Process Tech

Posted 11 July 2024
LocationHudson
Job type Permanent
Reference200582
Contact NameCameron Cyker

Job description

Job Summary:

The Process Technician will be responsible for supporting the manufacturing processes of our medical devices, ensuring they meet stringent quality standards. This role involves monitoring and optimizing production processes, troubleshooting issues, and implementing improvements to enhance efficiency and product quality.

Key Responsibilities:

  • Monitor Production Processes: Regularly observe and assess manufacturing processes to ensure they operate efficiently and effectively.
  • Troubleshoot and Resolve Issues: Identify and address any problems or defects in the production line to minimize downtime and ensure product quality.
  • Implement Process Improvements: Collaborate with engineering and quality teams to suggest and implement process enhancements.
  • Maintain Equipment: Perform routine maintenance on production equipment to ensure optimal performance and longevity.
  • Documentation: Accurately document all processes, changes, and maintenance activities in compliance with regulatory requirements.
  • Quality Assurance: Ensure all products meet the company’s quality standards and comply with industry regulations.
  • Training: Assist in training production staff on new processes, equipment, and quality standards.

Required Qualifications:

  • Education: Associate degree in Engineering, Manufacturing Technology, or a related field, or equivalent work experience.
  • Experience: Minimum of 2 years of experience in a similar role within the medical device or a regulated manufacturing industry.
  • Skills:
    • Technical Skills: Proficiency in using and maintaining manufacturing equipment, understanding of manufacturing processes and quality control.
    • Soft Skills: Strong problem-solving abilities, excellent attention to detail, effective communication skills.
  • Certifications: N/A (but any relevant certifications in manufacturing or quality control are a plus)

Preferred Qualifications:

  • Experience with Lean Manufacturing, Six Sigma, or other process improvement methodologies.
  • Knowledge of regulatory requirements for medical device manufacturing (e.g., FDA, ISO 13485).