Medical Device Quality Engineer Intern

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Skills you'll use

What you'll do

• Work on running quality processes and verification for regulated devices alongside the core team
• Apply ISO 13485 Compliance, CAPA Management, Risk Assessment (ISO 14971), Verification & Validation (V&V) Testing to live, production-facing problems
• Document your work clearly for reviewers and stakeholders
• Participate in reviews and act on the feedback you receive
• Collaborate across engineering, product, design or business as required
• Follow the team's quality, testing and documentation standards

Who can apply

• Pursuing or recently completed B.E./B.Tech (Biomedical / Mechanical / Electronics), M.Tech or B.Sc/M.Sc (Life Sciences) — 2026 freshers & final-year students welcome
• Working knowledge of ISO 13485 Compliance, CAPA Management, Risk Assessment (ISO 14971) (or a genuine willingness to learn them)
• Strong fundamentals in your discipline and clear problem-solving ability
• Care with detail and the discipline to document your work
• Clear written and verbal communication in English
• Based in or willing to work from Nagpur, Maharashtra

Perks & benefits

Interview & selection process

3 rounds — typical selection flow for this role:

1. 1Application screening & resume shortlisting by the talent team
2. 2Team-fit / behavioural interview with the team
3. 3HR discussion — stipend, start date, expectations and offer

About Cipla

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