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Senior Director, Technical Operations - Biologics

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-17
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 245987 - 303866 USD Yearly USD 245987.00 303866.00 YEAR
Job Description & How to Apply Below

Responsibilities

  • Develop and execute the global CMC and manufacturing strategy for AKB-097; align technical development with regulatory and program objectives.
  • Serve as CMC executive lead on the AKB-097 program team and represent Technical Operations in cross‑functional decisions.
  • Establish external manufacturing and lifecycle management strategies for global commercialization.
  • Oversee drug substance/drug product process development (cell line development, process development, formulation development, manufacturing).
  • Oversee analytical method development, product characterization, and product comparability.
  • Ensure scale‑up, technology transfer, process validation, and commercial readiness.
  • Build and manage a network of CDMOs/strategic manufacturing partners; lead governance with external manufacturers.
  • Ensure reliable clinical and commercial supply via planning, risk mitigation, and partnership with Supply Chain.
  • Lead CMC regulatory strategy for INDs/BLAs and global filings; partner with Quality/Regulatory to ensure GMP compliance; support agency interactions/inspections.
  • Build and lead a high‑performing biologics technical development/operations organization; recruit, mentor, foster continuous improvement, and partner cross‑functionally.
Qualifications
  • MS or PhD in Biochemistry, Chemical Engineering, Biotechnology, Pharmaceutical Sciences, or related field.
  • 12+ years in biologics process development, product characterization, manufacturing, and technical operations.
  • Proven leadership advancing biologics from development through late‑stage trials and commercialization.
  • Experience with product comparability (BLA support), and establishing/managing global manufacturing networks.
  • Experience with monoclonal antibodies, recombinant proteins, or other complex biologics modalities.
  • Deep expertise in biologics CMC (cell culture/purification, analytical, formulation, scale‑up) and strong GMP/regulatory knowledge.
Compensation

Targeted base: $245,987–$303,866. Additional benefits mentioned: health care, vision, dental, retirement, PTO, equity, and bonus/incentive programs (as applicable).

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Position Requirements
10+ Years work experience
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