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Job Description
- Plan, execute, and document validation protocols (IQ, OQ, PQ) for equipment, utilities, and processes.
- Ensure all validation activities comply with regulatory requirements and company SOPs.
- Prepare and review validation documentation, including protocols, reports, and risk assessments.
- Collaborate with cross-functional teams including QA, Production, and Engineering.
- Participate in audits and inspections related to validation processes.
- Maintain a validation master plan and ensure timely revalidation.
Job Requirements
- A bachelor’s degree in pharmacy is a must.
- Minimum of 3–5 years of experience in a pharmaceutical manufacturing environment.
- Strong knowledge of GMP, FDA, and international validation guidelines.
- Excellent analytical and documentation skills.
- Ability to work independently and within a team.