This permanent, full-time position is open at one of our offices in Sweden (preferably Stockholm or Uppsala)

LINK Medical is growing, and the Quality Assurance team is looking for a highly skilled and motivated Senior QA Manager with GDP expertise and RP experience. In this role, you will work closely with clients on QA projects and contribute to the development of LINK Medical’s QA services. You will have the opportunity to further develop LINK Medical’s competencies in different areas according to your aspirations and the customers’ needs. You will also participate in activities related to business development in close collaboration with members of various teams across the LINK Medical organization.

Responsibilities

• Acting as the Responsible Person (RP) for customers

• Ensure GDP compliance across all wholesale activities.

• Provide QA GDP expertise in customer services and projects. This may include QMS development, auditing, handling quality issues, training and advising in quality-related matters.

• Cooperate with colleagues at 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

• Degree in natural sciences or equivalent experience, preferably a M.Sc. Pharm. or alternatively B.Sc. Pharm

• Min 5 years’ experience from quality assurance within the pharmaceutical industry

• In depth knowledge within GDP and other GxPs

• Experience as Responsible Person (RP)

• Experience with pharmaceutical wholesale (GDP).

• Experience in auditing and QMS development

• Broad knowledge of quality assurance and regulatory requirements in the medicines or medical device area

• Fluent in one of the Scandinavian languages and English
  

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

• Identifies and creates business opportunities

• Performs high quality work while maintaining professionalism and a courteous attitude with clients and colleagues

LINK Medical Offers

We offer 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 Hilde K Holme, EVP Regulatory Services: hilde.holme@linkmedical.eu

All applications are treated confidentially.

Last application date: 2026‑04‑10