Pharmacy Jobs

Role & Responsibilities • Lead and execute medical affairs objectives for assigned therapeutic areas • Act as an internal medical and scientific resource for AbbVie products and disease areas • Build and maintain professional relationships with KOLs, academic centres and researchers • Present clinical and scientific data to healthcare professionals and institutions • Support clinical research initiatives in collaboration with R&D and Clinical Operations • Contribute to development of disease-state and product communication materials • Support advisory boards, round table meetings and scientific forums • Provide ongoing training to sales, medical affairs and internal stakeholders • Ensure accurate documentation of field medical activities • Maintain compliance with regulatory, ethical and internal company policies • Support pharmacovigilance, HEOR and global medical office activities • Collaborate closely with commercial and medical leadership teams • Travel extensively for field engagement (approximately 60% field time) Qualifications & Experience • MD / MBBS / PharmD • Minimum 2–3 years of experience in Medical Affairs or pharmaceutical / clinical research roles • Experience working in cross-functional and matrix organizations • Strong ability to interpret and communicate clinical data effectively Skills • Excellent scientific communication and presentation skills • Strong analytical and data interpretation abilities • Relationship building and stakeholder engagement expertise • Strategic thinking and planning capability • Proficiency in Microsoft Office and digital tools • Ability to learn quickly and convey complex medical information clearly About the Company • AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines • Core therapeutic areas include immunology, oncology, neuroscience and eye care

Role & Responsibilities • Lead and execute global medical affairs strategy for assigned therapeutic area and priority assets • Develop and own the Integrated Evidence Plan (IEP) across early and late asset lifecycle stages • Drive evidence generation including Interventional Studies, Non-Interventional Studies (NIS), Real-World Evidence (RWE) and implementation science projects • Define and implement global Medical Science Liaison (MSL) strategy and medical education programs • Lead scientific publication planning and Medical Expert/KOL network development • Represent Global Medical Affairs with internal stakeholders and external regulatory, investment and medical communities • Review and manage Managed Access Program (MAP) requests and define global treatment strategies • Develop Post Study Drug Supply (PSDS) treatment plans ensuring regulatory and safety compliance • Collaborate cross-functionally with Clinical Development, Regulatory, Market Access and Commercial teams Qualifications & Experience • MD preferred / PhD / PharmD in Health Sciences • Minimum 10 years of experience in Medical Affairs and/or Clinical Development within the pharmaceutical industry • Strong knowledge of GCP, clinical research methodology, protocol design and regulatory requirements • Proven experience in early asset lifecycle, pre-launch and launch medical strategy • Strong critical thinking, leadership and stakeholder management skills • Excellent written and verbal English communication skills Skills • Medical Affairs Strategy • Integrated Evidence Planning • Real-World Evidence (RWE) • Clinical Research & GCP Compliance • KOL Engagement & Medical Education • Publication Planning • Cross-Functional Leadership • Regulatory & Safety GovernanceAbout the Company • Novartis is a leading global innovative medicines company headquartered in Basel, Switzerland • It focuses on discovering, developing, and delivering breakthrough treatments across areas such as oncology, cardiovascular, neuroscience, immunology, and rare diseases

Role & Responsibilities • Support initiation, execution, monitoring, and follow-up of clinical studies and medical projects within oncology therapeutic area • Develop and deliver training PPTs, CMEs, and conference scientific materials based on updated clinical guidelines and recent evidence • Identify and engage Key Opinion Leaders (KOLs), expert speakers, and academicians for scientific programs • Create educational programs, scientific content, and disease awareness initiatives • Manage all medical and educational content related to assigned oncology products and disease states • Collaborate closely with marketing and sales teams to support medical strategy and execution • Review and approve promotional and local packaging materials as per SOPs and regulatory standards • Participate in interdisciplinary medical and commercial projects • Gather field insights from KOLs and submit strategic reports to Head Office for brand planning • Conduct medical trainings for field teams and address scientific queries • Maintain strong pharmacology and therapeutic knowledge in oncology Qualifications & Experience • Pharm D / B.Pharm / M.Pharm / MBBS / MD / BDS • Minimum 5 years of experience in Medical Affairs (mandatory) • 5–10 years of overall professional experience • Willingness for international travel as required Skills • Oncology medical affairs expertise • Scientific communication & KOL management • CME & training content development • Medical writing and guideline interpretation • Promotional material review & compliance • Cross-functional collaboration • Pharmacology knowledge • Presentation & communication skills • Strategic reporting & field insight analysisAbout the Company • Hetero is a fast-growing pharmaceutical company focused on delivering innovative oncology solutions across emerging and regulated markets

