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