JT381 - MANUFACTURING PROCESS TECHNICIAN

QUALITY CONSULTING

GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

Operating an automated and innovative manufacturing equipment for the packaging operations of our products. This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing and robotic automation. In addition to equipment operation and troubleshooting, the technician will ensure product quality as a result of the performance of the equipment. Based on their mechanical proficiency, the process technician will conduct machine troubleshooting and problem-solving skills in a fast-paced manufacturing environment. Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency. Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment. Assist as training resource on manufacturing tasks and equipment use Use human machine interfaces (HMIs) to identify alarms and correct line stoppages. Ensures components and products are available for a continuous operation. Carries out equipment inspections and generates emergency, corrective, or preventative work orders. Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes. Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs).

Qualifications:

Associate's degree (Educational Background in Mechanical, Electronic Engineering Technology or Industrial Mechanics) preferred. 2 years of technical experience in Pharmaceutical, Manufacturing, or Packaging environment Working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment. Excellent attention to detail, good organization, and capable of working independently. Ability to use computer systems to support the material inventory system (SAP transactions) and electronic batch records. Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills. (12 hour shifts 6pm-6:30am) Swing shift with alternating days Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.