support GCP compliance and regulatory requirements • Track site invoices and payment status • Handle vendor code generation and vendor tracking • Support site coordination and communication activities Qualification • Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Public Health / Related discipline • PG Diploma in Clinical Research (preferred) Experience • 0–2 years in Clinical Research • Freshers are eligible Skills • Basic understanding of GCP and clinical research documentation • Good organizational and coordination skills • Strong documentation and communication abilities • Proficiency in MS Office About the Company Sun Pharma is India’s largest pharmaceutical company and a global leader in specialty generics and innovative medicines.

Role & Responsibilities • Prepare and compile regulatory dossiers for drug registration submissions • Liaise with regional and global regulatory teams to obtain supporting documentation • Support DCGI and Health Authority submissions including PMS and Phase IV studies • Coordinate and review clinical study reports, stability protocols and non-clinical reports • Maintain regulatory dossiers, approvals and submission archives • Support lifecycle management activities for registered pharmaceutical products • Coordinate with regulatory consultants for effective submissions • Manage regulatory trackers and documentation for tenders • Ensure compliance with Indian regulatory requirements Qualification • Bachelor’s or Master’s degree in Pharmacy / Life Sciences / Related discipline Experience • Prior experience in Regulatory Affairs within pharmaceutical or healthcare industry • Hands-on exposure to DCGI submissions preferred Skills • Strong knowledge of Indian regulatory framework • Drug registration and lifecycle management expertise • Excellent documentation and coordination skills • Strong analytical and communication abilities • High attention to detail and compliance orientation About the Company Johnson & Johnson is a global healthcare leader committed to advancing patient care through innovative medicines, medical devices and regulatory excellence.

Role & Responsibilities • Review and evaluate adverse event reports (AERs) for regulatory reportability • Enter and maintain adverse event data in safety databases • Perform narrative writing and case documentation • Communicate with healthcare professionals to obtain follow-up safety information • Assist in preparation and submission of regulatory safety reports • Monitor safety literature related to company products • Collaborate with clinical research, regulatory affairs and PV teams • Support development and implementation of pharmacovigilance SOPs • Review safety profiles of new and existing products • Participate in risk management plan development and execution • Communicate with regulatory authorities and stakeholders on safety matters Qualification • B.Pharm / M.Pharm / Pharm.D / Life Sciences (preferred) Experience • Fresher / Entry-level candidates can apply Skills • Knowledge of pharmacovigilance and ICSR processing • Narrative writing skills • Basic understanding of regulatory safety reporting • Good communication and documentation skills • Attention to detail and analytical ability About the Company A life sciences organization engaged in pharmacovigilance, clinical research and regulatory safety operations, ensuring patient safety and regulatory compliance across products.

Role & Responsibilities • Oversee curriculum development, revision and delivery across D.Pharm, B.Pharm, M.Pharm and Ph.D. programs • Ensure compliance with PCI norms and accreditation standards • Promote innovative teaching methodologies and academic excellence • Encourage faculty research, publications and funded projects • Establish research collaborations with industries, hospitals and national institutions • Oversee laboratory facilities, equipment upgrades and research infrastructure • Manage faculty recruitment, onboarding, evaluation and professional development • Prepare academic calendars, timetables, workload distribution and faculty deployment • Oversee budgeting, resource allocation and departmental growth plans • Monitor student performance, mentoring and academic discipline • Build relationships with pharmaceutical companies, hospitals and regulatory bodies • Facilitate internships, industrial training, placements and MoU initiatives • Represent the institution at academic forums, conferences and meetings • Ensure adherence to PCI, AICTE, UGC and NAAC benchmarks • Prepare statutory reports, compliance documents and lead accreditation activities • Drive continuous improvement and institutional quality initiatives Qualification • Ph.D. in Pharmaceutical Sciences (mandatory) Experience • 10–15 years of teaching and research experience • Prior administrative leadership experience as HoD / Professor / Associate Dean / Dean Skills • Strong knowledge of PCI, AICTE, UGC and NAAC regulations • Proven academic leadership and research background • Excellent communication and people management skills • Strategic thinking and problem-solving ability • Strong decision-making and institutional governance skills About the Company A reputed academic institution committed to excellence in pharmaceutical education, research and professional development.

Role & Responsibilities • Conduct field visits for research activities • Collect patient and community health data • Administer questionnaires and surveys • Maintain accurate field records and reports • Coordinate with healthcare teams and participants • Support data validation and submission • Ensure compliance with research protocols Qualification • B.Sc / B.Sc Nursing / B.Pharm Experience • As per GMCH Field Investigator norms Skills • Field data collection • Communication skills • Documentation accuracy • Community coordination • Time management About the Company Government Medical College & Hospital (GMCH), Chandigarh is a premier government healthcare and academic institution delivering advanced medical care, education and research.Start Date05-01-2026Last Date15-01-2026Official Notification and Apply Online linkClick Here

