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Engineer III, Manufacturing Sciences - Purification

Job in Wilmington, New Hanover County, North Carolina, 28412, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-18
Job specializations:
  • Engineering
    Quality Engineering, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 79000 USD Yearly USD 79000.00 YEAR
Job Description & How to Apply Below

What You’ll Do

  • Serve as the downstream/purification technical lead for manufacturing issues during clinical, PPQ, and commercial processing, including impact assessments, investigations, and CAPA activities
  • Plan, execute, analyze, and communicate purification laboratory studies supporting tech transfers, process validation, investigations, and new capabilities
  • Perform data trending and statistical analysis for ongoing manufacturing campaigns using tools such as Tableau, Power BI, Statistica, or SIMCA
  • Observe and support critical downstream/purification manufacturing operations during tech transfers, PPQs, and investigations
  • Author and review technical protocols, reports, impact assessments, and GMP documentation
  • Drive continuous improvement initiatives and technical enhancement projects
  • Lead or support cross-functional sub-teams, escalating risks and roadblocks as needed
Who You Are

Self-driven engineer with strong technical judgment; comfortable working across manufacturing, laboratory, and quality environments; enjoys solving complex problems with data and collaborating cross-functionally.

Required Skills
  • Bachelor’s degree in relevant scientific or technical fields
  • At least 2 years of directly relevant industry or industry-adjacent experience
  • Protein purification experience (chromatography, filtration, and/or centrifugation)
  • Demonstrated self-motivation and ability to work independently
  • Ability to analyze complex data and identify process improvement opportunities
Preferred Skills
  • Experience designing, executing, and interpreting laboratory studies
  • Managing and influencing primary stakeholders
  • Experience supporting regulatory inspections
  • Experience working in a cGMP or regulated manufacturing environment
Benefits (if offered)
  • Base compensation range: $79,000.00–$
  • Medical, Dental, Vision, & Life insurances
  • Fitness & wellness programs
  • Disability insurance
  • Paid vacation and holidays
  • Sick time
  • Paid maternity/parental leave
  • 401(k) with match
  • Employee stock purchase plan
  • Tuition reimbursement up to $10,000/year
  • Employee Resource Groups participation
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