Regulatory Specialist II

As a Regulatory Affairs Specialist II, you will support new product developments/product modifications, IVDR implementation, and international product. Represent RA on global project teams for new or modified in vitro diagnostic devices (IVD). Manage global RA Change Request Process and ensure these are tracked in a log and all files completed and are audit ready. Create and maintain technical files in compliance with CE Marking. Support international product registrations: license updates and renewals in accordance with country specific requirements. Ensure labeling changes are implemented and communicated to the selling regions, as needed. Support Field Action activities and ensure all documentation is audit ready.Manage SAP product restrictions. Participate in review and implementation of new and/or revised external regulatory standards. Participate in review and approval of marketing materials. Support internal audits for MDSAP and IVDR requirements. Manage assigned tasks as needed.

Location: This position must be based in Irvine, California and requires the employee to be located within commuting distance of the office.

How You'll Make An Impact:

• Manage QS product global registration and licensing to support QS revenue.
• Effective communication skills, both written and oral with cross functional teams.
• Strong documentation, prioritization, and organization skills.
• Ability to work independently and as a team member under moderate supervision.
• Working with moderate complex issues under pressure.
• Good time management and ability to multitask.

What You Bring:

• Bachelor's degree in Biology, Chemistry, Medical Technology, or a related scientific discipline.
• Advanced degree and/or Regulatory Affairs Certification (RAC) preferred.
• 2-5 years of experience in domestic and international regulatory compliance, with experience in the medical device industry preferred (IVD experience strongly desired).
• Working knowledge of global regulatory requirements, including FDA and IVDR regulations.
• Experience supporting regulatory Field Actions, including corrections, removals, recalls, and related health authority communications.
• Knowledge of product labeling requirements and international product registration processes.
• Strong customer focus with the ability to support cross-functional and external stakeholders.
• Detail-oriented with strong technical and regulatory writing skills.
• Proficient in computer applications, including Quality Manament systems such as SAP.
• The ability to perform basic statistical analysis.
• Strong analytical, communication, problem solving, and critical thinking skills.
• Demonstrated ability to multitask and manage competing priorities across multiple timelines.

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 base salary range for this position is $86,600 - $119,200 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 also 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-PB1