Pharmacy Jobs

Roles & Responsibilities: • Support acquisition, validation, and standardization of structured and unstructured data. • Assist in maintaining data quality, integrity, and compliance with governance standards. • Apply company policies and procedures to routine data management activities. • Support analytics platforms, reporting systems, and data lifecycle processes. • Work on standard assignments involving basic analysis and problem-solving. • Refer to established policies, procedures, and best practices for guidance. • Escalate complex or unusual data issues to supervisors or senior team members. • Contribute to regulatory and business data compliance initiatives. Qualification: • Bachelor’s degree in Data, Analytics, IT, Life Sciences, Pharmacy, or a related field (or equivalent practical experience). Experience: • 0–1 year of experience; freshers are encouraged to apply. Skills: • Basic understanding of data management concepts and data governance frameworks. • Ability to follow standard operating procedures and guidelines. • Good communication and collaboration skills. • Attention to detail and willingness to learn enterprise data processes. • Basic analytical and problem-solving abilities. About the Organization: Cardinal Health is a global healthcare services and data-driven solutions company that supports hospitals, pharmacies, manufacturers, and healthcare providers worldwide. With a strong focus on trusted data, analytics, and regulatory compliance, Cardinal Health enables better healthcare outcomes while offering inclusive, growth-oriented career opportunities for early-career professionals and diverse talent.

Roles & Responsibilities: • Design and configure clinical databases using EDC systems such as Oracle Clinical and Medidata Rave. • Develop Case Report Forms (CRFs) aligned with formulation-specific clinical endpoints. • Perform data cleaning and query management, resolving discrepancies with clinical sites. • Conduct User Acceptance Testing (UAT) to validate database logic and edit checks. • Ensure data accuracy, consistency, integrity, and traceability throughout the clinical study lifecycle. • Support database lock activities and clinical data transfer to biostatistics teams. • Provide submission-ready clinical data to support global regulatory filings and formulation performance evaluation. • Collaborate with clinical, formulation R&D, and regulatory teams to ensure compliant data management practices. Qualification: • M.Pharm (Clinical) – Mandatory. Experience: • 2–5 years of experience in Clinical Data Management or Clinical R&D. Skills: • Hands-on experience with EDC systems (Oracle Clinical, Medidata Rave, or equivalent). • Strong understanding of GCP guidelines and clinical trial workflows. • Working knowledge of CDISC standards (SDTM/ADaM) preferred. • Excellent communication and cross-functional coordination skills. • Strong attention to detail and data quality mindset. About the Organization: Bachwell Pharma is a growing pharmaceutical company with a strong focus on formulation R&D for global regulatory markets. The organization supports development of tablets, injectables, and topical formulations, offering professionals the opportunity to work at the intersection of clinical research, data management, and regulatory submissions in a dynamic R&D environment.

Roles & Responsibilities: • Coordinate and support site-level clinical trial operations. • Act as a liaison between investigators, sponsors, CROs, and internal teams. • Track study timelines, milestones, and deliverables to ensure on-time execution. • Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements. • Support study start-up, ongoing trial management, and close-out activities. • Maintain accurate and complete clinical trial documentation and reports. • Assist in monitoring site performance and resolving operational challenges. • Support audits, inspections, and quality improvement initiatives. Qualification: • Bachelor’s or Master’s degree in Life Sciences, Medical Sciences, Pharmacy, or related field. Experience: • 3–4 years of experience as a Project Coordinator or Project Manager in Clinical Research. Skills: • Strong understanding of clinical operations and site management. • Excellent communication, coordination, and leadership skills. • High attention to detail and strong organizational abilities. • Ability to manage multiple activities and stakeholders effectively. • Commitment to research quality, compliance, and ethical standards. About the Organization: The organization is a growing clinical research organization focused on delivering high-quality clinical trial execution through strong site-level operations and regulatory compliance. It offers professionals an opportunity to work in a dynamic environment, collaborate with cross-functional stakeholders, and contribute to impactful clinical research projects.

