Pharmacy Jobs

Roles & Responsibilities • Develop, write, review, and finalize high-quality scientific publications including manuscripts, abstracts, posters, slide decks, and congress materials • Ensure scientific accuracy, data integrity, and strategic alignment across all publication deliverables • Collaborate with authors, clients, and internal stakeholders to ensure clarity, compliance, and impactful communication • Mentor and guide junior medical writers, providing constructive feedback and sharing best practices • Support development of digital scientific content such as infographics, summaries, and visual abstracts • Contribute to proposal writing, pitches, and new business development initiatives as required • Ensure adherence to publication ethics, authorship criteria, and industry guidelines Qualification • PhD / MD / PharmD / M.Pharm / M.Sc in Life Sciences or related discipline Experience • Minimum 4+ years of experience in scientific or medical writing with a strong focus on publications Skills • Excellent scientific writing, editing, and communication skills • Strong understanding of clinical trial data, literature evaluation, and data interpretation • Knowledge of publication standards and guidelines including GPP, ICMJE, and journal/congress requirements • Ability to manage multiple projects, meet deadlines, and work collaboratively with cross-functional teams About the Company VUEVERSE is a growing medical communications and scientific writing organization specializing in high-quality, compliant, and impactful publication solutions, supporting life sciences and healthcare clients across global markets.

Roles & Responsibilities • Manage end-to-end governance of raw material data management requests, ensuring initiation within 24 hours and adherence to defined TATs • Understand request objectives, seek clarifications when required, and ensure completeness before initiation • Coordinate effectively with suppliers, track responses, highlight delays, and escalate issues in a timely manner • Maintain and update the Global Request Tracker (GTR) as the single source of truth throughout the request lifecycle • Ensure timely, transparent communication with global stakeholders on request status and outcomes • Apply strong regulatory knowledge across raw material categories including Cosmetics, OTC, Drugs, and Food/Nutraceuticals • Support toxicology and safety data requirements in collaboration with Toxicology partners • Ensure right-first-time data collection, validation, and accurate system entry across all platforms • Take ownership to consistently meet quality, productivity KPIs, and on-time delivery Qualification • B.Pharm / M.Pharm • M.Sc (Life Sciences, Chemistry, Toxicology, or related disciplines) Experience • 0-3 years in Regulatory Affairs, Raw Material Compliance, Quality, or Data Management • Freshers with strong regulatory and compliance knowledge may apply Skills • Strong request and project management capabilities • High attention to detail with disciplined process execution • Effective written and verbal communication with internal teams and suppliers • Problem-solving and critical-thinking abilities • Sense of urgency, learning agility, and adaptability in fast-paced environments • Ability to work under pressure with resilience and accountability About the Company ClinChoice is a global clinical research and regulatory solutions organization providing end-to-end services across drug development, regulatory affairs, and data management, supporting life sciences companies with high-quality, compliant, and efficient delivery across global markets.

Role & Responsibilities • Conduct medical review and approval of selected scientific and literature articles • Review Individual Case Safety Reports (ICSRs) in the safety database • Perform medical labeling, causality assessment, and seriousness evaluation • Follow up with reporters to obtain missing or additional safety information • Review aggregate safety reports, including Periodic Safety Update Reports (PSURs) and Periodic Adverse Drug Experience Reports (PADERs) • Provide medical and scientific conclusions for benefit–risk assessments • Review and support Risk Management Plans (RMPs) • Contribute to signal detection and signal management activities • Ensure compliance with global pharmacovigilance regulations Qualification • MBBS or MD in Pharmacology Experience • 0–1 year of experience in pharmacovigilance or drug safety Skills • Strong understanding of ICSR processing and safety databases • Knowledge of global PV regulations (ICH, GVP, FDA, EMA) is an advantage • Prior experience in a regulated pharmaceutical company is a plus About the Company • Emcure Pharmaceuticals is a leading Indian pharmaceutical company, offering expertise in pharmacovigilance and drug safety operations globally.

