Associate R&D Process Engineer, Business Sustaining

<p><strong>Location - Vista, CA - On Site</strong></p> <p><strong>Salary - 84K - 89K</strong></p> <h3> </h3> <h3><strong>About Nordic Naturals</strong></h3> <p>At Nordic Naturals, we take pride in crafting foundational nutrients to help people all over the world live healthy lives. Our mission is to give people, pets, and families the highest-quality nutrients possible to be well and support optimal health. This seemingly simple mission of global health relies on a dedicated team of motivated employees who share our passion for nutrition and wellness. Join us and discover how rewarding it can be to make a living while contributing to a truly great cause.</p> <h3><strong>Position Summary</strong></h3> <p>The <strong>Associate R&D Process Engineer, Business Sustaining</strong>, supports material, formula & process sustainment activities across softgel, gummy, and packaging operations, ensuring robust, compliant, and efficient manufacturing processes. This role assists in implementing material and process changes, executing engineering trials, maintaining process documentation, and supporting cross‑functional investigations. Working under the guidance of the Senior R&D Process Engineer, the Associate contributes to scale‑up readiness, process optimization, and documentation accuracy across Product Development, Operations, and QA. The position is designed to grow into a full Process Engineer role, gaining increasing ownership of engineering trials, process improvements, and technical problem‑solving.</p> <p><strong> </strong></p> <h3><strong>Essential Functions & Core Responsibilities</strong><strong> </strong></h3> <p><strong>Material Qualification & Implementation</strong></p> <ul> <li>Support execution of material change projects across softgel, gummy, and packaging processes, ensuring compliance with cGMP and internal quality systems.</li> <li>Assist in drafting and maintaining change control documentation (change requests, qualification protocols, impact assessments, technical reports).</li> <li>Collaborate with Tech Ops, Manufacturing, QA, and PD Engineering to assess impacts and support material qualification activities.</li> </ul> <p><strong>Engineering Trials, Scale</strong><strong>‑</strong><strong>Up & Process Development</strong></p> <ul> <li>Own small‑scale engineering trials for softgels, gummies, and packaging‑adjacent processes, including data collection and parameter tracking under guidance.</li> <li>Support packaging trials and assist in softgel and gummy process development (encapsulation, cooking, drying, finishing, sampling).</li> <li>Support DOE studies, center‑lining, process capability assessments, and troubleshooting of process deviations.</li> </ul> <p><strong>Process Documentation & Continuous Improvement</strong></p> <ul> <li>Own updates to MMRs, SOPs, batch records, and work instructions; maintain documentation accuracy through change control processes.</li> <li>Support development of process flow diagrams, equipment specifications, and trial documentation.</li> <li>Own small process improvement initiatives and support RCA/CAPA investigations through data gathering, documentation, and analysis.</li> </ul> <p><strong>Cross</strong><strong>‑</strong><strong>Functional Collaboration & Operational Support</strong></p> <ul> <li>Work closely with Operations Engineering, Maintenance, PD Formulators, Process & Packaging Engineers, QA, and Supply Chain to support business‑sustaining activities.</li> <li>Provide technical support during production runs, helping troubleshoot material, process, and documentation issues.</li> </ul> <h3> </h3> <h3><strong>Position Qualifications</strong></h3> <ul> <li>BS in chemical engineering, industrial engineering, pharmaceutical engineering, food science, or related field.</li> <li>Experience in manufacturing, process development, or engineering (internships acceptable). Experience with dietary supplements, food, pharmaceutical, or regulated manufacturing preferred.</li> <li>Familiarity with SAP, PLM, or other manufacturing systems is a plus.</li> <li>Hands‑on experience with production equipment, pilot trials, or lab‑scale process work preferred.</li> <li>Must be able to read, interpret and create documents such as standard operating procedures, batch records, specifications, test reports and regulatory guidelines.</li> <li>Ability to learn and operate specialized instrumentation for product characterization and specification development.</li> <li>Ability to deal with complex problems with many variables.</li> </ul> <h3> </h3> <h3><strong>Other Preferred Skills & Abilities</strong></h3> <ul> <li>Meticulous attention to detail.</li> <li>Solution-focused.</li> <li>Ability to work in a dynamic environment and adapt to change.</li> <li>Ability to follow instructions to produce high-quality work with limited supervision.</li> </ul> <p> </p> <p><strong>Computer Skills:</strong></p> <ul> <li>Must be proficient with MS Office or Google Suite and have advanced Excel skills.</li> </ul> <p><strong> </strong></p> <p><strong>Certifications & Licenses: </strong>N/A</p> <p> </p> <h3><strong>Benefits</strong></h3> <p>Eligible employees may be offered a comprehensive benefits package, which may include medical, dental, vision, retirement benefits, paid time off, paid holidays, and other company-sponsored programs. Eligibility and offerings are subject to applicable plan documents and employment status.</p> <h3><strong>Physical Demands – Manufacturing</strong></h3> <p>This position operates on an active plant floor, requiring candidates to remain stationary or move throughout the facility for shifts up to 8–10 hours. Essential duties involve positioning self to operate tools, using fine motor dexterity to adjust components, and lifting or transferring materials weighing 10-50 pounds depending on the position. Work is performed in a manufacturing environment requiring strict compliance with mandatory safety protocols and Personal Protective Equipment (PPE). </p> <h3><strong>California Applicants</strong></h3> <p>The compensation range above applies to work performed in California and represents the employer’s good-faith estimate of the expected salary or hourly wage range for the position.</p> <h3><strong>Equal Employment Opportunity</strong></h3> <p>We are an equal opportunity employer committed to providing a workplace free from discrimination and harassment. We consider qualified applicants without regard to legally protected characteristics under applicable federal, state, or local law.</p> <h3><strong>Reasonable Accommodations Statement</strong></h3> <p>To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Reasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions.</p>