Quality engineer Work, Jobs in St Helens, Msy (with Salaries)

Junior QC & Validation Engineer
Sina Medical Glass Ltd —St Helens
- £31,000 - £34,000 a year
- Full-time
- Laboratory experience
- No experience needed
- Bachelor's degree
Quick apply
Quality, Health and Safety Engineer
Pyroguard UK Ltd. —Haydock
- £45,000 - £50,000 a year
- Continuous improvement
- IT
- Communication skills
Quality Inspection Engineer (Day shift)
Mini Gears Stockport Ltd —Stockport
- £38,000 - £40,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Free parking
- Annual leave
Quick apply
3d
QA Engineer
Clio —Manchester
- £50,200 - £67,800 a year
- Full-time
- Hybrid work
- Azure
- Engineering
- Bachelor's degree
- Life insurance
Quality Engineer - NGT (Felindre)
Bilfinger SE —Warrington
- Hybrid work
- Computer literacy
- Microsoft Office
- Computer skills
Quality Engineer - NGT (Alrewas)
Bilfinger SE —Warrington
- Hybrid work
- Computer literacy
- Microsoft Office
- Computer skills
Quality Engineer
Finova —Salford
- Hybrid work
- APIs
- AI
- Annual leave
- Employee assistance programme
Quality Engineer – Automotive Assembly
Rhenus SE & Co. KG —Manchester
- Full-time
- Assembly
- Bachelor's degree
- Communication skills
- Free parking
- Employee assistance programme
Apprentice Quality Engineer (18+)
Greif —Ellesmere Port
- Full-time
- English
10d
QA Engineer
The Granite Group —Liverpool
- Up to £50,000 a year
- Full-time
- Hybrid work
- Azure
- APIs
- Business
- Flexible schedule
Quick apply
Quality Engineer
Azenta —Manchester
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Process Engineer – UK Water/Wastewater – All Levels
Egis —Manchester
- Management
- Engineering
- Master's degree
7d
Quality Engineer / Responsible Weld Co-ordinator
Amentum —Risley
- Full-time
- Microsoft Powerpoint
- Travel
- Organisational skills
- Flexible schedule
Principal QA Engineer
The Very Group —Liverpool
- Full-time
- Hybrid work
- APIs
- Financial services
- Leadership
- Employee discount
Quick apply
Supplier Quality & Development Engineer - China
Oliver Valves —Knutsford
- English
- Travel
- In-person
Head of Quality – Engineering
BAE Systems —Warton
- £74,100 a year
- Hybrid work
- Engineering
- Continuous improvement
- No degree
5d
Project Compliance and Risk Engineer
Yokogawa —Runcorn
- Full-time
- Engineering
- Microsoft Office
- Analysis skills
Senior QA Engineer
SEFE Securing Energy for Europe GmbH —Manchester
- Hybrid work
- Analysis skills
- Software development
11d
Senior QA Engineer
Vix Technology —Manchester
- £40,000 - £65,000 a year
- Full-time
- Bachelor's degree
- APIs
- Agile
- Employee assistance programme
Quick apply
Graduate Mechanical Design/Project Engineer
Sonomatic Limited —Warrington
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply

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Junior QC & Validation Engineer

Sina Medical Glass Ltd
St Helens

Quick apply

Job details

Full-time
£31,000 - £34,000 a year

Qualifications

Laboratory experience
No experience needed
ISO 9001
Bachelor's degree
Technical writing
Document management systems
Leadership
Internal audits

Full job description

Job Description

Junior QC & Validation Engineer

About Sina Medical Glass

Sina Medical Glass, Ltd. is a UK-based start-up with an international team and a compelling mission: to ensure the production and ready supply of top-quality primary packaging (glass vials and cartridges), both within the UK and internationally. We are building our quality management infrastructure from the ground up and are looking for driven individuals who want to grow with us and make a real impact in the pharmaceutical supply chain.

Seniority level: Associate / Junior-Mid

Employment type: Full-time

Job function: Quality Assurance/ Quality Control

Industry: Medical Glass Industry

Salary: £31,000 – £34,000 depending on experience

Role overview

This is primarily a documentation and QMS role, with QC laboratory testing and validation support being equally important responsibilities. Your day-to-day focus will be writing and managing controlled documents such as SOPs, Work Instructions, forms, and quality records and supporting the build-out of our electronic QMS (eQMS) and performing hands-on physical and dimensional testing in the laboratory.

