Pharmacy Jobs

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Conduct signal detection and interpret emerging safety trends • Develop and review aggregate safety reports including PSURs, PBRERs and DSURs • Support benefit–risk assessments and safety strategy discussions • Ensure compliance with global pharmacovigilance regulations (ICH, EMA, US FDA) • Provide medical evaluation of case narratives and literature reports • Collaborate with cross-functional safety and quality teams • Contribute to clinical risk management and regulatory safety activities Qualification • MBBS / MD (Registered Medical Practitioner in India) Experience • Minimum 1+ year experience in Pharmacovigilance / Drug Safety Skills • Signal detection & aggregate reporting • ICSR medical review • Global PV regulatory knowledge • Analytical thinking & medical interpretation • Strong written and verbal communication About the Company • OrciMed Life Sciences is a pharmacovigilance and drug safety organization providing global safety services, signal detection, aggregate reporting and regulatory compliance solutions to pharmaceutical companies

Role & Responsibilities • Manage safety reconciliation and compliance monitoring activities for global clients • Perform reconciliation of Reference Safety Information (RSI) for assigned products • Conduct data mining and review of FDA Adverse Event Reporting System (FAERS) and other regulatory safety databases • Edit, review, and reconcile consolidated global product lists • Manage global exchange of safety information related to product approvals, launches, cancellations, and RSI updates • Maintain and update all documents related to safety reconciliation and compliance activities • Ensure adherence to global pharmacovigilance regulations and internal SOPs Qualification • B.Pharm / M.Pharm Experience • 5–8 years of experience in the Pharmacovigilance domain • Hands-on experience in safety reconciliation and compliance monitoring Skills • Pharmacovigilance compliance & reconciliation • FAERS database review • Reference Safety Information (RSI) management • Advanced MS Excel skills • Mailbox management & documentation • Strong analytical and communication skills About the Company • A global life sciences organization providing pharmacovigilance, regulatory, and compliance services across international markets

Role & Responsibilities • Initiate communication with internal business teams and subsidiaries for SDEA requirements • Follow up with third-party partners to establish and maintain SDEAs • Perform timely exchange of safety data with business partners • Conduct adverse event reconciliation with partners • Support case processing and safety writing activities • Ensure compliance with global pharmacovigilance standards • Stay updated with current PV regulations and scientific developments Qualification • B.Pharm / M.Pharm / BAMS / BHMS Experience • 3–4 years of experience in pharmacovigilance • Hands-on experience in case processing, safety writing and SDEA management • Experience in safety data exchange and reconciliation activities Skills • Knowledge of global pharmacovigilance regulations • SDEA management & reconciliation • Case processing & safety writing • Strong written and verbal communication skills • Presentation & documentation skills About the Company • A leading life sciences organization engaged in delivering high-quality pharmacovigilance and drug safety solutions across global markets

Role & Responsibilities Conduct detailed medical review and assessment of Individual Case Safety Reports (ICSRs) in safety databases Ensure accurate selection and coding of adverse events as per MedDRA guidelines Assess seriousness, expectedness, listedness and causality of reported cases Review suspect and concomitant medications, laboratory data, medical history and case narratives Prepare and provide Company Clinical Comments and medical narratives Ensure compliance with Good Pharmacovigilance Practices (GVP), Good Clinical Practice (GCP) and ICH guidelines Implement EMA and global regulatory requirements in safety reporting processes Maintain high quality and accuracy in safety case assessments Support audits, inspections and continuous quality improvement initiatives Qualification MBBS / MD or equivalent medical degree Experience Minimum 5–8 years of experience in Pharmacovigilance / Drug Safety / Medical Review roles Skills ICSR medical review and causality assessment MedDRA coding and narrative writing Strong knowledge of GVP, GCP, ICH and EMA guidelines Safety database handling (ARGUS, ARISg, etc.) Analytical skills and medical judgement Excellent documentation and communication skills About the Company The organization is a global pharmacovigilance and clinical research service provider delivering comprehensive drug safety, regulatory and clinical operations solutions to pharmaceutical and biotechnology companies worldwide, with a strong commitment to patient safety and regulatory compliance.

