07/05/2024 | Fulltime | | United Kingdom | CV-LibraryQC Analyst to join a GMP Manufacturing company in the Teeside area As a QC Analyst you will be responsible for testing finished products, raw materials and stability samples using a broad range of analytical techniques in a GMP accredited environment. Key Responsibilities Performing analytical
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 later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | In Ballina, Co. Mayo Reporting to the Immunoassay Supervisor this role shall be responsible for the following Conduct immunoassays in both an R and D and GMP environment. Assist in the development and validation of different immunoassays (ELISA, Western Blot, ELISPot, etc.) and activity based assays
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 later13/05/2024 | Fulltime | | United Kingdom | CV-Library | €23,000 - €26,000 / Year Please click apply or contact GMP Recruitment directly. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency
Save for later09/05/2024 | Fulltime | | United Kingdom | CV-LibraryCompanies in the UK. Location This role is located at their state of the art facilities near Woking. Summary of role As a QC Technician you will be supporting the team and working in a GMP environment. Your qualifications - skills Graduate in Biological degree or similar field. Experience working
Save for later14/05/2024 | Fulltime | | United Kingdom | CV-Library | €30,000 - €35,000 / Year As the Production Technician will be varied however the key duties and responsibilities are as follows 1. To adhere to GMP and H&S standards, including hygiene, environmental control and safe working practices. 2. To ensure that equipment is used in compliance with any maintenance, calibration and validation
Save for later17/05/2024 | Fulltime | | United Kingdom | CV-Library | €50,000 - €65,000 / Year Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. - Comprehensive experience with “quality management” within a technology company
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