Pharmacy Jobs

Roles & Responsibilities • Act as the US/EU local safety office representative and FDA/EMA point of contact • Prepare and submit Individual Case Safety Reports (ICSRs) to FDA, EMA, and business partners • Perform case review, quality checks, and escalation of case-level safety issues • Ensure timely expedited safety reporting in compliance with global regulatory timelines • Manage intake, triage, follow-up, and data entry queries related to ICSRs • Support vendor oversight for case intake, processing, reconciliation, and quality metrics • Conduct reportable event reconciliation for Amgen-sponsored clinical trials • Perform business partner safety reconciliations as per safety agreements • Provide LAO E2B support, including nullification and redistribution of cases • Review non-matching data across clinical and safety databases • Support audit readiness, health authority inspections, and internal audits • Undertake delegated activities from the QPPV in line with the PV System Master File • Assist in pharmacovigilance training and convention-related safety activities • Initiate unblinding requests and support literature case review processes Qualification • Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Clinical Research, or related field Experience • Bachelor’s degree with 2+ years of pharmacovigilance experience, or • Associate degree with 6+ years of directly related experience, or • High school diploma/GED with 8+ years of pharmacovigilance experience Skills • Strong knowledge of global pharmacovigilance regulations (US FDA, EMA, ICH) • Hands-on experience in ICSR case processing and regulatory reporting • Familiarity with clinical development and safety reporting workflows • High attention to detail and strong case quality management skills • Proficiency in safety databases and Microsoft Office (Word, Excel, PowerPoint, Outlook) About the Company Amgen is a leading global biotechnology company committed to discovering, developing, and delivering innovative medicines for patients with serious illnesses. With a strong focus on quality, compliance, and patient safety, Amgen offers a collaborative work environment and global exposure across pharmacovigilance and medical services functions.

Roles & Responsibilities • Prepare, review, and support development of high-quality clinical and regulatory documents • Assist in creation and review of CTD modules, Investigator’s Brochure (IB), protocols, ICFs, eCRF/CRFs, and safety reports • Ensure documents comply with SOPs, regulatory guidelines, and approved plans • Conduct literature searches and organize scientific data for clinical documentation • Perform quality control (QC) checks on clinical and regulatory documents • Support regulatory submission documentation activities • Ensure timely delivery of assigned documentation tasks Qualification • B.Pharm or M.Pharm from a recognized university Experience • 2-3 years of experience in clinical research documentation • Experience in a CRO or pharmaceutical industry preferred Skills • Knowledge of clinical trial documentation and regulatory requirements • Strong scientific writing, review, and QC skills • Ability to interpret clinical data and literature • Good attention to detail and time management • Strong communication and documentation skills About the Company Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations across India, USA, Canada, UK, Spain, and Poland. The company provides end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide, offering strong global exposure and long-term career growth opportunities in clinical research.

Roles & Responsibilities • Support timely global product launches for the Life Science business • Ensure compliance with global chemical regulations including GHS, SDS, chemical registration, and trade compliance • Collect, analyze, and validate product composition and physical property data • Review product formulations and hazard classification documentation • Collaborate with Product Management, internal regulatory teams, and external vendors • Coordinate with third-party vendors to ensure accuracy and completeness of regulatory data • Use SAP, JIRA, Palantir, and MS Office tools for regulatory data processing and tracking • Provide validated regulatory inputs to downstream compliance and processing teams Qualification • Master’s degree in Chemistry, Biochemistry, Toxicology, or Pharmacy Experience • Experience or academic exposure to regulatory affairs, chemical compliance, or product safety preferred • Familiarity with global regulatory frameworks is an advantage Skills • Understanding of chemical composition and hazardous characterization • Knowledge of GHS, SDS, and chemical regulatory compliance concepts • Data analysis, validation, and critical thinking skills • Experience with SAP, JIRA, and Palantir preferred • Strong communication, documentation, and vendor coordination abilities • Detail-oriented, collaborative, and quality-focused approach About the Company Merck is a global leader in Healthcare, Life Science, and Electronics, operating across multiple international markets. The company is known for its strong focus on innovation, regulatory excellence, sustainability, and inclusive work culture. Merck offers professionals the opportunity to work on globally impactful products while building a long-term career in regulatory affairs and life sciences.

