Pharmacy Jobs

Role & Responsibilities Maintain global oversight of unresolved sample discrepancies for incoming and outgoing shipments Coordinate with internal teams to resolve discrepancies within defined TAT and OTIF timelines Perform QC verification of biospecimen data in LIMS and inventory systems Conduct advanced QC checks and trend analysis on sample data Support study close-out activities including reconciliation of sample disposition Monitor patient sample collection schedules and protocol assessment windows Support study setup activities in LIMS including workflows and protocol configuration Prepare operational reports including inventory, kit tracking and site performance metrics Participate in RCA and CAPA activities Ensure compliance with QMS, SOPs and data privacy regulations Support ad-hoc analysis and cross-functional operational requests Qualification Bachelor’s or Master’s degree in Life Sciences or related discipline Experience Minimum 2–3 years of experience in clinical research, sample management or data operations Skills Strong understanding of drug, device and biologic development processes Hands-on experience with clinical databases and LIMS systems Expertise in data quality and compliance standards Proficiency in MS Excel, Word, PowerPoint and Outlook Excellent written and verbal communication skills Knowledge of GDPR, HIPAA and data privacy regulations About the Company Precision For Medicine is a global precision medicine organization supporting international clinical trials, biospecimen management and advanced clinical data operations

Role & Responsibilities Perform triage and initial validity assessment of adverse event cases Enter and manage safety data in global pharmacovigilance databases Conduct initial ICSR assessments as per regulatory requirements Evaluate cases for expedited reporting and regulatory timelines Prepare and submit CIOMS I, MedWatch and XML safety reports Draft follow-up queries to collect missing case information Maintain audit-ready documentation Retrieve and assess cases from EVWEB and health authority sources Support additional pharmacovigilance activities as assigned Qualification B.Pharm / M.Pharm BDS Life Science Graduate Experience Freshers / Entry-level candidates preferred Skills Strong written and verbal communication Attention to detail and compliance mindset Basic understanding of pharmacovigilance and drug safety Willingness to learn global PV regulations Time management and documentation skills About the Company Cencora, through PharmaLex India, is a global healthcare services organisation delivering regulatory, pharmacovigilance and risk management solutions while ensuring patient safety and compliance across international markets

Role & Responsibilities Author and support aggregate safety reports including PSURs, PBRERs, RMPs and Addendums Perform ICSR data entry, processing and management in global safety databases Conduct literature searches for individual case safety reports and periodic reports Ensure compliance with internal SOPs and global pharmacovigilance regulations Coordinate with global affiliates and cross-functional stakeholders Support safety signal detection and ongoing risk management activities Qualification B.Pharm / M.Pharm Experience 2 – 4 years of pharmacovigilance experience Skills PSUR, PBRER, RMP and AddCo authoring ICSR case processing and literature review Knowledge of ICH, GVP, US FDA and EMA guidelines Scientific writing and documentation Attention to detail and time management Strong communication and problem-solving abilities About the Company Mega Lifesciences is a global healthcare and pharmaceutical organisation delivering evidence-based medicines and operating robust pharmacovigilance systems to ensure patient safety and regulatory compliance across international markets

Role & Responsibilities Perform medical review and analysis of adverse event and adverse reaction reports Conduct signal detection, evaluation and ongoing safety surveillance Provide medical guidance to Drug Safety Associates and Specialists Review narratives for Clinical Study Reports and regulatory documents Prepare and review Benefit Risk Assessments, Safety Evaluation Reports, Clinical Overviews and Expert Statements Act as pharmacovigilance representative and safety scientist Maintain thorough knowledge of assigned product safety profiles Ensure compliance with global regulatory reporting timelines Communicate review issues with Project Managers and stakeholders Perform case medical review, causality assessment, seriousness and expectedness evaluation Conduct medical literature review for safety assessments Qualification Graduation / Post Graduation in Medicine (MBBS / MD) Experience Freshers or candidates with Pharmacovigilance / Drug Safety experience preferred Skills Strong knowledge of GCP, GVP and international PV regulations Excellent written and verbal communication skills Clinical data interpretation and medical judgment Case processing guidance and regulatory compliance Literature review and safety signal analysis Team collaboration and multitasking abilities About the Company A global pharmacovigilance and regulatory services organisation supporting multinational pharmaceutical clients in ensuring patient safety, compliance and lifecycle drug risk management

Role & Responsibilities Dispensing, counselling, immunisations Inventory, DAA, medication reviews Qualification Pharmacy Graduate eligible for internship Experience Community pharmacy experience preferred Skills Communication, teamwork, patient care, accuracyAbout the Company Biloela Discount Chemist is a community-focused regional pharmacy

Role & Responsibilities Minor ailment diagnosis, vaccinations, DAA, diabetes care UTI, BP monitoring, mobility solutions Community education & stock management Qualification Bachelor of PharmacyExperience Community pharmacy experience preferred Skills Communication, teamwork, patient care, accuracy About the Company SuperPharmacyPlus is an award-winning independent community pharmacy group focused on advanced clinical pharmacy services

