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Project QA/QC Lead - Construction
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting a Project QA/QC Lead - Construction for a pharmaceutical organisation. This role is on a contract basis and is located in Visp. The client is focused on allowing their clients to meet their deadlines and acknowledge the requirements of their patients.
Responsibilities:
- To distribute consistent developments in design, procurement and construction quality, which involves procedure effectiveness, you will recognise prospects.
- Assist the CQV team for the organisation vendor accomplishment of quality and creation record document to be involves in vendor turnover packages.
- Guarantee contractor's compliance with needs of welding and NDE.
- Contribute to evaluating/authenticating of all reports exhibiting either system accomplishment, scope of work achievement.
- You will select proficient Third-Party Inspectors (TPIs) and organise inspection staff and deployment rendering the vendor, manufacturing timetables.
- Supervise supplier notified body actions to guarantee surveillance actions are performed rendering to approved quality assurance needs.
- To obtain assurance that contractor work actions and apparatus meet particular necessities, the ideal candidate will perform conformity examination actions.
- To warrant that the project's evaluation, hold, or witness point(s) necessities have been recognised, you will assess vendor quality plans (ITP's).
- Other duties may be assigned to this role.
Skills & Requirements:
- Examination experience would involve know-how of codes and standards valid to pressure vessels and piping systems which involve pertinent PED directive and examination needs for piping works and apparatus installation.
- Ideally a trained auditor in ISO 9001 with experience in project auditing.
- At least 10 years of experience in a quality management position with knowledge in welding engineering and NDE examinations.
- Educated to a degree level in mech engineering is highly ideal.
- Familiarity with construction sites with the ability to socialise and communicate well.
- Knowledge of engineering topics, commissioning, compliance, qualification and validation.
- Validation procedure knowledge (IQ, OQ, PQ) with knowledge on present regulatory needs linked to E2500 and ISPE 2004.
- Past involvement operating within a GMP manufacturing setting,
- Fluency in the English language with knowledge in German.
- Understanding and acquaintance with construction quality, commissioning and qualification. S
- Management experience with the ability to conduct safety and quality actions.
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.
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#QACompliance
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