Roles & Responsibilities • Coordinate and oversee site-level clinical trial activities to ensure protocol compliance • Support end-to-end clinical research operations including planning, execution, tracking, and reporting • Act as a supervisory link between CRAs, site teams, and internal stakeholders • Monitor project timelines, deliverables, and quality metrics across assigned studies • Ensure compliance with ICH-GCP guidelines, SOPs, and applicable regulatory requirements • Identify operational risks and support implementation of corrective and preventive actions (CAPA) • Contribute to continuous quality improvement initiatives in clinical research operations Qualification • B.Pharm (Bachelor of Pharmacy), M.Pharm (Master of Pharmacy), Pharm.D (Doctor of Pharmacy), M.Sc, B.Sc, Life Sciences (related disciplines) Experience • 3-4 years of on-site experience as a Clinical Research Associate (CRA) • 4-5 years of total experience in clinical research operations • Minimum 2 years in a project management or supervisory role Skills • Strong knowledge of clinical trial operations and site management • Sound understanding of ICH-GCP and regulatory requirements • Leadership and team coordination skills • Excellent organizational, communication, and problem-solving abilities • Ability to manage multiple projects, timelines, and stakeholders effectively About the Company Hector Research & Archival Pvt. Ltd. is a clinical research organization committed to operational excellence and uncompromised quality in clinical trials, supporting site-level execution and regulatory compliance across India while driving high-quality clinical research outcomes.

Role & Responsibilities • Drive API sales and business development for Indian regulated customers • Build and maintain long-term relationships with key pharmaceutical clients across India • Collaborate with Regulatory Affairs, IP, Quality, and Supply Chain teams for smooth project execution • Monitor market trends and competitor activities, providing insights for business growth • Ensure compliance with US/EU regulatory guidelines and filings (DMFs, CEPs, etc.) • Travel regularly for customer visits and trade shows Qualification • 6 to 12 years of experience in API business development in Indian regulated markets Experience • Strong understanding of pharma regulatory landscape and documentation • Experience handling API business with Indian regulated market customers Skills • Excellent communication, negotiation, and relationship-building skills • Ability to work cross-functionally with multiple teams About the Company • Alembic Pharmaceuticals is a global leader in the pharmaceutical industry, specializing in the development and manufacturing of APIs and finished formulations, serving regulated markets worldwide.

Roles & Responsibilities • Prepare, review, and submit Ethics Committee (EC) applications and related regulatory documents • Coordinate with Principal Investigators and site teams at AIIMS Bhubaneswar for EC submissions • Maintain and regularly update EC submission trackers and documentation logs • Ensure compliance with ICH-GCP guidelines, Indian regulatory requirements, and internal SOPs • Support EC amendments, continuing reviews, annual reports, and EC correspondence • Assist in overall clinical trial documentation and record management at the site Qualification • B.Pharm, M.Pharm, Pharm.D, M.Sc / B.Sc / Life Sciences Experience • 1-2 years of experience as a Clinical Research Coordinator or in a similar clinical research role • Mandatory hands-on experience in Ethics Committee (EC) submissions Skills • Strong knowledge of GCP and regulatory documentation • Good understanding of clinical trial processes and site operations • Excellent communication and coordination skills • Strong organizational abilities and attention to detail • Ability to manage multiple submissions and timelines effectively About the Company Accede Clinicals is a growing clinical research services organization providing support across clinical trial operations, regulatory coordination, and site management, offering professionals valuable exposure to structured clinical research environments at reputed institutions like AIIMS.

Roles & Responsibilities • Assist Principal Investigators in day-to-day clinical trial activities • Coordinate with study participants and manage patient visits and follow-ups • Maintain essential clinical trial documents, study files, and investigator site files • Support compliance with GCP guidelines and regulatory requirements • Assist in preparation and maintenance of Case Report Forms (CRFs) and source documents • Ensure accurate documentation and maintenance of trial-related data and records Qualification • B.Pharm, D.Pharm, Life Sciences graduate Experience • Freshers are eligible to apply • Prior exposure to clinical research is an advantage but not mandatory Skills • Strong interest in clinical research and clinical trials • Basic understanding of GCP and clinical trial processes • Good communication and coordination skills • Attention to detail and documentation accuracy • Fluency in Kannada preferred • Candidates based in Mysuru will be given priority About the Company Daksun Clinical Research LLP is a growing clinical research organization focused on hands-on training and execution of clinical trials, offering aspiring professionals practical exposure to site operations, GCP compliance, and real-world clinical research with opportunities for long-term career growth.