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: • Lead and execute CMC regulatory strategies for post‑approval pharmaceutical products globally. • Prepare, review, and coordinate CMC documentation for post‑approval changes and lifecycle activities. • Assess scientific and technical data to evaluate regulatory impact and ensure risk-based, data-supported rationales. • Manage multiple CMC projects, ensuring timely, high-quality dossier submissions. • Collaborate with cross-functional teams (QA, QC, manufacturing, supply chain, packaging, device, analytics) and provide regulatory updates. • Translate complex technical concepts into clear regulatory justifications and influence cross-functional decisions. • Identify regulatory risks and opportunities and implement compliant solutions. • Participate in continuous improvement initiatives and maintain SOPs and internal guidelines. • Mentor junior colleagues and represent CMC regulatory function in project meetings. • Utilize MS Office and regulatory IT systems for efficient documentation management. Qualifications: • Bachelor’s or Master’s degree in Pharmacy, Science, or related field (advanced degree preferred). Experience: • 5-10 years of global Regulatory CMC experience. Skills: • Strong communication, regulatory strategy, and CMC documentation skills. • Cross-functional collaboration and stakeholder management. • Knowledge of pharmaceutical manufacturing, analytical testing, and quality systems. • Advanced MS Office and regulatory IT proficiency. • Leadership, mentoring, and project management abilities. About the Organization: Genpact is a global technology and professional services company that leverages deep industry expertise, advanced data, and AI-driven solutions to help enterprises transform and stay ahead. With a culture built on integrity, inclusion, and innovation, Genpact empowers over 140,000 professionals worldwide to solve complex business challenges, drive change, and deliver lasting value for clients across industries.

Roles & Responsibilities • Lead regulatory affairs for assigned franchise(s) from clinical development through lifecycle management • Develop and implement regulatory strategies, including risk mitigation and accelerated approval pathways • Drive SEC preparedness and support India’s inclusion in global clinical trials • Ensure 100% regulatory compliance, including post-approval commitments, labeling, site transfers, and biologics • Act as GRP Lead and ensure adherence to Good Regulatory Practices and quality management systems • Lead internal and external audits, ensuring deviations and CAPAs are addressed effectively • Collaborate cross-functionally with business, medical, QA, supply, and global regulatory teams • Support regulatory policy shaping, health authority advocacy, and industry association initiatives • Provide regulatory support to business development projects and oversee regulatory intelligence • Manage and develop regulatory team members (direct and indirect reports) Qualifications • Bachelor’s degree in Pharmacy (mandatory) • Post-graduate qualification in Pharmacy (preferred) Experience • Proven experience in regulatory affairs, drug development, and clinical trials • Prior people management and team leadership experience • Experience with innovative treatment modalities (desirable) Skills • Strong knowledge of Indian regulatory requirements • Strategic regulatory planning and risk management • Effective stakeholder management and cross-functional collaboration • Strong communication, leadership, and decision-making skills About the Organisation AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of innovative medicines. With a strong commitment to patient safety, scientific excellence, and ethical practices, AstraZeneca fosters an inclusive culture that encourages continuous learning, collaboration, and growth while advancing the future of healthcare worldwide.

Roles & Responsibilities • Perform medical and scientific data review for hematology clinical trials (e.g., myeloma, lymphoma) • Review standard data listings including adverse events, concomitant medications, efficacy and safety data • Conduct patient profile reviews, safety narratives, PD analysis, and scientific data evaluations • Support Lead Clinical Scientist and Medical Director in medical data review activities • Develop and contribute to Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans • Author medical data queries, review responses, and support query closure • Participate in medical and safety review meetings, including slide preparation • Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams • Identify data trends, risks, and subject safety issues; escalate concerns appropriately • Ensure compliance with ICH-GCP, data privacy standards, SOPs, and regulatory requirements • Support audits and trusted process meetings as required Qualification • Degree in Life Sciences: MSc, PharmD, PhD, MD, DMD or equivalent Experience • Relevant scientific or clinical research experience in clinical development • Exposure to medical data review, clinical trials, or drug development preferred Skills • Strong understanding of clinical trial data, scientific principles, and ICH-GCP guidelines • Excellent analytical, documentation, and problem-solving skills • Strong written and verbal communication abilities • Proficiency in MS Office (Word, Excel, PowerPoint) • Ability to manage multiple tasks in a regulated, fast-paced environment • Strong collaboration and stakeholder management skills About the Organisation Syneos Health® is a leading global biopharmaceutical solutions organization, supporting clinical development, medical affairs, and commercialization. With operations across 110+ countries and involvement in the majority of novel FDA and EMA approvals, Syneos Health partners with customers to accelerate the delivery of therapies that improve and save lives worldwide.

