Quality System Specialist

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob FunctionQualityJob Sub FunctionQuality SystemsJob CategoryProfessionalAll Job Posting Locations:Yokneam, Haifa District, IsraelJob DescriptionAbout CardiovascularFueled 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 Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtechWe are searching for a talented quality and compliance specialist to be in YokneamThis role is responsible for serving as the internal processes improvement agent and maintaining quality system comprehensive compliance.In This Role You Will BeResponsible for management and effectiveness of the CAPA process.Responsible for periodic monitoring of documents approaching the review period and notifications to document ownersOrganize and lead the Data Review Boards and Quality Systems Management Review.Responsible for maintaining updated list of applicable J&J internal standardsAssist in the development of quality metrics in order to achieve company's quality goals.Performs other duties assigned as neededRequirementsA minimun of Degree in engineering or life science.At least 3 years quality background, including previous roles.Experience as quality Specialist and/or quality assurance Specialist responsible for CAPA execution in medical devices and/or pharmaceutics companyAbility to build strong working relationship with internal partnersExperience managing international multi-disciplinary projects.Qualification in Quality Assurance as Quality Auditor, ISO and QSR standards/regulations for the medical devices or pharmaceutics industries (preferred)Required SkillsPreferred Skills:Analytical Reasoning, Business Alignment, Business Behavior, Collaborating, Communication, Compliance Management, Data Compilation, Data Quality, Data Savvy, Document Management, Execution Focus, Quality Auditing, Quality Control (QC), Quality Management Systems (QMS), Quality Services, Quality Standards, Systems Analysis, Training People