POSITION OVERVIEW
This role is responsible for designing and programming high-performance robotics automation, assembly, and inspection systems. The automation solutions support reagent dispensing systems, micro-plate test kits, and micro-fluidic assay cartridges utilized in biodefense, clinical, and life-science markets. The individual in this position will collaborate with cross-functional teams to drive innovation in new product development and enhance manufacturing capabilities through automation. Additional responsibilities include configuring, validating, and troubleshooting automation hardware and software.
PRIMARY RESPONSIBILITIES
- Configure, validate, and troubleshoot automation system hardware and software.
- Develop and maintain computer programs to control manufacturing and R&D equipment.
- Design and build automated assembly and process equipment.
- Support new product development initiatives.
- Provide equipment support for both the consumables manufacturing group and the assay development group.
- Work closely with cross-functional teams to enhance production capabilities through automation.
- Develop and implement fixtures for manufacturing and assay development.
- Engage with external vendors to source necessary equipment and components.
- Duties may shift based on department priorities and needs.
EXPERIENCE & QUALIFICATIONS
- Bachelor's degree in Computer Science, Electrical, Mechanical, or Systems Engineering required.
- Minimum of 5 years of experience in automation equipment design, design for manufacturing, and assembly; OR a Master's degree with at least 3 years of relevant experience.
- Prior experience in specifying, selecting, and integrating assembly, process control, and inspection instrumentation such as industrial robots, PLCs, machine vision/image processing, and digital/analog sensors is required.
- Proficiency in 3D CAD modeling (SolidWorks preferred).
KNOWLEDGE, SKILLS & ABILITIES
- Strong scientific and analytical background.
- Experience in full lifecycle software development for automation systems using programming languages such as C, C , C , or Visual Basic is preferred.
- Working knowledge of FDA-regulated device manufacturing and experience in the healthcare field is a plus.
- Demonstrated ability to develop, integrate, and validate systems in GMP, ISO, or other regulated production environments.
- Logical problem-solving skills with the ability to prioritize and structure tasks effectively.
- Strong interpersonal, written, and oral communication skills.
- Ability to work efficiently in a dynamic environment with shifting priorities.
- High level of creativity and adaptability.
PHYSICAL REQUIREMENTS
- Ability to communicate effectively and exchange information.
- Operate required equipment and move within the office setting.
WORK ENVIRONMENT
This position will operate in multiple environments, including:
- Standard office setting.
- Engineering lab environment.
- Cleanroom setting, with up to 50% of time spent in cleanroom conditions.