Pharmacy Jobs

Role & Responsibilities • Perform ICSR case processing and data entry. • Manage safety cases, triaging, and quality checks. • Handle literature screening, drug dictionary maintenance, and follow-up on queries. • Support the preparation of safety reports and documentation for audits. • Support xEVMPD and IDMP activities as required. • Ensure documentation compliance with TMF and PSMF. • Participate in internal and external PV audits. • Ensure adherence to ICH-GCP, GVP, and global safety regulations. Qualifications & Skills • Bachelor’s degree in Life Sciences / Pharmacy / Nursing. • 1 – 2.6 years of experience in Pharmacovigilance. • Familiarity with Argus Safety Database and safety case processing. • Strong attention to detail and multi-tasking ability. • Proficiency in MedDRA coding and medical terminology. • Excellent communication and time-management skills.Why Join Syneos Health? • Work with a leading global organization involved in 94% of novel FDA-approved drugs. • Exposure to international clinical trials and post-marketing safety programs. • Career development with structured training and mentoring. • Inclusive culture promoting diversity and well-being. • Opportunity to work on cutting-edge drug safety projects.

Role & Responsibilities • Perform ICSR case processing, booking, triage, and data entry. • Conduct quality review (QC) of ICSRs as per SOPs and GVP. • Enter, code, and review safety data in Argus / ARISg / LSMV. • Prepare accurate case narratives and follow up on queries. • Identify and manage duplicate safety cases. • Perform MedDRA coding for events, indications, and products. • Handle literature screening and drug dictionary maintenance. • Support xEVMPD, SPOR / IDMP activities. • Ensure documentation compliance with TMF and PSMF. • Participate in internal and external PV audits. • Ensure adherence to ICH-GCP, GVP, and global safety regulations. Qualifications & Skills • Bachelor’s degree in Life Sciences / Pharmacy / Nursing. • 3+ years of experience in Pharmacovigilance case processing. • Mandatory experience in Clinical Trial, PMS, and Spontaneous cases. • Strong working knowledge of Argus Safety Database. • Proficiency in MedDRA coding and medical terminology. • Excellent communication, accuracy, and time-management skills.Why Join Syneos Health? • Work with a leading global organization involved in 94% of novel FDA-approved drugs. • Exposure to international clinical trials and post-marketing safety programs. • Career development with structured training and mentoring. • Inclusive culture promoting diversity and well-being. • Opportunity to work on cutting-edge drug safety projects.

Role & Responsibilities • Dispense medications accurately as per prescriptions • Provide medication counseling to patients on usage and dosage • Monitor and maintain pharmacy inventory • Ensure compliance with pharmacy regulations and safety standards • Keep accurate records of dispensed medications Qualification • D. PharmVacancies no - 03 Experience • Experience in pharmacy operations preferredAge Limit • Minimum age: 18 years • Maximum age: 45 years Selection Process • Interview Salary • Minimum salary: Rs. 10,000/- per month • Maximum salary: Rs. 34,729/- per month Application Fee • No application feeAbout the Company • DHS Jamtara (District Health Society, Jamtara) is a government health organization focused on providing essential healthcare services to the people of Jamtara, Jharkhand. How to Apply • Visit the official website of DHS Jamtara • Read the notification and check eligibility • Fill out the application form and attach required documents • Submit the completed application before the last date Important Dates • Start date: 07-01-2026 • Closing date: 04-02-2026Official NotificationClick Here

Key Responsibilities • Manage pharmacy operations, ensuring compliance with DHA regulations • Develop and implement pharmacy policies and procedures • Oversee drug storage, dispensing, and inventory management • Secure permits for controlled drugs and maintain drug formulary • Serve as Co-chairman of the Pharmacy and Therapeutics Committee • Provide training and support to pharmacy staff • Collaborate with other departments for comprehensive patient care Qualifications • Pharmacy Degree (B.Pharm or equivalent) • 5 years of experience in hospital pharmacy (2 years in administration) • DHA license to practice in UAE • Strong English communication skills (Arabic preferred) Why Join NMC Healthcare? • Career growth opportunities in a leading healthcare provider • Competitive salary and benefitsAbout the Company NMC Healthcare is a leading private healthcare network in the UAE, offering high-quality care across 85 medical facilities and serving over 5.5 million patients annually.

