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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.

+ 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.

+ Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.

+ Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging.

+ Must follow Good Manufacturing Practices (GMPs).

+ Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.

+ Train fellow staff on the manufacturing processes, equipment, and general

+ Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.

Qualifications:

+ Associate's degree and 6 months work experience OR Bachelor's degree in Mechanical, Electronic Engineering Technology or Industrial Mechanics.

+ 2-3 years of experience or recent grad.

+ Working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment.

+ Excellent attention to detail, good organization, and capable of working independently.

+ Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions.

+ Able to follow written procedures.

+ Able to lift 35 pounds, stand or sit for extended periods of time.

+ Capable to diagnose malfunctions and perform equipment setup.

+ Experience working with Human Machine Interfaces (HMIs).

+ Working Shift: 12 hour shifts 6:00 pm - 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.

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