Please strictly adhere to the following resume naming convention:
Must Have TechnicalFunctional Skills
Experience managing medical-device market expansion projects, including entry of existing products
into new countries or regions and coordination of registration and launch readiness.
Proficiency in project charters, scope definition, work breakdown structures, integrated schedules,
critical-path analysis, resource planning, budget tracking, and governance reporting.
Working knowledge of ISO 13485, ISO 14971, FDA Quality Management System Regulation (QMSR
21 CFR Part 820), EU MDR, and country-specific registration requirements relevant to the target markets.
Ability to coordinate Regulatory Affairs, Quality Assurance, R&D, Clinical Affairs, Medical Affairs,
Manufacturing, Supply Chain, and regional commercial teams, with clear deliverable ownership.
Understanding technical documentation and design and development records, including DHF
documentation where used, risk management, verification and validation evidence, labeling, instructions for
use, and packaging documentation.
Understanding post-market surveillance and PMCF activities, and SSCP preparation
Experience managing risks, assumptions, issues, dependencies, change control, document review
cycles, and submission-readiness across multiple products and markets.
Proficiency in project scheduling and reporting tools such as Microsoft Project, Excel, PowerPoint
Desirable: Experience with orthopedic implants, surgical instruments, or other regulated medical-device portfolios. Exposure to regional regulatory submissions, notified-body review coordination Familiarity with UDI and device registration, labelling localization, and product lifecycle management systems. Familiarity with PLM system such as Wndchill.
Roles & Responsibilities
Lead end-to-end planning and execution of medical-device market expansion projects, from project initiation
and market-specific gap assessment through registration, launch readiness.
Develop and maintain an integrated project plan covering regulatory strategy and submissions, technical
documentation, clinical evidence, labeling and localization, manufacturing and supply readiness, and
commercial launch dependencies.
Coordinate market-specific documentation gap assessments with Regulatory Affairs, Quality, R&D, Clinical
Affairs, and Medical Affairs
Manage schedules, resources, budget forecasts, and critical-path dependencies maintain risks, assumptions,
issues, and dependencies logs and escalate constraints with mitigation options.
Facilitate cross-functional working meetings and governance reviews communication status, decisions,
actions
Generic Managerial Skills, If any
Strong cross-functional leadership and ability to influence stakeholders in an organization
Strong written and verbal communication skills, with the ability to provide clear, concise updates to senior leadership,
facilitate meetings, and accurately document key decisions.
Ability to negotiate with stakeholders to secure the required resources and adjust project plans when deadlines change.
Ability to solve problems systematically, make decisions based on risk, escalate issues promptly, and resolve conflicts
Ability to coordinate geographically distributed teams and maintain accountability for agreed actions and deliverables.
Key Words to search in Resume
Medical Device Project Manager Market Expansion Market Entry Product Registration Launch Readiness Regulatory Affairs Coordination EU
MDR FDA QMSR ISO 13485 Technical Documentation DHF PMP
Keyword:
Skills: EIS : Medical Device & RegulationsProject Management
Experience Required: 6-8
