Job Title: Research and Development Engineer Job Description The Research and Development Engineer leads research, design, and development of components and complex assemblies for critical bioprocessing applications. This individual supports innovation and product development through all stages, from ideation and concept, to prototyping, and through commercialization. The role involves working with the R&D team on new product introduction (NPI), supporting production and process engineering, creating manufacturing packages, and assisting with quality/customer complaints. Responsibilities + Translate business needs and market trends into product requirements and innovative engineering solutions. + Stay current with emerging technologies, materials, and industry trends to maintain competitive advantage. + Drive innovation by exploring new technologies, tools, and methodologies. + Support intellectual property strategies by identifying patentable technologies and collaborating with the legal team. + Partner with cross-functional teams to ensure successful product development and launch, adhering to established stage-gated process and governance model. + Effectively manage project timelines, budgets, and resources to deliver high-quality results. + Oversee the planning, design, development, prototyping, testing, and validation of new products and technologies. + Conduct risk assessments using the FMEA framework and drive risk mitigations as required. Lead design and drawing reviews as needed. + Ensure compliance with applicable regulatory, safety, and quality standards throughout the development process. + Lead problem-solving, corrective, and preventative actions around product concerns originating both external and internal to the organization. + Analyze data from validation tests to determine whether systems and processes meet required criteria and specifications. + Maintain technical records within design history files. + Drive continuous improvement in product performance, design for manufacturability (DFM), and design for cost-effectiveness. Implement engineering best practices, design standards, and documentation protocols. Author SOPs, Work Instructions, and Templates. + Support Product Delivery Teams (PDT), including creating and reviewing quality documents, participating in Corrective And Preventive Action (CAPA) implementation, and generating or supporting ECR (Engineering Change Request) & ECO (Engineering Change Order) activities. + Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications. + Perform other duties as assigned. Essential Skills + 7+ years of engineering experience within a biotechnology or pharmaceutical manufacturing facility. + 4+ years of Single-Use Technology (SUT) design experience, preferably with tubing, bags, and filling needles. + Expertise in the design of molded plastic parts and assemblies for fluid handling of leak-proof applications. + Thorough understanding of industry standards and regulatory guidelines, such as ISO. + Track record in product development, from concept through commercialization. + Ability to manage multiple projects in a fast-paced, collaborative environment. + Results-driven mindset with keen sense of urgency and ability to deliver ahead of deadlines. + Demonstrated attention to detail with excellent follow-up skills. + Self-motivated, adaptable to various work projects, and efficient working independently and as part of a team. + Strong knowledge of design controls, prototyping technologies such as 3D printing, testing, and validation methodologies. + Ability to read, comprehend, and interpret documents such as drawings, BOMs, blueprints, and operating procedures. + Ability to train and guide less experienced personnel on proper interpretation and best practices. + Maintain organized and controlled records of all drawings and BOMs. + Drive and facilitate assigned portions of product change management and control. + Solid understanding of mathematical fundamentals including plane and solid geometry, fractions, percentages, ratios, and proportions applied to practical situations. + Ability to interpret complex data sets, identify patterns, and draw meaningful conclusions. + Author scientific reports with conclusions and recommendations. + Use data to drive decisions tied to the business context. + Expert knowledge and demonstrated hands-on experience with CAD software, both 3D and 2D. + Proficient with Microsoft Office Suite or related software. Additional Skills & Qualifications + Exposure to both medical device and biopharma industries. + Opportunities for patent authorship. + Direct customer interaction. + Autonomy in design and testing. Work Environment The work environment offers a collaborative atmosphere where innovation is encouraged. Engineers have autonomy in design and testing, and there is exposure to both medical device and biopharma industries. The role involves direct customer interaction and provides opportunities for patent authorship. The environment is fast-paced, requiring efficient project management and adherence to regulatory standards. Dress code is professional Job Type & Location This is a Permanent position based out of Camarillo, CA. Pay and Benefits The pay range for this position is $110000.00 - $130000.00/yr. Internal company benefits provided Workplace Type This is a fully onsite position in Camarillo,CA. Application Deadline This position is anticipated to close on Feb 18, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.