16/05/2024 | Fulltime | | United Kingdom | CV-LibraryLarge scale projects within a pharmaceutical setting, to train and mentor existing staff. Delivering engineering and facility related projects whilst ensuring resource, cost management and timely completion are achieved, whilst meeting all regulatory and GMP requirements will also be your responsibility
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-Library | €40,000 - €50,000 / Year The audit function and supporting with supplier evaluation Requirements Experience working on a Chemical site Trained auditor to ISO and GMP Knowledge of QC principles Experience in a H&S role Extensive knowledge of Chemical RegulationsIf you would like to apply for this position, please use the link
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-Library | €33,000 / Year In ensuring the integrity, safety, and functionality of the site's infrastructure, including office environments, laboratories, and GMP production lines. Their primary responsibility is to oversee the maintenance, repair, and improvement of building fabrics to uphold regulatory compliance and operational
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-LibraryOf a willing mentee. You will be responsible for project planning, resource and cost management and progress reporting. Your background - experience gained within the pharmaceutical industry - experience of ensuring compliance with all EHS and GMP requirements - experience of writing SOP's - formal engineering
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-Library | €40,000 - €50,000 / Year Will include - Support with verification and validation activities to support global regulatory requirements. - Assist the quality and regulatory team in preparation of documents for the Global IVD regulations. - Maintenance of international quality certifications to ensure compliance (ISO13485, ISO17025, GMP
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-Library | €30,000 / Year Certifications including ISO 9001, ISO 45001, ISO 14001, ISO 50001, IATF 16949, AS 9100D & GMP Ability to host and support 2nd and 3rd party audits/inspections overall management systems Supporting departmental managers in the creation and maintenance of process definitions and work instructions Completing
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-Library | €13 / Hour Manufactured meet - exceed quality standards. - Allergen Control - GMP - Completing checks to ensure accuracy of labels and weights of finished products, and ensuring seals on finished articles are satisfactory - Supporting and training members of your team - Completing traceability and production paperwork
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-LibraryAssisting the factory in the preparation and delivery of successful Third-party audits including BRCGS - Ensuring the Quality Management System is fully implemented - Continuously improving factory standards and finished product quality with regards GMP and Hygiene, maintaining and updating procedures
Save for later16/05/2024 | Fulltime | | United Kingdom | CV-LibraryAs leading contractual negotiations in conjunction with the Senior Leadership Team. Requirements - Previous experience of multi-site operation. - Previous knowledge of contract models, eg. Cost plus, fixed price, shared savings, GMP, etc. - Experience of assisting with the development and management
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