Job Description

The successful candidate is responsible for designing, implementing, and optimizing manufacturing processes to improve efficiency and reduce costs. They will collaborate closely with cross-functional teams, train and support staff on new processes and equipment, and ensure compliance with safety policies and procedures.KEY RESPONSIBILITIESAssist in the planning, execution, and monitoring of capital and infrastructure projects, ensuring alignment with project goals, timelines, and budgets.Lead process and equipment validation ensuring regulatory compliance and consistent high-quality products.Monitor production data and Key Performance Indicators (KPIs) to highlight trends and opportunities for improvements.Ensure that all manufacturing processes and equipment meet the required standards and specifications through rigorous testing and validation.Follow IQ, OQ, PQ methodologies when applicable.Develop and manage qualification documentation for new equipment, processes, and systems, ensuring accuracy and completeness.Track the status of qualification activities and provide regular updates to stakeholders on progress and issues.Conduct assessments of packaging materials and processes to ensure they meet quality, safety, and compliance standards.Provide recommendations for packaging improvements and partner with suppliers and internal teams to implement changes.Identify and implement strategies and methodologies (Lean, Six Sigma) for continuous improvements, efficiency gains, and waste reduction including tracing performance of implemented changes.QUALIFICATIONSBachelors degree in mechanical or electrical engineering5+ years engineering experience working in a manufacturing company; pharmaceutical experience preferred.Certification in Lean Six Sigma or other process improvement methodologies would be considered an asset.Strong critical thinking and problem-solving skills to identify and implement improvements in production processesAbility to manage multiple projects and prioritize tasks effectivelyKeen attention to detail with strong documentation and organizational skillsExcellent communication and presentation skillsCompetent with MS Office and AutoCADFamiliarity with GMP (Good Manufacturing Practices) and other relevant regulatory standards in the pharmaceutical industry.Proven experience in managing projects from conception through completion, including budgeting and timeline management.Experience with manufacturing software and systems, such as ERP (Enterprise Resource Planning) systems.

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