Softpath System
Job Description:
Our company is seeking a team member to join our Hardware Manufacturing Team. In this role you will align, calibrate and execute test methods of varied complexity according to operational plans and customer demand. We're looking for associates whom thrive in a team-oriented, goal focused environment. We operate using Daily Management principles, providing immediate guidance and feedback to our associates and focusing on daily, monthly, and quarterly objectives. You'll be responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material and the execution of work orders to on-time completion. Looking for associates who meet the qualifications below. Our work delivers both instruments and reagents to customers in hospital and laboratory environments, supporting patient health.
Key responsibilities: • Must read, write and speak fluent English to understand the SOP/work instructions provided. Proficiency with Microsoft applications. • Experience with hand tools is a plus for some departments. Able to execute assembly tasks following standard operating procedures with supervision. Troubleshoot issues as they arise, escalating as necessary, Assure compliance with FDA Quality System Regulations (QSR). • Good Manufacturing Practices (GMP), and ISO regulatory requirements; Learn and participate in the company's lean manufacturing principles. Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality. Identify and recommend quality improvements including but not limited to production methods, equipment performance, product quality and efficiencies. Maintain a safe and clean working environment by complying with procedures, rules, and regulations. • Train new team members on equipment operations and work procedures as needed. Ability to complete appropriate paperwork, maintain accurate records of production and report status of work.
Education/Experience: • High school degree (or equivalent degree). • Must have 0-2 years' relevant experience. • Experience in a regulated industry preferred (e.g. FDA, ISO).
Key responsibilities: • Must read, write and speak fluent English to understand the SOP/work instructions provided. Proficiency with Microsoft applications. • Experience with hand tools is a plus for some departments. Able to execute assembly tasks following standard operating procedures with supervision. Troubleshoot issues as they arise, escalating as necessary, Assure compliance with FDA Quality System Regulations (QSR). • Good Manufacturing Practices (GMP), and ISO regulatory requirements; Learn and participate in the company's lean manufacturing principles. Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality. Identify and recommend quality improvements including but not limited to production methods, equipment performance, product quality and efficiencies. Maintain a safe and clean working environment by complying with procedures, rules, and regulations. • Train new team members on equipment operations and work procedures as needed. Ability to complete appropriate paperwork, maintain accurate records of production and report status of work.
Education/Experience: • High school degree (or equivalent degree). • Must have 0-2 years' relevant experience. • Experience in a regulated industry preferred (e.g. FDA, ISO).