Bilingual Quality Systems Supervisor – 2nd Shift

Quality Consulting Group, LLC; Hatillo (PR); On-site; USD 45,000 - 65,000; Full time

Job summary

Quality Consulting Group, LLC is seeking a dedicated professional in Hatillo, Puerto Rico, to oversee Quality Systems in manufacturing operations. The role requires a Bachelor’s degree and fluency in both English and Spanish, along with at least three years of experience in quality assurance and compliance within manufacturing environments.

Responsibilities include supporting quality documentation, managing deviations, and promoting a compliant work environment. If you have strong organizational skills and management experience, we encourage you to apply.

Qualifications

• 3+ years of experience in Quality Systems and Manufacturing environments.
• Experience with management and supervising teams.
• Ability to evaluate compliance issues and ensure company standards.

Responsibilities

• Support and oversee Quality Systems activities within manufacturing operations.
• Investigate and document deviations and non-conformances.
• Ensure compliance with quality standards and company procedures.

Skills

Bilingual (English & Spanish)

Quality Systems

Deviations and Manufacturing

Management and supervision

Organizational skills

Communication skills

Education

Bachelor’s Degree

Tools

SAP

Trackwise

MES

Job description

QUALITY CONSULTING GROUP, a leader inthe 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

QUALITY CONSULTING GROUP, a leader inthe 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