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Skills

Research and Development
Project Implementation
Regulatory Compliance
Production Engineering
Workflow
Manufacturing
Medical Devices
ISO 13485
Quality Management
ISO 9000
Risk Management
IQ
OQ
PQ
Documentation
Technical Writing
Collaboration
Management
Offshoring
Project Management
Preventive Maintenance
Performance Management
Profit And Loss

Summary

Summary:
We are seeking a highly skilled R&D/Validation Engineer with mandatory experience in the Medical Devices domain. The ideal candidate will be responsible for planning, leading, and coordinating project execution and validation activities in strict alignment
with ISO 13485 and ISO 14971 standards. This role requires a hands-on leader who can manage equipment, process, and product transfers while liaising with global teams and customers to ensure on-time delivery.

Roles & Responsibilities:

Project Leadership: Plan, lead, and coordinate project execution and validation activities, ensuring compliance with regulatory standards (ISO 13485, ISO 14971).
Validation Execution: Support and execute validation planning and protocols for equipment, process, and product transfers, specifically managing IQ (Installation Qualification), OQ (Operational Qualification),and PQ (Performance Qualification).
Documentation & Compliance: Author, review, and approve validation documentation, ensuring traceability and adherence to quality system regulations.
Cross-Functional Collaboration: Collaborate effectively with cross-functional teams (Quality, Production, Engineering) to resolve technical issues and streamline project workflows.
Stakeholder Coordination: Act as the primary point of contact, coordinating with customers, manufacturing plants, and off-shore teams to ensure project continuity and timely delivery.Strategic Contribution: Contribute as a Project Manager (PM) or Project Lead (PL) to drive project milestones is an added advantage.

Skills & Qualifications:

Domain Expertise: Mandatory prior experience in the Medical Devices industry.
Regulatory Knowledge: Deep understanding of ISO 13485 (Quality Management) and ISO 14971 (Risk Management).
Validation Expertise: Proven hands-on experience with IQ, OQ, and PQ protocols for equipment and process transfers.
Documentation: Strong technical writing skills for authoring and reviewing validation protocols/reports.
Coordination: Proven ability to manage cross-functional teams and global stakeholders (offshore and onshore).
Experience as a PM/PL handling full project lifecycles.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 67ee8e6da2fd4a41282ce96771c65f1f
Posted 22 days ago

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Senior Validation Engineer / Project Lead (Medical Devices)

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