Quality assurance Work, Jobs in Newmarket, Sfk (with Salaries)

Quality Assurance Specialist
TOGL (Holdings) Limited —Cambridge
- Full-time
- Engineering
- Microsoft Office
- Analysis skills
- Annual leave
Quick apply
1d
Laboratory Technician in Molecular Diagnostics for Colorectal Cancer Screening
TOGL (Holdings) Limited —Cambridge
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
Quick apply
Quality Assurance Lead
LGC Assure —Fordham
- Full-time
- Project management
- SharePoint
- Communication skills
Quick apply
4d
Quality Control Analyst - UK
Ascensus Specialties LLC —Newmarket
- Full-time
- Microsoft Word
- Microsoft Excel
- Laboratory experience
- Free parking
- Employee assistance programme
Academic Quality and Enhancement Administrator
CATS Global Schools —Cambridge
- £35,000 - £45,000 a year
- Bachelor's degree
- Communication skills
- School
- Employee assistance programme
- Referral programme
Quality Systems Coordinator
Hain Celestial UK —Cambridge
- Hybrid work
- Analysis skills
- Travel
- Organisational skills
- Annual leave
- Employee discount
Quick apply
QA Advisor - all levels
Resolian —Fordham
- Full-time
- No degree
- Communication skills
Junior Laboratory Technician
Reclinker —Cambridge
- £23,000 - £28,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
4d
Head Of Compliance And Quality Assurance
Medirest —Cambridge
- Hotel
- Analysis skills
- Leadership
- Employee discount
8d
AI Quality Analyst
Aykua Health —Cambridge
- £30,000 - £40,000 a year
- Full-time
- Hybrid work
- Laboratory experience
- Analysis skills
- Bachelor's degree
- Employee stock ownership plan
Quick apply
9d
Hardware Quality Assurance Engineer
Tait —Haverhill
- Full-time
- Engineering
- No degree
- Annual leave
- Employee assistance programme
Quality Control Analyst - UK
Ascensus Specialties —Newmarket
- Full-time
- Microsoft Word
- Microsoft Excel
- Laboratory experience
- Free parking
- Employee assistance programme
Quick apply
Head of Quality Assurance and Regulatory Affairs
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Project management
- Bachelor's degree
- Machine learning
- Annual leave
- Life insurance
Quick apply
2d
QA Night shift
elix sourcing solutions —March
- Up to £35,000 a year
- Overtime
- Data entry
- Employee assistance programme
- Life insurance
10d
Quality and Validation Engineer, Quality Department
CONTAMAC LTD —Saffron Walden
- £40,000 - £45,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Free parking
- Life insurance
Quick apply
1d
Quality Engineer Early Career Program
Hexcel Corporation —Duxford
- Full-time
- Microsoft Office
- Analysis skills
- Communication skills
QA Associate
Avantor —Cambridge
- Full-time
- Laboratory experience
- Bachelor's degree
- No degree
Technical Quality Manager
M Group —Bury St. Edmunds
- Analysis skills
- Construction experience
- Free parking
- Employee assistance programme
Customer Quality (Automotive) - Staff Engineer
Qualcomm —Cambridge
- Doctoral degree
- Computer Science
- Engineering
Quality Technician
AMOT —Bury St. Edmunds
- Microsoft Office
- Electrical Engineering
- Communication skills
Quick apply

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Quality Assurance Specialist

TOGL (Holdings) Limited
Cambridge

Quick apply

Job details

Full-time
1 day ago

Benefits

Annual leave
Company pension

Qualifications

Engineering
Quality management
Microsoft Office
Analysis skills
Quality assurance
Bachelor's degree
Continuous improvement
Business coaching

Full job description

TOGL(Holdings)Limited is a diagnostics company focused on diseases of the gastrointestinal tract. Our current research and validation programme targets accurate and efficient triage of patients with symptoms of colorectal cancer (CRC). We are looking for proactive, experienced, focused, and enthusiastic individuals who can make a significant contribution to the continued growth and success of our dynamic and forward-looking company. As we progress towards commercialising a test for CRC, we are looking for a Regulatory Manager to lead the development process through relevant regulatory pathways.

We are seeking a detail-oriented and experienced Quality Assurance Specialist with strong knowledge of ISO 13485 and electronic Quality Management Systems (eQMS), particularly Greenlight Guru. The successful candidate will support and maintain the Quality Management System (QMS), ensure compliance with regulatory requirements, and deliver effective training to users across all aspects of quality assurance processes. Excellent Training competence is required.

Key Responsibilities

Maintain and improve the Quality Management System in compliance with ISO 13485 and applicable regulatory requirements.
Administer and support the Greenlight Guru eQMS platform, including document control, CAPA, training records, audits, and change management.
Create, review, revise, and approve quality documentation such as SOPs, work instructions, forms, and policies.
Conduct internal audits and support external audits by notified bodies, customers, and regulatory agencies.
Manage CAPA investigations, non-conformances, deviations, and risk management activities.
Ensure proper document control and record retention processes are maintained.
Monitor quality metrics and prepare reports for management review.
Train employees and system users on quality assurance procedures, ISO 13485 requirements, and Greenlight Guru eQMS functionality.
Provide onboarding and refresher training to staff on QMS processes and compliance expectations.
Support supplier quality activities, including evaluations and audits where required.
Collaborate with cross-functional teams including Regulatory Affairs, Manufacturing, Engineering, and Operations.
Assist in continuous improvement initiatives and quality system enhancements.

Supplier Quality Management

Evaluate, qualify, approve, and monitor suppliers and contract manufacturers.
Conduct supplier risk assessments and maintain Approved Supplier Lists (ASL).
Lead supplier audits (remote and onsite) in accordance with ISO 13485 requirements.
Monitor supplier KPIs including quality, delivery, responsiveness, and non-conformance trends.

Requirements

Bachelor’s degree in Life Sciences, Engineering, Quality Management, or related discipline.
Proven experience working within an ISO 13485-certified environment.
Hands-on experience using Greenlight Guru or similar eQMS platforms.
Strong understanding of medical device quality management systems and regulatory compliance.
Experience delivering training and supporting users in quality systems and procedures.
Knowledge of CAPA, risk management, document control, and audit processes.
Excellent communication, organizational, and problem-solving skills.
Proficiency in Microsoft Office applications.

Preferred Qualifications

Internal Auditor certification for ISO 13485.
Experience in medical devices.
Familiarity with ISO 13485, ISO 14971, ISO 15189 and EU MDR requirements.

Key Competencies

Attention to detail
Regulatory awareness
Training and coaching ability
Analytical thinking
Strong documentation skills
Team collaboration
Continuous improvement mindset

Benefits

25 days annual leave (plus bank holidays).
Pension contribution.
Competitive Salary.
Employee wellbeing initiatives.

Quick apply

Refine Your Search

quality assurance jobs in newmarket, sfk

Quality Assurance Specialist

Laboratory Technician in Molecular Diagnostics for Colorectal Cancer Screening

Quality Assurance Lead

Quality Control Analyst - UK

Academic Quality and Enhancement Administrator

Quality Systems Coordinator

QA Advisor - all levels

Junior Laboratory Technician

Head Of Compliance And Quality Assurance

AI Quality Analyst

Hardware Quality Assurance Engineer

Quality Control Analyst - UK

Head of Quality Assurance and Regulatory Affairs

QA Night shift

Quality and Validation Engineer, Quality Department

Quality Engineer Early Career Program

QA Associate

Technical Quality Manager

Customer Quality (Automotive) - Staff Engineer

Quality Technician

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