Pharmacy Jobs

Roles & responsibility • Assist in planning, execution and monitoring of research projects • Conduct experiments, data collection, analysis and interpretation • Prepare research reports, technical documents and publications • Maintain research records, laboratory notebooks and documentation • Support proposal writing, project submissions and progress reports • Coordinate with faculty members, collaborators and project teams • Ensure compliance with institutional guidelines, SOPs and ethics • Assist in mentoring junior researchers or students when required Qualification • M.E. / M.Tech, M.Pharm, Ph.D., MDS, MD / MS Experience • Relevant research or academic experience preferred • Fresh PhD / postgraduate candidates may also be considered • Experience in funded research projects will be an added advantageImportant Date• Application Deadline: 30-01-2026 Skills • Strong research and analytical skills • Scientific writing and documentation skills • Data analysis and interpretation abilities • Good communication and presentation skills • Ability to work independently and in a team • Familiarity with research tools, software and methodologies About the company Indian Institute of Technology Delhi (IIT Delhi) is one of India’s premier institutes for higher education and advanced research, known for excellence in engineering, science, technology and interdisciplinary research, offering a dynamic environment that fosters innovation, academic growth and impactful research contributions.Official NotificationClick Here

Roles & Responsibilities• Provide high-quality medical or dental care to beneficiaries as per the post assigned• Conduct patient consultations, examinations, and assessments• Diagnose and manage medical or dental conditions according to standard protocols• Maintain accurate patient records and ensure compliance with clinical governance• Support healthcare teams in treatment planning, follow-up, and preventive care• Assist in administrative tasks related to patient care and departmental operations• Contribute to service improvement and operational planning within ECHS healthcare facilitiesSkills Required• Strong clinical knowledge and patient management skills relevant to the assigned post• Effective communication and interpersonal skills• Ability to work collaboratively in multidisciplinary healthcare teams• Attention to detail and commitment to patient-centred care• Organizational and documentation skillsQualifications• Medical Specialist: MD / MS• Medical Officer: MBBS• Dental Officer: BDS / MDS• Pharmacist: B.Pharm / D.Pharm• Nursing Assistant: GNM• Other posts: As per official notificationExperience After Qualification• Relevant post-qualification clinical experience preferredAdditional Requirements• Minimum age: 21 years; Maximum age: 45 years (age relaxation as per organization norms)• Willingness to comply with ECHS rules and professional standards• Eligibility to work in India• No application feeAbout the CompanyThe Ex-Servicemen Contributory Health Scheme (ECHS) provides accessible, high-quality healthcare services to ex-servicemen and their dependents. ECHS emphasizes patient-centred care, clinical excellence, and professional development. The organization maintains standards of safety, ethics, and operational efficiency while fostering multidisciplinary collaboration in healthcare delivery.Selection Process: InterviewImportant Dates:• Last Date of Application: 31-01-2026Official NotificationClick Here

Role & responsibilities • Assist faculty and research teams in ongoing research projects • Conduct literature review, data collection and experimental work • Support design, execution and documentation of research activities • Analyze experimental or computational data and prepare reports • Maintain proper records of research data, samples and observations • Assist in preparation of research papers, presentations and project reports • Support procurement, calibration and maintenance of laboratory equipment • Ensure compliance with institute guidelines, safety norms and project timelines • Participate in project meetings and academic discussions Qualification • B.E / B.Tech, B.Pharm, B.Sc / M.Sc, Ph.D Experience • Relevant research or academic experience as per project requirement • Freshers with strong academic background may also apply Age limit • Minimum age: 21 years • Maximum age: 45 years • Age relaxation applicable as per organization norms Important date • Application Deadline date: 24-01-2026 Skills • Strong analytical and problem-solving skills • Research methodology and data analysis knowledge • Good documentation and report writing skills • Ability to work independently and in a research team • Basic computer skills and familiarity with research tools • Good communication skills About the company Indian Institute of Technology Indore is a premier institute of national importance dedicated to excellence in education, research and innovation, fostering interdisciplinary research and contributing to scientific and technological advancement in India.Official NotificationClick Here

