Interim QA Coordinator

Main tasks and responsibilities:

• Assist with regulatory authority inspections/internal or external audits by providing administrative support
• Assist in preparing and conducting liaison meetings
• Manage QA intranet page
• Organize and attend drop-in sessions to support colleagues
• Management of procedures and ensuring they are up to date
• Manage QA general email inbox
• Create training materials as relevant
• Support IT staff with their quality-related tasks
• Responsible for QMS (QMapp and Veeva)
• Plan and prepare for Quality Management System (QMS) quarterly workshops
• Manage QA's documentary records (electronic and physical), e.g., qualification plans
• Prepare the Quality Management Review report/presentation
• Responsible for Physical Archive
• Take part in onboarding/offboarding
• Ensure the training matrix is updated
• Assist Line and Quality Managers with the planning and organizing of GxP Training

To be eligible for the role:

• Education in Life Sciences or similar
• Experience from the pharmaceutical/biotech/medtech industry
• Experience with Quality Assurance and systems such as QMapp and Veeva
• Speaking and writing Swedish and English fluently
• Good communicator and team player with a systematic approach

About the process:

The assignment starts as soon as possible and is expected to last for about 6 months at 100% FTE. The policy for working in the office/remotely is approximately 60/40.

We are presenting candidates to the client on Tuesday, September 17, and interviews will be held the following day.

Are you available and have the right profile? Apply today!

The recruiter responsible for this role is Lena Arrelöv, who collaborates with researcher Hedda Tornert.