GMP Quality Assurance Specialist – Onsite

Catalent, Inc.; Swindon; On-site; GBP 28,000 - 42,000; Full time

Benefits offered by this job

Site performance bonus

Pension scheme (8% matched)

Life assurance

Generous holiday entitlement

Job summary

Catalent, Inc. is seeking a Quality Associate to support audits, inspections, and compliance activities, ensuring high-quality standards are maintained.

You will contribute to continuous improvement and guide quality systems and processes, sustaining GMP compliance and a safe, ethical working environment. The role is an on-site position in Swindon, UK, with a Monday–Friday schedule and a focus on quality and regulatory adherence.

Qualifications

• 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.

Responsibilities

• Support customer audits, regulatory inspections, and compliance assessments.
• Conduct independent reviews of CAPAs and corrective actions to ensure timely closure.
• Participate in internal audits to assess compliance with quality systems and regulatory requirements.
• Drive continuous improvement and cross-functional projects to enhance quality and efficiency.
• Identify quality trends, risks, and recurring issues to support proactive quality management.
• Provide guidance on quality systems and processes to colleagues.

Skills

Attention to detail

Analytical skills

Strong communication

Effective organisation

Collaborative approach

Decision-making

Problem-solving mindset

Adaptability

Education

Degree/HND/HNC in a scientific discipline

Job description

Catalent, Inc. is seeking a Quality Associate to support audits, inspections, and compliance activities, ensuring high-quality standards are maintained.

You will contribute to continuous improvement and guide quality systems and processes, sustaining GMP compliance and a safe, ethical working environment. The role is an on-site position in Swindon, UK, with a Monday–Friday schedule and a focus on quality and regulatory adherence.