Senior Principal Engineer (WA)

Join a team! We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share a common goal and values, propelling us to provide essential care to millions of people globally. We seek dedicated individuals who share our sense of urgency, unity, and excellence.

We are looking for a trustworthy and respectful individual who consistently does the right thing. Someone who is imaginative and proactive, with a keen eye for what is possible. A perceptive and adaptive person who is action oriented. We need a disciplined, focused, and accountable team member. If you embody these values, come join our company and help us shape the future. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

Principle Responsibilities and Duties:

• Schedule, track, and report progress on regulatory processes for Bausch Health products.
• Understand Bausch Health product design and operation with respect to the regulatory approval process within each entity that BHC chooses to pursue regulatory approval.
• Provide product technical assistance for teams in every approval principality.
• Communicate test processes to labs, trouble shoot EMC and safety agency technical issues and work with design team to resolve regulatory issues proactively in a design for regulatory approval up front process.
• Read, write, review, and release documentation pertaining to EMC and safety agency approvals including: test plans, EMI/EMC reports, UL or equivalent safety test reports, operating manuals, drawings, and schematics.
• Work with product EMC, Safety, and medical device regulatory agencies to assure product approvals.
• Able to travel between the US and test venues when required with valid passport.
  
  

Experience, Education, Training, Skills, Traits:

• Must have excellent communications skills in English, other languages are a plus.
• BS Engineering degree in related discipline or equivalent experience.
• Minimum 10 years in regulatory technical product development or service, including experience in EMC regulatory approvals.
• Candidate should have laboratory EMI/EMC and safety agency testing experience.
• Experience working in a multidisciplinary environment including software, optical, RF, mechanical and project management disciplines.
• Capable of learning and differentiating multiple products with multiple configurations.
• Hands-on experience: The ability to debug electronics and EMC issues at the board and cable level is required;
• Familiarity with worldwide EMC and safety regulatory standards: 60601-x, ISO, FCC, or country equivalent agencies.
• Skilled in problem definition, analysis, data collection, generating solid conclusions, and recommendations.
  
  

Desired technical skills:

• Technically capable of dis-assembly and assembly of all products at the enclosure removal level.
• Technically capable of inspection with respect to assembly for EMC and safety compliance. Understands cable construction, design for EMC and safety compliance, and the principles of radiated, conducted, susceptibility, grounding, and ESD as it relates to product approvals.
• Familiar with EMC and safety testing laboratory practices and best practices for testing. A technical understanding of RF principles required for EMC spectrum analysis, antenna use, sniffer probe, oscilloscope use, and familiarity with other lab equipment such as power supplies, power meters, volt meters etc.
• Familiar with regulated/medical device documentation systems and change process. Able to submit change orders and track technical project progress.
• Basic understanding of product principles in ultrasound, lasers, optics, and RF.
  
  

As required by law, Bausch Health provides a reasonable range of compensation for roles that may be hired in the US. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location. For this role, the range of starting pay for this role is $130k to 195k per year.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, national origin, disability, military and/or veteran status, or any other Federal or State legally protected classes.

If a candidate needs a reasonable accommodation/adjustment due to physical or mental health impairment for any part of the application process, they are encouraged to send their request to humanresources@bauschhealth.com or call 908-927-1400 and let us know the nature of the request and their contact information. Please be sure to include the job requisition number.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please read Job Offer Fraud Statement (https://www.bauschhealth.com/siteassets/pdf/bausch-health-fraud-statement.pdf) .

Bausch Health is an EEO/AA employer M/F/D/V.