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Senior Specialist, Project Management - Chemistry Manufacturing & Controls; CMC - Hybrid

Job in Bethlehem, Northampton County, Pennsylvania, 18020, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-26
Job specializations:
  • Business
    Regulatory Compliance Specialist
Job Description & How to Apply Below
Position: Senior Specialist, Project Management - Chemistry Manufacturing & Controls (CMC) - Hybrid

Position Summary

CIPM Senior Specialist, Project Manager:
Lead project management efforts to support Chemistry Manufacturing & Controls (CMC) product development from First in Human to Transfer to Supply, driving line of sight across the development lifecycle.

Primary Responsibilities
  • Manage end-to-end development for moderate-complexity projects (or partner effectively on higher complexity efforts).
  • Guide creation, approval, and execution of integrated project plans appropriate to phase/complexity.
  • Build/maintain schedules and critical project information; integrate activities across functions; identify risks; ensure clear communication with stakeholders.
  • Leverage networks to improve team dynamics and remove obstacles.
  • Navigate corporate governance/process norms to enable informed decision-making.
  • Prepare for/facilitate key team meetings (agendas, participation, insights, and follow-through).
  • Participate in CIPM/GPAM initiatives to improve ways of working and cross-department interactions.
Required Qualifications
  • Bachelor’s degree required (scientific/applied preferred).
  • 3+ years project management (or related).
  • Experience planning/executing strategies for drug/vaccine registration and commercialization/lifecycle management.
  • Ability to work independently; be a resource to colleagues.
  • Strong interpersonal/collaboration skills.
  • Highly organized; strong problem-solving and alignment-building.
  • Excellent oral/written communication; know when/how to raise issues.
  • Ability to succeed in a dynamic environment.
Preferred Qualifications
  • Clinical drug development knowledge.
  • PMP certification and/or formal project management training.
Skills (Required)
  • Adaptability
  • Change Management
  • Clinical Supply Chain/Trial Management
  • Cross-Functional Leadership
  • Data Analysis
  • GMP
  • KPI
  • Risk Management
  • Supply Chain Systems
  • Technical Writing
Benefits (if applicable, as stated)
  • Annual bonus/long-term incentive (if applicable)
  • Comprehensive medical/dental/vision insurance
  • Retirement (401(k))
  • Paid holidays/vacation
  • Compassionate and sick days
Application

Apply via  (or Workday Jobs Hub). Final date to receive applications is listed on the posting.

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Position Requirements
10+ Years work experience
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