Pharmaceutical Quality Control Associate

2 weeks ago


Greenville, North Carolina, United States Disability Solutions Full time

Catalent is seeking a Quality Control Associate to support our Supplier Audits program in Greenville, N.C. As a Quality Control Associate, you will be responsible for conducting system-based audits and risk assessments for Supplies Audits and Internal Quality Systems.

Key responsibilities include:

  • Performing external supplier audits (Desktop, Virtual or On-Site) per schedule, communicating findings and ensuring CAPA plans are appropriate to address the findings.
  • Ensuring Supplier Audit Team members are properly qualified and assigning their roles and responsibilities; training staff to conduct or assist with audits and risk assessments.
  • Participating in Regulatory Inspections and assisting Inspection Readiness Teams with inspection preparation, including walkthroughs and gathering of documentation, per inspection agenda as required.
  • Assisting with the generation of the Internal Audit Schedule, preparation and execution of Internal Quality Audits of Catalent systems / subsystems.
  • Participating in process improvement projects and investigations, as required.

This role requires a strong understanding of cGMPs and experience working in a Quality Auditing function. The ideal candidate will have a Bachelor's degree in a technical field and at least 6 years of professional experience in the pharmaceutical industry, with 3 years of experience in a Quality Auditing function.

The salary range for this position is $80,000 - $110,000 per year, depending on experience.

Benefits include competitive medical benefits, 152 hours of PTO + 8 Paid Holidays, dynamic work environment, and opportunities for career growth and development.

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