Role & Responsibilities • Provide medical review, analysis, and guidance during the case handling and reporting cycle of Individual Case Safety Reports (ICSRs) and ADR reports for investigational and marketed products • Conduct detailed ICSR Medical Review to assess causality, seriousness, and completeness, ensuring compliance with regulatory requirements • Write safety sections of Aggregate Reports such as PSURs, CASRs, and PADERs, including benefit-risk assessments • Guide Drug Safety Associates on medical aspects of drug safety, including case assessments and aggregate analysis • Analyze ADRs during ongoing surveillance and signal detection • Participate in Safety Review Meetings and client discussions to provide medical insights and recommendations • Maintain personal readiness for internal audits or regulatory inspections Qualification • MBBS, MD in Pharmacology or equivalent Experience • Clinical research or pharmacovigilance experience • Strong understanding of ICSR processes and global safety regulations Skills • Analytical and problem-solving skills • Excellent verbal/written communication skills • Strong presentation skills • Client-focused approach to work • Excellent organizational and prioritization skills About the Company • Vizen Life Sciences Pvt Ltd is a leading company specializing in drug safety and pharmacovigilance, offering medical expertise to ensure regulatory compliance and the safety of investigational and marketed pharmaceutical products.

Roles & Responsibilities • Manage electronic Trial Master File (eTMF) activities including Trial, Country, and Site artifacts in line with TMF processes • Classify, review, and process documents through Smart Inbox and perform ARC reviews • Conduct visual quality checks to ensure document clarity, readability, and completeness • Perform Audit Ready Checks to maintain inspection-ready eTMF at all study stages • Track, process, and maintain final essential documents across the clinical study lifecycle • Ensure compliance with company SOPs, sponsor SOPs, GCP, ICH, and regulatory requirements • Support QA and sponsor audits, identify issues, and implement corrective and preventive actions • Collaborate with Business Process, Study, and cross-functional teams to meet project and client expectations • Participate in internal and external study meetings as required • Contribute to continuous improvement initiatives to enhance quality, productivity, and processes Qualification • Bachelor’s Degree in Life Sciences or Business • Master’s Degree in Life Sciences or Business preferred Experience • 6-12 months of experience in a clinical research environment • Equivalent clinical research experience may be considered Skills • Strong understanding of GCP, ICH guidelines, and regulatory documentation requirements • Proficiency in Microsoft Office, web-based applications, and Adobe Acrobat • Familiarity with clinical electronic systems is an advantage • Excellent communication, interpersonal, and organizational skills • High attention to detail and ability to manage multiple tasks About the Company Fortrea is a leading global Contract Research Organization dedicated to advancing clinical development through innovation, collaboration, and scientific excellence, helping transform lives by delivering high-quality clinical trials worldwide.

Roles & Responsibilities • Lead and execute analytical development activities using LC, LC-MS, HPLC, GC, and GC-MS as per departmental role • Perform method development, validation, and troubleshooting for pharmaceutical and related products • Handle analytical testing, data interpretation, documentation, and regulatory-compliant reporting • Support R&D activities including synthesis, formulation development, nano-material characterization, and technology evaluation • Operate and maintain advanced analytical instruments such as HPLC, LC-MS, GC-MS, NMR, XRD, AFM, and related systems • Conduct patent and market searches and contribute to selection of niche APIs and KSMs • Ensure compliance with GLP, NABL, and regulatory guidelines • Mentor junior team members and support laboratory setup, process improvement, and cross-functional collaboration Qualification • M.Sc / M.Pharm or equivalent • Ph.D in Nanotechnology preferred for R&D Manager role Open Positions & Requiremnets • Manager (LC, LC-MS - AD Department): 10-15 years • Research Associate - HPLC (AD&QC Department): 3-7 years • Manager - (R&D Department): 10-15 years • Research Associate / Sr. Research Associate (Method Development & Validation – HPLC, Analytical Dept.): 3-6 years • Research Associate / Sr. Research Associate (GC, GC-MS – AD&QC Dept.): 3-6 years Skills • Strong hands-on expertise in analytical techniques and instrumentation • In-depth knowledge of method development, validation, and regulatory documentation • Experience in pharmaceutical, CRO, or regulated laboratory environments • Analytical thinking, problem-solving, and attention to detail • Ability to work independently and lead teams where applicable About the Company Accuprec Research Labs Pvt Ltd is a NABL-accredited and GLP-certified Contract Research Organisation based in Ahmedabad, Gujarat, offering advanced regulatory testing and research services for pharmaceuticals, medical devices, herbal products, and allied industries, with a strong focus on quality, innovation, and scientific excellence.

