Director, Quality Control

med-in.at

Rahway, New Jersey, USA
Base: $173,200.00 - $272,600.00; bonus/equity: ann...
Hybrid (3 days on-site, 1 day remote)
Biologic critical reagents strategy
Gmp/gxp compliance and data integrity
Large molecule product lifecycle management
The Director of Quality Control at med-in.at in Rahway, NJ is a senior leadership role focused on the strategy, sourcing, development, and management of critical biological reagents for large molecule products. The position requires extensive experience in biologics development, strong leadership capabilities, and a commitment to quality and regulatory compliance

Job Summary

  • The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality.
  • This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision, retirement, paid holidays, vacation, and sick days.

Matching Summary

Match Score: 85

The Director of Quality Control at med-in.at in Rahway, NJ is a senior leadership role focused on the strategy, sourcing, development, and management of critical biological reagents for large molecule products. The position requires extensive experience in biologics development, strong leadership capabilities, and a commitment to quality and regulatory compliance.

Salary

Base: $173,200.00 - $272,600.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Biologic Critical Reagents strategy
  • GMP/GxP compliance and data integrity
  • Large molecule product lifecycle management
  • Vendor selection and performance management
  • Global SOP harmonization and standardization

Nice-to-have

  • Talent development and succession planning
  • Continuous improvement of operations
  • Cross-functional collaboration and influence
  • Modernization and standardization champion

Key Requirements

  • 10+ years in large molecule development/analytical sciences
  • 4+ years in leadership roles
  • Bachelor's degree in relevant scientific field
  • Advanced degree preferred
  • Experience with LIMS and electronic documentation systems

Work Rights

Not specified

Tailored Resume

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