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Validation (CQV) Engineer
Salary undisclosed
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Title: Validation (CQV) Engineer
Qualifications and Requirements
- Bachelor's degree in Engineering, Pharmaceutical Science, or related technical field
- 4-8 years of experience in a CQV role within pharmaceutical, biotech, or medical device industries
- Working knowledge of GMP regulations, Computerised System Validation and GAMP5
- Hands-on experience with qualification protocols for pharmaceutical manufacturing equipment and utilities
- Familiarity with automation systems used in pharmaceutical manufacturing
- Experience with pharmaceutical packaging lines and/or fill-finish operations utilizing PLC automation systems
- Experience in equipment commissioning and qualification documentation
- Good understanding of pharmaceutical manufacturing processes, clean utilities, and facility requirements
- Strong attention to detail and documentation skills
- Good problem-solving abilities and analytical thinking
- Effective written and verbal communication skills
- Ability to work collaboratively in cross-functional team environments
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job Title: Validation (CQV) Engineer
Qualifications and Requirements
- Bachelor's degree in Engineering, Pharmaceutical Science, or related technical field
- 4-8 years of experience in a CQV role within pharmaceutical, biotech, or medical device industries
- Working knowledge of GMP regulations, Computerised System Validation and GAMP5
- Hands-on experience with qualification protocols for pharmaceutical manufacturing equipment and utilities
- Familiarity with automation systems used in pharmaceutical manufacturing
- Experience with pharmaceutical packaging lines and/or fill-finish operations utilizing PLC automation systems
- Experience in equipment commissioning and qualification documentation
- Good understanding of pharmaceutical manufacturing processes, clean utilities, and facility requirements
- Strong attention to detail and documentation skills
- Good problem-solving abilities and analytical thinking
- Effective written and verbal communication skills
- Ability to work collaboratively in cross-functional team environments
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job