QC Incoming Associate

QRC Group; Gurabo (PR); On-site; USD 55,000 - 75,000; Full time

Job summary

QRC Group in Gurabo, Puerto Rico is seeking an experienced QC Incoming Associate to manage retain samples of materials and ensure traceability under regulatory standards. The role involves storage under controlled conditions, documentation, and periodic inspections of controlled substances.

Requirements include a bachelor’s degree in a scientific field, at least 3 years in pharmaceutical/biotech investigations, and bilingual (Spanish/English) communication skills.

Qualifications

• Bachelor’s degree in a scientific discipline is required.
• Bilingual in Spanish and English is required.
• Strong written and verbal communication and presentation skills are required.

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.

Skills

Bilingual (Spanish and English)

Strong written and verbal comms

Proficient in computer applications

Education

Bachelor’s degree in a scientific discipline

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.