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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.
Job Responsibility:
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
Requirements:
Pharmaconomist or laboratory technician with +5 years QA experience
+5 years of experience within the pharmaceutical industry
Solid experience with GxP QA work and QMS maintenance within a pharmaceutical company
Experience with Veeva Vault Quality Docs
Used to work in both English and Danish, written and spoken
What we offer:
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