Roles & Responsibilities • Manage day-to-day clinic operations to ensure smooth workflow • Dispense medicines accurately as per prescriptions • Handle patient enquiries, calls, registrations, and appointment scheduling • Maintain pharmacy stock, perform regular expiry checks, and keep proper records • Coordinate laboratory activities including sample collection and report management • Manage billing, cash handling, and basic accounting activities • Maintain patient files, medical records, and clinic documentation • Ensure cleanliness, organization, and efficient functioning of the clinic Qualification • 12th Pass / D.Pharm / B.Pharm from a recognized board or institute Experience • Minimum 1 year experience in a clinic, pharmacy, or healthcare setup Skills • Knowledge of medicine dispensing and clinic operations • Good communication and patient-handling skills • Ability to multitask and manage responsibilities independently • Basic computer skills and billing software knowledge • Organized, responsible, and service-oriented approach About the Company Vijra Family & Diabetic Clinic is a patient-focused healthcare clinic based in Gurugram, Haryana, providing comprehensive family medicine and diabetic care services. The clinic is committed to delivering quality treatment, efficient pharmacy services, and personalized patient care through well-managed clinical operations.

Role & Responsibilities • Manage affiliate safety mailboxes and reconciliation of safety reports as per defined processes • Perform written follow-ups for both serious and non-serious ICSRs • Oversee case identification, data entry, MedDRA coding, processing, submission, and follow-ups in safety databases • Ensure ICSR handling complies with global pharmacovigilance regulations and client SOPs • Review and monitor team performance, quality metrics, and timelines • Manage medium-sized PV teams and provide guidance and mentorship • Drive problem-solving for moderately complex PV operational challenges • Implement process improvements and new workflow solutions • Ensure compliance with client and regulatory requirements • Support rotational shift operations as required Qualifications & Experience • Bachelor of Pharmacy • 10–14 years of experience in Pharmacovigilance / Drug Safety Operations • Strong understanding of global PV regulations and ICSR lifecycle • Experience managing teams and safety workflows Skills • Pharmacovigilance operations & ICSR lifecycle management • MedDRA coding and safety database handling • Affiliate reconciliation and follow-up management • Global PV regulations & compliance • Team leadership and performance management • Process improvement & root cause analysis • Strong analytical and decision-making skills • Effective communication and stakeholder management About the Company • Accenture is a global professional services company delivering digital, cloud, security, consulting, technology, and operations solutions to life sciences and healthcare organizations across 120+ countries

Role & Responsibilities • Handle and process adverse event and serious adverse event reports from clinical trials and post-marketing sources • Determine appropriate action plans for incoming safety calls and reports • Collect, process, track, and document safety cases accurately • Prepare detailed safety narratives and reports • Maintain safety databases and track case follow-ups • Collaborate with internal teams and clinical research sites to ensure safety compliance • Support regulatory compliance and safety reporting activities • Maintain accurate safety documentation and timelines Qualifications & Experience • Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or Healthcare-related discipline • Clinical experience or Pharmacovigilance / Clinical Research experience preferred • Proficient English communication skills • Strong knowledge of medical terminology • Proficiency in Microsoft Office tools Skills • Pharmacovigilance case processing • Adverse event reporting and safety documentation • Safety database management • Medical terminology and narrative writing • Regulatory compliance and GCP understanding • Attention to detail and time management • Strong communication and coordination skills About the Company • Medpace is a global Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries across 40+ countries

