This position is open in one of our offices in Sweden (Uppsala, Stockholm, Lund), Norway (Oslo) and Denmark (Copenhagen).
LINK Medical is searching for a Senior QA Manager with a strong background in GCP, preferably combined with GMP experience. As our
company continues to grow and expand its portfolio of cross-functional projects, we are looking for a highly motivated Senior QA
Manager to join our team. In this role, you will work on QA projects in close collaboration with the customers ensuring compliance
with applicable GxP requirements and industry standards. You will play a key role in developing and strengthening LINK Medicals QA
capabilities, with a primary focus on GCP and preferably clinical-phase GMP activities according to the customer’s needs. The
position also offers opportunities to contribute to business development in close collaboration with members of several teams
across the LINK Medical organization.
Responsibilities
- Provide QA expertise in customer services and projects within GCP preferably in combination with GMP for clinical phase. This
may include QMS development, auditing, training and advising in quality-related matters.
- Fulfilling certain roles at the customer, e.g. Quality Manager, Qualified Person (QP) as applicable, based on the competency of
the consultant.
Cooperate with colleagues in LINK Medical, nationally and internationally.
Manage and execute projects in an efficient and timely manner and within budget.
Develop training material and conduct internal and external training.
Keep updated on quality-related regulations and topics.
Contribute to the development of LINK Medical’s business for quality assurance services
Desired qualifications
Natural science degree at college/university level
More than 7 years’ experience from quality assurance within the life science industry
Broad knowledge of quality assurance and regulatory requirements
In depth knowledge within GCP in addition to knowledge within GMP and possibly other GxPs.
Experience in auditing and quality system development
Fluent in one of the Scandinavian languages and English
Good IT skills and use of standard office tools
Personal characteristics
Takes initiative, acts with confidence and works independently
Takes responsibilities for actions and projects
Develops job knowledge and expertise through continual professional development.
Shares expertise and knowledge
Demonstrates an interest in and understanding of others, motivates and builds team spirit
Be flexible, structured, effective and customer focused.
Identifies and creates business opportunities
Performs high quality work while maintaining professionalism and a courteous attitude with clients and colleagues
LINK Medical offers
LINK Medical offers an exciting and challenging position in a European CRO and Regulatory Service Provider that has a strong local
presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be
given engaging assignments requiring efficient collaboration with industry partners, clinical and scientific teams and the
regulatory authorities. We offer a competitive compensation and benefit scheme for all employees.
Contact information
If you would like to know more or have any questions about the position, please contact Tina Madsen, Director QA Operations
(tina.madsen@linkmedical.eu). All applications are treated confidentially.
Last day for submitting your application: 2026-09-30