Roles & Responsibilities • Learn and follow Health Authority guidelines and local regulations for drugs, medical devices, cosmetics, and food/health supplements • Compile, prepare, and submit regulatory dossiers to Health Authorities (online and offline) • Track application status and follow up on dossiers, queries, and approvals • Respond to regulatory queries and coordinate meetings with Health Authorities for resolution • Represent clients for product registrations, audits, and FDA-related communications • Ensure proper maintenance and safe custody of original regulatory documents and records • Update internal regulatory documentation in line with current guidelines • Coordinate with internal teams and ensure effective communication with Health Authorities • Monitor project deliverables and ensure SOP compliance and updates • Verify application status through FDA portals and in-person follow-ups Qualifications • Bachelor of Pharmacy (B.Pharm) Experience • Up to 7 years of experience in Regulatory Affairs • Experience in regulatory submissions for drugs; exposure to cosmetics, medical devices, and food/health supplements preferred Skills • Knowledge of regulatory affairs and Health Authority submission processes • Understanding of FDA regulations, registrations, and audits • Strong documentation and coordination skills • Knowledge of CorelDRAW, Adobe Photoshop, and project management tools (added advantage) • Ability to work independently using a laptop• Willingness to be based in or relocate to NPT• Female candidates preferredAbout the Company Genedrift is a regulatory-focused organization providing end-to-end regulatory affairs and compliance support for pharmaceuticals, medical devices, cosmetics, and food/health supplements, working closely with Health Authorities to ensure timely approvals and adherence to local and international regulatory requirements.

Roles & Responsibilities • Design and deliver role-based onboarding and learning programs for CfDA teams • Coordinate learning programs with subject matter experts and learning partners • Maintain and update learning content, calendars, and training logistics • Track learning effectiveness using data, dashboards, and feedback • Act as point of contact for CfDA learning and onboarding initiatives • Ensure GxP and quality compliance in learning documentation • Support audit and inspection readiness through accurate records • Use automation and AI-enabled tools to improve learning operations Qualifications • Doctorate with 2+ years experience OR • Master’s degree with 6+ years experience OR • Bachelor’s degree with 9+ years experience Skills • Experience in regulated (GxP) learning environments • Knowledge of LMS platforms and learning operations • Strong coordination, project management, and stakeholder skills • Data and reporting literacy; experience with analytics dashboards • Familiarity with digital or AI-enabled learning toolsAbout the CompanyAmgen is a global biotechnology leader committed to advancing science and improving patient lives. Through its R&D Knowledge & Learning organization, Amgen fosters continuous learning, innovation, and capability building to support cutting-edge research and data-driven decision-making worldwide.

Roles & Responsibilities:• Provide high-level technical and strategic consultancy support to National Health Mission programs• Assist in planning, implementation, monitoring, and evaluation of national health initiatives• Contribute to policy formulation, program design, and health system strengthening activities• Prepare technical reports, presentations, and policy briefs as required• Coordinate with central and state government stakeholders, partners, and agencies• Support research, data analysis, and evidence-based decision-making• Participate in meetings, reviews, and capacity-building activitiesEducational Qualifications:• MBBS / BDS / BAMS / BHMS• B.Sc Nursing / B.Pharm / B.Sc• Post Graduation / MD / MS(Candidates with relevant postgraduate qualifications will be preferred)Age Limit:• Minimum Age: 21 years• Maximum Age: 50 yearsSelection Process:• InterviewImportant Dates:• Application Start Date: 13 January 2026• Last Date to Apply: 04 February 2026About the Organization:The National Health Systems Resource Centre (NHSRC) functions under the National Health Mission (NHM) and provides technical assistance to the Ministry of Health & Family Welfare, Government of India. NHSRC plays a key role in strengthening public health systems, improving healthcare delivery, and supporting policy development through research, innovation, and expert consultancy.Official Notification Click Here

