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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 dynamic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

+ Create a positive work environment through interactions with team members

+ Hands-on operations: set-up, operation, and sanitization of various manufacturing equipment

+ Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance

+ Using computer systems, performing and monitoring critical processes with the ability to perform basic troubleshooting

+ Performing in-process sampling of drug substance and operating analytical equipment (pH meters, conductivity meters, BGAs, etc.)

+ Working around high-pressure systems, occasionally work around/moving heavy equipment

+ Operate or comfortable learning to operate electric pallet jack

+ Performing parts washing and sterilization activities

+ Weighing out buffers/media per procedures.

+ Maintaining an organized and clean workspace

+ Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work

+ Recognize and raise hand for potential safety or quality concerns

+ Assisting in the review of documentation for assigned functions (equipment logs, batch records)

+ Initiating and being involved quality deviation reports, as required.

Qualifications:

+ High school/GED + 1 year of work or military experience or Associate degree.

+ Basic understanding of GMP principles

+ Direct experience utilizing Stand Operating Procedures to perform activities.

+ Experience working in teams

+ Understands the principles of safety culture and working with integrity

+ Lab exposure and worked in an environment where safety is top priority.

+ Track history of steady employment and timeliness.

+ Experience using computers or automated systems

+ Experience with manufacturing documentation

+ Strong eagerness to learn and shows a sense of ownership in their work or experiences

+ 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 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.

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