1 to 5 of 5 ISO/IEC 17025 Jobs in the East of England

Principal Analyst, GC / MS Location: Newmarket Type: Permanent Salary: upto £40,000 depending on experience Russell Taylor Group is working with a global testing company who are looking to recruit an experienced Senior Chemist ready to step up into a Principal role or an established PA looking for … laboratory team Respond to client queries in a prompt and professional manner, either directly, or in support of other colleagues To comply with ISO 17025:2017 and MCERTS requirements of your role, and perform any other reasonable duties. To assist others in the performance of their … of the role, and perform any other reasonable duties as required by the business. The Person: Will hold a Degree in a relevant - Scientific / Chemistry based discipline (or higher) 5+ years experience in an analytical - organic testing laboratory working to UKAS 17025 standards GC MS / more »

Key Tasks and Accountabilities Work with the Program / Project Managers and their teams to maintain all aspects of the QMS as we develop our diagnostic capability e.g. Change Controls, Non-Conformities, CAPAs, Customer Complaint Support continuous improvements in the Quality Management System (QMS) and maintain compliance of Quality … work in a dynamic environment Education and Training Degree level qualification within Life Sciences (or equivalent) Trained and competent lead auditor (internal audits) Experience / Knowledge Suitable working knowledge within a Pharmaceutical / Medical Device QA department Working knowledge, within Pharmaceutical / Medical Device business) of … GxP and Quality related regulations and standards Essential: ISO 9001, ISO 13485, GCP, Desirable: ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor (external audits more »

relating to the QMS. - Support Quality department initiatives as part of a multi-disciplinary team. Key Skills and Requirements: - Experience working within a Pharmaceutical / Medical Device Quality Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical / … Medical Device industry. - Familiarity with ISO 9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be beneficial. Interested or know someone who might be? Reach out to ­­­­Ben Godley using the following more »

Requirements: - Proven experience in instrument calibration, preferably in a field service role. - Strong knowledge of calibration techniques, measurement principles, and industry standards (e.g., ISO 17025). - Proficiency in using calibration software and equipment. - Excellent problem-solving skills with the ability to diagnose instrument malfunctions and implement more »

Requirements: - Proven experience in instrument calibration, preferably in a field service role. - Strong knowledge of calibration techniques, measurement principles, and industry standards (e.g., ISO 17025). - Proficiency in using calibration software and equipment. - Excellent problem-solving skills with the ability to diagnose instrument malfunctions and implement more »