1 to 25 of 28 GMP Jobs in the North West

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 ❯

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 ❯

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 ❯

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 ❯

based qualification and/or 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 across various teams and disciplines. More ❯

process, and packing checks. Provide coaching and development, closing skill gaps with tailored training plans. Foster a strong quality culture through effective leadership and clear communication. Maintain and enhance GMP standards through auditing, coaching, and root cause analysis. Ensure products meet both GMP and customer specifications. Manage internal and external audits in collaboration with the Technical Manager, resolving non-conformances 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 ❯

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 ❯

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 ❯

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 ❯

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 ❯

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 ❯

do spirit that’s spearheading 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 similar scientific environment 1 year 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 ❯

standards that guarantee product quality, 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). Skills and Qualifications Extensive 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 ❯

emerging from R&D Plan: 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 consolidating thinking and artefacts across More ❯

as a Senior Pensions Data Specialist to deliver data services to our clients, including data and benefit audits, preparing data strategies and plans, and undertaking pension rectifications such as GMP rectification and equalisation. While we continue to help clients meet their GMP objectives, the data challenges they face are becoming more diverse, giving you a chance to work across a More ❯

quality and production needs across 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 for emergencies. Use diagnostic tools 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 ❯