Role & Responsibilities • Process and review Individual Case Safety Reports (ICSRs) from multiple sources including literature, affiliates, and health authorities • Perform case triage, data entry, MedDRA coding, causality, seriousness, and expectedness assessment • Prepare medically accurate case narratives and perform quality checks • Manage follow-ups, reconciliation, and compliance tracking for safety reporting • Support expedited and periodic safety report submissions to regulatory authorities • Maintain regulatory databases and support product lifecycle management activities • Perform literature searches and maintain validated search strategies • Support audits, inspections, and compliance documentation • Collaborate with global PV teams and mentor junior team members Qualifications • Degree in Life Sciences / Health / Biomedical Sciences • Medicine, Dentistry, Nursing, Physiotherapy background is an added advantage • JLPT N2 or above (Japanese language proficiency) Experience • Prior experience in Pharmacovigilance / Drug Safety preferred • Experience with PMDA safety reporting and Japanese PV operations preferred Skills • Pharmacovigilance operations and ICSR processing • MedDRA coding and safety database handling • Japanese (JLPT N2+) and English communication • Regulatory compliance (ICH, EMA, PMDA, global PV regulations) • Literature review and safety data analysis • Quality control and audit readiness • MS Office and safety database proficiency • Analytical, documentation, and time management skills About the Company • Parexel is a global clinical research organization delivering clinical trials, regulatory, consulting, and market access services to advance life-changing therapies worldwide

Roles & Responsibilities • Dispense medicines as per doctor prescriptions following ECHS guidelines • Maintain proper storage, labeling, and documentation of medicines • Manage pharmacy inventory, stock levels, and expiry monitoring • Ensure compliance with medical, legal, and ECHS pharmacy procedures • Coordinate with medical officers and staff for smooth pharmacy operations • Maintain records for controlled drugs and daily issue registers • Support audits and inspections as required Qualification • B.Pharm or D.Pharm from a recognized institute Number of Openings: 05Walk-in Details: Stn HQs (ECHS Cell), BareillyImportant Dates: • Application Start Date: 13-01-2026 • Application Closing Date: 08-02-2026 Age Limit • Minimum: 18 Years • Maximum: 45 Years • Age relaxation as per organization norms Skills • Knowledge of medicines and medical terminology • Attention to detail and accuracy in dispensing • Basic computer skills for record maintenance • Good communication and teamwork skillsAbout the Company Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative under the Ministry of Defence, established to provide comprehensive medical care to ex-servicemen and their dependents through a network of polyclinics and empanelled hospitals across the country.Official NotificationClick Here

Roles & Responsibilities: • Dispense veterinary medicines accurately as per veterinarian prescriptions • Explain dosage, usage instructions, and precautions to pet parents when required • Ensure proper labeling, packaging, and documentation of medicines • Manage pharmacy inventory, stock levels, and expiry monitoring • Coordinate with purchase/inventory teams for timely replenishment • Ensure proper storage conditions for medicines and vaccines • Maintain pharmacy records, prescriptions, and controlled drug registers • Support audits, stock reconciliation, and monthly reporting • Maintain hygiene and cleanliness of the pharmacy area • Assist veterinarians and technicians by ensuring medicine availability • Follow SOPs, safety guidelines, and regulatory requirements • Provide courteous service and effective communication with customers and staff Qualifications: • D.Pharm or B.Pharm from a recognized institute • Valid Pharmacist License (Telangana – mandatory) Experience: • Experience in medical or veterinary pharmacy preferred Skills: • Good communication and customer service skills • Knowledge of veterinary medicines (added advantage) • Inventory management and basic computer proficiency About the Company: Crown Veterinary Services Pvt. Ltd. is a professionally managed veterinary healthcare organization providing high-quality clinical and pharmacy services. The company is committed to animal welfare, ethical practices, and delivering reliable veterinary care supported by trained professionals and standardized operating procedures.

Roles & Responsibilities • Dispense medications accurately and ensure patient safety • Provide professional medication counseling and healthcare advice • Ensure compliance with DHA regulations and UAE pharmacy laws • Manage daily pharmacy operations, records, and inventory • Use pharmacy software for dispensing, billing, and documentation • Maintain high standards of customer service and patient care Qualifications • B.Pharm or Pharm.D from a recognized university • Valid DHA license or DHA Eligibility Letter • Home country pharmacy council registration mandatory Experience: • Minimum 2 years of experience in retail or hospital pharmacy Skills • Strong communication skills in English (Arabic is an advantage) • Knowledge of UAE pharmacy laws and regulations • Proficiency in pharmacy management software • Customer-focused and detail-oriented Benefits • Health insurance as per UAE labor law • Visa sponsorship and residency processing • Annual/biennial air tickets • Paid annual leave and public holidays • End-of-service gratuityAbout the Company Ezee Healthcare is a Dubai-based healthcare recruitment and advisory firm with over 12 years of experience. The company specializes in placing qualified healthcare professionals with reputed hospitals, clinics, and pharmacies across the Gulf region, and also provides licensing assistance for DHA, MOH, and DOH to support smooth career transitions in the UAE.

