Process engineer Work, Jobs in Cambridge, Eng (with Salaries)

Process Engineer
Harvard Bioscience —Cambridge
- Full-time
- Engineering
- Bachelor's degree
- Continuous improvement
Quick apply
Graduate Process Engineer - Water - 2027 (Cambridge)
Stantec —Cambridge
- Hybrid work
- Engineering
- Bachelor's degree
8d
Manufacturing Engineer
Senior Aerospace Thermal Engineering —Royston
- Full-time
- Continuous improvement
- Manufacturing
- Communication skills
- Employee assistance programme
- Employee discount
Quick apply
Process commissioning engineer
Johnson Matthey —Royston
- Full-time
- Engineering
- No degree
Senior Special Process Engineer
Senior Aerospace Thermal Engineering —Royston
- Full-time
- Continuous improvement
- Team management
- Quality control
Quick apply
Senior RF Engineer
Filtronic —Cambridge
- Full-time
- Hybrid work
- Bachelor's degree
Quick apply
Higher Senior RF Engineer
Filtronic —Cambridge
- Full-time
- Bachelor's degree
Quick apply
Postdoctoral Research Associate in Chemical Process Engineering (Fixed Term)
University of Cambridge —Cambridge
- £34,610 - £46,049 a year
- Doctoral degree
- Engineering
- University
5d
Mechanical Design Engineer
Filtronic —Cambridge
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- No degree
Quick apply
11h

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Process Engineer

Harvard Bioscience -
Cambridge

Quick apply

Job details

Full-time

Qualifications

Technical troubleshooting
Mechanical engineering
Non-conformance investigation
Quality management change control procedures
Engineering
Mechanical Engineering
Quality control within general manufacturing industry
Technical support
Bachelor's degree
Continuous improvement
Quality control
Supplier quality management
Supply chain quality assurance
Manufacturing
Root cause analysis
ISO 13485

Full job description

Role Summary

The Process Engineer is responsible for the validation, engineering support and continuous improvement of manufacturing processes as well as product in our Cambridge, United Kingdom offices. You must live in this territory and position will be on site Monday - Friday.

This role requires a mechanical engineering background with hands‑on quality system experience, supporting day‑to‑day production activities while ensuring compliance with ISO 13485, applicable regulatory and internal QMS requirements.

The Process Engineer works cross‑functionally with Quality Control, Operations and QARA to ensure robust manufacturing processes, effective nonconformance management, and safe, compliant product release.

Key Responsibilities

Day‑to‑Day Quality Support for Production

Provide daily quality engineering support to manufacturing operations
Ensure production activities comply with:
- Approved procedures and work instructions
- ISO 13485 and other applicable requirements
Support line readiness, start‑up, and troubleshooting
Participate in production reviews, deviation assessments, and batch disposition support
Design Changes & Product Improvements

Coordinate and support design changes, design improvements, and process optimisations.
- Act as engineering representative for Design Change reviews and risk impact assessments.
- Ensure appropriate linkage between Design changes, Manufacturing process updates and Validation and verification activities.
- Support design transfer and continuous improvement initiatives
Manufacturing Process Validation & Control

Lead and execute manufacturing process validation activities, including IQ/OQ/PQ for production lines and equipment
Maintain validated state of manufacturing processes through change control and revalidation assessments
Support transfer of validated processes into routine production
Nonconformance (NC) & Deviation Management

Lead or support investigation of manufacturing‑related nonconformances
Coordinate root cause analysis using structured problem‑solving tools (e.g. 5‑Why, Fishbone)
Define and support implementation of corrective and preventive actions (CAPA) related to manufacturing processes
Interface with Quality to ensure timely closure and effectiveness verification
Cross‑Functional Coordination

Work closely with:
- Purchasing: support supplier quality issues related to manufacturing inputs
- QC Lab: support test method issues, failures, and investigations
- Warehouse: support material handling, traceability, and segregation of nonconforming product
- Repairs & Returns: analyse returned units and feed results into process improvements
- Technical Services: support field‑reported manufacturing issues
Provide technical and quality input for supplier‑related issues impacting manufacturing
Documentation & Compliance

Author and review controlled documents such as SOPs, Work Instructions, etc.
Support internal and external audits by providing process‑level evidence and explanations

Required Qualifications & Experience

Education

Bachelor's degree in Mechanical Engineering (or equivalent engineering discipline).

Experience

Experience in medical device or IVD manufacturing, strongly preferred or exposure to EU IVDR requirements.
Hands‑on experience with:
- Production support in a regulated environment
- Manufacturing process validation (IQ/OQ/PQ)
- Quality systems (ISO 13485)
- Supplier quality management
Experience supporting:
- Nonconformance investigations
- Change control and design changes
Ability to support ISO/ MDSAP/ regulatory audits

Structured problem‑solving mindset
Ability to work independently in a fast‑paced manufacturing environment
Comfortable interacting with Quality, Engineering, and Operations teams

Quick apply

Refine Your Search

process engineer jobs in cambridge, eng

Process Engineer

Graduate Process Engineer - Water - 2027 (Cambridge)

Manufacturing Engineer

Process commissioning engineer

Senior Special Process Engineer

Senior RF Engineer

Higher Senior RF Engineer

Postdoctoral Research Associate in Chemical Process Engineering (Fixed Term)

Mechanical Design Engineer

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