Eurofins is hiring a

Development Data Review Specialist

Indianapolis, United States
Full-Time

Employee Responsibilities:

Applies GMP/GLP in all areas of responsibility, as appropriate.

  • Perform verification of data and confirm resolution of issues identified
  • Independently engage and collaborate with coworkers, customers, and management
  • Must be able to identify problems and know when to solve proactively and seek advice
  • Strong computer, scientific, and organizational skills
  • Excellent written and oral communication with attention to detail
  • Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting
  • Ability to read, comprehend, and present complex subjects

Minimum Qualifications:

  • Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  • At least 2 years related GMP pharmaceutical experience in either operations or testing role
  • Authorization to work in the United States indefinitely without restriction or sponsorship
  • Ensure adherence to highest quality and efficiency standards in laboratory operations

 

Position is Monday- Friday 8:00 am- 5:00 pm. Overtime as needed.  Candidates currently living within a commutable distance of  Indianapolis, IN are encouraged to apply. 

  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • #LI-EB1
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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