QA Associate
Gilead - Foster City, CA

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Gilead Sciences is seeking a Quality Assurance professional, to be located in Foster City, CA, with experience in active pharmaceutical ingredients to support Gilead’s commercial programs.

Responsible for providing general QA support to QA Specialists, as required. Other key responsibilities include: coordinating site qualification activities and maintaining files (hard copy and electronic); coordinating Event Review Team sessions and maintaining associated records; maintaining general vendor files, such as audits, qualifications, correspondence; providing LIMS support for trending and COA issuance; reviewing executed batch records and preparing/approving IQS records. Duties may also include reviewing change request documentation and preparing/auditing related parameter comparison tables.

Essential Duties and Job Functions:
Performs a variety of activities to ensure compliance with internal processes and procedures. Supports, through routine tasks, investigations by more experienced QA colleagues and corrective and preventive action (CAPA) related to manufactured products. Normally receives direct instruction on routine work.

Knowledge, Experience and Skills:
0+ years of relevant experience in a GMP environment related field and an AA degree. Prior experience in the pharmaceutical industry is beneficial. Works on routine to moderately detailed assignments requiring the ability to recognize deviations from accepted practice and discrepancies in data. Must be able to balance multiple tasks in a busy and time-sensitive environment. Must have efficient ability using Word and Excel. Demonstrates good verbal, written, and interpersonal communication skills.

About this company
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Gilead Sciences has biotech balms for infectious diseases, including hepatitis, HIV, and infections related to AIDS. The company's HIV...