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

med-in.at

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
Oral solid dosage processing
Lead batch manufacturing
The position is for a Specialist in Process Engineering focusing on Oral Solid Dosage at med-in.at in Rahway, New Jersey. The role involves leading clinical supply manufacturing, ensuring compliance with GMP standards, and collaborating across teams to facilitate drug product development

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

The position is for a Specialist in Process Engineering focusing on Oral Solid Dosage at med-in.at in Rahway, New Jersey. The role involves leading clinical supply manufacturing, ensuring compliance with GMP standards, and collaborating across teams to facilitate drug product development.

Salary

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

Skills & Requirements

Must-have

  • GMP manufacturing facilities experience
  • Oral Solid Dosage processing
  • Lead batch manufacturing
  • Draft and execute GMP documentation
  • Quality investigations and change management

Nice-to-have

  • Foster collaboration, learning, and innovation
  • Build partnerships across work groups
  • Scientific rigor of processes
  • Flexibility and speed of pipeline

Key Requirements

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

Work Rights

Not specified

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