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Senthil Jayachandran is listed as Global Quality Leader in Healthcare | Pre-Market; Operations & Post-Market Quality Leadership | QMS | Supplier Quality | Acquisition Integration | MfgTransfer | Remediation | Audits at Medtronic, a with 10 employees, based in Minneapolis, Minnesota, United States. AeroLeads shows a work email signal at medtronic.com and a matched LinkedIn profile for Senthil Jayachandran.
Senthil Jayachandran previously worked as Sr Quality Director at Medtronic and Head of Compliance, QMS & Supplier Quality at Alcon. Senthil Jayachandran holds Master Of Business Administration - Mba from University Of Florida - Warrington College Of Business.
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AeroLeads found 2 current-domain work email signals for Senthil Jayachandran. Compare company email patterns before reaching out.
Email: Senthil.Jaya@icloud.com | Mobile: 904 629 9682I believe in adding my fingerprints on things I do, thereby, leaving a legacy. My leadership style is grounded on Gratitude; Commitment; Humility & People. I believe in keeping things simple and establish processes and tools to deliver consistent results, drive innovation and deliver improved outcomes. This with keeping People and their development at the core of everything I do. Successfully grown my career and delivered results in multiple organizations, cultures and in global setting. Managed & supported business growth from $600M to $900M+ in four years. Delivered operations stability, improved product quality & patient outcomes in a growing business and scaled manufacturing capabilities to enable business growth. Strong expertise in Lean and Six Sigma principles and practices, used in my roles across different organizations to deliver standard work, consistent results, and improved outcomes. Supported and delivered consistent audit outcomes with various regulatory agencies, including FDA, TUV, S.Korea FDA, Turkey HA and others. Experienced in 483 responses, warning letter remediation & inspections. Seasoned people leader with strong industry experience, grounded in values and people development
Listed skills include Fda, Quality System, Medical Devices, Design Of Experiments, and 9 others.
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A career timeline built from the work history available for this profile.
Minneapolis, Mn, Us
Responsible for Enterprise Field Corrective Action (FCA) and Product Hold Order (PHO) Process. Strategize, Plan, Communicate and Execute FCA activities globally in partnership with respective business units. Support and execute end-to-end PHO process.
Geneva, Switzerland, Ch
Manage and oversee Pharmacovigilance (PV) end-to-end process executed at turn-key vendor. Includes responses to Health Authorities across the globe, Safety Aggregate Reporting & Analytics, European Union Qualified Person Responsible For Pharmacovigilance (EU QPPV) oversight and Safety Monitoring. Global model with operations across the globe; also responsible for Vendor that manages Device Vigilance submission to global Health Authorities. Oversight includes Regulatory intelligence across the globe. Global operations in four strategic locations across the globe; Responsible for inspection oversight and audit responses. Drive strategic initiatives within the Vigilance and Pharmacovigilance process for improvements and effectiveness.
Minneapolis, Mn, Us
Perform remediation activities tied to Warning Letter and stabilize manufacturing for a combination bio-resorbable TYRX product family.
Minneapolis, Mn, Us
Leader of Operations Quality, and partner with operations team to support manufacturing. Lead and manage: Supplier Quality; Operations Quality Engineering; Calibration; Quality Control; Acquisition transfer and integration activities; Manufacturing transfers; Sterility Assurance. Overall 90+ in the organization; 54 exempts. Delegate for back-up management representative for Neurovascular Quality system
Minneapolis, Mn, Us
Managed Quality Operations and Quality Assurance functions. Provide guidance, support and directions to operations on improvement initiatives and quality issues at plant level. Direct oversight and control of all Quality Assurance processes, including product receipts, incoming inspection, in-process audits, sterile load build and subsequent release of finished goods to distribution center. Process owner for control of non-conforming product and process. Train and deploy First Time Quality (FTQ) principles and tools to reduce factory escapes.
