Become a key player in QA Compliance for plasma operations as a Specialist I. Your role will be essential in supporting high standards in pharmaceutical manufacturing.
As the Specialist I, you will provide quality assurance oversight, ensuring that all aspects of plasma sourcing, handling, and processing strictly comply with current Good Manufacturing Practices (cGMP) and regulatory guidelines. Your ability to conduct thorough audits and inspections will help maintain a state of readiness and support continuous improvement initiatives across the organization.
Key Responsibilities:
• Ensure compliance with cGMP in plasma operations
• Plan and execute internal quality audits
• Analyze documentation for regulatory adherence
• Report compliance metrics to leadership
• Guide quality improvement projects and initiatives
Requirements:
• Bachelor’s degree in Biological Science or equivalent
• At least 5 years of relevant QA experience
• Knowledge of FDA and cGM...