CQV Engineer

Proclinical are recruiting for a CQV Engineer to join a pharmaceutical organisation. This role is on a contract basis and is located in Visp.

Responsibilities:

• Offer aid in the execution of the installation commissioning process rendering to the project processes/regulations.
• Work/assist on any other C&Q action if deemed required.
• When necessary, you will carry out shift work.
• Implement actions for the company's pertinent systems rendering to the Vibe-X project processes/regulations.
• The ideal candidate will offer help in implementing design qualification for any other direct impact systems.
• Other duties may be assigned.

Key Skills and Requirements:

• Educated to a degree level in a life science or engineering field.
• Demonstrable experience within commissioning/qualification/validation such as QQ, IQ, OQ, commissioning actions, etc., within a pharmaceutical/biotechnology organisation.
• Familiarity within proves or utility equipment, such as either DSP, USP, Bioconjugates, or Clean Utilities.
• Exhibited experience within commissioning/qualification/validation of clean utilities systems.
• Acquaintance with DeltaV (Emerson).
• Fluency in both German and English.
• Communication skills both verbally and in writing.
• Expertise in cGMP and regulatory needs.
• Capable of working under minimal supervision to fulfil deliverables within target dates.
• Prior involvement with the client's commissioning/qualification approach.
• Former involvement with COMOS/KNEAT platforms.
• Willing to travel for business needs to vendors/contractors when necessary.

If you are having difficulty in applying or if you have any questions, please contact Chloe Jack at c.jack@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#Engineering