Quality Assurance Specialist
About the Role:
This is an excellent opportunity for a Quality professional with a minimum of 4 years' experience working in a GMP and/or sterile environment to oversee CAPA's, deviations, batch release review and change controls.
The successful candidate will be part of an established Quality team who promote collaboration and teamwork, ensuring all issues are investigated and approved by key management and stakeholders.
Key Responsibilities:
* Managing Deviations, CAPA and Non-conformances in Sterile Manufacturing facilities
* Batch record review and process improvement
* Audits and compliance documentation in line with regulations
Requirements:
* Experience in managing quality processes and investigations in a sterile product GMP manufacturing environment
* Demonstrated experience in Risk Analysis, Investigation, Problem Solving and critical thinking
* Proficiency with Microsoft Word, Excel, PowerPoint and electronic document systems
About You:
* Exceptional attention to detail and strong organizational skills
* Proven experience in cross-functional teamwork and decision-making
* Excellent interpersonal and communication skills, both written and verbal
Salary:$80,000 - $100,000 per annum