What are the responsibilities and job description for the Onsite Project Manager- Co-ordinator position at Cyient?
Key Responsibilities
- Lead and deliver complex NPD programs involving robotics, electromechanical systems, embedded software, and cloud applications.
- Own project execution including schedule, budget, risk management, and issue resolution.
- Form and lead cross‑functional teams across engineering, quality, regulatory, manufacturing, and commercial functions.
- Apply Agile and DevOps best practices for software and system development.
- Oversee cloud‑based and connected digital solutions in a regulated medical device environment.
- Ensure compliance with design controls, QMS requirements, and medical device regulations.
- Support Design History Files (DHF) and Phase Review governance.
- Provide clear executive‑level reporting on project status, risks, and opportunities.
- Partner with Franchise and Commercial leadership to shape product pipeline and commercialization strategy.
- Facilitate design reviews, requirements reviews, vendor meetings, and cross‑functional forums.
- Drive the development lifecycle of orthopaedic products from concept to launch.
- Develop detailed project plans, schedules, and budgets, setting timelines for design, verification, and validation.
- Manage sustaining engineering activities, including improvements, enhancements, and design changes.
- Lead cost‑reduction initiatives while maintaining quality and safety standards.
- Monitor and manage RAID logs (risks, assumptions, issues, dependencies).
- Act as primary point of contact for stakeholders, ensuring regular communication and reporting.
- Coordinate onsite/offsite teams, allocate resources, and ensure timely task execution.
Key Requirements
- Education: Bachelor’s or Master’s degree in Biomedical, Mechanical, or related engineering field.
- Experience: 10 years overall, with at least 5 years leading diverse projects in the medical device industry (orthopaedics preferred).
- Certifications: Project Management certification (PMP, PRINCE2, or Agile PM).
- Technical Skills: Proficiency in MS Office, project management tools, and CAD/design documentation.
- Domain Knowledge: Strong understanding of medical device design controls (21 CFR 820.30).
- Soft Skills: Excellent communication, proactive problem‑solving, and ability to thrive in fast‑paced environments.
Qualifications
Required
- 10 years of program/project management experience.
- Proven leadership of large, cross‑functional programs in medical device/MedTech.
- Experience with robotics, electromechanical systems, SaMD, MDDS, IoT, or connected systems.
- Strong knowledge of FDA‑regulated product development.
- Bachelor’s degree in engineering or related discipline.