In this role, you will represent Siegfried's quality management system at the Zofingen site to customers and authorities. You will gain a multifaceted overview of the technical and economic interrelationships in a pharmaceutical company.
Your tasks
* Plan and conduct audits of contract manufacturers, contract laboratories, and other service providers, including raw material suppliers and other suppliers.
* Qualify suppliers, evaluate audit results, follow up and rectify identified deficiencies.
* Respond to customer inquiries such as quality questionnaires, statements, and declarations.
* Collaborate in establishing and further developing processes and management systems.
* Conduct internal audits at the Zofingen site and closely collaborate with the Corporate Audits department.
Your profile
* Completed scientific studies (ideally with a doctorate).
* At least 3 years of professional experience as an auditor in a chemical, pharmaceutical, or similar environment.
* Comprehensive expertise in the field of quality, especially regarding ISO and GMP.
* Knowledge of cGMP, preferably in the production of active ingredients and/or finished medicinal products, is important in this position.
* Business fluency in German and English.
* Flexible and familiar with working in a matrix organization.
* Willingness to travel occasionally.
Main qualifications
* Business fluency in German and English.
* Familiarity with working in a matrix organization.
What we do in Zofingen
The production facility at our Zofingen headquarters supplies our customers around the globe with exemplary Swiss quality.
Main activities
* Development and commercial manufacture of active pharmaceutical ingredients (APIs) and corresponding intermediates.
* Fully compliant with cGMP and SHE standards.
Strategic importance
* Contract manufacturing of new active ingredients.