Regulatory specialist Work, Jobs in Glossop, Dby (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
Regulatory Affairs Specialist
Arxada —Manchester
- Part-time
- Bachelor's degree
Clinical Trials Co-ordinator
Manchester University NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Part-time
- University
- IT
- AI
2d
Regulatory Compliance Specialist
The Beauty Tech Group Trading Limited —Manchester
- Full-time
- Hybrid work
- Engineering
- Business
- Free parking
- Work from home
Quick apply
Regulatory Affairs Specialist
Luxfer MEL Technologies - UK —Swinton
- £32,000 - £40,000 a year
- Full-time
- Microsoft Excel
- Data analysis skills
- Travel
- Free parking
Quick apply
Head of College
Pure Innovations —Stockport
- £55,000 - £59,000 a year
- Full-time
- Bachelor's degree
- In-person
- Care plans
- Health & wellbeing programme
- Work from home
Quick apply
Flow Survey Validation & Verification Analysts
Detectronic —Sheffield
- Full-time
- Annual leave
- Employee assistance programme
Quick apply
5h
Scientist - Analytical Chemistry and Biological Monitoring (Band 5/EO)
Health and Safety Executive —Buxton
- £31,657 - £34,570 a year
- Part-time
- Data analysis skills
- Laboratory experience
- Analysis skills
6d
Regulatory Affairs Senior Specialist
Arxada —Manchester
- Full-time
- Doctoral degree
- English
- Master's degree
Tender & Bid Evaluation Specialist
Fortix —Sheffield
- £65,000 - £75,000 a year
- Full-time
- Presentation skills
- Organisational skills
- Contracts
Quick apply
11h
KYC Onboarding Specialist
Kroo Bank Ltd —Manchester
- Full-time
- Hybrid work
- Travel
- Banking
Quick apply
Senior Validation Specialist
Bespak —Holmes Chapel
- £43,000 a year
- Free parking
- Life insurance
Quick apply
1d
HSEQ Specialist - Systems
LANXESS Solutions UK Ltd. —Manchester
- Full-time
- Data analysis skills
- Life insurance
Crime & Regulatory - Solicitor
Keoghs —Manchester
- Full-time
- Hybrid work
- IT
- Communication skills
- Employee discount
Mechanical Design Engineer 3D CAD / SolidWorks
Sorption Wheel Services Ltd (Dehum) —Glossop
- £35,000 - £48,000 a year
- Full-time
- AutoCAD
- CAD
- Analysis skills
- Free parking
- Annual leave
Quick apply
9d
Mobility Technology Systems Specialist
Fragomen —Sheffield
- Full-time
- Hybrid work
- Organisational skills
- IT
- Communication skills
- Annual leave
- Employee assistance programme
L&D Manager
JaJa Finance Ltd —Manchester
- £45,000 - £55,000 a year
- Full-time
- Hybrid work
- Financial services
- AI
- Annual leave
- Employee assistance programme
Quick apply
Programme Manager
Barclays —Knutsford
- Agile
- Communication skills
- Negotiation
Assistant - Risk & Compliance
TLT —Town
- Full-time
- Analysis skills
- Organisational skills
- SharePoint
HR Systems Specialist
Together —Cheadle
- Full-time
- Microsoft Excel
- Analysis skills
- Human resources
Quick apply

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regulatory specialist jobs near glossop, dby

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

regulatory specialist jobs in glossop, dby

Quality Assurance Specialist

Regulatory Affairs Specialist

Clinical Trials Co-ordinator

Regulatory Compliance Specialist

Regulatory Affairs Specialist

Head of College

Flow Survey Validation & Verification Analysts

Scientist - Analytical Chemistry and Biological Monitoring (Band 5/EO)

Regulatory Affairs Senior Specialist

Tender & Bid Evaluation Specialist

KYC Onboarding Specialist

Senior Validation Specialist

HSEQ Specialist - Systems

Crime & Regulatory - Solicitor

Mechanical Design Engineer 3D CAD / SolidWorks

Mobility Technology Systems Specialist

L&D Manager

Programme Manager

Assistant - Risk & Compliance

HR Systems Specialist

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