Roles & Responsibilities • Review patient records from multiple Electronic Health Record (EHR) systems against predefined eligibility criteria • Identify and map eligible patients to relevant clinical studies with high accuracy • Prepare clear and comprehensive patient record summaries • Ensure data accuracy, consistency, and regulatory compliance • Support clinical research and clinical decision-support teams with structured data insights • Contribute to AI-driven healthcare and real-world data analysis initiatives Qualification • PharmD • M.Pharm (Pharmacology) Experience • Minimum 1 year of experience in clinical research–related domains • Experience in CROs, clinical pharmacy, medical coding, scientific writing, or related healthcare fields preferred Skills • Strong clinical and pharmacology knowledge • High attention to detail and data accuracy • Strong analytical and critical thinking abilities • Ability to interpret, analyze, and summarize clinical data • Proficiency in Google Workspace (Docs, Sheets, Slides) • Good communication and documentation skills About the Company Chisquare Lab is a fast-growing global organization specializing in AI, Data Science, Clinical Decision Support, and Healthcare Analytics, with operations in Kochi, the UK, and the US, and a strong team of 150+ professionals building next-generation healthcare decision-making platforms.

Roles & Responsibilities • Perform end-to-end pharmacovigilance case processing using Argus • Analyze, code, and enter safety data accurately • Handle all stages of case processing including triage, data entry, review, and follow-up • Ensure compliance with global and local PV regulations, SOPs, and Patient Safety policies • Execute and track follow-up procedures • Support implementation of new safety systems and process improvements • Contribute to a performance-driven work culture • Work collaboratively to meet strict timelines • Maintain clear written and verbal communication Qualification • B.Pharm(Bachelor of Pharmacy), B.Sc (Life Sciences), M.Pharm (Master of Pharmacy), M.Sc (Life Sciences) Experience • 1 to 4 years of Pharmacovigilance case processing experience Skills • Hands-on experience with Argus safety database • Knowledge of pharmacovigilance workflows and regulations • Strong analytical and data interpretation skills • Excellent written and verbal communication skills • Ability to work in a team and meet timelines About the Company Tata Consultancy Services (TCS) is a leading global IT services, consulting, and business solutions organization under the Tata Group, delivering end-to-end life sciences and pharmacovigilance solutions to global healthcare clients.

Roles & Responsibilities • Support automation of pharmacy processes including medication ordering, dispensing, and administration for inpatient and outpatient services • Act as a liaison between pharmacy/clinical users and IT teams to ensure effective system functionality • Monitor IT ticketing systems, follow up on issues, and ensure timely resolution • Manage system settings, access levels, and maintenance of assigned clinical modules • Support software testing, system upgrades, and vendor-related change requests • Maintain and upgrade pharmacy dictionaries and decision-support tools (alerts, order sets, CPOE) • Conduct end-user training and maintain updated training documentation • Ensure system downtime procedures and workflows are in place • Support workflow optimization and identify gaps during system implementation • Lead integration and implementation of safe clinical information systems • Assist in KPI data collection, reporting, and quality module incident handling • Participate in IT and clinical informatics projects as assigned Qualification • Bachelor of Pharmacy (B.Pharm) • Master of Pharmacy (M.Pharm) preferred • Bachelor’s Degree in Health Informatics preferred• DOH or MOH Registered Pharmacist • HIMSS Certification preferred Experience • 2-4 years of healthcare informatics experience • Minimum 1 year of inpatient hospital clinical experience post-certification Skills • Knowledge of hospital pharmacy workflows and clinical information systems • Exposure to Electronic Medical Records (Cerner preferred) • Experience with pharmacy automation and drug databases (e.g., First Data Bank) • Strong analytical, problem-solving, and decision-making skills • Excellent communication and coordination skills • Ability to train end users and manage system workflows • Organized, detail-oriented, and deadline-driven About the Company American Hospital Dubai LLC is a leading private healthcare provider offering advanced clinical services supported by state-of-the-art health information systems and international quality standards.

Roles & Responsibilities • Dispense medicines as per prescriptions and standard treatment guidelines • Maintain proper storage, handling, and inventory of medicines • Ensure compliance with pharmacy regulations and government norms • Assist in stock management, procurement, and record maintenance • Counsel patients on dosage, usage, and precautions of medicines • Support healthcare staff in pharmaceutical-related activities Qualification • B.Pharm or D.Pharm from a recognized institution Experience • Freshers and experienced candidates can apply (as per eligibility norms) Number of Openings: 03Age Limit • Minimum Age: 18 Years • Maximum Age: 38 Years Application Fee • Rs. 100/- for all candidatesImportant Dates • Application Start Date: 09-01-2026 • Application Last Date: 20-01-2026About the Organization Zilla Parishad is a local government body responsible for public healthcare and welfare services at the district level, ensuring accessible and affordable medical services for the community.Official NotificationClick Here

