Principal Scientist, Technical Director - Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Merck Sharp & Dohme Corp

Rahway, New Jersey, USA
Base: $173,200.00 - $272,600.00; bonus/equity: eli...
Hybrid
Gmp drug product processing
Solid oral dosage forms
Process robustness & validation
The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for a Principal Scientist / Sr. Principal Scientist / Technical Director – Process Engineering to lead clinical supply manufacturing, scientific rigor of processes, and ultimately to enable flexibility and speed of our Company's pipeline

Job Summary

  • The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for a Principal Scientist / Sr. Principal Scientist / Technical Director – Process Engineering to lead clinical supply manufacturing, scientific rigor of processes, and ultimately to enable flexibility and speed of our Company's pipeline.
  • This individual will also be responsible for driving new technology strategy, scientific understanding and capability build within the organization.
  • The salary range for this role is $173,200.00 - $272,600.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Matching Summary

The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for a Principal Scientist / Sr. Principal Scientist / Technical Director – Process Engineering to lead clinical supply manufacturing, scientific rigor of processes, and ultimately to enable flexibility and speed of our Company's pipeline.

Salary

Base: $173,200.00 - $272,600.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • GMP drug product processing
  • solid oral dosage forms
  • process robustness & validation
  • root cause analysis
  • deviation management
  • cGMP, FDA, EMA regulatory requirements

Nice-to-have

  • driving new technology strategy
  • scientific understanding and capability build
  • creativity to the position
  • advancing science and technology development
  • business process innovations

Key Requirements

  • 14 years relevant experience with BS
  • 10 years relevant experience with MS
  • 8 years relevant experience with PhD
  • Extensive knowledge in GMP drug product processing
  • Subject matter expert in drug deliveries/manufacturing technologies
  • Experience supporting GMP audits and CAPAs

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter