Compliance Coordinator, QA
KLIFO is a leading provider of Clinical Trial Supply (CTS) chain services to the international bio-pharma industry.
This is an exiting time to join our company. KLIFO moved our CTS business to a new 6.500 sq. m state-of-the-art facility located near the capital area in Denmark, expanding our team, our capacity and our range of services.
To help support our growth, KLIFO is strengthening our Quality Assurance Team.
Become part of an experienced and dedicated team.
KLIFO Quality Assurance helps manage and ensure the correct level of quality and integrity in the CTS and QA services. KLIFO provides you with the unique combination of interesting and challenging tasks related to our own CTS site in Brøndby and Senior QA specialist services for pharmaceutical clients.
You will be joining an experienced QA team of 11 highly specialised experts. We take pride in tailoring our solutions to suit each individual client. We provide practical consulting and operational services related to GMP, GDP, GCP, GLP and GVP to ensure that client projects can fulfil the complex regulatory requirements.
In the role as Compliance Coordinator, you’ll contribute to our growth with:
- Administration, Quality oversight and management of KLIFO’s Quality Management System in general and within QA
- Support in writing and updating of SOPs within the quality area
- Evaluation and approval of incoming goods
- Participate in the supplier management program
- Approval of quality related documents from GMP areas such as SOPs, Changes, Deviations, Complaints and CAPAs
- Occasionally assist with review of packaging batch documentation
Your Background and Qualifications
You possess a collaborative mindset and work in a structured way with an eye for detail. You enjoy working independently and conscientiously, and you are not afraid of taking responsibility. You are eager to share your knowledge, and thrive in a client focused and supportive role. You are diplomatic and accommodating, and you are able to motivate and communicate your points of view.
Furthermore:
- Preferably you are a pharmaconomist or laboratory technician with +5 years QA experience
- Have +5 years of experience within the pharmaceutical industry
- Possess solid experience with GxP QA work and QMS maintenance within a pharmaceutical company
- Experience with Veeva Vault Quality Docs
- Are used to work in both English and Danish, written and spoken
Why Join KLIFO?
- Join an organization where we value people and their expertise as the greatest asset
- Enter a flexible workplace with a culture based on trust, transparency and respect
- Work with some of the most experienced and dedicated colleagues in the life-sciences industry
- Contribute with your expertise across different therapeutic areas
- Develop tailor-made solutions based on cross-disciplinary collaboration
- Cultivate successful relationships with our clients
- Be part of an organization that sees knowledge-sharing as the road to success
Share Your Application
Share your application with us at job@klifo.com marked QA Compliance Coordinator, no later than 17th of April 2026. Kindly state how you heard about this position. Interviews will be carried out continuously.
If you have questions about the position, please reach out to Senior Director Erik Zobel at erik.zobel@klifo.com or 44 778 759 for more information.
KLIFO processes your application and all related personal data exclusively for the specific hiring process. Your data is processed as confidential information, cf. the current data protection law (GDPR).
For information on KLIFO’s processing of personal information see:
https://klifo.com/privacy-policy/
