Scientific Manager, Biologics Analytical Development

Johnson & Johnson MedTech

Malvern, Pennsylvania, United States
On-site
Lead a team for rmcr supply
Manage global storage and distribution
Drive rmcr qualification and requalification
Johnson & Johnson MedTech is seeking a Scientific Manager for Biologics Analytical Development in Malvern, Pennsylvania. This role involves leading a team responsible for managing reference materials and critical reagents to support analytical testing for biologics, requiring strong managerial and technical skills in a GMP environment

Job Summary

  • Lead a team to efficiently deliver on supply of Reference Materials and Critical Reagents (RMCRs) without impact to analytical testing timelines.
  • Drive qualification and requalification schedules for RMCRs, and work with analytical labs to acquire the data necessary to prepare qualification and requalification documents and issue Certificate of Analysis.
  • Author SOPs, protocols, and specifications to support project needs and drive continuous improvement and shaping future strategies.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Scientific Manager for Biologics Analytical Development in Malvern, Pennsylvania. This role involves leading a team responsible for managing reference materials and critical reagents to support analytical testing for biologics, requiring strong managerial and technical skills in a GMP environment.

Skills & Requirements

Must-have

  • Lead a team for RMCR supply
  • Manage global storage and distribution
  • Drive RMCR qualification and requalification
  • Collaborate with analytical testing labs
  • Author SOPs, protocols, and specifications

Nice-to-have

  • Continuous improvement and strategy
  • Adapt to evolving organizational dynamics
  • Strong technical credibility

Key Requirements

  • Bachelor's degree in Chemistry, Biology, Biochemistry or related scientific field with 8+ years of relevant industrial experience
  • Prior managerial experience
  • Experience in a GMP environment
  • Experience with analytical methods and critical reagents
  • Strong matrix leadership skills
  • Strong technical writing experience

Work Rights

Not specified

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