Process Engineer (Engineering) (contract)

Sanofi

Date: 21 hours ago
City: Framingham, Massachusetts
Contract type: Contractor
Job Title: Process Engineer II

Contract Length: 12 Months

Work Schedule: Hybrid (On-site & Remote)

Location: [Specify if known, otherwise "Hybrid role – Location TBD"]

Program: Sanofi FLEXT Direct – Contingent Workforce Program

Job Summary

Sanofi’s contingent workforce program, FLEXT Direct, is seeking a Process Engineer II for a 12-month contract. This hybrid role requires expertise in pharmaceutical manufacturing with a focus on tablet, ointment, and liquid dosage forms. The candidate will support manufacturing and quality operations, lead troubleshooting efforts, and contribute to continuous improvement and validation initiatives.

Key Responsibilities

  • Provide technical support for manufacturing operations related to tablets, ointments, and liquids.
  • Serve as Subject Matter Expert (SME) for investigations, including root cause analysis and resolution strategies.
  • Troubleshoot and analyze process-related issues using strong analytical and engineering skills.
  • Participate in and lead cross-functional teams to support ongoing production and quality improvements.
  • Contribute to the development, execution, and documentation of development, engineering, investigational, and process validation studies.
  • Provide input on critical process parameters and control strategies.
  • Support the commercialization of robust and compliant processes and test methods.
  • Communicate effectively with internal stakeholders and external partners.
  • Utilize process control strategies and apply engineering principles to optimize manufacturing systems.
  • Knowledge of product serialization is preferred.


Qualifications

  • Bachelor’s or Advanced Degree in Chemical or Biochemical Engineering; an advanced science degree is also acceptable with relevant experience.
  • 4–8 years of experience in:
  • Large-scale process equipment design
  • Scale-up implementation
  • Process validation in pharmaceutical manufacturing
  • Strong understanding of cGMPs, process controls, and manufacturing technologies.
  • Demonstrated experience in technical documentation, validation protocols, and study interpretation.
  • Excellent communication and collaboration skills.


Pay Rate Range

Min Pay Rate Max Pay Rate Currency Unit 50 66 USD hourly

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