Pharmacy Jobs

Roles & Responsibilities• Support PV system compliance and SOP implementation• Conduct quality checks and internal audits• Assist in inspection readiness and CAPA tracking• Maintain pharmacovigilance quality standardsQualification• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, or other Lifesciences degreeExperience• 4–6 years of relevant pharmacovigilance experienceSkills• Strong understanding of global pharmacovigilance regulations (ICH, GVP, FDA, EMA guidelines)• Experience with safety databases (Argus/ArisG preferred)• Strong analytical and documentation skills• Ability to work in a compliance-focused, quality-driven environmentAbout The CompanyMedifodil Smart Pharma Solutions is an expanding pharmacovigilance department offering high-growth opportunities in a quality-driven environment. With a focus on regulatory compliance and patient safety, Medifodil provides comprehensive solutions across ICSR, aggregate reporting, and PV Quality Assurance (QA).

Roles & Responsibilities• End-to-end ICSR case intake, processing, follow-up, and regulatory submissions• Provide medical review support and narrative writing• Perform MedDRA coding and case quality checks• Ensure compliance with global reporting timelines (FDA, EMA, MHRA)Qualification• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, or other Lifesciences degreeExperience• 4–6 years of relevant pharmacovigilance experienceSkills• Strong understanding of global pharmacovigilance regulations (ICH, GVP, FDA, EMA guidelines)• Experience with safety databases (Argus/ArisG preferred)• Strong analytical and documentation skills• Ability to work in a compliance-focused, quality-driven environmentAbout The CompanyMedifodil Smart Pharma Solutions is an expanding pharmacovigilance department offering high-growth opportunities in a quality-driven environment. With a focus on regulatory compliance and patient safety, Medifodil provides comprehensive solutions across ICSR, aggregate reporting, and PV Quality Assurance (QA).

Roles & Responsibilities• Advise patients on proper medication use and potential side effects• Collaborate with healthcare professionals to develop patient treatment plans• Monitor and manage medication inventories to ensure availability and prevent shortages• Provide patient education on disease management and healthy lifestyle choices• Compound specialized medications as needed• Conduct medication therapy management reviews to optimize patient outcomes• Participate in quality improvement initiatives to enhance patient safety and satisfaction• Maintain accurate and up-to-date patient records• Stay current on the latest developments in pharmaceuticals and healthcareQualification• Bachelor of PharmacyExperience• 1–7 years of experience in pharmacySkills• Strong knowledge of medication therapy management and patient counseling• Excellent communication and collaboration skills with healthcare professionals• Ability to manage medication inventories and optimize patient outcomes• Up-to-date knowledge of the latest pharmaceutical practicesAbout The CompanyNutripharm LLC is a leading pharmaceutical company in Dubai, UAE, focused on providing quality medications and healthcare services. The company is dedicated to supporting patient health through expert advice, personalized treatment plans, and high standards in pharmaceutical care.

Roles & Responsibilities• Engage customers with a warm welcome, actively listening to their needs and providing tailored product recommendations• Maintain an organized and visually appealing sales floor, ensuring that merchandise is displayed according to brand standards• Process transactions efficiently, handling cash, credit, and returns while ensuring accuracy and compliance with company policies• Monitor inventory levels and assist in restocking shelves, ensuring popular items are readily available for customers• Utilize point-of-sale systems to track sales data and analyze customer buying trends for effective merchandising• Share product knowledge confidently, educating customers on features and benefits to enhance their shopping experience• Resolve customer complaints and inquiries swiftly, turning potential issues into positive experiences to foster loyalty• Collaborate with team members during busy periods to ensure smooth operations and exceptional service• Participate in ongoing training sessions to stay updated on new products and sales techniquesQualification• High school diploma or equivalent, with a preference for candidates holding a degree in business or retail managementVacancies - 80Experience• 1-6 years of retail experience, with a proven track record of meeting or exceeding sales goalsSkills• Strong communication skills in English (additional language proficiency preferred)• Demonstrated ability to work effectively in a team environment and be self-motivated• Excellent problem-solving skills to address customer inquiries and resolve issues promptly• Positive attitude and strong interpersonal skills to build rapport with customers and colleagues• Flexibility to work various shifts, including evenings, weekends, and holidaysAbout The CompanyLife Pharmacy LLC is one of the leading healthcare groups in the UAE, providing a wide range of pharmaceutical and healthcare products. With a focus on customer care and high-quality service, Life Pharmacy is committed to meeting the needs of their diverse clientele across Abu Dhabi, Dubai, and Sharjah.

