Manager - Computer System Validation (CSV)

Syngene International Limited; Faridabad District; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Syngene International Limited invites applications for Manager – CSV in Faridabad, Haryana. You will support validation activities for GxP computerized systems and help maintain CSV lifecycle documentation.

The role requires 8–13 years of experience in CSV/regulatory environments and a Master’s in Science. You will ensure compliance with US FDA/EU GxP standards and contribute to quality management and audits.

Qualifications

• 8–13 years of experience in CSV, QA, or regulatory environments.
• Master’s in Science (M.Sc.) required.
• Experience with FDA/EU regulatory standards and compliance.

Responsibilities

• Support CSV validation activities for GxP computerized systems.
• Prepare and maintain URS, FS, TM, OQ, PQ, and VSR documentation.
• Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.
• Assist in audits and inspections and remediation actions.
• Support CAPAs, deviations, change controls, and audit observations.

Skills

CSV

Regulatory Compliance

GxP

Quality Management

Audit Support

Education

Master’s in Science (M.Sc.)

Job description

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Date: 28 Aug 2026

Location: Bangalore, KA, IN, 560100

Division: Discovery Services

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 ( www.syngeneintl.com ) 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:
• User Requirement Specifications (URS)
• Functional Specifications (FS)
• Traceability Matrix (TM)
• 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.

All employees will consistently demonstrate alignment with our core values

• Integrity
• Professionalism

Experience: 8 to 13 Years

Education: Master’s in Science (M.Sc.)

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.