Senior 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
Senior Manufacturing Engineer
Slingco —Rossendale
- Hybrid work
- Engineering
- Assembly
- Analysis skills
- Annual leave
- Employee assistance programme
Quick apply
Senior Systems Engineer
Assystem —Bolton
- In-person
Data Analyst
Bury Council —Bury
- £35,412 - £38,220 a year
- Full-time
- SQL
8d
Senior IT Director
Cloud Imperium Games —Manchester
- IT
- In-person
Senior Stress Engineer
Assystem —Bolton
- Hybrid work
- In-person
Senior Highways Design Engineer
Kier Group —Salford
- Full-time
- AutoCAD
- Civil engineering
Senior Systems Engineer
Babcock International —Warrington
- Full-time
- Hybrid work
- Engineering
- No degree
- Annual leave
- Employee assistance programme
Head of Engineering
Biorelate —Manchester
- Full-time
- Remote
- Laboratory experience
- Communication skills
Quick apply
Senior Principal Mechanical Engineer
Assystem —Bolton
- Hybrid work
- Travel
- In-person
- Leadership
Communications Lead - European Environmental Projects
Countryscape —Manchester
- £45,000 - £55,000 a year
- Full-time
- Hybrid work
- Project management
- Presentation skills
- Bachelor's degree
- Work from home
Quick apply
1d
Senior Process Engineer
Assystem —Bolton
- Hybrid work
- Engineering
- Travel
- In-person
Senior Project Manager
M Group —Rochdale
- Hybrid work
- Microsoft Outlook
- Microsoft Office
- Annual leave
- Employee discount
Senior QA Engineer
Vix Technology —Manchester
- £40,000 - £65,000 a year
- Full-time
- Bachelor's degree
- APIs
- Agile
- Employee assistance programme
Quick apply
Senior Project Engineer
Capgemini —Manchester
- Hybrid work
- Project management
- IT
- Leadership
Senior Test Engineer
UBDS Group —Manchester
- Hybrid work
- Azure
- Oracle
- SQL
Quick apply
Site Engineer
Costain —Bury
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
Senior Staff Process Engineer – Diffusion
Nexperia Germany GmbH —Manchester
- £62,000 - £69,000 a year
- 12 hour shift
- Microsoft Powerpoint
- Doctoral degree
- Microsoft Office
- Annual leave
- Employee assistance programme
Senior Verification Engineer
TechBiz Global GmbH —Manchester
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
1d
Senior Product Designer
Street Group —Manchester
- £50,000 - £68,000 a year
- Full-time
- Hybrid work
- Work from home
- Flexible schedule
Quick apply

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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

senior engineer jobs in whitefield, gtm

Quality Assurance Specialist

Senior Manufacturing Engineer

Senior Systems Engineer

Data Analyst

Senior IT Director

Senior Stress Engineer

Senior Highways Design Engineer

Senior Systems Engineer

Head of Engineering

Senior Principal Mechanical Engineer

Communications Lead - European Environmental Projects

Senior Process Engineer

Senior Project Manager

Senior QA Engineer

Senior Project Engineer

Senior Test Engineer

Site Engineer

Senior Staff Process Engineer – Diffusion

Senior Verification Engineer

Senior Product Designer

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