Sample Management

Eurofins•Upper Gwynedd Township, PA

12h•Onsite

About The Position

The Sample Management role supports Analytical Research & Development for major vaccine and biologics franchises. Responsibilities include physical sample handling and global distribution, management of biological critical reagents, equipment and records review, logistics coordination, maintenance of Research LIMS specifications, and support for analytical method transfer activities. The role requires compliance with regulatory expectations and applicable current Good Manufacturing Practices (cGMP). It is a full-time, permanent, onsite position in West Point, Pennsylvania, scheduled Monday through Friday, 8 a.m. to 5 p.m., with overtime as needed.

Requirements

Bachelor's degree in biology, chemistry, or another related degree concentration.
Authorization to work indefinitely in the United States without restriction or sponsorship.

Nice To Haves

Strong scientific and organizational skills.
Excellent oral and written communication skills.
High attention to detail, particularly in preparing GMP documentation and performing associated work.
Ability to work independently and as part of a team.
Self-motivation, willingness to contribute to the work, and ownership of projects.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Experience with classical biochemical assays and molecular biological techniques.
GMP experience.
Technical writing experience.
Experience with regulatory audits.

Responsibilities

Perform physical sampling, labeling, global sample distribution (import and export), and sample monitoring.
Aliquot biological critical reagents and document the work in ELN.
Perform quarterly equipment and logbook reviews.
Review equipment temperature data.
Serve as primary logistics coordinator for major vaccine and biologics franchises in Analytical Research & Development.
Perform second-scientist and second-person reviews as required.
Build and maintain Research LIMS specifications and specification lists for vaccine and biologics franchises.
As required, train on laboratory methods that support key analytical method transfer activities.
Ensure all work complies with regulatory expectations and follow applicable current Good Manufacturing Practices (cGMP).