QC Instrumentation Specialist

What are we looking for in our QC Instrumentation Specialist?

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.

About the Role: As a QC Instrumentation Specialist, you will play a vital role in managing laboratory instrumentation purchase, installation, qualification, and lifecycle management. Reporting to the QC Instrumentation Team Lead, you will oversee the calibration and maintenance of laboratory instruments, ensuring their accuracy and reliability for quality control processes.

Key Responsibilities:

• Provide calibration and maintenance services to the QC laboratory, including instrument calibrations, maintenance scheduling, and lifecycle management.
• Review and approve analytical instrumentation qualification, calibration, repairs, and documentation.
• Manage instrument-specific investigations such as calibration deviations and trend instrument performance.
• Participate in new instrument purchase and qualification, collaborating with QC Specialists, QA validation Specialists, and Computer System Validation personnel.
• Liaise with sister sites and vendors on instrumentation purchase, qualification, and lifecycle management.
• Ensure compliance with corporate policies, directives, and regulatory requirements for instrument qualification, calibration, and lifecycle management.
• Participate in the definition and establishment of instrument-related procedures and troubleshoot complex instrumentation issues.

Requirements:

• Bachelor's degree in a scientific discipline.
• Minimum of 3 years of experience, with at least 1 year related to instrument qualification in a GMP laboratory setting.
• Previous experience in technology transfers is advantageous.
• Strong teamwork, communication, time management, and organizational skills.
• Understanding of Data Integrity management (21 CFR 11/EU Annex 11) is desired.
• Fundamental understanding of protein biochemistry and technical expertise in biopharmaceutical analytical platforms.

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.

Interested?

Please click on APPLY today.

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