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The Quality Compliance and Systems team supports all activities associated with the sterile manufacture of pharmaceutical products at our facility in Swindon. In this role, you will support Quality Management Systems (QMS) designed to ensure high-level quality assurance for manufacturing operations. This position offers hands-on experience in a global organization, providing opportunities to address real-time problems, build interpersonal skills, and gain exposure to senior leadership.
Job Responsibility:
Engage with suppliers as a key part of the vendor assurance process
Support both internal and external audit activities to maintain regulatory standards
Collaborate with various departments regarding comprehensive document and record management
Monitor site metrics and follow up with action owners to ensure tasks are completed on time
Support on-site training curricula as a Qualified Subject Matter Expert (SME)
Perform trend analysis and report on performance data to drive quality improvements
Support Practical Process Improvements (PPI) and the issuance of a regular quality newsletter
Utilize key Quality Management Systems, including Trackwise, SAP, EDMS, and SFLMS
Requirements:
Currently pursuing a Bachelor's degree
0+ years of experience preferred
Ability to multi-task and strictly adhere to deadlines
Excellent communication and organizational skills
Goal-driven mindset with a high degree of flexibility in a rapidly changing environment