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:

• Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).
• Loading component into machine with possibility to learning/qualifying on other pieces of equipment.
• Maintaining strict adherence to SOP and cGMP requirements and expectations.
• Load components and materials into packaging equipment.
• Inspection and packaging of product-filled vials per procedures and batch records.
• Performing routine maintenance and cleaning of equipment.
• Assist in troubleshooting equipment and system errors as needed (or escalate to management).

Qualifications:

• High school/GED + 1 year of work or military experience or Associate degree
• Flexible schedule, strong work ethic
• Able to stand for extended periods of time, and able to occasionally lift up to 50lbs.
• No prior manufacturing experience is required but would be a plus.
• Filling and finishing manufacturing experience, preferably vial inspection
• Understanding of measurements, calculations and the metric system
• Basic GMP knowledge
• Candidate must be willing to work with 12 hours shifts

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.