Specialist Clinical Supplies Quality (m/w/d)

Key Responsibilities:

• Review and release of incoming label stock.
• Review and release of clinical finished goods, including printed and applied labels.
• Conduct GMP review of batch records and assess regulatory filings for final release.

Requirements:

• Previous experience in a similar role is highly appreciated.
• A university degree (bachelor’s or higher) is preferred.
• Experience in a regulated environment (pharma, medtech) is an advantage.
• Minimum of 2 years of experience in a regulated environment.

Language Skills:

• English (C1 level) is mandatory.
• German is a plus but not required.

Work Schedule & Hybrid Model:

• Three times per week, the day starts at 9 AM with a team meeting to discuss ongoing batch releases.
• Work primarily involves handling releases throughout the day.
• Hybrid work model: Initial full-time on-site training, followed by 2 days in-office and 3 days remote (subject to business needs).