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

Imsapharma Com Ar

Rahway, New Jersey, USA
Base: $71,900.00 - $113,200.00; bonus/equity: elig...
Hybrid (3 days onsite, 1 day remote)
Gmp documentation drafting and execution
Process data analysis for improvement
Root cause analysis and problem-solving
The Associate Specialist, Process Engineering position at Imsapharma Com Ar in Rahway, New Jersey, focuses on leading clinical supply manufacturing in a GMP pilot facility. The role requires a strong technical background in process engineering, particularly in oral solid dosage forms, and emphasizes collaboration, innovation, and quality assurance

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 person will lead 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 $71,900.00 - $113,200.00, with eligibility for annual bonus and long-term incentive, plus a comprehensive benefits package.

Matching Summary

Match Score: 85

The Associate Specialist, Process Engineering position at Imsapharma Com Ar in Rahway, New Jersey, focuses on leading clinical supply manufacturing in a GMP pilot facility. The role requires a strong technical background in process engineering, particularly in oral solid dosage forms, and emphasizes collaboration, innovation, and quality assurance.

Salary

Base: $71,900.00 - $113,200.00; 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 documentation drafting and execution
  • Process data analysis for improvement
  • Root cause analysis and problem-solving
  • Technical writing capabilities
  • Independent problem-solving
  • On-the-floor batch manufacturing leadership

Nice-to-have

  • Foster collaboration, learning, and innovation
  • Build partnerships across work groups
  • Continuous improvement mindset
  • Influence cross-functional teams

Key Requirements

  • Bachelor of Science degree in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field
  • Experience visualizing and analyzing data with Excel or comparable tools
  • Experience with Commissioning, Qualification and Validation
  • Experience with unit operations for solid oral dosage form manufacturing

Work Rights

Not specified

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