Job Description

• 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

Qualifications

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

Additional Information

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 options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.