Analytical QC Technology Transfer Specialist

LSC, Life Science Consultants; Munster; On-site; EUR 65,000 - 90,000; Full time

Job summary

Life Science Consultants in Ireland seeks an Analytical QC Technology Transfer Specialist to lead method transfer and verification with QC teams. You will coordinate with sending-site functions to secure packages, standards and data, while planning transfer timelines and supporting investigations into discrepancies.

The role requires 4+ years in a GMP QC/analytical setting and solid knowledge of validation/transfer principles (ICH Q2) and GMP documentation.

Qualifications

• Minimum 4+ years of experience in a QC/analytical role within a GMP pharmaceutical environment.
• Proven experience with analytical method transfer or verification processes.
• Working knowledge of analytical method validation/transfer principles (e.g., ICH Q2) and GMP documentation standards.

Responsibilities

• Own the analytical method transfer and verification protocols, coordinating directly with QC teams.
• Interface with sending-site analytical/QC functions to secure method packages, reference standards, and comparator data.
• Plan and track analytical transfer schedules in sync with overall process transfer timelines.
• Support investigations into analytical discrepancies encountered during method transfer or verification.
• Contribute analytical risk insights to overall product transfer risk assessments such as FMEA.

Skills

Analytical method transfer

GMP documentation

ICH Q2

Education

Degree in chemistry/biochemistry/pharmaceutical sciences

Tools

Analytical transfer trackers

Job description

Analytical QC Technology Transfer Specialist
Join us in shaping the future of pharmaceutical innovation as an Analytical QC Technology Transfer Specialist. This pivotal role offers a unique opportunity to lead and manage the analytical dimensions of product transfers, ensuring seamless method transfer and verification processes that uphold the highest quality standards. If you're passionate about advancing pharmaceutical sciences and thrive in a dynamic, collaborative environment, this is your chance to make a meaningful impact.
What You'll Do:

• Own the analytical method transfer and verification protocols, coordinating directly with QC teams.
• Interface with sending-site analytical/QC functions to secure method packages, reference standards, and comparator data.
• Plan and track analytical transfer schedules in sync with overall process transfer timelines.
• Support investigations into analytical discrepancies encountered during method transfer or verification.
• Contribute analytical risk insights to overall product transfer risk assessments such as FMEA.

Key Skills & Qualifications:

• Minimum 4+ years of experience in a QC/analytical role within a GMP pharmaceutical environment.
• Proven experience with analytical method transfer or verification processes.
• Working knowledge of analytical method validation/transfer principles (e.g., ICH Q2) and GMP documentation standards.
• Degree in chemistry, biochemistry, pharmaceutical sciences, or a related discipline.

Preferred Education & Experience:

• Direct experience managing analytical technology transfer trackers or leading method transfers for sterile injectables.
• Familiarity with analytical techniques like sterility testing, endotoxin, particulate matter, and container-closure integrity.
• Experience working with technical transfer teams such as Tech Transfer/NPI, Regulatory Affairs, and QC/Analytical.

Are you currently eligible to work in Ireland? As this is a contract opportunity, you will need to hold a Stamp 1G or Stamp 4 visa to apply. Apply via this advert or contact Siobhan Cummins on 021 4777329 if you have any questions about this role. Find out more about working with LSC at lscconnect.com