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Scientist Biostatistics, CPV-MSAT

Job in Summit, Union County, New Jersey, 07902, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-18
Job specializations:
  • Pharmaceutical
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Shift Available:

Monday–Friday, Hybrid Day Shift, 8:00 a.m.–4:30 p.m.

Responsibilities:
  • Assist in maintaining the site SPC program and support manufacturing performance trending/reporting.
  • Support multivariate analysis (MVA) modeling to improve process understanding/robustness.
  • Collaborate cross-functionally; support investigations with relevant data/analysis.
  • Support CPV and APQR by completing assigned tasks accurately and on schedule.
  • Develop/maintain process monitoring analytics under senior guidance.
  • Investigate/proactively address drift in product performance.
  • Represent MSAT CPV team in cross-functional forums as needed; prepare/review CPV/APQR site documents.
  • Support safe, compliant cGMP operations and inspection readiness.
  • Interact with Operational Excellence, PMO, site MSAT, Quality, Process Support/Engineering, Manufacturing Ops, and Supply Chain.
  • Stay current via training/best-practice forums; support Opex opportunities via data-driven evaluations.
Knowledge & Skills (required/preferred):
  • Statistical methods/tools for data-driven decisions in manufacturing.
  • Proficiency in statistical software/languages (R, JMP, Minitab, SAS; JMP preferred).
  • Detail oriented; strong time management.
  • Verbal/written communication; cross-functional teamwork.
  • cGMP and biopharmaceutical/cell therapy regulatory knowledge.
  • Familiarity with clean room/facility operations and manufacturing workflows.
  • Plus: single-use/closed systems/cold chain-cryogenic;
    Operational Excellence/Lean.
Minimum Requirements:
  • Bachelor’s required (science/engineering preferred); graduate degree preferred.
  • 4+ years biopharmaceutical/related manufacturing support.
  • 1+ year direct CPV and/or APQR reporting exposure (or relevant quality monitoring/trending).
  • 1+ year cell therapy/biologics/vaccine manufacturing/support exposure.
Working Conditions:

Adhere to BMS policies/procedures; gown to access classified manufacturing areas as needed.

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