100% onsite role at Thousand Oaks, CA - 9-5:30 (30 minute lunch)
Lab Based
Bachelor's degree.
Nice to have: documentation practices, GMP, previous lab experience.
Responsibilities:
Receive, clean, and evaluate product complaint return samples
Interface with various Amgen sites and business partners
Manage complaint return sample inventory
Author technical assessment reports
Requirements:
Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation according to company guidelines. Be self motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Written and verbal communication & collaboration skills. Strong word processing, database and spreadsheet application skills. Strong organizational skills with the ability to manage multiple projects or assignments. Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50lbs. Role may involve transporting samples to different buildings across campus.
Basic Qualifications
High school/GED + 4 years [Job Code Discipline OR Sub-Discipline] work experience OR Associate + 2 years [Job Code Discipline OR Sub-Discipline] work experience OR Bachelor + 6 months [Job Code Discipline OR Sub-Discipline] work experience Master
Top 3 Must Have Skill Sets:
Attention to Detail
Communication both written and oral
Self motivated
Pay Rate between $28 - $32/Hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"