Role & Responsibilities Lead product registrations and regulatory submissions including preparation of complex and routine filing packages Coordinate documentation, monitor timelines, and manage regulatory project activities Prepare responses to health authority deficiency letters Represent Regulatory CMC in cross-functional project meetings Monitor regulatory timelines and identify risks impacting project progression Maintain coordination with regional and affiliate regulatory teams Assess and approve lifecycle change requests and ensure ongoing compliance Develop Regulatory CMC strategies for assigned products and projects Identify and mitigate regulatory risks across product life-cycle Attend health authority meetings and provide licensing due diligence support Support process improvements, position papers, and regulatory work aids Maintain technical and regulatory knowledge of global and regional CMC requirements Qualification Bachelor’s degree in Pharmacy, Biology, Chemistry, Pharmacology, or related discipline Experience Minimum 10 years in Regulatory Affairs, R&D, Manufacturing, or related regulatory functions Skills Regulatory CMC strategy development Product registrations and lifecycle management Health authority interaction Risk management and compliance Cross-functional coordination Strong project management skills Technical regulatory documentation expertise Leadership, mentoring, and stakeholder management About the Company The organization is a global life sciences company engaged in pharmaceutical development and manufacturing, supporting worldwide regulatory compliance, product registration, and lifecycle management to deliver high-quality medicines to patients globally.

Role & Responsibilities • Prepare and review clinical study outlines, feasibility synopses, and clinical trial protocols (Phase I–IV, BA/BE) • Author and review Clinical Study Reports (CSRs) for regulatory submissions • Prepare Common Technical Documents (CTDs) and subject-facing documents (ICD, IBs, diaries, etc.) • Draft and review SAE narratives and regulatory submission documents (IND, NDA, BLA, MAA, 505(b)(2), biosimilar, hybrid applications) • Develop Module 2.4, 2.5, 2.6, 2.7 summaries, Clinical/Non-clinical Overviews, ISS/ISE, and briefing documents • Draft Pre-IND, Pre-NDA, SAM, orphan drug designation and expedited approval packages • Support cross-functional teams with SAPs, TLFs, eCRF outlines and study-specific documentation • Manage medical writing activities across studies and departments with minimal supervision • Ensure compliance with internal SOPs and global regulatory guidelines • Prepare and maintain departmental SOPs and quality documentation • Collaborate with Biostatistics, Data Management, Regulatory Affairs, and Medical Leads • Manage departmental administrative requirements and additional tasks as assigned Qualification PhD / MBBS / MD / M.Pharm / Pharm.D Experience Minimum 5 years of professional regulatory medical writing experience Skills • Expert knowledge of regulatory guidelines and submission requirements • Strong proficiency in MS Word, PowerPoint, Excel, and Adobe Acrobat/PDF editors • Understanding of publication processes and congress activities • Excellent interpersonal and communication skills • High attention to detail and scientific writing excellence • Strong multitasking, prioritization, and teamwork abilities About the Company A growing clinical research organization delivering high-quality regulatory medical writing, clinical documentation, and submission support services to global pharmaceutical and biotechnology clients

Key Responsibilities • Oversee adherence to Quality Management Framework procedures to ensure delivery of high-quality pharmacovigilance cases • Review and improve project Quality Management Systems and suggest process enhancements • Collaborate with Team Leads, Trainers and Medical Reviewers to implement new or enhanced quality processes • Coordinate with Quality Reviewers to maintain compliance with quality standards • Review late logs, perform Root Cause Analysis (RCA) and define Corrective and Preventive Actions (CAPA) • Ensure timely documentation and closure of late logs as per client SOPs • Conduct training, refresher sessions and awareness programs on case processing conventions • Work with Operational Excellence and Capability Development teams to enhance engagement quality • Support audits, inspections, SOP development and maintenance • Review safety case data for completeness and accuracy • Track, submit and distribute quality and compliance reports • Maintain client mailboxes, SharePoint, databases and safety tools • Drive zero quality deviations leading to regulatory submission delays • Support transitions, documentation archiving, and cross-functional coordination Skills & Competencies • Working knowledge of ICH, GCP, FDA, MHRA and global PV regulations • Strong attention to detail and data accuracy • Good understanding of medical terminology • Strong verbal and written communication skills • Proficiency in MS Excel, Word and PowerPoint • Strong interpersonal and stakeholder management skillsAbout Accenture Accenture is a global professional services company delivering Strategy & Consulting, Technology and Operations services across more than 120 countries. With industry-leading capabilities in digital, cloud and security, Accenture supports global life sciences clients through advanced technology and intelligent operations centers.

