COMPANY DESCRIPTION

medmix is a global leader in high-precision delivery devices. We occupy leading positions in the healthcare, consumer, and industrial end-markets. Our customers benefit from our dedication to innovation and technological advancement that has resulted in over 900 active patents. Our 14 production sites worldwide, together with our highly motivated and experienced team of nearly 2’700 employees provide our customers with uncompromising quality, proximity, and agility. medmix is headquartered in Baar, Switzerland. Our shares are traded on the SIX Swiss Exchange (SIX: MEDX).
www.medmix.swiss

JOB DESCRIPTION

We are seeking an experienced and highly skilled Manufacturing Automation Engineer to join us at medmix Healthcare US Inc., at our new Greenfield Site located in Flowery Branch, Georgia USA.
This role focuses on developing, implementing, and maintaining automated systems and equipment in the production of medical devices and products. The ideal candidate will have experience in automation, robotics, and control systems within the medical device manufacturing industry, ensuring compliance with regulatory standards such as FDA, ISO 13485, and Good Manufacturing Practices (GMP).

QUALIFICATIONS

Work experience: minimum 4 years of experience in automation, preferably within a medical device or regulated manufacturing environment
Education: Bachelor’s degree in mechanical engineering, industrial engineering or related field, or equivalent experience. Advanced degrees or certifications (e.g., Lean Six Sigma, Certified Automation Professional) are a plus

TECHNICAL SKILLS

• Proficiency in PLC programming and troubleshooting (Allen-Bradley, Siemens, etc.)
• Experience with robotics and vision systems integration (e.g., FANUC, KUKA, EPSON, ABB, Cognex, Keyence)
• Knowledge of SCADA systems and industrial networks
• Familiarity with automation-related software (e.g., AutoCAD, LabVIEW, etc.)

PROBLEM-SOLVING SKILLS

• Strong analytical and problem-solving skills, with the ability to troubleshoot complex automation systems and processes.

• Automation Systems Design & Implementation: design, implement, and maintain automated manufacturing systems for medical device production lines. This includes working with robotics, automated equipment, PLCs, SCADA, vision systems, and other automated technologies.
• Process Optimization: continuously monitor and improve manufacturing processes, utilizing automation to enhance efficiency, reduce variability, and improve quality control.
• System Integration & Troubleshooting: integrate automation equipment into existing production lines. Troubleshoot and resolve issues with automated systems, ensuring minimal downtime and maintaining system reliability. Mechanical or electrical troubleshooting of equipment.
• Regulatory Compliance: Ensure that all automation systems and processes comply with regulatory standards, including FDA regulations, ISO 13485, and GMP. Document design, validation, and testing processes for regulatory purposes.
• Collaboration with Cross-Functional Teams: work closely with engineering, production, quality assurance, and maintenance teams to ensure the successful deployment and maintenance of automation systems. Support qualification and validation activities related to any automation that required qualification Assist in evaluation, and selection of automation equipment based on production needs and cost-effectiveness.
• Training & Support: Provide training to production staff on new automation systems and equipment. Offer ongoing technical support and troubleshooting as needed.