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RA Spec III

  • 2025-36432
  • Seattle, Washington, United States
  • Qualidade e Regulatório
  • Remoto

Support Bio-Rad's commitment to quality and compliance by coordinating the internal and external audits as a Lead Auditor/Audit Coordinator. 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 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 Seattle Operations Regulatory Affairs 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.
  •  Drive change and transform the way we tackle challenge with support for additional quality and compliance activities,   including update to inter-divisional company agreements.
  •  Coordinate planning, approval, and execution of the annual internal Seattle Operations audit schedule and program.
  •  Document management: Maintains and stores current quality certificates, Memoradum of Understanding, contracts with auditing organizations, audit reports, Design History Files, and other records as assigned.

 What You Bring:

  • Bachelor's degree or equivalent in Biology, Chemistry, Medical Technology, or related field.

  • Qualified Lead Auditor withr Lead Auditor training.  Certification with a recognized accreditation body preferred.  (ASQ certification highly desired).

  • 5 years experience in regulated industry or equivalent combination of education and experience. Experience working in the area of quality management systems and/or regulatory affairs strongly preferred.

  • Working 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 annual salary for this position is $100,800 to $138,600 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 focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. 

 

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply.

 

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

 

Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. Click here for more information on this scam and how to avoid it. #LI-AK1

Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.

 

 

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