Role & Responsibilities • Oversee ICSR medical review activities performed by Global Service Providers (GSP) • Perform quality checks on medical review deliverables for regulatory and company compliance • Review listedness/expectedness and causality assessments • Lead training and competency development for medical reviewers • Act as liaison between SERM, ICSR processing teams and medical review vendors • Monitor KPIs, identify gaps, drive CAPA and continuous improvement initiatives • Support audit readiness, inspections, and regulatory compliance activities • Provide medical guidance on complex and high-risk safety cases • Support local operating companies on medical review processes when required Qualification • Advanced clinical degree preferred (MD / PharmD / Postgraduate Medical Qualification) Experience • 9–12 years of pharmacovigilance medical review experience Skills • Strong expertise in ICSR medical review, causality & listedness assessment • In-depth knowledge of MedDRA coding conventions • Expertise in quality management, KPI monitoring, and CAPA management • Strong understanding of global PV regulations and drug approval processes • Excellent medical judgment, analytical thinking, and communication skills • Leadership ability and stakeholder management in matrix environments • Experience with audits, inspections, CRO/vendor oversight About the Company GSK is a leading global biopharmaceutical company focused on vaccines and specialty medicines across respiratory, immunology, oncology, HIV and infectious diseases. With a mission to positively impact 2.5+ billion people by 2030, GSK unites science, technology and talent to deliver innovative, high-quality, patient-focused healthcare solutions worldwide.

Role & Responsibilities • Review biomedical literature to identify adverse reaction and non-individual case reports • Assess reportability, seriousness, and validity of safety cases using regulatory and internal guidelines • Perform relevancy assessment and ensure accurate identification of reportable safety information • Conduct narrative review and support MedDRA coding activities • Provide training and guidance to literature scanner teams on inclusion criteria and case standards • Collaborate with subject matter experts to maintain physician competency and compliance • Support quality, consistency, and regulatory adherence in safety case identification • Perform additional PV responsibilities as assigned by lead or manager Qualification • MBBS or MD Experience • 0–3 years in Pharmacovigilance / Drug Safety Skills • Strong knowledge of PV regulations and regulatory compliance • Literature case processing and medical review • Narrative writing and MedDRA coding • Sound pharmacological and clinical assessment skills • High attention to detail and strong communication skills About the Company Wipro is a leading global information technology, consulting, and business process services company delivering innovative solutions across industries, including life sciences and healthcare. Wipro partners with pharmaceutical organizations worldwide to support drug safety, regulatory compliance, and high-quality healthcare delivery.

Role & Responsibilities • Review published biomedical literature for identification of adverse reaction case reports and non-individual case reports • Apply regulatory and internal guidance to determine case validity and reportability • Perform relevancy assessment based on accepted pharmacovigilance guidelines • Provide training and guidance to literature scanners on inclusion criteria • Collaborate with subject matter experts to ensure team capability and compliance • Perform additional pharmacovigilance tasks as assigned by lead or manager Qualification • MBBS or MD Experience • 0–3 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of global PV regulatory guidelines • Narrative writing and medical case assessment • MedDRA coding proficiency • Understanding of pharmacological concepts About the Company Wipro is a leading global information technology, consulting, and business process services company that delivers innovation-led solutions to clients across industries, including life sciences and healthcare. With a strong presence worldwide, Wipro supports pharmaceutical organizations in ensuring drug safety, regulatory compliance, and patient-centric healthcare delivery.Interested candidates can share their resumes at varsha.kamalapurkar@wipro.com

