Pharmacy Jobs

Roles & Responsibility • Dispense medicines accurately as per valid prescriptions • Review prescriptions for correctness, dosage, and possible drug interactions • Ensure proper storage, labeling, and handling of pharmaceuticals • Maintain medicine stock, expiry tracking, and inventory records • Provide medication counseling and usage guidance to patients • Follow pharmacy SOPs, safety standards, and regulatory guidelines • Maintain pharmacy documentation, registers, and daily records • Coordinate with medical officers and healthcare staff for patient care Qualification • B.Pharm from a recognized university or institution Experience • Relevant pharmacy experience preferred • Experience in hospital or government healthcare setup will be an added advantage • Freshers fulfilling eligibility criteria may also apply Important Date• Application Deadline: 27-01-2026Skills • Sound knowledge of pharmaceutical products and practices • Attention to detail and accuracy in dispensing • Good communication and patient interaction skills • Ability to manage inventory and records efficiently • Basic computer knowledge • Understanding of pharmacy laws and safety protocols About the company National Ayush Mission (NAM), Dadra & Nagar Haveli and Daman & Diu (DNH & DD), works under the Ministry of AYUSH to strengthen AYUSH healthcare services through government health institutions, ensuring quality, affordable, and accessible traditional healthcare across the region.Official Notification and Application FormClick Here

Roles & Responsibility • Dispense prescribed medicines accurately as per physician orders • Review prescriptions for dosage accuracy, interactions, and contraindications • Maintain proper storage, labeling, and inventory of medicines • Provide medication counseling and usage instructions to patients • Ensure compliance with pharmacy laws, SOPs, and safety guidelines • Maintain pharmacy records, registers, and documentation • Coordinate with doctors, nurses, and healthcare staff for patient care • Monitor expiry dates and manage stock replenishment Qualification • B.Pharm from a recognized institution • D.Pharm from a recognized institution Experience • Relevant pharmacy experience preferred • Experience in hospital or clinical pharmacy will be an added advantage • Freshers meeting eligibility criteria may also applyImportant Date• Application Deadline: 30-01-2026 Skills • Good knowledge of medicines and pharmaceutical practices • Basic understanding of hospital pharmacy operations • Attention to detail and accuracy • Good communication and patient counseling skills • Ability to follow SOPs and regulatory guidelines • Basic computer knowledge for record keeping About the company Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative under the Ministry of Defence, providing comprehensive healthcare services to ex-servicemen and their dependents through a nationwide network of polyclinics, ensuring quality medical care with standardized systems and protocols.Official NotificationClick Here

Role & Responsibilities • Deliver high-quality, safe, and patient-centred medication management services across inpatient and outpatient settings. • Provide comprehensive pharmacy services including dispensing, clinical review, production, and patient counselling. • Undertake timely medication histories, daily medication reviews, and develop medication action plans to optimise therapy. • Exercise professional judgement and relative autonomy in dispensing and clinical decision-making in line with SA Health guidelines and legislation. • Provide expert medication advice and support to medical, nursing, and allied health professionals. • Supervise and support pharmacy technicians and assistants in daily pharmacy operations. • Respond to medication-related enquiries, prepare reports, and contribute to quality improvement, education, and research initiatives. • Ensure compliance with hospital policies, State and Federal legislation, and clinical governance requirements. Qualification • Bachelor of Pharmacy (or equivalent) from a recognised institution. • Current registration or eligibility for registration with the Pharmacy Board of Australia.Experience • Experience in hospital or clinical pharmacy practice is preferred. • Ability to work with relative autonomy while contributing effectively within a multidisciplinary healthcare team.Skills • Strong knowledge of clinical pharmacy practice, dispensing, production, and patient counselling. • Sound understanding of pharmacy legislation and hospital medication safety standards. • Excellent communication, organisational, and interpersonal skills. • High attention to detail with a strong focus on accuracy and patient safety. • Ability to work both independently and collaboratively, demonstrating flexibility, resilience, and initiative.About Company • Statewide Clinical Support Services (SCSS) is a public healthcare organisation under SA Health, providing specialist clinical services across South Australia. SCSS includes SA Pharmacy, SA Pathology, SA Medical Imaging, SA Dental, and BreastScreen SA, supporting health services and improving the health and wellbeing of South Australians across all stages of life.

