Senior QA Manager

This position is open at one of our offices in Norway (Oslo), Denmark (Copenhagen) or in Sweden (Uppsala, Stockholm, Lund).

LINK Medical is searching for a Senior QA Manager. Our company is growing, and the portfolio of cross-functional projects is increasing. As a Senior QA Manager, you will work on QA projects in close collaboration with the customers. You will have the opportunity to develop LINK Medical’s competencies in different GXP areas with main focus on GCP according to the customer’s needs and to participate in activities related to business development in close collaboration with members of several teams across the LINK Medical organization.
We are looking for a highly skilled and motivated person with previous experience from working with Quality Assurance within the Life Science sector. The person needs to be service minded with good cooperation and communication skills. It is also important to have good time management to drive performance. As a person it is important be flexible, structured, effective and customer focused.

• Provide QA expertise in customer services and projects. This may include QMS development, auditing, training and advising in quality-related matters.
• Fulfilling certain roles at the customer, e.g. Quality Manager, Responsible Person (RP), 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

• Natural science degree at college/university level
• Generally good IT skills and use of standard office tools
• Fluent in one of the Scandinavian languages and English
• Min 5 years’ experience from quality assurance within the life science industry
• Broad knowledge of quality assurance and regulatory requirements in the medicines
• In depth knowledge within GCP in addition to knowledge within other GXPs.
• Experience from auditing and quality system development

• 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
• Identifies and creates business opportunities
• Performs high quality work while maintaining professionalism and a courteous attitude with clients and colleagues

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.

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: 2025-04-30

Please apply to the job by filling out the application below: