We have an exciting opportunity for a Clinical Supplies Quality Specialist (m/f/d) in Switzerland
Tasks
- You are responsible for reviewing and approving incoming label stock.
- Your role involves meticulously reviewing and approving clinical finished goods ensuring accuracy in printed and applied labels.
- You conduct detailed GMP reviews of batch records and regulatory filings to ensure final release compliance.
Requirements
- A university degree (bachelors or higher) is preferred for this position.
- Your previous experience in a similar role is highly appreciated.
- Experience in a regulated environment will give you an advantage.
- minimum of 2 years of experience in regulated environments preferably in pharma or medtech.
Thank you for considering this opportunity. I look forward to connecting with you.