Key Responsibilities • Conduct patent searches including Prior Art, Patentability, and Freedom-to-Operate (FTO) analysis • Draft and file patent applications in coordination with internal teams and external counsels • Support patent landscaping and competitive intelligence studies • Coordinate with R&D teams to understand inventions and align patent strategies • Manage and maintain patent portfolios, databases, and timelines • Prepare and assist in responses to patent office actions and examiner queries • Ensure compliance with Indian and global IPR laws and guidelines • Support patent lifecycle management from filing to grant and maintenance Qualification • M.Pharm from a recognized university Experience • 1-3 years of experience in pharmaceutical IPR, patent analysis, or patent drafting Skills• Knowledge of patent databases and search tools • Understanding of pharmaceutical inventions and IPR regulations • Strong analytical and documentation skills • Attention to detail and organizational abilities • Effective communication and cross-functional coordination About the Company Cadila Pharmaceuticals Ltd. is a leading Indian pharmaceutical company focused on innovation-driven research and strong intellectual property protection, offering excellent career growth in pharmaceutical IPR.

Roles & Responsibilities • Perform medical device complaint investigations in compliance with ISO 13485 and ISO 14971 • Conduct risk assessments, hazard analysis, and FMEA • Support CAPA initiation, investigation, and closure activities • Prepare, review, and maintain high-quality investigation and compliance documentation • Ensure adherence to global regulatory and quality system requirements • Collaborate with cross-functional and global teams for complaint resolution • Support audit readiness and continuous quality improvement initiatives Qualifications • Any Life Science Graduate • For Kolkata location: B.Pharm / M.Pharm, Biomedical / Mechanical Engineering / B.Sc Medical Imaging & Radiology / M.Sc Molecular Biology / B.Sc Nursing / BDS Experience • Pune & Hyderabad: 3-9 years (Immediate joiners preferred) • Kolkata: 0-5 years (Relevant medical device investigation experience required) Skills • Medical Device Complaint Investigation • ISO 14971 Risk Management • ISO 13485 Quality Management Systems • CAPA, Root Cause Analysis • FMEA and Risk Assessment • Excellent English communication skills • Willingness to work rotational shifts and from office Walk-In Interview Details Hyderabad Dates: 12, 15 & 16 January 2026 Venue: Wipro Limited, Manikonda STPI, Tower 6, 3rd Floor, Gachibowli, Hyderabad – 500032 Contact: Pavan Pune Dates: 12, 14 & 16 January 2026 Venue: Unit 2, Plot No. 31, Hinjewadi Phase 2, Rajiv Gandhi Infotech Park, Pune – 411057 Contact: Riya / Varsha Kolkata Dates: 13, 15 & 16 January 2026 Venue: Gate 1, Plot 8 & 9, Block DM, Sector V, Salt Lake, Kolkata – 700091 Contact: Sarita Reporting Time: 10:00 AM – 12:30 PM Documents to Carry • Updated Resume • Original Government ID Proof • Mention source of walk-in information on top of CV About the Company Wipro Limited is a leading global information technology, consulting, and business services company with a strong presence in healthcare and medical devices. Wipro supports global clients with regulatory-compliant quality, safety, and post-market surveillance services, offering professionals exposure to international standards, advanced technologies, and long-term career growth opportunities.

Roles & Responsibilities • Prepare, review, and submit high-quality regulatory submissions to the US FDA within defined timelines • Maintain approved ANDA applications and manage Annual Reports in compliance with FDA regulations • Independently evaluate post-approval change controls (CCs) and ensure accuracy and completeness • Compile, publish, and submit annual reports and supplements for management review • Assist on complex supplements and independently handle simple supplements • Maintain regulatory databases, trackers, and documentation in real time • Stay updated with FDA post-approval guidance and regulatory requirements • Train and mentor Regulatory Affairs Associate I on internal processes and systems • Support additional regulatory projects as assigned Qualifications • Master of Pharmacy (M.Pharm)- Regulatory Affairs / Quality Assurance preferred • Bachelor’s degree in Pharmacy or related discipline Experience • Minimum 4+ years of experience in the pharmaceutical industry • Experience in Regulatory Affairs preferred; QA, Analytical, Production, or Lab exposure is an advantage Skills • Strong knowledge of FDA post-approval regulations and ANDA lifecycle management • Good understanding of regulatory documentation and submission processes • Proficiency in MS Word, Excel, and regulatory databases • Excellent written and verbal communication skills • Strong attention to detail, organization, and multitasking ability • Ability to work independently and collaboratively in cross-functional teams About the Company Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating across nearly 60 countries. With a mission to make healthcare more affordable and accessible, Teva supports the health of over 200 million patients worldwide every day through high-quality, essential medicines and a strong commitment to innovation, diversity, and inclusion.

