Oversee and optimize pharmaceutical manufacturing processes
Ensure process efficiency, robustness, and compliance with GMP and regulatory standards
Support production, technology transfer, and continuous improvement initiatives
Manage and optimize pharmaceutical manufacturing processes (drug substance and/or drug product)
Ensure compliance with GMP (Good Manufacturing Practices) and regulatory requirements (e.g., FDA, EMA, ICH)
Support process validation activities (IQ/OQ/PQ) and ongoing process verification (CPV)
Monitor process performance using data analysis and implement improvements
Collaborate with cross-functional teams including Manufacturing, Quality Assurance, Validation, and HSE

Bachelor’s or master’s degree in chemical engineering, Pharmaceutical Engineering, or related field
8+ years of experience in pharmaceutical manufacturing or process engineering
Strong knowledge of GMP and regulatory frameworks (FDA, EMA)
Experience with process validation and manufacturing support
Good understanding of data analysis and process monitoring tools
Strong problem-solving and organizational skills
Strong knowledge in automation applied to pharmaceutical process

Site Process Engineer

Key skills