Selection Process: Interview (Face to Face)
Interview Rounds: HR
Key Technical Skills:
- Expertise in injectables manufacturing
- Knowledge of regulatory requirements
- Experience with internal and regulatory audits
- Familiarity with industrial practices and current GxP processes
Key Duties and Responsibilities:
- Coordinate with cross-functional teams for execution of validation activities
- Develop procedures and policies
- Ensure plant QMS compliance status
- Manage major/critical deviations
- Handle change control and CAPA (Corrective and Preventive Actions)
- Provide quality responses as required
- Evaluate change controls
- Prepare, review, and execute various validation protocols
- Perform activities as assigned by the superior
- Follow up on day-to-day activities
Background of Job:
- Working experience in regulated markets focusing on sterile injectables, parenteral, ophthalmic, and vaccines
Interested candidates can share their resumes to Pooja.Thakkar@arcolab.com with the subject line “QA – Validation Resume”.
For more information about our company, visit our website at www.steri-science.com.
