1 to 25 of 30 Permanent QMS Jobs in the East of England

Systems (CDS), Laboratory Information Systems (LIS), Bioinformatics Software, Statistical Analysis Software, Image Analysis Software, Chemical Inventory Management Software, Lab Automation Software, Quality Management Software (QMS), Environmental Monitoring Software, Programmable Logic Controllers (PLCs), Distributed Control Systems (DCS), Supervisory Control and Data Acquisition (SCADA) systems, Human-Machine Interfaces (HMIs), Industrial Control Systems more »

The British flower market is worth £1.2bn and MM Flowers supplies fresh cut flowers and bouquets to the U.K.s and Europes leading flower retailers. We grow and source the highest quality and most beautiful blooms across the world, delivering colour more »

ensure a safe working environment for all employees. Key Accountability The engineer will ensure that we meet the requirements set out in our Quality Management System while ensuring that health and safety is a priority. Ensure that documentation (service reports etc) are completed and stored in the appropriate area within … the QMS and available for audit inspection. - Repairing Anprolene/EOGas sterilisers and purge probes both in-house and on-site - Annual servicing of Anprolene and EOGas Sterilisers in UK and Ireland - Installation of sterilisers in UK and Ireland Servicing and inspections of buildings and grounds are completed on time. more »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree more »

and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering, Manufacturing, and Biology teams to achieve regulatory submission and product more »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

Dairy free products. Role Overview: As a Compliance Technologist, you will play a crucial role in maintaining due diligence in the technical function. Updating QMS, accurate and up to date and accurate specifications. Supplier due diligence (supplier audits) HACCP validation which includes checking, providing, and validating legal info on the … printed packaging.Role Responsibilities: Quality management systems: HACCP team works with technical manager. Updating of QMS policies, procedures, and work instructions. Ensuring accuracy and useful training documents. Meeting BRC standards. Releasing updated and new QAS when gaps are identified. Working closely with factory. Working closely with the chemical supplier. QMS updated more »

large infrastructure projects. - Experience and understanding of project management. - Thorough understanding of H&S requirements. - Previous experience of working within an ISO 9001 Quality Management System (preferred but not essential). 3.3 Personal Qualities: - Highest levels of integrity, respectfulness and professionalism required at all times. - Open, trusting and in the more »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

Key Tasks and Accountabilities Work with the Program/Project Managers and their teams to maintain all aspects of the QMS as we develop our diagnostic capability e.g. Change Controls, Non-Conformities, CAPAs, Customer Complaint Support continuous improvements in the Quality Management System (QMS) and maintain compliance of Quality processes … QA staff, provide support to departments, e.g. reporting on Quality Metrics as well as assisting in training of personnel on matters relating to the QMS and Induction of new starters on Quality aspects. Support Quality department initiatives as required, as part of a multi-disciplinary team Competencies & Requirements for the more »

Our client is a leading manufacturing company based in Kings Lynn, due to their continued growth and development they are seeking to employ an Lead Production Planner to join their friendly and professional team. Competitive salary offered. Permanent role Hours more »

Main Duties (but not limited to): Completing technical checks in the factory (quality checks, carcase inspections, pH testing, steriliser checks etc) Reviewing and filing QMS paperwork from various production departments. Liasing with production teams in relation to paperwork completion, where necessary. Collating and registering all samples and results for microbiological more »

management of employee performance, absence management, and management of rostering Accountability for the clinical safety of the transfusion service, and operation of the quality management system, including compliance with the Blood Safety and Quality Regulations 2005 (as amended) and BS EN ISO 15189:2012 Liaison with the client, Mid and more »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree more »

ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators … Experience Degree in a relevant area of studies. 2 - 3 years’ experience in the role out of Quality policies. Knowledge of Quality Management Systems (QMS). Proven Auditing Skills. Continuous Improvement Mindset. Excellent interpersonal, verbal, and written communication skills. Experience of working at the headquarters of an international company. Fluent more »

and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering, Manufacturing, and Biology teams to achieve regulatory submission and product more »

in line with the QP/ITP schedule and are issued for inclusion in the LTR concurrent to the works completed. Undertake periodic Quality Management System audits both internal and external to ensure that the system and procedures are adhered to. Monitor Vendor Performance and carry out Supplier/Subcontractor more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working more »

team Facilitate project progress meetings with the project team Lead communications with suppliers and clients Contribute to sales activities, marketing materials and the Quality Management System as required What skills and knowledge can I bring? Experience managing the development of firmware for embedded products and systems (user interfaces, sensors, wireless more »

lyophilisation and quality control and production of small-medium scale batches. Handling receipt of reagents and chemicals -including aliquoting, storage and uploading onto the QMS as necessary. Working alongside CMO’s and in-house specialists to support the production scaling activities. Create and implement QC and validation protocols, ensuring that more »

Are you an experienced QMS Administrator looking for a part time role? If so, this interesting and flexible role could be just what you are looking for. The Client Established in the UK in 2000, but originally developed in California, USA, our client designs and manufactures a range of PH … renowned companies who are leaders in their specialised field. The Role They are now looking for an experienced QMS Administrator to ensure the Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure compliance with ISO 9001 and more »