Fantastic opportunity has arisen to join a world-leading pharmaceutical testing CRO.
We are looking for an enthusiastic Equipment Compliance Specialist with a broad knowledge of analytical chemistry equipment.
In this role, you will be responsible for: Checking instrument calibration & service data for multiple GMP analytical equipment (HPLC, dissolution, Karl Fischer, etc.) Updating & writing SOPs Supporting internal audits Liaising closely with analysts & team leaders to ensure GMP standards are adhered to Authorising quality documents (Installation Qualification (IQ), Performance Qualification (PQ), Operational Qualification (OQ)) Qualifications/Skills/Experience: Degree in Chemistry or related subject Pharmaceutical analysis experience in a GMP environment Strong knowledge of various analytical chemistry techniques and instrumentation Qualification and validation of analytical equipment is a plus! Strong communication and organisation skills If this role sounds like the right opportunity for you, apply today to be considered!
Keywords:
Pharmaceutical, Biopharmaceutical, API, Drug Product, Intermediate, GMP, cGMP, Good Manufacturing Practice, HPLC, UPLC, high performance liquid chromatography, LC, LCMS, LC-MS, GC, gas chromatography, Analytical Chemistry, analyst, SOP, documentation, validation, qualification, IQ, PQ, OQ, Wirral, Liverpool, Moreton, Cheshire, Manchester, North West, Ellesmere Port, Runcorn, Chester, Crewe, VRS8911MF
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Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
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We are looking for an enthusiastic Equipment Compliance Specialist with a broad knowledge of analytical chemistry equipment.
In this role, you will be responsible for: Checking instrument calibration & service data for multiple GMP analytical equipment (HPLC, dissolution, Karl Fischer, etc.) Updating & writing SOPs Supporting internal audits Liaising closely with analysts & team leaders to ensure GMP standards are adhered to Authorising quality documents (Installation Qualification (IQ), Performance Qualification (PQ), Operational Qualification (OQ)) Qualifications/Skills/Experience: Degree in Chemistry or related subject Pharmaceutical analysis experience in a GMP environment Strong knowledge of various analytical chemistry techniques and instrumentation Qualification and validation of analytical equipment is a plus! Strong communication and organisation skills If this role sounds like the right opportunity for you, apply today to be considered!
Keywords:
Pharmaceutical, Biopharmaceutical, API, Drug Product, Intermediate, GMP, cGMP, Good Manufacturing Practice, HPLC, UPLC, high performance liquid chromatography, LC, LCMS, LC-MS, GC, gas chromatography, Analytical Chemistry, analyst, SOP, documentation, validation, qualification, IQ, PQ, OQ, Wirral, Liverpool, Moreton, Cheshire, Manchester, North West, Ellesmere Port, Runcorn, Chester, Crewe, VRS8911MF
Follow VRS Recruitment on LinkedIn to view all our latest vacancies!
Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
#J-18808-Ljbffr
