
QA Specialist I
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Overview
Job Description
Duties
" Support final release of finished medical device products.
" Review Device History Records (DHR) for accuracy, completeness, and compliance.
" Verify that released products meet established quality standards prior to shipment.
" Review both 3rd floor Instrument products and ACP jobs.
" Identify documentation errors and escalate quality issues as needed.
" Collaborate with cross functional teams to resolve issues and support continuous improvement.
Required Experience
" 0 2 years of quality, manufacturing, or documentation review experience.
" Ability to work with minimal guidance and follow defined procedures.
Key Skills
" Strong attention to detail
" Quality Assurant background is a plus
" Effective communication
" Problem solving ability
" Teamwork and collaboration
" Ability to work independently with minimal supervision
Preferred Experience
" Quality Assurance (QA) experience
" Batch Release experience
" Non Conformance documentation
" Process improvement involvement
Education
" High School Diploma or equivalent required (Preferred BS)
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.
