Deviations Owner: Lead QA & CAPA in GMP

MENTOR Technical Group Corporation; Juncos (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

MENTOR Technical Group Corporation is seeking a professional specializing in deviation management in Juncos, Puerto Rico. This role involves leading deviation processes, coordinating with quality teams, and ensuring regulatory compliance in FDA-regulated environments.

The ideal candidate holds a Bachelor’s degree and has 5-10 years of relevant experience. Strong problem-solving and communication skills are essential. Join us in supporting life sciences clients with high quality and compliance standards.

Qualifications

• Minimum of 5–10 years’ experience in deviation management, quality assurance, or compliance in FDA‑regulated environments.
• Strong understanding of GMP, FDA regulations, and quality systems.
• Ability to collaborate effectively across teams.

Responsibilities

• Serve as the primary owner for deviations, ensuring proper documentation and resolution.
• Coordinate with production and QA/QC to evaluate deviations and implement corrective actions.
• Monitor deviation trends and provide reports to management.

Skills

Deviation management

Quality assurance

Analytical skills

Problem-solving skills

Communication skills

Education

Bachelor’s degree in Life Sciences, Engineering, Pharmaceutical Sciences, or related field

Tools

Deviation tracking systems

CAPA management

Electronic quality management systems (eQMS)

Job description

MENTOR Technical Group Corporation is seeking a professional specializing in deviation management in Juncos, Puerto Rico. This role involves leading deviation processes, coordinating with quality teams, and ensuring regulatory compliance in FDA-regulated environments.

The ideal candidate holds a Bachelor’s degree and has 5-10 years of relevant experience. Strong problem-solving and communication skills are essential. Join us in supporting life sciences clients with high quality and compliance standards.