Manufacturing Engineer
Cytek Biosciences Inc
Summary
The Manufacturing Engineer (ME) will be responsible for optimizing manufacturing processes to ensure efficient, high-quality production while maintaining compliance with standards and regulations. The ME will be expected to solve mechanical, electrical, and optical issues seen during the production of opto-electro-mechanical instruments, reduce downtime, lead projects, contribute new ideas, and find innovative methods to accomplish production goals.
Job description
Essential Duties and Responsibilities
- Develop and update work instructions, process documentation, and standard operating procedures.
- Design, develop, and optimize manufacturing processes, workflows, and production layouts.
- Improve production efficiency, reduce waste, and support cost-reduction initiatives.
- Select, install, qualify, and maintain manufacturing equipment, fixtures, and tooling.
- Ensure manufacturing processes meet quality, safety, and regulatory requirements.
- Troubleshoot production issues and implement corrective and preventive actions.
- Support new product introduction, process transfers, and production ramp-up activities.
- Collaborate with engineering design, quality, supply chain, and manufacturing teams.
- Improve product quality by leading root cause investigations and implementing Poka-Yoke solutions to reduce recurring manufacturing defects.
- Implement Lean manufacturing strategies and process enhancements to reduce labor hours per unit, improve throughput, shorten lead times, and decrease field installation.
- Analyze production data, yields, cycle times, and downtime to identify improvement opportunities.
- Lead or support Lean, Six Sigma, and other continuous improvement projects.
- Reduce equipment downtime and increase manufacturing output through technician training, coaching, and proactive problem-solving initiatives.
- Prepare and maintain required documentation for assigned duties, including validations, operating procedures, preventive maintenance schedules, engineering change notifications, spare parts lists, and related records.
Required Skills & Qualifications
- Bachelor's degree in Manufacturing, Electrical, Mechanical, Industrial Engineering, or a related field, with 3+ years of experience supporting system integration, manufacturing, assembly, and test in manufacturing operations.
- Experience in medical device manufacturing and familiarity with associated regulatory and quality requirements.
- Ability to read and interpret engineering drawings, specifications, and technical documents.
- Strong analytical, troubleshooting, and problem-solving skills.
- Knowledge of Lean manufacturing, Six Sigma, root cause analysis, and process validation.
- Strong written and verbal communication skills, teamwork and project management skills.
- Familiar with CAD tools, manufacturing documentation and production data analysis.
- Demonstrated ability to design, execute, and analyze experiments, translate data into actionable insights, and provide recommendations that improve product quality, process capability, and operational efficiency.
Preferred Qualifications
- Six Sigma Green Belt or Black Belt certification preferred, with demonstrated application of Lean and continuous improvement methodologies.
- Knowledge of Design for Manufacturing and Assembly.
- Knowledge of PCBA assemblies, laser systems, optics, fluidics, and electromechanical systems is highly desirable.
- Familiarity with ERP/MRP systems, statistical process control, and manufacturing metrics.
- Working knowledge of ISO 13485 and quality management systems within regulated manufacturing environments.
Requirements
- Bachelor's degree in Manufacturing, Electrical, Mechanical, Industrial Engineering, or a related field
- 3+ years of experience supporting system integration, manufacturing, assembly, and test in manufacturing operations
- Experience in medical device manufacturing and familiarity with associated regulatory and quality requirements
- Ability to read and interpret engineering drawings, specifications, and technical documents
- Strong analytical, troubleshooting, and problem-solving skills
- Knowledge of Lean manufacturing, Six Sigma, root cause analysis, and process validation
- Strong written and verbal communication skills, teamwork and project management skills
- Familiar with CAD tools, manufacturing documentation and production data analysis
- Demonstrated ability to design, execute, and analyze experiments, translate data into actionable insights, and provide recommendations that improve product quality, process capability, and operational efficiency
Company overview
Cytek Biosciences Inc is a leading cell analysis solutions company specializing in flow cytometry technology. Headquartered in Fremont, California, the company develops and manufactures innovative flow cytometry instruments, reagents, and software solutions that enable researchers to conduct high-parameter cell analysis. Cytek's proprietary full spectrum flow cytometry technology allows scientists to analyze up to 40 colors simultaneously, providing unprecedented depth in immune cell profiling and cellular characterization. The company's product portfolio includes the Cytek Aurora series, Northern Lights, Orion, and Muse Micro cell analyzers, along with cFluor reagents optimized for spectral cytometry. Cytek serves pharmaceutical companies, contract research organizations, academic institutions, and clinical researchers worldwide, supporting applications in immuno-oncology, infectious diseases, inflammatory diseases, drug discovery, and genomics. The company is committed to making advanced flow cytometry accessible and affordable while maintaining high ethical standards and fostering a culture of innovation and scientific excellence.