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SK pharmteco are seeking to recruit a Quality Control Instrumental Specialist to join the QC Department based in Swords, Co. Dublin on a permanent basis.
About the company?
SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France, and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion. Our mission is to ‘produce and deliver life-changing therapies that improve patient outcomes and save lives’. The SK pharmteco Small Molecule, Europe, facility located in Swords, Co Dublin, Ireland has led the way in the development, scale-up, and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities, and facilities, we have made some of the world’s most important medicines and continue to do so. Further information on SK pharmteco can be found at
Current Need:
The QC department is seeking to recruit a Quality Instrumental Specialist. This position is within the Instrumentation group in the QC Department.
Position Description:
Reporting to the QC Team Lead, the successful candidate will manage and control the laboratory instrumentation calibration and unplanned maintenance programme for the QC department. Responsibilities include:
* Liaising with Agilent to coordinate the calibration schedule
* Reviewing all Laboratory Calibration/Qualification documentation
* Reviewing all equipment unplanned maintenance reports
* Managing changes to instruments, instrument relocations, and decommissioning of instruments
* Troubleshooting laboratory equipment
* Managing the purchase of new instruments and related installation and operation qualification reports
* Managing laboratory instrument change controls
* Developing new procedures and ensuring equipment procedures are up to date
* Conducting all instrumentation calibration investigations
* Supporting the implementation and qualification of analytical instruments, and their routine/periodic maintenance
* Ensuring GMP compliance of laboratory operations and documentation
* Managing equipment supplier relations for new equipment and software used in the laboratory
* Fostering a culture of growth, enablement, and high performance
Qualifications and Experience:
* A BSc in Analytical Science, Chemistry, or a related discipline is required
* A minimum of 3 years’ experience in the pharmaceutical industry is required
* Knowledge of quality control operations
* Experience with regulatory agency audits and understanding of laboratory GMPs, FDA regulations, and their application to API manufacturing
* Experience in Equipment Validation and change control procedures is desirable
* Strong ability to manage workload, prioritize tasks, and meet timelines for calibrations, maintenance, and testing
* Excellent teamwork skills and motivation
Other Benefits:
* Opportunities for career growth and personal development
* Annual bonus linked to business results
* Comprehensive further education programs
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