Biologics Method Transfer & Validation Scientist

Eurofins; Sanford (NC); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins is seeking a focused analytical scientist to support method transfer and validation for biologic products at our Sanford, NC site. The role emphasizes collaboration with internal and external partners to ensure robust testing programs and regulatory compliance.

You will perform data analysis, generate protocols and reports, and troubleshoot instrumentation such as HPLC and ELISA while maintaining strict GMP standards.

Qualifications

• BS in Chemistry or similar field with a minimum of 2 years of experience in a laboratory environment.
• Experience with proteins or carbohydrates.
• Experience in a GMP/cGMP environment.
• Experience with analytical standards, reagents, and laboratory instruments.
• Strong pipetting skills.
• HPLC and Empower 3 experience.
• Familiarity with USP, EU guidelines.
• Excellent oral and written communication.
• Strong problem-solving 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.

Responsibilities

• Support analytical method transfer and validation activities to ensure robust and compliant testing of biologic products.
• Data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA.
• Ensure compliance with regulatory requirements in a GMP environment.

Skills

Oral and written communication

Problem solving

Independent work

Attention to regulatory requirements

Education

B.S. in Chemistry or related field

Tools

HPLC

Empower 3

Job description

Eurofins is seeking a focused analytical scientist to support method transfer and validation for biologic products at our Sanford, NC site. The role emphasizes collaboration with internal and external partners to ensure robust testing programs and regulatory compliance.

You will perform data analysis, generate protocols and reports, and troubleshoot instrumentation such as HPLC and ELISA while maintaining strict GMP standards.