Lilly is designing and building a new state of the art Parenteral, Device Assembly, and Packaging Facility in Concord, North Carolina, and requires a QA Specialist to support quality control and operations.
Requirements
- Demonstrated experience in a GMP facility
- Proficiency with computer systems including Microsoft Office products, SAP and MES
- Pass an annual vision test and be free of color blindness.
- Must be equivalent to 20 /20 correctable close vision acuity.
Responsibilities
- Ensure Good Documentation practices and compliance with inspection and operational related documents.
- Complete manual visual statistical sorting inspection for Concord Parenteral products in alignment with production schedule.
- Document defect classification information within manufacturing ticket associated with statistical inspection.
- Ensure appropriate sampling of final semi-finished product, delivering the samples to the appropriate laboratories and completing all associated documentation
- Support Operational inspection personnel with completion of required training and qualification activities.
- Support Operations and investigations related to appropriate classification of defects.
Other
- Demonstrated organizational skills
- Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
- Strong Attention to detail
- Experience in Pharmaceutical Production, QA or QC is desirable
