26 to 50 of 220 QMS Jobs in England

the site Ensure that the HACCP (HACCP/TACCP VACCP) program is maintained and aligned with best practice at all times Ensure that the QMS is effectively implemented and amended to ensure product standards are maintained Ensure the QA and Hygiene teams are run effectively and adequate technical resources are more »

Collaboration: Work closely with the sales and commercial teams to align technical aspects with market demands and business objectives. Quality Assurance: Oversee the quality management system, ensuring compliance with industry standards and regulations. Technical Leadership: Provide technical guidance and support to the production team, driving continuous improvement and operational excellence. more »

of in-house tools and process Support the wider company by answering technical questions Administration and maintenance of documentation forming part of the quality management system Review department KPIs to ensure targets are being hit Benefits: 25 days holiday + Bank Holidays New flexible holiday scheme Bupa Healthcare package Life 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 »

will be achieved by monitoring and maintaining quality assurance systems, food safety audits and HACCAP. Key Responsibilities.  Continually develop and maintain the Company quality management system and HACCP. with the assistance of our current BRC co-ordinator and administrator  Act upon legislation and guidelines to ensure that manufacturing is conducted more »

the following: Scientific, Technical and Professional To undertake work as you are assigned in compliance with current CPA/UKAS accreditation and TDL Quality Management System and H&S requirements. To adhere to all standard operating procedures at all times as relevant to the department in which you are working. more »

Lead, motivate and inspire QA team to achieve personal development and continuous improvement To promote a quality culture and help to develop the quality management system Experience Experience of leading a team Experience of working in a manufacturing environment Quality Assurance experience within a chilled environment Strong communication skills both more »

and assist production team with machinery assembly, to include working overtime as and when required. · Actively support continuous improvement. · Adherence to ISO 9001 Quality Management System compliance. · Be prepared to learn a diverse set of products from differing brands and continually improve your product knowledge. Required Skills: · Experience in a more »

development. Ophthalmic Knowledge: Knowledge of the ophthalmic field. GMP Experience: At least 2 years of experience working within a GMP environment, familiar with local QMS systems and compliant with EU GMP/EMA/ICH standards. Specialized Cell Culture: Experience in the generation, culture, and/or GMP manufacturing of 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 »

Ideally a qualified, certified Project Manager. Overview: Own ISO 9001 Plan Responsibilities, Policies, and Objectives of the Project Your Project Documentation to Launch Quality Management System Performance for Certification Improvement activities Key Responsibilities – Project Manager Quality Systems Health and Safety in the workplace above everything else, leading by example and more »

required in Quality Engineering in a manufacturing environment Role: Reporting to the Senior Quality Lead, you will be responsible for all aspects of Quality, QMS, Continuous Improvement and Business operating systems and play a key role in the day-to-day quality operations at our UK factory in Slough. The more »

the management and scheduling of all GCP supplier and site audits. Ensure a current schedule is maintained for these activities. Provide input into the QMS and at the regular Quality Management Review Meetings on GCP activities and metrics. To chair these in the absence of the Head of Quality. Represent more »

the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams, improve the QMS, provide expertise and guidance on changing regulatory landscape and input in operations that protects company reputation whilst maintaining product supply to market. The role holder more »

and effluent batches. Monitoring trends in data and reporting any issues directly to Quality Management. Assist Quality Manager in the maintenance of the Quality Management System as required. Reporting and managing of data on trends or certain batches declining if applicable, product quality and comms. Writing SOP and risk assessments. more »

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 in a QMS. Experience in writing deviations, change controls, CAPAs, complaints. Experience in supporting internal and external audits including BOH inspections. more »

in the South East market. We are seeking a dynamic and experienced Technical Sales Manager to support our sales efforts and oversee our quality management system, and maintain testing procedures to ensure excellence in our product offerings. Responsibilities: 1. Sales Strategy Implementation: Execute a sales strategy tailored to the South more »

wider finance team on an ad hoc basis (workload permitting) you will also adhere to company policy and working to the company ISO Quality Management system (9001 certification) and company security management system (27001 certification) and BSI standards at all times. Duties & Responsibilities Review and quality control of the POS more »

to detail and quality. • Problem Solving • Customer Focus • Functional/Technical Skills • Process Management • Understanding of program management, operations, distribution, delivery performance and quality management system • Understanding of root cause analysis, lean tools, procurement and supply chain management. • Familiarity with Sarbanes Oxley. • Exportation to international customers more »

attention to detail and with good communication skills to understand customer requirements and build products efficiently in line with our business objectives, our Quality Management system, Information Security Management system policies and Clinical Safety Frameworks. The candidate will have plenty of opportunity for growth with the possibility of becoming a more »

provided comprehensive language and technology solutions to help our clients communicate and conduct business more effectively in a global marketplace. Equipped with a quality management system certified to both the ISO 9001:2008 and EN 15038:2006 standards, TransPerfect provides a full array of language and business support services, including more »

eg GC, KF, UV-Vis, FT-IR. The use of a Chromatography Data System such as Empower in a regulated laboratory. Significant experience leading QMS driven aspects of a cGMP laboratory, Laboratory error investigation, OOS investigation, Deviation investigation and CAPA. Experience scheduling and planning workloads, resource and equipment including developing more »

the business. The Assurance Analyst will be responsible for the successful management and improvements of the Corporate Risk Register (RAID), the management of the QMS (ISO9001) and supporting the PMO. The Assurance Analyst will also be required to develop effective relationships with stakeholders across the business to deliver on objectives. … owners accountable for: Certifications Updating Partner Portal Ensuring objectives are being met in agreed timeframes QMS Management and continual improvement of the QMS (Quality Management System) Raise awareness of the QMS to the business and provide regular training and updates using corporate communication channels Hold Process owners to account for more »

or above Up to date & in-depth knowledge of quality and sub-specialist area within primary discipline. Desirable Evidence of understanding quality and the QMS within Pathology and being able to analyse and interpret quality data. Evidence of being able to perform audits. Equality, Diversity & Inclusion Essential Evidence of having more »

with a Life Science Organisation in the search for a Global Head of Quality. Deliverables To lead the build and continual development of the QMS to Quality standards Be the lead SME for Quality & Compliance related issues To shape, provide line management and run the Quality team To hold and more »