We are hiring an Analyst for a company in the pharmaceutical industry.Responsibilities:Organize and define daily priorities within assigned tasks to accurately and promptly perform allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs.Adhere to the laboratory testing schedule to achieve an efficient Quality Control (QC) system.Take responsibility for all data individually generated and ensure compliance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities.Maintain all checklists, laboratory records, and notebooks to an acceptable GMP standard and in accordance with company internal procedures.Maintain good hygiene and housekeeping within the laboratory.Perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required.Comply with high standards in the QC Laboratories.Report any discrepancies, deviations, or non-conformance in testing or work practice to QC management in accordance with internal procedures.Issue events and support the investigation of OOS/OOT/atypical results, deviations, and QC incidents generated in the QC Laboratories.Ensure appropriate communication with other internal departments regarding QC work by using the appropriate company processes and IT platforms.Assist with audits as required, following the instructions of QC Management.Undertake any additional tasks to support laboratory activities as needed.Seek out additional information when available information is insufficient.Follow all annual performance review requirements, including completion of the self-assessment.Carry out assigned tasks in a safe manner, complying with environmental, health & safety rules, procedures, regulations, and codes of practice.Ensure facility activities comply with all GMP, legal, and HSE regulations and applicable standards in the country of operation.Qualifications:Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related, or other science-related field (mandatory).Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory).Experience of GMP practices and HSE standards (preferable).Technical understanding of GMP practices, analytical theory, and techniques.Clear and open communication skills (written and verbal).Competent (written and verbal) English (preferable for sites where English is not the first language).Ability and availability to work in shift patterns as required by business needs.Computer literate with knowledge of the MS Office package.Must have the knowledge, experience, and skills to conduct tasks in accordance with established rules and procedures.
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