Education And/or Experience

BS Degree (engineering, science or pharmaceutical related discipline) with 8 -10 years of experience in medical device industry

Experience in the design and development of electromechanical devices is required.

Qualifications

- Demonstrated compliance knowledge in the areas of medical device and drug product development, change control, NCR CAPA, and risk management.
- Strong verbal and written communication skills
- Robust interpersonal/communication/influencing/negotiation skills required.
- Demonstrated leadership, teaming, and communication skills accomplishing success with large teams.
- Device regulation (design control) experience required
- Knowledge of FDA (21 CFR Part 210, 211, 820, 803, 806), ISO 13485, ISO 14971, IEC 60601, and standards for medical devices and therapeutics.
- Strong analytical and problems solving skills utilizing DMAIC tools, Six Sigma Engineering, ASQ or other certifications desirable.
- Proficient with Minitab or any equivalent statistical tool is required.
- Proficient in product and process change controls and risk management
- Apply DMAIC and statistical techniques to address issues and investigations
- Demonstrates ability to work independently

Essential Duties And Responsibilities

- Provides quality guidance and approval to product design and process change controls to ensure compliance to the required Product Development Process (PDP) deliverables, resulting in the development and sustaining of safe and effective medical devices




- Responsible for Quality Assurance of the Product Development and Lifecycle Management process.
- Supports product verification testing to ensure product reliability and conformance to specifications
- Organize and implement site support of corporate audits and Notified Body regulatory inspections. Act as front room lead for audits and inspections.
- Educates and trains on product body of knowledge and Vantive QMS principles
- Analyzes data from various sources (Non-Conformances, Field Corrective Actions, Medical Device Reports, and Complaints) to drive decisions
- Drive Quality culture mindset and provide input for code quality improvements.
- Identify and oversee specific process product improvement initiatives such as test case adequacy, requirement levelling and test automations.
- Reasonable Accommodation
- Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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📌 Principal Eng, Quality Assurance (Karnataka)
🏢 Foundit
📍 Karnataka