Roles & Responsibilities • Dispense prescription and OTC medications as per MOH guidelines • Counsel patients on medication usage, dosage, and side effects • Ensure safe storage and handling of medicines • Maintain pharmacy records, billing, and inventory • Support smooth daily operations of the pharmacy • Build strong customer relationships through professional service Eligibility & Qualifications • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D) • Valid MOH (Ministry of Health) Pharmacist License - mandatory Experience • Minimum 1 year of professional pharmacy experience (UAE or equivalent preferred) Visa Status • Candidates with own visa (Freelance / Partner / Dependent) preferred Skills • Excellent communication skills in English • Urdu/Hindi language skills are an advantage • Strong customer handling and interpersonal skills • Responsible, punctual, and well-organizedAbout the Company The hiring organization is a growing community pharmacy based in Ajman, UAE, associated with Reheal Pharmacy. It is committed to delivering high-quality healthcare services, authentic medicines, and personalized patient care, with a strong focus on customer satisfaction, ethical practices, and community well-being.

Roles & Responsibilities • Handle registration of medical devices and oral care products with the Ministry of Health (MOH) and Dubai Municipality • Prepare, submit, and track regulatory dossiers and product documentation • Coordinate with regulatory authorities to address queries and ensure timely approvals • Ensure compliance with UAE regulatory guidelines and updates • Maintain accurate records of product registrations and renewals • Support internal teams on regulatory requirements and compliance matters Qualification • Bachelor of Pharmacy (B.Pharm) • Doctor of Pharmacy (Pharm.D) preferred• Active pharmacist license from a recognized authority • MTM or BCPS certification preferred • Female candidates preferred • Nationalities: Arab, GCC, Indian, Emirati (UAE) Experience • 3-5 years of relevant experience • Minimum 2 years of clinical or retail pharmacy experience preferred Skills • Strong knowledge of UAE MOH and Dubai Municipality regulations • Understanding of medical device and oral care product registration processes • Good documentation and regulatory writing skills • Attention to detail and ability to manage multiple submissions • Effective communication and coordination skills About the Company Prevest DenPro Gulf General Trading LLC is a healthcare-focused organization specializing in dental, oral care, and medical products, with strong regulatory and market presence in the UAE.

Roles & Responsibilities • Lead and manage all hospital pharmacy operations including inpatient, outpatient, clinical pharmacy, and sterile compounding • Ensure safe, accurate dispensing, storage, and distribution of medications • Implement and monitor SOPs in line with hospital policies and regulatory standards • Promote medication safety, quality assurance, and inventory control • Collaborate with physicians and nursing teams to optimize medication therapy • Participate in clinical rounds, medication review, and therapeutic committees • Provide drug information and medication counseling to healthcare professionals and patients • Ensure compliance with DHA regulations, JCI/accreditation standards, and international guidelines • Oversee controlled drugs management and documentation • Prepare for and manage internal and external audits and inspections • Manage pharmacy department budgeting, procurement, and cost optimization • Lead recruitment, training, performance evaluation, and development of pharmacy staff • Monitor KPIs, lead quality improvement initiatives, and manage medication error investigations Qualification • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (PharmD) • Postgraduate qualification in Clinical/Hospital Pharmacy or related field preferred Experience • Minimum 8-10 years of hospital pharmacy experience • At least 3-5 years in a supervisory or leadership role Licensure & Eligibility • Eligible for Dubai Health Authority (DHA) license • Valid license from a recognized authority (DHA or eligible GCC license) Skills • Strong leadership and team management skills • In-depth knowledge of hospital pharmacy systems and clinical pharmacy practices • Expertise in pharmaceutical regulations, pharmacovigilance, and medication safety • Excellent communication, organizational, and decision-making abilities About the Company.The hospital is a multidisciplinary healthcare facility committed to delivering high-quality, patient-centered care while maintaining international standards in safety, quality, and clinical excellence.

