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:

• 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