that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that QualityManagementSystem ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »
the most important functions in the 300+ fte Quality organisation at this 1000+ fte site. A broad understanding of Quality (QA/QC/QMS) and Manufacturing would add value to how you manage the strategic and operational goals and clearly communicate your decisions to internal and external stakeholders. This more »
also be considered. At least five years of qualitymanagement experience and a track record of supporting businesses on their quality agenda. Experience in QMS implementation, HACCP and Trade Associations promoting good food quality business practice. A passion for delving deep to gather all the information available to support identifying more »
High levels of commitment to customer service. Strong written and verbal communication skills. Organisational skills to track and trend performance. Quality-minded focus/QMS experience. Our global team: We are a team of 66,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of whats more »
actively participating in their resolution to maintain quality standards. Track, assess, and approve Non-Conformances (NCs)/Incident Reports (IRs) through the electronic QualityManagementSystem (eQMS), driving continual quality enhancement. Review and approve Quality Documents to ensure adherence to ICH-GCP standards and process improvements, leveraging the eQMS. Prepare more »
London, England, United Kingdom Hybrid / WFH Options
i-Pharm Consulting
team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMSsystem Able to manage non-compliance issues and escalate when needed Have experience in the management of recalls Deal with customer, supplier, and vendor approvals more »
South East London, England, United Kingdom Hybrid / WFH Options
i-Pharm Consulting
of a global team.Other essential responsibilities include:Management of GMP and GDP complianceManagement of complaints, CAPAs, risk assessments, and validation protocolsReview and manage the QMS systemAble to manage non-compliance issues and escalate when neededHave experience in the management of recalls Deal with customer, supplier, and vendor approvals, including periodic 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 »
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 »
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 »
socially and professionally, with regular post-work events and regular group lunches. There is an atmosphere of openness and collaboration. We have a qualitymanagementsystem annually certified by the BSI to allow us to develop Software As a Medical Device, we have a machine learning operations created in-house more »
and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »
scale up of Manufacturing operations in line with GMP standards Draft and maintain SOP’s and batch recordsRecording all activities and deviations within the QMS Identify new working practices to streamline/standardise processesAct and support the team effort in identifying process risk assessments Maintain a clean and sterile working more »
up of Manufacturing operations in line with GMP standards Draft and maintain SOP’s and batch records Recording all activities and deviations within the QMS Identify new working practices to streamline/standardise processes Act and support the team effort in identifying process risk assessments Maintain a clean and sterile 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 »
and implement the policies for the maintenance and management of public parks and open spaces. to contribute to and follow the Service’s qualitymanagementsystem, ensuring all functions are carried out in accordance with them. to prepare and submit funding applications for external funds to support council capital funding more »
with existing and new requirements. Specify audit scopes to ensure compliance with legislation, industry standards, and company policies. Maintain and enhance the ISO9001 QualityManagementSystem and ISO14001 Environmental Management System. Approve engineering change documents and concessions, and monitor safety performance of fleet personnel and contractors. Ensure depot staff are more »
London, England, United Kingdom Hybrid / WFH Options
Comanos
any planned equity and debt raises. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and QualityManagementSystem, compliant with ISO standards. Required skills and qualifications: Prior project appraisal and business planning experience (ideally within renewable energy sector). Experience of project more »
prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 qualitymanagementsystem and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient outcomes! What skills and experience more »
the team and with external partners. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and QualityManagementSystem, compliant with ISO standards PERSON SPECIFICATION Required Experience Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »
PDA reports ensuring that it is correctly completed and procedures are followed within the required timescales - Work in line with the Company’s qualitymanagementsystem, industry standards and regulations and Health & Safety policy - Understand the importance of GDPR and the protection of sensitive customer information Professional Requirements: - Have a more »
job description carefully before applying, thank you) Primary Objectives: The Quality Assurance Associate is responsible for helping to maintain and improve the DnaNudge QualityManagementSystem as part of the Quality team by identifying potential improvements and efficiencies and helping to develop, revise and implement Quality procedures and policies. The … compliance of all regulatory requirements. Participate in the execution and support of internal and external regulatory audits and inspections. Support the maintenance of DnaNudge QMS program ensuring all processes are compliant to the relevant standards. · Manage some DnaNudge documentation associated with the QMS where required · Perform initial quality reviews of … internal auditor · (Desirable) Has worked in a similar role within the Medical Device/Pharmaceutical industry · (Desirable) Working knowledge and experience with a QualityManagementSystem, such as deviations, investigations, CAPA, and customer complaints. · (Desirable) Experience of ISO certified QMS (ISO13485) Knowledge (Essential) In depth understanding of approaches to qualitymore »
AWE is currently recruiting for a Commissioning Engineer to provide due governance and management to meet specifications and acceptance criteria, within the QMS and Project Delivery processes and procedures, whilst organising and managing commissioning activities. Location : Reading area Package : £33,850 - c£44,000 (depending on your suitability and level more »
East London, London, United Kingdom Hybrid / WFH Options
SOUTH WEST RECRUITMENT
employment as and when required. You will also receive a full company induction that will include many areas such as GDPR the DBF QualityManagementSystem and all other systems and soft skills training. About the Company Leading the way in Customer Interaction & process management the company are an international more »
to the Clinical Development teams, providing guidance on GCP activities related to quality. Primary Responsibilities: Defining, maintaining, and monitoring the GxP QualityManagementSystem (QMS). Making sure the QMS meets all the necessary regulatory requirements, with a strong focus on GCP compliance. Supporting and guiding the Clinical Development teams more »