Role & Responsibilities • Perform medical review of company, literature, and regulatory ICSRs • Select and assess adverse events for seriousness and expectedness • Conduct MedDRA coding review of adverse events • Review causality assessments and perform label assessment • Classify product role (suspect, concomitant, interacting) • Review medical history, concomitant conditions, and laboratory data • Evaluate case narratives for medical accuracy and completeness • Perform medical review and quality review of aggregate safety reports (PSURs, PADERs) • Conduct medical review of Risk Management Plans (RMPs) • Review Signal Management Reports and support signal evaluation Qualification • MBBS or MD (Pharmacology preferred) Experience • Relevant experience in pharmacovigilance medical review or drug safety preferred Skills • Strong knowledge of pharmacovigilance regulations and safety reporting standards • MedDRA coding proficiency • High attention to clinical detail and document quality • Strong written and verbal communication skills • Ability to work with global safety documentation and regulatory timelines About the Company The hiring organization operates in regulated pharmacovigilance and drug safety domains, supporting global pharmaceutical safety surveillance, aggregate reporting, and risk management activities aligned with international regulatory standards.

Role & Responsibilities • Design and manage clinical databases for RWE and interventional studies • Translate study protocols into structured data logic • Develop and maintain data dictionaries, coding standards, and variable mappings • Perform data cleaning, discrepancy management, and query resolution • Execute SQL-based data validation across EDC, EHR, and repository systems • Collaborate with data engineers and medical teams for ETL workflows • Maintain documentation and ensure regulatory compliance Qualification • Bachelor’s in Life Sciences, Pharmacy (B.Pharm preferred), Biomedical Engineering, Computer Science, or related field Experience • 2–4 years in clinical data management or EDC setup Skills • CDISC, SDTM, CDASH knowledge • ICD-10, MedDRA, SNOMED coding systems • SQL, Medidata Rave, Oracle Clinical, REDCap • Python/R, Power BI, Tableau (preferred) About the Company NeuroDiscovery AI is a health technology company leveraging AI-driven real-world evidence and clinical data analytics to advance precision medicine for neurological disorders including Autism, Alzheimer’s, Parkinson’s, and Migraine.

Role & Responsibilities • Support and conduct biomedical and biotechnology research projects • Assist in experimental design, data collection, and analysis • Prepare research documentation, reports, and scientific manuscripts • Maintain laboratory records and ensure compliance with research protocols • Coordinate with project investigators and multidisciplinary research teams • Ensure proper handling of laboratory equipment, samples, and reagents • Participate in project meetings, audits, and review activitiesName of the PostsNo.of VacanciesQualificationResearch Associate03MD/MS MDS, BDS/M.Pharm, M.V.Sc, M.E/ M.Tech Experience • Research exposure in biomedical, biotechnology, or related domains preferred • Fresh or experienced candidates eligible as per NABI norms Skills • Laboratory research and experimental handling • Data analysis and scientific documentation • Understanding of research methodologies and protocols • Attention to detail and regulatory compliance • Team coordination and communication About the Company The National Agri-Food Biotechnology Institute (NABI) is an autonomous research institute under the Department of Biotechnology, Government of India, dedicated to cutting-edge research in agri-food biotechnology, nutrition, and translational sciences aimed at improving national food security and public health.Date of Walk-in-Interview08-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Dispense medicines as per prescriptions • Maintain pharmacy stock, records and expiry tracking • Ensure proper storage of medicines and cold chain maintenance • Counsel patients on medication usage and safety • Maintain statutory registers and documentation • Coordinate with medical officers for medicine requirementsName of the PostsVacanciesEducationPharmacist02B. Pharm, D.Pharm Experience • Freshers or experienced candidates Skills • Dispensing and inventory management • Good communication and documentation skills • Knowledge of pharmacy regulations About the Company District Health and Family Welfare Society (DHFWS), Udupi operates under the National Health Mission to provide accessible and affordable public healthcare services across the district.Starting date31-12-2025Closing date16-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Dispense prescribed medicines to ECHS beneficiaries • Maintain pharmacy inventory and stock records • Ensure proper storage of medicines • Counsel patients on medication usage • Maintain prescription and dispensing records Qualification • B.Pharm / D.PharmVacancies no -17 Experience • Freshers or experienced pharmacists Skills • Drug dispensing and inventory management • Good communication skills • Knowledge of drug storage and handling About the Company ECHS operates polyclinic pharmacies delivering essential medicines to defence beneficiaries across India under government healthcare programs.Starting date02-01-2026Closing date28-01-2026Official NotificationClick HereApplication FormClick Here

