Manufacturing associate Work, Jobs in Wigan, Gtm (with Salaries)

Junior QC & Validation Engineer
Sina Medical Glass —St Helens
- £31,000 - £34,000 a year
- Full-time
- Data analysis skills
- No experience needed
- Analysis skills
Quick apply
4d
Supply Chain Graduate Programme 2026 - UK
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Anheuser-Busch —Preston
- Full-time
- Continuous improvement
- Training & development
- Leadership
- Annual leave
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Electrical Manufacturing Inspector
MBDA —Bolton
- £43,537 a year
- Overtime
- Hybrid work
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Technical Associate – Upstream Process Development
Elanco —Liverpool
- Continuous improvement
- Organisational skills
Quick apply
9d
IT Technician
Alkegen —Rainford
- Full-time
- Hybrid work
- No degree
- Travel
Scientist/Associate Scientist, Analytical Sciences (12 months Fixed Term Contract)
Pharmaron —Liverpool
- Laboratory experience
- Master's degree
- Bachelor's degree
Quick apply
11d
Associate Director Construction Planner - Programme Scheduler
Jacobs —Manchester
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R&D Tax Technical Manager/Associate Director
Sedulo —Manchester
- Full-time
- Hybrid work
- Engineering
- Team management
- Mentoring
- Work from home
- Flexible schedule
Quick apply
5d
Scientific Associate III, Analytical Sciences (Fixed term contract)
Pharmaron —Liverpool
- Master's degree
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Process Operator Apprentice
Ecolab Inc. —Northwich
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Research Microbiologist
Arxada —Manchester
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Associate
DWF —Manchester
- Full-time
- Hybrid work
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Rolls-Royce Fellow in Robust Nuclear Fuels
The University of Manchester —Manchester
- £47,389 - £58,225 a year
- Hybrid work
- Doctoral degree
- Engineering
- Research
- Annual leave
- Employee assistance programme
13d
Associate Director of TPM
AstraZeneca —Liverpool
- Monday to Friday
- Maintenance
- Continuous improvement
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10d
HR Business Partner - UK
Arxada —Manchester
- Full-time
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PDRA in Chemistry
University of Liverpool —Liverpool
- £39,906 - £46,049 a year
- Full-time
- Hybrid work
- Doctoral degree
- Research
- University
9d
Senior Area Sales Manager - North West England
Linx —Manchester
- Full-time
- CRM software
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Assoc Dir Global Category Manager Devices
Teva —Runcorn
- Communication skills
- Annual leave
PPI Engineer
M+A Matting UK —Manchester
- Engineering
- Microsoft Office
- Continuous improvement
Quick apply
10d

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Junior QC & Validation Engineer

Sina Medical Glass
St Helens

Quick apply

Job details

Permanent | Full-time
£31,000 - £34,000 a year
4 days ago

Qualifications

Document control
Quality management change control procedures
Data analysis skills
Quality control within general manufacturing industry
No experience needed
Analysis skills
Quality assurance
Bachelor's degree
HACCP
Quality control
Technical writing
Document control software
Document management
Document management systems
Leadership
ISO 13485
Internal audits

Full job description

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).

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

manufacturing associate jobs in wigan, gtm

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