Pharmacy Jobs

Roles & Responsibilities • Coordinate day-to-day clinical trial activities at the site • Support investigators during patient screening, enrollment, and follow-up • Maintain essential trial documents including ISF, CRFs, and study logs as per GCP • Ensure compliance with ICH-GCP, SOPs, and regulatory guidelines • Coordinate with sponsors, CROs, ethics committees, and study monitors • Support study initiation, monitoring visits, and close-out activities • Ensure accurate data collection and timely resolution of queries Qualification • B.Pharm or M.Pharm (Pharmacology) Experience • Freshers or candidates with prior clinical research experience Skills • Knowledge of clinical research processes and GCP principles • Strong documentation and communication skills • Proficiency in Gujarati, Hindi, and English • Willingness to work full-time at the Ahmedabad site About the Organisation Nirmit Clinical Research is a clinical research organization focused on conducting ethical, high-quality clinical trials while providing hands-on training and growth opportunities for aspiring clinical research professionals.

Roles & Responsibilities • Research global regulatory requirements for pharmaceuticals, medical devices, biologics, and nutraceuticals • Support preparation, review, and lifecycle management of CTD and eCTD dossiers • Assist with regulatory submissions, variations, renewals, and post-approval changes • Track global regulatory updates, approvals, guidelines, and policy changes • Maintain and update regulatory databases and regulatory intelligence tools • Support development of client presentations, regulatory reports, and internal knowledge content • Collaborate with senior regulatory consultants on active client projects • Assist in documentation review, data analysis, and compliance-related activities Qualification • Pursuing or recently completed B.Pharm, M.Pharm, MSc (Life Sciences), Biotechnology, or Regulatory Affairs Experience • Freshers or students with academic exposure to Regulatory Affairs are encouraged to apply • Prior internship, project work, or coursework in regulatory affairs is an advantage Skills • Strong interest in global regulatory frameworks including USFDA, EMA, CDSCO, and ICH • Good understanding of regulatory documentation and submission processes • Proficiency in MS Word, Excel, and PowerPoint • Strong research, analytical, and documentation skills • Detail-oriented with good written and verbal communication • Ability to work independently and adapt in a startup consulting environment About the Organisation ArtiXio is a fast-growing life sciences consulting startup delivering regulatory affairs, compliance, and regulatory intelligence solutions to global pharmaceutical, medical device, and biotech companies. With a strong focus on practical learning and real-world exposure, ArtiXio provides interns and professionals the opportunity to work on live regulatory projects while building industry-relevant skills in a dynamic consulting environment.

Roles & Responsibilities • Act as the primary surgical point of contact for Roche’s Port Delivery System (PDS) within the Ophthalmology community • Provide operating room support during ophthalmic procedures, including hands-on device support, training, and ensuring safe and effective device use • Support ophthalmology clinical trials by assisting with site set-up, investigator and site staff training, and sharing key clinical data • Build and maintain strong relationships with ophthalmology stakeholders including Vitreo-Retinal surgeons, Medical Retinal specialists, General Ophthalmologists, Optometrists, ORDMs, and surgical theatre staff • Deliver high-quality medical education on surgical ophthalmology devices to healthcare professionals and patient organizations • Act as a connector between external clinical experts and Roche internal teams to support scientific exchange and collaboration • Gather expert insights, share best practices, and contribute to strategies that improve patient outcomes and inform lifecycle planning • Explore and support partnership opportunities such as joint working initiatives, patient safety programs, education, and data generation • Ensure full compliance with regulatory, quality, and industry standards in all activities • Travel within Canada up to 60% to support clinical, educational, and stakeholder engagement activities Qualification • Degree or certification in a scientific or related discipline • Postgraduate qualification (PhD, PharmD, MSc, MD, or MBA) preferred Experience • Minimum 7 years of experience in the pharmaceutical or healthcare sector • At least 2 years of experience in ophthalmology • Hands-on experience in ophthalmic surgery or surgical device support • Experience supporting clinical trials and engaging with medical experts Skills • Strong knowledge of clinical trials, regulatory requirements, and compliance standards including GCP, PV, and industry codes (e.g., IMC) • Excellent communication, presentation, and relationship-building skills • Strong project management and cross-functional collaboration abilities • Customer-focused mindset with demonstrated scientific credibility • Proficiency in both English and French is required • Ability to work independently in a field-based role and manage extensive travelRelocation benefits are not available for this posting. About the Organisation Roche is a global, research-driven healthcare company committed to advancing science to prevent, stop, and cure diseases while ensuring access to healthcare for all. Roche fosters a culture of inclusion, open dialogue, and respect, where every individual is encouraged to bring their authentic self to work. Through innovation in pharmaceuticals and diagnostics, Roche continues to shape the future of healthcare and improve patient lives across generations.