Role & Responsibilities • Dispense medications to patients as per prescriptions • Provide patient counseling on proper medication usage • Ensure compliance with pharmacy regulations and safety standards • Maintain accurate patient records and documentation • Assist in inventory management and stock controlName of the PostsVacanciesEducationPharmacist11D. Pharm Experience • Relevant experience in pharmacy operations preferredAge Limit • Minimum age: 18 years • Maximum age: 45 years Selection Process • Interview Application Fee • Open Category Candidates: Rs. 150/- • Reserved Category Candidates: Rs. 100/- Salary • Minimum salary: Rs. 17,000/- per month • Maximum salary: Rs. 40,000/- per month About the Company • National Health Mission (NHM) Raigad is a government initiative aimed at improving healthcare delivery across India, with a special focus on rural and underserved areas.How to Apply • Fill out the application form and pay the application fee (if applicable) • Attach required documents and submit the completed form by the last dateAddress • National Health Mission Office, Raigad Zilla Parishad, Alibaug, Kunte Bagh, Near Collector’s Office, Alibaug, District Raigad, Pin 402201 Important Dates • Start date: 07-01-2026 • Closing date: 13-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Dispense prescription and over-the-counter medications accurately, ensuring patient safety and compliance with regulatory standards. • Provide expert pharmaceutical care, medication counseling, and healthcare advice to patients and customers. • Review prescriptions for accuracy, appropriateness, interactions, and contraindications. • Manage pharmacy inventory, including procurement, storage, expiry monitoring, and stock control. • Supervise and guide pharmacy staff to ensure smooth daily operations and adherence to SOPs. • Ensure full compliance with DOH/MOH regulations, company policies, and legal requirements. • Handle prescription-related queries, insurance claims, and documentation with confidentiality and professionalism. • Participate in health awareness programs, promotional activities, and community engagement initiatives. • Maintain accurate records and reports related to dispensing, inventory, and regulatory audits. Qualifications • Bachelor’s Degree in Pharmacy (B.Pharm / Pharm.D or equivalent). • Valid and active DOH or MOH Pharmacist License (mandatory). • Strong knowledge of pharmacy laws, ethics, and best practices. Experience • 3 to 8 years of relevant experience in a pharmacy setting. • Retail pharmacy experience is highly preferred. • Proven experience in managing pharmacy operations and regulatory compliance. Skills & Competencies • Excellent communication and patient counseling skills. • Strong organizational ability with high attention to detail. • Customer-focused mindset with a commitment to service excellence. • Ability to work efficiently in a fast-paced, team-oriented environment. • Leadership skills to supervise and mentor pharmacy staff. Perks & Benefits • Competitive salary with performance-based incentives. • Staff discounts on pharmacy products and services. • Comprehensive health and insurance coverage. • Continuous professional development and training opportunities. • Supportive work environment with a strong team culture. • Work-life balance-friendly policies.About the Company We are a trusted and patient-focused healthcare organization committed to delivering high-quality pharmacy services and promoting safe and effective medication use. Our pharmacy operates with strong ethical standards, regulatory compliance, and a customer-centric approach.

Role & Responsibilities • Dispense medications accurately and provide patient counseling • Ensure compliance with pharmacy regulations and safety standards • Maintain proper documentation and manage pharmacy inventory • Collaborate with doctors, nurses, and other healthcare staff for patient care • Monitor and track medication usage and patient outcomes • Provide support in the development and improvement of pharmacy services Qualifications & Experience • Bachelor’s degree in Pharmacy (B.Pharm) or equivalent • Valid license/registration to practice pharmacy in the respective region (preferred) • 3-5 years of prior experience in retail or hospital pharmacy (preferred) Skills • Strong knowledge of medications, dosage, and safety regulations • Excellent communication skills for patient counseling • Ability to work collaboratively with a healthcare team • Attention to detail and high standards of compliance Preferred • Hindi-speaking candidates are preferred About the Company • Apex Medical Center LLC is a renowned healthcare provider in the UAE, committed to delivering high-quality medical services and patient care. The center focuses on providing personalized care with a team of skilled professionals across various specialties.

Role & Responsibilities • Communicate therapeutic area-related, product-related, and clinical information to external       stakeholders • Develop long-term relationships with opinion leaders and key stakeholders • Support clinical research, including investigator-initiated trials (IITs) and RWE projects • Capture market insights to support Field Medical Plans and business strategies • Provide medical expertise to commercial teams and assist in regulatory submissions • Ensure compliance with industry regulations and company policies • Support Patient Support Programs (PSPs) and patient awareness initiatives Qualification • MBBS, MD, or Pharm D Experience • 1-2 years in medico marketing or related field Skills • Strong communication and presentation skills • Excellent relationship-building ability with healthcare professionals • Proficiency in English and ability to manage cross-functional projects Why Join Domnic Lewis • Career growth in a leading healthcare company • Collaborate with experts in the therapeutic area • Contribute to global medical strategies and patient outcomes

Role & Responsibilities • Assist in processing Adverse Events (AE) and endpoint data, including intake, tracking, and workflow distribution • Track safety case timelines and ensure timely submissions to clients and stakeholders • Support Lifecycle Safety database entry, quality control, and report generation • Coordinate safety report submissions to regulatory authorities and investigators • Maintain project files, case folders, and document control systems • Assist with project start-up activities, system access, and administrative workflows • Archive safety data and manage records post-study closure • Support database validation, user testing, and ad-hoc data searches • Coordinate meetings, courier dispatch, and administrative logistics • Mentor junior administrative staff and support continuous process improvement Qualification • Degree in Life Sciences, Pharmacy, Healthcare, or an allied scientific discipline Experience • Minimum 1 year of relevant experience in pharmacovigilance, clinical research, or safety operations Skills • Good understanding of GCP, ICH guidelines, SOPs, and safety workflows • Working knowledge of medical terminology • Proficiency in Microsoft Office and web-based applications • Strong organizational, multitasking, and time-management skills • Excellent written and verbal communication skills • High attention to detail, accuracy, and compliance About the Company • IQVIA is a globally recognized leader in clinical research, pharmacovigilance, and healthcare intelligence, supporting life sciences companies in the development and commercialization of innovative medical treatments.

Role & Responsibilities • Manage end-to-end ICSR lifecycle, including data entry into pharmacovigilance databases • Book and triage ICSRs, ensuring compliance with PV regulations • Perform medical coding (MedDRA, WHO-DD) and narrative writing for safety reports • Generate follow-up letters to reporters and ensure timely case closure • Review scientific and medical literature to identify valid ICSRs • Perform quality checks (QC) on safety cases to ensure data accuracy and completeness • Assist in the preparation of aggregate safety reports (PSUR, PBRER, DSUR, if applicable) • Support signal detection activities and ADR trend analysis • Ensure compliance with SOPs, project guidelines, and global pharmacovigilance regulations • Stay updated with regulatory changes impacting pharmacovigilance activities • Coordinate with cross-functional teams and affiliates to resolve safety queries Qualification • B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences Experience • 2–5 years of experience in Pharmacovigilance, particularly in ICSR processing, safety data entry, and medical coding Skills • Knowledge of global pharmacovigilance guidelines (ICH, GVP, FDA, EMA) • Proficiency in MedDRA and WHO-DD coding systems • Strong experience in narrative writing and case quality review • Excellent written and verbal communication skills • Ability to perform quality checks and ensure regulatory compliance Why Join Apcer Life Sciences? • Work with a globally recognized pharmacovigilance and regulatory services company • Exposure to international pharmacovigilance projects and a strong focus on career development

Role & Responsibilities • Perform end-to-end pharmacovigilance case processing for clinical trial safety cases • Collect, assess, process, and submit adverse event (AE) and serious adverse event (SAE) reports • Ensure timely and accurate data entry in LSMV (LifeSphere MultiVigilance) database • Maintain compliance with global pharmacovigilance regulations (ICH-GCP, GVP, FDA, EMA) • Support signal detection activities and risk management assessments • Collaborate with cross-functional teams on safety queries and investigations • Stay updated with the latest drug safety guidelines and industry standards Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline Experience • Minimum 2+ years of experience in pharmacovigilance case processing • Hands-on experience in Clinical Trial Safety Cases or LSMV/Argus/Safety Databases Skills • Strong analytical skills with high attention to detail • Excellent written and verbal communication skills • Proven commitment to quality, compliance, and patient safety About the Company • ICON plc is a global leader in healthcare intelligence and clinical research, specializing in providing comprehensive clinical development and outsourcing solutions to the pharmaceutical, biotechnology, and medical device industries.

Role & Responsibilities • Dispense prescription and over-the-counter medications to patients • Provide medication counseling and ensure safe and effective use of medications • Maintain accurate records of all prescriptions and patient interactions • Ensure compliance with local regulations and pharmacy policies • Monitor medication stock levels and manage inventory • Assist with clinical duties and provide support during health consultations • Collaborate with healthcare professionals to optimize patient care Qualification • MOH Oman License (Mandatory) • Bachelor of Pharmacy (B.Pharm) / Doctor of Pharmacy (PharmD) / Master of Pharmacy   (M.Pharm) Experience • 3+ Years Clinical experience is preferred but not mandatory Skills • Strong knowledge of pharmacy practices and regulations • Ability to work independently and as part of a team • Good communication skills, with fluency in English • Attention to detail and accuracy in dispensing medications Salary & Benefits • Salary: OMR 500 – 550 per month • Accommodation provided • Immediate joining preferred • Interviews will be conducted online About the Company • Thashkeel is a recruitment agency facilitating placements in various industries, including healthcare. This position is part of a healthcare recruitment drive for a clinic in Sohar, Oman.How to Apply • Interested candidates can apply by sending their resume to cv@thashkeelindia.com WhatsApp +91 89212 66205

Role & Responsibilities • Dispense medications with proper labeling and instructions regarding usage, dosage, and other relevant information • Ensure medication stock levels and storage practices are maintained according to company standards and best practices • Follow accurate patient billing processes • Implement JCIA standards for pharmacies • Contribute to enhancing the patient experience by adhering to best practices and principles • Manage stock control and ensure compliance with UAE healthcare regulatory frameworks and related requirements Qualification • B.Pharm degree from an accredited educational institution Experience • At least 2 years of relevant experience in a hospital or clinic pharmacy Skills & Knowledge • Knowledge of JCIA standards for pharmacies • Patient experience principles and related best practices • Stock control principles and management • Familiarity with the UAE healthcare regulatory framework and related requirements About the Company • Mediclinic is a leading private healthcare group in the UAE and part of Mediclinic International.

Role & Responsibilities • Receive, prepare, and submit Individual Case Safety Reports (ICSRs) to global regulatory authorities • Ensure all safety reports comply with country legislation and regulatory timelines • Lead large-scale safety reporting projects and monitor submission performance • Contribute to the development and continuous improvement of SOPs and procedural documents • Collaborate with internal teams on safety reporting activities • Act as the primary point of contact for safety reporting projects • Mentor and guide new team members and junior colleagues • Produce safety metrics and support limited financial project activities • Participate in internal and external meetings related to pharmacovigilance operations Qualification • Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline Experience • Minimum 2+ years of experience in safety reporting or pharmacovigilance • Strong understanding of global safety reporting requirements • Proven skills in ICSR submissions, regulatory timelines, and safety reporting processes Skills • Global safety reporting and pharmacovigilance compliance • ICSR submission and regulatory timelines management • SOP development and cross-functional collaboration • Proficiency in Microsoft Office and safety databases • Strong attention to detail and multi-tasking ability • Ability to influence and collaborate across teams Benefits & Work Environment • Fully remote work model • Standard Monday–Friday schedule • Exposure to global pharmacovigilance projects • Opportunity to work with senior international stakeholders • Career growth in a regulated, high-impact safety environment About the Company • Thermo Fisher Scientific is a leading global life sciences organization, providing innovative solutions and cutting-edge technology in the fields of biotechnology, life sciences, and drug safety.

Role & Responsibilities • Deliver lectures and coaching to students preparing for the Prometric Exam • Provide academic support and guidance to students on pharmacy practices • Engage with students to clarify doubts and offer practical knowledge • Offer regular feedback to students to enhance their learning • Foster a positive and encouraging learning environment for students Qualification • Doctor of Pharmacy (Pharm D) with KAPS/OPRA qualification Experience • Strong knowledge of pharmacy practices • Teaching experience is a plus Skills • Excellent verbal and written communication skills • Fluency in English is essential • Ability to engage and motivate students Additional Information • Job Type: Full-time • Work Schedule: Monday to Saturday (Day Shift) About the Company • Pharma International Institute is an educational institution offering coaching and training for pharmacy students, particularly focusing on the preparation for exams like Prometric. • The institute provides hands-on experience in pharmacy practices and academic excellence in a collaborative environment.

