DESCRIPTION:

• Support qualification of sterile ophthalmic product in a new container closure system and multiple commercial-driven projects from feasibility to implementation.
• Lead process improvement initiatives (yield, quality, throughput, cost reduction).
• Analyze process data using statistical methods; develop action plans to increase robustness and prevent product loss.
• Provide technical support for shop floor issues and lead structured investigations of deviations.
• Prepare technical justifications, reports, and regulatory documentation.
• Manage small projects or sub-projects, including coordination, reporting, and communication.
• Support process validation, technology transfers, and introduction of new processes/materials.
• Maintain compliant process documentation and support audits/inspections.
• Actively support EHS compliance.

QUALIFICATIONS:

• BS/MS in Chemistry or Engineering (Chemical, Mechanical, Biochemical).
• 5–7 years’ experience in Process/Manufacturing/Project Engineering.
• Strong background in sterile/aseptic pharmaceutical processes (ophthalmic experience preferred).
• Hands-on experience with process validation, design control, and technology transfers.
• Strong data analysis and problem-solving skills (Six Sigma a plus).
• Knowledge of sterile GMP, IND/BLA submissions, and regulatory compliance.
• Excellent communication skills in English.
  Job Type: Contract
  Pay: $65.00 per hour

Benefits:

• Health insurance

Work Location: In perso

Please refer the Job description for details