Role & Responsibilities • Dispense prescribed medicines accurately • Maintain pharmacy stock and inventory records • Ensure proper storage, labeling, and documentation of medicines • Assist in procurement and stock verification activities • Support doctors and nursing staff in medication management • Monitor expiry dates and ensure safe drug handling • Maintain compliance with pharmacy laws and safety guidelines • Participate in audits and inventory reconciliationName of the PostsVacanciesEducationAssistant Pharmacist 01D.Pharm, B. PharmPharmacist Grade IV01Pharmacist Grade III01Pharmacist Grade II01Pharmacist Grade I0 Experience • Freshers & experienced candidates can apply Skills • Drug dispensing • Inventory & stock management • Knowledge of pharmacy laws • Documentation and record keeping • Communication skills • Basic computer proficiency About the Company HLL Lifecare Limited is a Government of India enterprise engaged in healthcare products, services, and infrastructure development, contributing significantly to national public health programs and healthcare delivery across India.Interview Address : Chanakya BNR Hotel, Station Rd, Sirom Toly, Kishan Singh Colony, Gosaintola, Ranchi, Jharkhand 834011Starting date05-01-2026Closing date08-01-2026Official NotificationClick Here

Role & Responsibilities • Dispense medicines as per valid prescriptions • Maintain medicine inventory and stock records • Verify dosage, directions and drug interactions • Ensure proper storage of medicines • Counsel patients regarding medication usage • Maintain pharmacy documentation and registers • Ensure compliance with drug safety regulations Qualification • B.PharmVacancies No - 05 Experience • Freshers & experienced candidates can apply Skills • Knowledge of pharmaceuticals and drug safety • Inventory management • Documentation skills • Patient counselling • Computer literacy About the Company Northern Coalfields Limited (NCL) is a Government of India enterprise under Coal India Limited supporting mining and healthcare operations across its locations.Starting date01-01-2026Closing date30-01-2026Official Notification and Application FormClick Here

Role & Responsibilities Prepare aggregate safety reports including PBRERs, PSURs, Addendum PSURs, ACOs, PADERs and PSUR line listings Perform quality checks of aggregate safety reports in line with client conventions and regulatory requirements Conduct signal detection activities including cumulative analyses, issue-based event analyses, SERs and Drug Safety Reports Review published literature and case listings for safety surveillance Maintain vigilance over important and designated medical events Interact with client teams to discuss potential safety signals and emerging issues Support preparation and maintenance of Risk Management Plans (RMPs) Perform follow-up with clients to obtain incomplete or missing safety information Perform medical review of Individual Case Safety Reports (ICSRs) Perform medical review of narratives for Clinical Study Reports (CSRs) Provide medical guidance to drug safety scientists on ICSR and CSR narrative processing Maintain up-to-date knowledge of product safety profiles, labeling documents and SOPs Ensure compliance with global regulatory reporting timelines and requirements Maintain accurate safety records in compliance with guidelines and SOPs Qualification MBBS or MD (preferably in a clinical branch) Experience Pharmacovigilance / drug safety experience preferred Skills Strong ability to prepare concise and accurate medical synopses and narratives Ability to evaluate and interpret safety data independently Excellent written and spoken English communication skills Proficiency in MS Word, Excel, PowerPoint and web-based safety applications Strong typing, transcription accuracy and attention to detail About the Company Continuum is a leading contract research organization providing services in Pharmacovigilance, Regulatory, Evidence Evaluation and Technology The organization employs scientists and physicians to support global safety and regulatory operations

Role & Responsibilities Manage processing, follow-up, analysis and regulatory reporting of AEs and SAEs for marketed and investigational human and veterinary products Perform medical evaluation of safety cases in compliance with global regulatory requirements Prepare aggregate safety reports including PBRERs, PSURs, Addendum PSURs, ACOs, PADERs and PSUR line listings Perform quality checks of aggregate safety reports Conduct signal detection related analyses including cumulative and issue-based event analyses Ensure compliance with client conventions, SOPs and global pharmacovigilance guidelines Maintain accuracy, consistency and timelines for all safety deliverables Qualification Master’s degree in Life Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics) BDS / B.V.Sc. / M.V.Sc. Experience Pharmacovigilance industry experience preferred Skills Strong knowledge of medical terminology and pharmacovigilance processes Excellent written and spoken English communication skills Ability to prepare concise and accurate medical synopses and narratives Ability to evaluate safety data independently and draw conclusions Proficiency in MS Word, Excel, PowerPoint and web-based safety applications Strong analytical and documentation skills About the Company Continuum is a leading contract research organization providing services in Pharmacovigilance, Regulatory, Evidence Evaluation and Technology The organization employs scientists and physicians to support global safety and regulatory operations

Role & Responsibilities • Perform initial assessment and medical review of ICSRs in safety databases • Review seriousness, causality, labeling, narratives, MedDRA coding and medical history • Verify suspect drug, concomitant medications and laboratory data • Respond to case owner queries and document medical review comments • Identify and escalate complex case issues to team leads or line managers • Determine follow-up requirements and ensure proper documentation • Train and mentor PV associates on safety conventions and event capturing • Maintain current knowledge of product safety profiles across therapeutic areas Qualification • MBBS / MD (PG degree preferred) Experience • Minimum 8 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of ICSR medical review • Good understanding of MedDRA coding and global PV regulations • Excellent communication and documentation skills • Strong organizational and mentoring abilities • Ability to work under pressure and meet timelines About the Company • Cencora is a global healthcare solutions organization delivering regulatory, pharmacovigilance and medical safety services through its affiliate PharmaLex India Private Limited, supporting safer medicines and improved patient outcomes worldwide