QA specialist
Dentsply Sirona
**Requistion ID** : 81565
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.
**Bringing out the best in people**
As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us.
Working at Dentsply Sirona you are able to:
**Develop faster** - with our commitment to the best professional development.
**Perform better** - as part of a high-performance, empowering culture.
**Shape an industry** - with a market leader that continues to drive innovation.
**Make a difference** -by helping improve oral health worldwide.
**QA Specialist – Bar-Lev Site, Israel**
**Join MIS Implants, part of Dentsply Sirona — a global leader in dental implant solutions.**
We are looking for a **QA Specialist** to lead quality processes, drive continuous improvement, and ensure supplier and internal compliance across our manufacturing operations.
**What You Will Do**
+ **Supplier Quality Management** – qualification, ongoing monitoring, risk assessments, and continuous communication with supplier QA representatives.
+ **Data Analysis** – trend analysis, statistical tools, and identifying opportunities for quality improvement.
+ **Lead Quality Improvement Projects** across manufacturing, engineering, supply chain, development, and validation teams.
+ **Manage CAPA Processes** – investigations, root cause analysis, corrective & preventive actions.
+ **Ensure QMS Compliance** with ISO 13485, GMP, FDA and additional regulatory requirements.
+ **Write and Update Procedures & Work Instructions** .
+ **Conduct Internal Audits** (subject to certification and company procedures).
+ Collaborate with internal stakeholders: Quality Coordinators, Validation teams, Engineering, Technology, Supply Chain, Production staff, and cross-company interfaces.
+ Work with external partners: regulatory auditors, corporate Dentsply functions, suppliers, subcontractors, and distributors.
**Success in This Role Means**
+ Deep understanding of MIS products and core production processes.
+ Strong knowledge of relevant standards and regulatory requirements.
+ Ability to identify trends and improvement opportunities through analytics and statistical tools.
+ Meeting defined timelines and KPIs in supplier quality management.
+ Effective execution of CAPA and investigation processes.
**What We’re Looking For**
+ **B.Sc. in Engineering – required.**
+ **At least 2 years of experience in Quality Assurance** — strong advantage for medical devices.
+ Experience with **QMS, ISO 13485, GMP, FDA requirements** .
+ High analytical ability, problem‑solving skills, and strong attention to detail.
+ Ability to work cross‑functionally and manage multiple tasks simultaneously.
+ Strong statistical and analytical capabilities.
+ **High level of English – required.**
**Personal Qualities**
+ System-wide perspective and ability to understand complex processes.
+ Strong self-management, independence, and accountability.
+ Assertiveness paired with excellent communication skills.
+ High professionalism, work ethic, and reliability.
+ Precision, detail orientation, and ability to work under pressure.
**Why Join MIS?**
MIS, part of the **Dentsply Sirona Group** , designs and manufactures advanced, innovative dental implant solutions that set global standards.
Join a strong, multidisciplinary team where your expertise directly impacts product quality, patient safety, and global customer satisfaction.
Be part of a company where **quality is not a department — it’s a mindset** .
**Apply now and help us drive excellence in every product we deliver.**
Dentsply Sirona is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona.
Dentsply Sirona Canada welcomes and encourages applications from all backgrounds, including individuals with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.
If you need assistance with completing the online application due to a disability, please send an accommodation request to careers@dentsplysirona.com (careers@dentsply.com) . Please be sure to include “Accommodation Request” in the subject.
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