Inspector
Date: Mar 31, 2026
Location: Tianjin, CN, 300457
Company: Dentsply Sirona, Inc
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Requistion ID: 82897
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Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over a century 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 dental care. Dentsply Sirona’s headquarter is located in Charlotte, North Carolina. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.dentsplysirona.com for more information about Dentsply Sirona and its products.
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SUMMARY OF POSITION
Finished product and raw material inspection, package inspection，in-process inspection, laboratory related work, as well as complaint handling related work, and the ability to timely and effectively handle various abnormalities before and post market according to the non-conforming product control process. Able to effectively supervise and identify and control related risks during the production process, ensuring that the factory can supply and deliver in a qualified, compliant and timely manner. Effectively monitor the production in the controlled workshop to ensure that the biological load of the products, as well as the aseptic inspections, all meet the requirements.
DUTIES & RESPONSIBILITIES
1. Conduct daily inspection and verification of raw materials, packaging materials, intermediate products in the production validation process, and finished products in coordination with related work.
2. Responsible for the inspection and testing work required for the evaluation of new material suppliers.
3. Verify the inspection and calibrationinstruments for internal measurement.
4. Supervise the quality of each process in the production process, effectively monitor and identify and control related risks during the production process.
5. Review and organize daily quality records for archiving.
6. Assist in conducting various research and development inspections and testing work.
7. Provide timely testing data support for the validation of new equipment and processes, and conduct relevant feasibility reviews.
8. Assist in investigating technical issues during the production process and provide testing data support.
9. Strengthen service awareness and do a good job in all relevant service work for internal and external customers.
10. Cooperate to complete the re-examination of complaints, as well as complete related work such as complaint investigation..
11. Timely handle various abnormalities before and post market according to the non-conforming product control process.
12. Make changes to inspection related documents.
13. Support related work such as domestic and foreign registration.
14. Comprehensively identify and control the risks associated with automated projects and the changes during the process.
15. Complete other tasks assigned by the manager.
KNOWLEDGE , SKILLS & EXPERIENCE
Education Background
College degree or above in relevant fields.
Experience Work Experience
More than three years of experience in inspection related work, preferably with experience in medical device inspection.
Specific Knowledge /skills
Specific Knowledge/Skills Specific Professional Skills
Master the abilities of chemical testing, physical testing, performance testing, etc
Master the process related to document changes
knowthe inspection control points related to microbiological testing and clean room environmental control.
Understand the basic knowledge of measuring instrument management, internal and external measurement, etc
Having laboratory testing qualifications, metrology qualifications, and clean room testing experience is preferred
COMPETENCIES 能力要求:
Proactive, innovative, with good teamwork, personnel management, and cross departmental coordination and communication skills;.
Good learning and computer skills
Good file modification ability
Timely and effectively handle various abnormalities and changes in the production process
Can effectively supervise and guide the production site to fill in records and standardize operations
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Equal Opportunity Employer: Dentsply Sirona is an Equal Opportunity Employer. All qualified applicants will be considered without unlawful discrimination or regard for race, color, religion, sex, sexual orientation, sexual or gender identity, national or ethnic origin, age, marital status, disability, genetic factors, military and veteran status, or any other characteristics protected by applicable local law. Eligibility: All successful applicants must be eligible to work in the country the position is based. Assistance: If you need assistance with completing the online application due to a disability, please send an accommodation request to accommodationrequest@dentsplysirona.com. Agencies: Please note that Dentsply Sirona does not accept or respond to unsolicited requests or applications submitted by Recruitment Agencies/ Search Firms. Notice on Fraudulent Job Offers: Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information: careers.dentsplysirona.com.
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