Job Description

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: Bachelor's Degree (BA/BS) from four-year college/university plus 1+ year experience in regulatory affairs or Master's Degree in regulatory sciences from a college/university. Skills & Attributes: Open-minded and willing to take an educated risk to drive innovation, fail fast and try again. Challenge the status quo and seek opportunities to set new standards. Committed to team engagement, respectful collaboration, and shared success. Ability to take accountability of his/her work, good or bad. Takes initiative to make a positive difference and win with our customers and co-workers. Maintains a sense of urgency and attention to detail. Must have "can do" attitude and be a team player. Ability to be flexible and adaptable. Know when to ask questions. Have a positive attitude. Demonstrate a commitment to getting the job done right and on time. Be able to successfully manage multiple projects and product families. Must be comfortable dealing with ambiguity, relying on critical thinking to accomplish project goals. Maintain a professional demeaner under pressure. Begin to demonstrate problem-solving skills and creativity. Ability to persuade coworkers in a positive, partnership perspective. Effective collaborator with department and cross-functional team members and comfortable working independently with limited direction/supervision. Demonstrated organizational problem-solving skills, project coordination skills and computer literacy in Microsoft Office suite, databases and electronic document management systems. Enthusiastic self-starter with excellent verbal, written, and interpersonal skills. Highly organized, detail-oriented "mindset" and ability to be flexible and multi-task in a dynamically changing environment. The ability to interpret and provide guidance on regulations from various countries. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Physical Demands: While performing the duties of this job, the employee is frequently required to sit. The employee is occasionally required to stand and walk. The employee is occasionally required to sit. The employee is frequently required to walk. The employee is occasionally required to stand. The employee must occasionally lift and/or move up to 10 pounds. 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. 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. Arkansas Staffing

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