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