Roles & Responsibilities• Plan, implement, and monitor clinical research studies according to regulatory and institutional guidelines• Coordinate with investigators, study teams, and stakeholders to ensure smooth study execution• Maintain accurate documentation of clinical trial activities and prepare reports• Ensure compliance with Good Clinical Practice (GCP) and study protocols• Support data collection, quality checks, and regulatory submissions• Assist in training and mentoring junior research staff• Contribute to service improvement and operational planning for research projectsSkills Required• Strong understanding of clinical research protocols and regulatory requirements• Excellent communication and interpersonal skills• Ability to manage multiple studies and meet deadlines• Attention to detail and commitment to high-quality data management• Effective collaboration with multidisciplinary research teamsQualifications• M. Pharm, MBBS, BDS, BHMS, BAMS, or B.E./B. Tech• Relevant certifications or experience in clinical research is preferredExperience After Qualification• Prior experience in clinical research coordination or monitoring preferredAdditional Requirements• Minimum age: 21 years; Maximum age: 45 years (age relaxation as per organization norms)• Willingness to adhere to institutional and regulatory guidelines• Eligibility to work in India• Application Fee: ₹590 (OBC/Unreserved), ₹118 (Reserved/Women)About the CompanyThe Translational Health Science and Technology Institute (THSTI) is a premier research organization dedicated to advancing human health through cutting-edge research, innovation, and technology translation. THSTI focuses on multidisciplinary collaboration, clinical studies, and translational research, promoting excellence in scientific and clinical practices. The institute emphasizes professional development, ethical research, and high-quality contributions to health science.Important Dates:• Starting date: 15-01-2026• Closing date: 04-02-2026Official NotificationClick Here

Roles & responsibility • Dispense medications accurately as per prescriptions • Review prescriptions for dosage, interactions and appropriateness • Counsel patients on correct medication use, side effects and precautions • Manage pharmacy inventory, stock control and expiry monitoring • Ensure compliance with UAE pharmacy regulations and safety protocols • Maintain accurate documentation and pharmacy records • Coordinate with doctors and healthcare staff for optimal patient care • Follow standard operating procedures and quality guidelines Qualification • Bachelor’s degree in Pharmacy (B.Pharm) • Doctor of Pharmacy (PharmD) preferred • Valid UAE Pharmacist license Experience • 3+ years of experience in hospital or community pharmacy • UAE pharmacy experience preferred Skills • Strong knowledge of pharmaceuticals and drug safety • Inventory management and documentation skills • Excellent communication and patient counseling abilities • High attention to detail and accuracy • Ability to work independently and within a healthcare team About the company The organization operates within the medical and healthcare sector, delivering patient-centric pharmaceutical and clinical services while maintaining high standards of quality, safety, regulatory compliance and professional healthcare practices.

Role & responsibilities • Dispense prescribed medicines accurately as per standard guidelines • Ensure proper storage, labeling and inventory management of medicines • Review prescriptions for correctness and compliance • Counsel patients on dosage, usage, side effects and storage of medicines • Maintain pharmacy records, stock registers and documentation • Monitor expiry dates and ensure safe disposal of expired medicines • Coordinate with doctors, nurses and healthcare staff for patient care • Ensure compliance with pharmacy laws, AYUSH guidelines and SOPs • Maintain cleanliness and safety standards in the pharmacy Qualification • B.Pharm, D.Pharm Age limit • Minimum age: 21 years • Maximum age: 30 years Important date • Application deadline: 27-01-2026 Skills • Knowledge of pharmacy operations and drug handling • Understanding of AYUSH medicines and formulations • Attention to detail and accuracy • Good communication and patient counseling skills • Record keeping and basic computer skills • Ability to work in a healthcare environment About the company The Ministry of AYUSH is a Government of India body responsible for the development, regulation and promotion of traditional systems of medicine including Ayurveda, Yoga & Naturopathy, Unani, Siddha and Homoeopathy, supporting quality healthcare delivery across the country.

