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Roles & Responsibilities: • Perform quality control of vigilance cases. • Conduct medical evaluation of safety reports. • Data entry of vigilance cases into agreed databases/formats. • Follow-up of vigilance cases via phone and email. • Pre-analysis of complex cases prior to data entry. • Medical evaluation of files including coding, causality assessment, expectedness, and seriousness of events. • Identify submission requirements for each case. • Validate documents prepared by Data Managers/Vigilance Associates. • Close vigilance case files in compliance with regulations. • Define and implement ICSR/MLM filters and applicable changes. • Analyze inclusion/exclusion of EV/MHRA cases. • Provide medical information support and handle safety-related calls. • Review medical information queries and quality complaints to identify safety information. • Act as key contact for specific clients and prepare quality documents as required. Qualification: • Doctor of Pharmacy / Pharmacist Experience: • 1–3 years of experience in a similar Pharmacovigilance role • Knowledge of Pharmacovigilance is an advantage Skills: • Experience with safety databases preferred • Knowledge of current PV regulations • Process-oriented, detail-focused, and team player • Proficient in Microsoft Office tools • Strong multitasking and flexibility • Excellent communication skills in French and English About the Organisation: ProductLife Group is a global life sciences consulting and services company providing integrated solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the entire product lifecycle.

Role & Responsibilities • Perform quality control (QC) of pharmacovigilance cases • Conduct medical evaluation of adverse event reports • Enter vigilance case data into agreed databases and formats • Perform follow-up of cases via phone and email • Pre-analyse complex cases prior to data entry • Evaluate cases for medical coding as per applicable dictionaries • Assess causality between suspect product and reported events • Determine seriousness and expectedness of events • Identify regulatory submission requirements for each case • Validate documents prepared by Vigilance Associates or Data Managers • Close vigilance case files in compliance with timelines • Support setup and review of ICSR / MLM filters • Analyse inclusion or exclusion of EV / MHRA cases • Provide medical input to the Medical Information division • Support client-specific pharmacovigilance activities within the business unit Qualification • Doctor (MBBS or equivalent) or Pharmacist by training Experience • Minimum 3 years’ experience with service providers in pharmacovigilance • Hands-on experience in QC of safety cases • Experience with SafetyEasy database (mandatory) Skills • Strong knowledge of global pharmacovigilance regulations • Experience working with safety databases • Process-oriented and detail-focused approach • Ability to multitask and manage multiple priorities • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills in English • Strong teamwork and collaboration skills • Flexible and adaptable in a dynamic environment About the Company • ProductLife Group is a global life sciences consulting and services company , Supports pharmaceutical, biotech, and medical device companies across the product lifecycle.

Roles & Responsibilities: • Manage administrative tasks for non-linguistic Pharmacovigilance (PV) projects, including file transfers, internal process checks, and client deliverables. • Monitor project progress, communicate updates, and ensure strict adherence to deadlines. • Uphold Good Pharmacovigilance Practices (GVP) and Good Documentation Practice in all projects. • Support the Production team in day-to-day project coordination. • Complete tasks assigned by managers or supervisors. Qualification: • Minimum Bachelor’s degree. Experience: • Prior experience in project coordination or administrative support is a plus. • Exposure to pharmaceutical, healthcare, or PV-related environments is advantageous. Skills: • Superior written and spoken English communication. • Proficiency in Microsoft Office (Word, Excel, Outlook). • Quick learner with aptitude for various technology platforms. • Strong problem-solving and critical thinking skills. • Excellent attention to detail and organizational skills. • Ability to multitask in a fast-paced environment. • Can work independently or as part of a team. • Strong interpersonal skills and ability to collaborate with diverse teams. About the Organisation: TransPerfect is a global leader in language and technology solutions, providing translation, localization, and compliance support across industries such as healthcare, life sciences, and legal, with a focus on quality, innovation, and client satisfaction, offering opportunities for professional growth in a multicultural work environment.

