Compliance Coordinator


KLIFO is looking for a Compliance Coordinator for our Glostrup office

KLIFO wants to engage a Compliance Coordinator into a dynamic and experienced team within Clinical Trial Supply (CTS) and the area of Business Support.

KLIFO is a service provider of drug and device development competences and operational services to the pharmaceutical, biotech and med-tech companies in Europe, US and Asia. The areas covered by KLIFO include Clinical Operations Solutions, Pharmacovigilance Solutions, Clinical Trial Supply Solutions, Regulatory Affairs Solutions, QA Solutions, CMC Development Solutions and Drug Development Counselling.

The position as Compliance Coordinator:

  • Lead/facilitate compliance processes and engages with crossfunctional to ensure execution and completion
  • Develop guidance information, policies, procedures and process training
  • Quality management, Deviations, Complaints, Change Requests and CAPAs
  • Perform Risk Assessments/Root cause analysis in cooperation with the responsible department
  • QAP follow up and execution.
  • Participating in process improvement initiatives
  • Participate in all aspects of authority inspections

You will have daily interaction with all functions in the CTS area, and Quality department in KLIFO A/S.

The qualifications of the Compliance Coordinator:

In order for you to be a success in your new position you should possess

  • Experience within GMP and GDP
  • Have a systematic problem-solving approach
  • Good sense for details and have a natural curiosity
  • Quality mindset
  • Good communication skills in Danish and English
  • Experience in MS Office
  • Experience with Veeva Vault (is an advantage)
  • Experience in handling of deviations, change controls and complaints
  • A background from Pharma, Life Science or similar

Personally you are

  • Cooperative, and great at creating relations
  • Skilled within project management
  • Structured
  • Responsible

We offer:

A position in Business Support, with great opportunity to further develop and set the agenda for support in the CTS organisation.

The right candidate will be welcomed by a team of highly skilled colleagues and a business unit with a variety of daily tasks.

The team has an informal working environment, with respect for each other.

The chance to join a dynamic company, with a flat organization structure.

A company with a clear direction of being an international drug and device development consultancy, enabling clients to maximise their opportunities in each projects.

Location:

KLIFO has offices in both Denmark, Germany, Sweden and The Netherlands. This position is located at our headoffice in Glostrup, Denmark. 

Contact:

For more information, please contact Jørgen Rigtrup, Director CTS Business Support +45 44778 757 or Christina Vinum CTS Vice President+45 44 222 960.

Applications should be sent to:

moc.ofilk@boj, marked Compliance Coordinator. 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). 

Deadline

31 October 2022

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