CVP QMS Partner - CMC Development

Category: Project Management & Agile

Location:Måløv, Capital Region of Denmark, DK

• Ensuring high-level GMP overview and report quality trends to management.

• Driving preparation for, participate in and follow-up on authority inspections and internal audits

• Responsible for the Quality Management Review (QMR).

• Supporting daily operations and ensure the relevant level of GMP and training

• Be the go-to person on quality subjects; you actively identify and drive quality improvement initiatives, and support as needed by applying systematic problem-solving, process mapping, or other LEAN methodologies
  
  

• Master's degree in pharmacy, biochemistry, production engineering or similar

• At least 5 years of GMP experience from the pharmaceutical industry (manufacturing/QC/QA)

• Strong understanding of GMP regulations and requirements

• Excellent communication and interpersonal skills

• Ability to work independently with a pragmatic mindset

• Experience with project management

• Preferably c LEAN certified

• Ability to manage multiple projects and priorities

• Full professional proficiency English, Danish is an advantage, but not required.