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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:        

• 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

• Champion Lean Transformation and OE initiatives; facilitate the drive towards continuous improvement in all Manufacturing areas.

• Support DI&B initiatives to increase inclusion, connectivity, and engagement within the team

Qualifications:

• Bachelors degree or Associate degree

• 1-3 years work experience in manufacturing or operations.

• Experience working in a team.

• Comfortable handling chemicals or can demonstrate the importance of lab safety.

• Able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work

• Experience with Systems MS office suite

• Good written communication

• Experience with troubleshooting (does not need to be biotech)

• Available to work various shifts (day/nights) as dictated by the production schedule Able to work in teams to complete operational tasks

• Night Shift 6:45PM - 6:45AM

• C and D Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days. Candidates must be available to work weekends.

  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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