In_senior Associate_csv,qms_rc - Internal Audit_advisory_noida

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Noida, India
Computer system validation (csv)
Instrument qualification iq oq pq
Regulated industry experience 1-3 years
The role involves assisting in the planning, execution, and documentation of Computer System Validation activities within pharmaceutical or biotech industries

Job Summary

  • The role involves assisting in the planning, execution, and documentation of Computer System Validation activities within pharmaceutical or biotech industries.
  • Candidates will support instrument qualification for laboratory equipment ensuring compliance with regulatory requirements such as FDA 21 CFR Part 11.
  • PwC offers a vibrant community focused on trust, innovation, and inclusive benefits including mentorship and flexibility programmes.

Matching Summary

The role involves assisting in the planning, execution, and documentation of Computer System Validation activities within pharmaceutical or biotech industries.

Skills & Requirements

Must-have

  • Computer System Validation (CSV)
  • Instrument Qualification IQ OQ PQ
  • Regulated industry experience 1-3 years
  • GxP compliance FDA 21 CFR Part 11
  • Validation lifecycle documentation

Nice-to-have

  • LIMS and MES familiarity
  • Strong attention to detail
  • Cross-functional collaboration skills
  • Ability to manage multiple tasks
  • Willingness to learn in fast-paced environment

Key Requirements

  • Bachelor of Technology degree
  • 1-3 years CSV experience
  • Experience with HPLCs and GCMS instruments

Work Rights

Not specified

Tailored Resume

Cover Letter