Quality Officer - Compliance and Process Support - FTC
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (42.0%).
Occupation Type
Quality assurance and regulatory professionals
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£48,200
(£24.72 per hour)
Occupation rate applies
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Description
Quality Officer - Compliance & Process Support (Quality Assurance)
Leicester | Sterile Manufacturing
15-Month Fixed Term Contract | 37 hours per week | Immediate Start
Are you a detail-driven QA professional ready to make a real impact in sterile manufacturing?
Inizio Engage is partnering with a leading organisation to recruit a Quality Officer - Compliance & Process Support to join a high-performing Quality Assurance team. This is an exciting opportunity to play a pivotal role in safeguarding patient safety while working at the forefront of sterile pharmaceutical and medical device manufacturing.
Reporting to the Principal Quality Officer, you will act as the primary QA liaison for the manufacture of both marketed and investigational medicinal products. This is a visible, hands-on position where your expertise will directly support compliance, quality excellence, and continuous improvement across the sterile manufacturing operation.
What You'll Be Doing
In this varied and impactful role, you will:
Leicester | Sterile Manufacturing
15-Month Fixed Term Contract | 37 hours per week | Immediate Start
Are you a detail-driven QA professional ready to make a real impact in sterile manufacturing?
Inizio Engage is partnering with a leading organisation to recruit a Quality Officer - Compliance & Process Support to join a high-performing Quality Assurance team. This is an exciting opportunity to play a pivotal role in safeguarding patient safety while working at the forefront of sterile pharmaceutical and medical device manufacturing.
Reporting to the Principal Quality Officer, you will act as the primary QA liaison for the manufacture of both marketed and investigational medicinal products. This is a visible, hands-on position where your expertise will directly support compliance, quality excellence, and continuous improvement across the sterile manufacturing operation.
What You'll Be Doing
In this varied and impactful role, you will:
- Lead GMP and Quality Systems compliance within Sterile Manufacturing
About You
You are a proactive and quality-focused professional who thrives in regulated environments and enjoys working cross-functionally to uphold high standards.
Essential Requirements:
- Science-based degree
- Experience within aseptic pharmaceutical or medical device manufacturing
- Strong working knowledge of ISO 13485
- Good understanding of EudraLex Volume 4, Medicines Regulations (as amended), and 21 CFR
- Join a highly skilled QA team within a sterile manufacturing environment
- Gain exposure to regulatory inspections and client audits
- Broaden your experience across pharmaceuticals and medical devices
- Contribute directly to patient safety and product quality
- Work in a collaborative, quality-driven culture
Apply today.
Please note: If you have not heard from the Recruitment team within 7 days of your application, unfortunately your application has not been successful on this occasion.