Sr. Quality Compliance Engineer- Shockwave Medical

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, and solutions are personal.

Through our expertise in Innovative Medicine and Med Tech, 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.

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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 Description:

Johnson & Johnson is hiring for a Senior Quality Compliance Engineer– Shockwave Medical to join our team in Santa Clara, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, 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

The Senior Quality Compliance Engineer maintains quality compliance, assists in release of final product, assists in maintaining the Receiving Inspection system, NCR system, Supplier controls, Competency Assessment Activity, Audit activities and compiling quality metrics for periodic reviews. This position may also provide quality engineering support for manufacturing but not limited to managing the calibration system and ensuring that the environmental monitoring of the clean rooms remain in compliance.

• Review Production and Sterilization Records and release of Final Product to inventory
• Review Production Records for accuracy and good documentation practice and compliance to respective Manufacturing Instructions
• Compile and monitor process control data
• Review sterilization records and lot release test data to ensure product can be released to inventory
• Ensure non-conformances/deviations and rework orders are resolved
• Manage Equipment and Tool Calibrations
• Lead the activities to implement and validate new Equipment Control software.
• Implement IQ and Calibration requirements in accordance with Manufacturer recommendation and internal requirements
• Harmonize equipment specifications, Installation Qualification and Calibration requirements
• Coordinate with calibration vendors and equipment manufacturers to ensure all tools and equipment are calibrated prior to their calibration due dates
• In the event of an out of tolerance condition, work cross-functionally to assess the risk and product impact, and how to resolve the situation
• Work with the Manufacturing Engineering group to ensure Preventive Maintenance is performed as scheduled.
• Incoming Inspection
• Work with R&D and Manufacturing Engineers to draft and maintain Incoming Inspection Plans
• Identify and implement Incoming Inspection measuring equipment.
• Train QA inspectors on such equipment
• Environmental Monitoring
• Ensure periodic Environmental Monitoring of the clean rooms are scheduled and performed by an approved supplier
• Review Environmental Monitoring test results to ensure compliance, and work cross-functionally to address any non-conformances as needed
• Responsible for coordinating Bioburden/Quarterly Dose Audit builds and ensuring sterility testing is performed per schedule.
• Review test data to ensure validated sterilization parameters are valid
• Perform ongoing review of Janitorial and Pest Control Records
• Manage Competency program
• Ensure Technician and Assembler competency program is implemented using a risk-based approach
• Assist with…