Lancaster, PA, USA
Full-time
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.
- Review 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
- 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 experience.
- Strong 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.
Additional Information
Position is Full-time, Monday‑Friday, 8:00 a.m.‑4:00 p.m., with overtime as needed.
Benefits
- 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.