CQ Engineer

☞ Proclinical Staffing

View: 149

Update day: 21-03-2024

Location: Visp Valais VS

Category: High Technology Mechanical / Technical Electrical / Electronics IT - Software

Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing

Position: Entry level

Job type: Contract

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Job content

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.

#QACompliance

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Deadline: 05-05-2024

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