Clinical Supplies Quality Specialist (a) 100%

Our client, a leading global player in the pharmaceutical industry with modern offices in the Lucerne area is looking for a service oriented Specialist in Clinical Supplies Quality (a) who will support the Clinical Supplies Quality Team. The candidate holds an important role within the team and contributes significantly to the team's overall success.

Description

The selected candidate will be responsible for the primary following activities:

• Review and release of incoming label stock
• Review and release of clinical finished good, including review of the printed and applied label
• GMP review of the batch record and review of the regulatory filings and the final release
• Coordination with cross-functional teams (e.g., Regulatory Affairs, Manufacturing, and Packaging) to resolve discrepancies identified during label stock or batch record review
• Oversight of deviation and CAPA processes related to labeling errors or documentation issues

Profile

To be considered for this position, the ideal candidate must have:

• BA/BS or higher academic education

• Minimum of 2 years experience in a regulated environment (pharma, medtech preferred)

• Service- & customer-oriented mindset

• Excellent communication skills and fluency in English, German is a plus

• Immediate availability

Job Offer

This is a unique opportunity to immediately join a renowned international company and become an integral part of the team within a short time.