
Pharmaceutical Commissioning and Validation Professional
3 days ago
We are seeking a highly skilled Commissioning, Qualification & Validation (CQV) engineer to join our team.
Job Description:The successful candidate will be responsible for planning and executing CQV activities for pharmaceutical/biotech manufacturing facilities, utilities, and process equipment. This includes leading commissioning, qualification, and validation efforts to ensure GMP compliance and timely project execution.
The ideal candidate will have strong technical expertise in CQV processes and experience working with cross-functional teams. They will also have excellent communication skills and the ability to coordinate projects effectively.
Required Skills and Qualifications:- Bachelor's degree in engineering, Life Sciences, or a related field.
- 2-5 years of industry experience in commissioning/qualification/validation within pharmaceutical or biotech industries.
- Familiarity with GMP, GAMP 5, ISPE Baseline Guides, and pharmaceutical regulations.
- Attractive remuneration package and comprehensive benefits.
- Generous annual leave of at least 14 days.
- Opportunity to work in a rapidly growing industry with cutting-edge technology.
Ready to take the next step? Click apply now to submit your resume and share your availability and expected salary.
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