Quality Assurance Manager Q&V (Quality Partner Infrastructure) (80-100%) — Roche
NewCHF 85'500 - 129'500
Roche · Basel (BS)
- Location
- Basel
- Contract
- full-time
- Posted
- 2 days ago
SalaryCHF 85'500 - 129'500
Role overview
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
- At Roche you can show up as yourself, embraced for the unique qualities you bring.
- Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
- You are an autonomous, agile, and open-minded team player with the ability to assert yourself, backed by excellent judgment, negotiation, and communication skills. We provide A great and enthusiastic team An inspiring working environment Substantial fringe benefit
What the company offers
- You are an autonomous, agile, and open-minded team player with the ability to assert yourself, backed by excellent judgment, negotiation, and communication skills. We provide A great and enthusiastic team An inspiring working environment Substantial fringe benefit
Company and context
- They develop cutting-edge in-vitro medical devices, assays, laboratory information solutions and cloud-based offerings in the medical domain and include R&D, manufacturing and end user service organizations.
- Our new global modular quality management brings a radical simplification of our process landscape and provides our validation and qualification teams with more freedom and ability to shape our future, while preserving our high quality standards. The Opportunity
- Act as an independent Quality Partner for our qualification & validation business teams
- Enable our business partners to develop and execute compliant and efficient qualification & validation strategies based on our global quality management system
- Perform comprehensive and independent feedback, review and approval of all validation and qualification artifacts involved in the system life cycle
- Based on a deep understanding of our global quality management system: act as ambassador of the global quality assurance processes and thereby enable our business partners to deliver high class medical products
- Shape, live and defend our global quality management system
- Take controlled risks and help in the defense during audits Who You Are
- Educational Background: Technical or scientific degree or completed education in a technical profession.
- Professional Experience: At least 3 years of practical expertise in the area of qualification and/or validation in GxP environments, with experience or a high level of affinity with quality management in the area of medical devices or in vitro Diagnostics (based on ISO 13485 and FDA’s Quality Systems Regulations) regarding Equipment Qualification/Management and data integrity.
Additional details
- Our new global modular quality management brings a radical simplification of our process landscape and provides our validation and qualification teams with more freedom and ability to shape our future, while preserving our high quality standards.
- You are an autonomous, agile, and open-minded team player with the ability to assert yourself, backed by excellent judgment, negotiation, and communication skills. A great and enthusiastic team An inspiring working environment Substantial fringe benefit
Notes and original content
- The Opportunity
- You are an autonomous, agile, and open-minded team player with the ability to assert yourself, backed by excellent judgment, negotiation, and communication skills.
- We provide
- A great and enthusiastic team
- An inspiring working environment
- Substantial fringe benefit
