About this role
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 documentationData analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISAThe role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environmentThis 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.Experience working with proteins or carbohydrates.Experience working in a Good Manufacturing Practices {also cGMP} environmentExperience working with analytical standards, reagents, and laboratory instrumentsStrong pipetting skillsHPLC and Empower 3 experienceFamiliarity with USP, EU guidelinesEffective oral and written communicationStrong problem-solving skillsExcellent oral and written communication skills as well as strong computer skillsMust 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.