Senior Computer System Validation (CSV) (Bangalore, Karnataka, IN)

Biopharma Careers; Bengaluru; On-site; INR 3,000,000 - 4,200,000; Full time

Job summary

Bayer in Bengaluru is seeking a Senior Computer System Validation (CSV) Engineer to lead validation activities for local R&D software tools in a regulated medical device software environment. Ensure compliance with 21 CFR Part 11, data integrity, and internal quality standards across the system lifecycle.

The role collaborates with global teams to support audit readiness, lifecycle management, and effective documentation. A proactive leader will drive outcomes in a fast-paced environment.

Qualifications

• Bachelor-level or higher in CS/IT/Electronics/Biomedical Engineering or related field.
• 5+ years’ experience validating computer systems in a regulated environment.
• Strong CSV knowledge and risk-based validation methodologies.
• Experience with GxP regulated systems in pharma/med device.
• Ability to author and maintain validation documentation.

Responsibilities

• Lead CSV activities for regulated R&D software tools (JIRA, Confluence, Jama, etc.).
• Develop and maintain validation deliverables and risk assessments.
• Execute IQ/OQ/PQ and UAT testing for GxP systems.
• Draft and update SOPs to comply with GxP and internal standards.
• Coordinate with global teams for audits and lifecycle management.

Skills

CSV experience

GxP

Data integrity

Cross-functional collab

Documentation

Education

Engineering degree

Tools

JIRA/Confluence

IBM ELM

Jama

GitHub

JFrog Artifactory

Job description

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Senior Computer System Validation (CSV)

POSITION PURPOSE:

We are seeking a Senior Computer System Validation (CSV) Engineer to lead and manage validation activities for local R&D business software applications used in a regulated medical device software development environment. This role is responsible for ensuring GxP and non- GxP systems comply with regulatory requirements, data integrity and security principles, and internal quality standards across the full system lifecycle.

This role works closely with global, cross functional teams to support compliant implementations, documentation, effective lifecycle management, and audit readiness. The ideal candidate will be a proactive leader who can drive outcomes and align with Bayer's mission and values.

YOUR TASKS AND RESPONSIBILITIES:

• Lead and perform computer system validation activities for regulated R&D software tools, including Atlassian suite (JIRA, Confluence, Crowd), IBM ELM Suite (RQM, DNG), Jama, GitHub, and JFrog Artifactory.
• Develop, execute, and maintain validation deliverables such as user requirement specs, validation plans, test protocols, test scripts, test reports, risk assessments, and change documentation.
• Execute formal validation testing activities (UAT, IQ, OQ, PQ) for GxP relevant systems.
• Draft, review, and update SOPs and procedural documentation in compliance with GxP requirements and internal quality processes.
• Apply risk based validation approaches to ensure efficient, compliant validation activities.
• Support system lifecycle management, change control, and impact assessments for validated systems.
• Ensure compliance with 21 CFR Part 11, GxP regulation, and data integrity expectations.
• Support and coordinate user access management and administrative activities for validated tools.
• Manage tool related service (new requests, project efforts, and break-fix) and administration requests via ServiceNow.
• Collaborate closely with Software Quality Management, IT, Engineering, and other stakeholders to ensure audit readiness.
• Support internal and external audits, access reviews, and inspections by providing validation evidence and subject matter expertise.
• Participate in deviation management, CAPA activities, and continuous improvement initiatives related to validated systems.

WHO YOU ARE:

Required

• Bachelor of Engineering (BE), Bachelor of Technology (BTech), Bachelor of Science (BSc), or equivalent degree in Computer Science, Information Technology, Electronics, Biomedical Engineering, or a related technical discipline.
• Greater than 5 years’ experience with computer software validation in a regulated environment.
• Strong understanding and prior experience with Computer System Validation (CSV) and CSA risk based validation methodologies.
• Strong experience working with GxP regulated systems in pharmaceutical, medical device, or similarly regulated industries.
• Working knowledge of data integrity principles.
• Hands on experience authoring and maintaining validation documentation, including:
  • User Requirements Specifications, Configuration Specifications, Test Scripts
  • UAT, IQ, OQ, PQ
  • Test protocols and reports
  • Change records and risk documentation
• Knowledge of application change control, deviation handling, and CAPA processes.
• Ability to collaborate and communication effectively with global, cross functional teams.
• Accountable, willing to go the extra mile style of working.

Preferred

• Familiarity with tools such as IBM's Engineering Lifecycle Management, Atlassian's suite (JIRA, Confluence), GitHub, and JFrog Software Supply Chain, at an administrator level.
• Prior experience with internal or external audits and inspections.
• Prior experience supporting regulated R&D software environments.
• Previous Scrum Master experience utilizing Jira is a plus

Ever feel burnt out by bureaucracy? Us too. That's why we're changing the way we work- for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here https://www.bayer.com/enfstrategyfstrategy

Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext.

Please don’t rely upon any unsolicited email from email addresses not ending with domain name bayer.com or job advertisements referring you to an email address that does not end with bayer.com. For checking the authenticity of such emails or advertisement you may approach us at [e-mail].

Bayer is an equal opportunity employer that strongly values fairness and respect at work.

We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc.

We are committed to treating all applicants fairly and avoiding discrimination.

Location: India : Karnataka : Bangalore

Division: Pharmaceuticals

Reference Code: 884301

Contact Us

+ 022-25311234