Quality auditor Work, Jobs in Kettering (with Salaries)

Quality Assurance Manager
Activinsights Ltd —Kimbolton
- Full-time
- Bachelor's degree
- No degree
- In-person
- Free parking
- Life insurance
Quick apply
3d
Practice Lead Audit Officer
Cambridgeshire County Council —Huntingdon
- £46,956 - £50,157 a year
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
- Employee discount
12d
Quality & Technical Manager – Asbestos Consultancy
Acorn Analytical Services —Northampton
- £50,000 - £60,000 a year
- Full-time
- Management
- Up to 50% travel
- Microsoft Office
- Annual leave
- Work from home
Quick apply
9d
Inventory & Audit Coordinator - UK
Rhenus SE & Co. KG —Lutterworth
- Full-time
- Microsoft Excel
- Oracle
- Analysis skills
4d
Quality Engineer
Wabtec —Northampton
- Full-time
- Bachelor's degree
Quick apply
9d
Packaging Technologist
pladis —Wigston Magna
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
Asbestos Site Auditor
Rentokil Initial Group —Milton Keynes
- £40,000 - £48,000 a year
- Full-time
- Contracts
- IT
- Annual leave
- Employee assistance programme
Quick apply
QHSE Advisor
Framatome —Cranfield
- Full-time
- Presentation skills
- No travel
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Head of Finance & Procurement
British Association for Counselling & Psychotherapy —Lutterworth
- £76,551 a year
- Full-time
- Analysis skills
- Leadership
- Communication skills
11d
SHEQ Advisor
March —Peterborough
- £0.01 a year
- Continuous improvement
- Travel
- Communication skills
Quick apply
5d
Co-op Store Manager
University of Leicester Food and Drink —Leicester
- £36,000 a year
- Weekend availability
- Hospitality
- Marketing
- Customer service
Quick apply
3d
ISACA Instructor
BPP Holdings —Wyboston
- Hybrid work
- Communication skills
- Time management
- Annual leave
- Employee discount
Finance Business Partner – Retail
Mitie —Northampton
- Full-time
- Microsoft Excel
- Communication skills
Project Buyer
Rexroth —St. Neots
- Full-time
- Microsoft Office
- Organisational skills
- Communication skills
- Free parking
- Employee assistance programme
Quick apply
Audit Assistant Manager
Grant Thornton UK LLP —Milton Keynes
- Full-time
- Project management
Interim Finance Accountant (3 Month FTC)
ABAgri —Peterborough
- Temporary
- Microsoft Excel
- ERP systems
- Accounting
2d
Senior Treasury Manager
Soho House & Co. —Milton Keynes
- Microsoft Excel
- Oracle
- Supervising experience
- Employee discount
Quick apply
Audit and Compliance Lead
Weetabix —Burton Latimer
- Full-time
- Annual leave
Quick apply
5d
Practice Auditor - fixed-term for two years
Cambridgeshire County Council —Huntingdon
- £34,434 - £36,363 a year
- Microsoft Office
- Analysis skills
- Communication skills
- Annual leave
- Employee discount
4d
Project & Quality Engineer
King Trailers —Market Harborough
- PMP
- Military
- Travel
- Annual leave
- Employee assistance programme

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Quality Assurance Manager

Activinsights Ltd
Kimbolton

Quick apply

Job details

Full-time | Fixed term contract
3 days ago

Benefits

Free parking
Company pension
Company events
Private medical insurance
Life insurance
On-site parking

Qualifications

Quality management
Information security
Quality assurance
Bachelor's degree
Root cause analysis
FDA regulations

Full job description

Role Purpose

The Quality Manager leads the effective operation, maintenance and continual improvement of ActivInsights’ Quality Management System (QMS), ensuring that products, services and business processes meet applicable regulatory, quality and customer requirements.

Reporting to the Regulatory Affairs Manager, the role owns the day-to-day management of the QMS and provides quality leadership across the business. The Quality Manager escalates significant quality and compliance risks and supports regulatory strategy, technical documentation, inspections and certification activities while maintaining clear accountability between Quality and Regulatory Affairs.

Responsibilities

QMS Leadership & Governance

Lead the operation, maintenance and continual improvement of the QMS in accordance with ISO 13485:2016, the FDA Quality Management System Regulation (QMSR), 21 CFR Part 820, and other applicable requirements.
Coordinate management review, prepare QMS performance information and analyse quality metrics, trends and risks to support effective decision-making.
Support the continued development and effective use of the electronic Quality Management System (eQMS).
Monitor relevant quality standards and regulatory developments, working with the Regulatory Affairs Manager to assess and implement required changes.

