CQV Qualification + Documentation Management Lead

☞ Proclinical Staffing

View: 151

Update day: 25-04-2024

Location: Visp Valais VS

Category: Administrative / Clerical / Assistant

Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing

Position: Entry level

Job type: Contract

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Job content

Proclinical are recruiting a CQV Qualification + Documentation Management Lead for a pharmaceutical establishment. This role is on a contract basis and is located in Visp. The client is focused on permitting a healthier society.

Responsibilities
  • Handle COMOS / KNEAT / DMS interfaces for the CQV group.
  • Manage System Boundary development surveillance.
  • Plan qualification development, supervision and sanction which involves the release for IQ.
  • Support the evaluation of project risk and analysing the efficiency of mitigation approaches implemented.
  • Document crucial deliverables and dates and bring into line with crucial indicators within the projects critical path.
  • You will handle qualification group approval (Qualifizierungsleiter).
  • Guarantee reporting reliability across CQV group.
  • Manage the CQV training program both directly and indirectly.
  • The ideal candidate will prioritise and implement responsibilities in a fast-paced setting such as GQV Qualification and documentation management lead additional deliverables.
  • Offer assistance to implement the design qualification for all immediate impact systems.
  • If needed, will operate / assist other C&Q actions.
  • Document and assist in providing project matter solutions.
  • Execute and handle training procedures.
  • Free to travel for business needs.
  • Other duties may be assigned to the role.
Skills & Requirements
  • Educated to a degree level in s life science or engineering discipline.
  • At least 6+ years of experience in commissioning / qualification / validation such as DQ, IQ, OQ, Commissioning actions in the pharmaceutical/biotech business.
  • Knowledge in HVAC/Proven utility/process system, CIP, and SIP.
  • Familiarity with DeltaV or Emerson.
  • Fluency in the English language.
  • Communication abilities both verbally and written.
  • Know-how of regulatory needs as well as cGMP.
  • Capable of operating under minimal supervision completing deliverables in objective timelines.
  • Knowledge of the German language.
  • Acquaintance with the clients Commissioning / Qualification Approach.
  • Previous involvement with COMOS/KNEAT platforms.
  • Knowledge of biopharmaceutical.
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: 09-06-2024

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