Katalyst CRO
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Manufacturing Engineer
role at
Katalyst CRO .
Responsibilities
Manufacturing Engineer, GMP, FDA, KPI, ISO Standards, Six Sigma, Lean Methodology, Risk management, Validation processes, Manufacturing Automation.
Lead manufacturing programs to drive process improvements, cost reductions, and quality enhancements.
Collaborate with R&D, Quality, Supply Chain, and Manufacturing teams to ensure seamless transition from product development to manufacturing.
Develop comprehensive project plans, timelines, and budgets to meet business objectives.
Identify risks and develop mitigation strategies to avoid delays and ensure compliance with regulatory standards.
Monitor KPIs and generate reports to stakeholders.
Ensure manufacturing processes adhere to Good Manufacturing Practices (GMP) and ISO standards.
Drive continuous improvement initiatives within manufacturing operations.
Facilitate communication and collaboration across departments to align project goals and milestones.
Support validation, qualifications, and regulatory submissions related to manufacturing processes.
Experience in leading manufacturing Automation programs.
Exposure to AI/Gen AI technologies and implementation in the manufacturing site.
Requirements
Strong knowledge of GMP, FDA, ISO standards, and regulatory requirements.
Demonstrated project management expertise, preferably PMP or equivalent certification.
Excellent leadership, communication, and interpersonal skills.
Ability to manage multiple projects in a fast-paced, dynamic environment.
Proficiency with manufacturing/ERP software and MS Office Suite.
Experience in the Medtech Industry. Cardiovascular device manufacturing experience preferred.
Six Sigma, Lean Methodology, or other continuous improvement certifications.
Knowledge of risk management and validation processes.
Experience in leading manufacturing Automation programs.
Seniority level
Associate
Employment type
Contract
Industries
Pharmaceutical Manufacturing
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Manufacturing Engineer
role at
Katalyst CRO .
Responsibilities
Manufacturing Engineer, GMP, FDA, KPI, ISO Standards, Six Sigma, Lean Methodology, Risk management, Validation processes, Manufacturing Automation.
Lead manufacturing programs to drive process improvements, cost reductions, and quality enhancements.
Collaborate with R&D, Quality, Supply Chain, and Manufacturing teams to ensure seamless transition from product development to manufacturing.
Develop comprehensive project plans, timelines, and budgets to meet business objectives.
Identify risks and develop mitigation strategies to avoid delays and ensure compliance with regulatory standards.
Monitor KPIs and generate reports to stakeholders.
Ensure manufacturing processes adhere to Good Manufacturing Practices (GMP) and ISO standards.
Drive continuous improvement initiatives within manufacturing operations.
Facilitate communication and collaboration across departments to align project goals and milestones.
Support validation, qualifications, and regulatory submissions related to manufacturing processes.
Experience in leading manufacturing Automation programs.
Exposure to AI/Gen AI technologies and implementation in the manufacturing site.
Requirements
Strong knowledge of GMP, FDA, ISO standards, and regulatory requirements.
Demonstrated project management expertise, preferably PMP or equivalent certification.
Excellent leadership, communication, and interpersonal skills.
Ability to manage multiple projects in a fast-paced, dynamic environment.
Proficiency with manufacturing/ERP software and MS Office Suite.
Experience in the Medtech Industry. Cardiovascular device manufacturing experience preferred.
Six Sigma, Lean Methodology, or other continuous improvement certifications.
Knowledge of risk management and validation processes.
Experience in leading manufacturing Automation programs.
Seniority level
Associate
Employment type
Contract
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr