Job-type Interim / Contract
Salary £33k - 36k per year + Package
Contact Mike Butler
Call Mike
Email mike.butler.331675233.0@applybe.com
Reference MCB-QVEMAN

Quality Engineer

1 year fixed term contract 

Factory manufacturing and validation support

Direct Report To: Quality Team Manager

Location: Greater Manchester

Client: Consumer healthcare and FMCG solutions on a Global scale

Rewards? £32k - £36k Band  awesome Package

Working within the site quality team, in this newly created role and due to expansion, you’ll do challenging work, everyday!

At the heart of an operational technical team; a team that values  quality and product innovation.

Our client is a growing,  global organization expanding through £MM site investment.

This is a diverse and challenging role, promoting product quality improvements, compliance& validation  and efficiency improvement projects & new product introductions, to improve product quality.

You will play a key role to improve people’s lives and develop cutting edge healthcare solutions.

Your new challenge!

  • Measuring and monitoring of performance against agreed KPI's including collating and sharing of information/data
  • Facilitate risk assessments (PFMEA/FMEA) to assist in improving both product and processes
  •  QA lead on CAPA projects, ensuring product/process improvements are executed
  • Support the change control process ensuring compliance with ISO/Corporate guidelines and championing process improvements
  • Support quality assurance improvement activities by evaluating products, processes, and data to develop control or improvement strategies intended to improve the customer’s experience
  • Participate in the development and maintenance of product risk
  • Develops and review risk assessments and risk strategies, validation management
  • Able to effectively use risk assessment tools like FMEAs and FTAs

Is this you?

  • Degree in a scientific or engineering discipline
  • Knowledge of ISO9001/13485/ or equivalent standards
  • Experience of FMEA/PFMEA an advantage
  • Experience with Quality Improvement Tools (5 Why/pareto analysis)
  • Experience of CAPA processes & problem solving within Process/Product Improvement
  • Work independently and with project teams to develop design control deliverables including quality plans, manufacturing & inspection documentation
  • Experience in a Quality Engineering role at an engineering, regulated pharmaceutical or medical device manufacturer
  • Quality Auditor experience
  • Validation experience , factory experience, process and equipment validation
  • Proficient in the knowledge of applicable Quality System Regulations and ISO quality requirements
  • QA, Manufacturing, Validation, Change Control, and Design Control processes

would suit applicants from pharmaceutical, FMCG, medical and related regulated industries such as automotive and aerospace, Manufacturing, FMEA, quality engineer, quality officer, validation engineer

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