Roles & Responsibilities: • Perform daily website review and pharmacovigilance compliance monitoring for Europe, UK, WHO, and ROW markets (India, Kazakhstan, South Africa, Ukraine, etc.). • Identify safety-related updates and share with relevant stakeholders: ICSR updates with Case Processing team, PSUR updates with PSUR team, and signal-related updates with Signal Management team. • Draft, review, and update SOPs in line with evolving global pharmacovigilance regulations. • Coordinate with QPPV and Local Responsible Persons (LRPs) for regulatory queries and training activities. • Archive emails and documents as per pharmacovigilance compliance requirements. • Collect safety data from cross-functional teams for compliance report preparation. • Prepare, review, and circulate compliance reports as per approved templates and SOPs. • Conduct and support compliance meetings with QPPV, draft Minutes of Meeting (MoM), and track action items. Qualification: • M.Pharm in Pharmacology or Pharmaceutics. Experience: • 1–2 years of hands-on experience in Pharmacovigilance compliance, website review, and global regulatory reporting. Skills: • Strong knowledge of GVP Modules and global PV regulations (EU, UK, USFDA, India, MHRA, ROW). • Hands-on understanding of PSMF, ICSR, PSUR, and RMP. • Excellent written and verbal communication skills. • Strong documentation, time management, and coordination abilities. • Ability to work effectively in cross-functional pharmacovigilance teams. About the Organization: Macleods Pharmaceutical Ltd is a leading Indian pharmaceutical company with a strong global presence and a robust R&D focus. Known for its commitment to quality, compliance, and patient safety, Macleods operates across multiple regulated markets and offers professionals an opportunity to work on global pharmacovigilance systems in a dynamic and growth-oriented environment.

Roles & Responsibilities • Support project monitoring and coordination using project management tools • Prepare study safety documents including SAE reporting forms and guidelines • Develop training materials for investigator meetings and safety trainings • Generate progress reports, listings, and study-related outputs for PVSM and clients • Assist in SAE and ICSR processing as per protocols, SOPs, and regulatory guidelines • Maintain and update internal safety databases • Follow up with investigator sites for query resolution • Prepare high-quality case narratives for safety reporting • Distribute ICSRs to Ethics Committees, Investigators, and MAHs • Prepare and circulate 6-monthly SUSAR line listings • Support preparation and submission of DSURs to Competent Authorities and Ethics Committees • Assist with MedDRA coding in coordination with Data Management and Statistics teams • Support additional pharmacovigilance activities as per departmental requirements Qualification • Degree in Pharmacy, Life Sciences, or related discipline Experience • Relevant experience in Pharmacovigilance, Clinical Research, or Safety Operations Skills • Pharmacovigilance processes and SAE / ICSR reporting • Safety database handling and case processing • MedDRA coding knowledge • ICH, EMA, and FDA regulatory guidelines • Microsoft Office and database management tools • Strong documentation, coordination, and communication skills About the Organisation Veeda Clinical Research is a leading global CRO providing comprehensive clinical research, bioanalytical, and pharmacovigilance services. The organization is known for its regulatory expertise, quality-driven processes, and strong presence in domestic and international clinical research.

Roles & Responsibilities • Ensure compliance with global pharmacovigilance regulations (EMA, EU GVP, ICH E2A/E2B, FDA, local guidelines) • Maintain and update pharmacovigilance documentation including SOPs and PV Master File (PSMF) • Assist during regulatory inspections, audits, and CAPA implementation • Support preparation, review, and submission of safety documents:  ICSRs, PSURs / PBRERs, DSURs, Risk Management Plans (RMPs) • Submit safety reports to EudraVigilance and other global safety databases • Perform literature screening and safety data evaluation • Assist in signal detection, risk minimization activities, and safety review meetings • Support preparation of SmPC, PIL, and package leaflets • Code and review adverse events using MedDRA and WHO-DD • Maintain accurate safety databases, trackers, and compliance logs • Complete mandatory PV trainings and stay updated with evolving regulations Qualification • B.PharmExperience • 0–1 year of experience in Pharmacovigilance • Freshers with PV training are eligible Skills • Basic understanding of pharmacovigilance regulations (EMA, EU GVP, ICH, FDA) • Knowledge of ICSR processing and safety reporting • Familiarity with MedDRA and WHO-DD coding • Strong attention to detail and documentation accuracy • Good written and verbal communication skills • Compliance-oriented and proactive learning mindset About the Organisation Lincoln Pharmaceuticals is a well-established Indian pharmaceutical company with a strong presence in domestic and international markets. The company is committed to quality, patient safety, and regulatory excellence, offering strong career growth opportunities in pharmacovigilance, regulatory affairs, and drug safety operations.

