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Guerbet, a leader in medical imaging, seeks an In-Process Quality Control Chemist to support its Dublin manufacturing operations. The role involves utilizing various analytical techniques for quality control, alongside potential training responsibilities within a globally diverse team. A third-level degree in a relevant field is sought, with experience in analytical instrumentation as a bonus.
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At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.
We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years, we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.
Achieve, Cooperate, Care and Innovate are the values that we share and practice on a daily basis.
Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.
For more information on Guerbet, go to www.guerbet.com and follow Guerbet on LinkedIn, Twitter, Instagram and Youtube
Role purpose :The In-Process Quality Control Chemist is responsible but not limited for the provision of analytical support to 24/7 manufacturing operation at Guerbet Dublin. This will involve the use of wide variety of analytical techniques working a Panama Shift pattern (12-hour shifts on a fixed rotation cycle). Additional testing responsibilities shall be assigned, and will include testing of raw materials.
Your responsibilities :
• Perform In-Process control activities to support API manufacturing; such analysis to include chromatographic techniques, equipment control and calibration, peer review
• Perform QC analysis of raw material bulk tankers.
• Record results accurately and interpret correctly.
• Apply all relevant laboratory techniques and methods used to verify manufacturing process control and therefore, product quality.
• Train other QC analysts in laboratory methods and procedures when required.
• Perform all work under cGMP.
• Escalate OOS/OOT results and other non-conformances, and assist with associated investigations.
• Comply with EHS procedures and policies as they apply to the site and laboratory.
• Other work as determined by Site Quality Lead, QC Lead and/or Quality Control Supervisor.
Education Requirements :
• Must have a third level degree qualification in Quality or Science discipline
Experience :
• Previous experience is not essential although 6- 12 months relevant industrial experience is an advantage
• Familiarity with HPLC, GC and other analytical instrumentation is an advantage
• LIMS/Empower experience advantageous
• Good computer skills.
Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to careers@guerbet.com or you can also call this number+19843443717