Our Swindon facility houses our Zydis® fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability.
Position Summary
We have an opportunity for a Quality Associate to join our team. In this role, you will support audits, inspections, and compliance activities to ensure high-quality standards are maintained. You will contribute to continuous improvement initiatives and provide guidance on quality systems and processes. This position plays a key part in maintaining compliance with Good Manufacturing Practice requirements and promoting a safe, ethical working environment.
Shift: Monday - Friday 09.00 - 17.00
Location: Swindon, UK
100% Onsite
The Role
Support customer audits, regulatory inspections, and compliance assessments.
Conduct independent reviews of Corrective and Preventive Actions and corrective actions to ensure effective issue resolution and timely closure.
Participate in internal audits to assess compliance with quality systems, procedures, and regulatory requirements.
Drive continuous improvement and cross-functional projects that enhance quality, compliance, efficiency, and business performance.
Identify and escalate quality trends, risks, and recurring issues to support proactive quality management.
Provide guidance and support to colleagues on quality systems and processes.
Maintain compliance with Good Manufacturing Practice requirements, quality standards, company procedures, and organisational values.
Promote a safe working environment by adhering to Health, Safety, Environmental, Security, and ethical standards.
Report hazards, incidents, and unsafe practices in a timely manner.
Undertake any other reasonable duties commensurate with the role as assigned by the Line Manager.
The Candidate
Minimum Requirements
Degree, Higher National Diploma, Higher National Certificate, or equivalent in a scientific discipline, or relevant industry experience.
Experience working within a Good Manufacturing Practice-regulated pharmaceutical, biotechnology, medical device, or similar environment.
Knowledge of Quality Management Systems and quality processes.
Ability to review technical and quality documentation accurately.
Understanding of data integrity requirements and good documentation practices.
Proven success working with cross-functional teams.
Preferred Skills & Background
Attention to detail and accuracy.
Analytical skills to identify risks and compliance issues.
Strong communication with stakeholders, customers, and auditors.
Effective organisation and ability to manage priorities.
Collaborative approach across teams and functions.
Confident decision-making and independent quality oversight.
Problem-solving mindset with a focus on continuous improvement.
Adaptability in a fast-paced, regulated environment.
Why You Should Join Catalent
Our Swindon facility houses our Zydis® fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability.
Competitive Salary – Reflecting your experience and skills.
Bonus & Benefits – Includes a site performance bonus, a pension scheme matching up to 8% and life assurance. Enjoy a generous holiday entitlement that increases with tenure, with the option to purchase additional leave. Plus, gain access to Reward Gateway, offering discounts at many national retailers.
Career Development – Access high-quality training, mentoring, and cross-functional opportunities within Catalent’s global network. Benefit from a subscription to LinkedIn Learning, providing access to 10,000+ online courses.
Health & Wellbeing – Includes an employee assistance programme, on-site canteen facilities, and an active safety and “Patient First” culture. Take advantage of a Cycle to Work Scheme and an Electric Vehicle car scheme.
Excellent Location – Just a two-minute drive from J16 of the M4, with free on-site parking.
Catalent offers rewarding…