Regulatory Affairs Associate

Regulatory Affairs Associate

The Regulatory Affairs Associate (RAA) supports the RA team in creating, evaluating and completing regulatory tasks related to worldwide product registration submissions, facility registrations, special projects and strategy to drive market growth worldwide. This individual is responsible for driving global regulatory registrations / approvals based on company objectives, collaborating with cross-functional departments to ensure country-specific requirements are met and integrated throughout post-product launch activities. The ideal candidate brings a strong sense of urgency, attention to detail, and a passion for regulatory excellence. This entry-level position is ideal for a motivated self-starter who thrives in a fast-paced environment, demonstrates creative problem-solving, and actively contributes to a collaborative team culture.

This position is required to be on-site at minimum three days a week in Brea, CA

Primary Duties & Responsibilities :

• Monitor and interpret current and emerging regulations issued by relevant authorities, assess their impact on the organization, and provide timely regulatory guidance and support to ensure compliance.
• Develop and maintain procedures, standard operating procedures (SOPs), and technical documentation to support regulatory operations and ensure clear, compliant, and auditable processes.
• Support the preparation of Technical Files and compilation of technical documentation required for global product registrations, collaborating with international registration teams to facilitate timely approvals across a diverse product portfolio.
• Prepare and maintain regulatory submissions, product and facility registrations, and certifications in accordance with country-specific requirements to support global product approvals.
• Coordinate with distributors, in-country consultants, inter-company affiliates, and commercial partners to ensure fulfillment of regulatory requirements for product registrations in target markets.
• Support the review and evaluation of product, manufacturing, and labeling changes to determine regulatory reporting requirements and ensure ongoing compliance.
• Follow Envista CIRCLe values and incorporate into daily work. Be customer centric and build ethical, supportive relationships with customers.
• Any duties or tasks that your Leader assigns.

Job Requirements : Qualifications :

Skills & Attributes :

Physical Demands :

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is frequently required to sit. The employee is occasionally required to stand and walk. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Target Market Salary Range : $60,000 - $90,000

Operating Company : Ormco

Ormco is a global leader and innovator of high-quality orthodontic products and solutions, including brackets and wires. For more than 60 years, our team has partnered with the orthodontic community to help create over 20 million smiles in more than 140 countries. We build trusted relationships. Each one is rooted in respect and understanding. We take that approach when we help orthodontists achieve their clinical and practice management objectives. We take the same approach when we help our team bring their personal best to work each day, ready to make a difference and reach their full potential.

Envista and all Envista Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The "EEO is the Law" poster is available at : http : / / www.dol.gov / ofccp / regs / compliance / posters / pdf / eeopost.pdf.