Roles & Responsibilities • Support clinical studies through coordination of study data and documentation • Assist in development, testing, and maintenance of case report forms (CRFs), databases, and study reports • Verify clinical study data, resolve discrepancies, and ensure timely completion of study forms • Process subject compensation and resolve related discrepancies • Create, organize, and maintain clinical study files in compliance with regulatory requirements • Support internal and external audits to ensure accuracy and completeness of study documentation • Communicate with internal teams and stakeholders to provide updates and clarifications • Provide guidance and support to new or entry-level team members as required Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline Experience • Minimum 2 years of experience in clinical research, clinical studies coordination, data coordination, or document management • Experience working with clinical study documentation and data verification processes Skills • Strong organizational, communication, and problem-solving skills • Ability to work under moderate supervision using established processes • Familiarity with clinical data management systems and regulatory documentation • Attention to detail and ability to manage multiple tasks effectively About the Organisation Medtronic is a global leader in healthcare technology, committed to alleviating pain, restoring health, and extending life. With a strong focus on innovation and patient-centered solutions, Medtronic supports clinical research that drives safe, effective, and transformative medical technologies worldwide.

Roles & Responsibilities • Dispense medicines accurately as per valid prescriptions • Ensure safe storage, handling, and distribution of medicines • Maintain pharmacy stock, batch records, and expiry monitoring • Follow FIFO / FEFO practices in medicine management • Provide basic medication guidance to beneficiaries when required • Maintain proper documentation and pharmacy records • Ensure compliance with ECHS guidelines and standard operating procedures • Support audits, inspections, and inventory verification activities Qualification • B. Pharm Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organisation norms Important Date • Application Deadline: 12-02-2026 About the Organisation ECHS (Ex-Servicemen Contributory Health Scheme) is a Government of India healthcare scheme providing comprehensive medical care to ex-servicemen and their dependents through a network of polyclinics and empanelled hospitals across the country.

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and ECHS guidelines • Maintain proper records of medicines, stock, batch numbers, and expiry dates • Ensure correct storage of medicines following FIFO/FEFO practices • Issue medicines to beneficiaries against authorized prescriptions • Monitor inventory levels and prevent stock shortages or expiries • Maintain cleanliness and hygiene of the pharmacy area • Support audits, inspections, and documentation as per organizational norms • Ensure compliance with pharmacy laws, safety standards, and ethical practices Qualification • Diploma in Pharmacy (D.Pharm) • Bachelor of Pharmacy (B.Pharm) Age Limit • Minimum Age: 18 Years • Maximum Age: 45 Years • Age relaxation applicable as per ECHS / Government norms No. of Vacancies: 19Important Date • Application Deadline: 10-02-2026 About the Organisation The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative under the Ministry of Defence, providing comprehensive medical care to ex-servicemen and their dependents through a wide network of polyclinics, empanelled hospitals, and diagnostic centers across the country.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and institutional guidelines • Ensure proper storage, labeling, and inventory management of pharmaceutical products • Maintain records of drug receipt, issue, and stock levels • Ensure compliance with pharmacy laws, safety standards, and university regulations • Provide basic medication-related guidance to patients/staff when required • Monitor expiry dates and ensure timely replacement of medicines • Coordinate with procurement and administrative departments for smooth pharmacy operations Qualification • Diploma in Pharmacy (D. Pharm) from a recognized institution • Registration with the State Pharmacy Council is mandatory Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organisation norms Important Date • Application Deadline: 30-01-2026Skills • Good knowledge of medicines, dosages, and dispensing practices • High attention to detail and accuracy • Basic computer skills for record keeping • Strong organizational and documentation abilities • Good communication and interpersonal skills About the Organisation Kerala Veterinary and Animal Sciences University (KVASU) is a reputed academic and research institution dedicated to veterinary education, animal healthcare, and scientific advancement in the livestock sector.Official Notification Click Here

Join a leading tertiary care hospital. Responsibilities include medication therapy management.

