About this role
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment.
Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact. Your Role: The Site Quality Head is responsible of managing the QA and QC departments, ensuring the compliance with the overall strategy of Quality. He/She is responsible of managing the department in terms of operations, projects, resources and policies.
Main responsibilities of the Site Quality Head are: 1. Ensure compliance with GMP regulations of conduct standards, ISO13485 requirements, ICH guidelines and Siegfried (Quality Manual), as well as SOPs in all site operations. 2.
Manage the QA/QC department. 3. Ensure compliance to GMPs, ISO 13485 and Global Siegfried regulations of the site products, projects, strategies, processes and decisions.
4. Act as SPOC in all issues related to Global Quality of Siegfried. Responsible for implementation and compliance to the principles and practices of the Siegfried Manual.
5. Define, execute and monitor/adherence to the annual budget. Ensure the adequate use of human and economic resources in order to achieve the department goals in an efficient manner.
6. Encourage Quality Culture at the site and excellence in Quality Management Control at the site 7. Final responsible for ensuring the quality, safety and efficacy of products manufactured at the site.
8. Lead the implementation of Local Quality Plan, review of the Quality Management systems with the Site Leadership Team and with Siegfried Pharma Division. 9.
Act as Medical Devices management representative having the associated responsibility and authority collected in the ISO13485 standard. 10. Ensure compliance with SHE regulations.
11. Ensure and sustain a MRP Class A for all the site. Your Profile: Education: - Pharmacy degree - MBA will be valued - Knowledge in FDA, MHRA, EMA, WHO, GxP and ICH regulations Local language and English advanced.
Minimum 10 years experience in Quality in the Pharmaceutical Industry. Experience in managing large teams. Your Benefits: Annual Bonus Company car Free parking Subsidized canteen on-site or restaurant ticket: to use when eating out or working from home Medical, life, and accident insurance Access to "Club Siegfried": an exclusive platform with discounts and offers on over 400 services.
If you’re excited by the idea of joining our group , we’d love to hear from you. Apply today and be part of building something extraordinary! Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents.
With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.