QC Microbiology Scientist II – GMP Pharma Lab

Regulatory Toolkit; Greenville (NC); Sur place; USD 75 000 - 100 000; Plein temps

Résumé du poste

Thermo Fisher Scientific seeks a QC Scientist II – Microbiology in Greenville, NC to support pharmaceutical manufacturing operations. You will perform microbiological testing of raw materials, components, and finished oral solid dosage products in a GMP environment, review data, and contribute to investigations and CAPAs.

You will collaborate with cross-functional teams, mentor junior staff, and help ensure product quality and patient safety while maintaining compliance with USP standards and

Qualifications

• Requires advanced degree or bachelor’s with experience in GMP QC.
• Experience with compendial microbiological testing (USP <61>/<62>).
• Strong attention to detail and analytical problem-solving.

Responsabilités

• Perform and review microbiological testing for product release and stability.
• Conduct microbial identification using MALDI-TOF and MicroSeq.
• Support raw materials, components, finished products, and environmental monitoring testing.
• Review data and author/revise GMP documentation.
• Troubleshoot issues and participate in investigations and CAPAs.
• Collaborate with cross-functional teams and mentor staff.

Connaissances

Microbiology testing

GMP compliance

MALDI-TOF identification

Technical documentation

Data review

Troubleshooting

Cross-functional collaboration

Formation

Advanced degree in Biology/Microbiology

Bachelor's degree in Biology/Microbiology

Outils

MALDI-TOF

MicroSeq

LIMS

Microsoft Office

Description du poste

Thermo Fisher Scientific seeks a QC Scientist II – Microbiology in Greenville, NC to support pharmaceutical manufacturing operations. You will perform microbiological testing of raw materials, components, and finished oral solid dosage products in a GMP environment, review data, and contribute to investigations and CAPAs.

You will collaborate with cross-functional teams, mentor junior staff, and help ensure product quality and patient safety while maintaining compliance with USP standards and