Manchester Area, United Kingdom Hybrid / WFH Options
Wilde Analysis Ltd
Ambitious and experienced engineer initially focused on nuclear-related applications, with specific involvement in an embedded team delivering a national project currently at concept phase. Background Wilde Analysis is a multi-disciplined consultancy and software channel partner, specializing in simulation more »
Directive 2001/83/EC , with previous operational QP experience. Additional responsibilities will include : Acting as GMP Subject Matter Expert for QMS site compliance Maintaining QMS systems, leading by example to implement and coordinate updates accordingly. Leading and coaching QA Team Ensuring all activities are completed in line with more »
Engineering Harwell About the Role We have an exciting opening for a Graduate Space Systems Software Engineer to join our growing team based at Harwell. Reporting to the Chief Engineer you'll be responsible for specifying, developing, integrating and verifying more »
Cranleigh STEM is working with a medical device and diagnostics manufacturer with a global reach. We are looking for a driven production manager to join our client’s team at their site in Berkshire. As a production manager, you will more »
Job summary PREVIOUS APPLICANTS NEED NOT APPLY This is a new role in an expanding department. Please note that this is an operational role, the holder of this post is expected to always work on one of the Trust sites more »
estimation Perform the responsibilities of Management Appointments relevant to post Perform additional Management Activities as required Undertake audits on UKAS aspects of the QualityManagementSystem Attributes, Qualifications & Experience HNC in Science or equivalent qualifications plus experience Demonstrable experience in lab areas Good interpersonal and communication skills Good general safety more »
of the following: Good standard of education – GCSE/A-Level or equivalent Ideally six sigma green belt certified Good knowledge of ISO9001 & AS9100 QMS Standards QA experience in manufacturing setting (ideally automotive/aerospace) Understanding of QA/CI tools e.g 5 why, FMEA, DMAIC etc. Customer service oriented more »
daily support to inspections and operations teams. Perform Internal Audits against ISO 9001, internal procedures, and customer requirements. Follow audit schedule to conduct workstation & QMS audits inclusive of follow up activity. Awareness of the requirements of ISO 9001 with experience applying the standard Experience using Microsoft Office (Word, Excel, PowerPoint more »
Job Title: QMS Manager (Part-time) Salary: £30,000 Pro Rata (18-22 hours per week) Location: Ashford Overview: An excellent opportunity has arisen with my client, a leading Insurance firm operating across the UK. We are seeking an experienced QMS Manager who is looking to operate on a part … QMS), driving efficiencies and continuous improvement across domestic operations. Duties include: Develop and maintain QMS documentation, maintaining the quality data collection and reporting system, performing QMS audits, and providing QMS training Ensure quality standards are met throughout the entire agency and ensure compliance to applicable regulations Prepare effective and high … business strategy and enhance customer experience Attending whole team meetings The successful candidate will have/be: Proven track record in developing and maintaining QMS systems Experience of carrying out audits on a qualitysystem Strong research and analytical skills Focus on continuous improvement, able to use own initiative Able more »
in line with the QP/ITP schedule and are issued for inclusion in the LTR concurrent to the works completed. Undertake periodic QualityManagementSystem audits both internal and external to ensure that the system and procedures are adhered to. Monitor Vendor Performance and carry out Supplier/Subcontractor 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 »
is required. You will need to be conversant with the main laboratory information managementsystem, and with middle-ware packages. There is a qualitymanagementsystem to ISO 15189 standards, within which you will be required to operate, particularly getting involved in audit and the investigation of adverse occurrences. The more »
to detail and quality. • Problem Solving • Customer Focus • Functional/Technical Skills • Process Management • Understanding of program management, operations, distribution, delivery performance and qualitymanagementsystem • Understanding of root cause analysis, lean tools, procurement and supply chain management. • Familiarity with Sarbanes Oxley. • Exportation to international customers more »
provided comprehensive language and technology solutions to help our clients communicate and conduct business more effectively in a global marketplace. Equipped with a qualitymanagementsystem 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 »
University College London Hospitals NHS Foundation Trust
The post holder will be expected to work closely with the Radiotherapy/PBT QualityManagement Team in the maintenance of the overall qualitymanagementsystem and under oversight of the services quality manager. About us University College London Hospitals NHS Foundation Trust (UCLH) is one of the most complex more »
Royal Sutton Coldfield, England, United Kingdom Hybrid / WFH Options
WEG Tech
in an engineering and/or manufacturing environment. Conversant with the process of attaining and maintaining accreditations to ISO 9001 and ISO 45001 Experienced QMS/H&S auditor This is a great opportunity to join a fast growing SME organisation and be a key member of their Senior Managementmore »
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 »
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 »
Hounslow, England, United Kingdom Hybrid / WFH Options
Trinity Resource Solutions
quality incidents, safety occurrences, and customer complaints, and implement corrective and preventive actions as necessary. Provide support during regulatory inspections, customer audits, and qualitymanagementsystem certifications. What you will need: Strong knowledge of QA methodologies, tools, and best practices including Part 145 Safety Management Systems. Extensive experience in qualitymore »
compliance of product manufactured Off-Site and complete the relevant reporting on timely manner. Ensure the Subcontractors/suppliers maintain a robust documented QualityManagementSystem that meets the requirements of the Works Information and supports self-certification. Perform frequent inspections of the construction elements to ensure their acceptance. This more »
To conduct the administrative aspect of the Technical Department taking responsibility for the day-to-day management of some or all of the following; QMS, HACCP, Legislation, Customer Specifications, Raw material specification. · Technical kpi generation and interpretation, including, non-conformance, customer complaints, microbiological performance · Helping to develop and maintain change more »
considered) Work Timings : US Timings (EST -3 days and PST -2 days) Job Responsibilities- 1.Compliance with working SOPs within the framework of the QualityManagementSystem and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. 2. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP more »
clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the QualityManagementSystem (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working more »