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  • Job title:

    Freelance QA Auditor

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Role: QA Auditor
Location: Oss
Type: Freelance / Fixed Term Contract
Length: Contract till 31-12-2022 , with option for extension
Start: within now and 6 weeks

Experience should be in the pharmaceutical/chemical industry or government drug-regulatory agency with a working knowledge of cGMP regulations. Effective communications (oral/written) and interpersonal skills are necessary.

The Quality Auditor conducts routine audits of data, information, procedures, equipment and systems (including computer systems), and/or facilities to ensure the compliance with SOPs and GMPs 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. In addition, the Auditor communicates and resolves audit comments with client areas. Under supervision, or as part of a team, perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards. Issue reports summarizing deficiencies and work with areas to execute remedial action. Notify appropriate management of inspection result. Minimal work direction needed, highly skilled and knowledgeable to the position