QC Incoming Associate

QRC Group, LLC; Gurabo (PR); On-site; USD 52,000 - 68,000; Full time

Job summary

QRC Group, LLC in Gurabo, Puerto Rico is seeking an experienced QC Incoming Associate to manage reserve samples in regulated environments. You will ensure traceability, perform visual inspections of controlled substances, and support investigations with data gathering.

Requirements include a bachelor’s degree in a scientific discipline, 3+ years in pharma/biotech investigations, bilingual Spanish/English, and proficiency with computer systems.

Qualifications

• Bachelor’s degree in a scientific discipline.
• 3+ years of pharmaceutical/biotech investigations experience.
• Bilingual in Spanish and English with strong written and verbal communication.

Responsibilities

• Manage retain samples of Raw Materials, Finished Goods and Bulk.
• Store reserve samples under specified conditions to preserve integrity.
• Document reserve samples in logbooks and electronic systems for traceability.
• Conduct periodic visual inspection of Controlled Substances and reserve samples.
• Document and report findings from visual evaluations of customer complaints samples.
• Prepare reports on inventory and expiration of Controlled Substances and reserve samples.
• Identify when reserve samples have reached retention period and dispose per regulatory standards.
• Contribute to investigations by gathering data and reviewing evidence.

Skills

Communication skills

Bilingual

Computer proficiency

Education

Bachelor's degree in science

Tools

Electronic systems

Job description

Gurabo, Puerto Rico | Posted on 08/06/2026

We are looking for an experienced QC Incoming Associatewith experience in regulated industries.

Responsibilities:

• Managing retain samples of Raw Materials, Finished Goods and Bulk.
  
• Storing reserve samples under specified temperature and humidity conditions, preventing loss of integrity.
  
• Documenting reserve samples on logbooks and electronic systems, ensuring traceability.
  
• Conducting periodic visual inspection of Controlled Substances and reserve samples.
  
• Documenting and reporting findings from visual evaluations of customers complaints samples, detailing defect categories to aid corrective actions.
  
• Preparing reports regarding inventory and expiration of Controlled Substances and reserve samples.
  
• Identifying when reserve samples have met or exceeded their retention period and disposing them utilizing the corresponding documentation and regulatory standards.
• Contributing to investigations by gathering data and reviewing evidence.
  

Requirements

• Bachelor’s degree in a scientific discipline and at least 3 years of experience in pharmaceutical/biotech investigations.
  
• Bilingual (Spanish and English).
  
• Strong written and verbal communication skills, including facilitation and presentation abilities.
  
• Proficient in computer applications and systems.