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22 minutes ago
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Full time
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process validation regulatory cmc drug product

๐Ÿ“‹ Description

  • Lead drug product CMC strategy and execution for small molecule programs from early clinical
  • Direct phase-appropriate formulation and process development for oral solid dosage forms.
  • Provide technical leadership for technology transfers, process characterization, process
  • Select, onboard, and provide technical oversight of CDMOs and external partners.
  • Establish expectations, work plans, timelines, budgets, and performance measures for external
  • Provide technical oversight of GMP manufacturing campaigns.

๐ŸŽฏ Requirements

  • Advanced degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Pharmaceutics, or
  • Demonstrated success leading therapeutic product formulation and process development.
  • Strong technical expertise in formulation development, process development, scale-up, technology
  • Experience supporting drug product early-stage development through commercialization; commercial
  • Strong knowledge of drug product manufacturing, analytical testing, stability, specifications, and
  • Ability to interpret complex data and make technical and business decisions.

๐ŸŽ Benefits

  • Fully remote working environment from anywhere.
  • Full-time, exempt position with significant technical and strategic leadership responsibility.
  • Expected salary range of $200,000โ€“$260,000 USD, based on experience, qualifications, geographic
  • Potential discretionary annual bonus based on individual and organizational performance.
  • Opportunity to lead drug product strategy across full development lifecycle from early clinical
  • High-impact collaboration with CMC, Quality, Regulatory, Analytical Development, Clinical Supply
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