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Manager, Process Engineering

Organogenesis
Full-time
Remote friendly (Canton, MA)
United States
$128,000 - $160,000 USD yearly
Operations

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Role Summary

Manager, Process Engineering. Responsible for managing projects ranging from small equipment customization to large bio-process scale-up. Lead a team to design systems and execute experimental protocols, develop and execute validations, and communicate findings across functional departments. Travel up to 20% for vendor qualifications, design reviews, and factory acceptance testing; some off-hours and weekend work may be required to support startup and validation schedules.

Responsibilities

  • Manage complex cross-functional programs and coordinate with multiple stakeholders
  • Evaluate new manufacturing systems and process changes to improve yield, capacity, and reduce production costs
  • Build and lead a team to design systems and execute experimental protocols, collect and evaluate data, and summarize findings in written reports
  • Develop and execute validations
  • Communicate across functional departments and mentor/train engineering staff
  • Ensure adherence to timelines, budgets, and quality standards

Qualifications

  • Required: B.S. in Chemical Engineering, Biomedical Engineering, or related field
  • Required: 7–10 years of industry experience with 2–3 years of engineering team management
  • Required: Knowledge of aseptic processing methods and aseptic technique
  • Required: Understanding of industry process systems under GMP
  • Required: AutoCAD proficiency; Electromechanical system debugging
  • Required: Proficiency in MS Office (Word, Excel, PowerPoint)
  • Required: Ability to work in a cleanroom environment, fully gowned for up to 6 hours per day
  • Required: Strong planning, organizational, and communication skills; hands-on problem solving; ability to mentor and lead an engineering team
  • Preferred: Experience mentoring and leading cross-functional teams; strong cross-functional collaboration

Skills

  • Process development and scale-up
  • Project management and cross-functional leadership
  • Laboratory and manufacturing validation execution
  • Data collection, analysis, and reporting
  • Clear written and verbal communication

Education

  • B.S. in Chemical Engineering, Biomedical Engineering, or related field

Additional Requirements

  • Up to 20% travel required for vendor qualifications, design reviews, and factory acceptance testing
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