Title: Quality Assurance Specialist – GMP
Location: Los Angeles, CA
Duration: End date 08/31/2022 (Possible extension)
Description:
Title: Trackwise Specialist
Onsite Expectations: Onsite training, first few months. Opportunity to transition partial, possibly fully remote. No gowning required. Must be able to work overtime as required.
Primary Responsibilities: The primary responsibility of this role is to manage deviation and CAPA records in Trackwise. Role requires performing administrative duties such as filing timely extensions and progressing records through the action and effectiveness phases. Must be able to manage multiple records at once. Must be comfortable communicating with different departments to get updates on action items. Able to follow general writing template and receive feedback. Opportunity to develop and/or implement sustainable tracking system to manage records. Other responsibilities may include trending, data compilation, and other similar tasks as assigned.
Job Requirements:
Skills/Qualifications:
Must have strong organizational skills
Must have solid writing skills
Must have strong attention to detail
Trackwise experience preferred
Pharmaceutical background preferred