This position is responsible for supporting analytical method transfer and validation activities to ensure robust and compliant testing of biologic products.
• Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation
• Data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA, PCR
• The role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environment
This role is onsite in Sanford, NC. There are no public transportation options to the site. Ability to support outside standard hours may be needed.
• BS in Chemistry or similar field with a minimum of 2 years of experience working in a laboratory environment.
• Strong pipetting experience is required
• 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
• 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
This position is Full-Time, Sunday to Wednesday 7 am - 7 pm. Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply.
• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.