Role & Responsibilities • Organize and maintain the pharmacy for easy and quick product identification • Ensure proper stocking, labeling, and delivery of medicines and products • Monitor the condition of medications to prevent expiration or deterioration • Maintain accurate pharmacy records and documentation • Provide medication counseling and ensure proper drug storage • Ensure compliance with pharmacy regulations and standards Qualification • Pharmacy license (Delhi Pharmacy Council) Experience • Previous experience in pharmacy operations preferred Skills • Strong knowledge of pharmaceutical products and treatments • Inventory and stock management • Excellent organizational and communication skills • Patient counseling and customer service Salary • ₹20,000 – ₹30,000 per month Benefits • Health insurance • Provident Fund About the Company • Sharp Sight Center, Preet Vihar, Delhi • Reputed healthcare center specializing in vision care • Offers a supportive and growth-oriented work environment

Role & Responsibilities • Dispense prescription and over-the-counter medications • Provide medication counseling and educate patients on drug use • Ensure proper medication storage and handling • Maintain accurate pharmacy records and manage inventory • Collaborate with healthcare professionals to ensure effective patient care Qualification • B.Pharm Experience • Prior experience in pharmacy operations Skills • Prescription validation and medication dispensing • Patient counseling and drug interaction analysis • Inventory management and regulatory compliance Age Limit • Minimum age: 18 years • Maximum age: 45 years Selection Process • Interview Application Fee • No application fee How to Apply • Visit the official website • Check for the relevant job post • Read the notification carefully and verify eligibility • Send your resume and required documents to the address specified in the official notification Important Dates • Last Date of Application: 13-01-2026About the Company • ECHS (Ex-Servicemen Contributory Health Scheme) • A healthcare initiative under the Ministry of Defence, India, providing medical services to veterans.Official NotificationClick Here

Role & Responsibilities • Assist in the coordination and administration of clinical trials • Ensure compliance with study protocols and regulatory requirements • Maintain and organize clinical trial documentation and regulatory submissions • Support preparation of study-related materials such as informed consent forms and case report forms • Collaborate with cross-functional teams for smooth trial execution • Track and report clinical trial metrics and milestones to management Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or healthcare-related field Experience • Freshers or candidates with prior experience in clinical trials Skills • Strong understanding of GCP guidelines and clinical trial processes • Excellent organizational, communication, and multitasking skills • Ability to work in a fast-paced, collaborative environmentPerks & Benefits • Comprehensive health insurance plans for employees and families • Competitive retirement and savings plans • Generous annual leave and flexible working options • Global Employee Assistance Program (TELUS Health) • Country-specific benefits (gym memberships, travel passes, childcare vouchers) • Inclusive workplace fostering diversity, equity, and belonging About the Company • ICON plc, a global leader in healthcare intelligence and clinical research • Provides cutting-edge solutions in clinical development • Offers a supportive and inclusive workplace focused on career growth

Role & Responsibilities • Author, review, and approve Clinical Evaluation Reports (CER) in compliance with EU MDR • Prepare and maintain Periodic Safety Update Reports (PSUR) • Develop Post-Market Clinical Follow-up (PMCF) plans and evaluation reports • Create Trend Reports and other post-market surveillance documentation • Ensure compliance with global medical device regulations in regulatory documents • Collaborate with cross-functional regulatory, clinical, and quality teams • Maintain document traceability, version control, and audit readiness • Support regulatory submissions and responses to health authority queries Qualification • Graduate in Pharmacy or Biomedical Engineering, OR • Post-Graduation in Life Sciences Experience • 2 to 15 years in medical device medical writing • Proven hands-on experience in CER, PSUR, PMCF, and post-market documentation Skills • Strong understanding of EU MDR, post-market surveillance, and regulatory writing standards • Experience with regulatory document creation and management • Excellent written communication skills • Ability to collaborate effectively across teams About the Company • Hiring through Wipro • Pune-based, multinational organization • Focused on global medical device regulatory projects and post-market surveillance