Roles & Responsibilities • Monitor adherence to prescribed dose status across global clinical trial sites • Identify dose discrepancies and drive timely, traceable follow-ups with sites • Document dose-related risks and maintain inspection-ready records • Conduct routine and ad-hoc dose surveillance reviews as per protocol • Collaborate with Trial Managers, Clinical Medical Managers, and Medical Advisors • Support site engagement through clear communication and data insights • Coach site staff on dose compliance, documentation quality, and protocol adherence • Communicate findings to trial teams and contribute to continuous improvement initiatives Qualification • Graduate degree in Life Sciences: M.Pharm, PharmD, Pharmacy, BDS/MDS, or MSc Nursing Experience • Minimum 2 years’ experience in clinical trials (Pharma/Biotech/CRO/Hospital) • Exposure to global clinical operations and trial systems Skills • Strong understanding of ICH-GCP and clinical trial conduct • Analytical mindset with ability to interpret clinical data • Excellent communication and stakeholder management skills • Ability to work independently in dynamic environments • Coaching and influencing skills with strong attention to detail About the Organisation Novo Nordisk is a global healthcare company with a strong legacy in clinical research and innovation. Through its Global Business Services in Bangalore, the company supports worldwide clinical development with advanced risk-based monitoring, data quality, and patient safety initiatives, contributing to high-quality and compliant clinical trials across the globe.

Roles & Responsibilities • Perform publishing and technical validation of regulatory submissions (eCTD/CTD/NEES/Paper) for the US market • Conduct final technical quality review of submission dossiers • Dispatch submissions to health authorities or affiliates as per regulatory timelines • Handle post-submission activities including acknowledgements, receipts, and metadata capture in RIM systems • Upload and manage health authority correspondence, commitments, and related documentation • Ensure compliance with ICH and FDA guidelines in a regulated, process-driven environment • Coordinate with internal stakeholders and ensure timely communication of submission status Qualification • Bachelor’s degree in Pharmacy, Medicine, Chemistry, or related Life Sciences discipline Experience • Relevant experience in Regulatory Affairs Operations / Regulatory Publishing within the pharmaceutical industry Skills • Strong knowledge of ICH and FDA guidelines (US market) • Hands-on experience with eCTD, CTD, NEES, and paper submissions • Expertise in publishing tools such as Liquent, DocuBridge, or similar systems • Advanced English communication skills • Good understanding of RIM systems and regulatory workflows • Time management, organizational, and multitasking skills • Attention to detail and quality-focused mindset • Flexibility to adapt in a fast-changing environment About the Organisation Genpact is a global advanced technology services and solutions company that helps leading enterprises drive digital transformation through data, technology, and AI. Known for its strong regulatory, life sciences, and operations expertise, Genpact supports global pharma companies with end-to-end regulatory and compliance solutions while fostering innovation and continuous growth.

Roles & Responsibilities • Support clinical data management activities across clinical trials • Assist in data collection, validation, cleaning, and processing as per protocols and SOPs • Ensure accuracy, consistency, and completeness of clinical trial data • Work with standard guidelines to resolve routine data-related issues • Maintain and update clinical databases using approved systems and tools • Collaborate with team members and report to direct supervisors on assigned tasks • Follow detailed instructions for daily activities and new assignments • Contribute as an individual team member within a defined scope of work • Support regulatory compliance and quality standards in clinical data services • Work in rotational shifts as per business requirements Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of relevant experience in clinical data management or related roles Skills • Clinical Data Management concepts • Data collection, validation, and processing • Understanding of clinical research and trials • Attention to detail and data accuracy • MS Office and clinical data systems • Basic understanding of regulatory guidelines • Good communication skills (English – Intermediate) • Ability to work in a team-based environment About the Organisation Accenture is a global professional services company with strong capabilities in digital, cloud, and security. With a presence in over 120 countries, Accenture supports leading life sciences organizations across R&D, clinical trials, regulatory services, and pharmacovigilance, helping them deliver better patient outcomes through data-driven solutions.

Roles & Responsibilities • Secure regulatory approvals for new products (NDA, LCM) within defined timelines • Manage product lifecycle activities including submissions, variations, and renewals • Prepare and review regulatory submission dossiers and application forms as per country-specific Health Authority requirements • Coordinate with distributors, affiliates, and health authorities to ensure regulatory compliance • Handle regulatory documentation for tenders and special submissions • Update and maintain regulatory information in Veeva Vault within agreed timelines • Support labeling development, review promotional materials, and ensure compliance with local regulations • Monitor regulatory environment changes and support post-approval regulatory activities Qualification • Post-Graduation or equivalent degree in Science Experience • Minimum 5+ years of experience in Regulatory Affairs within the pharmaceutical industry • At least 3 years of experience working in cross-functional, international or affiliate environments • Experience handling interactions with Health Authorities preferred Skills • Regulatory submissions and lifecycle management • Health Authority interactions • Regulatory documentation and compliance • Veeva Vault (Regulatory systems) • Project management and prioritization • Cross-functional collaboration and stakeholder management About the Organisation Novo Nordisk is a global healthcare company with over a century of experience in developing innovative treatments for chronic diseases. Driven by a strong patient-centric mission, the organization focuses on delivering high-quality, compliant, and sustainable healthcare solutions across international markets.

