Description
About the Opportunity
We are seeking a highly motivated and detail-oriented Regulatory Affairs professional to join our team. This position supports the development, registration, commercialization, and lifecycle management of innovative in vitro diagnostic (IVD) products designed to address emerging infectious diseases and biothreats.
The ideal candidate has a strong understanding of U.S. and international regulatory requirements for diagnostic products and is experienced in preparing regulatory submissions and supporting cross-functional product development teams. You are proactive, organized, and capable of managing multiple priorities while working collaboratively with scientific, quality, manufacturing, and commercial teams. If you enjoy solving complex regulatory challenges and helping bring impactful diagnostic solutions to market, we encourage you to apply.
This is a regular full-time position that will be supported by project-based funding. The anticipated duration of the funded project is approximately one (1) year. While InBios hopes to retain successful team members beyond the initial project period, continued employment will depend on business needs, project requirements, and the availability of future funding through contract renewals, expanded programs, or new initiatives.
About UsInBios International Inc. has been advancing diagnostic solutions since 1996, specializing in the design, development, and manufacturing of assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded programs, with a strong focus on innovation, quality, and compliance.
Based in Seattle, WA, we offer a collaborative, mission-driven culture where employees contribute to meaningful work that impacts lives worldwide.
About the Position- Position Title: Regulatory Affairs Associate II
- Location: Seattle, WA
- Employment Type: Full-time, exempt | On-site (Hybrid option may be available after employee is established in the position.)
- Position Pay Range: $91,500 - $125,000 annually (based on knowledge, skills, and experience)
- Represent and/or lead Regulatory Affairs in project teams throughout product life cycle.
- Write/review protocols for analytical studies in support of regulatory submissions.
- Assist in the preparation and submission of EUAs, pre-submissions, 510(k)s for class II products.
- Support international registrations, create and maintain technical files, and prepare product dossiers.
- Prepare and maintain Design History Files.
- Lead Risk Management effort.
- Prepare and review labeling and marketing materials to ensure regulatory compliance.
- Help set the regulatory strategy for new product development.
- Keep abreast with the latest regulatory requirements and trends.
- Communicate with the FDA and other regulatory bodies concerning product submissions.
- Bachelor's or Master's degree in Life Sciences, Bioengineering, Regulatory Affairs, or a related discipline.
- Minimum of 5 years of regulatory affairs experience within an FDA-regulated IVD manufacturing environment, or a Ph.D. with at least 2 years of applicable industry experience.
- Certification in regulatory affairs preferred.
- Excellent knowledge of US and international IVD regulations.
- Strong written and verbal communication skills.
- High attention to detail.
- Technical system skills (e.g., MS Office, SharePoint, statistical packages, online research).
- Ability to manage multiple projects and deadlines.
- Strong understanding of statistical analysis.
- Ability to identify compliance risks and escalate when necessary.
- Prior experience in regulatory submissions (pre-submissions, EUA, 510(k), De Novo, PMA) for lateral flow and real-time PCR assays is required.
- Professional office environment with extensive computer-based work.
- Occasional work in a GMP-regulated manufacturing environment and Biosafety Level 2 (BSL-2) laboratory setting.
- Medical, dental, vision, life & disability insurance
- 401(k) + Roth IRA + FSA options
- 2 weeks paid vacation + 11 paid holidays (including winter break)
- Competitive pay and growth opportunities
- Supportive, team-oriented culture focused on innovation and impact
Join a dedicated team committed to advancing diagnostic technologies that improve lives worldwide. Bring your regulatory expertise, collaborative mindset, and passion for quality to help deliver innovative solutions for infectious disease detection and global public health.
Skills Required
- Bachelor's or Master's degree in Life Sciences, Bioengineering, Regulatory Affairs, or related discipline
- Minimum of 5 years regulatory affairs experience within an FDA-regulated IVD manufacturing environment, or Ph.D. with at least 2 years applicable industry experience
- Certification in regulatory affairs
- Excellent knowledge of US and international IVD regulations
- Prior experience preparing regulatory submissions (pre-submissions, EUA, 510(k), De Novo, PMA) for lateral flow and real-time PCR assays
- Strong understanding of statistical analysis
- Technical system skills (MS Office, SharePoint, statistical packages, online research)
- Strong written and verbal communication skills
- High attention to detail
- Ability to manage multiple projects and deadlines
- Ability to identify compliance risks and escalate when necessary
- Experience preparing and maintaining Design History Files and leading Risk Management efforts
What We Do
InBios International Inc. specializes in the design, development and manufacture of diagnostic assays for emerging infectious diseases and biothreats. Located in Seattle, Washington, InBios offers superior quality products which are accurate, easy to use and cost effective. InBios is GMP compliant, FDA registered, USDA licensed and ISO 13485:2016 certified. For more information, visit http://www.inbios.com.