Roles & Responsibilities • Manage day-to-day administrative activities for non-linguistic pharmacovigilance projects • Coordinate file transfers, internal quality checks, and client deliveries • Track project progress and ensure adherence to timelines and deadlines • Support PV production teams to deliver high-quality outputs • Implement and maintain Good Pharmacovigilance Practices (GVP) • Ensure compliance with Good Documentation Practice (GDP) • Provide project support activities as assigned by the supervisor or manager Qualification • Bachelor’s degree (Life Sciences, Pharmacy, or related field preferred) Experience • Fresh graduates or candidates with relevant exposure to pharmacovigilance, literature monitoring, or PV operations • Strong interest in pharmacovigilance and drug safety domain Skills • Excellent written and spoken English communication skills • Proficiency in MS Word, Excel, and Outlook • Strong attention to detail and documentation accuracy • Ability to learn and adapt to PV systems and technology platforms • Good problem-solving and critical-thinking abilities • Strong organizational and multitasking skills • Ability to work independently and in a team-oriented environment About the Organisation TransPerfect is a global leader in language, content, and life sciences solutions, supporting pharmaceutical and biotech companies worldwide. Its Pharmacovigilance Solutions team delivers high-quality, compliant safety services, offering professionals a structured work environment, global exposure, and long-term career growth in the drug safety and pharmacovigilance domain.

Roles & Responsibilities • Maintain thorough knowledge of Pharmacovigilance and Medical Information procedures, legal requirements, and quality documents • Handle adverse event reports and PV data in line with local regulations and company standards • Provide accurate and timely safety information to Health Authorities and relevant stakeholders • Support the Country Safety Head in local safety surveillance, risk management, and safety issue handling • Manage product alerts and market research programs with appropriate regulatory communication • Respond to Medical Information inquiries from healthcare professionals, patients, and customers with high-quality, compliant responses • Collaborate effectively with internal teams and external third parties within PV and Medical Information functions • Actively contribute to North Europe Cluster PV & Medical Information projects and daily operations Qualification • University degree in Pharmacy, Medicine, or an equivalent scientific discipline Experience • Prior experience in the pharmaceutical industry or equivalent • Experience in Pharmacovigilance, Drug Safety, or Medical Information preferred Skills • Strong knowledge of pharmacovigilance regulations and medical information processes • Excellent planning, organization, and attention-to-detail skills • High accuracy and compliance-oriented work approach • Strong interpersonal and communication skills for interaction with HCPs, patients, and internal teams • Proficiency in MS Office and relevant safety/MI systems • Ability to work collaboratively in cross-functional and multicultural teams • Fluency in English and Norwegian (written and spoken) About the Organisation Sanofi is an R&D-driven, AI-powered global biopharmaceutical company dedicated to improving lives through innovative medicines and vaccines. With deep expertise in immunology and a strong pipeline across diabetes, transplant, cardiovascular, and specialty care, Sanofi delivers treatments to more than 100 million people annually, combining global scale with local impact and a strong culture of collaboration, inclusion, and scientific excellence.

Roles & Responsibilities • Analyze organizational processes, business models, and system integrations with technology • Act as Subject Matter Expert (SME) in Drug Safety and Pharmacovigilance for Veeva Vault Safety • Lead requirement-gathering workshops and define system requirements for Veeva Vault implementation • Assess current-state processes and define future-state business solutions aligned with regulatory needs • Design and configure Veeva Vault to meet FDA, EMA, and ICH regulatory requirements • Document business and system requirements including URS, FS, and user stories • Develop test scripts and support system validation and UAT activities • Serve as the primary liaison between customers, stakeholders, and delivery teams • Collaborate with Product Owners to manage backlogs, prioritize user stories, and support agile delivery • Participate in RFPs and support business development initiatives • Ensure compliance with global Drug Safety and Pharmacovigilance regulations • Provide post-implementation support and optimization for Veeva Vault Safety solutions • Lead change management activities to support client transition to Veeva Vault • Define deployment strategies and post–go-live support plans • Mentor and guide cross-functional teams to ensure successful project delivery Qualification • 15 years of full-time education (Bachelor’s degree or equivalent) Experience • Minimum 5 years of experience in Business Requirements Analysis • Hands-on experience as a Life Sciences / Pharmacovigilance Business Analyst • Experience working on Drug Safety and Pharmacovigilance systems preferred Skills • Strong expertise in Business Requirements Analysis • In-depth knowledge of Pharmacovigilance & Drug Safety Surveillance • Hands-on experience with Veeva Vault Safety • Familiarity with PV systems such as Argus, ArisGlobal • Knowledge of GxP, ICH, FDA, EMA, and global safety regulations (ICH E2E) • Understanding of medical terminology and safety dictionaries (MedDRA, WHO Drug) • Experience with Agile delivery models and backlog management • Proficiency in tools such as JIRA, Confluence, HP-ALM, Q-Test • Working knowledge of SQL, Oracle, XML, Medidata, TMF, eCRF • Strong documentation, communication, and stakeholder management skills • Leadership, mentoring, and cross-functional collaboration abilities • Strong analytical, critical thinking, and problem-solving skills About the Organisation The organization operates at the intersection of life sciences and digital transformation, delivering technology-enabled solutions for Pharmacovigilance, Drug Safety, and regulatory compliance. With a strong focus on Veeva Vault implementations and global regulatory standards, it supports pharmaceutical and life sciences clients in optimizing safety operations, ensuring compliance, and driving efficient, high-quality system delivery across global programs.

