QA Associate
TalentZok
San Diego, CA
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JOB DETAILS
SALARY
$20–$32 Per Hour
LOCATION
San Diego, CA
POSTED
6 days ago
QA Associate - Simply Biotech
OVERVIEW
Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below.
Immediate opening for a QA Associate in San Diego, CA who possess:
- Experience working in an ISO 1345 environment
- Experience writing and maintaining control documents
- 1+ years of QA experience in med device
Email resumes to
tness@simplybiotech.com
or call 858.258.6501.FULL DESCRIPTION: We are seeking a quality assurance associate to monitor the effectiveness of our QA system on an ongoing basis, recommending and implementing any changes that promote continual improvement, validating processes; and completing and organizing documentation. Our ideal candidate can think big- helping to develop our infrastructure, while also acting on improving upon our operational systems.
The selected candidate will be responsible for:
- Create and maintain Company Quality Management System documentation, including but not limited to: quality manual, quality procedures, work instructions and any related forms.
- Manage and maintain the Company quality inspection and product release programs for incoming and in-process materials, components, production processes and finished goods.
- Interface with Purchasing to assure that applicable quality requirements are included on all purchasing documentation.
- Perform Supplier Evaluation audits at the facilities of potential suppliers.
- Serve as Lead Auditor for Quality Management System internal audits.
- Serve as the designated representative of the Quality Manager for Material Review Board activities.
- Interface with Engineering and Operations to assure that the transfer to Production of new products is in accordance with approved procedures.
- Evaluate customer complaints and participate in Corrective and Preventive Action reviews
- Provide Root Cause Analysis for conditions found to be adverse to quality.
- Serve as the Company Safety Engineer regarding the processing of Hazardous Materials, interfacing with applicable federal, state and local authorities and maintaining records of these activities.
- Maintain and update, as required, facility schematic diagrams.
- Spearhead Company continuous improvement activities to enhance the Quality Management System, utilizing tools such as: 5S, Six Sigma and total process improvement (TPI) techniques.
The selected candidate will also possess:
- High school diploma and/or GED
- Proficiency with Microsoft Office, Word, and Excel
- Well organized, flexible and enjoy the administrative challenges of supporting an office of diverse people
- Keen attention to detail and eye for improvement
- Due to small business environment, must be able to assume responsibilities beyond scope of job description.
- Leadership and coordination skills.
- Flexible and organized. Able to plan and organize activities accordingly and handle various tasks simultaneously.
- Decision making skills and ability to work independently in a start-up environment.
- Strong verbal and written communication skills
Salary Range: $20.00 - $32.00/hour
For immediate and confidential consideration, please email your resume to
For immediate and confidential consideration, please email your resume to
tness@simplybiotech.com
or call 858.258.6501More information can be found at www.simplybiotech.com
About the Company
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