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A leading company in IT Services and Consulting is seeking a Senior Quality Assurance Associate to join their team. The ideal candidate will have a Bachelor's degree in life sciences and 2+ years of experience in quality assurance within the GMP pharmaceutical or medical device industry. Responsibilities include evaluating product complaints and authoring technical reports. This entry-level contract position offers a dynamic work environment focused on quality and compliance.
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Bachelor's degree. Nice to have: documentation practices, GMP, previous lab experience.
Hiring Manager Intake Notes
Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2+ years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operations according to company guidelines. Be self-motivated, attentive to details, and able to prioritize and meet deadlines. Basic statistical skills including data trending. Basic project management skills. Ability to understand, follow, and implement instructions independently. Strong communication, collaboration, word processing, database, and spreadsheet skills. Good organizational skills to manage multiple projects. Role may involve prolonged sitting, standing, lifting up to 50 lbs, and transporting samples across campus.
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Locations and salary ranges vary, including Camarillo, Los Angeles, and Simi Valley, CA.