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Head of Science and Engineering Recruitment at CK QLS
Specialist Clinical Supplies Quality, Lucerne
Duration: 12-month contract. Possibility of an extension.
Home Office: We do have a hybrid work model. The candidate will start for training purposes fully on-site and then switch to hybrid (currently 2 days in the office, 3 days home office).
The Clinical Supplies Quality team is responsible for the release of the packaged and labelled drugs for use in clinical studies. The team is responsible for the release of clinical and commercial drugs for packaging, incoming label stock and primary packaging components to the release of clinical finished goods.
Responsibilities:
1. Review and release of incoming label stock
2. Review and release of clinical finished goods, including review of the printed and applied label
3. GMP review of the batch record and review of the regulatory filings and the final release
Candidate’s requirements:
1. Previous experience in a similar role is highly appreciated, university degree (bachelor or higher) is preferred, experience in regulated environment is an advantage
2. Minimum of 2 years experience in a regulated environment (pharma, medtech preferred)
3. English C1 mandatory, German is nice to have
Day in the job:
3 times per week, the day starts at 9 am with a team meeting to discuss ongoing jobs to be released (batch). During the day, the person will work on releases.
Seniority level:
* Mid-Senior level
Employment type:
* Contract
Job function:
* Quality Assurance
Industries:
* Pharmaceutical Manufacturing
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