Analytical QC Technology Transfer Specialist

LSC, Life Science Consultants; Munster; On-site; EUR 60,000 - 90,000; Full time

Job summary

LSC, Life Science Consultants in Ireland invites a seasoned Analytical QC Technology Transfer Specialist to lead method transfer and verification within GMP pharmaceutical environments. You will coordinate analytical aspects of product transfers, ensuring robust transfer packages and compliant documentation.

The role requires strong experience in QC/analytical operations, exposure to ICH Q2, and collaboration with Tech Transfer, Regulatory Affairs, and QC teams.

Qualifications

• 4+ years in a QC/analytical role within a GMP pharmaceutical environment.
• Experience with analytical method transfer or verification processes.
• Knowledge of analytical method validation/transfer principles (ICH Q2) and GMP documentation.

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

QC/Analytical experience

Method transfer

ICH Q2 knowledge

GMP documentation

Education

Chemistry/Pharmaceutical degree

Tools

Sterility testing

Endotoxin testing

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.