Roles & Responsibilities • Perform initial screening of newly submitted manuscripts for journal scope and editorial policy compliance • Evaluate submissions for clinical trial registration, ethics approvals, and reporting standards • Review English language quality to ensure scientific clarity and accuracy • Identify issues such as salami slicing, redundancy, plagiarism, and research integrity concerns • Recommend suitable alternative journals when submissions are out of scope • Coordinate with authors and internal editorial teams to ensure smooth workflow • Support improvements in customer engagement and publication processes • Manage editorial tasks independently from coordination to execution Qualification • M.Pharm, M.Sc, PhD, or Postgraduate degree in Life Sciences, Biotechnology, Nutrition, Public Health, Physiotherapy, Healthcare Management, Physician Assistant, Dialysis Therapy, Echocardiography, MLT, or related disciplines Experience • Experience in scientific publishing, peer review services, or editorial support roles • Background as Editorial Assistant / Journal Editorial Office (JEO) / Research Support Executive (RSE) / Desk Transfer roles preferred Skills • Strong understanding of scientific research, medical concepts, and clinical trials • Knowledge of publication ethics and editorial policies • Excellent written and verbal English communication skills • Strong attention to detail and analytical ability • Ability to work independently and manage multiple tasks efficiently About the Company Macmillan Publishers India Pvt. Ltd. is part of a globally renowned publishing group with a strong presence in academic, scientific, and educational publishing. The company is committed to advancing knowledge by supporting high-quality research dissemination through robust editorial standards and ethical publishing practices.

Roles & Responsibilities: • Lead formulation development activities for ophthalmic products for ROW markets • Plan, execute, and review product development in line with ROW regulatory requirements • Oversee scale-up, technology transfer, and commercialization activities • Coordinate with Analytical R&D, QA, Regulatory Affairs, Production, and Packaging teams • Ensure timely delivery of development milestones and regulatory submissions • Handle troubleshooting during development, scale-up, and validation stages • Review and approve development reports, protocols, and technical documentation • Support regulatory queries, variations, and lifecycle management activities • Ensure compliance with cGMP, ICH guidelines, and internal quality standards • Mentor and guide team members to achieve functional and project goals Qualification: • M.Pharm (Master's of Pharmacy) Experience: • 14+ years of experience in ophthalmic formulation development Key Skills: • Strong expertise in ophthalmic dosage forms and sterile formulations • In-depth knowledge of ROW regulatory guidelines • Leadership and cross-functional coordination skills • Strong problem-solving and project management abilities About the Company: Ajanta Pharma Ltd is a globally recognized pharmaceutical company with strong R&D capabilities, focused on developing high-quality, differentiated formulations, including ophthalmic products, for regulated and emerging markets.

Role & Responsibilities • Act as US/EU local safety office and FDA/EMA point of contact • Submit ICSRs to FDA, EMA, and business partners • Perform case review, quality checks, and escalation of safety issues • Ensure timely expedited safety reporting • Support vendor oversight for case intake, triage, processing, and quality metrics • Conduct clinical trial and business partner reconciliations • Manage ICSR intake, triage, data entry queries, and E2B support • Support audit readiness, health authority inspections, and internal audits • Assist in PV training delivery and delegated QPPV activities Qualifications & Experience • Bachelor’s degree with 2+ years of pharmacovigilance experience, or • Associate degree with 6+ years of relevant experience, or • High school diploma/GED with 8+ years of pharmacovigilance experience Skills • Strong knowledge of global pharmacovigilance regulations • Experience in ICSR case processing and reporting • Proficiency in safety databases and MS Office tools • High attention to detail and compliance orientation About the Company • Amgen is a global biopharmaceutical leader delivering innovative therapies and maintaining world-class pharmacovigilance operations

