Biotech Change Control Project Lead

BioPharma Consulting JAD Group

Boston, Northern (MA, KY)

Hybrid

USD 120,000 - 150,000

Full time

13 days ago
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Job summary

BioPharma Consulting JAD Group is seeking a Change Control Project Manager to support cross-functional teams executing change controls for cell and gene therapy programs. You will track scope, timeline, and milestones, escalating risks and coordinating with leadership to ensure on-time delivery.

The role requires a strong background in biopharma project management, GMP knowledge, and experience with regulatory pathways.

Qualifications

  • Bachelor’s degree in engineering, life sciences or related field.
  • 8+ years of biopharmaceutical industry experience.
  • 6+ years in project management of biopharmaceutical products.
  • Working knowledge of GMPs, regulatory environments and drug development lifecycle.
  • Ability to lead cross-functional teams in a matrixed environment.
  • Strong communication and presentation skills; proficient with MS Office and PM tools.

Responsibilities

  • Partner with functional area leads to maintain and monitor integrated project plans.
  • Track milestones and drive completion of changes with project team members.
  • Communicate status, risks, and mitigation plans to stakeholders.
  • Organize team communications including meeting agendas, notes, tasks, and risk analyses.
  • Update project status tools and risk registers; create templates for team use.
  • Develop and deliver project management tools and SOP-aligned processes.

Skills

Cross-functional collaboration
Communication
Analytical thinking
Regulatory knowledge
Risk management

Education

Bachelor's degree in engineering or life sciences

Tools

Microsoft Project
PowerPoint
SharePoint
Word
Excel
Outlook
Smartsheet
Power BI

Job description

BioPharma Consulting JAD Group is seeking a Change Control Project Manager to support cross-functional teams executing change controls for cell and gene therapy programs. You will track scope, timeline, and milestones, escalating risks and coordinating with leadership to ensure on-time delivery.

The role requires a strong background in biopharma project management, GMP knowledge, and experience with regulatory pathways.

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