Loughborough, Leicestershire, East Midlands, United Kingdom Hybrid / WFH Options
Almac Group (Uk) Ltd
as part of the Quality Assurance team based in our Charnwood site in Loughborough, you will be responsible for supporting the QualityManagementSystem (QMS) and verifying the adherence of manufactured products for human use, in line with current Good Manufacturing Practice (cGMP). As part of a busy team more »
are experts in Asset Lifecycle Management, offering our clients innovative software solutions, service contracts and consultative expertise through our own, proprietary QualityManagementSystem (QMS). We deliver our best-in-class asset and resource management software and consultancy services to a broad range of clients across multiple sectors. Location more »
Work with Customer Success Team to deploy and maintain client solution environments & configuration. Provide Tier 2 support. Ensure compliance with CYTE QualityManagementSystem (QMS), including training assignments. In order to perform this role, individuals must have the following qualifications, competencies and personal qualities: Bachelor s degree, or equivalent, in more »
Work with Customer Success Team to deploy and maintain client solution environments & configuration. Provide Tier 2 support. Ensure compliance with CYTE QualityManagementSystem (QMS), including training assignments. In order to perform this role, individuals must have the following qualifications, competencies and personal qualities: Bachelor’s degree, or equivalent, in more »
be able to hold their own within a QMS. The ideal candidate must have at least two years of experience in a Pharmaceutical QualityManagementSystem and understand and be able to complete QMS activities including: Change control Deviations CAPA QMRs Recalls Returns Training The role involves: Review, update and … bona fide reviews, reviewing Technical Agreements etc. Requirements: Experience/knowledge in the following is useful – Sage, Outlook, Microsoft 365, import of pharmaceuticals, pharmaceutical QMS or PLPI would be useful but not essential. The company has a MIA for PLPI as well as a WDA with a single QMS, so more »
operational issues within the PPA areas. Supports with project related document and technical review. Generation and monitoring of data streams and analysis to support QMS maintenance and inform decision making across business. Work alongside internal customers to support in on-going compliance to internal QMS and external standard/regulation more »
and products under change control due to continuous improvement and product evolution. The successful candidate will be experienced in working with QualityManagement Systems (QMS) related to the medical device industry, and the reviewing of technical engineering documentation. They will be able to review and understand from a quality perspective … the following: M&E Maintenance Engineer, M&E, Mechanical and QualityManagement, Mechanical, Electrical, Maintenance Engineer, Electrical Engineering, Electrical Engineer, Mechanical Engineering, Mobile Engineer, QMS, Design Engineer, CAD Design Engineer, Design Quality, Technical Engineer etc REF more »
Quality Assurance Manager – Project Lead. FTC until end of Dec 2024 (3 days a week). Salary Negotiable dependent on experience plus benefits. My client are an expanding pharmaceutical manufacturing organisation seeking a highly motivated and experienced Quality Assurance Manager more »
Huntingdon, Cambridgeshire, East Anglia, United Kingdom
MM Flowers Ltd
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 »
Knowledge of robotics and lights out methodologies for machining. • Working knowledge of qualitysystem models such as ISO9001, AS9100 into a QualityManagementSystem (QMS), Aerospace Regulations • Able to use/familiarity of ERP systems • Understanding of Project Management processes and systems What we can offer They offer an attractive more »
Knowledge of robotics and lights out methodologies for machining. • Working knowledge of qualitysystem models such as ISO9001, AS9100 into a QualityManagementSystem (QMS), Aerospace Regulations • Able to use/familiarity of ERP systems • Understanding of Project Management processes and systems What we can offer They offer an attractive more »
QMS Co-ordinator Irlam Mon-Fri 08:00-16:30 £30,000 QMS Co-ordinator The Role My client is a leading manufacturer in their field. They are going through an exciting period of growth, with a true vision to develop their machinery, capabilities and facilities – it is an opportunity … not to be missed! They are looking to employ an experienced QMS Co-ordinator, with knowledge of BRC and experience with auditing. QMS Co-ordinator Main Responsibilities Ensure all Safety rules and procedures are adhered to. Encourage a safe and clean work area at all times. Follow operating, health and … all Work Stations. Monitor Employee Training Records and re-train where necessary. Maintain Records for BRCGS Audit including internal audits. Amend agreed changes to QMS documents and procedures. Participate in BRCGS and other Customer audits. Mentoring Production Staff to get the best out of them, showing them best practice. Working more »
central role in the continued implementation & improvement of the ISO 9001 QualityManagement System. You will work across functions to help integrate the new QMS into our everyday processes. You will have the opportunity to have a broad range of quality responsibility & make a significant contribution to the growth of … across the company to continue the implementation, maintenance, & improvement of the ISO 9001 QualityManagement System. Ensure that the processes needed for the qualitymanagementsystem are operated in such a way that a culture of quality is developed & maintained. Drive training activities on Quality processes. Taking ownership of the … electronic QMS & administration the system. Ensure that quality documents & records are appropriately managed within the eQMS. Update policies & procedures as part of continual improvement activities. Drive the nonconformance & CAPA systems & acting as a subject matter expert for quality assurance in CAPA investigations. Engage with product development & operations teams on supplier more »