Non-conformances, CAPA & Complaints

Manage non-conformances, corrective and preventive actions (CAPA), audit findings and root-cause investigations, ensuring actions are proportionate, effective and completed within agreed timescales.
Analyse quality issues and performance data to identify trends, reduce recurrence and drive continual improvement.
Support complain handling and post-market quality activities, ensuring significant issues are escalated and regulatory reporting requirements are considered with Regulatory Affairs.
Maintain effective change-control, document-control and record-control processes.

Audits & Supplier Quality

Plan and conduct the internal audit programme and host external certification, customer and regulatory audits or inspections.
Coordinate timely responses to audit and inspection findings and monitor resulting actions through to effective closure.
Manage supplier quality activities, including qualification, monitoring, audits and supplier non-conformances, in collaboration with relevant operational teams.

Product, Process & Risk Management

Ensure applicable cGMP requirements and quality procedures are implemented and maintained throughout the business.
Provide quality input into design and development, verification and validation, risk management, product or service changes and technical documentation.
Support the application of medical-device risk-management principles, including ISO 14971 where applicable.
Coordinate quality training and monitor completion and effectiveness of required QMS training.

Collaboration & Quality Support

Work with the Regulatory Affairs Manager to define and implement the quality strategy and provide quality support for regulatory compliance activities.
Support customers during vendor audits, respond to quality queries, demonstrate compliance and help manage complaints.
Work with operational and development teams to ensure the QMS is understood, implemented and maintained and that new or changed products and services are appropriately verified and validated.
Support information security management activities, including ISO/IEC 27001 requirements, where these interface with the QMS.
Undertake other reasonable duties and general office activities appropriate to a small and growing team.

You will work with:

Regulatory Affairs Manager

Senior Leadership Team

Development and Product teams

Manufacturing, Operations and Logistics

Commercial and Data Services teams

Employees across the wider business

Suppliers and other external service providers

Certification bodies, auditors and regulatory authorities

Candidate Attributes

· Relevant degree, professional qualification or equivalent practical experience in medical-device quality management.

· Significant experience managing or leading quality assurance activities within a regulated medical-device environment.

· Strong working knowledge of ISO 13485:2016 and the FDA Quality Management System Regulation (QMSR), 21 CFR Part 820.

· Practical experience of QMS management, CAPA, non-conformance investigations, root-cause analysis, internal and external audits, document control and quality metrics.

· Ability to work autonomously, prioritise effectively and make sound, evidence-based judgements while escalating material risks appropriately.

Skills & Behaviours

· Methodical and analytical, with strong attention to detail and a practical approach to problem-solving and continual improvement.

· Clear and confident written and verbal communicator, able to explain quality requirements and work collaboratively across the business.

· Able to influence constructively, maintain professional judgement and meet agreed targets and timescales.

Desirable Experience & Knowledge

· Experience within the electronics, engineered-device or connected-health sectors.

· Knowledge of ISO 14971 medical-device risk management and experience supporting design, verification and validation activities.

· Experience implementing, administering or improving an eQMS.

· Experience of information security management systems, including ISO/IEC 27001:2022.

Benefits:

Company events
Company pension
Free parking
Life insurance
On-site parking
Private medical insurance

Ability to commute/relocate:

Kimbolton PE28 0LF: reliably commute or plan to relocate before starting work (preferred)

Application question(s):

Do you have excellent knowledge of ISO13485 and 21 CFR 820

Education:

Bachelor's (preferred)

Experience:

medical device quality management: 3 years (required)

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

quality auditor jobs in kettering

Quality Assurance Manager

Practice Lead Audit Officer

Quality & Technical Manager – Asbestos Consultancy

Inventory & Audit Coordinator - UK

Quality Engineer

Packaging Technologist

Asbestos Site Auditor

QHSE Advisor

Head of Finance & Procurement

SHEQ Advisor

Co-op Store Manager

ISACA Instructor

Finance Business Partner – Retail

Project Buyer

Audit Assistant Manager

Interim Finance Accountant (3 Month FTC)

Senior Treasury Manager

Audit and Compliance Lead

Practice Auditor - fixed-term for two years

Project & Quality Engineer

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