Senior Manufacturing Engineer - Medical Devices

Newton Colmore; Cambridge; On-site; GBP 50,000 - 70,000; Full time

Job summary

A medical devices company in Cambridgeshire is seeking a Senior Manufacturing Engineer to lead process development and support product launches. You will collaborate with multidisciplinary teams while ensuring quality manufacturing practices. The role offers a generous compensation package with additional perks, in an innovative environment that champions professional growth.

Benefits

Generous compensation package

Monetary bonuses

Collaborative environment with world-class engineers

Qualifications

• Minimum of 5 years of experience in manufacturing in a medical devices environment.
• Expertise in process development and quality assessment.
• Proven ability to collaborate with multidisciplinary teams.

Responsibilities

• Lead manufacturing process development and identify improvements.
• Support design for manufacture as products are developed.
• Model product costs and identify potential suppliers.

Skills

Hands-on experience with design and manufacturing

Understanding of ISO 13485 and GMP

Manufacturing process improvement methodologies

Strong network of CMOs and tooling specialists

Job description

Overview

Senior Manufacturing Engineer - Medical Devices. A medical devices company based in Cambridgeshire is looking for a senior manufacturing / new product introduction engineer to join their fledgling team and help take their first products from development through to production. The company aims to transform patients' lives by providing step-change in real-time personalised health information via their novel sensor technology.

Responsibilities

• Take lead on manufacturing process development, controlling each stage of the process and planning experimental work with prototypes to identify improvements for the product and processes.
• Assess manufacturing quality and support design for manufacture as products are developed.
• Model product costs, identify potential suppliers, and support supplier audits.
• Apply knowledge to design verification activities, including procurement of prototypes for testing and specification and validation of jigs and fixtures.
• Collaborate with a multidisciplinary team and contribute to shaping working practices and team culture as the company grows.

Qualifications

• Hands-on experience with design and manufacturing.
• Understanding of ISO 13485 and GMP.
• Familiarity with manufacturing process improvement methodologies (advantageous).
• Strong network of CMOs and tooling specialists (advantageous).

Benefits

The company offers a generous and tailored compensation package with a variety of perks, including monetary bonuses. You will be joining a multidisciplinary team, working alongside world-class engineers and scientists in an innovative environment that supports success in your role.