Role & Responsibilities • Dispense medications accurately, verifying prescriptions for dosage, interactions, and allergies • Counsel patients on proper medication usage, side effects, and storage • Oversee pharmacy operations: inventory management, ordering, and stock maintenance • Provide clinical pharmacy services including medication therapy management • Collaborate with healthcare professionals to ensure safe and effective medication use • Maintain accurate patient records and comply with regulatory standards • Stay updated on new medications, treatment guidelines, and pharmacy practices • Prepare and compound medications using sterile and non-sterile techniques • Ensure a clean, organized, and regulation-compliant pharmacy environmentQualification • Bachelor of Pharmacy (BPharm) / Master of Pharmacy (MPharm) / Doctor of Pharmacy (PharmD) / PhD • Valid UAE license to practice pharmacy (DHA or MOH registration)Vacancies: 50Experience • Minimum 2 years in hospital, retail, or clinical pharmacy settingSkills & Competencies • Strong knowledge of pharmaceutical calculations, drug interactions, and therapeutics • Proficient with pharmacy software and electronic health records • Excellent communication and interpersonal skills • Strong problem-solving and critical-thinking abilitiesAbout Company • Life Pharmacy is a leading pharmacy chain in the UAE providing patient-centered care and advanced pharmaceutical services • Committed to safe, effective, and high-quality medication management

Roles & Responsibilities • Handle medical and drug-related queries through Medical Information Contact Center (MICC) operations • Support pharmacovigilance and medical information documentation activities • Ensure accurate data collection, case intake, and safety information reporting • Adhere to SOPs, GxP, and applicable regulatory guidelines during all activities • Coordinate with internal medical, pharmacovigilance, and safety teams for query resolution • Maintain strict confidentiality and data integrity in line with compliance standards Qualification • B.Pharm / M.Pharm / Pharm.D Skills • Basic understanding of Pharmacovigilance and Medical Information processes • Good verbal and written communication skills • Willingness to work in night shifts • Strong attention to detail and documentation accuracy • Eagerness to learn and ability to work in a regulated environment About the Company Mitocon Biopharma is a growing pharmaceutical organization focused on delivering high-quality healthcare and safety solutions. The company offers structured training, real-world exposure, and strong career development opportunities in pharmacovigilance and medical information services. This paid internship provides a solid entry point into the drug safety and pharmaceutical industry, with potential for permanent employment based on performance.

Roles & Responsibilities • Assist in preparation, formatting, and compilation of clinical trial documents such as Protocols, Investigator Brochures (IB), Informed Consent Forms (ICF), and Clinical Study Reports (CSR) • Support senior medical writers and medical leads in reviewing documents for accuracy, clarity, and regulatory compliance • Ensure documents align with ICH-GCP guidelines, ethical standards, and medical writing best practices under supervision • Coordinate document review cycles and track comments from Clinical Operations, Data Management, and Regulatory teams • Assist in compiling documentation for regulatory submissions including INDs and NDAs • Support ongoing clinical trials with documentation related to safety data, protocol amendments, and medical queries • Conduct literature searches and summarize scientific and clinical information • Maintain version control and document management records as per quality standards • Assist in preparing presentations, reports, and client-facing materials • Adhere to patient safety, data confidentiality, and ethical research practices at all times Qualification • Educational background in Pharmacy, Life Sciences, Biotechnology, Clinical Research, or related disciplines Skills • Basic understanding of clinical trials and medical writing concepts • Familiarity with ICH-GCP guidelines (preferred but not mandatory) • Strong written communication skills and attention to detail • Willingness to learn regulatory and clinical documentation standards • Good coordination and time management skills • Availability for immediate joining in Bengaluru About the Company Samahitha is a growing organization in the clinical research and healthcare domain, focused on delivering high-quality clinical and regulatory documentation services. The company provides hands-on learning opportunities, professional mentorship, and real-world exposure to clinical trials and medical writing, making it an ideal place for fresh graduates to begin a career in medical writing and clinical research.

