Associate Specialist, Quality Assurance
$52,800–$66,000 year
On-siteTustin, California, United States
Job Summary
Manage administrative tasks for Avid's electronic document and training systems, including assigning curricula, generating reports, and revising training materials. Reconcile equipment and laboratory logbooks, issue controlled documents, and file or retrieve items from the QA archive. Deliver formal and informal training to coworkers on quality systems, training, and GMPs while enforcing Good Documentation Practices. Support customers with document revisions and requests, collaborate on departmental initiatives, and maintain inspection readiness during regulatory audits. This full-time onsite role requires Monday through Friday hours (8:00 a.m. to 5:00 p.m.) with potential overtime or weekend work.
Required Qualifications
- B.A. or B.S. degree (preferably in Life Science)
- Minimum of 1+ years of experience in the biopharmaceutical industry
- Knowledge of CGMPs or equivalent regulations
- Ability to interpret Quality standards for implementation
- Skills to independently evaluate situations and propose potential solutions
- Must have the ability to work overtime and/or weekends when necessary
- You have a 'bring it on!' team player approach
- You have an unshakable positive attitude
- Your written and verbal skills are out of this world
- You communicate with clarity and confidence
- You have exceptional multitasking skills
- You have an unparalleled attention to detail
- You are a master at building relationships
- Your visual acuity, including close, distance, and color vision, will be essential
Desired Qualifications
- preferably in Life Science
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