Your new company

Your new role

• Lead the planning and execution of analytical method transfers for IPC testing, ensuring adherence to project timelines and objectives.
• Serve as the primary point of contact for all IPC technical transfer activities, liaising between internal analytical teams, manufacturing sites, and external partners.
• Coordinate the development and validation of IPC analytical methods, including protocol design, execution, and documentation.
• Conduct risk assessments and troubleshooting activities to address IPC technical challenges and ensure the successful implementation of analytical methods.
• Generate and review technical documents, including IPC transfer protocols, reports, and standard operating procedures (SOPs), to support IPC method transfer activities.

What you'll need to succeed

• B.A. / B.Sc. or equivalent in Biological Sciences, Chemistry or other biotechnical science or equivalent experience in a regulated industry.
• Minimum of 10 years of laboratory experience in a GMP laboratory environment.
• 5 years of analytical instrument validation/qualification experience preferable.
• Proven leadership of laboratory staff and experience in a GMP laboratory
• Proven ability to work in a matrixed organisation.
• In-depth understanding of current regulatory requirements for IPC or QC, including analytical testing, data integrity, and cGMP laboratory equipment validation.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.