Manager - Computer System Validation (CSV)

JOB DESCRIPTION Job Title: Manager – CSV Job Location: Translational Health Science and Technology Institute (TSHTI) - Faridabad, Haryana Department: Human Pharmacology Unit - Translational & Clinical Research About Syngene: Syngene ( ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Role Accountabilities: Computer System Validation Support validation activities for GxP computerized systems and applications. Prepare, review, and maintain CSV lifecycle documentation including: Validation Plans (VP) User Requirement Specifications (URS) Functional Specifications (FS) Risk Assessments Traceability Matrix (TM) Installation Qualification (IQ) Operational Qualification (OQ) Performance Qualification (PQ) Validation Summary Reports (VSR) Execute and document validation testing activities. Regulatory Compliance & Quality Ensure compliance with: US FDA 21 CFR Part 11 EU Annex 11 GAMP 5 Guidelines Data Integrity requirements GxP regulations (GCP, GLP, GMP) Support Electronic Records and Electronic Signatures (ERES) assessments and remediation activities. Participate in Data Integrity assessments and compliance initiatives. Assist in maintaining systems in a validated state through change management activities. Quality Management System (QMS) Support investigation, documentation, and closure of: Deviations CAPAs Change Controls Audit Observations Participate in periodic review activities for computerized systems. Ensure validation deliverables comply with internal procedures and quality standards. Audit & Inspection Support Support internal, customer, and regulatory audits. Assist in preparation and presentation of CSV documentation during audits and inspections. Support remediation activities related to audit findings. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: 6 to 13 Years Education: Master’s in Science (.) Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.