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**Job Function: **
Quality
**Job Sub Function: **
Quality Control
Job Category:
Professional
All Job Posting Locations:
Nes-Ziona, Center District, Israel
Job Description:
About Biosurgery
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Quality Control Analyst position for our Ness Ziona site.
Position Summary
This role is intended for an analyst who works hands-on at the bench.
This Role:
- Performs QC analytical testing in accordance with GMP, approved methods, and procedures (Enzymatic/Protein assays Experience - significant adv.)
- Develops and supports implementation of laboratory practices.
- Mentors, coaches, and trains QC staff through hands-on guidance and knowledge sharing.
- Supports development and tracking of QC metrics to monitor and improve product and system quality.
- Prepares quality control reports, technical summaries, and documentation as required.
- Operates in full compliance with GMP, Israel labor law regulations, J&J policies, values, and Code of Conduct.
- Drives operational excellence.
- Communicates quality-related risks, issues, and improvement opportunities to management as needed.
- Performs additional duties as assigned to support business and quality objectives.
Job Requirements
- B.Sc. in Chemistry, Life Sciences, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum 2+ years of hands-on experience as a QC Analyst in a GMP-regulated pharmaceutical, biotech, or medical device environment - significant advantage.
- Enzymatic/Protein assays Experience - significant advantage
- Proven experience working under GMP, including documentation, data integrity, investigations, and audit support.
- High quality and compliance mindset.
- Ability to work independently while contributing effectively to a team.
- Strong written and verbal communication skills.
- High level English (reading, writing, speaking) is a MUST.
**Required Skills: **
Preferred Skills:
Administrative Support, Communication, Compliance Management, Controls Compliance, Execution Focus, ISO 9001, Persistence and Tenacity, Problem Solving, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Standard Operating Procedure (SOP), Teamwork, Technologically Savvy