Entry Level Microbiology Data Review

Eurofins•Lancaster, PA

2d•Onsite

About The Position

This entry-level laboratory role focuses on reviewing departmental microbiology testing experiments, data, and reports. The employee completes training and works with an experienced analyst or mentor on analyses of biopharmaceutical ingredients and products. Duties may include preparing or reviewing reagents, samples, and standards; operating laboratory equipment independently or with guidance; and ensuring client data is accurate, clear, and compliant with GMP and/or GLP requirements. This is not a data science role. The position requires a technical understanding of microbiology and a commitment to quality, accurate documentation, laboratory procedures, and client service. The employee performs laboratory operations and maintenance, processes data, prepares reports, and works with moderate supervision after training. The role is full-time, first shift, Monday through Friday, 8 a.m. to 5 p.m., and is not remote. Candidates within commuting distance of Lancaster, Pennsylvania are encouraged to apply; relocation assistance is not provided. Travel of up to 25% may be required.

Requirements

Bachelor's degree in chemistry, biology, biochemistry, or a related degree concentration.
Technical understanding of microbiology.
No previous laboratory experience is required.
Ability to work in the United States without immediate or future sponsorship.
Good dexterity.
Positive attitude and solution-driven approach.
Organized, efficient, careful, safety-conscious, and accurate work habits.
Attention to detail and sound scientific logic.
Good oral and written communication skills.
Understanding of instrumentation.
Client-service focus and organizational skills.
Ability to work with moderate supervision after training on assigned tasks.
Ability to handle multitasking.

Responsibilities

Complete all required training in a timely and complete manner.
Work with an experienced analyst or mentor to perform tasks and analyses of biopharmaceutical ingredients and products.
Prepare or review standards and samples for analysis and operate equipment or instrumentation independently or with guidance.
Review departmental testing experiments, laboratory data, and reports for accuracy, clarity, and compliance with GMP and/or GLP regulations.
Apply GMP/GLP requirements and the highest quality standards in areas of responsibility.
Plan and multitask proactively to maximize productivity and meet quality and productivity metrics.
Perform laboratory operations using sound technique, dexterity, accuracy, and precision.
Prepare or review reagents, samples, and standards according to procedures.
Document testing, observations, deviations, and results clearly, completely, and in compliance with regulatory requirements.
Understand and perform calculations required by test methods.
Read and understand compendial and client-supplied analytical procedures and internal SOPs.
Use computers to access information, perform calculations, process data, generate reports, and prepare reports.
Use Microsoft Windows applications, including Excel, Word, and Outlook.
Communicate effectively orally and in writing and demonstrate client service, teamwork, and collaboration.
Perform laboratory maintenance and maintain a neat, clean, and orderly workspace.
Work occasional overtime as workload requires.