Manufacturing Associate (GMP-Deviation) (Boston)

Description

• Support coordination of QC and manufacturing investigations by gathering data and tracking progress.
• Assist with documentation updates in eQMS, including deviations and corrective action tracking.
• Prepare initial summaries and investigation logs under senior staff guidance.
• Escalate issues and provide status updates to ensure timely closure of quality events.
• Participate in cross-functional meetings for investigation follow-up and compliance activities.
• Maintain organized records and ensure documentation aligns with GMP standards.
• Coordinate with cross-functional stakeholders and follow up on action items.
• Develop an understanding of root cause analysis methodology and quality processes.