Role & Responsibilities • Report safety information from India & South Asia cluster to Global Safety • Perform follow-ups with reporters for additional safety information • Monitor and review Pharmacovigilance safety mailbox • Conduct monthly PV reconciliation and compliance checks • Prepare and submit Periodic Safety Update Reports (PSURs) as per regulations • Prepare regulatory dossiers for new products, clinical trials, variations, renewals, and query responses • Coordinate with global teams for regulatory submissions and approvals • Support regulatory authority and expert committee meetings • Prepare and maintain regulatory submissions for South Asia countries • Update and maintain product labeling and promotional material compliance • Ensure timely updates in regulatory and pricing databases (NPPA) • Update and maintain local SOPs and Safety Agreements • Support lifecycle management and inform commercial teams on key milestones Qualification • Bachelor’s degree in Pharmacy • OR Life Sciences / Microbiology / Chemistry or related disciplineExperience • Minimum 1+ year experience in Regulatory Affairs and Pharmacovigilance • Experience in Indian pharma or biotech industry preferredSkills • Strong knowledge of Indian regulatory and PV requirements • Familiarity with PSURs, safety reporting, and compliance processes • Good coordination and communication skills • Attention to detail and documentation accuracy • Ability to work cross-functionally with global teamsAbout Company • Ferring India M&S is part of the global Ferring Pharmaceuticals group,     Focused on research-driven, specialty biopharmaceutical products

Role & Responsibilities • Draft and revise Pharmacovigilance Agreements (PVAs) ensuring alignment with company requirements • Review PVAs for quality and consistency with global and local regulatory standards • Address comments from company and collaborating partners on PVAs • Manage dedicated PVA mailbox and respond to queries • Announce new or revised PVAs to all relevant client stakeholders • Maintain PVA tracker for all active global PVAs, including reconciliations and updates • Perform compliance monitoring of PVAs and prepare dashboards for management review • Assist Project Manager in managing project-related documents and trackers • Upload and maintain PVAs and associated documentation in company repository • Attend team meetings to provide status updates and report any issues with PVAs Qualification • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field • Strong knowledge of global pharmacovigilance regulations (ICH, GVP)Experience • Minimum 2–3 years of experience in pharmacovigilance • Hands-on experience with global and local PVAs and contractual pharmacovigilanceSkills • Expertise in drafting, reviewing, and maintaining PVAs • Knowledge of global pharmacovigilance standards and compliance monitoring • Excellent written and verbal communication skills • Strong organizational and document management skills • Attention to detail and ability to manage multiple tasks concurrentlyAbout Company • Tata Consultancy Services (TCS) is a leading global IT and consulting services organization , Provides solutions across Life Sciences, Healthcare, and technology domains

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.

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.

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 • 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 • 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.

Roles & Responsibilities•Draft new and revised Pharmacovigilance Agreements (PVAs) as per company and regulatory requirements •Review PVAs to ensure quality, accuracy, and global pharmacovigilance compliance •Address internal and collaborating company comments on PVAs •Manage and monitor the dedicated PVA mailbox •Announce new and revised PVAs to relevant stakeholders •Maintain and update global PVA trackers and reconciliations •Perform compliance monitoring of effective PVAs and prepare dashboards •Support Project Managers in maintaining project documents and trackers •Upload, archive, and maintain PVAs in the company repository •Participate in team meetings and provide regular status updatesQualifications•B.Pharm, M.Pharm, B.Sc, M.ScExperience •Minimum 3-7 years of hands-on experience in Pharmacovigilance•Prior experience in drafting and managing Global and Local Pharmacovigilance AgreementsSkills •Strong knowledge of ICH & GVP regulations•PVA drafting and management •Life sciences domain expertise•Documentation skills•Stakeholder coordination•Good communication skillsAbout the CompnayTata Consultancy Services (TCS) is a global leader in IT services, consulting, and business solutions, headquartered in India and part of the Tata Group. With operations in over 50 countries, TCS serves clients across industries including life sciences, healthcare, pharmaceuticals, banking, and manufacturing. The company is known for its strong focus on innovation, digital transformation, regulatory-compliant solutions, and employee development, delivering high-quality services that help organizations improve efficiency, compliance, and business performance worldwide.