Vandana Arestad

Background

About Vandana Arestad

I am a Versatile Director who delivers high impact strategies, product realization, process optimization within the medical device and pharmaceutical market sectors. My strengths… Skilled in navigating strategic roadmaps, implementing Lean methodologies – continuously improving efficiencies in rapid-growth GMP environments. A collaborative team builder and mentor successful in leading cross-functional groups and evaluating complex quality analytics – consistently surpassing key performance metrics. Efficient site management leader – ensuring full compliance with 21 CFR Part 820, ISO 13485 and ISO 14971 requirements through third-party audits for Class I and Class II medical devices. Strong abilities in negotiating critical programs with C-level management, thought leaders and multiple departments – while delivering enterprise solutions within time and budget. Specialties include: Organizational Improvements | Operational Streamlining | Turn-around Strategy | Platform Redesign | Strategic Planning | Operational Excellence | Multisite Operations | Continuous Improvement | Regulatory Affairs | Process Optimization | Resource Allocation | Relationship Building | Policies and Procedures | Stakeholder Buy-In | Lean Methodology | Class I and II Medical Devices | Validation Processes | Data Analytics | Executive Reporting | Comprehensive Audits | Market Knowledge | Research and Development