16 of 16 GMP Jobs in the North of England

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 ❯

related function within either the 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 the post. It is not More ❯

We're Looking For Degree in a life science field or relevant experience in quality assurance/quality control. Experience in the pharmaceutical or healthcare industry preferred. Knowledge of GMP requirements for sterile manufacturing (clean room) is desirable or general experience of working within a GMP environment. Familiarity with sterile operations or compounding is a plus. If you're passionate More ❯

client's biotechnology start-up facility in North East England. This role offers the opportunity to be part of a high-performing automation team delivering critical systems in a GMP-regulated environment. Responsibilities: Executing FAT/SAT/IOQ protocols including generation of protocols and reports. Design, configure, and support Emerson DeltaV PCS and/or BMS platforms for bioprocessing … qualification, and validation of automation systems in collaboration with CQV and Operations teams. Participate in the development, testing, and deployment of automation changes, and maintain documentation in compliance with GMP requirements. Provide technical input during design reviews, FATs, SATs, and system walkdowns. Qualifications & Experience: Bachelor's degree in Automation Engineering, Software Engineering, or a related field. Prior experience in a More ❯

Overseeing a liquid manufacturing facility, the Technical Operations Manager will lead 10 direct reports across various departments. This position holds overall responsibility for ensuring site compliance with MHRA and GMP guidelines. The role involves leading continuous improvement and change management initiatives, as well as acting as the site lead on CAPA projects. Job Details: Pay: £50,000 per annum Hours … Friday, 8am - 4.30pm Duration: Permanent Essential Skills & Experience: Previously held a Senior Technical Manager, Manufacturing Manager or similar role in a regulated industry Sound knowledge of Good Manufacturing Practices (GMP), regulatory compliance, and pharmaceutical manufacturing Background in chemical manufacturing, pharma, or other highly regulated industries Desired Skills & Experience: Experience in oral dosage production Previous involvement in pharmaceutical manufacturing Essential Qualifications More ❯

continuous improvement. You will lead a skilled team of operators, technicians, and supervisors, overseeing day-to-day plant operations while ensuring production targets, quality standards, and regulatory compliance (MHRA, GMP, Home Office) are consistently met. This is a hands-on leadership role, requiring a balance of strategic insight, technical expertise, and operational execution. Key Responsibilities Lead the operations of a … pharmaceutical manufacturing facility. Drive continuous improvement, process optimisation, and operational excellence. Ensure GMP compliance and uphold the highest quality standards. Provide hands-on technical support and troubleshoot production issues. Collaborate cross-functionally with Quality, R&D, Supply Chain, and Engineering. Champion Lean principles and eliminate waste through process improvement. Lead investigations, CAPAs, and Change Control processes. Mentor and develop team … What We're Looking For We're seeking someone with experience in a senior technical or operational management role within pharmaceutical manufacturing. You'll have a deep understanding of GMP, regulatory compliance, and dosage form production. Essential: Proven leadership within a pharmaceutical manufacturing setting. Strong knowledge of GMP, MHRA regulations, and pharmaceutical manufacturing. Track record of process improvements, cost control More ❯

used in implant and instrument manufacturing Good understanding of the design process and tools used Experience in DFMEA, PFMEA, 6 sigma and Lean Experience of working with GMP(Good Manufacturing Practice). Experience in project management and problem solving Knowledge of quality systems, regulatory requirements and related standards, with demonstrated understanding of the practical application of these requirements Excellent planning More ❯

ensuring efficient, compliant, and high-quality production. This senior leadership role involves overseeing daily operations, driving continuous improvement, and managing cross-functional teams. The ideal candidate will have strong GMP knowledge, proven leadership in regulated manufacturing, and a focus on process optimisation and regulatory compliance. Technical Operations Manager Job Responsibilities: Oversee daily manufacturing operations to ensure production runs efficiently, safely … standards. Lead, support, and develop a skilled team while promoting a culture of accountability, collaboration, and continuous improvement. Implement process enhancements, resolve technical challenges, and maintain full compliance with GMP and regulatory requirements. Work cross-functionally with key departments to coordinate seamless operations, manage new product launches, and uphold safety and quality standards. Champion Lean initiatives, lead root cause investigations More ❯

a QA role within a 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 Offer: An attractive salary of More ❯

for example). Working collaboratively with all operations teams within the business, such as Quality and Health and Safety to uphold the stringent protocols necessary along with adhering to GMP and Data Integrity at all times. Your background: BSc or equivalent in a Life Science discipline. Demonstrable experience in a business development role, from within the Biologics or Pharmaceutical Manufacturing More ❯

detail. Excellent computer skills (MS Office, particularly Excel and Word). Strong communication and interpersonal skills to work with cross-functional teams. Ability to work independently Experience in a GMP-regulated manufacturing environment. Basic knowledge of maintenance trades (mechanical, electrical, utilities). Experience in generating reports and dashboards using CMMS or BI tools. Benefits Holiday 24 days plus 8 stat 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 ❯

and implement Siemens automation solutions (PCS7, SIMATIC SCADA, TIA Portal, MES). Program and troubleshoot PLC (S7-1500, S7-1200) and DCS for optimized process control. Ensure compliance with GMP, GAMP, FDA guidelines in automation projects. Oversee commissioning, validation, and maintenance of automation systems. Collaborate with process engineering, IT, and quality teams to enhance automation efficiency. Stay updated on emerging … . Required Technical Skills: 5+ years in pharmaceutical automation with Siemens systems. Strong expertise in PCS7, SCADA, MES, and PLC programming (TIA Portal) . Deep knowledge of regulatory standards (GMP, GAMP, FDA) . Experience managing automation projects, validation, and troubleshooting . More ❯

Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of GMP requirements for automated systems. The role requires delivery of results on time, in accordance with client standards and health and safety procedures. The successful candidate will be a self-starter More ❯

Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of GMP requirements for automated systems. The role requires delivery of results on time, in accordance with client standards and health and safety procedures. The successful candidate will be a self-starter 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 ❯