CQV Engineer job in Visp, Schweiz

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Job type: Permanent

Discipline: Validation

Location: 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:

Be included in all validation actions, which may include facilities, utilities, validation life cycle, implementation, technical documentation procedure, GAP analysis, risk assessment, etc.
Author and/or revise processes suitable to the engineering actions.
Implement IQ/OQ and PQ for equipment, systems and utilities, as well as author reports of accomplished validation actions.
Operate to implement lessons learned and stay notified of industry regulatory alterations as it affects equipment/facility validation.
Assist the engineering group to prepare the validation, requalification, and maintenance programs.
Conduct allocated quality systems actions which involves document management system, change control, non-conformities, and CAPAs.
Other duties may be assigned.

Key Skills and Requirements:

Educated to a degree level in a scientific or technical discipline.
Fluency in the English language.
Demonstrable experience in a pharma organisation.
Communication skills both verbally and in writing.
Able to work in a precise, detailed and timely manner.
Works well independently.
An organised individual with the ability to manage own time efficiently.

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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