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.