Roles & Responsibilities • Oversee end-to-end clinical trial delivery ensuring quality, timelines, and budget compliance • Monitor project performance and provide operational guidance to project and functional teams • Prepare and present study status reports to sponsors and senior management • Manage study documentation, correspondence, and operational compliance • Lead, mentor, and manage clinical operations teams to achieve productivity and quality targets • Develop resource and staffing plans aligned with project requirements • Conduct quality reviews of deliverables, including site-level and centralized activities • Act as primary liaison with sponsors and internal stakeholders • Support proposal development, project bids, and client presentations • Ensure adherence to ICH-GCP, regulatory requirements, and Parexel SOPs • Drive process improvements and operational excellence initiatives Qualification • Bachelor’s degree in Pharmacy, Life Sciences, Biological Sciences, or related healthcare discipline • Nursing or equivalent clinical background may be considered Experience • Extensive experience in clinical research operations, clinical monitoring, or data management • Proven people-management and leadership experience in a CRO or similar environment • Strong exposure to global clinical trial operations Skills • Strong leadership, team management, and decision-making abilities • Excellent written and verbal English communication skills • Solid understanding of ICH-GCP and global regulatory requirements • Client-facing skills with experience in stakeholder and sponsor management • Ability to work independently under senior management supervision About the Company Parexel is a leading global clinical research organization dedicated to improving patient outcomes through innovative clinical development solutions. With a strong global presence and a commitment to quality, compliance, and people development, Parexel offers long-term career growth opportunities in clinical operations, leadership, and global clinical research management.

Roles & Responsibilities • Coordinate GLP toxicology studies with CROs, including timelines, tracking, and review of study reports • Support CMC readiness by compiling specifications, development data, and technical documentation • Assist in preparation of IND/CTA submissions with focus on nonclinical and CMC sections • Manage cross-functional coordination with R&D, QA, CROs, and external partners • Maintain regulatory-ready documentation, trackers, and development logs • Support IND-enabling activities for late preclinical development programs Qualification • MS / M.Pharm / M.Sc in Life Sciences, Pharmacy, or Biotechnology Experience • 2-3 years of experience in clinical development, preclinical development, or regulatory support • Hands-on exposure to GLP toxicology coordination, CMC documentation, or IND submissions Skills • Strong understanding of GLP toxicology and CMC development workflows • Working knowledge of CDSCO and/or US FDA IND processes • Excellent documentation, organizational, and follow-up skills • Ability to work effectively in cross-functional and CRO-facing environments • Good communication and coordination abilities About the Company Utopia Therapeutics is an emerging biopharmaceutical company focused on advancing innovative therapies through robust preclinical and clinical development. With active IND-enabling programs and a science-driven culture, the company provides hands-on exposure, close collaboration with senior scientists, and strong career growth opportunities in clinical development and regulatory affairs.

Roles & Responsibilities • Develop new formulations including powders, syrups, tablets, and capsules • Conduct stability studies, scale-up, and commercialization support activities • Perform literature review and patent searches for formulation development • Maintain GMP and GLP-compliant laboratory practices • Prepare R&D documentation, technical reports, and presentations • Ensure regulatory compliance for Ayurvedic and Nutraceutical products • Support cross-functional teams during product development and validation Qualification • M.Pharm (Pharmaceutics) • OR PhD in a relevant pharmaceutical discipline Experience • 0-6 years of experience in formulation R&D • Experience in Nutraceutical or Ayurvedic industry is preferred Skills • Strong knowledge of formulation development and R&D instruments • Understanding of stability studies and scale-up processes • Familiarity with GMP, GLP, and regulatory requirements • Good documentation, reporting, and presentation skills • Analytical thinking and problem-solving abilities About the Company Patanjali Research Foundation (PRF) is a NABL, DSIR, and DBT-accredited research institute engaged in advanced Ayurvedic and nutraceutical research. With state-of-the-art R&D facilities, PRF focuses on innovation, scientific validation, and regulatory-compliant product development, contributing to the growth of evidence-based traditional and modern healthcare solutions.

Roles & Responsibilities • Perform data stewardship for monthly/quarterly Master Data Management processes • Maintain pharma data and business rules based on market, dataset, and client requirements • Deliver error-free periodic reports to internal and client stakeholders • Conduct rapid ad-hoc analyses to support senior management decisions • Create dashboards and visualizations using Excel, Power BI, Tableau, or Qlik Sense • Identify data quality issues, gaps, or biases and assess their reporting impact • Build strong client communication and take ownership of assigned tasks • Share ideas for process improvements and efficiency enhancements • Lead or support team members to ensure timely and high-quality delivery Qualification • Bachelor’s or Master’s degree in Pharmacy or a related pharma/life sciences discipline Experience • 2-4 years of experience working with pharma datasets and therapy areas • Prior exposure to datasets such as IQVIA MIDAS, Prescription Data, Channel Dynamics, Evaluate Pharma preferred Skills • Strong pharma data analysis and visualization expertise • Proficiency in Excel/VBA, Power BI, Tableau, or Qlik Sense • Working knowledge of SQL; Python/R is an added advantage • Strong analytical, problem-solving, and automation skills • Excellent verbal and written communication in English • Detail-oriented, organized, proactive, and client-focused mindset About the Company Evalueserve is a global leader in AI-powered analytics and managed services, supporting smarter decision-making for over 30% of Fortune 500 companies across 45 countries. With deep domain expertise in pharma and life sciences, Evalueserve offers a collaborative, innovation-driven culture, hybrid work flexibility, global exposure, and strong opportunities for learning and career growth.

