Specialist QA

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

Job summary

QRC Group in Juncos, Puerto Rico is seeking a QA Specialist to support quality and manufacturing operations, including batch record review, GMP documentation, electronic systems management, and inventory control. The ideal candidate is detail-oriented, able to work independently in a fast-paced environment, with strong communication, organizational, and problem-solving skills.

The role requires experience with GMP, GDP, data integrity, SAP inventory management, and eBR systems, and involves

Qualifications

• Perform comprehensive Batch Record Review for completeness, accuracy, and GMP compliance.
• Experience with GMP-regulated environments and Data Integrity requirements.
• Strong ability to manage multiple priorities with minimal supervision.

Responsibilities

• Review batch records for completeness and compliance.
• Assist quality operations in GMP/documentation management.
• Participate in manufacturing and quality operations meetings.

Skills

Batch record review

GMP compliance

Data integrity

Communication

Organizational skills

Problem solving

Independent work

Education

Doctorate or Masters + 2 years

Bachelor's + 4 years

Tools

SAP inventory management

PAX

eBR systems

Job description

Juncos, Puerto Rico | Posted on 09/03/2026

We are seeking a QA Specialist to support Quality and Manufacturing operations through batch record review, GMP documentation compliance, electronic systems management, inventory control, and quality decision-making. The ideal candidate is detail-oriented, able to work independently in a fast-paced environment, and possesses strong communication, organizational, and problem-solving skills.

Requirements

• Education: Doctorate or Masters + 2 years of directly related experience or Bachelors + 4 years of directly related experience.
• Perform comprehensive Batch Record Review to ensure completeness, accuracy, compliance, and adherence to approved procedures and GMP requirements.
• Experience performing Batch Record Review in a GMP-regulated environment.
• Strong knowledge of GMP, GDP, and Data Integrity requirements.
• Experience with SAP inventory management and material reconciliation.
• Experience using PAX and/or Electronic Batch Record (eBR) systems.
• Ability to assess quality/compliance issues and apply risk-based decision making.
• Experience participating in manufacturing and quality operations meetings.
• Strong organizational skills and ability to manage multiple priorities with minimal supervision.