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Quality Engineer

£45,000 - £52,000 per annum
Location

Gloucestershire

Contract type

Full Time

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Location - Gloucestershire

Salary - £35k - £40k

Job Type - Permanent

To maintain and support the quality management systems within a manufacturing environment.

Maintains product quality standards across all manufacturing processes, focusing on those where deficiencies are known/occur. Supports teams to work accurately and effectively to eliminate/reduce the probability and severity of faults, failures and scrap.

Working as part of a team which strives to define and develop manufacturing solutions from the early phases through to production working with the Engineering team. This will include working as part of a project core team with respect to design control, as well as working with the operational team on continuous improvement projects.

• Environmental monitoring control

• Reporting/completing of quality metrics monthly and filling out dashboard

• Supporting quality control team and monitoring performance and output

• Ensure quality is maintained across manufacturing

• Performing process validations

• Maintaining the efficiency of the Quality Management System (QMS) and implementing continuous improvement.

• Maintaining processes and creating procedures related to incoming inspection, quality assurance and quality compliance.

• Work with the Technical teams to ensure the proper deployment of Engineering Changes.

• Plan and carry out Process Validation for existing and new products.

• Qualified as an internal auditor. Part of the internal quality audit team by auditing the quality and manufacturing processes to ensure both internal and external regulations.

• Maintain working knowledge of Regulatory and Quality System requirements.

• Support customer & 3rd party audits, including yearly QMS audit.

• Writing and updating documentation for maintenance of the quality management system.

• Contribute to CAPA system, complaint management process and documentation control.

• Train and provide assistance to the other QA teams on quality procedures, protocols, and documentation.

• Coordinate investigation of quality issues with customers and suppliers

• Assist with the monitoring, measurement and recording of environmental conditions significant to preservation of product and for packaging of product to be sterilised

• Leads Quality related projects and represents quality as and when required on projects across operations

Qualifications & experience:

• Scientific or engineering degree with experience in the medical device or pharma industry, in a quality related position.

• Certification, such as Quality Engineer, Quality Auditor, Six Sigma, or Quality Improvement Associate, is preferred

• Project management desirable

• Formulating and execution of corrective action programs

• Superb computer competence, including experience with databases and Microsoft Office

• Knowledge of QA terms, tools, and methodologies

If this is of interest please contact Ryan Kline on (phone number removed) or (url removed)

Omega Resource Group is acting as an Employment Agency in relation to this vacancy.

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By applying a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

By applying a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

Apply now in a few quick clicks

By applying a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

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