QA & QC Oversight Specialist – GMP, HPLC/GC

Eurofins; Sanford (NC); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions in Sanford, NC seeks a QA professional to oversee QC activities in a biotech/pharma setting. GMP experience is required, with hands-on oversight over method validation, equipment qualification, and change controls.

You will support investigations into QC deviations, drive process improvements, and ensure compliance with regulatory requirements. A BS/BA with 4+ years in biotech/pharma quality is expected.

Qualifications

• Requires BS/BA in a related field and minimum 4 years of experience in manufacturing, laboratory, quality, technical or engineering within biotech/pharmaceutical industry.
• GMP experience is required for this QA oversight role.
• Direct experience with method transfer validation, investigations, change controls, and equipment qualification is needed.

Responsibilities

• Provide QA oversight of QC activities.
• Review and approve QC method validation, equipment qualification, protocols, reports, process control documents, and new/existing procedures.
• Support evaluation and resolution of QC deviations and investigations; contribute to process improvement initiatives.
• Position is full-time with standard hours; commuting distance to Sanford, NC is required.

Skills

GMP Experience

QC Oversight

Method Validation

Equipment Qualification

Change Controls

HPLC/GC Testing

Investigations

Pharmacopoeia knowledge

Education

BS or BA in a related field

Job description

Eurofins USA PSS Insourcing Solutions in Sanford, NC seeks a QA professional to oversee QC activities in a biotech/pharma setting. GMP experience is required, with hands-on oversight over method validation, equipment qualification, and change controls.

You will support investigations into QC deviations, drive process improvements, and ensure compliance with regulatory requirements. A BS/BA with 4+ years in biotech/pharma quality is expected.