Associate Analytical Data Reviewer
3 semanas atrás
We are hiring an Associate Analytical Data Reviewer for a leading company in the pharmaceutical industry. If you have a strong attention to detail and experience in reviewing analytical data, this is your chance to contribute to critical processes in a dynamic and growing sector.
Responsibilities:Responsible for data from chemical analyses such as HPLC, GC, DSC, XRPD, PSD;Rigorously manage, execute and support all assigned projects in accordance with applicable GMP, quality operational standards and legal regulations;Propose new methodologies considering project demands;Execute project specific analytical tasks and act as a stakeholder liaison;Ensure all assigned analytical tasks are well managed and delivered on time, safely, efficiently, reliably, and cost-effectively;Solve analytical problems by providing collaborative and timely support, initiating escalation when necessary;Ensure effective flow of information between the Analytical team and internal/external stakeholders;Review work generated by the team ensuring all procedures are followed;Create, investigate and evaluate CAPAs, incidents, and deviations;Perform equipment maintenance, internal calibrations, and qualifications on designated laboratory instruments;Accurately use and maintain all laboratory information systems;Maintain good hygiene and housekeeping within the laboratory;Maintain all laboratory records, project and general logbooks to an acceptable GLP standard;Fulfill and promote all applicable GMP requirements and HSE regulations;Be an advocate for safe operating and high-quality performance, alerting colleagues to potential risks or discrepancies;Assist with audits/investigations as required;Support the reporting of KPIs for the team;Develop and accumulate strong analytical chemistry expertise;Maintain high standards in the QC Laboratories;Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC);Interpret data and analysis to ensure compliance with strict documentation guidelines;Work collaboratively in cross-functional teams;Execute professional activities in compliance with GMP and HSE guidelines;Carry out assigned tasks in a safe manner, complying with health and safety rules;Minimum Requirements:University or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar field (mandatory);Educational/training experience in a QC laboratory environment;Hands-on experience in Analytical Chemistry and QC procedures (desirable);Training and experience of GMP and ICH guidelines standards (desirable);Knowledge on HPLC and GC, and familiarity with Empower Software (desirable);Technical understanding of GMP practices, analytical theory, and techniques;Documentation skills and attention to detail - Fluency in English is a requirement;Computer literate with good working knowledge of the MS Office package.
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Associate Analytical Data Reviewer
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