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

Nerdgigs

Rahway, New Jersey, US
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
Process optimization
Nerdgigs is seeking a Specialist in Process Engineering for their Oral Solid Dosage team at the FLEx Center in Rahway, New Jersey. The role involves leading clinical manufacturing processes, ensuring safety and quality, and drafting GMP documentation, requiring a background in Chemical Engineering or related fields with experience in GMP manufacturing

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.
  • The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

Nerdgigs is seeking a Specialist in Process Engineering for their Oral Solid Dosage team at the FLEx Center in Rahway, New Jersey. The role involves leading clinical manufacturing processes, ensuring safety and quality, and drafting GMP documentation, requiring a background in Chemical Engineering or related fields with experience in GMP manufacturing.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • GMP manufacturing facilities experience
  • Oral Solid Dosage processing
  • Process optimization
  • cGMP Guidelines
  • Pilot Plant Operations

Nice-to-have

  • Collaboration and innovation culture
  • Independent problem-solving willingness
  • Technical reports and presentations
  • Cross-functional partnerships

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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