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Senior​/Principal Scientist Cell Potency Assay

Job in Lexington, Middlesex County, Massachusetts, 02173, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-12
Job specializations:
  • Quality Assurance - QA/QC
  • Research/Development
Salary/Wage Range or Industry Benchmark: 150000 - 230000 USD Yearly USD 150000.00 230000.00 YEAR
Job Description & How to Apply Below

Join as a Senior/Principal Scientist, Cell Based-Potency Assay Development. Provide technical leadership for cell-based potency assay development, qualification, validation, transfer, and lifecycle management across biologics programs. Translate mechanism of action insights into phase-appropriate analytical methods supporting product characterization, process development, GMP release/stability, comparability, regulatory submissions, and analytical control strategy. Lead and troubleshoot potency assays and mammalian cell culture work; perform statistical analysis (relative potency, dose-response modeling, curve fitting, parallelism/similarity, reference standard comparison) and establish assay acceptance criteria.

Prepare/review technical documentation (reports, SOPs, protocols, CMC/regulatory sections). Coordinate with cross-functional and external stakeholders (Process Development, QC, Analytical Sciences, QA, Regulatory, CROs/labs) and independently resolve complex assay/cell culture/data/transfer issues. Provide training and mentoring; present results internally/externally as appropriate.

Qualifications (What you bring):

Ph.D. (3+ years for Senior/7+ for Principal), MS (9+/13+), or BS (11+/15+) in relevant fields. Advanced expertise in cell-based potency assays/functional bioassays and MOA-driven methods for biologics/vaccines/cell/gene therapy. Advanced statistical expertise for bioassays (4-parameter logistic/nonlinear dose-response, parallelism/similarity, reference standard comparison, system suitability, acceptance criteria). Strong mammalian cell culture expertise and proficiency with readouts (luminescence/fluorescence/absorbance, ELISA, MSD, flow cytometry, reporter/neutralization assays). Knowledge of assay qualification/validation and GMP, data integrity, ELN/LIMS, SOPs, and regulatory expectations.

Ability to lead complex work streams and communicate/present; experience with regulatory/transfer documentation and working with CROs/labs; ability to mentor and work independently.

Benefits:
  • Medical/dental/vision
  • 401(k) match
  • short-/long-term disability
  • basic life insurance
  • tuition reimbursement
  • paid volunteer time off
  • holidays
  • well-being benefits
  • up to 80 hours sick time and up to 120 hours paid vacation (new hires)
Position Requirements
10+ Years work experience
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