Roles & Responsibilities • Generate and convert leads from pharmaceutical, nutraceutical, MedTech, and healthcare organizations • Promote market access services, pricing intelligence, product launch support, and healthcare research solutions • Build and maintain strong client relationships by understanding customer needs and business objectives • Prepare business proposals, presentations, and conduct follow-ups to close deals • Maintain and monitor the sales pipeline to achieve assigned business development targets • Coordinate with internal consulting, research, and delivery teams to ensure smooth project execution • Track market trends and identify new business opportunities in healthcare and life sciences Qualification • Graduate or Postgraduate in Pharmacy, Life Sciences, Healthcare, or Business Management Experience • 1–3 years of experience in business development, healthcare sales, or consulting services Skills • Basic understanding of pharmaceutical drugs, nutraceutical products, and healthcare markets • Strong communication, negotiation, and client relationship management skills • Ability to work in a target-driven, client-facing environment • Good presentation and proposal development skills • Self-motivated with a proactive approach to business growth About the Company Mark8Access is a leading healthcare intelligence and market access consulting firm that partners with pharmaceutical, nutraceutical, MedTech, and healthcare organizations. The company supports clients across pricing intelligence, market access strategy, product launch planning, scientific content services, and healthcare research, helping them make informed decisions and achieve successful market entry and growth.

Roles & Responsibilities • Collaborate with the Clinical Supplies Manager, Regulatory, and Clinical Operations teams to manage labeling, packaging, re-labeling, and shipment activities • Develop and execute drug distribution strategies aligned with recruitment trends, supply forecasts, and study timelines • Initiate and manage IMP and non-IMP packaging and sourcing activities with external vendors • Prepare, review, and maintain accurate clinical supply forecasts • Support IMP plans, including temperature excursion management to ensure product integrity • Coordinate with vendors for sourcing, labeling, packaging, and shipment in compliance with GMP and quality standards • Monitor vendor deliverables and resolve issues related to timelines, specifications, or quality • Initiate, track, and manage Import License (IL) processes, including submissions, renewals, and follow-ups • Ensure compliance with Quality Management Systems (QMS), Information Security Management Systems (ISMS), and global regulatory requirements • Maintain adherence to GMP, GCP, data protection laws, and applicable national and international regulations Qualification • Any Graduate • Life Sciences, Pharmacy, or related discipline preferred Experience • 3–5 years of relevant experience in clinical supplies, IMP/IP logistics, or clinical trial operations Skills • Strong knowledge of GMP and clinical supply chain processes • Hands-on experience in label generation, packaging, and shipment activities • Understanding of drug distribution strategies and supply forecasting • Experience working with CROs, sponsors, and third-party vendors • Familiarity with regulatory documentation and import licensing procedures • Strong coordination, documentation, and communication skillsAbout the CompanyVeeda Clinical Research (Veeda CR) is a leading global Contract Research Organization (CRO) headquartered in Ahmedabad, Gujarat, delivering end-to-end clinical research services across bioavailability/bioequivalence (BA/BE), clinical trials, clinical supplies, and regulatory solutions. Known for its strong quality culture, regulatory compliance, and global footprint, Veeda supports pharmaceutical and biotech companies in advancing safe and effective therapies worldwide.

Roles & Responsibilities • Perform triage and initial validity assessment of safety cases including spontaneous, health authority, clinical trial, and literature cases • Enter and process case data accurately in pharmacovigilance (PV) safety databases • Conduct initial ICSR assessment and determine applicability for expedited reporting • Evaluate reporting requirements and timelines for submission to health authorities and client partners • Prepare standard regulatory reporting forms such as CIOMS I, MedWatch forms, and XML files • Generate, send, and track follow-up requests to obtain complete safety information • Submit Individual Case Safety Reports (ICSRs) to global health authorities and client partners • Ensure complete case documentation and timely case closure as per SOPs • Perform quality checks on ICSRs to ensure compliance with project requirements, regulatory standards, and best practices • Conduct ICSR search and retrieval activities from EVWEB and perform company versus non-company case assessments • Mentor and support new team members by guiding them on processes and fostering a collaborative learning environment • Execute additional responsibilities as assigned by the supervisor in line with process requirements Qualification • University degree in Life Sciences such as Pharmacy, Biotechnology, Clinical Research, or a related discipline Experience • Minimum 2 years of hands-on experience in pharmacovigilance • Strong working knowledge of ICSR processing, case triage, and safety reporting workflows Skills • Good written and verbal communication skills • Ability to identify issues and suggest practical solutions within area of expertise • Strong attention to detail and quality-focused mindset • Good understanding of global PV regulations and reporting timelines • Ability to work independently and collaboratively within a team About the company Cencora is a global healthcare solutions organization dedicated to improving patient outcomes by supporting pharmaceutical and life sciences companies across the product lifecycle, and through its affiliate PharmaLex India Private Limited, it delivers specialized services in pharmacovigilance, regulatory affairs, and compliance, with a strong commitment to quality, ethics, and patient safety worldwide.

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.