QC Method Transfer and Validation Scientist (Sun-Wed)

Eurofins USA PSS Insourcing Solutions•Sanford, NC

1d•Onsite

About The Position

This position supports analytical method transfer and validation activities to ensure robust, compliant testing of biologic products. The scientist collaborates with internal and external partners to execute method qualification, validation protocols, and transfer documentation. Responsibilities also include data analysis, protocol and report generation, and troubleshooting analytical techniques such as HPLC, CE, ELISA, and PCR. The role requires technical expertise and attention to regulatory requirements in a GMP-compliant environment. It is onsite in Sanford, North Carolina; public transportation is not available to the site. Support outside standard hours may be needed. The schedule is Sunday through Wednesday, 7 a.m. to 7 p.m.

Requirements

Bachelor of Science in Chemistry or a similar field.
At least 2 years of experience working in a laboratory environment.
Strong pipetting experience and skills.
Experience working with proteins or carbohydrates.
Experience working in a Good Manufacturing Practices (GMP/cGMP) environment.
Experience working with analytical standards, reagents, and laboratory instruments.
HPLC and Empower 3 experience.
Familiarity with USP and EU guidelines.
Effective oral and written communication skills.
Strong problem-solving and computer skills.
Organized, self-motivated, and able to work independently or collaboratively.
Authorization to work indefinitely in the United States without restrictions or sponsorship.
Ability to support work outside standard hours may be needed.

Responsibilities

Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation.
Analyze data and generate protocols and reports.
Troubleshoot analytical techniques, including HPLC, CE, ELISA, and PCR.
Support activities in a GMP-compliant environment and adhere to regulatory requirements.