Butler Rose are seeking a Quality Engineer to join one of our clients, a Plymouth based manufacturer.
This role is ideal for an existing Production, Process, Metrology or Quality Engineer, or for an existing Technician level person to progress into a more senior position within a progressive, high technology organisation.
The ideal candidate must be enthusiastic, data driven, extremely flexible and tenacious, training will be provided to the right candidate.
We are looking for a Quality Engineer on a permanent basis in the Plymouth area with experience in the Manufacturing Industry.
Your main duty will be to carry out Process Improvement projects as well as deal with day to day Manufacturing Quality issues within the various processes.
50,000 per annum plus benefits (dependent on experience)
To work in line with Quality, Safety and Environmental Policies, Procedures and Instructions.
General
An experienced Quality Engineer who has strong experience within Quality tools like 8D, investigations, FMEA's PPAP and SPC is required for a large and reputable Manufacturing business based in Plymouth.
Our client is able to offer a long term and progressive career within a Multi-National organisation.
Excellent opportunity for a Quality Engineer to join a market-leading, international company where you will have the chance to develop your career and work on advanced engineering projects.
The company are a well-established, highly revered manufacturing company in the Plymouth area with sites across the world that not only are renowned for the quality of their products but also for being a leading and progressive employer within the area.
£42,000 - £45,000 Bonus 25 Days Holiday Bank Holidays Pension Extra Benefits
Be part of our ambition to be the world's leading Pharmacy-led retailer.
Our patients are at the heart of everything we do, and we're proud to offer legendary care every day; it's what sets us apart from other UK Pharmacy chains.
Maintaining compliance to relevant regulations and quality standards such as cGMP, FDA QSR 21 CFR 820, ISO13485, and European Medical Devices Directive MDD94/42/EEC.
General
This will be an onsite role, due to the crucial part you will play as the liaison between quality and production.
Adecco are working with a Medical Device manufacturer hiring a Quality Engineer into the team.