
Quality Process Specialist
14 hours ago
Job Overview:
This role is integral to ensuring compliance with regulatory and GMP requirements at a compounding centre. Key responsibilities include investigating incidents, preparing reports, participating in audits, and training staff on quality procedures.
About the Position:
We are seeking an experienced Quality Associate to join our team. The successful candidate will have a strong background in GMP compliant pharmaceutical manufacturing, experience in sterile compounding environments, and competency in IT software such as MS Word and Excel.
Key Responsibilities:
- Investigate incidents, deviations, and complaints
- Participate in risk assessments, change control, validation, and internal audits
- Conduct training for staff on quality procedures
- Maintain and organize the site micro laboratory
- Support Environmental Monitoring activities and perform quality assessments
Requirements:
- Experience in GMP compliant pharmaceutical manufacturing environment
- Experience in sterile compounding environment (desirable)
- Experience with regulators of pharmaceutical manufacture
- Competency in common IT software
What We Offer:
- A supportive and collaborative team environment
- A permanent full-time position with reasonable overtime and possible weekend work
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