Roles & Responsibilities• Dispense prescription medications accurately and safely• Review prescriptions for correctness, interactions, and allergies• Counsel patients on proper medication use, side effects, and storage• Collaborate with physicians and other healthcare professionals• Maintain medication records and ensure compliance with laws and regulationsQualification• Any GraduationExperience• 2–5 years of experience in pharmacySkills• Strong knowledge of medications, interactions, and side effects• Ability to collaborate effectively with healthcare professionals• Good communication and counseling skillsAbout The CompanyJoyce Pharmacy is a trusted pharmacy in Zouk Mosbeh, Lebanon, dedicated to providing quality pharmaceutical services and healthcare support. The pharmacy focuses on patient care, medication safety, and collaboration with healthcare providers to ensure the best outcomes for patients.

Roles & Responsibilities• Review and interpret medication orders (verbal and written) for clarity, rationality, dosage form, allergies, interactions, incompatibility, etc.• Communicate with healthcare providers for clarification and discrepancies about the medication order and document the intervention properly• Transcribe to computerized patient medication profiles accurately and maintain complete patient medication profiles• Report medication errors• Provide drug information and assist in instructing nursing and medical staff and pharmacy students• Perform inspections of nursing units, discuss service problems, and recommend solutions to Pharmacy Supervisor• Develop and coordinate the Quality Improvement Program within the area of responsibility• Fulfill the requirement of 24-hour pharmacy service within the Pharmacy schedule• Attend pharmacy continuing education programs and departmental meetings• Serve as a role model and represent the department professionally• Be cooperative, motivated, and considerate of others' perspectives• Participate in patient and family education to help them better understand and make informed care decisions• Perform other applicable tasks as required by the roleQualification• Bachelor’s Degree in Pharmacy from an accredited college of pharmacy• Valid professional registration certificateExperience• 2–7 years of experience in hospital pharmacy (preferred)Skills• Knowledge of computerized pharmacy systems, I.V admixture, and unit dose systems• Communication skills and the ability to counsel patients• Experience in Middle East healthcare facilities (desirable)About The CompanyDallah Health is a leading healthcare provider in Saudi Arabia, offering comprehensive medical services across multiple specialties. With a focus on patient-centered care, Dallah Health ensures that patients receive high-quality treatment in a supportive and professional environment.

Roles & Responsibilities• Monitor and route incoming safety information to project teams• Perform accurate ICSR data entry and case processing in safety databases• Track and record all safety documentation per sponsor guidelines• Redact patient-identifiable data as per ICH-GCP and GVP requirements• Support literature and clinical trial (CT) case processing• Assist in translation coordination for safety source documents• Support query follow-up and safety submission processes• Maintain case files (electronic and paper)• Conduct daily workflow reconciliation activities• Follow SOPs, WIs, global PV regulations, and study plansQualification• B.Pharm / M.Pharm / PharmD / BDSExperience• Minimum 1 year of Pharmacovigilance case processing or full data entry role (mandatory)• Experience in Clinical Trial (CT) cases and Literature cases preferred• Knowledge of safety databases and medical terminology preferredSkills• Strong documentation accuracy• Ability to manage multiple tasks• Team collaboration• MS Office (Word, Excel, PowerPoint, Outlook) proficiency• Familiarity with document management systems• Understanding of ICH Guidelines, GVP Modules, and global drug safety regulationsAbout The CompanySyneos Health is a global, mid-sized Contract Research Organization (CRO) providing integrated biopharmaceutical solutions to help customers accelerate the development of their drugs. With operations in over 110 countries, Syneos Health has been involved in 94% of novel FDA-approved drugs in the last five years, offering unparalleled exposure to global regulatory standards and drug safety regulations.

