Documentation engineer Work, Jobs in Whitefield, Gtm (with Salaries)

Quality Assurance Specialist
ELS Recruitment Ltd —Heywood
- £40,000 - £56,000 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Quality control
- Free parking
Quick apply
Data Engineer
First Choice Homes Oldham —Oldham
- £50,000 a year
- Full-time
- Hybrid work
- Microsoft Access
- Azure
- SQL
- Annual leave
- Employee assistance programme
Quick apply
13d
Research Assistant
Holiferm —Trafford
- £31,000 a year
- Full-time
- Hybrid work
- Life insurance
Quick apply
5d
Trainee Field Engineer - Radio
Avoira Limited —Bury
- £26,228 - £28,000 a year
- Full-time
- Driving
- Organisational skills
- IT
Quick apply
Administration Assistant
Hart Process Services —Stockport
- £13.25 an hour
- Part-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Free parking
- Flexitime
Quick apply
1d
Document Controller
AECOM —Manchester
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Project management
Product Test and Technical Document Engineer
EDM Ltd —Manchester
- £37,000 - £40,000 a year
- Full-time
- Microsoft Office
- Analysis skills
- Travel
- Work from home
- Life insurance
Quick apply
5d
QA Engineer
Zellis —Manchester
- Azure
- Master's degree
- AWS
- Annual leave
Business Systems Support Engineer I
Brand Addition —Manchester
- Full-time
- Hybrid work
- Software troubleshooting
- ERP systems
- SQL
Quick apply
AI Engineer
JDSPORTS —Bury
- Full-time
- APIs
- AI
- Python
- Employee discount
Quick apply
Agile Release Engineer
interactive investor —Manchester
- From £55,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Agile
- Annual leave
- Employee discount
Quick apply
Document Controller
Babcock International —Warrington
- Full-time
- Hybrid work
- Computer literacy
- Communication skills
- Annual leave
8d
Cyber Security Engineer
PayStream Accounting Services —Altrincham
- £35,000 - £55,000 a year
- Full-time
- Hybrid work
- English
- IT
- Communication skills
- Work from home
Quick apply
SCADA Engineer
EMR Integrated Solutions —Manchester
- Full-time
- Hybrid work
- Management
- Programmable logic controllers
- IT
- Sick pay
Quick apply
UC Systems Engineer
Avoira Limited —Bury
- £32,496 a year
- Full-time
- Sales
- IT
- In-person
Quick apply
Site Reliability Engineer
CGI —Manchester
- Full-time
- DevOps
- Scripting
- In-person
Quick apply
Assistant Signal Sighting Engineer
WSP —Manchester
- Part-time
- Hybrid work
- Analysis skills
- Communication skills
- Flexitime
- Work from home
Test and Verification Engineer
Azenta —Manchester
- Full-time
- Communication skills
Junior Systems Engineer
ENWL —Blackburn
- £33,775.20 - £39,819.24 a year
- Microsoft Word
- Microsoft Outlook
- Microsoft Office
- Annual leave
- Employee assistance programme
6d
SolidWorks Design Engineer
Envair Technology —Heywood
- £28,000 - £30,000 a year
- Full-time
- Hybrid work
- AutoCAD
- Assembly
Quick apply
21h

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documentation engineer jobs near whitefield, gtm

Quality Assurance Specialist

ELS Recruitment Ltd
Heywood

Quick apply

Job details

Permanent | Full-time
£40,000 - £56,000 a year

Benefits

Free parking
Company pension
Private medical insurance
On-site parking

Qualifications

GCSE
Quality management
ISO 9001
Analysis skills
Quality assurance
Bachelor's degree
Quality control
Internal audits

Full job description

Quality Assurance Specialist

Medical Devices / ISO13485 Quality Management Systems - Essential

Location: Heywood

Salary: depending on experience

PLEASE NOTE

To be considered for this position, you must have:

✔ Previous Quality Assurance experience within a Medical Device environment

✔ Significant experience working with ISO13485 Quality Management Systems

This is a documentation, compliance and quality systems role. It is not a laboratory, inspection, testing or hands-on Quality Control position.

Applicants without Medical Device and/or ISO13485 experience are unlikely to be considered.

The Role

Our client is seeking a Quality Assurance Specialist to support and continually improve their Quality Management System within a regulated Medical Device manufacturing environment.

This is a predominantly office-based role focused on:

Quality Management Systems (QMS)
ISO13485 compliance
Internal auditing
CAPA management
Complaint investigations
Documentation control
Regulatory compliance
Process improvement

The successful candidate will work closely with senior management and regulatory bodies to ensure ongoing compliance and quality excellence.

Key ResponsibilitiesQuality Management Systems

Maintain and improve the company's Quality Management System (QMS)
Develop, review and update quality procedures, policies and work instructions
Identify gaps within existing quality systems and implement improvements
Manage document control processes and quality documentation
Support the maintenance of the electronic Quality Management System

Auditing & Compliance

Coordinate and manage the internal audit programme
Support external audits by regulatory and accreditation bodies
Track audit findings and ensure agreed actions are completed
Monitor compliance with ISO13485, ISO9001 and Medical Device regulatory requirements

CAPA, Complaints & Non-Conformances

Investigate customer complaints and non-conformities
Coordinate CAPA activities through to closure
Monitor complaint and non-conformance trends
Support root cause investigations and corrective actions

Regulatory Support

Act as a key contact for quality and compliance matters
Support communications with MHRA and Notified Bodies
Assist with regulatory compliance activities and reporting

Supplier & Quality Administration

Maintain approved supplier and contractor records
Review supplier risk assessments
Monitor calibration and service schedules
Ensure product literature and artwork meet regulatory requirements

Experience Required

Essential

Previous experience in a Quality Assurance role
Medical Device industry experience and/or strong ISO13485 experience
Experience maintaining Quality Management Systems
Experience with internal audits
Experience managing CAPAs, complaints and non-conformances
Strong documentation and procedural writing skills

Desirable

Experience liaising with MHRA and/or Notified Bodies
ISO9001 experience
Lead Auditor qualification
Experience within a regulated manufacturing environment

Suitable Backgrounds

We would particularly like to hear from candidates currently working as:

Quality Assurance Specialist
Quality Systems Specialist
Quality Compliance Officer
Quality & Regulatory Officer
Quality Systems Coordinator
QA Engineer (Medical Devices)
Quality Manager (Medical Devices)

Not Suitable For

This role is not focused on product inspection, laboratory testing or production-based quality control. Applicants whose experience is solely within Quality Inspection or Quality Control may not be suitable.

Please note that only shortlisted applicants will be contacted

Pay: £40,000.00-£56,000.00 per year

Benefits:

Company pension
Free parking
On-site parking
Private medical insurance

Work Location: In person

Quick apply

Refine Your Search

documentation engineer jobs in whitefield, gtm

Quality Assurance Specialist

Data Engineer

Research Assistant

Trainee Field Engineer - Radio

Administration Assistant

Document Controller

Product Test and Technical Document Engineer

QA Engineer

Business Systems Support Engineer I

AI Engineer

Agile Release Engineer

Document Controller

Cyber Security Engineer

SCADA Engineer

UC Systems Engineer

Site Reliability Engineer

Assistant Signal Sighting Engineer

Test and Verification Engineer

Junior Systems Engineer

SolidWorks Design Engineer

I want to receive the latest job alerts for documentation engineer in whitefield, gtm

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