Bristol, Avon, South West, United Kingdom Hybrid / WFH Options
Staffbase Recruitment
for the position of Quality Assurance & Safety Manager. The successful candidate will be responsible for the maintenance and development of the company's qualitymanagementsystem and to oversee the health & safety system associated with the design, assembly, manufacture of automated machinery and after-sales servicing activities. The Role: Reporting … initiatives throughout the business. Your duties will include but is not limited to the the following; Maintain, develop and improve the company's qualitymanagementsystem Oversee safety and environment compliance Monitor, report and develop KPI's Lead & develop continuous improvement throughout all areas of the business Deploy quality improvement more »
Senior Buyer (Manufacturing) Location : Oxfordshire Job Type: Full time Contract Type: Permanent Salary: Competitive Benefits: Private healthcare, pension, income protection, life assurance, 27 days holiday + bank holidays, equity scheme Are you an experienced Senior Buyer of electronic components & electro more »
Job summary The Manchester University NHS Foundation Trust includes major teaching hospitals. A wide range of equipment is used for medical work - diagnosis, monitoring, therapy and technical work - throughout its wards, theatres, andclinical departments. The Clinical Engineering Department deliver high more »
This is an exciting opportunity for a Technical Manager to join a world-leading provider of vertical access equipment. This role involves managing and further developing a focused Technical Support offering that delivers value to the UK business and client more »
Quality Engineer should demonstrate: 3 years experience in an automotive manufacturing environment Degree or similar qualification (or qualified by experience) Trained in standards for QMS: IATF16949, Application of QMS tools and techniques Application of QMS tools and techniques APQP, FMEA, Inspection planning, SPC, DOE, QFD, Six Sigma Knowledge in PC more »
Job Summary QA Specialist is responsible for ensuring continued compliance of the QualityManagementSystem of the company with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities Provide day-to-day support and be responsible to … maintain the effectiveness of the QualityManagementSystem, including, but not limited to, Document Control, CAPA, Vigilance, Risk Management, Internal Audit, Post-Market Surveillance, Supplier Monitoring and Assessment and Product Release activities Contribute to strategic improvement projects to improve business processes in line with the applicable regulatory requirements and Medicareplus … times To show initiative in problem solving by identifying and recommending solutions to problems encountered To maintain a personal knowledge of the current QualityManagementSystem and Regulatory Requirements Please note that the duties and responsibilities within this role may change over the course of employment, which will require flexibility. more »
Bishop's Stortford, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
HR GO Recruitment - Bishop's Stortford
compliance with ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other regulations. Prepare and maintain QMS and regulatory documentation. Assist QA Admin team with product approvals for UK and international markets. Evaluate suppliers and conduct approval audits. Document quality audits to … in a production/manufacturing environment. Internal and external quality auditing experience to ISO 13485. Passion for quality excellence. Previous quality assurance experience, including QMS documentation. Knowledge of CAPA and root cause analysis tools. Practical problem-solving approach. Understanding of ISO 14971 quality risk management principles. Self-motivated and team more »
a QA officer in either the Pharmaceutical, Medical Device, Biotechnology, Life Sciences or Specialty chemicals industry. You will have experience in Deviations, CAPA, Audits, QMS or batch release. To apply for QA Officer role please send your CV to Peter at Rowland Talent. Please note candidates must have the right … to work in the UK Key words Quality, QMS, Deviations, CAPA, Audits, batch release, SOPs, Documents, GMP, QA, change controls more »
and knowledge. Manage HSE policy and system framework in coordination with Group Health and Safety and client EHS representatives. Oversee the QualityManagementSystem (QMS) in line with contract and scope of QMS requirements. Ideal Candidate: Location: Based in either UK, Ireland, Spain, Belgium, Switzerland, or Netherlands. Experience: Solid background more »
required corrective actions Ensure products and ingredients are evaluated against specification Support the promotion of a quality culture and help to develop the qualitymanagementsystem Coordinate QA requirements for product launches e.g. update of required documentation/systems, liaison with Process team/line support to ensure product is … manufactured to correct standard Plan and co-ordinate work of the QA team to meet requirements of the qualitymanagementsystem and the needs of the business About you. Ideally you will have a good practical working knowledge of food safety legislation and quality requirements. A strong QA background is more »
conformance reports (NCRs). Final review of all fabrication and assembly documentation. Collate and update SQEP files. Conduct audits on the QualityManagementSystem (QMS). Requirements: CSWIP 3.1 certified is essential. Experience within Nuclear or MOD highly advantageous. Experience with Life-Time Quality Records (LTQRs) Pay Rate: circa more »
and spoken Ability to interact at all levels Customer facing experience AS9100, BSEN ISO9001 experience Are you familiar with ISO 9001:2015 and AS9100 QMS standard … requirements? As the Quality Assurance Supervisor for the companys Avonmouth operation, you will be required to flow down the requirements of the company QualityManagementSystem & AS9120 to site employees and advise on any relating queries. This is a new role for the company where you will: Monitor and measure more »