1 to 12 of 12 GMP Jobs in the North West

Note: Applicants must be authorised to work in the UK Our client is a leading pharmaceutical distributor with multiple GDP distribution facilities and a GMP assembly unit. They are committed to maintaining the highest standards of Good Manufacturing and Distribution Practice (GDP) and regulatory compliance. Their dedication to quality, safety … to move forward with your application. Other suitable skills and experience include Responsible Person (RP), Quality Affairs Specialist, Compliance Manager, Pharmaceutical Quality Control Manager, GMP Auditor, Distribution Manager, Pharmaceutical Consultant, Quality Systems Coordinator. more »

corrective actions Collecting micro-samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/fabric audits Temperature checks Quality checks The nature of this role requires a flexible approach to working hours. Core working hours are: Monday to more »

vacuum cooler. Help with maintaining the plant to ensure we are hitting our consent. Ensure all maintenance equipment is fit for purpose. Compliance to GMP, QMS, 5'S, BRC Person Specification ONC in a related subject or equivalent experience Recognised apprenticeship Experience of working in an FMCG environment Electrical engineering more »

area highlighting any stock issues to the engineering team manager To maintain standards of hygiene and good housekeeping appropriate to a quality food manufacturer. GMP standard of workshops and engineers tool boxes is maintained at a high level About you. Strong people management experience A multi skilled background Experience completing more »

compensated at an enhanced overtime rate) Experience in some or all of the following areas is highly desirable: ISO 9001 Quality systems Working under GMP conditions Maintaining and certifying equipment to British, European, or International Standards (BS EN 12469, ISO 14644, HTM03-01, GMP) PLC-based control systems IIE 18th more »

you a skilled technical assistant with a passion for food manufacturing? Do you have a keen eye for systems and specifications, and experience in GMP and supplier approval? If so, we have an exciting opportunity for you! About the Role: We are seeking a Technical Assistant for our esteemed client … maintaining high standards and ensuring compliance with industry regulations. Key Responsibilities: Manage and maintain technical systems and specifications. Ensure compliance with Good Manufacturing Practices (GMP). Conduct supplier approval processes and audits. Collaborate with various departments to ensure seamless production and quality control. Provide technical support and expertise where needed. … Requirements: Proven experience in a technical role within food manufacturing. Strong understanding of systems and specifications. Knowledge of GMP and experience in supplier approval processes. Excellent attention to detail and organizational skills. Must have an indefinite right to work in the UK. Why Join Us? Competitive salary up to more »

a Quality Director to head up a Quality department. The Quality Director will promote and integrate quality into every aspect of the business ensuring GMP compliance and meeting the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams … the business and provide support to sister company for regulatory inspections and conduct self-inspection program Oversee the Pharmaceutical Management System. Implement the current GMP regulations and industry best practices, where applicable Support and develop the QA team Support/lead manufacturing deviation or testing out-of-specification/out … of-trend investigations Audit the contract manufacturing organisation and laboratory against EU GMP and relevant regulations and guideline Qualifications and Skills: Qualified Person (QP) Knowledge and experience in manufacturing and testing of oral dosage forms and topical products Experience in releasing medicinal products in a fast-paced environment Experience in more »

PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous more »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role. Main Responsibilities So, what will you be … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

company dedicated to improving health and wellness through cutting-edge products. Committed to excellence, they operate to the highest standards of Good Manufacturing Practices (GMP). Key Responsibilities: Oversee and maintain the Quality Management System (QMS) to ensure compliance with GMP standards. Conduct thorough internal audits and participate in external … reviews to identify areas for improvement and ensure continuous quality enhancement. Collaborate with cross-functional teams to implement quality processes and provide training on GMP compliance. Develop and update quality policies, procedures, and documentation to align with industry best practices. Requirements: Bachelor's degree in a relevant field (e.g., Life … Sciences, Pharmacy, Quality Management). Proven experience in quality systems management within the Medical Nutrition or Pharmaceutical industries. In-depth knowledge of GMP standards and regulatory requirements. Strong analytical skills with a keen eye for detail. Excellent communication and interpersonal abilities to work effectively with various teams. Experience in leading more »

of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply more »

Lab Analyst/Senior Lab Analyst Serving Society through Science, Tata Chemicals Europe (TCE) is one of Europes leading producers of sodium carbonate, salt and sodium bicarbonate and other products, from our plants in Cheshire, UK. British Salt has been more »