Job Summary: We are seeking a Clinical Supplies Quality Specialist to join our team. This role is responsible for the release of clinical and commercial drugs, review and approval of incoming label stock and clinical finished goods, and GMP review of batch records and regulatory filings.
The ideal candidate will have previous experience in a similar role, a university degree, and experience in a regulated environment. They must also be proficient in English (C1 level) and have basic knowledge of German.
* Release clinical and commercial drugs for packaging, incoming label stock, and primary packaging components;
* Review and approve incoming label stock;
* Review and approve clinical finished goods, including printed and applied labels;
* GMP review of batch records and regulatory filings.
Requirements:
* University degree (bachelor or higher);
* Previous experience in a similar role;
* Minimum 2 years in a regulated environment (pharma, medtech preferred);
* English C1 mandatory, German is nice to have.
Working Conditions:
* 6 months duration;
* Full-time employment;
* Entry-level position.
Industry: Pharmaceutical Manufacturing.