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CQV Engineer
- Contract
- Validation
- Switzerland
This vacancy has now expired. Please see similar roles below...
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 implementing design qualification for other direct impact systems.
- Supply assistance within the execution of the installation commissioning process rendering to project process/regulations.
- Provide help on any other C&Q actions if required.
- When needed, you will carry out shift work.
- Other duties may be assigned.
Key Skills and Requirements:
- Willing to travel for business needs.
- Educate to a degree level in a life science or engineer field.
- Demonstrable experience within commissioning/qualification/validation such as DQ, IQ, OQ, commissioning, etc., actions within a pharmaceutical/biotech organisation.
- Expertise on clean utilities.
- Exhibited familiarity within commissioning/qualification/validation of clean utilities systems.
- Acquaintance with DeltaV (Emerson).
- Fluency in the English language.
- Communication skills both verbally and in writing.
- Know-how of cGMP and regulatory needs.
- Capable of working well while under minimal supervision fulfilling deliverables within target dates.
- Prior involvement with client's commissioning / qualification approach.
- Familiarity with COMOS/KNEAT platforms.
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
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