JT844 - 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:        

• Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
• Weighing out buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
• Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
• Performing and monitoring critical processes with the ability to perform basic troubleshooting
• Performing in-process sampling of equipment and operating analytical equipment
• Performing parts washing and sterilization activities
• Maintaining an organized and clean workspace
• Initiating and being involved quality deviation reports, as required
• Drafting and revising documents (SOPs, MPs)
• Identifying, recommending, and implementing improvements related to routine functions
• Assisting in the review of documentation for assigned functions (equipment logs, batch records)
• Working around high-pressure systems, occasionally work around/moving heavy equipment with powered industrial vehicles
• Perform routine manufacturing process operations (equipment cleaning, dispensing of raw materials/components, material reconciliation etc.)
• Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs)

Qualifications:

• Associate degree OR High school diploma / GED
• 1 year of Manufacturing or Operations experience
• Ability to follow Standard Operating Procedure (SOP)
• Experience in a technical field
• Experience with advance computer systems
• Understands the principles of safety culture and working effectively on a team, lab exposure and worked in an environment where safety is top priority.
• Experience in Biotech cross lateral could be anything with batch chemicals or chemical processing
• Night Shift: 6:45pm 6:45AM
  Swing Shift - Week 1 is 5 working days Week 2 is 2 working days.
  Candidates must be available to work weekends and holidays.

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.