Roles & Responsibilities• Develop and implement national market access strategies and plans to support launch readiness and long-term access• Build and maintain trusted relationships with public payers, private insurers, hospital procurement teams, and other local stakeholders• Identify access barriers and design practical, evidence-led solutions, including local pilots or partnership programs• Lead preparation of reimbursement dossiers, value stories, and evidence summaries aligned with local and regional needs• Provide regular market and payer insights to inform commercial, medical, and policy decisions• Work across functions to ensure coordinated execution and compliance during negotiations, tenders, and contracting processesQualification• Bachelor’s degree in pharmacy, life sciences, health economics, public health, or a related fieldExperience• Minimum 3 years of experience in pharmaceutical market access, government affairs, tender management, or payer engagement• Experience working with Saudi public sector payers, hospital procurement, or private insurersSkills• Fluent in Arabic and strong English communication skills• Proven track record of building and managing stakeholder relationships with healthcare and policy decision makers• Strong analytical skills and experience using evidence to build value propositionsAbout The CompanyGSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade. GSK focuses on four therapeutic areas: respiratory, immunology and inflammation, oncology, HIV, and infectious diseases.

Roles & Responsibilities• Monitor investigator sites using risk-based monitoring (RBM)• Ensure compliance with protocol, ICH-GCP, SOPs, and regulations• Conduct site initiation, monitoring, and close-out visits• Perform SDV, SDR, and CRF reviews for data accuracy• Maintain essential documents and audit readiness• Communicate with sites, sponsors, and project teams• Prepare monitoring reports, follow-up letters, and status updatesQualification• Bachelor’s degree in Life Sciences or Registered NursingExperience• 2+ years of experience as a Clinical Research MonitorSkills• Strong knowledge of ICH-GCP and clinical trial regulations• Proficiency in MS Office and CTMS toolsAbout The CompanyThermo Fisher Scientific is a global leader in serving science, providing innovative solutions for life sciences, diagnostics, and applied materials. With a strong commitment to supporting researchers and healthcare professionals, Thermo Fisher offers a comprehensive range of tools and services that enable the advancement of scientific discovery.

Roles & Responsibilities• Dispense medications to inpatient wards and provide pharmaceutical care• Review and monitor patient medication profiles for safety and efficacy• Collaborate with healthcare providers to optimize medication therapy• Provide patient education on medications and their proper use• Ensure compliance with hospital policies, procedures, and regulatory guidelines• Maintain accurate and updated medication recordsQualification• Bachelor’s degree in PharmacyExperience• Previous experience in inpatient pharmacy within a hospital is preferredSkills• Strong knowledge of pharmaceutical practices and hospital pharmacy operations• Excellent communication and interpersonal skills• Ability to work effectively as part of a multidisciplinary team• Attention to detail and strong organizational skillsAbout The CompanyAl Jazeera Hospital is committed to providing quality healthcare and exceptional medical services. We offer a wide range of healthcare services with a focus on patient care, safety, and innovation.

Roles & Responsibilities• Handle pharmacy operations and ensure the availability of medicines• Oversee medication dispensing and ensure proper storage• Monitor inventory levels and manage procurement for the pharmacy• Provide pharmaceutical care and counseling to patients• Ensure compliance with PCI and hospital standards• Collaborate with healthcare providers for effective patient careQualification• D.Pharm / B.Pharm• Valid Telangana PCI RegistrationExperience• Freshers may applySkills• Strong knowledge of pharmaceutical practices and medication management• Excellent communication and interpersonal skills• Ability to manage inventory and handle procurement• Good organizational skills and attention to detailAbout The CompanyAnkura Hospital for Women & Children, Hyderabad, is committed to clinical excellence and providing quality healthcare to women and children. As part of our growth, we are expanding our pharmacy department and are seeking dedicated professionals who share our vision for patient care and operational excellence.

Roles & Responsibilities• Support research activities related to clinical studies.• Assist in organizing and conducting research trials.• Maintain accurate patient records and research documentation.Qualification• BDS/BAMS/BHMS/BUMS with PGDCR is mandatory.• Pharm D.Experience• Research experience in clinical or healthcare-related fields is desirable.Skills• Understanding of clinical research methodologies.• Ability to handle research documentation and patient data.• Strong communication and analytical skills.About The CompanyTata Memorial Centre is one of India’s leading research institutions focused on cancer care and research. The center plays a key role in educating healthcare professionals and advancing research for better cancer treatment.Last date of online application: 13/02/2026, up to 05:30 p.m.

