Regulatory Affairs Associate - Entry Level, FDA Submissions

Valid8 Financial, Inc.; Tustin (CA); On-site; USD 68,000 - 75,000; Full time

Benefits offered by this job

Medical, Dental, Vision, and Life

EAP Sessions

401(K) with matching

Employee Referral Bonus

Complimentary fruit, snacks, and Bevar

Complimentary catered lunches on Thrus

EV Charging

Cell phone stipend

Job summary

Zymo Research is seeking an entry-level Regulatory Affairs Associate to join our team in California. You will help support regulatory activities, document maintenance, and compliance tasks under experienced guidance, contributing to high-quality regulatory processes.

The role emphasizes learning, coordination with cross-functional teams, and facilitating registrations and submissions to regulatory bodies including FDA. Onsite work in Tustin, CA offers growth in a dynamic scientific environment.

Qualifications

• Bachelor’s degree in a science or related discipline preferred; entry-level candidates encouraged to apply.
• Demonstrates initiative, ownership, and willingness to take on new responsibilities.
• Flexible and adaptable with ability to research regulatory questions.
• Highly organized with strong time management and detail orientation.

Responsibilities

• Support registrations and device listings in domestic and international markets.
• Assist with IVDD/IVDR technical documentation and registrations.
• Support FDA submissions including 510(k) as applicable.
• Research regulations and summarize findings for review.

Skills

Interest in regulatory affairs

Attention to detail

Organizational skills

Time management

MS Office proficiency

Independent work

Education

Bachelor’s degree in science or related field

Tools

MS Office

Job description

Zymo Research is seeking an entry-level Regulatory Affairs Associate to join our team in California. You will help support regulatory activities, document maintenance, and compliance tasks under experienced guidance, contributing to high-quality regulatory processes.

The role emphasizes learning, coordination with cross-functional teams, and facilitating registrations and submissions to regulatory bodies including FDA. Onsite work in Tustin, CA offers growth in a dynamic scientific environment.