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CQV CIP Engineer
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Location | Switzerland |
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Job Type | Contract |
Blackfield Associates are looking for 4+ CQV Engineers to be based in Visp for initially a one year contract with a strong focus on CIP.
Responsibilities
- Perform the following tasks for the relevant systems, ensuring compliance with project procedures and guidelines:
- Prepare, execute, and approve Design Qualification, including release for IQ.
- Prepare, execute, and approve Installation Qualification, including release for OQ.
- Prepare, execute, and approve Operational Qualification, including release to operations.
- Conduct GMP Risk Assessments (GMP-RA).
- Prepare, execute, and approve commissioning activities, including overseeing vendor testing scope and quality.
- Support the execution of Design Qualification for other directly impacted systems.
- Assist in the implementation the Installation and Commissioning process in accordance with project procedures and guidelines.
- Be flexible to work on or support other C&Q activities as needed.
- Willing to work shifts as required.
- Willing to travel to vendors/contractors when required.
Requirements
- Bachelor’s degree in Life Sciences or Engineering.
- At least 4 years of experience in commissioning, qualification, and validation (DQ, IQ, OQ, Commissioning) within the pharmaceutical or biotech industry.
- Demonstrated experience in performing IQ and OQ qualifications on CIP skids.
- At least 2+ years of experience in commissioning, qualification, and validation of CIP
- Familiarity with DeltaV (Emerson)
- Familiarity with COMOS/KNEAT platforms.
- Proficient in written and verbal communication in English.
- Strong knowledge of cGMP and regulatory requirements.
- Ability to work independently and meet deadlines with minimal supervision.
- Fluency in German is advantageous
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If this position interests you, and you would like to learn more or explore other available jobs that could also match your skill set, please apply today or email vi@blackfieldassociates.com