PE Global is currently recruiting for a CQV Engineer for a leading multi-national pharma client based in Switzerland. This is an initial 12 month contract position. The CQV Engineer is primarily responsible for the preparation and the execution of the CQV activities as per below responsibilities.
Responsibilities (includes but is not limited to): Execution of the following activities for the relevant systems in accordance with Project procedures/guidelines: System Boundary development Design Qualification preparation, execution and includes release for IQ. GMP-RA's. Commissioning preparation, execution and includes vendor supervision on their testing scope and quality. Installation Qualification preparation, execution and includes release for OQ. Operational Qualification preparation, execution and includes release to OPS. Provide support in execution of Design Qualification for other direct impact. Provide support in the implementation of the Installation Commissioning process in accordance with Project procedures/guidelines. Shall be able to work/support another C&Q activity if deemed necessary. Carry out shift work, where required. Available for travel to vendors/contractors, where required. System Responsibilities: The list of the systems for which the CQV Engineer is responsible depends on the assigned equipment group and will be shared with the holder of the position at job start. The equipment group for which the candidate will get assigned to will be evaluated during the interview and communicated to the candidate with the job offer. The system scope for which the CQV Engineer will be responsible may evolve over time and may get updated as the project progresses.
Minimum requirements: Minimum Bachelor's degree in Life Sciences or Engineering. Minimum of 2+ years of experience in commissioning/qualification/validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry. Proven experience in performing qualification (IQ and OQ) on CIP skids. Minimum 2+ years of experience in commissioning/qualification/validation of Clean Utilities. Experience with DeltaV (Emerson). Fluent English language written and verbal communication. cGMP knowledge and knowledge of regulatory requirements. Able to work with minimum oversight fulfilling deliverables within target. Interested candidates should submit an updated CV. Please click the link below to apply, or alternatively send an up-to-date CV to ******.
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