Role & Responsibilities • Provide technical and programmatic support to health programs under National Health Mission • Assist in planning, implementation and monitoring of national and state health initiatives • Analyze health data, program reports and indicators for informed decision-making • Support preparation of policy documents, guidelines and operational frameworks • Coordinate with central, state and district health authorities • Conduct field visits, reviews and assessments of ongoing programs • Prepare presentations, reports and official communications for stakeholders • Support capacity building, training and technical discussions as required • Ensure compliance with government norms, policies and timelines Qualification • MBBS / BDS / BAMS / BHMS / BUMS • B.Sc Nursing / B.Sc / B.Pharm • Post Graduation / MD / MS Experience • Relevant professional or program experience in healthcare, public health or health systems • Experience working with government health programs will be preferred Age limit • Minimum age: 21 years • Maximum age: 45 years Important dates • Application Deadline date: 04-02-2026 Skills • Strong analytical and problem-solving skills • Good communication and presentation skills • Ability to work with multidisciplinary teams • Knowledge of public health systems and government programs • Proficiency in documentation, reporting and data interpretation About the company National Health Mission works towards strengthening public health systems in India by improving access to quality healthcare services, implementing national health programs, and supporting states in achieving key health outcomes through policy, planning and technical assistance.Official Notification Click Here

Role & Responsibilities • Plan, execute and support research projects under assigned scientific programs • Assist in experimental design, data collection and data interpretation • Maintain accurate documentation of research activities and results • Prepare technical reports, research summaries and project updates • Ensure compliance with institutional guidelines, ethical standards and safety norms • Coordinate with internal teams, investigators and external collaborators • Support procurement, calibration and maintenance of laboratory equipment • Analyze experimental data using appropriate scientific tools and methodologies • Contribute to publications, presentations and project deliverables • Assist in monitoring project timelines and milestones Qualification • M.Sc / M.Tech / M.Pharm / Ph.D in relevant discipline Experience • Relevant research or project experience as per institutional norms Age limit • Minimum age: 21 years • Maximum age: 40 years Skills • Strong research and analytical skills • Good documentation and reporting skills • Ability to work independently and in a team • Proficiency in scientific tools and laboratory practices • Good communication skills About the company Postgraduate Institute of Medical Education and Research (PGIMER) is a premier medical and research institute dedicated to excellence in medical education, advanced research, and high-quality healthcare services, contributing significantly to national and global medical advancements.Official NotificationClick Here

ROLES & RESPONSIBILITIES • Develop, implement and maintain an effective Quality Management System (QMS) • Monitor and evaluate existing QMS processes for continuous improvement • Conduct internal audits and assessments to ensure regulatory compliance • Coordinate with cross-functional teams to maintain quality control measures • Draft, review and update Standard Operating Procedures (SOPs) • Ensure SOPs are aligned with regulatory and industry best practices • Implement and monitor Change Control related to SOPs • Support risk management activities and mitigation plans • Participate in external audits and regulatory inspections • Perform vendor audits during onboarding and periodic reviews • Collect and analyze quality performance data and metrics • Prepare quality reports and track trends • Identify gaps and recommend process improvements • Investigate non-conformances and quality incidents • Implement and monitor Corrective and Preventive Actions (CAPA) • Ensure effective closure of CAPA and Change Control activities QUALIFICATION • Post Graduation - Master of Pharmacy (M.Pharm) • Graduation - Bachelor of Pharmacy (B.Pharm) EXPERIENCE • Up to 6 years of relevant experience SKILLS • Strong knowledge of QMS, SOPs, CAPA and audits • Good communication and coordination skills • Fluency in English • Strong documentation and analytical skills ABOUT THE COMPANY The company is a quality-focused organization committed to maintaining robust quality systems, regulatory compliance, and continuous improvement to support high standards across pharmaceutical operations.

