1 to 25 of 30 GMP Jobs in the North West

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

pharmaceutical/healthcare or related industry Experience of aseptic operations is desirable, if possible aided by experience in aseptic compounding activities Good knowledge of GMP requirements specifically for manufacturing and control of aseptically produced products as laid down in the Orange Guide This job description reflects the present requirements of More ❯

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 More ❯

in project management activities. Document process impacts with business partners. Execute test scenarios. Maintain Standard Operating Procedures for systems. Support validation/requalification of GMP/cGMP systems. Perform other duties as assigned. All employees are responsible for compliance with health, safety, environmental, and quality management systems. Requirements Bachelor's More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

our success, bring those unique qualities, with the following skills and qualifications/experience: Excellent Computer skills including proficiency in the Microsoft Office Suite GMP knowledge - understand how to work to process (if you have some experience, even better!) Qualification in a scientific principal and/or experience in a More ❯

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 More ❯

manufacturing environment. Strong leadership and people management skills. In-depth knowledge of QA processes (QC experience desirable but not essential). Familiarity with ISO, GMP, or similar standards. Excellent communication, organisation, and problem-solving skills. Ability to manage multiple tasks and priorities in a fast-paced setting. What's on More ❯

safety, and legality. Participate in digitalisation initiatives to improve communication, data collection, efficiencies, and culture, including system implementation and enhancement. Ensure site compliance with GMP, BRCGS, ISO9001, ISO14001 standards to maintain product quality. Collaborate with the Compliance Manager and departments to review and update the internal IMS (Integrated Management System More ❯

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 More ❯

Supply chain planning and optimisation Source: Procurement of externally sourced materials and contract manufacturing Make: Manufacturing and quality release of medicines in a validated (GMP) environment Delivery: the delivery of medicines to patients The role will focus on the definition and governance of enterprise information architectures, strategies, designs, models and More ❯

all facilities on site. Specific duties include: Isolation and de-isolation of 3.3KV equipment. Fault finding on 415vac equipment. Fault finding and calibrations to GMP standards on pressure, temperature, flow, pH, humidity etc loops and individual local instrumentation. Response to and interrogation of Fire alarm systems, support ERMT in details More ❯

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 More ❯

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 More ❯

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 ❯

experience in a scientific support role Experience with electronic laboratory notebooks or similar systems. Familiarity with supporting laboratory operations. Understanding of Good Manufacturing Practice (GMP) regulations and quality assurance processes. Ability to adapt to changing workflows and contribute to process improvement efforts. Strong interpersonal skills, with the ability to collaborate More ❯