As a Regulatory Affairs Specialist, you will support Bio-Rad's commitment to quality and compliance by coordinating the internal and external audits as a Regulatory Specialist. As part of Bio-Rad's Seattle Operations RA team, you'll apply your strong leadership skills and knowledge of regulatory requirements to ensure that our QMS and the products we distribute 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 SO RA team and cross functional teams to ensure all the non-conformances are resolved and corrective actions 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 Internal, External and Customer Audits including regular meetings to prepare, follow up on action items and escalate as needed.Maintain the consistency of high quality standards across Bio-Rad by aligning local and regional procedures with our global processes and expectationsDrive change and transform the way we tackle challenge with support for additional quality and compliance activities, including update to inter-divisional company agreements.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 fieldQualified Lead Auditor per Lead Auditor training and certification with a recognized accreditation body (ASQ certification preferred).5 years experience in regulated industry or equivalent combination of education and experience with 3 or more years working in the area of quality management systems and/or regulatory affairsWorking knowledge of global governing regulations, requirements, and standards such as 21 CFR Parts 803, 806, 820, 11, ISO 13485, ISO 14971, European IVD Regulation, and the Medical Device Single Audit Program / participating country regulations.Experience with AI (Artificial Intelligence) is preferred.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 $95,700 to $131,600 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 achievement of your individual objectives and Company performance.Who We Are: For 70 years, Bio-Rad has focus