Roles & Responsibilities • Respond to medical and product-related inquiries from healthcare professionals, consumers, and internal teams • Document medical inquiries and responses accurately in approved databases and formats • Support development and updating of standard response letters, FAQs, and reference materials • Collect, document, and route adverse event (AE) information in compliance with drug safety SOPs • Perform medical literature searches using databases such as PubMed, OVID, and EMBASE • Maintain and update product and medical information databases • Assist in creation, review, and maintenance of SOPs and procedural documents • Prepare weekly and monthly reconciliation and activity reports • Ensure compliance with project guidelines, SOPs, and regulatory requirements • Coordinate with internal stakeholders and clients for timely and accurate medical responses Qualification • B.Pharm or M.Pharm (any specialization) • PhD (Pharmacy) – optional Skills • Medical information services and scientific communication • Medical literature review and data interpretation • Basic understanding of pharmacovigilance and adverse event intake • Familiarity with PubMed, OVID, and EMBASE databases • Strong written and verbal communication skills • Attention to detail and compliance-oriented mindset About the Company Apcer Life Sciences is a global provider of pharmacovigilance, regulatory, medical information, and clinical research services, supporting pharmaceutical, biotechnology, and medical device companies with compliant, technology-driven solutions across the product lifecycle.

Roles & Responsibilities • Collaborate with the eTMF Team Lead to proactively meet TMF business and study requirements • Act as document creator, QC reviewer, and primary TMF contact for assigned clinical studies • Manage end-to-end TMF activities including document processing, indexing, filing, and reconciliation • Ensure continuous TMF completeness, accuracy, and inspection readiness • Perform discrepancy identification and resolution as per SOPs, timelines, and regulatory expectations • Support internal audits and external regulatory inspections • Contribute to TMF-related SOPs, guidelines, and system user documentation • Communicate TMF risks, issues, and status updates to senior stakeholders in a timely manner Qualification • Degree in Life Sciences, Pharmacy, Clinical Research, or a related discipline Experience • 1-3 years of hands-on experience in eTMF, TMF operations, or clinical documentation roles Skills • Strong knowledge of ICH-GCP guidelines and TMF lifecycle management • Understanding of regulatory inspection preparedness and compliance requirements • High attention to detail with a strong quality and audit-focused mindset • Good communication skills and ability to collaborate with cross-functional clinical teams About the Company Tata Consultancy Services (TCS) is a global leader in IT services, consulting, and life sciences solutions, supporting pharmaceutical and clinical research organizations worldwide with technology-driven, compliant, and scalable solutions across clinical operations, regulatory affairs, and digital transformation.

Roles & Responsibilities • Recruit and enroll eligible study participants as per approved protocols • Coordinate patient visits, procedures, follow-ups, and study schedules • Enter, review, and maintain accurate clinical data in EDC systems • Act as primary point of contact for study participants and address protocol-related queries • Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements • Prepare, maintain, and update essential study documents and trial files • Manage proper filing and archival of CRFs and study-related documentation • Coordinate with sponsors, ethics committees, investigators, and multiple study sites • Support Principal Investigators (PI) for smooth conduct of clinical studies Qualification • Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, Nursing, Pharmacy, or related discipline • Diploma in Clinical Research is an added advantage Experience • 1-5 years of experience in clinical research coordination or site operations • Hospital-based or site-level research experience preferred Skills • Strong knowledge of clinical trial processes and documentation • Working understanding of ICH-GCP and regulatory requirements • Good data management, organizational, and planning skills • Proficiency in MS Word and MS Excel • Strong communication and interpersonal skills • Ability to coordinate with multiple stakeholders and sites About the Company Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations, known for its extensive national presence, patient-centric approach, and commitment to clinical excellence, research, and ethical medical practices in assisted reproductive technologies.

