Specialist QA Compliance
Infos sur l'emploi
- Date de publication :04 septembre 2024
- Taux d'activité :100%
- Type de contrat :Durée indéterminée
- Langue :allemand (Courant)
- Lieu de travail :Oberriedstrasse 68, 3174 Bern
For us, it is all about improving and saving lives
We are a fully integrated vaccine company focused on the development, manufacturing, and commercialization of vaccines, and our vision is to become one of the largest pure-play vaccine companies in the world. At Bavarian Nordic, you will be part of a global team of +1600 dedicated colleagues worldwide, all passionate about making a difference. We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and we welcome people who are passionate about saving lives. If you are open-minded and have the willpower to succeed, we might just be a perfect fit.
At Bavarian Nordic Berna, the Swiss affiliate there are - beside manufacturing activities - professionals in Quality Assurance, Quality Control, Supply Chain and Regulatory affairs working. On the Swiss site in Thörishaus / Bern there are approx. 160 dedicated and committed professionals working locally and globally.
To complement and strengthen our Quality Assurance Team we are looking for a
Specialist QA Compliance 80 - 100% (f/m/d)
Responsible, as QA representative in multidisciplinary teams, to oversee the following topics:
- Deviation, Change Control, CAPA Management, Continuous improvements
- Process Validation
- Product Quality Review (PQR)
What is in the role for you:
- Reviews and approves deviations, investigations, CAPAs and Change Controls
- Reviews and approves process validation documents including risk assessments
- Oversees site manufacturing activities (oral and parenteral)
- Establishes annual Product Quality Reviews
- Ensures regulatory compliance and continuously improves the allocated quality systems and procedures
- Participates in audits and inspection within the area of responsibility
What do you bring to it:
- Master's degree preferrably in Life Sciences or related field
- Minimum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology industry
- Solid computer skills including MS Office required / SAP, LIMS, Quality Management Systems skills are a plus
- Analytical thinking and problem-solving attitude
- Multilingual - at least German and English, written and spoken
We provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our dedicated and agile QA team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and academic skills
We look forward to receiving your application directly on our recruiting portal!