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Job type: Contract

Discipline: Design

Location: Switzerland

Proclinical is seeking a dedicated and innovative C&Q Engineer to join our team. This role is an excellent opportunity for someone passionate about making a significant impact within the Life Science industry. This a 6-month contract role. The successful candidate will be involved in various aspects of engineering, including checking specifications, understanding different statuses of PIDs, and generating CQV related documents.

Responsibilities:

Familiarity with the client's SOP-Visp and Q-doc templates.
Experience with COMOS, specifically in checking specifications for TP and Real-Equipment and understanding the differences.
Ability to read and understand PIDs in various statuses like B, C, D, and E.
Proficiency in using Excel.
Generation of CQV related documents: DQ-TP, IQ-EQ, IQ-Montage & Betrieb, IH-Doku, GMP-RA, FS, uCQP, OQ, and PQs.
Initiation of AWF in DMS.
Handling of DMS, controlled copy printing, and wet-signature.

Key Skills and Requirements:

Experience in CQV, preferably with the client's Visp onsite CQ-document handling.
Strong understanding of engineering principles and practices.
Excellent communication and organisational skills.
Ability to work independently and as part of a team.

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