Roles & Responsibilities:• Convert patient medical records into accurate alphanumeric medical codes• Review doctors’ notes, diagnoses, procedures, and treatment details• Assign ICD-10, CPT, and HCPCS codes as per coding guidelines• Ensure accuracy and compliance in medical documentation• Support medical billing and insurance claim processes• Maintain confidentiality of patient health information• Follow quality standards and productivity benchmarksQualifications:• UG / PG in Life Science or Paramedical streams• Eligible degrees include BPT, MPT, BDS, BHMS, BAMS, BNYS, BSMS, BUMS, Nursing, Pharmacy, Biotechnology, Microbiology, Zoology, Botany, Biomedical, and related fields• Knowledge of Anatomy and Physiology is mandatoryExperience:• Freshers are encouraged to apply• Candidates with up to 3 years of experience can also applyKey Skills:• Medical Coding fundamentals• Anatomy & Physiology knowledge• ICD-10 / CPT basics• Medical documentation review• Basic computer skills• Attention to detailCompensation & Benefits• Performance-based incentives (₹3,000 and above)• 5-day work week (Saturday & Sunday off)• Day shift only• Food and cab facilities provided• Medical expenses covered• Provident Fund & Gratuity benefits• Salary increment within 6 months (for experienced candidates)• Abroad opportunities available• Referral bonusesAbout the Company:Achievers Spot is a well-established, ISO 9001:2015 certified medical coding training and placement organization based in Chennai. The company specializes in building careers for Life Science and Paramedical graduates by providing industry-oriented medical coding training and placement support. With experienced trainers and strong ties to leading healthcare BPOs and MNCs, Achievers Spot enables candidates to secure long-term, stable careers in the healthcare industry.

Roles & Responsibilities • Assist in delivering comprehensive pharmacy services under the supervision of a registered Pharmacist • Support dispensing of prescriptions and individual patient medication supply for inpatients • Manage ward imprest supply and maintain medication availability in assigned wards • Assist with clinical documentation including adverse drug reaction records • Repack medications as per pharmacy requirements and guidelines • Maintain stock levels through imprest systems with minimal supervision • Support stock control activities including receipt, storage, and inventory maintenance of pharmaceuticals • Contribute to health equity initiatives, supporting culturally safe and inclusive healthcare practices Qualification • Relevant pharmacy support qualification or equivalent healthcare-related education (as per hospital requirements) Experience • Prior experience in a hospital or healthcare pharmacy setting preferred • Fresh or early-career candidates with relevant exposure may be considered Skills • Basic understanding of pharmacy dispensing and medication handling • Strong attention to detail and accuracy • Ability to work under supervision and follow standard procedures • Good documentation and organizational skills • Team-oriented mindset with commitment to patient safety and equity About the Company Metro North Hospital & Health Service is a Queensland Government health organization delivering world-class public healthcare across Brisbane’s north, known for its commitment to innovation, equity, cultural safety, professional development, and a supportive work environment that prioritizes patient care and employee wellbeing.

Roles & Responsibilities • Maintain confidentiality of sponsor and clinical trial information • Coordinate with subcontractors such as labs, translators, and document vendors • Prepare and customize study documents including SMP, monitoring plans, ICFs, IMP labels, and trial forms • Manage regulatory submissions, approvals, and related documentation • Support investigator meetings and study-related communications • Handle adverse event (AE) reporting during trial conduct • Manage clinical trial supplies, drug accountability, and site documentation • Develop, maintain, and ensure completeness of the Trial Master File (TMF) • Plan and coordinate site initiation, monitoring, and close-out visits • Coordinate with CRAs/CTAs, review monitoring reports, and support study databases • Support data clarification, co-monitoring visits, and regular study updates Qualification • Degree in Pharmacy, Life Sciences, Clinical Research, or related discipline Experience • 0-6 months of experience in clinical research or clinical trial coordination • Freshers with relevant academic exposure are eligible Skills • Basic knowledge of ICH-GCP and clinical trial processes • Understanding of regulatory documentation and TMF management • Strong communication, documentation, and coordination skills • Ability to work with cross-functional teams and multiple stakeholders • Willingness to join immediately About the Company Samahitha is a growing clinical research organization focused on delivering high-quality clinical trial support services, offering early-career professionals hands-on exposure to end-to-end clinical research operations in a structured and learning-driven environment.

