HR Admin/Recruiter at INSTRUMENTATION AND CONTROL SOLUTIONS
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ICS - CSV Validation Engineer (1-5 yrs)
The CSV Engineer will be responsible for ensuring compliance with regulatory requirements and industry standards for computerized systems used in pharmaceutical manufacturing.
Key Responsibilities:
1. Develop, execute, and maintain validation protocols for computerized systems, including IQ, PQ, and CSV.
2. Ensure compliance with regulatory requirements, including 21 CFR Part 11, GXP, and GAMP5.
3. Validate equipment and computerized systems used in pharmaceutical manufacturing.
4. Conduct risk assessments to identify potential hazards and develop mitigation strategies.
5. Develop and maintain validation documentation, including protocols, reports, and SOPs.
- Key Skills:
- GAMP5
- IQ, PQ, CSV
- Validation of equipment
- 21 CFR Part 11
- GXP assessment
- Soft Skills: Excellent communication, problem-solving, and analytical skills.
Interested candidates can share your resume
For more details, please connect or drop your CV at 9109188946
