Eurofins BioPharma Product Testing North America

Scientist (Data Review)

LANCASTER, PAPosted a month ago

Job summary

  • Job post source

    This job is directly from Eurofins BioPharma Product Testing North America

  • Job overview

    The Scientist (Data Review) role involves reviewing scientific reports to ensure compliance with cGMP guidelines and regulatory standards, impacting the quality and accuracy of data reporting within the company.

  • Responsibilities and impact

    The role requires reviewing scientific reports for regulatory compliance and data accuracy, assisting with internal audits, collaborating with lab operations staff daily, and having final authority for report sign-off.

  • Unique job features

    This position is distinct from data science or analytics roles, focusing specifically on scientific data review under regulatory guidelines.

Company overview

Eurofins BioPharma Product Testing North America is a leading provider of laboratory services to the biopharmaceutical industry. They specialize in analytical testing, bioanalytical services, and microbiology testing to ensure the safety, identity, purity, and quality of pharmaceutical products. The company generates revenue by offering a broad range of testing services that support drug development and manufacturing processes. Founded as part of the global Eurofins Scientific network, they leverage extensive expertise and advanced technologies to serve clients efficiently and reliably.

How to land this job

  • Tailor your resume to emphasize your experience in reviewing scientific data and reports within cGMP or similar regulatory frameworks, showcasing your attention to detail and commitment to quality assurance.

  • Highlight your ability to collaborate with lab operations and your responsibility in final report approvals, demonstrating your capacity to work cross-functionally and make authoritative decisions.

  • Apply through multiple platforms including Eurofins BioPharma Product Testing North America's corporate careers page and LinkedIn to maximize your chances of being noticed by recruiters.

  • Connect with current employees in the Quality Assurance or Scientific Review divisions on LinkedIn, using ice breakers like commenting on recent company news or asking about their experience with report review under cGMP guidelines.

  • Optimize your resume for ATS by incorporating keywords such as 'cGMP,' 'scientific report review,' 'quality assurance,' 'audit assistance,' and 'final report sign-off' to ensure it passes initial screenings effectively.

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