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Job Summary:
The
Process Enginee r will support the design, optimization, and continuous improvement of manufacturing processes within a pharmaceutical production environment. This role ensures that processes meet quality, safety, and regulatory standards while maximizing efficiency and reliability. The ideal candidate will collaborate closely with cross-functional teams to troubleshoot issues, implement process improvements, and support technology transfer and scale-up activities.
Responsibilities: Develop, optimize, and validate manufacturing processes to ensure consistent product quality and compliance with cGMP standards. Lead process investigations and implement corrective and preventive actions (CAPAs). Support technology transfer, scale-up, and new product introduction activities. Analyze process data to identify trends and recommend process improvements. Collaborate with Quality, Validation, and Production teams to ensure smooth manufacturing operations. Author and review technical documentation, including SOPs, batch records, and process validation protocols. Ensure adherence to safety, environmental, and regulatory requirements.
Qualifications: Bachelors degree in Chemical Engineering, Pharmaceutical Engineering, or related field. Minimum of 3 years of experience in a pharmaceutical manufacturing environment. Strong understanding of cGMP, process validation, and regulatory compliance. Proficiency in process modeling, data analysis, and continuous improvement methodologies (e.g., Lean, Six Sigma) preferred.
Process Enginee r will support the design, optimization, and continuous improvement of manufacturing processes within a pharmaceutical production environment. This role ensures that processes meet quality, safety, and regulatory standards while maximizing efficiency and reliability. The ideal candidate will collaborate closely with cross-functional teams to troubleshoot issues, implement process improvements, and support technology transfer and scale-up activities.
Responsibilities: Develop, optimize, and validate manufacturing processes to ensure consistent product quality and compliance with cGMP standards. Lead process investigations and implement corrective and preventive actions (CAPAs). Support technology transfer, scale-up, and new product introduction activities. Analyze process data to identify trends and recommend process improvements. Collaborate with Quality, Validation, and Production teams to ensure smooth manufacturing operations. Author and review technical documentation, including SOPs, batch records, and process validation protocols. Ensure adherence to safety, environmental, and regulatory requirements.
Qualifications: Bachelors degree in Chemical Engineering, Pharmaceutical Engineering, or related field. Minimum of 3 years of experience in a pharmaceutical manufacturing environment. Strong understanding of cGMP, process validation, and regulatory compliance. Proficiency in process modeling, data analysis, and continuous improvement methodologies (e.g., Lean, Six Sigma) preferred.