Quality Systems Specialsist
Collabera
Apply to this job Goleta, CA, us on site Until 8/23/2026 H-1B sponsor history First posted March 22, 2025 Last posted March 22, 2025
Job description
- Experience in a Medical Device manufacturing environment working with Quality System processes such as Corrective and Preventive Action (CAPA).
- Experience using Trackwise software for tracking of quality system records. 4 year degree required Experience working with cross functional teams to identify and address quality issue root causes.
- Experience and ability to produce clear, concise quality records. Ability to articulate information when communicating with others.
All your information will be kept confidential according to EEO guidelines.
About this role
Summary
Manage quality system processes, track records, and collaborate on root cause analysis in medical device manufacturing.
Job title
Quality Systems Specialist
Experience level
4+ years
Industry
healthcare
Location requirements
On-site in Goleta, CA, no remote work allowed.
Salary
Not specified
Visa sponsorship
H-1B sponsor history
Management role
No
Skills & keywords
Required skills
quality system processesCAPAtrackwisecommunication
Preferred skills
None specified
Specializations
quality systemsCAPAtrackwisemedical device
Locations
Structured locations inferred from the posting.
Goleta, CA, USA
On-site City
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