Are you an experienced quality professional ready to step into a global QA role? Join a dynamic organization where your expertise in GMP and regulatory requirements will be valued, and your ability to support and challenge colleagues will help drive our success. We offer opportunities for growth and learning in an environment that celebrates collaboration and innovation. If you’re eager to make an impact and grow with us, apply now!
About us
PolyPeptide Group AG and its consolidated subsidiaries (“PolyPeptide”) is a specialized Contract Development & Manufacturing Organization (CDMO) for peptide- and oligonucleotide-based active pharmaceutical ingredients. By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world. PolyPeptide serves a fast-growing market, offering products and services from pre-clinical through to commercial stages. Its broad portfolio reflects the opportunities in drug therapies across areas and with a large exposure to metabolic diseases, including GLP-1. Dating back to 1952, PolyPeptide today runs a global network of six GMP-certified facilities in Europe, the U.S. and India. PolyPeptide’s shares (SIX: PPGN) are listed on SIX Swiss Exchange.
Our Values
Trust: We build and maintain trust in all our relationships – both with each other and with our customers. We support each other and work as a team.
Innovation: We are curious and driven by finding smart solutions to the challenges we face.
Excellence: We always strive to deliver high quality and adapt to meet the needs of our customers.
About the role
As a global QA Specialist, you will work with and support the organization with activities related to supplier & material qualification, global quality documents, changes and deviations.
Main duties
- Leading regular meetings with the team for follow-up on supplier qualification activities
- Preparation of global annual audit and re-qualification plans
- Coordination of activities related to the vendor audit plans
- Support supplier audits and supplier qualifications
- Creating and updating global quality procedures, forms, templates
- Support management of global quality documents, changes and deviations
About you
We believe that you are ready for new and exciting challenges in a global QA role. You have several years of experience with quality work within the pharma or medical device industry. You have high GMP understanding as well as knowledge of regulatory requirements and guidelines.
You enjoy supporting and coach co-workers but are also able to challenge procedures and introduce alternative options.
Your profile:
- Minimum 5 years’ experience within Pharma or Medical Device industry
- Minimum 3 years’ experience within a quality function
- Bachelor/Master/PhD degree in scientific life sciences, or equal
- Strong understanding of Good Manufacturing Practices (GMP) and regulatory compliance standards.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
- Excellent written and verbal communication skills in English.
Find this interesting?
If you are ready for your next challenge and want to work in an environment where you will be part of a great team this could be the right position for you. We want our business and our co-workers to grow together, so if you like to be part of that, we look forward to your application.
For more information, please contact Ina Altrell, Global Director Quality, at [email protected]. For union information contact the local union chairman for Akademikerföreningen or Unionen, please call 040-36 62 00 for support. We will review applications ongoing so please submit your application as soon as possible. Latest day to apply is 31/8.
