14 of 14 GMP Jobs in Manchester

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

with diverse cultures. Necessary legal status to work in the UK. Beneficial requirements: The closest relevant experience would be MES/EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers. Experience of different project delivery methodologies including waterfall and agile. Experience of client account management. Knowledge of software delivery projects. Knowledge of Computer System Validation is an advantage. More ❯

low/no-code tools is advantageous but not essential. Proven track record of leading MES projects from start to finish. Understanding of Pharma/Biotech processes and regulations (GMP, FDA 21 CFR Part 11, GAMP5). Strong problem-solving and communication skills. Willingness to travel to client sites. What We Offer: Competitive salary and benefits. Growth and development opportunities. More ❯

You Bring 5+ years delivering MES solutions (Tulip or similar platforms - e.g. Siemens, Rockwell, Koerber, etc.) Strong experience in integration: ERP, lab systems, IoT, machines A practical grasp of GMP, GAMP5, and 21 CFR Part 11 Familiarity with business process mapping from URS to validation Confident working across Fit-Gap, presales, and improvement phases Curious, modern mindset — excited by low More ❯

You As Senior/Principal Architect - Life Sciences you will have experience in delivering projects from concept to detailed design in the life science sector for both laboratories and GMP manufacturing facilities. You will be part of an enthusiastic and committed team of Architects and Technicians who will deliver high quality output on projects. To be successful you will exhibit More ❯

You As Senior/Principal Architect – Life Sciences you will have experience in delivering projects from concept to detailed design in the life science sector for both laboratories and GMP manufacturing facilities. You will be part of an enthusiastic and committed team of Architects and Technicians who will deliver high quality output on projects. To be successful you will exhibit More ❯

relevant technical documentation and records to ensure audit readiness. Support the implementation and maintenance of the site’s Quality Management System. Quality & Food Safety Support Assist with internal audits (GMP, hygiene, traceability, etc.). Support the Technical team in complaint investigations, non-conformance reporting, and root cause analysis. Help monitor CCPs and PRPs in line with HACCP plans. Data & Reporting More ❯

partner with our customers to implement one of Veeva’s newest products - Veeva Vault LIMS . Passionate about bringing disruptive technology to customers and have novel ideas for successful GMP software implementation? This role will allow you to help our clients to drive new product adoption through successful implementations. This is a remote, full-time permanent role with Veeva. This More ❯

in a fast-moving environment providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations. Practical knowledge of the Pension Protection Fund (PPF). Circumstances Working hours: Monday to Friday, 37.5 hours per week with additional hours as and when required. More ❯

Developing specifications and leading multidisciplinary teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What You’ll Be Doing Designs, defines More ❯

or service. Experience of PLC, Fieldbus network, LAN, drives and controls. Experience in fault-finding, both mechanical and electrical. Competent in Microsoft based software. Experience of SAT, IQOQ and GMP procedures. Must possess excellent communication skills and the ability to interface effectively with customers and peers. An ability to resolve problems and make independent decisions based upon the priority of More ❯

plans that can be presented clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics) Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher landscape Are analytical, flexible and More ❯

and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