Full Job Description
As a Quality Assurance Associate I, you will have a strong desire to be part of our Quality Team and assist in the administration of the Document Control and Quality Management System (QMS). As well as perform Quality Assurance (QA) product release. You will possess strong attention to detail and have a collaborative and team-oriented disposition.
Administer the Document Control system.
Perform QA product release.
Support development and updates for SOPs, work instructions and other quality documentation.
Review records and documents, for completeness and compliance with QSR and ISO requirements.
Assist Quality Management with various projects, as required
Support the eQMS electronic documentation system, as needed
0-3 years of related experience in a GMP and/or FDA regulated industry
Bachelor's degree in engineering, science, business, or liberal arts
Strong communication skills (written, oral, and listening)
High level of initiative with the ability to self-manage
Strong interpersonal skills with the ability to work independently and as part of a team
Excellent analytical skills
Working knowledge of FDA Quality System Regulation, ISO Standards, and other regulatory agencies
Experience in the medical device and/or pharmaceutical industry
NanoString is an Equal Employment Opportunity and Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. NanoString does not accept unsolicited agency resumes and will not pay fees to any third-party agency or company that it does not have a signed agreement with.
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