• Coordinate with Clinical, Regulatory, Safety, DevOps, and Submissions teams • Review and validate safety data for accuracy, consistency, and regulatory compliance • Compile aggregate reports using electronic authoring and document management tools • Manage cross-functional reviews, approvals, and resolution of comments • Ensure timely submissions to global health authorities (FDA, EMA, etc.) • Support process improvements, special projects, and UAT activities • Complete mandatory training under Pfizer Safety Information Management curriculum Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, or related discipline Experience • Experience in pharmacovigilance, safety aggregate reporting, clinical research, or pharmaceutical industry • Exposure to global regulatory submissions preferred Skills • Strong knowledge of global safety regulations (ICH, FDA, EMA) • Proficiency in MS Word, Excel, Adobe Acrobat, ISI Toolbox, SharePoint • Business Objects knowledge is an added advantage • Excellent written and verbal communication skills • Strong coordination, project management, and problem-solving abilities • High attention to detail and data accuracy About the Company Pfizer is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative medicines and vaccines. With a strong focus on science, quality, and patient safety, Pfizer offers dynamic career opportunities and global exposure across drug development, pharmacovigilance, and regulatory operations.

Roles & Responsibilities • Support Project Managers in eClinical system design, setup, and study configuration • Assist in creation and maintenance of study-specific documentation and quality records • Track, monitor, and report study metrics, timelines, and progress • Coordinate with clients to collect requirements and resolve system-related queries • Perform assigned eClinical and data management support activities to ensure data accuracy and compliance Qualification • Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or other health-related discipline Experience • 1-2 years of experience in a pharmaceutical company or CRO environment (preferred) • Freshers with strong aptitude for clinical research may also be considered Skills • Strong attention to detail and accuracy • Proficiency in Microsoft Excel and Word • Working knowledge of medical terminology • Good communication and coordination skills • Ability to work effectively in a global, process-driven environment About the Company Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services. Known for scientific rigor and operational excellence, Medpace supports biotechnology, medical device, and pharmaceutical companies worldwide, offering strong career growth opportunities in clinical research and data management.

Roles & Responsibilities • Work on pharma, biotech, and medical device research projects supporting strategic decision-making • Design and execute research strategies aligned with client objectives • Analyze scientific literature, clinical trials, market entry, opportunity assessments, and competitive landscapes • Conduct competitor analysis, benchmarking, newsletters, and company profiling • Collect data from public sources and through primary interviews with industry experts • Map industry professionals and generate analytical insights • Present findings in client-ready formats (Word, Excel, PowerPoint) Qualification • Graduate or Postgraduate degree from a reputed institution (Life Sciences, Pharmacy, or related fields preferred) Experience • Consultant: Minimum 1 year relevant experience (freshers from reputed institutes may be considered) • Senior Consultant: Minimum 3+ years of experience in pharma/life sciences research or consulting Skills • Strong written and verbal communication skills (English) • Excellent analytical and quantitative abilities • Experience in market research, competitive intelligence, or strategy analysis • Ability to manage multiple projects and work in unstructured environments • Strong stakeholder interaction and presentation skills About the Company Axience is a professional business services firm delivering integrated, bespoke research and consulting solutions. With a strong focus on pharmaceuticals, life sciences, and diagnostics, Axience supports global corporates and consulting firms through high-quality strategic, market, and competitive research, offering employees exposure to global standards and strong learning opportunities.

Role & Responsibilities • Assist in providing pharmaceutical care to patients • Ensure compliance with DHA, MOH, and DOH regulations • Provide expert advice on medication usage and dosage • Support the pharmacy team in dispensing medications and managing inventory • Assist in inventory management and stock control Qualification • Pharmacy degree (B.Pharm / Pharm.D) • DHA, MOH, or DOH license preferred Experience • Freshers or up to 1 year of experience in a pharmacy settingAbout the Company • Life Pharmacy is a dynamic, customer-focused organization dedicated to health, wellness, and exceptional customer care, With a strong commitment to innovation and excellence, Life Pharmacy offers a wide range of health-related products and services.