Roles & Responsibilities:• Regulatory query management and responses• Scientific and technical justification preparation• Compliance and regulatory documentation• Cross-functional coordination with internal teams• CAPA handling and continuous improvement activities• Maintaining confidentiality and ethical standardsQualification:• M.Pharm in Regulatory AffairsExperience:• 3 to 5 years in Regulatory Affairs (Pharma)Skills:• Expertise in regulatory query management• Strong scientific and technical writing skills• Familiarity with compliance and regulatory documentation• Ability to work cross-functionally• Strong attention to detail and confidentialityAbout the Company:Accuprec Research Labs Pvt. Ltd. is a leading contract research organization (CRO) dedicated to providing regulatory, clinical research, and pharmaceutical solutions to the global healthcare market. Based in Ahmedabad, Gujarat, the company specializes in regulatory affairs and aims to ensure compliance with all relevant standards and regulations.

Roles & Responsibilities:• Liaise with business partners, country medical teams, and medical leads• Maintain strong relationships with internal stakeholders across regions• Coordinate regularly with FMV leads and tier validators• Ensure accurate transfer of HCP data into tiering systems• Perform data quality checks and remediation of identified errors• Prepare monitoring, verification, and compliance reports within timelines• Support quarterly scientific expert and customer engagement reporting• Manage and prioritize requests via centralized mailbox/platform• Review HCP and non-HCP tiering documentation• Analyze expert credentials to determine appropriate tier levels and FMV• Support local process training, tools, and continuous improvementsQualification:• Bachelor’s or Master’s degree required• B.Pharm / M.Pharm / Life Sciences preferredExperience:• 1–2 years of experience in pharma or life-science companiesSkills:• Strong proficiency in MS Excel, Word, PowerPoint, Outlook, Access• Experience in data handling, reporting, and documentation• Stakeholder and project management skills• Strong communication (written & spoken English)• Analytical thinking, planning ability, and teamwork mindsetAbout The Company:Sanofi is a global pharmaceutical leader, centralizing and streamlining global medical processes to reduce dependency on external vendors and strengthen internal expertise. The company focuses on improving the quality of life for patients worldwide by delivering innovative medicines and therapies. Sanofi offers an inclusive, diverse, and equal-opportunity workplace with structured career growth and skill development opportunities.

Roles & Responsibilities:• eCRF development, testing, and maintenance• Clinical data validation and query management• Preparation of CDM documentation (DMP, DVP, eCCG)• Data reconciliation activities and user training• Medical coding using standard dictionaries• Handling EDC systems and related tools (IWRS, ePRO)• Supporting end-to-end clinical data management activitiesQualification:• M.Pharm (Pharmacology / Quality Assurance)• BDS / BAMS / BHMSExperience:• Site-level experience as a Clinical Research Coordinator (CRC)• Hands-on experience in late-phase clinical trials• Working knowledge of EDC systems and CDM processes• Exposure to IWRS, ePRO, and clinical data toolsSkills:• Strong knowledge of clinical data management processes• Proficiency in handling eCRFs, IWRS, and ePRO systems• Expertise in medical coding using standard dictionaries• Strong analytical and problem-solving skills• Excellent communication and training skillsAbout The Company:Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad. Lambda operates across India, USA, Canada, UK, Spain, and Poland, offering clinical research services with a focus on late-phase clinical trials. With competitive compensation and global exposure, Lambda provides a structured career growth path in the clinical research industry.

Roles & Responsibilities:• Perform systematic literature searches for regulatory and scientific documents• Assist in preparing pre-clinical and clinical sections of Marketing Authorization Dossiers (CTD/eCTD)• Support toxicology documentation including PDE, OEL, and other risk assessments• Contribute to medical-scientific documents such as publications, product rationales, and medico-marketing materials• Collaborate closely with senior medical writers and regulatory managers• Handle additional responsibilities aligned with role capabilitiesQualification:• Degree in Pharmacy, Life Sciences, or related disciplineExperience:• FreshersSkills:• Strong interest in medical writing and regulatory affairs• Basic understanding of EU marketing authorization procedures• Awareness of economic principles related to healthcare/pharma• Excellent written and spoken English communication skills• Proficiency in MS Word, Excel, PowerPoint, and scientific literature review• Ability to work independently with high accuracy and attention to detail• Strong teamwork, responsibility, and interpersonal skillsAbout The Company:Cencora offers global exposure in regulatory medical writing. The company provides structured training and mentorship for early-career professionals, working on international regulatory submissions. With a commitment to an inclusive and equal opportunity workplace, Cencora offers competitive compensation and long-term career growth opportunities within its global ecosystem.

