Northwich, Cheshire, North West, United Kingdom Hybrid / WFH Options
Dechra
or preparation of responses to deficiencies) and on-site presence as required. Develop audit systems to ensure key elements of the Dechra GxP QualityManagementSystem and the requirements of the product licences/marketing authorisations are effectively implemented throughout the internal and external manufacturing network (as required) across the … and GMP/GDP regulatory compliance. Disseminate regulatory intelligence related to industry best practice, upcoming regulations, audit/inspection trends as well as general QMS training and product quality knowledge. Support the QMS Manager in the configuration of the eQMS supplier qualification, audit, and inspection processes within the eQMS system. more »
Greater Cheshire West and Chester Area, United Kingdom
Kintec Global Recruitment
wider responsibilities, on behalf of the TA team, for delivery of specific business processes. For example these could include TA Continuous Improvement, TA QualityManagementSystem or TA Materials Management. Organisation: Reports to Turnaround manager Key Accountabilities Turnaround Preparation and Planning: Scope Definition/Optimisation and Formulation of the Budget more »
for a Quality Engineer to join the major projects located in Warrington The Quality Engineer is responsible for: Maintaining, managing and improving the QualityManagementSystem in accordance with the requirements of BS-EN-ISO-9001 and other qualitymanagement standards and specifications as required. Ensure additional customer requirements are … phases of construction. Ability to develop client and supplier relationships ensuring compliance with relevant standards, specifications and instructions. Ability to develop the company QualityManagementSystem ensuring compliance with the latest National and European standards. Excellent knowledge and understanding of Nuclear Quality requirements for Lifetime Records and delivery of goods. more »
QP qualification essential Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies. Significant experience working with cGxP regulations Previous management/supervisory experience in a quality setting Important Information: We endeavour to process your personal data 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 »
Info about what the role entails Some of the key responsibilities of the role include: Assist in refining and evaluating the extant Project QualityManagementsystem by establishing requisite protocols, blueprints, and operational directives as necessary. Supervise the enactment of the Asset/Project/Function QualityManagementSystem through … periodic audits and evaluations. Provide backing and oversight in implementing Yokogawas CDM QMS on projects. Generate project-specific quality documentation for client ratification, such as Quality Plans, ITPs, and Databooks with appropriate frameworks. Participate in and furnish input for technical HSE and integrity reviews. Establish and track Key Performance Indicators more »
Alderley Edge, Cheshire, North West, United Kingdom
Russell Taylor Group Ltd
or maintaining and archiving documentation Supporting and executing external audits where applicable Supporting management when hosting regulatory audits Working on executing and maintaining the QMS, including but not limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant more »