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 documentation
- Data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA
- 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.
- 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.