Roles & Responsibilities • Manage warehouse operations including receiving, dispensing, storage, and documentation through online systems • Handle eLog, eBRMS, WDS, SAP, and eWMS for effective inventory and warehouse control • Perform quality control activities such as FP & stability testing, dissolution, and analytical testing using HPLC and UV • Operate and manage LIMS, Empower software, and Waters HPLC systems • Execute quality assurance functions including IPQA for manufacturing and packing areas • Monitor shop-floor activities, line clearance, and review BMR, BPR, and equipment audit trails • Ensure strict compliance with GMP, SOPs, and regulatory guidelines Qualification • Officer / Sr. Officer: M.Sc / B.Pharm / M.Pharm / B.Com / B.Sc / D.Pharm • Quality Control: M.Sc / B.Pharm • Quality Assurance: M.Pharm / B.Pharm Experience • 2 to 6 years of relevant experience in Warehouse, QC, or QA functions within formulation manufacturing Skills • Strong knowledge of GMP-compliant operations and documentation • Hands-on experience with analytical instruments and quality systems • Familiarity with SAP, eWMS, WDS, LIMS, Empower, and electronic documentation systems • Good attention to detail and ability to work in regulated manufacturing environments Walk-in Interview Details • Date: 18th January 2026 (Sunday) • Venue: RE:GEN:TA Central Harimangla, ABC Circle, Old NH-8, Bholav, Bharuch, Gujarat – 392015 • Note: Carry updated resume, educational certificates, experience letters, passport-size photographs, and ID proof. Interviews are on a first-come, first-served basis. About the Company Alkem Laboratories is a leading Indian pharmaceutical company with a strong global footprint, known for high-quality generics, formulations, and nutraceuticals, offering employees exposure to advanced manufacturing facilities, innovation-driven culture, and long-term career growth opportunities.

Roles & Responsibilities • Support the business process owner for literature surveillance activities • Manage training documentation and user access for literature surveillance and reconciliation systems • Perform operational activities including literature reconciliation, quality control of non-ICSR literature, and article uploads • Conduct ICSR reconciliation, quality monitoring, and safety spot checks in collaboration with cross-functional teams • Handle team mailboxes and ensure timely action on all pharmacovigilance communications • Ensure end-to-end compliance with global pharmacovigilance regulations across the literature surveillance lifecycle Qualification • B.Pharm / M.Pharm / Pharm.D / MSc / BSc / Life Sciences / Medicine Experience • Minimum 3 years of experience in a pharmacovigilance environment • Proven experience in literature safety surveillance and ICSR reconciliation • Exposure to global drug safety regulations for clinical and post-marketing products Skills • Strong knowledge of global pharmacovigilance regulations and safety reporting requirements • Hands-on experience with literature surveillance and reconciliation processes • Experience with ArisG Safety Database (preferred) • Excellent written and verbal communication skills • Ability to work effectively in a global, cross-functional matrix environment About the Company Merck is a global science and technology leader operating across healthcare, life science, and electronics, committed to innovation, patient safety, and advancing human health through cutting-edge research and global collaboration.

