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Quality Auditor

Switzerland   •  Contract/Temporary, Full time

CK QLS are recruiting for 2 Quality Auditors to join a leading pharmaceutical company at their site based in Lucerne on a contract basis for 12 months, with the possibility of extension.
Quality Auditor Role:
The main purpose of the role will be to:

  • Conduct routine audits of data, information, procedures, equipment and systems (including computer systems), and/or facilities to ensure the compliance with SOP\'s and GMP\'s and worldwide regulations.
  • Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots (bulk and packaged) to ensure conformance to appropriate regulatory requirements.
  • Perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards.

Your Background:
In order to be considered for this role, you will be required to have the following qualifications, skills and experience:

  • Previous experience within the pharmaceutical/chemical industry or government drug-regulatory agency.
  • A working knowledge of cGMP regulations.
  • Effective communications (oral/written) and interpersonal skills are necessary.
  • Fluency in German would be a huge advantage.

This is an excellent opportunity to join a global pharmaceutical organisation.

For more information or to apply for these Quality Auditor positions, please contact CK Group, quoting job ref 48827.

Please could you send any correspondence in English.

It is essential that applicants hold entitlement to work in Switzerland.

You MUST be eligible to work in Switzerland. Learn more

  • Agency: CK Group
  • Contact: Jocelyn Blackham
  • Phone: 01438 723 500
  • Reference: 48827
  • Posted: 4th September 2020
  • Expires: 2nd October 2020

CK Group

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