Quality Systems Manager

Expiring today

Recruiter
Anonymous
Location
Southend-on-Sea
Salary
50000.00 - 60000.00 GBP Annual + GBP50000 - GBP60000/annum
Posted
05 Feb 2017
Closes
19 Feb 2017
Function
Consultant
Contract Type
Permanent
Hours
Full Time
Our clients Manufacturing Business Centre plays a key role in the development and manufacture of new, sophisticated medical and industrial products. Working with colleagues in Europe, the USA and Japan, our multi-disciplinary team of R&D engineers is fully equipped with the latest computer-aided design and modelling technologies, to enable them to develop medical workstations and fluid management products & accessories, and industrial Remote Visual Inspection devices.

Producing world class products in terms of Quality, Cost and Delivery isn't just desirable, it's essential. Therefore, in today's fast moving, ever changing world, we continue to invest in both our people and the latest equipment and processes to remain at the forefront in manufacturing technology.

Your Responsibilities:
• Participate in the design and manufacturing process to ensure products meet SQCD requirements.
• Deputise for the Quality Management Systems Representative.
• Assures that quality systems procedures, processes, practices and controls are properly developed, implemented and maintained.
• Assures that all products represent the maximum quality and reliability attainable.
• Routinely provides guidance and leadership to engineers, inspectors and/or technicians for the duration of a project assignment.
• Key role in ensuring product issues are promptly investigated and adequate corrective/preventive action implemented e.g. customer complaints, out of specification components, etc.
• Ensures the CAPA systems are operating effectively and close out of corrective actions meets expected deadlines.

Your Qualifications:

• Degree, or equivalent, in an Engineering or Life-Sciences Discipline.
• Five in a Quality Systems and/or Engineering role within an Electro-Mechanical or Electronics or Sterile Medical Devices Manufacturing environment.
• Experience in a Medical Device facility and knowledge of FDA Quality System Regulations (21 CFR 820), EU MDD, JPAL, ISO13485 and ISO9001.
• Proven track record in a supervisory role