A company is looking for a Specialist Manufacturing.
Key Responsibilities :
Own and manage quality records : Deviations, CAPAs, Change Controls, Supplier Investigations
Lead root cause analysis and defect material evaluations
Collaborate with suppliers and internal teams to drive timely closure
Required Qualifications :
Bachelor's degree with 4+ years of experience (or equivalent combination of education and experience)
Strong experience in quality record ownership
Familiarity with TrackWise or Veeva systems
Biotech or pharmaceutical industry background
Basic project management skills
Quality Specialist • Charleston, South Carolina, United States