Change Control Jobs in East Anglia

4 of 4 Change Control Jobs in East Anglia

Senior Configuration Engineer

stevenage, east anglia, United Kingdom
Hybrid / WFH Options
Eclectic Recruitment Ltd
a British Citizen or Dual UK National (including British Citizenship). Key responsibilities will include: Manage Configuration Management (CM) processes, ensuring accurate documentation and control of product configurations. Lead engineering change management, including preparation and presentation of changes in change control meetings. Collaborate with cross-functional … teams to maintain configuration integrity throughout the product lifecycle. Support supplier audits to ensure CM compliance across the supply chain. Maintain and control technical data, including BOMs, drawings, and CAD models. Produce and review CM documentation to ensure compliance with governance standards. The successful candidate will have: A background … in Configuration Control or Technical Data Management within a Defence or Aerospace industry or similar. Evidential experience in interpreting technical data and Bills of Materials for large and complex product assemblies. Familiar with the principles of Configuration Management within an aerospace or defence setting; preparing and handling Configuration Management More ❯
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Project Manager

st albans, east anglia, united kingdom
Outsourced Professional Administration Limited (OPAL)
performance, process/systems/service improvements within Project Team. People – Demonstrates integrity, respect, teaming, leadership and management of handling of all Project and Change Control work. Resilience is required during the pressures of project delivery and in such cases as conflicting priorities or where customer satisfaction is … OPAL operate in. The ability to motivate a project team to meet tight deadlines Good People Management skills as follows: - Anticipates and reacts to change - Possesses good judgement - Able to manage conflict - Persuasion, Resource Management, Time Management, Vision Ability to adapt to change with a flexible approach. Experience … of delivering software change and technologies Additional Knowledge required to become fully competent Understanding of the product particulars in the Protection and Investment space Competent knowledge of the Software Development Lifecycle Acquire a technical understanding of the software, architecture and infrastructure of OPAL solutions Acquire and implement knowledge and More ❯
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Quality Validation (CSV) Specialist

hertfordshire, east anglia, United Kingdom
CK Group
global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for ensuring that electronic systems within the Quality Control Laboratory and the Quality Systems operate in accordance with the requirements of the departmental Standard Operating Procedures Key duties will include : Ensure the Electronic … Quality Management System (QMS) and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and company expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required … and Validation documentation. Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data and ensure continuous system availability and functionality. Support the Management of the relationships with external system providers for technical and More ❯
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Quality Validation Specialist

hatfield, east anglia, united kingdom
CK Group
global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for ensuring that electronic systems within the Quality Control Laboratory, and the Quality Systems operate in accordance with the requirements of the departmental Standard Operating Procedures Key duties will include : Ensure the Electronic … Quality Management System (QMS) and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and company expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required … and Validation documentation. Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data and ensure continuous system availability and functionality. Support the Management of the relationships with external system providers for technical and More ❯
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