Quality Officer & Compliance & Process Support

Inizio Group; Leicester; On-site; GBP 30,000 - GBP 40,000; Full time

Job summary

A leading pharmaceutical company in Leicester is seeking a Quality Officer for a 15-month fixed-term contract. You will act as the primary liaison for QA in sterile manufacturing, ensuring compliance with regulatory standards. Essential requirements include a science-based degree and experience in aseptically manufactured products. This is a full-time role with an immediate start in a highly visible team that impacts product quality and patient safety.

Benefits

Exposure to client audits

Development of QA expertise

Impact on patient safety

Qualifications

• Detail-oriented QA professional with experience in regulated pharmaceutical or medical device environments.
• Experience working with aseptically manufactured pharmaceuticals or medical devices.
• Strong working knowledge of ISO 13485.

Responsibilities

• Managing Quality Systems and GMP compliance within Sterile Manufacturing.
• Investigation and review of Quality Incidents.
• Delivering and coordinating training sessions.

Skills

Attention to detail

Knowledge of ISO 13485

Proficiency in Microsoft Office

Good understanding of EudraLex Volume 4

Education

Science-based degree

Tools

Q-Pulse

TrackWise

Job description

Quality Officer - Compliance & Process Support (Quality Assurance)

Leicester | Sterile Manufacturing

15-month Fixed Term Contract | Full time (37 hours/week)| Immediate Start

Inizio Engage has an exciting opportunity for a Quality Officer - Compliance & Process Support to join our Client's Quality Assurance team, supporting our Sterile Manufacturing facilities.

Reporting to the Principal Quality Officer - Compliance and Process Support, you will act as the primary QA liaison for sterile manufacture of marketed and investigational medicinal products, playing a key role in maintaining regulatory compliance and quality excellence.

About the role

You will work closely with Sterile Manufacturing to ensure ongoing compliance with GMP, ISO 13485, 21 CFR, Medicines Regulations, and internal procedures. This is a highly visible role with significant interaction across manufacturing, microbiology, clients, and auditors.

Key responsibilities include:

• Managing Quality Systems and GMP compliance within Sterile Manufacturing
• Investigation and review of Quality Incidents, Deviations, OOS results, and Customer Complaints
• Performing regular Gemba walks across manufacturing areas
• Supporting microbiology investigations
• Tracking and closing CAPAs and effectiveness checks
• Instigating, reviewing, and approving Change Controls
• Planning, performing, and closing out internal audits
• Delivering and coordinating training sessions
• Reviewing and updating SOPs
• QA review of Batch Manufacturing & Packaging Records and Aseptic Process Simulations

About you

You are a detail-oriented QA professional with experience in regulated pharmaceutical or medical device environments.

Essential:

• Science-based degree
• Experience working with aseptically manufactured pharmaceuticals or medical devices
• Strong working knowledge of ISO 13485
• Good understanding of EudraLex Volume 4, Medicines Regulations (as amended), and 21 CFR
• Proficiency in Microsoft Office and electronic QMS (e.g. Q-Pulse, TrackWise)

Why join Nova Laboratories?

• Be part of a highly skilled QA team in a regulated sterile manufacturing environment
• Gain exposure to client audits, regulatory inspections, and new product introductions
• Develop your QA expertise across pharmaceuticals and medical devices
• Make a real impact on patient safety and product quality

How to apply

Interested? Apply now!

Please note if you have not heard from Recruitment within 7 days of submitting your application, your application has been unsuccessful.