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:        

• Work in a dynamic production environment at site supporting development, clinical, and launch activities.

• Under general supervision, employee will perform operations in the Manufacturing area.

• Operations will be performed according to Standard Operating Procedures (SOPs).

• Performing in-process sampling of equipment and operating analytical equipment

• Performing washroom activities: clean small- and large-scale equipment used in production activities.

• Maintaining an organized and clean workspace.

• Initiating quality reports.

• Drafting and revising documents (SOPs, MPs)

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

• Review/complete training daily

• Attend and Participate in daily shift huddles

• Perform and complete assigned tasks safely

• Elevate concerns, processes concerns, and questions to lead and manager

Qualifications:

• Bachelor’s Degree in Science

• Four (4) years of relevant experience

• Safety Minded

• Quality Minded

• Organizational Skills.

• Shift is Sunday - Wednesday 6am -5pm

• Available to work various shifts (weekends, holidays, 4x10hrs)

  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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