Roles & Responsibilities • Assist in dispensing medicines as per prescriptions under pharmacist supervision • Support pharmacists in daily pharmacy operations • Handle medicine storage, labeling, and inventory management • Ensure compliance with pharmacy regulations and safety standards • Provide basic medication-related information to customers • Maintain cleanliness and organization of the pharmacy area • Support documentation and record-keeping activities Qualification • Diploma in Pharmacy (D.Pharm) • Bachelor of Pharmacy (B.Pharm) • Doctor of Pharmacy (Pharm.D) Experience • Freshers or experienced candidates may apply (experience preferred) Skills • Basic knowledge of medicines and dosage forms • Good communication and customer-handling skills • Attention to detail and accuracy • Ability to work under supervision • Basic computer and billing knowledge About the Organisation The hiring pharmacy operates in the UAE and provides quality pharmaceutical services focused on patient safety, accuracy, and professional care. 📧 Interested candidates can send details to: asstpharmacyjobsuae@gmail.com

Roles & Responsibilities • Manage and process clinical trial data including collection, validation, and review • Perform routine clinical data management tasks as per SOPs and standard guidelines • Ensure accuracy, consistency, and integrity of clinical trial data • Resolve data queries under supervision and follow predefined processes • Support data storage, integration, and analysis activities • Collaborate with internal team members and report to the direct supervisor • Follow regulatory, quality, and compliance requirements • Work as an individual contributor within a defined scope • Be flexible to work in rotational shifts when required Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of experience in Clinical Data Management or Clinical Data Services Skills • Clinical Data Management fundamentals • Clinical trial data collection and validation • Understanding of CDM processes and workflows • Attention to detail and data accuracy • Basic knowledge of regulatory requirements • Proficiency in MS Office and clinical databases • Good communication skills About the Organisation Accenture is a leading global professional services company with capabilities across digital, cloud, data, AI, and security. With operations in over 120 countries, Accenture supports life sciences organizations through end-to-end solutions spanning clinical research, pharmacovigilance, regulatory services, and patient-centric innovations.

Roles & Responsibilities • Manage and process clinical trial data including collection, validation, and review • Perform routine clinical data management activities as per SOPs and guidelines • Ensure data accuracy, consistency, and integrity across clinical databases • Resolve data queries and support issue resolution under supervision • Work with clinical data systems and specialized CDM tools • Collaborate with team members and report progress to the direct supervisor • Follow regulatory, quality, and compliance requirements • Operate as an individual contributor within a defined scope of work • Be flexible to work in rotational shifts if required Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of experience in Clinical Data Management or Clinical Data Services Skills • Clinical Data Management fundamentals • Data collection, validation, and quality checks • Understanding of clinical trial processes • Familiarity with clinical data systems and databases • Attention to detail and analytical thinking • Basic knowledge of regulatory compliance • Good communication skills About the Organisation Accenture is a global professional services company with strong capabilities in digital, cloud, data, AI, and security. Serving clients in over 120 countries, Accenture supports organizations across industries through Strategy & Consulting, Technology, Operations, Industry X, and Song. Its Life Sciences R&D practice enables leading biopharma companies to improve patient outcomes by delivering high-quality clinical, pharmacovigilance, and regulatory solutions.

Roles & Responsibilities • Manage and process clinical trial data including data collection, validation, and reconciliation • Ensure accuracy, consistency, and integrity of clinical data as per defined guidelines • Perform routine data management tasks by following standard operating procedures • Support data review, query management, and issue resolution activities • Work with clinical data systems and tools used in clinical research • Collaborate with team members and report progress to the direct supervisor • Adhere to regulatory, quality, and compliance requirements • Operate as an individual contributor within a defined scope of work • Be flexible to work in rotational shifts as required Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of experience in Clinical Data Management or Clinical Data Services Skills • Clinical Data Management fundamentals • Data validation and data quality checks • Understanding of clinical trial processes • Attention to detail and analytical skills • Familiarity with clinical data systems and tools • Basic understanding of regulatory compliance • Good communication skills Language Requirement • English (Intermediate – Domestic) About the Organisation Accenture is a global professional services company with expertise across digital, cloud, security, technology, and operations. Serving clients in over 120 countries, Accenture’s Life Sciences R&D practice supports clinical trials, pharmacovigilance, regulatory services, and patient solutions—helping leading biopharma companies improve patient outcomes through data-driven innovation.

