Validation & Process Engineer – Medical Device Moulding

Meridian Medical Limited

Littlehampton

On-site

GBP 50,000 - 70,000

Full time

40 hours ago
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Benefits offered by this job

Employee health cash plan
Company pension
Onsite parking
Free tea and coffee provided
2 annual parties
All bank holidays paid and offsite

Job summary

Meridian Medical Limited is seeking an experienced Process & Validation Engineer in Littlehampton, West Sussex. The role focuses on developing and implementing best-practice validation and statistical methodologies across MouldShop and Cleanroom Production areas.

You will organise moulding validations, support new product introductions, improve validation systems and ensure proper documentation and handover into production.

Qualifications

  • Solid background in validation and/or product quality control.
  • Strong understanding of validation principles, methodologies and documentation.
  • Experience with statistical analysis and Minitab is advantageous.
  • Ability to read and understand CAD data.

Responsibilities

  • Organise and execute injection moulding validation protocols, including risk management.
  • Develop and maintain validation documentation and ensure requirements are met.
  • Ensure complete handover packages after validation.
  • Oversee metrology and validation activities for projects.
  • Contribute to Validation Master Plan and procedures.
  • Monitor production scrap and identify improvement opportunities.
  • Provide technical and validation support to Quality team.

Skills

Process engineering
Validation
Metrology
Quality control
Injection moulding
Statistical methods
CAD data reading
Problem solving

Education

Relevant technical degree

Tools

Minitab
Microsoft Office
CAD software

Job description

Meridian Medical Limited is seeking an experienced Process & Validation Engineer in Littlehampton, West Sussex. The role focuses on developing and implementing best-practice validation and statistical methodologies across MouldShop and Cleanroom Production areas.

You will organise moulding validations, support new product introductions, improve validation systems and ensure proper documentation and handover into production.

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