51 to 60 of 60 GMP Jobs

for usability, performance, quality, and manufacturability. Use CAD software (preferably SolidWorks) to create models, drawings, and layouts. Ensure compliance with applicable medical device regulations and quality systems (e.g., ISO, GMP, GLP). Partner with Legal and IP teams to identify and support opportunities for intellectual property protection. Minimum Requirements: Education Bachelor's degree in Engineering or a related field. Work … development. Strong ability to manage and execute design objectives independently. Proficiency in CAD (SolidWorks preferred). Experience with design tools such as FEA, DFSS, DFM, ISO/CE Mark, GMP, GDP, ASME Y14.5, and GD&T. Knowledge plastic film processing, pressure-sensitive adhesives, and other medical-grade materials. Understanding of regulatory standards (ISO 13485, ISO 14971, IEC 60601). Strong More ❯

We are seeking an experienced Quality Operative/GMP Co-ordinator to join … a leading food manufacturing business, ensuring products meet strict safety, hygiene, and compliance standards. In this MondayFriday role, youll carry out quality checks, support production teams, and maintain Good Manufacturing Practice across all processes. With steady hours, full PPE, and the potential to go permanent, this is a great opportunity to build on your food industry expertise. What Youll Be … Doing: Carrying out GMP and quality checks across production processes Collecting and testing product samples to meet exacting standards Conducting hygiene audits to maintain compliance Supporting and mentoring colleagues on quality procedures Printing and verifying labels for accuracy and compliance Working in a temperature-controlled environment (811C) to ensure product integrity What Were Looking For: Proven experience in quality within More ❯

product in a timely and cost effective manner. Analyse production data to identify trends, deviations, and performance metrics. Assist in the execution of cleaning validation protocols in line with GMP requirements. Bring in SQL/Power BI approaches to improve the site approach to data. Support sampling, documentation, and coordination of validation activities. Your Background : GMP experience is essential Have … degree (e.g., Biochemistry, Biotechnology, Chemical Engineering, Pharmaceutical Sciences). Understanding of cleaning validation principles and documentation practices. Experience with data handling and analytics Knowledge of HSE, bio-safety standards, GMP regulations as well as main tools and principles of operational excellence Company: Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one More ❯

used in pharmaceutical packaging. Responsibilities include on-site service, vendor coordination, project materials management (SAP/CRM), customer training, line audits, and system upgrades. Ensure compliance with SHEQ and GMP standards while supporting both European and U.S. equipment. Requirements Associate degree + 3-5 years' experience or 8+ years in a GMP environment Strong knowledge of PLCs, HMIs, SCADA, and More ❯

opportunity to be part of a company that values innovation, collaboration, and the flawless execution of ideas that genuinely improve the world! Key responsibilities: Generate and revise documentation for GMP manufacturing to ensure technical accuracy and GMP compliance. Provide technical support to develop required process documentation in collaboration with internal customers. Independently manage the creation of new documents and revise … GMP documents according to detailed procedures. Use and maintain the Documentation Management System (DMS) according to detailed procedures. Produce and process batch documentation according to standard timelines, coordinate review, approval, and issuance ensuring availability for use in Manufacturing per production schedule. Monitor progress of document creation and communicate with relevant parties to resolve potential issues in a timely manner. Manage … training to others during routine document revision. Understand and align with company policies, departmental practices, regulatory, and statutory requirements. Key requirements: Proven experience as a Technical Writer in a GMP manufacturing environment. Outstanding ability to generate and revise technical documentation with attention to detail. Comprehensive knowledge of DMS and standard methodologies for documentation. Ability to manage multiple tasks and projects More ❯

recruit an Associate Expert Bioprocess DSP (m/f/d) to join the Pilot Plant Downstream Process team starting at the next possible date at our Research and GMP Production Site in Heidelberg. Associate Expert Bioprocess DSP (m/f/d) What's the best thing about working with us? A permanent position in full-time (40 hrs. … development and process transfer from laboratory to pilot scale Planning and execution of DSP unit operations at pilot scale in technical and clinical campaigns (cleanroom class D + C, GMP regulated environment) Development and implementation of new process technologies within the framework of process optimization Creation of process risk analyses, control strategies, process mappings, batch protocols, development plans, and reports More ❯

We are currently recruiting for a QA Supervisor based at our Llanidoles site, this will be a 5 day onsite role. The successful candidate will be responsible for leading a small QA team to ensure the efficient and effective operation More ❯

GMP Recruitment are proud to be in partnership with a long-established and reputable defence engineering firm based in the Birmingham area. We are currently recruiting on their behalf for an experienced IT Support professional to join their I.T Department on a full-time, permanent basis. This position offers a salary of up to £35,000 Per annum based on … obtain BPSS and SC clearance. AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

We are seeking an experienced Quality Operative/GMP Co-ordinator to join … a leading food manufacturing business, ensuring products meet strict safety, hygiene, and compliance standards. In this MondayFriday role, youll carry out quality checks, support production teams, and maintain Good Manufacturing Practice across all processes click apply for full job details More ❯

Work on the cleaning crew on weekends as needed Working knowledge of HACCP plan and HACCP checks Working knowledge of SOP plans and SSOP checks LOTO trained Know all GMP's and plant rules Must know how to GMP audits Water and ice monitoring-help collect samples and send to lab E-Coli Sampling procedure Complete various checks, collections, and More ❯