Sample Processing Associate
5555 Valley Blvd Los Angeles, CA 90032 US
Job Description
Summary: Responsible for transporting and distributing samples to different QC laboratories for testing, packaging and shipping samples for outside lab testing.
Primary Responsibilities:
-Transport samples from Valley Blvd. manufacturing plant to QC Labs using a golf cart.
-Pick up and drop off QC documentation to and from QC.
-Log the samples into LIMS (Laboratory Information Management System).
-Distribute the samples to QC laboratories for testing and make entries on the sample tracking forms and sample log forms in each lab
-Package samples and schedule delivery of samples to contract laboratories for testing.
-To assist in other duties, such as filling and archiving documents, that is deemed necessary by the supervisor
Knowledge, Skills and Abilities:
Knowledge of computer applications and basic computer skills (MS Office, Outlook, Word, Excel). Knowledge of LIMS (Laboratory Information Management System) is a plus.
Must have valid driver’s license. Good organizational skills with ability to perform multiple priorities efficiently and effectively. Excellent verbal and written communication. Must be able to read, write, and speak English. Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner. Ability to manage multiple projects simultaneously, meet deadlines, and handle an ever changing, fast paced critical work environment. Strong organizational, analytical and problem-solving skills. Ability to analyze details and perform structured decision-making on a daily basis. Self-starter with good work ethic and ability to work independently with minimum supervision and use good judgment, or as a contributing member of a team. Must be proactive, results oriented, and have strong attention to detail. Ability to keep neat, accurate and complete records and logs.
Education: Minimum High School Diploma or GED
Experience: Experience in an FDA regulated manufacturing facility - pharmaceutical, biologics, biotech, or medical device industry, with knowledge of cGMPs, FDA regulations, and industry guidelines is preferred
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