Responsibilities may include the following:
- Design manufacturing processes, procedures, and production layouts for assemblies, equipment installation, machining, and material handling
- Develop and optimize workflow and sequence of operations to improve efficiency and productivity
- Design equipment and facility layouts to maximize production capabilities
- Adapt machine and equipment designs to meet manufacturing and production requirements
- Incorporate inspection and testing requirements into production processes
- Evaluate equipment performance and implement corrective actions to resolve issues
- Support statistical process control (SPC) and continuous improvement initiatives
- Provide engineering support for design concepts and manufacturability
- Ensure compliance with FDA, ISO, and GMP regulations
- Collaborate with cross-functional teams including Quality, Operations, and R&D
*Other duties may be assigned.*
Requirements
- Bachelor’s Degree in Engineering (Mechanical, Electrical, Chemical, or related)
- 0–3 years of experience in manufacturing, engineering, or related roles
- Bilingual (English & Spanish)
- Experience in Computer System Validation (CSV)
- Experience working in a regulated environment (Medical Devices or Pharmaceutical industry)
- Basic knowledge of manufacturing processes and equipment
- Strong organizational, communication, and technical writing skills
Preferred:
- Knowledge of Process Validation (IQ/OQ/PQ)
- Experience with Statistical Tools (Minitab or equivalent)
- Familiarity with MES systems (e.g., FactoryWorks)
- Knowledge of risk management tools (FMEA)
*Willing to work 100% On-Site, weekend and other shifts when necessary.*
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