Medical Device Process Engineer: Validation & Improvement

Intersurgical; Wokingham; On-site; GBP 40,000 - 60,000; Full time

Job summary

Intersurgical UK is seeking an experienced Process Engineer to develop, optimise and validate manufacturing processes within the Site Engineering Department. You will coordinate IQ, OQ and PQ activities and support continuous improvement across production and quality practices.

You will apply medical device quality requirements (ISO 13485) and work with cross‑functional teams to resolve process issues, document protocols, and drive compliant, efficient manufacturing.

Qualifications

• Experience in process validation and qualification incl. IQ/OQ/PQ.
• Experience in process optimisation and continuous improvement.
• Knowledge of ISO 13485 and medical device quality requirements.

Responsibilities

• Develop, optimise and improve manufacturing processes.
• Plan and execute IQ/OQ and PQ activities.
• Support validation and qualification projects to ensure compliance.
• Collaborate with cross‑functional teams to resolve process issues.

Skills

IQ/OQ/PQ

Process validation

Process optimisation

Documentation

Quality systems

Education

Engineering degree

Tools

Microsoft Office

Quality Management Systems

Job description

Intersurgical UK is seeking an experienced Process Engineer to develop, optimise and validate manufacturing processes within the Site Engineering Department. You will coordinate IQ, OQ and PQ activities and support continuous improvement across production and quality practices.

You will apply medical device quality requirements (ISO 13485) and work with cross‑functional teams to resolve process issues, document protocols, and drive compliant, efficient manufacturing.