Quality Assurance Scientist

7 days ago


Chaska, United States TalentBurst Full time
Job Title: Quality Assurance Scientist - Senior
Duration: -3 month(s)
Location: Chaska MN

Description/Comment: The Senior Quality Assurance Scientist initiates, designs, develops and implements product design improvements and changes where analysis of situations or data requires a review of identifiable factors
The incumbent organizes and monitors field evaluations of current and new products for customer acceptance and validation; develops, recommends and reviews system design evaluations, service/maintenance plans and procedures, operator manuals and reliability requirements; directly assists customers on product performance issues; teams with Engineering and other departments to troubleshoot instrument and chemistry problems; assists with product definition and specification development; develops and executes test protocols to assess feasibility of product modifications; and prepares service documents
The Senior Quality Assurance Scientist represents QA on current business or product improvement projects
Assure accuracy of product labeling and compliance
Generate, prepare and issue complex data for assigned quality reports
Responsibilities include complaint management activities and failure investigation quality oversight.BS, BA in a Life Science or related studies with 5+years in IVD industry or experienced with medical devices
Knowledge of ISO/FDA requirements experience preferred.

Additional Job Details:
The Quality Assurance Scientist- Senior for ** responsible for Reagent Manufacturing Quality Assurance
This position is part of the Reagent Quality team located in Chaska and will be an on-site position
Our vision is to advance healthcare for every person
You will be working on the Reagent Quality team led by the Quality Assurance Manager responsible for Reagent Manufacturing Quality
If you thrive in a role that prioritizes teamwork and collaboration and want to work to build world-class medical devices—read on.
In this role, you will have the opportunity to:
Provide Quality Assurance support for Reagent manufacturing of medical devices.
Ensure compliance to design change procedures, corporate policies, and global regulations (FDA QSR, ISO, etc.) and make decisions/provide guidance to prevent a deviation or non-conformance
Work with cross-functional team to identify, contain and disposition non-conforming product
Effective interaction with development, technical operations, and manufacturing staff to ensure quality, strive to minimize the costs of reworking or waste and maximize customer satisfaction with the products
Establish and drive to daily management actions for quality processes that support corporate initiatives
Evaluate quality system performance and lead kaizen events to improve process efficiency
The essential requirements of the job include:
BS, BA in a Life Science or related studies with 5+years in IVD industry or experienced with medical devices.
Experience working in a regulated industry It would be a plus if you also possess previous experience in:
Experience working in Quality Assurance
Experience with medical device industry

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