KLIFO A/S
Vigtige datoer:
Oprettet:22. februar 2026
Ansøgningsfrist:15. marts 2026
Virksomheden tilbyder
Fast ansættelse
Fuldtid
Kontakt person
Arbejdsgiver
KLIFO A/S
Danmark
Annoncen er hentet fra Jobnet
Annonce ID
E10947048
Senior QA Specialist, Supplier Management - Klifo
Senior QA Specialist, Supplier Management - Klifo 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. Deadline for Application | 15th March 2026 Location Brøndby, Denmark Employment Full time 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, you will contribute to our growth 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 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 with the title being Business Development Manager, no later than 16th of March 2026. Interviews will be carried out continuously throughout the process. If you have questions about the position, please reach out to Martin Lamb, Senior Business Development Director, CTS at martin.lamb@klifo.com or +44 7361 862 684 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/ About KLIFO At KLIFO, passion and professionalism define our culture. With years of dedication to their fields, our teams take pride in finding effective solutions and bringing that mindset into every client partnership. Each project is unique, and we tailor our work to deliver compliant, cost-effective solutions that meet specific needs. Together, the four values to the right side define how we work — and how we create results for our clients. KLIFO 130+ employees. Offices in Denmark and Sweden. Headquartered in Glostrup, Denmark. Clinical Trial Supply When running a Clinical Trial Supply, every detail matters. Reliable delivery of Clinical Trial supplies (CTS) is critical to Clinical Trial Supply success. At KLIFO, we combine strategic insight with operational excellence to manage your clinical supply chain end-to-end ensuring you deliver for your sites, your patients, and within your budget. Advisory KLIFO Advisory provides experienced guidance from early drug development to market. We combine deep scientific insight with hands-on know-how, helping you navigate complex decisions with confidence. Get in touch with us We understand that every project is unique. Our experts are available to provide tailored support — from early development to post-market activities as well as world class clinical trial supply. Departments Advisory CTS Sitemap About News Career Contact KLIFO A/S Smedeland 36 2600 Glostrup Denmark KLIFO A/S - Clinical Trial Supply Abildager 24 2605 Brøndby Denmark info@klifo.com +45 44 222 900 Emergency contacts GMP QP: Jens Harry Jespersen +45 48 80 55 78 Christina Vinum: +45 20 99 95 68 © Copyright KLIFO. All Rights Reserved. Contact us We’re always ready to answer your questions We understand that every project is unique. Our experts are available to provide tailored support — from early development to post-market activities. Write to us write to us We’re always ready to answer your questions We understand that every project is unique. Our experts are available to provide tailored support — from early development to post-market activities. Book a meeting Book a meeting Book a meeting Notifications
