FULL_TIME

FEED

OTHER

If you are motivated by building robust processes, solving problems on the production floor, and mentoring other engineers and technicians, this role provides the responsibility and support to grow your technical and leadership skills. This company partners closely with eye care professionals to continually refine how products are engineered, packaged, and delivered, ensuring they are reliable in the operating room and everyday clinical practice.

This Jobot Job is hosted by: Tyler May Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $110,000 - $130,000 per year A bit about us: Our client is a specialized medical device manufacturer focused on innovative eye care products that support better vision and long‑term ocular health. For more than three decades, this company has designed and produced a broad portfolio of ophthalmic and optometric supplies, instruments, and disposables used in procedures such as cataract, refractive, and dry eye treatments. Operating from an ISO 13485–certified facility in Southern California, the organization maintains rigorous quality standards that align with U.S. and international medical device regulations. The manufacturing and quality systems are built to comply with 21 CFR 820 and comparable global requirements, allowing the company to serve clinicians and patients in both domestic and international markets. This company partners closely with eye care professionals to continually refine how products are engineered, packaged, and delivered, ensuring they are reliable in the operating room and everyday clinical practice. With hundreds of SKUs spanning dry eye therapies, surgical accessories, and other vision care solutions, our client combines precision manufacturing with a mission‑driven culture centered on improving patient outcomes. Why join us? Joining our client means stepping into a stable, growth‑oriented medical device business where your engineering decisions have a direct impact on patient comfort and clinical results. You will own complex manufacturing processes for highly specialized ophthalmic products, giving you visibility across the full product life cycle—from concept and scale‑up through sustained production and continuous improvement. As a senior manufacturing engineer, you will collaborate daily with R&D, quality, operations, and regulatory teams in a close‑knit environment where ideas can move quickly from the cleanroom to the customer. The company’s ISO 13485–compliant environment offers the chance to deepen your experience with regulated manufacturing, validation, and documentation while still maintaining an agile, hands‑on culture. Our client offers a comprehensive benefits package typical of established medical manufacturers in the region, including health coverage, retirement plans, and paid time off, along with opportunities for professional development and cross‑functional leadership. If you are motivated by building robust processes, solving problems on the production floor, and mentoring other engineers and technicians, this role provides the responsibility and support to grow your technical and leadership skills. Job Details Core responsibilities: Lead the design, development, and optimization of manufacturing processes for ophthalmic medical devices and related components in a regulated environment. Drive new product introduction (NPI) from an operations standpoint, including process definition, pilot builds, scale‑up, and transition to full production. Develop and maintain process documentation such as work instructions, standard operating procedures (SOPs), process flow diagrams, PFMEAs, and control plans in alignment with ISO 13485 and 21 CFR 820. Analyze production data to improve yield, reduce scrap, and enhance process capability using statistical tools, root‑cause analysis, and structured problem‑solving methodologies. Specify, qualify, and implement new equipment, tooling, and fixtures; lead IQ/OQ/PQ protocols and coordinate with quality and validation teams. Provide day‑to‑day technical support to manufacturing, troubleshooting nonconformances and process deviations, and implementing both immediate containment and long‑term corrective actions. Collaborate with R&D to influence product designs for manufacturability, reliability, and cost‑effectiveness while maintaining critical performance requirements for eye care applications. Champion continuous improvement initiatives leveraging Lean and Six Sigma principles to shorten lead times, reduce costs, and standardize best practices across production lines. Train and mentor operators, technicians, and junior engineers on new processes, equipment, and documentation requirements to ensure consistent execution on the floor. Qualifications: Bachelor’s degree in mechanical engineering, manufacturing engineering, biomedical engineering, or a related technical discipline; an advanced degree is a plus. 5+ years of experience in manufacturing or process engineering, preferably in medical devices, pharmaceuticals, or other highly regulated, precision manufacturing environments. Proven track record developing and sustaining processes under ISO 13485 or comparable quality management systems, with working knowledge of FDA quality system regulations (21 CFR 820). Hands‑on experience with process validation (IQ/OQ/PQ), equipment qualification, and statistical process control in a cleanroom or controlled manufacturing environment. Demonstrated ability to use structured problem‑solving tools (5 Whys, fishbone diagrams, DMAIC, DOE, etc.) to resolve complex production issues and improve capability. Familiarity with Lean manufacturing concepts such as 5S, visual management, standard work, and flow optimization; Six Sigma certification is a plus. Comfortable reading engineering drawings and specifications, including GD&T, and working with ERP and document control systems common to medical device manufacturers. Strong communication skills, with the ability to interface effectively with production, quality, R&D, supply chain, and regulatory stakeholders. Ability to manage multiple projects simultaneously, prioritize effectively in a fast‑paced environment, and take ownership of deliverables with minimal supervision. Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy

