Commissioning & Qualification Specialist
vor 1 Tag
We are seeking a highly skilled Commissioning & Qualification Specialist to join our team at Randstad. The ideal candidate will have a strong background in engineering and technical services, with a minimum of 5 years of experience in a C&Q/CQV equivalent position within the pharma industry.
Key Responsibilities:
- Develop and implement Commissioning & Qualification plans and protocols for new or modified GMP utilities, facilities, and process equipment.
- Conduct DQ, IQ, OQ, and PQ activities, including protocol deviations, investigation, and corrective action activities.
- Coordinate and execute FAT/SAT, commissioning activities for new GMP systems in collaboration with internal and external partners.
- Prepare, review, and approve technical and GMP-related documentation.
Requirements:
- Bachelor's or Master's degree in Engineering, technical, or natural sciences.
- Minimum 5 years of working experience within the pharma industry in a C&Q/CQV equivalent position.
- Knowledge of Qualification requirements according to cGMP regulations.
- Excellent communication and analytical skills.
Working with us:
We offer a dynamic and challenging work environment, with opportunities for professional growth and development. If you are a motivated and experienced professional looking for a new challenge, please submit your application.
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