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Artech Information System LLC Verified 53m ago

Associate Process Engineer/Scientist

New Brunswick, NJ On-site

Salary not listed
PaySalary not listed
TypeContract
Work settingOn-site
Verified listing

JobFig found this opening at its original source and checks that it remains available.

About the role

Title: Associate Process Engineer/Scientist Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology The Process Engineer/Scientist conducts product and process characterization studies; collaborates with research and development in drug product process development of sterile parenteral and biologics drug product and works with manufacturing sites to characterize, troubleshoot or optimize processes for lifecycle products. This position is accountable for the design and execution of process characterization to ensure design and transfer of robust manufacturing processes for new products and key life cycle management products, development of new technology for optimization and continuous improvement in manufacturing operations, and providing specialized expertise as necessary to complement site capabilities for critical investigations or process improvements.

What you'll bring

  • Bachelor’s degree in relevant science or engineering discipline (chemistry, pharmaceutical sciences, pharmacy, biology, chemical engineering).
  • Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and process development and commercialization in a global environment.
  • Key Skills and Experience
  • Hands-on experience in the laboratory and in-depth understanding in sterile and liquid products, particularly biologics, formulation development, analytical methods, commercial manufacturing, and their unit operations.
  • In-depth understanding of Quality by Design (QbD), Design of Experiments (DOE), multivariate analysis, PAT, critical process and material attributes and CQA's.
  • Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS).
  • Able to design and execute scientifically sound, hypothesis driven experiments
  • Skilled in writing and reviewing complex study plans and scientific reports.
  • Overall knowledge of parenteral technology: aseptic processing, sterilization, isolator processing, lyophilization, pre-filled syringe operations, etc.
  • Strong understanding of project management systems and tools
  • Master or advanced degree preferred.
  • Six Sigma Green/Black Belt certification desirable