Process Engineer - Basingstoke, United Kingdom - Thermo Fisher Scientific

Thermo Fisher Scientific Basingstoke, United Kingdom

3 weeks ago

OTHER

Description

Job Description

Title: Process Engineer

Location: Basingstoke

Hours: Monday - Friday, 8am - 4pm

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit

Role summary

Working in the Basingstoke Production Leadership team; the Process Engineer is accountable for driving improvements in performance within manufacturing departments to deliver outstanding customer service safely and compliantly.

Responsibilities:

EHS:

For changes implemented ensure that Safe Systems of Work are In Place though use of risk assessment. Control measures built in through engineering controls, PPE requirements or procedural controls.

Promote safe working through either coaching or mentoring of staff

Quality:

Investigation of deviation and non-conformances in a timely manner owning Corrective and Preventive Actions.

Quantify and mitigate risk ensuring quality is built into production processes.

Customer Service:

Understand capacity constraints in the departments you support - Use of Plan Do Check Adjust cycle to drive continuous implement to solve worthy problems.

Key Performance indicators are in place to identifying underlying performance losses in an area that drive poor customer service

Ownership of actions as part of daily tier process where performance is not at expected level using appropriate problem solving tools working collaboratively with shift teams / peer group / wider site.

Cost:

Identify waste in processes and implement corrective actions to eliminate.

Gain business approval for worthy business improvements requiring capital expenditure.

Work with project engineers through project process to ensure capital expenditure delivers expected return on investment.

People:

Continuous improvement culture fully in Place and promoted through both JDI and Kaizen activities to deliver resolution to worthy business problems.

Working with team leaders communicate the need for change to production team creating advocates within the business

Work collaboratively with your peer group to ensure proposed changes are introduced safely and compliantly.

Minimum Qualifications:

Understanding of health and safety legislation and its practical application in the workplace backed up by IOSH qualification.

Demonstrate an understanding of GMP & Quality related medical device and / or pharmaceutical regulations & standards

Practical application use of lean manufacturing tools and techniques within a production environment – typically within pharmaceutical, medical device or FMCG industry.

Preferred Qualifications:

Green Belt Qualification or equivalent

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