Roles & Responsibilities • Support Lead Data Manager and act as backup for end-to-end CDM activities • Perform CRF review, specifications development, and database build/UAT support • Conduct clinical data review, query management, and line listing reviews • Perform medical coding and AE/SAE reconciliation • Maintain data management documentation with version control • Coordinate with EDC vendors and third-party stakeholders • Support database lock, metrics reporting, and process improvements • Train study teams on CRF, EDC, and study-specific processes Qualification • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Computer Applications, or related discipline Experience • Relevant experience in Clinical Data Management within a CRO or sponsor setup • Hands-on experience across the clinical trial lifecycle Skills • Strong experience with EDC systems (Medidata Rave, Veeva Vault preferred) • Good knowledge of ICH-GCP and clinical trial processes • Experience in medical coding, data review, and database lock • Strong analytical, documentation, and communication skills About the Company Precision For Medicine is a global CRO focused on precision medicine and advanced clinical research, delivering innovative data-driven solutions to accelerate drug development across complex and rare diseases.

Roles & Responsibilities • Execute day-to-day production activities in API and Formulation units in compliance with SOPs and cGMP • Handle IPQA activities, QA documentation, QMS implementation, PV support, and regulatory compliance • Perform QC activities including analytical testing, validation, stability studies, and GLP documentation • Manage stores operations such as receipt, dispensing, inventory control, and inward/outward movements • Operate and maintain formulation and injectable equipment including vial filling & sealing, autoclave, tunnel, vial washing, and dry powder injection systems • Support engineering and technical operations related to HVAC, utilities, instrumentation, and electrical systems • Ensure data integrity, audit readiness, safety compliance, and adherence to regulatory standards Qualification • B.Pharm / M.Pharm • M.Sc (Chemistry / Organic Chemistry) • B.Sc / B.Com / M.Com (for Stores roles)Experience • Typically 2-8 years, depending on role and department • Relevant exposure to API and/or Formulation manufacturing in regulated pharmaceutical environments Walk-In Interview Details • Date: 18 January 2026 (Sunday) • Time: 09:00 AM onwards • Venue: Reyansh Pride Hotels, P-18, MIDC Boisar, Next to Orange Hospital, Tarapur Road, Boisar (W), Dist. Palghar – 401506 • Registration: Mandatory via official linkSkills • Strong knowledge of cGMP, SOPs, and pharmaceutical regulatory requirements • Hands-on experience with manufacturing, QC, QA, or injectable operations • Good documentation practices and attention to detail • Ability to work in shifts and collaborate across cross-functional teams About the Company Macleods Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong domestic and global footprint. Known for its quality-driven manufacturing, regulatory excellence, and wide therapeutic portfolio, Macleods offers professionals a stable work environment, advanced manufacturing exposure, and long-term career growth opportunities.

Role & Responsibilities • Manage aggregate safety reporting and benefit-risk assessments • Lead pharmacovigilance projects and submissions to regulatory authorities • Coordinate with global safety stakeholders to ensure timely reporting and compliance • Ensure inspection readiness and adherence to regulatory requirements Qualification • MBBS / MD Experience • Strong experience in aggregate reporting and pharmacovigilance project management Skills • Excellent knowledge of safety data review and submission processes • Proficient in managing pharmacovigilance teams and regulatory interactions • Strong organizational and leadership abilitiesAbout the Company • Sun Pharmaceutical Industries Ltd. is one of India’s largest global pharmaceutical companies. • It is a leader in the manufacturing of specialty and generic medications, with a focus on drug safety, regulatory compliance, and patient health.

Role & Responsibilities • Lead safety activities for New Chemical Entities (NCE) and innovator products • Perform signal detection and risk management activities • Author/review PSURs, PBRERs, DSURs, and other safety reports • Review Safety Management Plans (SMPs) and study protocols • Collaborate with global cross-functional teams to ensure safety monitoring Qualification • MBBS / MD Experience • 3–4 years of Pharmacovigilance experience • Prior exposure to NCEs or innovator molecules Skills • Expertise in signal detection and benefit-risk assessment • Strong experience with global regulatory reporting and safety risk management • Proficient in writing and reviewing safety documents like PSURs and DSURsAbout the Company • Sun Pharmaceutical Industries Ltd. is one of India’s largest global pharmaceutical companies.

