Process Engineer at Flexible Medical Packaging
Lancaster LA1 4XS, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

27 Nov, 25

Salary

40000.0

Posted On

27 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Mechanical or Industrial Engineering

Description

ABOUT US

Flexible Medical Packaging Limited (FMP) is the part of Clinimed Holding Limited, a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group.
Flexible Medical Packaging (FMP) Limited are offers a first-class turnkey service of sterile and non-sterile products, for the Healthcare provision. It is our mission to ensure that our customers are completely satisfied with the quality of our work and service. Supported by years of experience and extensive industry knowledge, we are confident in our ability to provide a level of service that will surpass our customers’ expectations.

JOB SUMMARY

The Process Engineer plays a key role in supporting the Engineering department with both ongoing and new projects. This includes leading cross-functional teams to ensure timely and successful project delivery. A major focus of the role is facilitating effective communication between departments and coordinating efforts to review and improve processes. The Process Engineer will also be responsible for conducting and documenting process trials on both existing and new products.

Responsibilities
  • Evaluate current manufacturing processes and identify opportunities for improvement.
  • Design, modify, and implement process enhancements to reduce defects and improve efficiency.
  • Analyse production data to propose and implement improvement measures and track the effectiveness of these changes.
  • Assist in the selection, implementation, and testing of new or upgraded manufacturing equipment.
  • Lead and manage projects related to the introduction of new equipment and processes.
  • Research and support the procurement of new manufacturing technologies and equipment.
  • Collaborate with project teams to define validation requirements for new equipment or processes.
  • Manage process validation and trials, including OQ/PQ activities, as well as day-to-day management of process improvement trials.
  • Work closely with production teams to identify performance constraints and implement actions to increase Overall Equipment Effectiveness (OEE)
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