Quality improvement specialist Work, Jobs in Baildon, Wyk (with Salaries)

Quality Assurance Specialist
ELS Recruitment Ltd —Heywood
- From £40,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- In-person
- Free parking
- Health & wellbeing programme
Quick apply
1d
Clinical Governance and Quality Improvement Facilitator
Spectrum Community Health CIC —Wakefield
- £39,959 - £48,117 a year
- Full-time
- Annual leave
- Employee assistance programme
8d
Lead for Falls Improvement
Bradford Teaching Hospitals NHS Foundation Trust —Bradford
- £57,528 - £64,750 a year
- Full-time
11d
Multichannel Cx Agent
Vintage.com —Morley
- £26,250 a year
- Full-time
Quick apply
Quality Technician
Omega Proteins —Halifax
- From £12.71 an hour
- Overtime
- Laboratory experience
- English
- Analysis skills
- Free parking
- Referral programme
Quick apply
4d
EPRR Manager
Bradford District Care NHS Foundation Trust —Bradford
- £57,528 - £64,750 a year
- Full-time
Head of PPC
Vintage.com —Gildersome
- £60,000 - £80,000 a year
- Full-time
- Remote
- Analysis skills
- AI
- Leadership
Quick apply
Risk Innovation Specialist
Yorkshire Building Society —Leeds
- Up to £54,600 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
Learning & Development Co-ordinator
BAPP INDUSTRIAL LTD —Barnsley
- £32,000 - £35,000 a year
- Full-time
- Sales
- Presentation skills
- Human resources
- Free parking
- Referral programme
Quick apply
3d
Continuous Improvement Manager
Capita —Leeds
- Full-time
- Hybrid work
- Analysis skills
- Continuous improvement
- Driving
1d
Technical Specialist
Glanua —Wakefield
- Full-time
- Engineering
- Laboratory experience
- Business development
Quick apply
QC Project Analyst
Dechra Pharmaceuticals PLC —Skipton
- £32,000 - £37,000 a year
- Monday to Friday
- Bachelor's degree
- Organisational skills
- Communication skills
- Free parking
- Annual leave
3d
PMO Officer - Securing the Future programme
Airedale NHS Foundation Trust —Keighley
- £49,387 - £56,515 a year
- Full-time
- SharePoint
- Annual leave
- Employee assistance programme
4d
QC Technical Specialist
Dechra Pharmaceuticals PLC —Skipton
- Computer literacy
- Maintenance
8d
Quality Manager
Ceratex Engineering Limited —Barnoldswick
- £40,000 - £50,000 a year
- Full-time
- C++
- IT
- In-person
- Free parking
Quick apply
4d
SHEQ Manager
Dawsongroup —Brighouse
- Full-time
Quick apply
Service Delivery Manager
Leeds City Council —Leeds
- £41,700 - £66,318 a year
- Full-time
- Rehabilitation centre
- Leadership
19h
Specialist, EH&S
Avient —Barnsley
- Full-time
- Sales
- Computer literacy
- In-person
8d
QC Team Leader Raw Materials and Sampling
Dechra Pharmaceuticals PLC —Skipton
- £45,000 a year
- Day shift
- Continuous improvement
- Leadership
- Communication skills
- Free parking
- Annual leave
9d
Large and Complex Loss Handler
Leeds City Council —Leeds
- £46,142 - £500,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
8d

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quality improvement specialist jobs near baildon, wyk

Quality Assurance Specialist

ELS Recruitment Ltd
Heywood

Quick apply

Job details

Permanent | Full-time
From £40,000 a year
1 day ago

Benefits

Free parking
Health & wellbeing programme
Company pension
Private medical insurance
Life insurance
On-site parking

Qualifications

Quality management
Quality assurance
Bachelor's degree
HACCP
Internal audits

Full job description

Quality Assurance Specialist

Medical Devices / ISO13485 Quality Management Systems - Essential

Location: Heywood

Salary: £40K+

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.

Role focuses on:

Continued regulatory compliance to ISO13485, whilst assisting with Technical Documentation under (EU)2017/745, (EU)2017/746 to maintain device compliance.
Maintain and improve the company's Electronic Documentation Management System (EDMS) by Progressing, reviewing and update quality procedures, risk assessments and work instructions.
Key contact for quality/compliance whilst hosting external regulatory and accreditation bodies.
Coordinate and manage the internal/process audit programme to drive improvement assisted alongside external consultancy.
Manage document control processes and quality documentation through the EDMS.
Monitor/Investigate customer complaints and non-conformities along with CAPA/root cause activities.
Track audit findings and Identify gaps within existing quality systems and implement improvements ensuring agreed actions are completed in timely manner by stakeholders.
Enhance compliance with ISO13485, ISO9001 and Medical Device requirements using initiative.
Approving product literature and artwork to ensure they meet regulatory requirements

The successful candidate will work closely with senior management, whilst corroborating with external consultancy team to drive compliance for the company.

Essential

Previous experience in Quality Assurance or managing a QMS within a regulated environment.

Experience managing CAPAs, complaints and non-conformances

Strong documentation and procedural writing skills

Desirable

Experience with internal auditing

ISO13485 experience within MD environment.

PLEASE NOTE

To be considered for this position, you must have:

✔ Previous Quality Assurance experience preferably within a Medical Device environment

AND/OR

✔ Experience working with ISO13485 Quality Management Systems.

This is a documentation, compliance and quality systems role with some external travel and some hybrid working will be considered after probationary period. Laboratory, inspection, testing experience will only be considered where significant involvement within Quality System/documentation can be demonstrated.

Please note that only shortlisted applicants will be contacted

Pay: From £40,000.00 per year

Benefits:

Company pension
Free parking
Health & wellbeing programme
Life insurance
On-site parking
Private medical insurance

Experience:

managing CAPAs, complaints and non-conformances: 3 years (required)
strong documentation and procedural writing: 3 years (required)
Quality Assurance or managing QMS: 3 years (required)
QA within Medical Devices and/or ISO13485: 3 years (required)
QA or managing QMS within a regulated environment: 3 years (required)

Work Location: In person

Quick apply

Refine Your Search

quality improvement specialist jobs in baildon, wyk

Quality Assurance Specialist

Clinical Governance and Quality Improvement Facilitator

Lead for Falls Improvement

Multichannel Cx Agent

Quality Technician

EPRR Manager

Head of PPC

Risk Innovation Specialist

Learning & Development Co-ordinator

Continuous Improvement Manager

Technical Specialist

QC Project Analyst

PMO Officer - Securing the Future programme

QC Technical Specialist

Quality Manager

SHEQ Manager

Service Delivery Manager

Specialist, EH&S

QC Team Leader Raw Materials and Sampling

Large and Complex Loss Handler

I want to receive the latest job alerts for quality improvement specialist in baildon, wyk

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