Senior Bioassay Scientist - cGMP ELISA & Validation

Eurofins BioPharma Product Testing North America

Columbia (PA)

Vor Ort

USD 90.000 - 140.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical coverage
Life insurance
Disability insurance
401(k) with match
Paid holidays
Vacation
Dental and vision

Zusammenfassung

Eurofins BPT-Columbia is seeking a Sr. Scientist to join our Biotech group in Columbia, MO. You will serve as a subject matter expert for testing Drug Substances and Drug Products, performing method establishment and validation under cGMP guidelines, including ELISAs and multiplex ELISAs using ECL.

Success requires strong data analysis, clear communication of results, and the ability to train junior staff while meeting project timelines and complying with SOPs and regulatory requirements.

Qualifikationen

  • Bachelor’s degree in chemistry/biochemistry/biology with 5 years in a cGMP lab.
  • Master’s degree with 3 years in a cGMP lab.
  • PhD with at least 1 year in a cGMP lab.

Aufgaben

  • Design and perform experiments per regulatory SOPs.
  • Establish and validate methods including multiplex ELISAs using ECL.
  • Analyze data and communicate results.
  • Train and mentor junior staff.
  • Use LIMS for data management.
  • Ensure on-time delivery per schedule.

Kenntnisse

cGMP knowledge
Data analysis
Training/mentoring
Communication

Ausbildung

Bachelor’s degree in chemistry/biochemistry/biology
Master’s degree in related field
PhD in related field

Tools

Molecular Devices Softmax Pro
LIMS
ELISA
ECL platforms

Jobbeschreibung

Eurofins BPT-Columbia is seeking a Sr. Scientist to join our Biotech group in Columbia, MO. You will serve as a subject matter expert for testing Drug Substances and Drug Products, performing method establishment and validation under cGMP guidelines, including ELISAs and multiplex ELISAs using ECL.

Success requires strong data analysis, clear communication of results, and the ability to train junior staff while meeting project timelines and complying with SOPs and regulatory requirements.

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