QC Incoming Associate

QRC; Gurabo (PR); On-site; USD 60,000 - 95,000; Full time

Job summary

QRC Group, LLC is seeking an experienced QC Incoming Associate with regulated industry experience. You will manage and document reserve samples, perform visual inspections, and support investigations with data and evidence in a pharmaceutical/biotech setting.

Role requires a scientific degree, 3+ years in investigations, and bilingual Spanish/English communication. Strong documentation and computer skills are essential for maintaining traceability and regulatory compliance.

Qualifications

• Bachelor's degree in a scientific discipline and at least 3 years in pharma/biotech investigations.
• Bilingual Spanish and English.
• Strong written and verbal communication, facilitation and presentation skills.
• Proficient with computer applications and systems.

Responsibilities

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

Skills

Bilingual Spanish and English

Communication skills

Computer proficiency

Education

Bachelor's degree in a scientific discipline

3+ years of pharma/biotech investigations experience

Job description

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Job Description

We are looking for an experienced QC Incoming Associate with 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 on investigations by gathering data and reviewing evidence.

Qualifications

• 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.

Additional Information

Benefits

• Opportunities for learning, development, and professional growth.
• A collaborative and supportive work environment.
• The opportunity to work with industry-leading clients on impactful projects.

Your information will be kept confidential according to EEO guidelines.