When needed, you will also support equipment qualification and validation activities alongside the Deputy Quality Manager, helping to prepare and maintain validation protocols and reports.

This role suits someone from a GMP-regulated background ideally within medical glass, pharmaceutical, or medical device industries who writes clearly, works methodically, and is ready to get stuck in at a start-up where the systems are still being built.

Key Responsibilities

Technical Writing & Document Control — Primary Focus

Author, review, and maintain controlled documents including SOPs, Work Instructions (WIs), forms, templates, and quality records.
Support the build-out and day-to-day management of our eQMS, ensuring documents are structured, version-controlled, and audit-ready.
Ensure all documentation aligns with ISO 9001, ISO 15378, and GMP requirements.
Manage document lifecycle drafting, review cycles, approval, issuance, and archiving in line with document control procedures.
Support the development and rollout of training materials linked to new or revised documents.

QC Laboratory & Product Testing – Primary Focus

Perform physical and dimensional testing on vials, cartridges, and glass tubing to defined specifications.
Conduct visual inspection of finished product in line with acceptance criteria.
Test to relevant standards including USP <660>, <790>, <1660> and applicable ASTM methods.
Record and trend test results and raise non-conformances where required.
Maintain lab equipment calibration records and testing logs.

Validation & Equipment Qualification — Supporting Role

Assist in the preparation and formatting of IQ/OQ/PQ qualification protocols and summary reports under the direction of the Deputy Quality Manager.
Maintain and organise validation documentation within the eQMS.
Support scheduling and coordination of qualification activities with operations and equipment suppliers.
Help track open validation actions and ensure documentation is completed and closed in a timely manner.

Quality Assurance Support

Assist with internal audit preparation, including document retrieval and evidence collation.
Support CAPA, non-conformance, and change control processes by maintaining records and tracking actions to closure.
Contribute to quality metrics and data trending reports.

Essential Requirements

2–3 years of experience in a Quality, documentation, or quality systems role within a GMP-regulated industry (medical glass, pharmaceutical, medical device, or primary packaging manufacturing preferred).
Demonstrable technical writing skills. Candidate must be able to independently produce clear, structured, audit-ready GMP documents (SOPs, WIs, forms, templates).
Experience working within a document control system or eQMS platform.
Working knowledge of ISO 9001 and GMP principles; familiarity with highly regulated manufacturing environments (for example ISO 15378, ISO 13485) is a bonus.
Understanding of validation concepts (IQ/OQ/PQ/IOPQ/IOQ). Validation leadership experience is not required, but experience supporting validation process is a necessary.
Knowledge of USP <660>, <790>, <1660> and applicable ASTM standards.
Degree (BSc or equivalent) in a relevant field: chemistry, pharmaceutical sciences, engineering, life sciences, or similar.
Organised, detail-oriented, and comfortable building processes in an evolving environment.

Desirable Qualifications

Direct experience in glass manufacturing or primary pharmaceutical packaging
Experience with eQMS administration (system setup, user management, workflow configuration).
Experience supporting regulatory submissions or inspections.
Familiarity with ISO 14971 (risk management).

This role reports to the Deputy Quality Manager. Please feel free to contact Ayshi with any questions at

[email protected]

How to apply

Please submit your CV and a brief cover letter explaining your validation and technical writing experience to:

[email protected]

In your cover letter, please provide a brief example of a GMP document you have written from scratch (SOP, WI, or similar), describe any hands-on laboratory testing experience, and outline any exposure to validation or qualification activities.

Pay: £31,000.00-£34,000.00 per year

Work Location: In person

Quick apply

Refine Your Search

quality engineer jobs in st helens, msy

Junior QC & Validation Engineer

Quality, Health and Safety Engineer

Quality Inspection Engineer (Day shift)

QA Engineer

Quality Engineer - NGT (Felindre)

Quality Engineer - NGT (Alrewas)

Quality Engineer

Quality Engineer – Automotive Assembly

Apprentice Quality Engineer (18+)

QA Engineer

Quality Engineer

Process Engineer – UK Water/Wastewater – All Levels

Quality Engineer / Responsible Weld Co-ordinator

Principal QA Engineer

Supplier Quality & Development Engineer - China

Head of Quality – Engineering

Project Compliance and Risk Engineer

Senior QA Engineer

Senior QA Engineer

Graduate Mechanical Design/Project Engineer

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