Senior QA Specialist, Supplier Management
KLIFO is a leading provider of Clinical Trial Supply (CTS) chain services to the international biopharma industry.
This is an exciting 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 Senior QA Specialist, Supplier Management you’ll contribute by:
Ensuring that our suppliers are in a state of control and you will be the QA Subject Matter Expert on Supplier Management which includes:
- Development and maintenance of the Supplier Management Program
- Qualification, assessment and evaluation of suppliers
- Perform supplier audits
- Auditing of a wide variety of project/clients suppliers/manufacturers/vendors.
- Some travelling must be expected
- Write up and maintain Quality Agreements for our suppliers
- Approval of quality related documents
- QA handling of Supplier Complaints
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 accomodating, and you are able to motivate and communicate your points of view.
Furthermore, you have:
- Experience as Lead Auditor
- Experience with Supplier Management
- +5 years’ experience from the Biopharmaceutical industry or similar
- Experiences with interpretation of global cGMP rules concerning manufacturing and quality assurance of biopharmaceutical products and API
- Relevant academic background within pharmacy, biotechnology or similar
- Experience working in both English and Danish, written and spoken
Why join KLIFO?
- Join an organisation 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-science 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 organisation that sees knowledge-sharing as the road to success
Share your application
Share your application with us at job@klifo.com marked Senior QA Specialist, Supplier Management no later than 15th March 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/disclaimer-privacy-policy/.