Role & Responsibilities Dispensing and OTC counselling Stock control, DAA preparation and dispensary admin Vaccinations, wound care, sleep apnoea services Work with allied health professionals Qualification Bachelor / Master of Pharmacy Experience Community pharmacy experience preferred Skills Communication, teamwork, patient care, accuracy About the Company Wizard Pharmacy Mosman Park is a busy metropolitan community pharmacy offering professional clinical services with structured intern training support

Role & Responsibilities Review and assess individual case safety reports from clinical trials, spontaneous and solicited sources Determine regulatory reportability and perform case triage Assess seriousness, causality and relatedness of adverse events Review narratives, MedDRA coding, labeling and adverse event selection Escalate complex safety cases to client medical review teams Assess litigation and special case scenarios Coordinate with client therapeutic teams for case resolution Maintain up-to-date product safety profile knowledge Ensure compliance with global health authority regulations Perform additional drug safety activities as assigned Qualification MBBS / MD MCI / State Medical Council Registration Mandatory Experience 1 – 3 years in Pharmacovigilance as Medical Reviewer Skills Safety database handling and MedDRA coding Case triage and regulatory compliance Customer and stakeholder communication Presentation and people management skills Strong organizational, leadership and time management abilities About the Company A leading pharmacovigilance and drug safety services organization supporting global pharmaceutical clients in ensuring patient safety and regulatory compliance

Role & Responsibilities Ensure high quality and regulatory-compliant case processing by vendors Perform quality review of ICSRs and device event reports Review and update vendor SOPs and working procedures Monitor weekly and monthly quality data and identify training needs Review AE/SAE and device event reports for pre and post-marketed products Clarify medical issues, revise MedDRA coding and ensure accurate narratives Coordinate with vendors and internal medical teams for case resolution Support audits, inspections, CAPA documentation and vendor oversight Maintain vigilance documentation and archival processes Train and guide vendor vigilance staff Implement process improvements and corrective actions Qualification BS / MS / Doctorate in Pharmacy, Nursing or related healthcare discipline Experience Minimum 3 years in Pharmacovigilance or Materiovigilance Prior experience in ICSR or device event review preferred Skills Strong knowledge of global PV & MV regulations Experience with safety databases (LSMV, CATSWeb preferred) Excellent communication and interpersonal skills High attention to detail and strong organizational skills Ability to work cross-functionally and manage workflow priorities About the Company A global healthcare organization operating within Global Pharmacovigilance & Risk Management, focused on regulatory-compliant safety surveillance, risk management and medical device vigilance across international markets

Role & Responsibilities Dispense medicines and manage pharmacy stock Provide patient counselling Maintain pharmacy records Qualification B.Pharm or D.Pharm Experience As per norms Skills Dispensing, stock management, patient counsellingAbout the Organisation District Health Society Ranipet – Government Health Services Start Date17-12-2025Last Date06-01-2026Application formClick HereOfficial NotificationClick Here

Role & Responsibilities Support safe and effective use of specialist medicines Provide medication therapy management and clinical services Deliver personalised, high-quality patient care Dispense and review specialist medications Work across fertility, chemotherapy, macular degeneration and GLP-1 weight management services Maintain accurate clinical and dispensing records Collaborate with healthcare teams to ensure optimal treatment outcomes Qualification Bachelor of Pharmacy Valid AHPRA Registration (Australia) Experience Minimum 1 year experience as a registered pharmacist Skills Strong communication and attention to detail Ability to work under pressure Willingness to learn and adapt Leadership and team management abilities Organisational and time management skills About the Company A modern, fast-growing specialist pharmacy and supply organisation delivering personalised care, clinical pharmacy services and technology-driven healthcare solutions across multiple high-impact therapeutic areas

Role & Responsibilities Dispense medicines accurately as per prescriptions Maintain pharmacy inventory, stock records and expiry tracking Ensure compliance with Pharmacy Act and hospital SOPs Provide medication counselling to patients and caregivers Monitor storage conditions and drug safety standards Maintain computerized pharmacy records Support night shifts and rotational duty schedules as required Qualification Diploma in Pharmacy (D.Pharm) or Bachelor of Pharmacy (B.Pharm) Must be a Registered Pharmacist under the Pharmacy Act, 1948 Experience Minimum 1 year of experience preferred Freshers can apply if registeredSalary ₹20,000 – ₹22,000 per monthVacancies 21 Position Skills Sound knowledge of medicines and dispensing Inventory and stock management Patient counselling and communication skills Basic computer proficiency Ability to work in rotational shifts About the Company Homi Bhabha Cancer Hospital & Research Centre is a premier oncology healthcare institution providing advanced cancer diagnosis, treatment and research services under Tata Memorial Centre, focused on patient-centric and evidence-based medical careHow to Apply Walk-In Interview 📍 Venue: Homi Bhabha Cancer Hospital & Research Centre Shri Krishna Medical College & Hospital Campus Umanagar, Muzaffarpur, Bihar – 842004 Reporting Time: 9:00 AM – 10:00 AM Reporting Date - 19-01-2026

