Analytical Scientist - Biologics Assays & Method Transfer

Real Staffing Group

United States

Sur place

USD 70 000 - 95 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Health insurance
Health savings accounts
Retirement savings plans
Life and disability insurance
Paid leave

Résumé du poste

Real Staffing Group in the United States is seeking an Analytical Scientist to provide analytical support for upstream and downstream manufacturing labs, performing in-process sample testing in a non-GMP environment and reporting data accurately.

You will execute and troubleshoot ELISA, qPCR, potency assays, and support assay transfers, development, and implementation of new methods, using HPLC/UPLC and capillary electrophoresis for biologics characterization.

Qualifications

  • Provide analytical support for upstream and downstream manufacturing labs by performing in-process sample testing in a non-GMP environment, ensuring accurate data reporting.
  • Execute and troubleshoot analytical assays including ELISA, qPCR, potency assays, and support assay transfers, development, and implementation of new analytical methods.

Responsabilités

  • Maintain electronic lab notebooks, document results, prepare technical reports, and present findings to cross-functional teams.
  • Collaborate with manufacturing and analytical teams on method transfer, qualification, validation, and troubleshooting activities.
  • Preferred background includes experience with monoclonal antibodies, protein therapeutics, and mammalian-cell bioprocessing.

Connaissances

ELISA
qPCR
Potency Assays
HPLC/UPLC
Capillary Electrophoresis
Method Transfer/Validation
Biologics Characterization
Monoclonal Antibodies
Protein Therapeutics
Technical Reporting

Formation

BS in Biochemistry/ Biotechnology
MS in related field

Outils

HPLC/UPLC
Capillary Electrophoresis

Description du poste

Real Staffing Group in the United States is seeking an Analytical Scientist to provide analytical support for upstream and downstream manufacturing labs, performing in-process sample testing in a non-GMP environment and reporting data accurately.

You will execute and troubleshoot ELISA, qPCR, potency assays, and support assay transfers, development, and implementation of new methods, using HPLC/UPLC and capillary electrophoresis for biologics characterization.

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