About this role
*THIS IS NOT A DATA SCIENCE POSITION*
Employee Responsibilities:
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
The Ideal Candidate would possess:
One to two years experience in molecular and/or cell biology, mainly real-time PCR, ddPCR, ELISA, cell based plate reader, and nucleic acids sequencing.
GMP experienceStrong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
Bachelor’s degree in molecular/cellular biology or other related degree concentration, or equivalent directly-related experience.
At least one to two years hands on experience in a molecular/cell biology laboratory; industry and/or contract testing experience desired
Familiarity or experience with GMP setting highly preferred
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is Full-time, Monday-Friday, 8:00 a.m.-4:00 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lancaster, Pennsylvania 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 holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.