QUALITY CONSULTING GROUP, a leader inthe 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 :

• Following Good Manufacturing Practices (GMPs) and applicable regulations from the Code of Federal Regulations (CFRs).
• Reporting any discrepancies to the Team Leader or Production Supervisor to ensure quality standards and safety.
• Ensuring quality & compliance through a Right First-Time mentality.
• Receiving and preparing components for use in manufacturing.
• Feeding components into equipment and performing sanitation activities.
• Documenting appropriate paperwork, understanding Overall Equipment Effectiveness (OEE) / performance metrics, and participating in daily performance meetings.
• Use of pallet jacks and manual wrapping of pallets.
• Use of computer systems to support material inventory and electronic batch record.
• Partnering with cross-functional teams to drive improvement opportunities.
• Ensuring components and products are available for continuous operation.

Qualifications :

• Associate degree or High school diploma / GED
• 1 year of Manufacturing or Operations experience
• 1 plus years of experience in a GMP / other regulated environment.
• Demonstrated knowledge of GMP principles.
• Drug substance manufacturing experience.
• Ability to stand or sit for extended periods of time.
• Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.
• Ability to document process tasks in electronic batch records.
• Ability to perform assignments with a high degree of focus / attention to detail.
• Ability to work anyshift and12-hour shifts if needed.
• 1st shift is 630am - 3pm
• 2nd shift is 230pm -11pm
• 3rd Night shift 10 : 30pm - 7am

Last updated : 2024-05-17