76 to 100 of 256 Permanent QMS Jobs

Level 5 as SHEQ Manager Minimum of 4 to 5 Years experience in Health and Safety management Knowledge of ISO9001:2015 or, equivalent Quality Management System Fantastic communication skills with good influential and analytical skills An enthusiastic and dynamic personality with a highly ‘proactive attitude'. A ‘natural ability' to more »

plant Business Management System. Support the roll out of the Business Systems strategic improvement business plan. The maintenance and development of the companys quality management system documentation, including control and supervision of all amendments and revisions. Work effectively within various business units both in house and externally to improve the more »

weights, surface area, dimensions, radii, clearances, tolerances, leverages and location of holes Checks drawings, specifications, procedures, and bills of material in accordance with quality management system processes and procedures Coordinates with offshore design office for their work assignments Interfaces with internal customers to understand their project/design requirements & discuss more »

Quality Control of Radiotherapy Equipment Treatment Planning of Radiotherapy Patients Experience with complex computing systems and basic Microsoft Office skills Working within a quality management system Skills Essential Ability to use complex computerised Ability to use complex computerised Treatment Planning Systems and a range of radiotherapy equipment Computer literate Highly more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »

FID experience (general - Gas Chromatography experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT more »

Management of the destructive and non-destructive testing activity. Management and control of the product and system auditing. Management and control of all relevant QMS systems ISO9001, ISO14001 etc.. Lead and manage the development of preventative/corrective actions. Manage proactively any technical queries with customers providing all necessary guidance. more »

environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of more »

environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of more »

standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (eg ISO14001:2018, Lead the creation and more »

standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (e.g. ISO14001:2018, Lead the creation and more »

standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (eg ISO14001:2018, Lead the creation and more »

quality incidents, safety occurrences, and customer complaints, and implement corrective and preventive actions as necessary. Provide support during regulatory inspections, customer audits, and quality management system certifications. What you will need: Strong knowledge of QA methodologies, tools, and best practices including Part 145 Safety Management Systems. Extensive experience in quality more »

that arise as quickly and efficiently as possible to prevent compromising quality and safety standards. Ensure compliance and assist with adherence to the Quality Management system (ISO9001/AQAP2110) Report on Key Performance Indicators (KPIs) in order to adhere to process and prevent occurrence of any non-conformity relating to more »

Checking and reviewing of data in compliance with Data Integrity requirements Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner Supporting the team leader where required Skills/Experience Required: Degree or equivalent in a relevant scientific discipline Experience in more »

compliance of product manufactured Off-Site and complete the relevant reporting on timely manner. Ensure the Subcontractors/suppliers maintain a robust documented Quality Management System 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 »

the administrative aspect of the Technical Department taking responsibility for the day to day management and maintenance of some or all of the following; QMS, HACCP, legislation, specifications, Technical Reports, Contaminants & Non Conformance Logs, complaints, microbiological & nutritional surveillance, this work includes data entry, trending, filing, information requests, co-ordination of more »

from personal or Sonardyne work activities. To ensure awareness, understanding and adherence to all Sonardyne Policies and Procedures including Health & Safety, Anti Bribery, ISO9001-QMS and Operational requirements at all times. To take an active part in the Sonardyne Continuous Improvement Process, through providing suggestions for corrective actions, suggestions, initiatives 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 »

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 »

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 »

Overview: To ensure that all the products produced are assessed in accordance with the companys and customers requirements, the site Quality Management System and HACCP System, in order that the quality, safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position 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 Quality Management System 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 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 »