Roles & Responsibilities • Ensure compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements • Manage and review QMS documentation including SOPs, batch manufacturing records, and quality reports • Support preparation and execution of internal, external, customer, and regulatory audits • Handle batch release activities in coordination with Production and Quality Control teams • Identify, investigate, and implement CAPA for deviations, OOS/OOT results, and quality complaints • Support data integrity practices and maintain accurate, traceable quality records • Participate in continuous improvement initiatives to strengthen quality systems Qualification • B.Pharm or M.Pharm from a recognized university Experience • 1–3 years of experience in a Quality Assurance role within the pharmaceutical industry Skills • Strong knowledge of GMP, GLP, and regulatory guidelines (USFDA, WHO, CDSCO preferred) • Hands-on experience with QMS, CAPA, deviations, and batch release activities • Good documentation, audit-handling, and compliance skills • Proficiency in MS Office and quality management systems • Effective communication and coordination abilities About the Company Ceph Lifesciences Pvt. Ltd. is a well-established pharmaceutical company specializing in the manufacturing of high-quality cephalosporin-based products, driven by robust quality systems, regulatory compliance, and a commitment to excellence in pharmaceutical manufacturing.

Roles & Responsibilities • Handle Quality Management System (QMS) activities including Deviations, CAPA, Change Control, and OOS/OOT documentation • Ensure compliance with cGMP, regulatory guidelines, and internal SOPs • Prepare, review, and maintain quality documents and records in line with injectable manufacturing standards • Support internal audits, regulatory inspections, and compliance assessments • Coordinate with QC, Production, and Engineering teams for investigation closure and corrective actions • Monitor effectiveness of implemented CAPA and quality improvements • Support continuous improvement initiatives within the quality system Qualification • B.Pharm or M.Pharm (preferred) Experience • Experience in QMS activities within pharmaceutical manufacturing • Prior exposure to injectable/sterile facilities is preferred • Freshers with strong academic background and interest in QA/QMS may also be considered Skills • Good understanding of QMS, GMP, and regulatory requirements • Knowledge of deviation management, CAPA, and change control systems • Strong documentation and compliance skills • Attention to detail and problem-solving ability • Good communication and coordination skills About the Company Nitin Lifesciences Limited is a reputed pharmaceutical company specializing in sterile injectable formulations, known for its quality-driven manufacturing practices and compliance with global regulatory standards, offering professionals a stable and growth-oriented career environment in injectable manufacturing.

Roles & Responsibilities • Provide timely regulatory support for Skin Health and Essential Health portfolios • Ensure right-first-time dossier submissions and compliant product registrations • Review and approve product artworks through the Artwork Management System • Manage regulatory submissions and authority responses (CDSCO, State FDAs, ASCI) • Track and interpret Indian regulatory changes for cosmetics, OTC, and commodities • Support policy shaping and proactive regulatory risk mitigation • Ensure audit readiness with zero critical regulatory observations • Review and approve product claims and promotional materials as per regulations Qualification • Master’s degree in Pharmacy or Science • PG Diploma or Certification in Regulatory Affairs Experience • 6-7 years of hands-on experience in Indian cosmetics and commodities regulatory affairs • Exposure to drugs regulations (including NPPA) preferred • Experience with medical device regulations is an added advantage Skills • Strong knowledge of Indian regulatory frameworks and compliance requirements • Expertise in dossier preparation and regulatory submissions • Excellent regulatory interpretation and documentation skills • Effective stakeholder communication and coordination abilities • Ability to manage multiple priorities in a fast-paced environment About the Company Kenvue is a global consumer health leader behind trusted brands such as Neutrogena, Aveeno, Tylenol, Listerine and Johnson’s, combining science-led innovation with a strong commitment to care, quality, and regulatory excellence to improve everyday health worldwide.

Roles & Responsibilities • Review and interpret prescription orders to ensure accuracy and appropriateness • Provide medication counseling on usage, side effects, and interactions • Conduct medication reviews and resolve drug therapy–related issues • Coordinate with healthcare professionals to support effective patient care Qualification • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.) • Active pharmacist license as per local regulatory requirements Experience • 0-3 years of professional pharmacy experience • At least 2 years of experience in a cosmetic pharmacy preferred • Exposure to cosmetic and aesthetic pharmacy practices is an added advantage Skills • Strong pharmaceutical and medication management knowledge • Excellent patient counseling and communication skills • High attention to detail and clinical accuracy • Ability to work collaboratively in a healthcare team About the Company Care Medical Center is a healthcare provider in Riyadh committed to delivering high-quality medical and pharmaceutical services, with a strong focus on patient safety, personalized care, and adherence to clinical and regulatory standards.