Roles & Responsibilities:• Assist Principal Investigator (PI) in site feasibility assessments• Support pre-trial documentation and regulatory readiness• Collect and maintain updated CVs of site staff• Ensure timely completion of financial disclosure forms, PI undertaking, and confidentiality agreements• Coordinate with IRB/IEC for faster approvals and timely submission of safety reports and protocol amendments• Assist PI & Co-Investigators in Informed Consent Process• Prepare for Site Initiation Visits (SIV)• Maintain Site Master File (SMF) and patient files• Handle patient recruitment, screening, enrollment, and follow-ups• Complete CRF and clinical data entry• Coordinate patient follow-up visits (physical & telephonic)• Report and follow-up on SAE (Serious Adverse Events)• Manage drug accountability and inventory tracking• Maintain study budget sheets and track IRB fees, site administration fees, lab costs, and patient reimbursementsQualification:• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, LifesciencesExperience:• 1–4 years in clinical research / clinical trialsSkills:• Knowledge of ICH-GCP Guidelines• Experience with IRB/IEC Submissions• SAE Reporting & Drug Safety• CRF Completion & Clinical Data Management• Patient Recruitment & Site CoordinationAbout The Company:Max Healthcare is one of India’s leading hospital networks, offering an advanced research ecosystem for clinical trials. The company is focused on providing comprehensive healthcare and pioneering clinical research that adheres to global standards, promoting patient safety and the highest standards of care.

Roles & Responsibilities• Handle batch manufacturing and filling activities in sterile area (Injectables, BFS, Eye drops)• Operate ampoule/vial washing (Macofar), Rota filling, BFS machines and Autoclave• Conduct media fill studies and equipment qualification• Lead qualification studies in sterile manufacturing (QA senior roles)• Perform QC testing for finished products and stability samples• Conduct analytical method validation and method transfer• Handle QMS documentation and compliance activities• Perform microbiological testing including sterility testing, MLT, environmental monitoring• Ensure adherence to regulatory and GMP guidelinesQualification• B.Pharm / M.PharmExperience• Freshers (QC – male candidates only)• 0–12 years depending on role• Production: 2–8 years• QA: 3–10 years• QC: 0–6 years• Microbiology: 6–12 yearsSkills• Sterile manufacturing exposure• Media fill & validation knowledge• Equipment qualification handling• Analytical testing & stability studies• QMS & regulatory documentation• Environmental monitoring• GMP & compliance awarenessAbout The CompanyMicro Labs Limited is a leading Indian pharmaceutical company specializing in sterile formulations including injectables and ophthalmic products. The organization operates in regulated markets and provides strong exposure to quality systems, GMP compliance, and large-scale pharmaceutical manufacturing.

Roles & Responsibilities• Dispense medicines as per prescription in accordance with hospital protocols• Ensure safe storage, handling and distribution of pharmaceuticals• Maintain proper drug inventory and stock registers• Monitor expiry dates and ensure compliance with pharmacy regulations• Provide medication counselling to patients where required• Maintain accurate clinical and pharmacy documentation• Ensure compliance with Pharmacy Council and statutory norms• Assist in hospital pharmacy operations at NLC India HospitalQualification• Full-time Bachelor’s Degree in Pharmacy (B.Pharm)• Registration with Pharmacy Council of India / State Pharmacy Council• Qualification must be from a recognized Indian University/InstituteVacancies no - 15 (UR – 8, EWS – 1O, BC – 4, SC – 2)Experience• Experience as per eligibility criteria mentioned in official notification• Candidates must meet age and statutory eligibility conditions• Preference as per Government of India norms (if applicable)Skills• Strong knowledge of pharmaceutical sciences and drug dispensing• Understanding of hospital pharmacy operations• Knowledge of drug storage and inventory systems• Familiarity with regulatory compliance and statutory guidelines• Good communication skills• Proficiency in Tamil (local/regional language requirement)• Documentation and record-keeping skillsSalary• Pay Scale: ₹22,000 – 3% – ₹90,000 (W-5 Grade)• Approx. CTC: ₹6.13 Lakhs per annum• Additional benefits: Unified Incentive Scheme, Free medical treatment for self & dependents, Group Insurance• Residential accommodation subject to availabilityAbout the CompanyNLC India Limited is a ‘Navratna’ Government of India Enterprise engaged in Mining (Lignite & Coal), Thermal Power Generation, and Renewable Energy. With a consolidated annual turnover of ₹15,282.96 Crores (FY 2024-25), the organization operates NLC India Hospital at Neyveli, Tamil Nadu, providing comprehensive healthcare services.