Process engineer Work, Jobs in Brampton, Cam (with Salaries)

Process Engineer
Harvard Bioscience —Cambridge
- Full-time
- Engineering
- Bachelor's degree
- In-person
Quick apply
Lead Process Engineer
Costain —Peterborough
- Full-time
- Remote
- Engineering
- Master's degree
- IT
12d
Mechanical Design Engineer
Filtronic —Cambridge
- Full-time
- Hybrid work
- CAD
- Engineering
- System design
Quick apply
Senior Mechanical Design Engineer
Filtronic —Cambridge
- Full-time
- Hybrid work
- CAD
- System design
- Bachelor's degree
Quick apply
Engineering Buyer
A4 Plus Limited —Sandy
- £45,000 - £48,000 a year
- Engineering
- ERP systems
- Organisational skills
- Sick pay
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13d
Equipment Engineering Technician
Bourns —Bedford
- Computer literacy
- Continuous improvement
- Organisational skills
11d

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Process Engineer

Harvard Bioscience -
Cambridge

Quick apply

Job details

Full-time

Qualifications

Mechanical engineering
Engineering
Mechanical Engineering
Quality management
Bachelor's degree
Root cause analysis

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

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process engineer jobs in brampton, cam

Process Engineer

Lead Process Engineer

Mechanical Design Engineer

Senior Mechanical Design Engineer

Engineering Buyer

Equipment Engineering Technician

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