Healthcare Instrumentation Specialist

Exciting Career Opportunity Alert! 🔬 Looking for a QC Instrumentation Specialist in Dublin 15 - 12 months contract

Russell Tobin is proud to partner with a leading global biologics manufacturer dedicated to enhancing the health and well-being of patients and staff. Renowned for its commitment to excellence, this company is at the forefront of driving positive change in its daily operations.

We are seeking a QC Instrumentation Specialist to execute Laboratory Instrumentation Purchase, Installation, Qualification and Lifecycle management. Reporting to the QC Instrumentation Team Lead, the specialist will manage the purchase and qualification of laboratory instruments and will be responsible for providing an Instrument Calibration and Maintenance service to the QC laboratory teams.

The candidate must have strong experience in all aspects of instrument management in a GMP environment, in addition to an understanding of the needs and best practices of routine biopharmaceutical drug product and drug substance laboratories. They will have responsibility for establishment of project plans and instrument qualification procedures.

The main responsibilities for this position include;

• Providing a Calibration and/or Maintenance Service to the QC laboratory that includes instrumentation calibrations, scheduling and tracking of instrument maintenance and instrument lifecycle management.

• Review and approve analytical instrumentation qualification, calibration, repairs and documentation.

• Ensure instrument maintenance and verification is appropriate to the use of the instrument

• Manage all instrument specific investigations such as calibration deviations

• Trend lab instrument performance and lifecycle management.

• Participate in new instrument purchase and qualification

• Participate as part of a team of QC Specialists, QA validation Specialists and Computer System Validation personnel to deliver on the qualification of new instruments.

• Liaise with sister sites and vendors on instrumentation purchase, qualification and lifecycle management.

• Ensure compliance with corporate policies, directives and current regulatory requirements for laboratory instrument qualification, calibration and lifecycle management.

• Participate in definition and establishment of instrument related procedures.

• Participate in troubleshooting complex instrumentation issues.

Requirements:

The ideal candidate should hold a minimum of a B.Sc. in scientific related discipline and must have at least 3 years’ experience, at least 1 of which should be related to instrument qualification experience in a GMP laboratory setting.

Previous experience in technology transfers would be advantageous.

The successful candidate must demonstrate the ability to contribute to and lead in a team-based collaborative environment, as well as the ability to prioritise objectives from multiple projects.

The successful candidate must demonstrate time management and organisational skills and excellent communication is essential.

A strong fundamental understanding of protein biochemistry is desirable, in addition to technical expertise in the following Biopharmaceutical analytical platforms (HPLC/UPLC, CE, cIEF, SDS-PAGE, Biacore, HIAC, KF, Liquid Handlers).

Experience in Data Integrity management (21 CFR 11/EU Annex 11) is desired.

What’s on offer:

• 12-month contract with potential for extension.
• Pay rate: €25-30/hour PAYE
• Opportunity to work with a leading global pharmaceutical company dedicated to improving patients' futures.
• You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.

Interested? Apply Now! or tag someone who might be a perfect fit!

If you are passionate about making a difference in the pharmaceutical industry and possess the necessary skills and experience, we want to hear from you! Apply now to join our dynamic team and contribute to meaningful projects that impact lives.