JT001 - QUALITY SUPERVISOR

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:

• Support and oversee Quality Systems activities within manufacturing operations
• Investigate and document deviations, non-conformances, and quality events
• Ensure compliance with company procedures and quality standards
• Collaborate with Manufacturing and Quality teams to support continuous improvement initiatives
• Review and maintain quality documentation and records
• Assist in audits, inspections, and corrective action follow-up activities
• Promote a safe and compliant work environment

Qualifications:

• Bachelor’s Degree required
• Fully bilingual (English & Spanish)
• Minimum of 3 years of experience in: Quality Systems, Deviations and Manufacturing environments
• Must have management and supervisor experience
• Quality Professional with Manufacturing Process Audit and Batch Record Review experience
• Ability to evaluate compliance issues
• Able to perform review, approval and tracking of cGMP processes, procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise; including but not limited to Deviation’s, CAPAs, and validations
• Strong organizational and communication skills
• Available to work administrative shift
• Support 2nd shift if needed