Job 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.

Log on now to our website http://www. qrcgroup.com to learn more about our services and solutions!

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

What We Offer

• 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.