Position Summary:
Join our team as a Process Engineer I! You will play a key support role in the cGMP manufacture of active pharmaceutical ingredients (APIs). Working closely with project teams, you’ll help translate cutting-edge chemical processes into successful manufacturing operations. Projects span small-scale development, technology transfer, pilot-scale production, validation, and commercial manufacturing support.
Key Accountabilities & Responsibilities:

• Perform scaling calculations for unit operations and assist with conceptual process design.
  

• Participate in process reviews to ensure operability, safety, and quality requirements are met.
  

• Provide support to both external clients and internal stakeholders.
  

• Support production campaigns through in-person observation and analysis.
  

• Analyze production and laboratory data for process understanding and troubleshooting.
  

• Assist with quality investigations and implement corrective and preventive actions (CAPA).
  

• Support process improvement initiatives focused on reducing cycle time, increasing yield, and enhancing quality.
  

• Draft critical manufacturing documents such as process flow diagrams, batch records, validation protocols, standard operating procedures, quality investigations, and campaign reports.

Requirements:

• B.S. degree in Chemical Engineering or a related field.
  

• Experience in a chemical manufacturing environment, especially pharmaceutical, is preferred.

What We Offer:

• Competitive per diem rates.
  

• 8-month contract, with the possibility for extension or future opportunities.
  

• Valuable hands-on experience in pharmaceutical process engineering.
  

• Mentorship and guidance from experienced engineers and scientists.
  

• Exposure to a range of projects from development to commercial manufacturing.

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