About Us
CTC is a specialized search and recruitment partner for the Life Sciences industry, dedicated to serving clients and candidates since 1997. We connect talented professionals with meaningful career opportunities and support our clients in engaging, retaining, and developing the right talent when necessary.
Client Overview
Our client is a highly regarded specialist biotherapeutics manufacturer with over a century of experience in treating various diseases on a global scale. They are committed to providing solutions for patients with coagulation disorders, immunological diseases, enzyme deficiency diseases, and other rare diseases.
Main Responsibilities
- Execute GxP supplier qualification activities.
- Lead vendor qualification processes, including document review and audit execution.
- Ensure the qualification of vendors providing GxP-relevant equipment and services.
- Act as Quality Delegate / Change Coordinator for Vendor Qualification Change Controls.
- Establish and maintain an overview of already qualified and to-be-qualified vendors.
Qualifications and Experience
- Relevant working/residency permit or Swiss/EU citizenship required.
- A degree in life sciences and/or engineering.
- At least 5 years of experience as a professional in the pharmaceutical industry or an equivalent combination of education and experience.
- Proven experience in quality assurance and regulatory compliance with GxP, Swissmedic, US FDA, TGA, EU, and other regulatory agency guidelines in the manufacturing of biologics.
- Direct experience in quality oversight of GxP-compliant vendor qualification processes, including planning, documentation review, and audit execution.
- In-depth knowledge of GMP and global regulatory requirements, including GMP, FDA, EU, and other relevant GxP regulations.
- Effective collaboration skills with internal and external stakeholders.
- Fluency in English (spoken and written).
Engage with Us
If you are interested in learning more about CTC and the outlined opportunity, we invite you to connect with us for further details.