Roles & Responsibilities: • Dispense medications accurately as per prescriptions • Provide clear medication counselling and dosage instructions to customers • Deliver excellent customer service with a patient-first approach • Support pharmacy operations while ensuring regulatory compliance • Maintain professional communication with customers and healthcare providers • Uphold Aster Pharmacy’s service quality and care standards Qualification: • DHA / MOH license or eligibility required Skills: • Strong communication and interpersonal skills • Multilingual ability preferred • Customer-centric mindset and service excellence • Attention to detail and professional ethicsWalk-in Interview Details: 📅 Date: Saturday, 17th January 2026 📧 Shortlisted candidates will receive venue details via email by 14th January 2026 About the Company: Aster Pharmacy is part of Aster DM Healthcare, one of the leading healthcare providers in the Middle East and India. Known for quality care and patient trust, Aster Pharmacy offers strong career growth and a professional work environment.

Role & Responsibilities • Deliver high-quality online lectures and coaching for pharmacy competitive and licensing exams • Use student-centric teaching approaches including case-based learning, problem-solving, and exam-        oriented strategies • Provide academic mentoring and conceptual clarity in pharmacy subjects and real-world practices • Actively engage with students to resolve doubts and motivate consistent learning • Offer regular feedback and performance guidance to improve student outcomes • Create educational video content for YouTube, Instagram, and other digital platforms • Collaborate with academic and content teams to design engaging, high-impact learning materials • Contribute innovative ideas to improve teaching delivery and digital education qualityQualifications • Master of Pharmacy (MPharm) or Doctor of Pharmacy (Pharm D) • GPAT / KAPS / OPRA / PEBC / BCPS / SPLE qualification preferredExperience • 1–5 years of relevant academic, teaching, or mentoring experience • Strong conceptual knowledge of pharmacy subjects and practices • Prior teaching or academic mentoring experience is an advantage • Passion for teaching, mentoring, and student success is essential Skills Required • Excellent verbal and written communication skills • Fluency in English (spoken and written) is mandatory • Ability to simplify complex pharmacy concepts for online teaching • Confidence in front of camera for video-based lectures and content • Tech-friendly mindset with familiarity in LMS, Zoom, and digital tools • Strong ability to engage, motivate, and inspire students• Work Schedule: Monday to Saturday (Day Shift) What We Offer • Competitive salary based on skills and performance • Opportunity to work closely with Dr. Akram Ahmad • Clear career growth into senior academic and leadership roles • Exposure to global healthcare education and international licensing exams • Supportive, fast-paced, and result-driven work culture • Be part of a global healthcare brand creating real impact in professionals’ livesAbout Academically Global • Fast-growing Healthcare EdTech platform focused on global career transformation • Led by Dr. Akram Ahmad, internationally recognised healthcare career coach with 1M+ followers                   across social media • Supports Doctors, Dentists, Pharmacists, Physiotherapists, Optometrists, and Nurses • Offers licensing exam preparation, industry upskilling programs, and study-abroad pathways • Founder-led, mission-driven, and fast-scaling global healthcare education brand

Role & Responsibilities: • Assist in dispensing medicines as per valid prescriptions • Learn and follow proper dosage, labeling, and medication handling practices • Support prescription handling and verification processes • Maintain pharmacy records and documentation • Check medicine expiry dates and ensure proper storage of drugs • Assist in inventory management and stock organization • Adhere to pharmacy safety standards and regulatory guidelines • Support day-to-day pharmacy operations under supervision Eligibility / Qualification: • Final semester students pursuing D.Pharm or B.Pharm Internship Details: • Duration: 3 or 6 months • Stipend: No stipend • Certificate: Internship/Experience certificate will be issued upon successful completion Skills Gained: • Hospital Pharmacy Operations • Prescription Handling & Dispensing • Inventory & Drug Storage Management • Pharmacy Documentation & Compliance About the Company: • PVS Sunrise Hospital is a multi-specialty healthcare institution in Calicut, Kerala, committed to delivering quality patient care and providing practical learning opportunities for future healthcare professionals.