GMP Laboratory Technician Role

About the role ESP Medical is seeking a GMP Laboratory Technologist to join our dynamic team. This is a hands‑on role involving the testing of raw materials and finished products in the laboratory whilst supporting GMP‑compliance across the wider business. We are seeking an experienced, enthusiastic individual with a strong background in GMP‑compliant analytical testing and laboratory operations. The successful candidate will have a demonstrated ability to operate complex laboratory instruments, undertake GMP‑compliant analysis and laboratory operations, and support lot and batch release from production. A strong preference will be given to candidates with a demonstrated ability independently troubleshoot and problem‑solve analytical and quality issues in a GMP‑compliant manner. Key responsibilities Perform scheduled testing of raw materials and finished products in accordance with approved laboratory procedures and GMP requirements. Operate analytical instruments, including HPLC, GC, and UV spectrophotometers. Prepare reagents, standards, and test solutions required for analysis. Ensure analytical results are accurate, reliable, and completed within required timelines. Support routine operations and procedures required to maintain GMP compliance, including: Environmental monitoring Inventory management Maintenance and calibration Ensure both the laboratory environment is clean, organized, and GMP‑compliant. GMP Responsibilities Accurately document laboratory activities and analytical results in accordance with GMP documentation practices. Identify, report, and assist in the investigation and reporting of Out-Of-Specification (OOS) results, Non-Conformances (NCR), and deviations. Investigate, troubleshoot, and problem‑solve to resolve analytical and quality issues in conjunction with the preparation and review of GMP‑compliant records and reports of these activities. Prepare and complete the documentation required to ensure GMP‑compliance, including: Standard operating procedures (SOPs) Laboratory testing records and results reports Inventory control records Maintenance and calibration records Inwards Goods Quality Control (IGQC) records QMS records such as schedules, change controls, deviations, and supplier evaluations. Manage inventories of laboratory and production materials (e.g., consumables, reagents, standards, production raw materials) and maintain the associated records. Support and maintain any other QMS‑related activities and processes required to maintain certification to and compliance with Regulatory Standards (e.g., ACVM GMP, ISO 13485), as well as internal and external specifications for results, products, raw materials, and facilities. About you A Bachelors or Masters-level tertiary qualification (or equivalent experience) in Pharmaceutical Science, Chemical or Biochemical Process Engineering, Biochemistry, Chemistry, or a closely related scientific discipline. At least 3 years' practical experience in a laboratory environment certified to ACVM GMP (or more a stringent GMP standard) or ISO 17025. Sound experience with the execution and troubleshooting of analytical techniques, GC, HPLC, and UV spectroscopy. A preference will be given to candidates with strong GC experience. A sound understanding of GMP documentation and laboratory compliance requirements. Excellent attention to detail and strong organizational skills. The ability to work independently and as part of a collaborative team in a fast‑paced environment. A willingness to work flexible or extended hours when required to meet testing or regulatory priorities. A proactive attitude and a strong willingness to learn and develop. #J-18808-Ljbffr