Entry-Level Data Review Scientist - Biopharma GMP/GLP

Eurofins; Lancaster (Lancaster County); Presencial; USD 55 000 - 75 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical, dental and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Resumo da oferta

Eurofins Biopharmaceutical in Lancaster, PA, is seeking an Associate Scientist to support Data Review for the Biochemistry team. This entry‑level role offers hands‑on development in daily lab activities under prescribed SOPs and CGMP guidelines.

You will review scientific reports, assist with internal audits, and help track data to ensure regulatory requirements are met. The position provides exposure to both laboratory operations and data management in a collaborative team environment.

Qualificações

• Bachelor's degree in life sciences (chemistry/biochemistry/biology) required.
• Authorization to work in the United States without sponsorship.
• Experience in a laboratory or GMP pharmaceutical setting preferred.
• Ability to review data for GMP/GLP compliance and accuracy.
• Strong organizational, communication, and documentation skills.
• Ability to work independently and as part of a team.

Responsabilidades

• Review laboratory data for accuracy, clarity, and GMP/GLP compliance.
• Review data across multiple areas according to SOPs; ensure procedures are followed.
• Assist with internal audits and regulatory requirements.
• Data tracking and reporting.
• Balance schedule supporting both lab and data tracking operations.

Conhecimentos

Data review

GMP/GDP compliance

Attention to detail

Communication

Teamwork

Documentation

SOP understanding

Independent learner

Laboratory data analysis

Adaptability

Formação académica

Bachelor's degree in Life Sciences

Ferramentas

Microsoft Excel

Descrição da oferta de emprego

Eurofins Biopharmaceutical in Lancaster, PA, is seeking an Associate Scientist to support Data Review for the Biochemistry team. This entry‑level role offers hands‑on development in daily lab activities under prescribed SOPs and CGMP guidelines.

You will review scientific reports, assist with internal audits, and help track data to ensure regulatory requirements are met. The position provides exposure to both laboratory operations and data management in a collaborative team environment.