Roles & Responsibilities • Perform wet chemistry sample extraction as per study protocols and SOPs • Handle centrifugation, evaporation, freezing, storage, and aliquoting of biological samples • Prepare reagents, solvents, mobile phases, calibration standards, and QC samples • Support method development and validation of drugs and metabolites using LC/MS/MS • Execute validation parameters including accuracy, precision, recovery, matrix effect, and stability studies • Carry out routine bioanalysis for bioequivalence and subject sample analysis • Operate and maintain LC/MS/MS, HPLC, and ICP-OES instruments • Perform system suitability checks, troubleshooting, and basic instrument maintenance • Complete analytical worksheets, QC sheets, raw data records, and logbooks accurately • Ensure compliance with GLP, SOPs, and regulated bioanalytical guidelines • Support audits, inspections, and mandatory training activities Qualification • M.Pharm / M.Sc / MS (Science) – Any Specialization Experience • Hands-on exposure to LC/MS/MS bioanalysis preferred • Experience with biological matrices such as plasma, serum, and urine is an advantage • Regulated bioanalytical lab exposure is desirable (not mandatory) Skills • LC/MS/MS operation and troubleshooting • Wet chemistry and bioanalytical workflows • Bioanalytical method development and validation • GLP compliance and documentation practices • Data integrity and basic MS Office skills About the Organisation Cliantha Research is a leading global Contract Research Organization (CRO) providing integrated clinical research, bioanalytical, and regulatory services. The organization is known for its strong compliance culture, advanced analytical capabilities, and commitment to quality-driven clinical research.

Roles & Responsibilities • Plan and conduct clinical trial audits in compliance with ICH-GCP, regulatory guidelines, and internal SOPs • Review and maintain Quality Management Systems (QMS) documentation and processes • Lead CSV validation and qualification activities related to clinical systems • Ensure audit and inspection readiness for sponsor, regulatory, and internal audits • Manage sponsor interactions and audit responses effectively • Identify compliance gaps and drive CAPA implementation • Lead and mentor QA audit teams to meet project timelines • Monitor audit timelines and ensure timely closure of audit findings • Support continuous quality improvement initiatives across clinical operations Qualification • M.Sc / B.Pharm / M.Pharm / Other relevant life science qualifications Experience • 10 – 15 years of experience in Clinical QA, auditing, and compliance Skills • Regulatory guidelines and compliance requirements • Clinical QMS and auditing practices • CSV validation and qualification • Audit and inspection readiness • Team leadership and timeline management • Sponsor handling and communication About the Organisation Cliantha Research is a globally recognized clinical research organization providing integrated clinical, bioanalytical, and regulatory services. The company is known for its strong quality culture, regulatory expertise, and commitment to delivering compliant and reliable clinical research solutions.

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 • Handle OOS, OOT, deviations, CAPA, and laboratory investigations • Review analytical data generated from HPLC, GC, UV, and IR instruments • Ensure compliance with Quality Management Systems (QMS) and SOPs • Perform documentation review and maintain data integrity in lab operations • Use Chromeleon Software 7.2 for chromatography data handling and review • Support internal, regulatory, and customer audits (FDA, USFDA, MHRA) • Ensure timely closure of lab incidents and implementation of corrective actions • Contribute to continuous improvement in laboratory quality systems Qualification • B.Pharm / M.Pharm / M.Sc (Chemistry or Analytical preferred) Experience • Relevant experience in Pharmaceutical Lab QA / QC environment Skills • OOS, OOT, CAPA, deviations handling • QMS and SOP compliance • HPLC, GC, UV, IR instrumentation • Chromeleon Software 7.2 • Regulatory audit exposure (FDA, USFDA, MHRA) • Documentation and data integrity About the Organisation IPCA Laboratories is one of India’s leading pharmaceutical companies with a strong global presence. The company is known for its commitment to quality, regulatory compliance, and excellence in manufacturing, offering professionals a stable and growth-oriented work environment.