JT691 - ASSOCIATE 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:

• Load components and materials into packaging equipment.
• Operating a variety of packaging equipment (Assembly, labeler, cartoner, case packer, autoinjector testing, ID testing)
• Maintaining strict adherence to SOP and cGMP requirements and expectations
• Assist in troubleshooting equipment and system errors as needed (or escalate to management).
• Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).
• Specific responsibilities include inspection and packaging of product-filled vials per procedures and batch records.  
• Routine maintenance and cleaning of equipment
• Assisting or participating in other manufacturing operations (e.g., filling support activities)
• Internal support operations (e.g. stocking items, tracking inventory, material movement)
• Recognizing and reporting malfunctions and making necessary adjustments to equipment. 
• Training new MPTs on routine tasks.
• Reconcile components and products and calculate product exposure to room temperature.

Qualifications: 

• High school/GED 1 year of work or military experience or Associate degree
• Required to know, comprehend, and apply packaging configurations, as well as understand, follow and document batch records for the inspection and packaging process.
• Tech Savy and have good attendance record is required.
• Pharma experience is preferred but not required.
• Has a track record of being fluent in technology (navigating computer systems and software beyond just Microsoft products) and using those skills in a fast-paced manner.
• Prior experience in cGMP environments.
• Filling and finishing manufacturing experience, preferably vial inspection
• Understanding of measurements, calculations and the metric system
• Candidate must be willing to work with 12 hours rotational shift with breaks. 6AM - 6:30PM

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.

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