17 QMS Jobs in the East of England

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 »

company procedures and policies to ensure smooth delivery of our service. Producing reporting on time and to agreed standards. Adhering to the companys quality management system and recycle correctly and responsibly. Required Skills: Experience in the installation, configuration and maintenance of access control and door entry systems. Basic IT Skills more »

quality reports on TrackWise Investigate OOS records in coordination with SMEs, and ensure the timely progression of reports. Participate in internal and external audits. QMS administration activities. What you'll need to succeed Our client is … looking for an individual with strong experience as a Quality Assurance Officer within a GMP Pharmaceutical/Cleanroom environment. Other key desirables include: Quality Management System activities and maintenance. Experience in participating in internal/external audits. Be able to work independently as well as within a cross-functional environment. more »

implementing our Food Safety. Quality and Hygiene systems in line with business growth and development. The role will be responsible for ensuring the company QMS is maintained and up to date. Ensuring compliance with BRC and Customer technical standards/codes of practice. Key responsibilities : Goods in checks. Paperwork checking more »

the development and validation of biomarker assays and Precision Medicine Solutions. Facilitate/participate in projects to deliver improvements to the clinical laboratory Quality Management System through collaboration with R&D Understand the business needs of PM departments, with respect to technology infrastructure, third party work and human biological sample more »

Consultant to join their team in Cambridgeshire, UK for a 6-12 month assignment contract, working on an exciting project. 🔸 Your responsibilities: GAP analysis QMS maintenance Transition to IVDR FDA audit support Remedial action in the following areas: Supplier & raw material controls, Process Validation, Equipment (Qualification, SOPs, Software Validation) 🔹 Your 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 »

with the existing software development team. Follow all relevant medical device directives and EU GMP Annex 11 with regards to software. Keep relevant Quality Management System documentation up to date. Qualifications & Experience: 2+ years of experience creating software for a regulated field such as medical devices. 2+ years of experience 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 »

The Quality Assurance Specialist will be responsible for ensuring the standards of the Quality Management System (QMS) at CGT Catapult Stevenage are maintained in a fit for purpose state of control, and improved, for a multi-purpose, multi-client facility. This will involve maintenance and improvement of associated procedures for … Maintain processes, including GMP document control and training, needed for successful site compliance to the QMS. Participate in the review the performance of the QMS at planned intervals and provide regular reporting to ensure its continuing suitability, adequacy and effectiveness and propose improvements. Participate in the execution of a GMP … actions and a process to track their completion. Experience: Demonstrable experience in an Operational Quality Assurance role providing product impact assessments as part of QMS processes. Demonstrable experience in sterile manufacturing processes, ideally ATMP’s or biologics (Desirable). Previous exposure to R&D interfacing environment (Desirable). Demonstrable experience more »

Human Medicines Regulations 2021 relevant MHRA Guidelines, legal requirements, and updates Ensure compliance with ISO 9001: 2015 and ISO 13485: 2016 standards. Ensure the QMS is implemented and maintained. The RP must approve, sign and date, all GDP SOPs/Documentation. Annual review of SOPs/Documentation will be carried … team and liaise with relevant department heads to ensure full regulatory compliance at all times To ensure that the business has in place a QMS that is compliant with all relevant regulatory requirements. Assess and approve new OEM’s, product specifications and artwork/labelling is in accordance with legal … advice on regulatory requirements. To ensure that the company has suitable of Quality Agreements in order to meet regulatory requirements. Lead the creation of QMS compliant processes and procedures to further improve the internal governance of our QMS systems, compliance with required Skills & Experience Relevant experience in Medical Device regulatory more »

for a perm role on behalf of our client based in Stanford le Hope. Duties and Responsibilities: Maintain the company's Environmental and Quality Management System frame work and ensure ongoing compliance with accredited ISO90001, ISO14001 and any other ISO standards as applicable. Manage day to day operation of the more »

ready to step up into a Principal role or an established PA looking for a change in their career. The Role: Adherence to the QMS including root cause analysis and communicating with clients on technical matters. Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical more »

quality, and delivery and to ensure continuity of supply. Role Understand, implement, and adhere to all relevant procedures included in the company's Quality Management System Become conversant with the part numbers, descriptions and application of the company's products and parts Become conversant with the capabilities of all assigned more »

/FDA regulated environment. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Collaborate with the Engineering and quality departments to ensure test method, equipment and materials are available in line with company timelines. Analyse and more »

your engaging management skills, audit ready mentality and practical approach will be a great compliment to the team. You'll be well versed with QMS, third party accreditation including BRC, HACCP, Retailer COP's, team management and open to change with the confidence to share your ideas! Your responsibilities will more »

facility in Bedfordshire. The primary purpose of the Quality Manager, Bedfordshire role will be to manage and proactively develop and maintain the Company Quality Management System in accordance with regulatory, customer and business requirements. Furthermore, the Quality Manager shall seek to improve the efficiency and effectiveness of the Quality System more »