CQ Engineer job in Visp, Switzerland

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Validation

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting a CQ Engineer for a pharmaceutical organisation. This role is on a contract basis and is located in Visp. The client is focused on enabling remedies that preclude illness and assist in healthier lifestyles.

Responsibilities:

Offer assistance in the execution of the installation commissioning procedure rendering to project ORCA processes/regulations.
When needed, carry out shift work.
Handle commissioning planning, implementation and sanction which involves supplier oversight on their testing scope and quality.
Manage installation qualification planning, implementation and consent which involves release for OQ.
You will design qualification planning, implementation and sanction which involves the release for IQ.
Handle System Boundary development + agreement.
The ideal candidate will manage the planning, implementation and sanction od operational qualification, which involves release for OPS.
You will offer assistance in the implementation of design qualification for any other direct influence systems.
Other duties may be assigned to this role.

Skills & Requirements:

Educated to a degree level in a life science or engineering discipline.
At least 6+ (Lead) / 4+ (Senior) / 2+ (Intermediate) years of experience in commissioning / qualification / validation such as DQ, IQ, OQ, Commissioning actions in the pharmaceutical or biotech organisation.
Knowledge in upstream system, CIP and SIP.
At least 6+ (Lead) / 4+ (Senior) / 2+ (Intermediate) years of experience in commissioning / qualification / validation of Upstream systems.
DeltaV (Emerson) experience.
Fluency in the English language with knowledge in German.
Communication abilities both written and verbally.
Knowledge of cGMP and of regulatory needs.
Capable of working under minimal supervision completing deliverables within target dates.
Familiarity with the company's commissioning/qualification strategy.
Acquaintance with COMOS/KNEAT platforms.

If you are having difficulty in applying or if you have any questions, please contact Sasha Botha at +41 61 568 79 88.

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.

#LI-SB6

#QACompliance