Roles & Responsibilities • Assist in scientific, laboratory, and technical activities as per departmental requirements • Support sample handling, testing, data recording, and documentation • Maintain laboratory equipment, records, and inventory • Ensure compliance with SOPs, safety guidelines, and quality standards • Coordinate with doctors, scientists, and technical staff • Assist in reporting, audits, and routine operational tasks Qualification • B.Pharm (Bachelor of Pharmacy) or B.Sc Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years Walk-in Details Date: 29-01-2026 Location: Homi Bhabha Cancer Hospital & Research Centre, New Chandigarh, Medicity, SAS Nagar, PunjabAbout the Company Tata Memorial Centre is a premier institution under the Government of India, dedicated to cancer treatment, research, and education, operating state-of-the-art oncology hospitals and research centers across the country.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines as per prescriptions and ECHS guidelines • Maintain proper storage, stock control, and inventory records • Ensure availability of medicines and medical supplies • Verify prescriptions for accuracy and compliance • Maintain pharmacy documentation and registers • Follow SOPs, safety standards, and regulatory requirements • Coordinate with medical officers and ECHS staff Qualification • D.Pharm Age Limit • Minimum Age: 18 Years • Maximum Age: 45 Years • Age relaxation applicable as per organization rules Important Dates • Application Start Date: 08-01-2026 • Application Closing Date: 13-02-2026 About the Organization Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative providing comprehensive healthcare services to ex-servicemen and their dependents through a nationwide network of ECHS polyclinics and empanelled hospitals.Official NotificationClick Here

Roles & Responsibilities • Support research activities as per the project objectives • Conduct experiments, data collection, and data analysis • Prepare technical reports, research documentation, and publications • Assist in laboratory work, validation studies, and result interpretation • Coordinate with project investigators and research team members • Maintain research records and ensure compliance with institute guidelines • Support presentations, reviews, and project-related meetings Qualification • M.Sc, M.Tech, BDS, M.Pharm, Ph.DAge Limit • Minimum Age: 21 Years • Maximum Age: 35 Years Important Date • Last Date to Apply: 13-01-2026 About the Organization Indian Institute of Technology Jodhpur is a premier autonomous institute of national importance, dedicated to advanced education, cutting-edge research, and innovation across science, engineering, and technology disciplines.

Roles & Responsibilities • Dispense prescribed medicines to ECHS beneficiaries as per medical prescriptions • Maintain accurate records of medicines issued and received • Ensure proper storage, labeling, and handling of drugs • Monitor stock levels and assist in inventory control • Ensure compliance with pharmacy regulations and ECHS guidelines • Provide basic medication counseling to patients when required • Support medical officers and healthcare staff in daily operations Qualification • B.Pharm & D.Pharm Experience • As per ECHS recruitment norms (Freshers / experienced candidates may apply) Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years Important Date • Last Date to Apply: 28-01-2026 About the Organization The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India healthcare initiative that provides comprehensive medical care to ex-servicemen and their dependents through a nationwide network of polyclinics and empaneled hospitals.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines or provide nursing care as per hospital protocols • Ensure safe medication administration and patient care • Maintain medical, pharmacy, and patient records accurately • Follow hospital SOPs, safety standards, and ethical practices • Support doctors and healthcare teams in clinical activities • Monitor patient conditions and report abnormalities • Maintain inventory, equipment, and ward/pharmacy cleanliness • Ensure compliance with regulatory and institutional guidelines Qualification • B.Pharm, B.Sc Nursing, GNM Experience • Freshers and experienced candidates can apply (as per AIIMS norms) Number of Openings: 01Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per government rulesImportant Dates • Application Start Date: 09-01-2026 • Application Closing Date: 29-01-2026 About the Organization All India Institute of Medical Sciences (AIIMS) is a premier government healthcare institution dedicated to excellence in medical education, research, and patient care, providing high-quality healthcare services across India.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines as per valid prescriptions • Ensure correct storage and handling of drugs • Maintain pharmacy stock records and inventory • Check expiry dates and ensure safe medication practices • Counsel patients on dosage, usage, and precautions • Ensure compliance with pharmacy rules and regulations • Maintain proper documentation and reporting Qualification • D.Pharm Experience • Freshers and experienced candidates can apply Number of Openings: 17Age Limit • Minimum Age: 18 Years • Maximum Age: 45 Years • Age relaxation as per KSCCF norms Important Dates • Application Start Date: 09-01-2026 • Application Closing Date: 07-02-2026 About the Organization Karnataka State Co-operative Federation (KSCCF) is a government-supported cooperative organization engaged in public service and welfare activities across Karnataka, ensuring quality services through skilled professionals.Official NotificationClick Here