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As a Regulatory Affairs Specialist, you will support Bio-Rad's commitment to quality and compliance by coordinating the Domestic and International Registration Requests as a Regulatory Specialist. As part of Bio-Rad's Seattle Operations Regulatory Affairs team, you'll apply your strong leadership skills and knowledge of regulatory requirements to ensure that we register and distribute products that are in compliance to local and international regulations and applicable standards, escalate issues as necessary, complete necessary documentation and optimize our processes and procedures. You'll also work closely with Seattle Operations Regulatory Affairs team and cross functional teams to ensure all the product and facility registration activities are complete and change assessments are documented as needed. How You'll Make An Impact Help to create and foster a quality environment and mindset throughout the business by coordinating the Domestic and International Regulatory Registrations, Regulatory Change Assessment including weekly meetings, workflows and documentation, and escalations. Maintain the consistency of high quality standards across Bio-Rad by aligning local and regional procedures with our global processes and expectations. Drive change and transform the way we tackle challenge with support for additional quality and compliance activities, including audits and inspections. What You Bring: While this list of qualifications may help an employee to succeed in this position, capable candidates may have a wide range of backgrounds or skills. If you have experience that aligns with the responsibilities of this role, we encourage you to apply! Bachelor's degree, or equivalent, in Biology, Chemistry, Medical Technology, or related field. Advanced Degree and/or Regulatory Affairs Certification preferred. Minimum of 10 years experience in Regulatory Affairs, or equivalent combination of education and experience relating to IVD/Medical Devices/Biologics. Proficiency in interpretation and application of US and international regulatory requirements for IVD/Medical Devices/Biologics and related submissions experience. Experience with high-risk class IVD products (e.g. U.S. BLA/PMA, EU Class D and C, etc...) preferred. Ability to manage multiple complex projects with defined timelines. Excellent written and verbal communication skills required for negotiation with internal and external parties. Total Rewards Package: At Bio-Rad, we're empowered by our purpose and recognize that our employees are as well. That's why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee's work and life cycle. Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! Compensation: The estimated hourly range for this position is $140,100 to $192,600 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon ac