Intern, R&D & PMO - CR
Position Overview
Support MVCR R&D organization in the development of medical device products with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements.Support MVCR Project Management Office (PMO) organization, which requires exceptional project management skills and a deep understanding of the management and execution to ensure successful project delivery across the organization. Job duties:
- Develop new product concepts and products.
- Provide engineering design and process development.
- Partially self-directed and capable of meeting project goals with supervision.
- Foster a culture of collaboration, accountability, knowledge sharing, and continuous improvement across the organization.
- Oversee the planning, execution, and monitoring of projects, ensuring adherence to timelines, budget, and quality standards.
- Manage project risks, issues, and dependencies, implementing proactive measures to mitigate potential obstacles.
- Establish project management best practices, tools, and methodologies to enhance project outcomes and efficiency.
- Conduct regular reviews of projects to identify risks, issues, and dependencies, and implement mitigation strategies.
- Collaborate closely with cross-functional teams, including R&D, regulatory affairs, manufacturing, quality assurance, and marketing, to drive project success.
- Facilitate effective communication and collaboration between internal and external stakeholders, ensuring alignment and shared objectives.
- Provide regular updates on project status, milestones, and risks to senior leadership and key stakeholders.
- Stay current with industry trends, regulations, and best practices in medical device project management, and apply them to improve project delivery.
- Implement project performance metrics and dashboards to track progress, identify areas for improvement, and report on key performance indicators.
- Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
- Perform additional duties as assigned.
- Advanced student of careers in Engineering or Scientific field.
- Strong written and verbal communication skills.
- Proficient English Language skills (writing, reading, listening, and speaking; 80%).
- Proficient computer skills including MS Word, Excel, Outlook, Teams, and CAD (SolidWorks or PRO/E proficiency required).
- Ability to learn about design and development of medical devices.
- Ability to read and prepare technical documentation.
- Knowledge of standard machine shop equipment and processes, and ability to learn of medical device manufacturing equipment and processes.
- Ability to learn about medical and technical development.
- Ability to acquire strong knowledge of medical device development processes, regulatory requirements, and quality management systems.
- Excellent analytical skills to produce accurate data and solution proposal.
- Use of computer assisted engineering, design software, and equipment to perform engineering and design tasks.
- Computer software and coding skills.