Sr. Process Engineer

Syner-G BioPharma Group

Wilmington, United States
Base: market competitive base salary; bonus/equity...
On-site
Oral solid dose manufacturing processes
Technology transfer support
Process validation and ppq activities
Syner-G enables its people to build careers that positively impact their quality of life through expertise, consulting, and management skills accelerating breakthrough science and life-enhancing therapies

Job Summary

  • Syner-G enables its people to build careers that positively impact their quality of life through expertise, consulting, and management skills accelerating breakthrough science and life-enhancing therapies.
  • The Senior Process Engineer will lead process optimization, support technology transfer, troubleshoot complex issues, and provide technical leadership during PPQ and process verification activities in oral solid dose manufacturing.
  • Employees enjoy a total rewards program including competitive salary, benefits, flexible paid time off, company-paid holidays, flexible working hours, and fully remote work options for most positions.

Matching Summary

Syner-G enables its people to build careers that positively impact their quality of life through expertise, consulting, and management skills accelerating breakthrough science and life-enhancing therapies.

Salary

Base: Market competitive base salary; Bonus/Equity: Annual incentive plan; Benefits: Robust benefit offerings, flexible paid time off, company-paid holidays

Skills & Requirements

Must-have

  • Oral solid dose manufacturing processes
  • Technology transfer support
  • Process validation and PPQ activities
  • Troubleshooting process deviations
  • Collaboration in GMP environments
  • Process documentation and data analysis
  • Mentoring junior engineers

Nice-to-have

  • Strong communication skills
  • Continuous improvement initiatives
  • Ability to manage multiple priorities
  • Support commissioning and qualification
  • Cross-functional technical leadership

Key Requirements

  • 8+ years oral solid dose manufacturing experience
  • BS or MS in Chemical, Mechanical, or Pharmaceutical Engineering
  • Hands-on experience with tablet presses and granulators
  • Experience supporting tech transfer and commercial operations
  • Involvement in PPQ and continued process verification
  • Knowledge of GMP requirements and pharmaceutical regulations
  • No visa sponsorship available

Work Rights

Not specified

Tailored Resume

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