Minimum 3 years of industry experience in a GMP-regulated biotech or pharmaceutical environment
Strong knowledge of quality systems and QC lab operations
Experience in writing, owning, and closing quality records (deviations, CAPAs, change controls)
Excellent technical writing, grammar, and investigation leadership skills
Detail-oriented, proactive, and able to manage shifting priorities in a fast-paced environment
Comfortable working cross-functionally and leading meetings/investigations independently
Experience with Veeva Quality Systems is highly desirable
Part of the QC Deviation & Change Control team supporting startup and operations of the ANC facility
Collaborate with Quality and QA teams to manage quality systems in DQMS (Veeva)
Write, own, and manage deviations and change controls in Veeva
Lead investigation teams and track/report system metrics
Review validation documents for equipment and computerized systems
Author, revise, and review:
SOPs
Test methods
Safety assessments
Trend reports
Qualification/validation summary reports
Technical reports
Support GMP QC lab startup activities
Provide support during weekends and public holidays as needed
High School Diploma/GED + 2 years of experience
OR
Associate’s Degree + 6 months of experience
OR
Bachelor’s Degree
3+ years of GMP experience
Deviation ownership with strong technical writing skills
QC laboratory experience
Experience with Veeva Quality Systems
Deviation ownership
Change control ownership and management
No GMP experience
No QC lab experience
Virtual interview
1–2 rounds