Manufacturing EngineerCompany Overview This organization is a global healthcare and medical technology leader dedicated to safeguarding and improving patient outcomes. With a strong footprint in regulated manufacturing, automation, and pharmaceutical and medical device production, the company delivers high‑quality, innovative solutions used in critical care, infusion therapy, and sterile manufacturing environments worldwide. Its culture emphasizes safety, quality, continuous improvement, and engineering excellence, supported by robust quality systems and advanced automated production technologies. Position Summary The Manufacturing Engineer is responsible for supporting and improving automated production systems in a highly regulated environment. This role leads or supports investigations, corrective and preventive actions, and continuous improvement initiatives while providing technical expertise for production troubleshooting and equipment reliability. The Manufacturing Engineer collaborates closely with cross‑functional teams to ensure operational efficiency, product quality, and compliance with regulatory and safety standards. Key Responsibilities + Lead or support Corrective and Preventive Actions (CAPAs), Non‑Conformances (NCs), and Investigation Reports (PIRs) to drive effective issue resolution, risk mitigation, and continuous improvement. + Provide technical expertise to troubleshoot production issues, perform root cause analysis, and resolve equipment failures and process variances in automated manufacturing environments. + Collaborate with cross‑functional teams including mechanics, automation technicians, operators, quality, and engineering to implement robust and sustainable solutions. + Evaluate, implement, and optimize new technologies, tools, and methodologies to improve operational efficiency, including predictive maintenance strategies and enhanced quality control standards. + Supervise testing, commissioning, and validation of new or upgraded equipment and systems. + Analyze manufacturing and equipment performance data to develop reports and insights that support strategic decision‑making and continuous improvement initiatives. + Ensure compliance with safety regulations, FDA requirements, industry standards, and environmental guidelines in all engineering activities. + Conduct equipment health assessments, predictive maintenance, and upgrades on automated production equipment such as blow molders, fillers, conveyors, and integrated packaging systems. + Lead or support cross‑disciplinary projects, including equipment installations, upgrades, and process improvements. + Provide ongoing technical support and guidance to operators and technicians to improve equipment reliability and production performance. Required Skills & Competencies + Manufacturing engineering in automated or high‑volume production environments + Process improvement and continuous improvement methodologies + Reliability engineering and failure analysis + Data analysis and performance metrics reporting + Root cause analysis and structured problem‑solving techniques + CAPA and investigation management + Experience working in FDA‑regulated or highly regulated industries + Preventive and corrective maintenance principles + Automation systems, controls, and industrial equipment + Lean Manufacturing, Six Sigma, and Kaizen methodologies Education & Qualifications + Bachelor’s degree in Mechatronics, Electrical Engineering, Mechanical Engineering, or a related multidisciplinary engineering field. + 7+ years of experience in manufacturing engineering, automation, or systems engineering, with exposure to robotics, controls, and complex industrial processes. + Strong communication, collaboration, and project management skills. + Demonstrated ability to troubleshoot and support customized, complex manufacturing equipment. + Certifications in automation, reliability, Lean Six Sigma, or project management (e.g., PMP) are preferred. + Ability to work effectively in dynamic production environments, including clean rooms and manufacturing facilities. #LI-1 Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay range for this position is $60.00 - $75.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irvine,CA. Application Deadline This position is anticipated to close on Feb 4, 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.