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LifeBondAn ISO 13485 certified, leading medical device company located in Caesarea is searching for a QA Engineer to lead QMS activities for the development and manufacture of a line of bio-surgical medical device products
A successful candidate must have experience in:
-Familiar with medical device regulations.
-Establishing and maintaining procedures related to all aspects of life science company operations.
-Establishing and maintaining company’s QMS process such as Document & Record Control, Internal Auditing, Training, Complaints, Nonconformance, Process Deviations & Waivers, MRB, CAPA, Supplier Control, Calibration & Maintenance, Complaints, Quality Planning, etc.
-Participate and perform internal audits.
-Working with Company departments to ensure QMS compliance.
-Producing medical products to meet operating requirements.
-Working in accordance with a detailed work plan.
-Provide quality training.
-Contributing to multi-disciplinary tasks of the company.
*Qualified candidates can submit a cover letter along with their resume or CV in English.
Job Requirements:- At least 2-3 years’ experience in a quality affairs position.
- Experience in GMP environment.
- Fluency in technical English – ability to easily converse, produce and revise documents.
- A BSc/BA degree in a relevant academic field of study (biomedical engineering, biotechnology, chemistry, biochemistry, chemical engineering, etc.).
- References from previous employers or managers.
Required Experience:3-4 שנים
Sub Categories:ביוטכנולוגיה, כימיה, אבטחת איכות