Minneapolis, Mn, Us
Responsible for Complaints & MDRs for products manufactured at various facilities. Interact with business partners across the globe to drive consistency for complaint reporting and improving overall product quality. Represent at management reviews for Complaints, CAPAs and MDRs. Successfully supported and experienced with internal and external regulatory agency audits, including FDA and TUV. Assisted other manufacturing facilities during FDA inspection and helped with FDA 483 response plans. Drive product improvements through customer feedback. Utilize Lean tools to drive process improvements within complaint handling. Identify early product failures and support any corrections or corrective actions. Represent business unit at the corporate councils to drive process and complaint handling tool enhancements.Acted an interim manager for CAPA dept. from June 2013 to January 2014. Partner with other functional groups within the business to drive CAPA files to closure with robust root-cause analysis, implementation of corrective actions and verifying effectiveness. Manage the CAPA board meetings to ensure decisions are made with objective evidence and robust investigations.
Minneapolis, Mn, Us
Lead cross-functional project team on various projects. Supported new product development projects from, product feasibility to commercial launch and post launch monitoring. Experienced with process development activities, such as, process characterization, qualification & validation. Performed supplier selection and qualification of sourced raw materials and components. Skilled in collecting Voice of Customer (VOC) feedback, for new product development projects during cadaver lab to develop Design Inputs (DI).
Minneapolis, Mn, Us
Support New Product Development team through product feasibility to commercial launch and post launch monitoring. Coordinate with Manufacturing Engineer to develop a process, characterize, and qualify for production. Develop monitoring process for special processes.
Minneapolis, Mn, Us
Support operations in daily production and drive process improvements. Participate in Rapid Improvement Events (RIE) and improve process efficiencies. Assist with non-conformance and supplier issues. Coordinate/partner with R&D Engineer to improve current product feature’s and function.
Warsaw, Indiana, Us
Support production processes and disposition non-conforming products. Participate in new product development project. Drive process improvement, and perform supplier qualification.
Investigate product quality issues, determine root-cause and action plan. Drive process improvement, and monitoring.
Other employees you can reach at medtronic.com. View company contacts for 10 employees →
Marina R.
Colleague at MedtronicSan Diego County, California, United States
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Nguyen Anh Dung
Colleague at MedtronicVietnam, Viet Nam
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이승현
Colleague at MedtronicNorth Jeolla, South Korea, Korea, Republic Of
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Brock Johnson
Colleague at MedtronicAnchorage, Alaska, United States
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Rimmy Lim
Colleague at MedtronicPittsburg, California, United States
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Souraya Bouzari
Colleague at MedtronicNew Haven, Connecticut, United States
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Cabot Rogers
Colleague at MedtronicShreveport, Louisiana, United States
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Andrea Avalos Sandoval
Colleague at MedtronicShinagawa-Ku, Tokyo, Japan
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Diana Carolina Almanza Ochoa
Colleague at MedtronicColombia
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Stephen Hayden
Colleague at MedtronicPortland, Connecticut, United States
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Quick answers generated from the profile data available on this page.
Senthil Jayachandran works for Medtronic.
Senthil Jayachandran is listed as Global Quality Leader in Healthcare | Pre-Market; Operations & Post-Market Quality Leadership | QMS | Supplier Quality | Acquisition Integration | MfgTransfer | Remediation | Audits at Medtronic.
AeroLeads has found 2 work email signals at @medtronic.com for Senthil Jayachandran at Medtronic.
Senthil Jayachandran is based in Minneapolis, Minnesota, United States while working with Medtronic.
Senthil Jayachandran has worked for Medtronic, Alcon, Biomet Mircrofixation, and B.G Sulzle.
Senthil Jayachandran's colleagues at Medtronic include Marina R., Nguyen Anh Dung, 이승현, Brock Johnson, and Rimmy Lim.
You can use AeroLeads to view verified contact signals for Senthil Jayachandran at Medtronic, including work email, phone, and LinkedIn data when available.
Senthil Jayachandran holds Master Of Business Administration - Mba from University Of Florida - Warrington College Of Business.
Senthil Jayachandran is listed with skills including Fda, Quality System, Medical Devices, Design Of Experiments, Spc, Quality Assurance, Lean Manufacturing, and Capa.
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