Bioassay Scientist III: Cell Potency & ELISA Expert

Alcami Corporation

Wilmington (NC)

On-site

USD 90,000 - 120,000

Full time

14 days+
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Job summary

Alcami Corporation is seeking a Scientist III, Bioassay to drive pharmaceutical development and manufacturing testing. Expect routine and non-routine work, method development, and data analysis to support assay validation and product quality.

The role emphasizes cell-based potency assays, ELISA, real-time PCR, enzymatic assays, and related techniques, with on-site requirements and strong collaboration with teams and clients under cGMP guidelines.

Qualifications

  • Associate's degree and 16+ years of related experience.
  • Bachelor's degree and 6+ years of related experience.
  • Master's degree with 2+ years of related experience.
  • PhD with 0+ years of experience required.
  • 2+ years of experience in Pharmaceutical, CDMO, or cGMP preferred.

Responsibilities

  • Performs laboratory analysis of pharmaceutical and biopharmaceutical products utilizing analytical instrumentation and documents data as per Alcami SOPs.
  • Documents results in electronic laboratory notebook.
  • Performs cell-based potency assays, ELISA, real-time PCR and other biochemical testing methods.
  • Supports troubleshooting and problem solving for cell-based and biochemical tests.
  • Evaluates and interprets generated data and writes SOPs, test procedures and reports.
  • Maintains instrumentation knowledge and safe work practices; manages waste and supplies.
  • Interacts with team, management, and clients to discuss data and progress; complies with cGMP.

Skills

Cell-based Bioassays
ELISA
Real-time PCR
Enzymatic Activity Assays
Laboratory Documentation
cGMP
Data Analysis
Microsoft Office

Education

Associate's degree
Bachelor's degree
Master's degree
PhD
2+ years of related experience in Pharma/CDMO

Tools

SoftMax
Empower

Job description

Alcami Corporation is seeking a Scientist III, Bioassay to drive pharmaceutical development and manufacturing testing. Expect routine and non-routine work, method development, and data analysis to support assay validation and product quality.

The role emphasizes cell-based potency assays, ELISA, real-time PCR, enzymatic assays, and related techniques, with on-site requirements and strong collaboration with teams and clients under cGMP guidelines.

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