Associate Director, Engineering- Small Molecule

Merck & Co., Inc.

Base: $129,000.00 - $203,100.00; bonus/equity: eli...
Hybrid
Small molecule portfolio leadership
Pharmaceutical packaging development
Cross-functional team leadership
The Associate Director will be accountable for defining and executing packaging strategies that meet global network needs while ensuring technical rigor and regulatory compliance

Job Summary

  • The Associate Director will be accountable for defining and executing packaging strategies that meet global network needs while ensuring technical rigor and regulatory compliance.
  • This role offers a hybrid work model with three days on-site per week and includes a comprehensive benefits package with medical, dental, vision, retirement, and paid time off.
  • Merck & Co., Inc. is committed to inclusion and equal opportunity, encouraging diverse experiences and perspectives to drive breakthrough innovation.

Matching Summary

The Associate Director will be accountable for defining and executing packaging strategies that meet global network needs while ensuring technical rigor and regulatory compliance.

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
  • Pharmaceutical packaging development
  • Cross-functional team leadership
  • Risk assessment tools usage
  • Project management in fast-paced environment
  • Regulatory compliance knowledge
  • Packaging system design and qualification

Nice-to-have

  • Medical device and combination product packaging
  • Quality risk management and QbD
  • Standard work process definition
  • Packaging materials specification and characterization
  • Strong interpersonal and communication skills
  • Ability to influence senior leaders
  • Willingness to learn pharmaceutical product development

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
  • Ability to manage multiple complex projects
  • No relocation required
  • No visa sponsorship
  • 10% travel requirement

Work Rights

US and Puerto Rico residents only

Tailored Resume

Cover Letter