QC Method Transfer Project Manager

QCS Staffing Ltd; København; On-site; DKK 800,000 - 1,200,000; Full time

Job summary

QC Method Transfer Project Manager in Denmark for an initial 8-month contract within the Life Sciences sector. Lead analytical method transfers, focusing on bioassays, and act as PM and primary liaison for internal transfers.

Coordinate across functions, plan meetings, track milestones, and manage lab capacity with local PM and teams. Strong cGMP, ICH knowledge and hands-on transfer experience required.

Qualifications

• Strong scientific background with hands-on experience in analytical method transfer and validation.
• Ideally strong knowledge of bioassays.
• Previous QC laboratory experience within a cGMP environment.
• Good understanding of ICH guidelines.
• Strong project management/project coordination experience.

Responsibilities

• Lead the analytical tech transfer of methods, particularly bioassays, between client facilities.
• Act as the Project Manager and primary liaison for internal analytical method transfers.
• Coordinate activities across functional, tactical and operational levels.
• Plan and facilitate project meetings and track key milestones/progress.
• Coordinate laboratory capacity, resources and timelines with the local PM and wider teams.

Skills

Project management

Bioassays

cGMP

ICH guidelines

Analytical method transfer

Job description

QC Method Transfer Project Manager - Denmark - Initial 8-Month Contract - Life Sciences

Our client, a global organisation within the pharmaceutical sector, is seeking an experienced QC Method Transfer Project Manager to support the delivery of their large-scale CAPEX project based in Denmark. This is an initial 8-month contract offering the opportunity to contribute to a high-impact life sciences programme.

What You'll Deliver

• Lead the analytical tech transfer of methods, particularly bioassays, between client facilities.
• Act as the Project Manager and primary liaison for internal analytical method transfers.
• Coordinate activities across functional, tactical and operational levels.
• Plan and facilitate project meetings and track key milestones/progress.
• Coordinate laboratory capacity, resources and timelines with the local PM and wider teams.

Experience required:

• Strong scientific background with hands-on experience in analytical method transfer and validation.
• Ideally strong knowledge of bioassays.
• Previous QC laboratory experience within a cGMP environment.
• Good understanding of ICH guidelines.
• Strong project management/project coordination experience.

Don't miss your chance to be part of something extraordinary, and let's talk!