About Role & Responsibilities • Act as a liaison between clinical trial sites, supporting rapid identification and referral of eligible patients • Drive recruitment acceleration strategies at the site level, collaborating closely with investigators, study coordinators, and site staff • Engage in patient finding activities through site-based engagement, outreach to the medical community, and data-driven approaches • Provide education and continuous communication to sites regarding eligibility criteria, enrollment processes, and recruitment barriers • Proactively identify and address enrollment challenges, escalating risks and proposing mitigation strategies • Track recruitment progress, providing regular updates and insights to the sponsor and TFS study team Qualifications • Background in Life Sciences, Pharmacy, Nursing, or a related healthcare field • Proven experience in supporting patient recruitment for Phase 2/3 clinical trials • Expertise in hematology and/or rare diseases; experience with Myelofibrosis or other rare hematologic malignancies is a plus • Strong understanding of site-based patient identification and recruitment methodologies in India • Excellent communication and relationship-building skills with investigators and site teams • Willingness to travel to sites across the country (living near an airport is desirable) What We Offer • A chance to make a direct, measurable impact on patient enrollment in a critical late-stage clinical trial • Work closely with an experienced global study team in a fast-paced, results-driven environment • Clear objectives and decision-making authority focused on successful enrollment

About Role & Responsibilities • Assist customers with general pharmacy inquiries and provide excellent customer service • Support the dispensary with scripts in/out, ensuring accurate and timely processing • Replenish stock and maintain inventory levels to ensure pharmacy operations run smoothly • Multitask in various areas of the pharmacy to support team and customer needs Qualification • Previous experience in a pharmacy environment is essential • A good understanding of Point of Sale Systems (MINFOS software is beneficial) • Certificates I - III in Community Pharmacy or S2 & S3 training (preferred but not essential) Skills • Strong interpersonal and communication skills • Self-motivated, organised, and enthusiastic about providing outstanding customer service • Genuine passion for the pharmacy industry and delivering professional health advice About the Company Chempro Chemists is one of Australia’s fastest-growing pharmacy groups, with over 150 locations across the Gold Coast, Tweed Coast, and Brisbane. We are dedicated to providing exceptional healthcare solutions to Australians and are committed to customer service excellence.

About Role & Responsibilities • Lead delivery operations for pharmacovigilance and drug safety services • Ensure adherence to global pharmacovigilance standards and timelines • Collaborate with teams to manage client relationships and regulatory compliance Qualification • B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences Experience • 3+ years in pharmacovigilance or related operations roles Skills • Leadership and team management skills • In-depth knowledge of pharmacovigilance processes and regulations About the Company Arcolab is a leader in pharmacovigilance and drug safety services, offering comprehensive solutions to the pharmaceutical industry

About Role & Responsibilities • Process pharmacovigilance cases in various languages, including Japanese, Vietnamese, French, Arabic, or Persian • Ensure timely processing of adverse event reports in accordance with regulatory requirements • Collaborate with cross-functional teams to ensure accurate data entry and reporting Qualification • B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences Experience • Freshers welcome to apply Skills • Fluency in one or more of the listed languages • Attention to detail and strong analytical skills About the Company Clinovo is a global leader in clinical research, specializing in pharmacovigilance and medical writing

About Role & Responsibilities • Assist with evidence synthesis and health economics-related tasks • Conduct data analysis and report preparation for clinical studies • Work with cross-functional teams to support decision-making Qualification • M.Pharm, M.Sc, or related discipline / MBBS, MD Experience • 0-2 years of experience in evidence synthesis or related roles Skills • Strong analytical and data interpretation skills • Proficiency in health economics methodologies About the Company Sanofi is a global healthcare leader providing innovative treatments in various therapeutic areas

About Role & Responsibilities • Perform pharmacovigilance activities such as signal detection and risk management • Ensure compliance with regulatory requirements for drug safety • Assist in preparing safety reports and presenting findings Qualification • B.Pharm Experience • 0-2 years in pharmacovigilance Skills • Strong understanding of pharmacovigilance processes • Good communication and report writing skills About the Company Cosette Pharma specializes in the development and commercialization of pharmaceutical products

About Role & Responsibilities • Dispense prescribed medications and provide pharmaceutical care • Assist in maintaining pharmacy inventory • Offer counseling to patients on drug use and side effects Qualification • D. Pharm / B. Pharm Experience • 0 – 2 years Skills • Pharmaceutical dispensing • Patient care • Inventory managementAbout the Company DHS Nilgiris provides healthcare services in the Nilgiris regionStart Date27-12-2025Last Date06-01-2026 Official Notification and Application FormClick Here