Marco Toro
Senior Director of Manufacturing at Jubilant Cadista Pharmaceuticals (a Jubilant Life Sciences Company)
- Role
- Senior Director of Manufacturing at Jubilant Cadista Pharmaceuticals
- Location
- Salisbury, MD, US
- LinkedIn followers
- 500 followers
About Marco Toro
A result oriented, “hands on” executive with more than 20 years in the pharmaceutical and medical device industry. Experience spans general management, manufacturing, packaging operations, with site management responsibility for all support activities (Equipment / Facilities Maintenance; Calibration, Documentation Configuration / Control; Engineering, Environmental, Health and Safety). A proven leader whose style encourages high engagement, trusted partnering, team building, drives accountability and alignment while creating an environment that supports innovation, risk taking, continuous improvement and learning. Excellent track record in identifying and developing talent among subordinates at all levels. Well versed in quality systems and committed to compliance. Experienced in the implementation of cross-functional teams and lean manufacturing programs. A skilled, data driven and process oriented problem solver, especially strong in the areas of new product introductions, rapid scale up, cost effective manufacturing and process improvements.Specialties: Solid Dose ManufacturingLiquid and Soft-Gel ManufacturingPackaging of Liquid and Solid Dose Tablet and CapsulesProductivity & Process ReengineeringEnvironmental, Health and SafetyExcellent Process TroubleshootingcGMP ManufacturingEngineering ManagementFacilities & Maintenence ManagementContinuous ImprovementsConstruction & Project ManagementPLC Programing & AutomationVendor Negotiations
Experience
Senior Director of Manufacturing
Jubilant Cadista Pharmaceuticals
Jan 2013 — Present
Education
Universidad Tecnológica de Pereira
Bachelor of Science, Electrical Engineering
Skills
- Change Control
- Six Sigma
- Gxp
- Quality Auditing
- Pharmaceutics
- Continuous Improvement
- Engineering Management
- Regulatory Requirements
- Glp
- 21 Cfr Part 11
- Validation
- Cgmp Manufacturing
- Process Improvement
- Contract Manufacturing
- Manufacturing Operations
- Design of Experiments
- Manufacturing
- Quality Assurance
- Computer System Validation
- Troubleshooting
- R&D
- Environmental Awareness
- Iso 13485
- Quality System
- V&V
- Process Simulation
- Dmaic
- Operational Excellence
- Quality Control
- Regulatory Affairs
- Gmp
- Lean Manufacturing
- Quality Management
- Spc
- Fda Gmp
- Process Engineering
- Iso
- Pharmaceutical Industry
- Sop
- Fda
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