Role & Responsibilities • Review and perform medical assessment of Individual Case Safety Reports (ICSRs) • Conduct causality assessments and MedDRA coding • Review literature cases and write safety narratives • Support the preparation of Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs), and aggregate safety reports • Ensure compliance with global pharmacovigilance (PV) regulations Qualification • MBBS / MD Experience • 1–2 years of Pharmacovigilance experience • Hands-on experience in ICSR review and aggregate reporting Skills • Strong knowledge of MedDRA coding and causality assessment • Proficient in safety narrative writing and literature review • Familiarity with global PV regulationsAbout the Company • Sun Pharmaceutical Industries Ltd. is one of India’s largest global pharmaceutical companies.

Roles & Responsibilities • Conduct in-process, on-site, and off-site audits to ensure trial activities are performed, recorded, analyzed, and reported in compliance with regulatory, organizational, and client requirements • Perform system audits as per the annual audit calendar to ensure compliance with Lambda SOPs, quality systems, protocols, and applicable regulations • Carry out retrospective audits of study raw data including ICFs, protocols, project management plans, IMP plans and release checklists, SMPs, CSRs, and medical imaging documents • Support completion of assigned system audits and preparation of detailed audit reports • Review and contribute to SOPs related to Clinical Data Management and Quality Assurance • Audit clinical databases and CDM documents prior to database lock • Calculate clinical database error rates and communicate findings to CDM; prepare CDM audit status for audit certificates and QA statements • Review Data Management Plans, SAPs (CDM aspects), and CRF/eCRF designs for assigned projects • Conduct system audits of Clinical Data Management functions and report outcomes • Review TMF, SMF, site selection visit reports, and IMP release documentation Qualification • M.Pharm Experience • 2-3 years of experience in late-phase Quality Assurance within clinical research Skills • Strong knowledge of ICH-GCP, regulatory guidelines, and clinical trial quality systems • Experience in CDM audits, database reviews, and SOP compliance • High attention to detail with strong analytical and reporting skills • Effective communication and documentation abilities About the Company Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization headquartered in Ahmedabad, India, with operations across India, the USA, Canada, Europe, and the UK, delivering end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide.

Roles & Responsibilities • Execute manufacturing activities for transdermal patches, semi-solids (cream, ointment, lotion), ODF, and MDI as per GMP guidelines • Perform equipment qualification, calibration, and routine maintenance • Operate and monitor production machines for coating, blending, filling, and solid oral dosage forms • Carry out in-process checks and maintain batch manufacturing and packing records • Conduct analytical testing using HPLC, GC, KF titration, and related instruments (QC roles) • Maintain accurate documentation in LIMS and ensure GLP compliance • Support shift-based operations and coordinate with cross-functional teams • Follow safety, quality, and regulatory standards at all times Qualification • ITI / Diploma / B.Sc / BE / B.Tech / B.Pharm / M.Sc (relevant disciplines) Experience • 1-7 years for Officer / Executive / Analyst roles • Freshers or up to 1 year experience eligible for FTE / FTA / Apprentice roles Skills • Knowledge of GMP, GLP, and pharmaceutical manufacturing practices • Hands-on exposure to semi-solid preparations, transdermal systems, or QC instruments preferred • Ability to operate and troubleshoot production equipment • Good documentation, communication, and teamwork skills • Willingness to work in shifts About the Company Zydus Lifesciences Limited is a leading Indian pharmaceutical company with a strong global presence, known for innovation, high-quality manufacturing, and specialized dosage forms, offering stable careers and long-term growth opportunities.

Roles & Responsibilities • Production: Operate and monitor API manufacturing processes, handle equipment, maintain batch records, ensure GMP compliance, and meet production targets • Quality Control (QC): Perform sampling, testing, and analysis of raw materials, in-process and finished products; operate analytical instruments and ensure data integrity • Quality Assurance (QA): Review batch manufacturing records, ensure GMP/GLP compliance, support audits, maintain quality documentation, and implement quality systems • Environment, Health & Safety (EHS): Implement safety protocols, conduct risk assessments, manage environmental compliance, train employees on safety practices, and handle incident reporting Qualification • B.Sc / M.Sc (Chemistry) • B.Pharm / M.Pharm • Other relevant science or pharmacy qualifications as per role Experience • Production / QC / QA: 0-8 years (freshers can apply) • EHS: 4-5 years of relevant experience • Prior experience in API or pharmaceutical manufacturing preferred Skills • Strong knowledge of API manufacturing processes and GMP guidelines • Understanding of quality systems, safety regulations, and compliance standards • Good communication and teamwork skills • Attention to detail and commitment to quality • Willingness to work in a dynamic manufacturing environment About the Company Spica Laboratories Pvt Ltd is a growing API manufacturing company based in Telangana, known for its focus on quality, regulatory compliance, safety, and innovation, offering professionals strong exposure to regulated pharmaceutical manufacturing and long-term career growth opportunities.