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Onsite Principal Engineer, Biologics Process Development

Job in Bedford, Middlesex County, Massachusetts, 01730, USA
Listing for: Sarepta Therapeutics
Full Time position
Listed on 2026-08-26
Job specializations:
  • Pharmaceutical
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 136000 - 170000 USD Yearly USD 136000.00 170000.00 YEAR
Job Description & How to Apply Below

Sarepta Therapeutics is seeking a Principal Engineer, Process Development on site in the United States. You will lead development and scale-up for AOC and AAV drug substances, overseeing technology transfer and external manufacturing to ensure GMP readiness and product quality.

The role requires deep expertise in complex biologics, analytical methods (HPLC), and cross-functional leadership to drive programs from development through late-stage production.

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