Compliance Coordinator, QA

KLIFO is a leading drug development consultancy with significant experience in partnering with biotech and pharmaceutical companies to advance their drug development project. KLIFO provides consultancy and operational solutions within all areas of clinical research, clinical trial supply, regulatory affairs, pharmacovigilance, CMC Development, QA and development of pharmaceutical and biotech products and medical devices
We want to engage a person with a positive, proactive, flexible and self-confident personality, who would like to work in a consulting environment.

The Compliance Coordinator, QA will be responsible for:

  • Administration, Quality oversight and management of KLIFO’s QA Management System
  • Responsible for maintaining an archiving system
  • SOP updates and writing of new SOPs within the quality area
  • Approval of quality related documents from GMP areas as SOPs, Deviations, Complaints and CAPAs
  • For the right person there will be opportunity in this position to become a Delegate Qualified Person and to be trained and qualified as GMP auditor

The Compliance coordinator, QA must have a academic background and some experience from working with medicinal products. You must be service minded and fond of systems and organization. You must be used to communicating in English

We offer:

  • GXP compliant quality system and production
  • Variation in the job
  • Diverse client pool (pharmaceutical companies, established biotech, inexperienced, virtual biotech,
  • Opportunity to utilize many pharmaceutical competences
  • An interactive, open and positive working environment
  • High level of transparency – and influence
  • Room for individual planning

The position is new and there will be possibilities influence the job content so it will fit the experience of the selected person.

For information about the position you can contact Director, QA – Anne Ploug Jørgensen +45 44 222 982



Applications for the job must be send to; moc.ofilk@boj



February 18, 2019.