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Jobot

Senior Manufacturing Engineer

Best Practices

Biomedical Engineering

Biotech and Pharmaceutical

Cataract

Cleanroom

Clinical Outcomes

Code of Federal Regulations

Communication Skills

Continuous Improvement

Control Systems

Corrective Action

Cost Control

Cost Effectiveness Analysis

Data Analysis

Document Control

Documentation

ERP (Enterprise Resource Planning)

Engineering Drawing

Establish Priorities

FDA Requirements

Geometric Dimensioning and Tolerancing

ISO (International Organization for Standardization)

Identify Issues

Lean Manufacturing

Lean Six Sigma

Legal

Machine Tool

Manufacturing

Manufacturing Design

Manufacturing Engineering

Manufacturing Process Engineering

Manufacturing Requirements

Manufacturing Systems

Manufacturing/Industrial Processes

Mechanical Engineering

Medical Equipment

Mentoring

Multitasking

Ophthalmology

Patient Care

Problem Solving Skills

Process Capability

Process Development

Process Flow Diagram (PFD)

Process Improvement

Process Validation

Product Design

Product Engineering

Product Lifecycle

Product Support

Product/Service Launch

Productivity Management

Project/Program Management

Quality Management

Quality Metrics

Regulations

Research & Development (R&D)

Root Cause Analysis

Six Sigma Certification

Six Sigma Champion

Six Sigma DMAIC

Standard Operating Procedures (SOP)

Statistical Process Control

Stock Keeping Unit (SKU)

Supply Chain

Technical Support

United States Department of Energy (DOE)

Validation Documentation

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. 4. Extensive knowledge and hands-on experience with sensors, valves, solenoids, electrical systems, troubleshooting, pneumatics, extrusion, and injection molding.

Seeking Manufacturing Engineer to work with R&D Team This Jobot Job is hosted by: Tim Sargious Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $110,000 - $135,000 per year A bit about us: Our Client has been around over 50 years Manufacturing the highest quality rubber that is sold to Fortune 500 companies and used in their products. Why join us? <ul><li>Competitive Salary</li><li>Great Benefits (Medical, Dental and Vision)</li><li>401k Match </li><li>Generous paid time off</li><li>Training</li><li>Career Advancement</li><li>Fun, energetic working environment</li></ul> Job Details Job Details: We are seeking a dynamic and innovative Manufacturing Engineer (Electro-Mechanical) to join our team. This is a permanent, full-time position that offers the opportunity to work with cutting-edge technology in the manufacturing industry. You will be a key player in developing, implementing, and optimizing manufacturing processes to ensure efficiency and effectiveness. This role requires a blend of technical expertise in electro-mechanical systems and a deep understanding of manufacturing principles. Responsibilities: 1. Design, develop, and test all aspects of mechanical components, equipment, and machinery related to electro-mechanical systems. 2. Apply knowledge of engineering principles to design products such as sensors, valves, solenoids, and other electro-mechanical systems. 3. Collaborate with design engineering and manufacturing team to develop and implement new product manufacturing, assembly processes, and equipment. 4. Troubleshoot and resolve technical issues related to production processes and equipment, including electrical and pneumatic systems. 5. Implement improvements to existing manufacturing processes, focusing on enhancing productivity, quality, and efficiency. 6. Develop and maintain detailed work instructions for assigned products/processes. Disseminate these instructions to the production floor to ensure that the workforce is well-trained and capable. 7. Use SolidWorks or equivalent CAD software to design, test, and validate tools and equipment used in the manufacturing process. 8. Execute and analyze tests to inspect product performances and adjust processes as needed. 9. Participate in cross-functional teams to execute product development plan. 10. Conduct root cause analysis for manufacturing process deviations and perform corrective actions. Qualifications: 1. Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field. 2. A minimum of 5 years of experience in a manufacturing engineering role, specifically in electro-mechanical systems. 3. Proficient in the use of SolidWorks or equivalent CAD software for designing, testing, and validating tools and equipment. 4. Extensive knowledge and hands-on experience with sensors, valves, solenoids, electrical systems, troubleshooting, pneumatics, extrusion, and injection molding. 5. Strong understanding of manufacturing processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods. 6. Excellent problem-solving skills, with a knack for technical innovation and creative engineering solutions. 7. Strong communication skills, both written and verbal, with the ability to effectively collaborate with team members and present ideas clearly and effectively. 8. Ability to manage multiple projects simultaneously, prioritizing tasks based on company needs. 9. Proven track record of driving continuous improvement in process capabilities, product yield, and production volumes. 10. Must be a self-starter, with the ability to work independently or as part of a team. Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy

Full Time Manufacturing Jobs in Cucamonga, CA

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Full Time Manufacturing Jobs in Cucamonga, CA

Senior Manufacturing Engineer Jobot

Manufacturing Engineer (Electro-Mechanical) Jobot

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