Role & Responsibilities • Perform accurate data entry of safety and pharmacovigilance cases • Ensure completeness and correctness of case-related information • Follow SOPs, quality standards and regulatory timelines • Identify, document and escalate data discrepancies • Maintain data confidentiality and integrity • Support workload management during high-volume periods Qualification • B.Pharm / M.Pharm / Pharm.D Experience • 2 – 3 years in pharmacovigilance case processing or safety data entry Skills • Strong data accuracy and documentation skills • Good knowledge of SOPs and regulatory requirements • Attention to detail and time management skills • Ability to work in quality-driven environments About the Company Mitocon Biopharma is a Hyderabad-based pharmaceutical organization focused on regulated pharmacovigilance operations, offering pharmacy professionals structured growth, compliance exposure and a professional work environment.

Role & Responsibilities • Review pharmacovigilance case processing for accuracy, completeness and regulatory compliance • Perform quality checks and identify gaps, deviations and trends • Ensure adherence to SOPs, global PV guidelines and defined TATs • Maintain quality metrics, reports and compliance documentation • Provide feedback, mentoring and training to case processing teams • Support audits, inspections and continuous improvement activities Qualification • B.Pharm / M.Pharm / Pharm.D Experience • 3 – 5 years in pharmacovigilance case processing or quality review Skills • Strong understanding of PV regulations and SOP compliance • High attention to detail and analytical skills • Good documentation and reporting ability • Effective communication and mentoring skills About the Company Mitocon Biopharma is a Hyderabad-based pharmaceutical organization engaged in regulated pharmacovigilance operations, providing high-quality drug safety services with strong focus on compliance, audits and continuous quality improvement.

Role & Responsibilities • Oversee pharmacovigilance vendors and CRO partners in a sponsor environment • Review, manage and approve SAEs, SUSARs and ICSR submissions • Support preparation and medical review of DSURs and aggregate safety reports • Provide safety input into clinical protocols, Investigator’s Brochures and trial documents • Coordinate with Clinical Operations, QA and Regulatory Affairs teams • Support inspection readiness, audits and safety governance meetings • Manage long-term follow-up and safety activities specific to Cell & Gene Therapy trials • Ensure compliance with ICH-GCP, ICH E2 and global PV regulations Qualification • Degree in Pharmacy, Life Sciences or related discipline Experience • Experience in Pharmacovigilance and Clinical Trials • Prior exposure to sponsor oversight or CRO/vendor management preferred Skills • Strong understanding of clinical safety reporting and PV regulations • Ability to work in cross-functional sponsor teams • Good documentation, coordination and communication skills • Exposure to Cell & Gene Therapy, Oncology or Rare Disease programs preferred About the Company This is a growing sponsor organization focused on developing innovative Cell & Gene Therapy programs, driving advanced clinical research with strong regulatory compliance and patient safety governance at its core.

Role & Responsibilities • Review high-value and complex medical claims for up-coding, unbundling, duplication, and misrepresentation • Prevent fraudulent, abusive, and non-compliant claim payments • Apply CPT and diagnosis coding knowledge during claim investigations • Ensure compliance with CMC guidelines, benefit plans, and client-specific policies • Identify provider aberrant behavior and risk patterns • Support reporting, audits, and special investigative projects • Maintain adherence to state and federal healthcare regulations Qualification • BPT / MPT • BHMS / BAMS / BUMS • BDS / B.Sc Nursing (minimum 1 year corporate experience mandatory) Experience • 6 months – 4 years in healthcare, claims review, or medical auditing roles Skills • Strong analytical and investigation skills • Understanding of healthcare documentation and billing systems • High attention to detail and quality orientation • Good communication and reporting skills About the Company Optum is a global healthcare and analytics organization delivering data-driven insights, technology, and services to improve healthcare quality, efficiency, and patient outcomes worldwide.