101 to 113 of 113 Permanent GMP Jobs in England

and collaboration with Operations and Quality teams. Major Responsibilities Under the QC Manager's direction, the Incoming QC Team Leader will: Ensure GDP/GMP compliance within Incoming Inspection and Quarantine areas through inspection of incoming goods against specifications. Create and maintain incoming inspection procedures and work instructions. Manage QC … external audits (e.g., BSI, FDA). Support and complete other tasks set by the QC Manager. Skills and Experience Working knowledge of GDP/GMP requirements. Ability to create and write Standard Operating Procedures and Work Instructions/Specifications. Understanding of inspection criteria and the use of drawings/specifications. … area for medical devices. Knowledge of SAP (desirable). Knowledge of Master Control (desirable). Strong written and oral communication skills. Good understanding of GMP compliance requirements in Quality Control. Attention to detail. Promotes a collaborative working environment. Understanding of using basic measurement tools (e.g., calipers/jigs and gauges more »

role for you! As a Technical & Quality Coordinator, you will be: Updating and developing technical documentation. Ensuring the organisation remains compliant with food safety, GMP, quality, ACCP , and health and safety procedures . Conducting, and supporting with, internal and external audits and finished product traces . Recording all findings and … in food science or related field. Previous experience in a Quality & Technical role within food manufacturing . A strong understanding of HACCP, BRCGS, and GMP standards and food legislation . Computer literate with MS Office. Able to work well independently and part of a team. If you believe you meet more »

its capabilities. This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying … protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline Qualifications related to validation and quality compliance (GMP/ICH/FDA/USP/EP policies). Experience of validating manufacturing/laboratory equipment, facilities/utilities and processes, including the generation more »

The Role - Development/GC MS/HPLC Scientist The Salary - Competitive The Location - Yorkshire Russell Taylor group has a brand-new opportunity for a chromatography scientist. If you think this role would be of interest, apply now to avoid more »

Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »

Practice Leader - Head of GMP London Company client partnered with a leading pensions consultancy in the UK, who have seen continuous growth in 2024 and looking to continue with ambitious objectives. This consultancy is seeking a Practice Lead as Head of GMP. This role provides opportunity to lead the Actuarial … GMP team, leading a team of actuaries towards innovative solutions in GMP reconciliation, equalisation, and rectification for UK Defined Benefit Pension Schemes clients. Key Responsibilities: * Leading a mid-sized team, with numerous direct reports- supporting on projects covering GMP. * Provide high quality Actuarial and pensions expertise to clients * To contribute more »

if required), considering safety, quality, integrity and legality. Ensure all procedures/process deviations are analysed and actioned in a safe & legal manner. Hygiene & GMP: Ensure that the company has up to date, consistent and appropriate cleaning and GMP procedures that meet the requirements of BRC/Customers. Ensure that more »

Desirable) Time served Engineer. NVQ Level 3 Qualification or above Electrical Bias The Role Carry out duties ensuring the site achieves and maintains required GMP standards. Ensure all work conforms to statutory & safety requirements. Ensure that risk assessments are completed and actioned. Carry out site maintenance activities and ensure GMP more »

of your role ensuring that all areas of the factory site are maintained to exceptional standards of hygiene process improvements, working to KPI's, GMP standards, food safety and health and safety standards. The overall focus of the role will be to manage and develop the hygiene standards, your team … food manufacturing sector although this is not essential A can-do attitude, able to communicate effectively at all levels A comprehensive understanding of modern GMP Experience operating to BRC standards The ability to multi task and balance multiple priorities Proficient in MS Office Knowledge of CIP systems Excellent Problem-solving 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 »

and filling support. Key Responsibilities of Production Technician: * Produce bulk products and manage stock solutions, dispensary operations, and filling support. * Complete documentation adhering to GMP standards. * Operate within cleanroom environments and maintain compliance with media qualifications. * Organise and prioritise tasks to meet production schedules. * Demonstrate adherence to company values and … behaviours. Requirements of Production Technician: * Strong focus on GMP standards with attention to detail. * Problem-solving skills and the ability to gather necessary information. * Ability to work methodically and multi-task. * Meet targets and deadlines effectively. * Punctual and flexible with working hours. * Team player with good written, verbal communication, and more »

Records Manager – Inside IR35 Contract Term: 6 months Contracting Authority: Greater Manchester Police Location: Hybrid – Manchester 2-3 days per week Greater Manchester Police (GMP) is the territorial police force responsible for law enforcement within the metropolitan county of Greater Manchester in North-West England. GMP employs almost … officers, PCSOs and Special Constables together with just over 3,500 police staff making GMP the second biggest police force in England and Wales. GMP are replacing their Records Management System (RMS). An RMS is the system on which police forces manage cases through to completion and maintain records … the people, objects, locations, and events that the force has interacted with. The RMS will join that data to paint a rich picture that GMP’s officers can use to mitigate risk and protect the citizens of Greater Manchester. We’re looking for someone with a specific records management background more »

addition, this role may develop into encompassing the following: Promoting HACCP principles throughout the Group; Carrying out Internal Audits including UKAS (ISO 17025) and GMP audits as required; Assisting with the development and understanding of Food Hygiene Standards and Practices and GMP throughout the Group. Assisting with the development and more »