Associate Director, Engineering- Small Molecule

microsatsystems.biz

Base: $129,000.00 - $203,100.00; bonus/equity: eli...
Hybrid
Small molecule portfolio leadership
Packaging system design and development
Cross-functional team leadership
The Associate Director will lead packaging development for new oral solid dosage and parenteral products in the small molecule portfolio, ensuring robust packaging designs and efficient processes

Job Summary

  • The Associate Director will lead packaging development for new oral solid dosage and parenteral products in the small molecule portfolio, ensuring robust packaging designs and efficient processes.
  • This role requires collaboration across CMC areas and accountability for packaging strategies that meet global network needs while driving risk understanding and reduction prior to product launch.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, and vacation, with a hybrid work model for office-based U.S. employees.

Matching Summary

The Associate Director will lead packaging development for new oral solid dosage and parenteral products in the small molecule portfolio, ensuring robust packaging designs and efficient processes.

Salary

Base: $129,000.00 - $203,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation

Skills & Requirements

Must-have

  • Small molecule portfolio leadership
  • Packaging system design and development
  • Cross-functional team leadership
  • Pharmaceutical development process knowledge
  • Regulatory compliance and quality standards
  • Project management in fast-paced environment

Nice-to-have

  • Medical device and combination product packaging
  • Quality Risk Management and Quality by Design
  • Standard work process definition
  • Packaging materials specification and characterization
  • Strong interpersonal and communication skills
  • Ability to influence senior leaders

Key Requirements

  • Bachelor’s degree with 10 years pharmaceutical experience or Master’s with 8 years
  • Experience with oral solid dosage forms (tablets, capsules)
  • Knowledge of US and global pharmaceutical regulations and standards
  • Project management experience
  • Ability to manage complex programs
  • US and Puerto Rico residency required

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter