quality engineer Work, Jobs in edinburgh (with Salaries)

Quality Systems Engineer
AliveDx —Penicuik
- Full-time
- Bachelor's degree
- Annual leave
Senior Quality Engineer
Opus 2 —Edinburgh
- £50,000 - £60,000 a year
- Full-time
- Hybrid work
- Java
- AWS
- APIs
- Employee assistance programme
Quick apply
23h
Senior Quality Engineer
Oceaneering —Rosyth
- Full-time
- Microsoft Office
- Continuous improvement
Salesforce Senior Quality Assurance Engineer
Trustpilot —Edinburgh
- Azure
- Salesforce
- Analysis skills
- Employee assistance programme
- Employee discount
Quality Systems Engineer
Rexroth —Glenrothes
- Full-time
- Microsoft Office
- Time management
- Employee discount
Quick apply
Quality Assurance Engineer
NAVANTIA UK —Methil
- Full-time
- Spanish
Quick apply
Senior Quality Assurance Engineer
Spacelabs —Edinburgh
- Engineering
- Bachelor's degree
- Business
Senior Quality Assurance Engineer
OSI Systems, Inc. —Edinburgh
- Engineering
- Bachelor's degree
- Business
Graduate Placement - Quality Engineering
Rexroth —Glenrothes
- Full-time
- Engineering
- Microsoft Office
- Organisational skills
- Employee discount
Quick apply
Project Manager
Ground Control —Falkirk
- Hybrid work
- Civil engineering
- Engineering
- Project management
- Annual leave
- Life insurance
Quick apply

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Quality Manager
City of Glasgow College —Glasgow
To be successful, you should understand what is involved in the checking and maintaining of assessment standards, able to work in a disciplined manner with…
£44,583 - £48,267 a year
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Due diligence testing- Conduct regular product testing of replenishable products and maintain records. Ensure product level compliance for all selling regions.

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Quality Systems Engineer

AliveDx -
Penicuik

Apply Now

Job details

Permanent | Full-time

Benefits

Additional leave
Cycle to work scheme
Annual leave

Qualifications

Quality management
Quality assurance
Bachelor's degree
Root cause analysis
Document management systems

Full job description

At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.

QUALITY SYSTEMS ENGINEER

AliveDx is recruiting for a Quality Systems Engineer to join the Quality and Regulatory Affairs team based at our ARC site near Penicuik, EH26 0BF.

The role is a full-time, permanent position working 37.5 working hours.

Job Purpose

Reporting to the Head of QMS, the Quality Systems Engineer is responsible for managing and overseeing three foundational QMS processes: document control, change control and failure investigations. This includes ensuring the proper creation, revision, approval, distribution, and archiving all quality-related documents, facilitating the change control process from end to end and applying root cause analysis methodologies to failure investigations. The role plays a critical part in ensuring that all processes meet regulatory, customer, and internal requirements within the medical device industry.

YOUR MISSION

Your main responsibilities will include:

Manage the document control system, including document creation, review, approval, distribution, and retrieval processes, in compliance with ISO 13485 requirements.
Ensure that all documents are maintained according to the company's quality management system (QMS).
Establish and enforce version control to maintain accurate and up-to-date documents.
Manage the change control process; receive, log, evaluate and route engineering change requests.
Chair change control board meetings and guide change.
Manage product and process failure investigations.
Ensure root cause analysis methodologies are being used and coach cross-functionally to ensure competency in root cause analysis.
Support external audits.
Ensure that all documentation is maintained in compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable regulatory requirements.
Implement and maintain a secure system for archiving and retaining quality records according to regulatory and company retention policies.

YOUR COMPETENCIES

Bachelor's degree in a related field (Quality Assurance, Life Sciences, Engineering) or equivalent experience.
Minimum of 3 years of experience in a document control or quality assurance role within an ISO 13485 GMP or 21CFR part 820 -compliant environment, preferably in the medical device or pharmaceutical industry.
Experience with document management systems and electronic quality management systems.

WHAT WE OFFER

A highly dynamic and growing environment.
An opportunity to live your passion for intrapreneurial mindset, where cultivating innovation and customer centricity are at the heart of everything we do.
A flexible working environment where applicable and a range of core and flexible benefits ranging from private medical cover, life assurance, additional annual leave, cycle to work, technology and access to marketplace discounts.

Interested? We look forward to receiving your application.

Closing date: May 21st 2026

AliveDx is an equal opportunity employer and welcomes applications from all qualified individuals regardless of nationality, sex, disability, region/belief, sexual orientation or age. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on competences, performance and business

Apply Now

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