Senior Bioassay Scientist - cGMP ELISA Expert (ECL)

Eurofins

Columbia (PA)

In loco

USD 95.000 - 130.000

Tempo pieno

6 giorni fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

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

Descrizione del lavoro

Eurofins USA BioPharma Services in Columbia, MO, is seeking a Senior Scientist to join the Biotech department. You will serve as a subject matter expert for Drug Substances and Drug Products, performing method establishment and validations for ELISAs using ECL, and training junior staff.

The role requires strong data analysis, regulatory knowledge, and the ability to work in a cGMP environment with timely results and clear communication to Eurofins clients.

Competenze

  • Bachelor’s degree in chemistry, biochemistry, or biology with 5 years in cGMP lab OR Master’s with 3 years in cGMP lab OR PhD with 1 year in cGMP lab.
  • Authorization to work in the U.S. without restriction or sponsorship.

Mansioni

  • Design, perform and optimize simple and complex experiments per regulatory SOPs.
  • Perform method establishment and validations on ELISAs with ECL platforms.
  • Analyze data and communicate results clearly.
  • Train and mentor junior staff.
  • Utilize LIMS and other lab systems effectively.
  • Ensure timely delivery and adhere to schedules.

Conoscenze

Data analysis
Training/mentoring
ELISA & multiplex ELISA
SoftMax Pro
LIMS proficiency
Results communication
Regulatory knowledge (cGMP)

Formazione

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

Strumenti

Molecular Devices SoftMax Pro
LIMS

Descrizione del lavoro

Eurofins USA BioPharma Services in Columbia, MO, is seeking a Senior Scientist to join the Biotech department. You will serve as a subject matter expert for Drug Substances and Drug Products, performing method establishment and validations for ELISAs using ECL, and training junior staff.

The role requires strong data analysis, regulatory knowledge, and the ability to work in a cGMP environment with timely results and clear communication to Eurofins clients.

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