Manufacturing engineer
Thermo Fisher Scientific
Paisley
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When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation. With revenues of $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Position Objective:
The positions objective is to assist in delivering all engineering key initiatives on time and within scope. The Manufacturing Engineer will work closely with the manufacturing, QA & EHS departments to deliver projects to enhance quality, productivity, safety and cost. The primary function of the manufacturing is to ensure that manufacturing process continues to deliver world class products as efficiently as possible through continuous improvement initiatives within the manufacturing areas.

Essential Functions:
The role of the manufacturing engineers is drive continuous improvement initiatives using PPI methodology and other Process excellence techniques.

Participate as a team member in complex multi-functional projects taking the lead role when required on engineering actions and sub project.

Lead Kaizen events and short to medium projects to completion ensuring all deliverables are delivered on time and on cost

Ensure day to day manufacturing issues are resolved and auctioned in a timely manner

Collaborate and share best practice and knowledge across functions and if required across

sites

Analyse daily metrics and use data driven decision to improve processes and generate reports to document

Ability to write and perform validation of process and equipment

Work with other departments to develop and improve current process equipment and systems to deliver change and improve key metrics

Key Skills required for this specific Role

Good Technical knowledge of process and equipment

Excellent communication skills – works across functions

Result driven

Team player and self-starter

Ability to learn and develop current skills and behaviours to progress within the function and lead by example.

Ability to set up relationships with current and new vendors to develop processes and system to drive continuous improvement within manufacturing process

Knowledge of process excellence techniques including lean , Six sigma and SPC

Good working knowledge of validation of medical devices ( IQ/ OQ/ PQ)

Minimum Requirements/Qualifications:
Experience

Minimum HND or higher in technical / scientific discipline

Experience working within a medical device manufacturing environment or cGMP manufacturing environment.

Previous experience of working within team and delivering projects deliverables essential

Working Conditions

Role could require occasional travel and out of hours working

Role will require working in controlled environments e.g. Cleanroom
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