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Senior Quality Engineer. QMS

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
Quality Systems

Job Category:
Professional

All Job Posting Locations:
Athens, Georgia, United States of America

Job Description:

The Senior Quality Engineer provides technical quality leadership for computerized systems, equipment, and digital solutions used within a regulated environment.

This role is responsible for developing and executing Computerized System Validation (CSV) strategies, applying risk-based approaches to qualification and validation, providing quality guidance with change management, and ensuring systems and processes maintain appropriate data integrity throughout their lifecycle.

The Senior Quality Systems Engineer partners with Quality, Manufacturing, Engineering, IT, Automation, system owners, and business process owners to ensure that systems are fit for intended use, appropriately controlled, and maintained in a validated state.

The position serves as a subject matter expert and provides practical, risk-based guidance that balances compliance requirements, patient/product risk, and operational needs

Key Responsibilities


* Support qualification and validation activities for equipment, systems, including computerized systems used in regulated business and manufacturing processes.


* Apply a risk-based approach to determine the appropriate scope and rigor of qualification and validation activities.


* Review and approve lifecycle documentation such as validation plans, user requirements, functional and configuration specifications, risk assessments, test protocols/scripts, traceability documentation, validation reports, and system retirement documentation.


* Provide change management direction and guidance on appropriate validation strategies based on intended use, system complexity, regulatory impact, and risk.


* Provide quality oversight for implementation, upgrades, configuration changes, integrations, migrations and retirement of computerized systems.


* Support investigation and resolution of validation discrepancies, test failures, and system-related quality issues.


* Ensure validated systems remain in a controlled state throughout thei...




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