Quality Release Specialist
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (27.0%).
Occupation TypeIT business analysts, architects and systems designers
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£54,900
(£28.15 per hour)
Occupation rate applies
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Description
Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world.
We are currently 1,100 people headquartered in the UK with global offices in the US, EU, JAPAC and South Africa. Clinigen has grown rapidly since it began in 2010 and is positioned well for an exciting future of continued expansion.
We are seeking a proactive and detail‑driven Quality Release Specialist to support our Quality and Warehouse teams. This role plays a key part in ensuring compliance with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP), supporting the effective operation of the Quality Management System (QMS), and safeguarding product quality and patient safety.
You will work closely with cross‑functional teams, external partners and regulators, providing both technical and administrative quality support across a wide range of activities.
Requirements
Key Responsibilities:
We are currently 1,100 people headquartered in the UK with global offices in the US, EU, JAPAC and South Africa. Clinigen has grown rapidly since it began in 2010 and is positioned well for an exciting future of continued expansion.
We are seeking a proactive and detail‑driven Quality Release Specialist to support our Quality and Warehouse teams. This role plays a key part in ensuring compliance with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP), supporting the effective operation of the Quality Management System (QMS), and safeguarding product quality and patient safety.
You will work closely with cross‑functional teams, external partners and regulators, providing both technical and administrative quality support across a wide range of activities.
Requirements
Key Responsibilities:
- Manage day‑to‑day activities within the Quality Management System (QMS), partnering with cross‑functional teams to investigate, review and close quality records within the electronic QMS.
- Create, review and approve quality documentation, including SOPs, work instructions and forms, ensuring compliance with Good Documentation Practice.
- Maintain GMP and GDP standards, managing accurate paper and electronic quality records in line with company procedures and regulatory requirements.
- Investigate quality issues and customer complaints, working collaboratively to identify root causes, prioritise actions and implement pragmatic, compliant solutions.
- Communicate quality system requirements effectively to employees, support quality‑related training, and influence others to achieve quality objectives.
- Degree in Life Sciences, Pharmacy or Chemistry (or equivalent)
- Experience in a Quality Assurance or related role
- Knowledge of GMP and GDP guidelines for human medicinal products
- Understanding of WDA(H), MS and MIA(IMP) licence requirements
- Strong organisational, planning and administrative skills
- Excellent IT skills, particularly Microsoft Office
- Confident communicator, able to engage at all levels
- Solutions‑focused with the ability to adapt and manage changing priorities
- High levels of accountability, accuracy and attention to detail
- 27 days holiday plus 8 bank holidays
- Pension contributions 4.5% matched
- Life assurance 4 x annual salary
- Flexible Benefits Platform with £25/month Company contribution
- Annual salary review
- Independent financial advice service
- Enhanced Employee Assistance Programme
- Shopping discounts with retailers
- Long service awards
- Recognition scheme & employee of the year awards