What are the responsibilities and job description for the JT472 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN position at Quality Consulting Group?
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:
- 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. - Perform basic, routine manufacturing process operations such as dispensing of raw
materials, material reconciliation, line clearance, basic analytics, and record transactions - Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs,
area audits and batch records) - 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 as needed in the Maximo system. - Troubleshoot and identify potential solutions for mechanical errors, safety issues or general
operating inefficiencies within the production processes. - Partner with cross-functional teams to help drive improvement opportunities.
Qualifications:
- Associate degree or High school/GED 1 year of related work experience
- Experience in manufacturing or operations.
- Able to use computer systems to support material inventory system (SAP transactions) and
electronic batch records. - Knowledge of equipment/process validation protocols independently.
- Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging.
- Must follow Good Manufacturing Practices (GMPs).
- Shift is 6:00am - 6:30pm (1st and 12hrs)
- Schedule is 3 days week 1 Mon, Thurs, Friday - 4 days week 2 Tues, Wed, Sat, Sun
Must work every other weekend
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.
