Pharma Lab Scientist: GMP Analytics & Method Transfer

Eurofins

Portage (MI)

On-site

USD 52,000 - 75,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, and vision options
401(k) with company match
Paid vacation and holidays
Life and disability insurance

Job summary

Eurofins USA BioPharma Services in Portage, MI is seeking a full-time analytical lab specialist to perform physical, chemical, and instrumental analysis of APIs and finished pharmaceutical products, including tablets, capsules, parenterals, devices, liquids, creams, and gels.

The role requires hands-on operation of HPLC, Karl Fischer, UV/Vis, and dissolution systems, method transfer, data review for GMP/GLP compliance, and collaboration with vendors.

Qualifications

  • Bachelor's degree in biology or chemistry, or equivalent directly-related experience.
  • 1-2 years of previous laboratory experience.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

  • Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels).
  • Prepare standards and samples for analysis; operate instrumentation independently including HPLC, Karl Fischer, UV/Vis, and dissolution apparatus.
  • Execute method transfer protocols and maintain monthly equipment maintenance.
  • Ensure client data quality by reviewing laboratory data for GMP/GLP compliance and accuracy.
  • Train others in laboratory procedures and lead project/test areas.

Skills

Laboratory experience
Attention to detail
Documentation

Education

Bachelor's degree in biology or chemistry, or equivalent experience

Tools

HPLC
Karl Fischer
UV/Vis spectrophotometry
Dissolution apparatus
Chromatography systems

Job description

Eurofins USA BioPharma Services in Portage, MI is seeking a full-time analytical lab specialist to perform physical, chemical, and instrumental analysis of APIs and finished pharmaceutical products, including tablets, capsules, parenterals, devices, liquids, creams, and gels.

The role requires hands-on operation of HPLC, Karl Fischer, UV/Vis, and dissolution systems, method transfer, data review for GMP/GLP compliance, and collaboration with vendors.

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