Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Vetamc

Rahway, New Jersey, USA
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid (3 days onsite, 1 day remote)
Gmp manufacturing facilities experience
Drug product processing knowledge
Oral solid dosage manufacturing
Vetamc is seeking a Specialist in Process Engineering for its Non-Sterile Process Engineering team, focusing on clinical manufacturing of oral solid dosage forms. The role requires hands-on leadership in batch manufacturing processes and a strong understanding of GMP documentation

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products, leveraging pharmaceutical unit operations.
  • This role will lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
  • The salary range for this role is $87,300.00 - $137,400.00, with eligibility for annual bonus and long-term incentive, plus a comprehensive benefits package.

Matching Summary

Match Score: 85

Vetamc is seeking a Specialist in Process Engineering for its Non-Sterile Process Engineering team, focusing on clinical manufacturing of oral solid dosage forms. The role requires hands-on leadership in batch manufacturing processes and a strong understanding of GMP documentation.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • GMP manufacturing facilities experience
  • Drug product processing knowledge
  • Oral Solid Dosage manufacturing
  • Process Engineering leadership
  • GMP documentation drafting and execution

Nice-to-have

  • Culture of collaboration and innovation
  • Flexibility across shifts
  • Independent problem-solving willingness

Key Requirements

  • Bachelor of Science with 2 years experience or Master's with 1 year experience
  • Experience in executing in GMP manufacturing
  • Experience leading quality investigations and change management

Work Rights

Not specified

Tailored Resume

Cover Letter