Duties & Responsibilities

- Lead, develop, and execute comprehensive Computer System Validation (CSV) strategies, plans, and protocols (IQ/OQ/PQ) in compliance with FDA and global regulatory requirements.

- Oversee validation activities for GxP-regulated computerized systems including ERP, QMS, MES , manufacturing equipment software, data integrity systems, and custom applications.

- Ensure systems meet 21 CFR Part 820, 21 CFR Part 11, and ISO 13485 requirements for software validation and electronic records/electronic signatures.

- Partner with cross-functional teams (Quality, IT, Engineering, R&D;, Manufacturing) to ensure compliant system lifecycle management aligned with GAMP 5 guidelines.

- Drive validation documentation creation, review, and approval, ensuring traceability and regulatory readiness.

- Ensure systems used in support of GxP activities are validated and maintained appropriately in compliance with applicable FDA, EU and other international regulations

- Serve as the SME during internal audits, supplier audits, and FDA/Notified Body inspections regarding CSV and data integrity.

- Assess system changes, conduct impact analyses, and ensure controlled execution of validation activities in accordance with established change control procedures.

- Maintain strong understanding of data integrity controls aligned with ALCOA + principles and applicable global guidance documents.

- Develop and improve CSV processes, templates, and procedures to enhance compliance, consistency, and operational efficiency.

- Participate in change control processes to assess impact upgrades and changes on validated systems; Oversee execution of change actions.





- Coordinate and execute periodic reviews of validated systems per defined schedule; support development of remediation plan, if needed.

Minimum & Preferred Qualifications and Experience:

Minimum Qualifications:

- 5+ years of experience in Computer System Validation within a regulated medical device, pharmaceutical, or biotechnology workplace preferred.

- Advanced knowledge of and hands-on experience with: 21 CFR Part 11, Part 820, ISO 13485, ISO 14971, GAMP5 guidelines, FDA guidance on risk-based software validation and computer software assurance.

- Proven leadership in planning, executing, and documenting validation of enterprise and manufacturing systems.

- Strong understanding of data integrity requirements, audit trails, and system security principles.

- Experience developing validation documentation including URS, design specifications, traceability matrix, validation plans, IQ/OQ/PQ, summary reports, and controlled procedures .

- Excellent analytical, technical writing, and communication skills.

Preferred Qualifications:

- Familiarity with: EU MDR, Annex 11 (EU guidelines on computerized systems) and ISO 27001 (Information Security Management).

- Hands-on experience with validation of cloud-based or SaaS systems .

- Prior experience supporting FDA and Notified Body inspections as a CSV subject matter expert.

- Experience developing or enhancing CSV/QMS processes.

Education

- Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or related technical field required.

Language Requirements:

- Advanced English proficiency (written and verbal) required to collaborate effectively with global stakeholders, prepare technical documentation, and participate in regulatory audits and inspections.

Location

- This position is located at our Bengaluru, India office.

📌 Engineer, Computer Software Assurance (India)
🏢 Masimo
📍 India