About this role
Ensure that the client receives high quality data and reports that adhere to client and good manufacturing process (GMP) requirements.Reviewing laboratory documentation for accuracy, consistency, and clarity.Gain a technical understanding of the techniques for the assays in which review is being performed
Begin to gain industry knowledge of the testing being completed within the department
Document work as required for GMP compliance
Minimum Qualifications:
Bachelor’s degree in molecular/cellular biology or other related degree concentration, or equivalent directly-related experience.
Familiarity or experience with GMP setting higly preferred
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is Full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with additional hours, as needed. Candidates currently living within a commutable distance of Lancaster, PA 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 BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.