1 to 25 of 70 GMP Jobs in the UK

Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required. … or supplier complaints are satisfactorily investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills, we are looking for Candidates who 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 ❯

in process control skills, including some of the following: PLC (AB Rockwell, Siemens), SCADA systems (Rockwell Historian), CAD, Trend BMS/Set, Lighthouse EMS, JDEdwards. Experience: Good Manufacturing Practice (GMP) experience. Attributes: Proactive, methodical, and a strong problem solver. Why You Should Join Catalent: Competitive Salary - Reflecting your experience and skills. Bonus & Benefits - Includes an annual performance bonus, a pension More ❯

User Requirement Brief (URB) and User Requirement Specification (URS) with the end customer as required by the project and interfaces with validation. Co-ordination of design reviews, safety studies, GMP reviews and constructability assessments to shape the design and planning process. Preparation of Pre-Construction Information (PCI) for accountable projects as well as client HSE requirements (e.g. F10 notification). More ❯

asubject matter expert in automation, ensuring seamless integration of digital manufacturing approaches beyond traditional automation boundaries. Your contributions will support system reliability, performance optimization, and continuous improvement initiatives within GMP-regulated environments. Working under the technical supervision of your line manager and senior technical colleagues, you will ensure regulatory compliance, system validation, and effective automation strategies that align with MMIC … Automation for Pharma strategy into practical deliverables within the Operational Technology ( OT ) team to meet business objectives. Compliance & Documentation: Ensure full compliance with Safety, Health, and Environmental ( SHE ) regulations, GMP standards, and best practices. Maintain clear and documented records of technical data, validation master plans, and experimental testing plans within the MMIC GMP framework. Technical Leadership: Act as arecognized authority … GAMP 5 approach to GxP Computerised System Validation. Knowledge of functional safety systems within automated machinery. Chartered/registered status with arelevant professional institution. Have industrial experience within a GMP environment. What does CPI offeryou? At CPI , we offer awide range of benefits to our employees, this includes: Up to 36 days holiday, including bank holidays - Plus aholiday purchasing scheme 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 ❯

in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National Regulatory Authority (AIFA) and is compliant with the FDA More ❯

basic understanding of computer system validation in the pharmaceutical sector Experience and knowledge of working in a regulated environment, specifically with regards to record retention Knowledge of GCP and GMP with regards to QMS activities Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures Responsible … for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions are closed timely and in a RFT state Job Background Minimum of 3 years experience working in More ❯

day-to-day operations with long-term strategic planning. This involves ensuring that advanced instrumentation, automation, and control engineering techniques are implemented across the Barnard Castle Site in a GMP compliant manner to meet both local and global requirements. By integrating robust management practices with strategic initiatives, the site can optimize operational efficiency, maintain regulatory compliance, and achieve sustainable growth. … with maintenance technicians, fostering a collaborative and innovative work environment. System Design and Implementation: Lead the design, development, and implementation of advanced automation systems, including PLCs, SCADA, and DCS. GMP Compliance: Ensure all automation systems and processes comply with Good Manufacturing Practices (GMP) and regulatory requirements. Training and Development: Develop and deliver training programs to ensure staff are proficient in More ❯

and embedded analytics for production KPIs Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.) Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs Ability to translate complex operational processes into streamlined SAP-enabled solutions Excellent More ❯

and embedded analytics for production KPIs Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.) Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs Ability to translate complex operational processes into streamlined SAP-enabled solutions Excellent 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 ❯

and embedded analytics for production KPIs Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.) Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs Ability to translate complex operational processes into streamlined SAP-enabled solutions Excellent More ❯

Looking For: Degree in Food Science, Microbiology, or a related field (or equivalent experience). Experience in a QA role within the food manufacturing industry. Strong knowledge of HACCP, GMP, and food safety regulations. Excellent communication and problem-solving skills. Detail-oriented with a proactive approach to continuous improvement. What We Offer: A supportive and collaborative work environment. Opportunities for More ❯

Participating in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Auditing compliance against Quality Management Systems, GMP and HACCP controls - raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participating in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Auditing compliance against Quality Management Systems, GMP and HACCP controls - raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

standards set nationally and by our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

standards set nationally and by our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

Importance Extensive experience in facilities management, focusing on support services and operations Essential Strong track record in contract management, supplier performance monitoring, and budget oversight Essential Extensive knowledge of GMP catering contract models Essential Proven ability to lead security, soft services, insurance administration, and business continuity functions Essential Strong experience in Soft FM and building management Essential Extensive experience in More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

practice etc ). In support of this develop process standards, SOP's and work instructions for key maintenance activities to ensure compliance to standard and ongoing maintenance of our GMP compliance and standard. - Track/Monitor and report upon utility costs and consumption data for R&D site ensuring that all invoicing, payment and consumption tracking is maintained accurately in … background and knowledge of mechanical & electrical systems is essential. - Strong knowledge of evaluating and vendor selection based on quality, compliance and cost effectiveness and the ability to meet specific GMP requirements. - Experience in systems and building management, around certification in Legionella & Asbestos Management - Knowledge of Pharmaceutical manufacturing processes and understanding of GMP requirements is advantageous. - Extensive work-based experience with More ❯

meet quality and regulatory standards. Ensure consistency in automation design and execution between all Sanofi facilities, adhering to a uniform approach. Identify and manage risks proactively, ensuring compliance with GMP and minimizing disruptions to project timelines and costs. About you Experience : Proven track record of managing complex manufacturing systems involving automation, robotics, and advanced technologies, in the pharmaceutical sector. Technical 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 ❯

z2bz0 years in programme/project management, ideally in pharmaceutical manufacturing or supply chain Strong background in managing large-scale planning or capital investment programmes Knowledge of GMP, tech transfers, regulatory frameworks, and operational readiness Skills: Excellent at critical path planning and integrated project time-lines Confident managing senior stakeholders and driving decisions Robert Half Ltd acts as an employment More ❯