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Engineer, MS&T – Aseptic Drug Product

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-08-30
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Quality Engineering, Pharmaceutical Manufacturing, Regulatory Compliance Specialist
  • Engineering
    Validation Engineer, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 89600 - 166400 USD Yearly USD 89600.00 166400.00 YEAR
Job Description & How to Apply Below

Key Responsibilities:

  • Monitor and analyze process performance data to support continued process verification and product quality.
  • Lead technical investigations and provide scientific expertise to resolve manufacturing process challenges.
  • Trend critical quality attributes and process parameters to identify risks and drive improvements.
  • Support technology transfer activities for new products and processes into commercial manufacturing.
  • Identify and implement continuous improvement opportunities that enhance operational performance.
  • Partner with Quality teams to maintain a compliant and inspection-ready manufacturing environment.
  • Collaborate with Manufacturing to troubleshoot production issues and ensure reliable product supply.
  • Support process changes and improvements with cross-functional Engineering, Validation, and Operations teams.
  • Contribute to the startup and implementation of new equipment, software, and manufacturing processes.
  • Provide technical support for strategic projects, remediation initiatives, and process optimization efforts.
Essential Requirements:
  • Bachelor’s in Biochemistry, Chemical Engineering, Bioengineering, or related field with 4+ years biopharmaceutical GMP manufacturing (including aseptic fill-finish); or 3+ years direct Novartis Gene Therapies experience with aseptic fill-finish; or Master’s with 2+ years relevant aseptic fill-finish or engineering experience.
  • Knowledge of GMP requirements, pharmaceutical manufacturing regulations, and validation/qualification principles.
  • Experience supporting aseptic drug product manufacturing, MS&T, process engineering, or related technical operations.
  • Strong technical writing skills for accurate, compliant documentation.
  • Proven ability to collaborate across cross-functional teams and communicate with diverse stakeholders.
  • Ability to travel up to 10%.
Benefits (explicitly stated):
  • Salary expected range: $89,600–$166,400 annually; performance-based cash incentive; eligibility for annual equity awards (depending on level).
  • US-based comprehensive benefits (health, life/disability), 401(k) match, time off (vacation, personal days, holidays, other leaves).

Onsite in Durham, NC; no relocation support—apply only if location is accessible.

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