QA & QC Specialist: GMP Oversight, Validation & Transfers

Eurofins USA PSS Insourcing Solutions; Sanford (NC); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Medical, dental, and vision coverage

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a QA professional to oversee QC activities and ensure GMP standards. The role involves reviewing method validation, equipment qualification and change controls to support pharmaceutical manufacturing processes.

Candidates should have a BS/BA in a scientific field with at least 4 years in biotech/pharma settings, and be authorized to work in the United States. On-site in Sanford, NC, with full-time hours and comprehensive benefits.

Qualifications

• BS or BA degree in a scientific field, with a minimum of 4 years of experience in manufacturing, laboratory, quality, technical or engineering within biotech or pharma.
• GMP experience required.
• Direct experience with Method Transfer Validation, Investigation, Authoring Change Controls, Equipment Qualification.

Responsibilities

• Provide QA oversight of QC activities and ensure compliance with regulations.
• Review and approve QC method validation, equipment qualification, protocols, reports and procedures.
• Support evaluation and resolution of QC deviations and investigations, and contribute to process improvement initiatives.

Skills

QA oversight

QC method validation

Equipment qualification

Change controls

Deviations investigations

Process improvement

Biotech/pharma industry experience

Education

BS or BA degree in a scientific field

Tools

HPLC

GC

Raw materials testing

Job description

Eurofins USA PSS Insourcing Solutions is seeking a QA professional to oversee QC activities and ensure GMP standards. The role involves reviewing method validation, equipment qualification and change controls to support pharmaceutical manufacturing processes.

Candidates should have a BS/BA in a scientific field with at least 4 years in biotech/pharma settings, and be authorized to work in the United States. On-site in Sanford, NC, with full-time hours and comprehensive benefits.