1 to 25 of 113 Permanent GMP Jobs in the UK excluding London

CY Partners are currently looking to recruit an Analytical Team Leader on behalf of a growing County Durham based Pharmaceutical CDMO on a permanent basis. As well as routine analysis on raw materials, intermediates and finished products, this quality department more »

disposition. The QA officer will ensure assigned tasks are performed in a timely manner to meet batch disposition, supply chain and all associated international GMP/GDP requirements. Key Responsibilities will include: To compile & review batch document sets for completeness & compliance to EU GMP, Pfizer internal requirements and regulatory dossier … s degree in a related scientific discipline with relevant experience (Preferably Biology/Chemistry/Pharmacy/Life Sciences) 2-3 years in a GMP environment Basic experience in pharmaceutical manufacturing, distribution, and control measures Basic experience in Quality administered systems. Previous use of TrackWise® QMS beneficial. Experience in operating more »

to help our patients. We value and encourage learning and development. As the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing, testing and release of the product. … companies QMS. · Support with assessment of deviation event investigations. · Support closure to plan of Change Controls and CAPA actions. · Issue, review and approval of GMP batch manufacturing records to support certification and release. · Assist in performance of internal self-inspection audits. · Support the Company’s Quality Meetings. · Assist in maintaining … the Company’s quality certifications, e.g. GMP, GDP, HO approvals, etc. · Assist in preparation for inspections from MHRA and other Competent Authorities · Provide quality review and input to manufacturing and business activities. · Ensure compliance with the Company’s Quality Standards. · Engage with the wider team and sector to gain wider more »

selecting and acquiring equipment to ensuring its proper validation. Providing technical support to Manufacturing Operations during troubleshooting and investigations. Conducting data integrity assessments for GMP equipment , safeguarding the accuracy and reliability of collected data. Maintaining the qualification life-cycle of all GMP equipment by performing re-qualification activities as necessary. … a Doctorate (PhD) in a Life Science or Engineering field. Proven experience in validating manufacturing equipment and processes. Solid understanding of Good Manufacturing Practices (GMP) regulations. Experience in collaborating effectively with internal and external stakeholders. Adept at multitasking and thriving in a busy environment. Strong relationship builder with excellent communication more »

from a Pensions background and ideally Team Leading people working on similar projects as listed below. - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

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 »

Develop and implement comprehensive quality management strategies, policies, and procedures to ensure compliance with regulatory requirements (e.g. FDA, EMA, etc.) and industry standards (e.g. GMP, GDP, GCP). Provide leadership and direction to the quality assurance and quality control teams, fostering a culture of quality excellence, accountability, and continuous improvement. more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

degree level or above in life sciences, chemistry or a related file with experience of working in a regulated laboratory environment (e.g. GLP or GMP) • Experience in using and troubleshooting ELISA analytical systems as well as the ability to develop and validate analytical methods using ELISA. • The ability to document more »

is a particular need for this role/location An understanding of the principles of Chemistry, Degree/HNC in Chemistry preferred Knowledge of GMP procedures and best practices Valid, clean UK driving license Ability to travel in the UK and willingness to attend training in EU or USA The … responsibilities of the Field Service Technician – Analytical Instruments: Duties include Fault diagnosis, repair, routine servicing, certification, and installation of equipment in accordance with GMP guidelines 80% of your time will be spent on pre-planned maintenance visits and circa 20% breakdown support which will enable you to manage your time more »

profile and past history: 1. Relevant degree in a chemistry related discipline. 2. Proven industry experience in development activities for drug development in a GMP environment. 3. A working knowledge and practical experience with management of an analytical chemistry function/facility in the pharmaceutical industry. Hyper Recruitment Solutions Ltd more »

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go 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 Be the Engineering point of contact during & out of hours Respond to more »

facilitate change. The ability to present information coherently, accurately and persuasively. PC literate Experience within food manufacturing, advanced Food Hygiene Certificate & good understanding of GMP/hygiene standards Please click ' Apply Now' to be considered for this fantastic opportunity and to become part of our Proud Bakkavor family. #LI-HF1 more »

staff on quality protocols. Responsibilities: Develop and improve quality assurance policies and procedures to ensure compliance with regulatory requirements and industry standards (e.g. BRC, GMP) Conduct regular audits and inspections of laboratory and manufacturing processes, equipment, and documentation to identify areas for improvement. Gain expert knowledge of the business management more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »

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) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

focus on compliance within a specific bakery, working with the teams to identify non-compliance and full engagement and support to ensure company processes. GMP and procedures are fully understood. Work with the bakeries to ensure compliance with relevant customer standards and codes of practice. Conduct physical factory audits (outside … safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and any non-conformances raised to bakery management. Verify that close out actions are robust and complete. Communicate more »

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) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

monitoring good manufacturing practices, applying HACCP principles and preventing reoccurrence of non-conformance against these standards. To audit compliance against Quality Management Systems and GMP, raising all non-conformances against relevant standards with objective evidence enabling the operational teams to take the appropriate and necessary corrective action, to follow up more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and 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 »

development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of 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 »

the wider Quality group at Alba Bioscience, part of AliveDx, and its primary role is to ensure that all aspects of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) compliance are met through effective control of the Quality Management System (QMS). The role is a full-time temporary … by the business . Participate in an 'in-house' programme of continuous training and assessment. Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements including statutory Health & Safety legislation and internal practice. Perform any other duties as reasonably requested from the more »