QC Method Transfer and Validation Scientist

Eurofins•Sanford, NC

20h•Onsite

About The Position

This position is responsible for supporting analytical method transfer and validation activities to ensure robust and compliant testing of biologic products. The role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environment.

Requirements

BS in Chemistry or similar field with a minimum of 4 years of experience working in a laboratory environment
Experience working with proteins or carbohydrates
Experience working in a Good Manufacturing Practices also cGMP environment
Experience working with analytical standards, reagents, and laboratory instruments
Strong pipetting skills
HPLC and Empower 3 Experience
Familiarity with USP, EU guidelines
Effective oral and written communication
Strong problem-solving skills
Flexible to support outside standard hours and potential for weekend support
Excellent oral and written communication skills as well as strong computer skills
Must be organized, self-motivated, and capable of working independently or in a collaborative environment
Authorization to work in the United States indefinitely without restrictions or sponsorship

Nice To Haves

Pathogen safety experience
Background with regulatory landscape

Responsibilities

Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation.
Perform data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA.