QA Officer Medical
Anacura, a family-owned, growing center of excellence in healthcare with over 300 employees consists of 4 independent business units: Labo Nuytinck, active in medical analytics and Anabiotec, OHMX.bio and Discovery Studio, active in drug development. The labs have their main activities in a state-of-art building in a green surrounding near Ghent, Belgium.
We pride ourselves on our flexibility, dedication and scientific approach, and operate as an extension of our clients. To achieve this, Anacura has been designed as an open-door workplace, where our staff are encouraged to work as a team to continuously improve and grow, and to actively contribute to the company’s objectives.
Role
- As a QA Officer, you and your colleagues serve as the primary point of contact for medical laboratory staff regarding quality matters.
- You help maintain, implement, and improve the quality system within the lab in accordance with applicable quality guidelines and regulations (ISO 15189, clinical biology practice guidelines).
- You monitor the management of quality documents in the electronic system.
- You provide support in documenting and investigating quality deviations, complaints, and changes, as well as in initiating corrective and preventive actions, and you monitor their progress.
- In addition, you conduct reviews of method validation and other documents, as well as the associated raw data.
- You will conduct internal audits throughout the entire process and report on them to ensure the quality of the analyses and services. You will also assist the QA Manager in preparing for, organizing, and overseeing external audits.
- You will provide QA training to (new) lab staff and raise their awareness of quality-conscious practices.
- Finally, you’ll have the opportunity to actively collaborate on a project basis with the lab and other departments within the organization from within the Quality Department, with the goal of continuously improving the quality of our services. In this role, you'll support the management and optimization of the eQMS by monitoring existing processes and workflows, as well as setting up and digitizing new ones. You'll assist colleagues in using the system and continuously seek ways to make processes more efficient and user-friendly.
- You will work at least 80% of full-time hours and report to the QA Manager.
Profile
- You hold a master’s degree—or have equivalent experience—in a scientific field and have prior experience in a quality assurance department or are familiar with the day-to-day operations of a (preferably medical) laboratory.
- Your colleagues know you as a true team player who enjoys collaborating and communicates constructively.
- You work analytically, systematically, and meticulously, with an eye for detail. You value quality but never lose sight of practical feasibility, and you always seek pragmatic solutions.
- You work independently, take responsibility, and enjoy bringing structure to processes and documentation. In addition, you are curious, eager to continue learning, and actively seek opportunities to continuously improve processes and results.
- You have an excellent command of Dutch.
Offer
- You will be part of the anacura group, a family owned, long term focused and ambitious laboratory organization.
- You will join a dynamic team and have a position with autonomy and responsibility with opportunities to take initiatives to support further growth.
- You will be offered a competitive salary with fringe benefits, a green work environment and the possibility to join our bike lease program, flexible working hours, a healthy lunch, and a pleasant fun club.
- You are stimulated in your personal growth; we build on your talents in accordance with our ambitions.
Interested?
Please send us your CV and a compelling cover letter via jobs@anacura.com. We will handle your application with care and in strict confidence. The recruiter for this role is Marthe Vereecke. For further information, please contact her on 09/257 15 07.
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