Roles & Responsibilities • Approve and schedule Individual Case Safety Reports (ICSRs) in the Argus database for submission to Health Authorities • Submit safety cases to Health Authorities, Business Partners, and Affiliates as per regulatory requirements • Ensure strict adherence to internal and external timelines to maintain regulatory compliance • Schedule and approve regulatory reports based on defined reporting obligations • Perform quality review of ICSRs to ensure accuracy, completeness, and compliance with PV guidelines • Support regulatory submission activities and maintain high-quality pharmacovigilance standards Qualification • B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)Experience • 4 to 6 years of relevant Pharmacovigilance experience • Mandatory hands-on experience in ICSR Quality Review and Regulatory Submissions • Strong working experience with the Argus Safety Database Skills • Strong knowledge of global Pharmacovigilance regulations and reporting guidelines • Expertise in ICSR quality review, compliance, and regulatory submissions • High attention to detail with strong analytical skills • Excellent communication, coordination, and time management abilities About the Company Vizen Life Sciences is a growing life sciences organization focused on delivering high-quality pharmacovigilance, regulatory, and safety solutions, supporting global healthcare and regulatory compliance standards.

Roles & Responsibilities • Manage clinical study documents in line with client, regulatory, and ICON requirements • Perform document receipt, review, quality checks, scanning, indexing, filing, and archiving in the Trial Master File (TMF) • Ensure continuous compliance with ICON SOPs, work procedures, and applicable regulatory guidelines • Collaborate with study teams, clients, and internal ICON departments to support study deliverables • Participate in internal and external audits and support inspection readiness activities • Prepare and maintain TMF status reports and tracking logs • Identify gaps or issues in TMF documentation and support corrective actions • Participate in training programs to enhance TMF and clinical research knowledge • Support special projects and additional responsibilities as assigned by the Manager Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences or related disciplines Experience • 1-15 years of experience in TMF management or clinical document management • Strong understanding of clinical trial documentation and TMF processes Skills • Strong oral and written communication skills • Excellent attention to detail and document accuracy • Good interpersonal and stakeholder coordination skills • Strong organizational and time management abilities • Working knowledge of clinical trial regulations and documentation standards About the Company ICON plc is a global leader in clinical research and healthcare intelligence, committed to advancing clinical development through innovation, partnership, and integrity, while fostering an inclusive work environment focused on improving patient lives worldwide.

Role & Responsibilities • Perform data QC and editing for regulatory documents, including Clinical Study Reports   (CSR), Investigator’s Brochures (IB), Protocols, and more • Ensure adherence to ICH-GCP guidelines and internal quality standards • Collaborate with CROs and sponsor companies to deliver high-quality outputs Qualification • Strong experience in medical editing and QC for regulatory documents Experience • Experience in clinical research or pharmaceutical industries • Familiarity with regulatory documents and editing processes Skills • Excellent written and verbal communication skills • Ability to manage multiple projects under tight timelines • Attention to detail and strong understanding of clinical research processes Preferred Skills • Familiarity with publishing tools and regulatory submission platforms About the Company • Syneos Health is a global, full-service biopharmaceutical solutions organization committed to advancing clinical research for pharmaceutical and biotechnology companies worldwide.

Roles & Responsibilities • Lead end-to-end Clinical Data Management (CDM) activities for single or multi-service clinical studies • Gather and analyze study setup requirements in collaboration with sponsors and internal stakeholders • Oversee data collection, data cleaning, validation, and database lock activities • Validate and manage new device and system integrations with minimal supervision • Ensure all study deliverables meet sponsor expectations, quality standards, and timelines • Track project progress, identify risks and issues, and implement corrective and preventive actions • Lead study kick-off meetings, internal team meetings, and sponsor audits • Support onboarding and training of new team members • Collaborate with programming and technology teams to drive automation and process improvements • Contribute to the development, review, and maintenance of SOPs and work instructions Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences, Health Sciences, Clinical, Biological, Mathematical Sciences, or related discipline Experience • 3-4 years of clinical data management experience • Minimum 1 year of experience as a CDM Project Lead preferred Skills • Strong understanding of the drug development lifecycle and overall clinical research process • Hands-on expertise in clinical data collection, validation, and reporting • Proficiency in Microsoft Excel, Word, and Outlook • Strong spoken and written English communication skills • Good leadership, problem-solving, and stakeholder management skills • Ability to manage multiple priorities and meet project timelines About the Company IQVIA is a global leader in clinical research, healthcare analytics, and life sciences intelligence, supporting pharmaceutical, biotechnology, and healthcare organizations worldwide through advanced analytics, technology-enabled solutions, and deep scientific expertise to improve patient outcomes and accelerate innovation.

Roles & Responsibilities • Promote pharmaceutical products to doctors, pharmacies, and healthcare professionals in assigned territories • Build and maintain strong professional relationships with healthcare stakeholders • Achieve sales targets through effective product detailing and regular field visits • Conduct product presentations and explain benefits, indications, and usage • Collect market intelligence, competitor information, and customer feedback • Prepare daily visit reports and sales performance updates • Ensure compliance with company policies and Qatar healthcare regulations Qualification • B.Pharm / M.Pharm / Pharm.D from a recognized institution Experience • Minimum 1 year of experience as a Medical Representative Skills • Strong communication and persuasion skills • Good knowledge of pharmaceutical products and sales techniques • Ability to work independently and meet sales targets • Willingness to travel extensively within assigned areas • Valid driving skills (Qatar Driving License required for enhanced salary) Walk-in Interview Details • Dates: 2nd & 3rd February • Location: Kochi, Kerala About the Company The opportunity is with a well-reputed pharmacy group in Qatar, offering attractive salary growth, international exposure, and long-term career prospects in pharmaceutical sales through a direct walk-in interview process conducted in Kochi

Roles & Responsibilities • Dispense prescribed medicines accurately in compliance with Qatar pharmacy regulations • Provide professional counseling to patients on dosage, usage, and precautions • Ensure safe storage, handling, and inventory control of medicines • Maintain accurate records, documentation, and stock registers • Coordinate with healthcare professionals to ensure optimal patient care • Follow pharmacy SOPs, quality standards, and regulatory guidelines • Deliver excellent customer service and support day-to-day pharmacy operations Qualification • B.Pharm / M.Pharm / Pharm.D from a recognized institution Experience • Minimum 2 years of relevant pharmacy experience Walk-in Interview Details • Dates: 31st January & 1st February • Location: Kochi, Kerala Skills • Strong knowledge of pharmaceutical products and dispensing practices • Good communication and patient counseling skills • Ability to work efficiently in a retail or hospital pharmacy environment • Attention to detail and commitment to accuracy and compliance • Team-oriented with a professional and ethical approach About the Company The hiring organization is a well-reputed pharmacy group in Qatar, offering stable career opportunities, competitive salary packages, and exposure to international pharmacy practice standards through a direct interview process conducted in Kochi.

Roles & Responsibilities • Draft new and revised Pharmacovigilance Agreements (PVAs) in line with company and regulatory requirements • Review PVAs to ensure accuracy, quality, and compliance with global standards • Address internal and collaborating company comments on PVAs • Manage the dedicated PVA mailbox and stakeholder communications • Announce new or updated PVAs to relevant client and internal stakeholders • Maintain and update the global PVA tracker, including reconciliations • Perform compliance monitoring of active PVAs and prepare dashboards • Upload and maintain PVAs and related documents in the company repository • Support Project Managers by maintaining project documents and trackers • Participate in team meetings and provide regular status updates Qualification • Bachelor of Pharmacy (B.Pharm) • Bachelor of Science (B.Sc – Life Sciences) Experience • 3 to 7 years of Pharmacovigilance experience • Hands-on experience with Global and Local Pharmacovigilance Agreements Skills • Strong knowledge of ICH and Good Pharmacovigilance Practice (GVP) modules • Expertise in pharmacovigilance contractual arrangements • Excellent documentation and compliance monitoring skills • Strong analytical, communication, and coordination abilities • Ability to manage multiple priorities and stakeholders About the Company Tata Consultancy Services (TCS) is a global leader in IT services, consulting, and business process services, providing end-to-end pharmacovigilance and life sciences solutions to leading global pharmaceutical and healthcare organizations.