Manufacturing Process Engineer

Thermo Fisher Scientific seeks a Manufacturing Process Engineer to develop and optimize dosage form manufacturing processes for therapeutic and diagnostic products. The role involves process validation, technology transfer, scale-up activities, and cross-functional collaboration to ensure robust, compliant production.

Responsibilities

• Lead development and implementation of manufacturing processes for solids, liquids, and semi-solid dosage forms
• Manage process scale-up, validation, and technology transfer activities across internal and external teams
• Serve as primary technical representative on client projects and conduct technical discussions with stakeholders
• Create and validate scientific methodologies using experimental design for clinical, scale-up, and registration batches
• Investigate technical challenges, implement problem-solving activities, and document manufacturing processes

Requirements

• Bachelor's degree in chemical engineering, chemistry, pharmacy, or related science field
• 1–3 years of manufacturing or process development experience; advanced degree acceptable with no prior experience
• Strong knowledge of cGMP requirements and regulatory compliance
• Experience with process validation, technology transfer, and scale-up activities
• Project management experience with minimum 1 year in related activities
• Proficiency with Microsoft Office and manufacturing/quality systems software
• Risk assessment and root cause analysis capabilities