Senior Quality Engineer, Jobs, Scotland, Glasgow, 5328

Engineering, Manufacturing & Supply Chain Recruitment

Senior Quality Engineer - Glasgow

Engineering & Manufacturing - Engineering & Manufacturing
Ref: 5328 Date Posted: Thursday 15 Feb 2018
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Nine Twenty Engineering are assisting in the recruitment of a Senior Quality Compliance Engineer for our West Central Scotland based Client. Our Client requires an enthusiastic and skilled individual to be responsible for Providing guidance and support. 

The Role:

Support key QA processes to ensure that these are compliant with required regulations and company policies and procedures. 

Support and manage the coordination of external audits by OEM customers and regulatory bodies including: 
•Leading advanced preparation of all notified audits 
•Developing a process for managing of unannounced audits 
•Responding to any identified findings from customer / regulatory audits 
•Following up on audit findings and tracking through to completion 
•Ensuring site audit readiness at all times 

Support and coordination of company internal audit programme including: 
•Management of internal audit schedule 
•Trending and reporting of internal audit findings 
•Performing Internal Audits as required 

Provide trending data and reports upon request to senior management, functional managers, regulatory authorities and customers. 

Work towards meeting departmental and facility objectives 

Development of effective internal and external customer relationships to ensure quality and regulatory compliance for the business. 

Oversight of new and updated quality and regulatory requirements to ensure the site retains a state of compliance in a changing environment. 
 

Essential Skills and Experience:

Relevant Science/Engineering Degree, or similar qualification 

Proven experience in Quality Management Systems in a similar role within a medical devices or a similar regulated environment 

Lead or Internal auditor qualified with proven audit experience 

Strong analytical and problem solving skills 

Knowledge and experience of FDA regulations 

Thorough knowledge of regulatory standards, Quality Management Systems and global regulations for medical devices 

Excellent facilitation, coordination, prioritization, presentation and communication skills 

Proven ability to manage and prioritise work load, meet deadlines and work in a pressurised environment 

Competence in the use of IT technology, such as Microsoft Office applications, and ability to learn other IT systems used in the QA department 

If you have the skills and Experience required for this role please submit your CV  to Nicole Lavelle for consideration.