9 Jobs für Identity Verification Specialist in Berlin
Stellenangebote Identity Verification Specialist in Berlin Jobs
Job am 12.01.2026 bei Jobleads gefunden
• Berlin
[. .. ] and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Senior Regulatory Affairs Specialist, youll be working to obtain government approval for new products. Your responsibilities will include analyzing compliance regulations and ensuring product and process compliance. Additionally, youll carry out compliance and inspection activities, report on findings, and make recommendations. Primary Responsibilities Medical device approval Selfresponsible compilation of registrationrelevant documents on request of [. .. ] file as part of the design steering process. Review/approval of regulatory documents in the context of design governance, in particular: Risk Analysis/ Risk Management, Clinical Evaluation, Design Validation/ Design Verification Plans and Protocols, Software Documentation, Instructions for Use and Product Labels. Processing of change processes and checking for relevance to approval General inquiries regarding RA and contact person for interpretation of standard requirements e. g. for sterivalidation, biocompatibility, electrical safety etc. Customers and externals Interface to the RA departments of [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. #J-18808-Ljbffr 74562966 [. .. ]
Job am 12.01.2026 bei Jobleads gefunden
Senior Regulatory Affairs Specialist Medical Devices (m/f/d)
• Berlin
Senior Regulatory Affairs
Specialist Medical Devices (m/f/d) page is loaded # # Senior Regulatory Affairs Specialist Medical Devices (m/f/d) locations: Berlin, Germanytime type: Full timeposted on: Posted 2 Days Agojob [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requisition id: R008858Build a career powered by innovations that matter At Novanta, our innovations power technology products that are transforming [. .. ] file as part of the design steering process. Review/approval of regulatory documents in the context of design governance, in particular: Risk Analysis/ Risk Management, Clinical Evaluation, Design Validation/ Design Verification Plans and Protocols, Software Documentation, Instructions for Use and Product Labels. Processing of change processes and checking for relevance to approval General inquiries regarding RA and contact person for interpretation of standard requirements e. g. for steri-validation, biocompatibility, electrical safety etc. Customers and externals: Interface to the RA departments [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. Solving complex challenges, delivering innovations that matter is a leading [. .. ]
Job am 10.09.2025 bei Jobleads gefunden
• Berlin
[. .. ] between the individual departments Technical management of the technical project components and content-related support of the associated work packages (target definition, Do D) together with the project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manager and the specialist departments Creation and maintenance of technical documentation together with the project manager Responsible for product-specific risk management in cooperation with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of equipment and hose set construction (Alpha, Beta, Vali) Transfer (design transfer) of products into production Responsible for the review and approval of assembly instructions Responsible for standard testing of the device and hose sets Support of manufacturing processes up to the pilot [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. Seniority level Mid-Senior level Employment type Full-time Job [. .. ]
Job am 21.01.2026 bei Neuvoo gefunden
Novanta
• Berlin
[. .. ] the departments. Preparation and maintenance of technical documentation together with the project manager. Responsible for product-specific risk management in cooperation with the risk manager. Responsible for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] product-specific verification plans and their successful implementation. Technical management of the equipment and hose set constructions (Alpha, Beta, Vali) . Transfer (design transfer) of the products to production. Responsible for the review and approval of assembly instructions. Responsible for the standard tests of the device and tube sets. Support of manufacturing processes [. .. ] (e. g. project acquisition General Tasks Strict compliance with the quality, occupational safety, and environmental regulations. Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist. Required Experience, Education, Skills, Training and Competencies Training/ Education:Dipl. -Ing. / Master of Medical Technology/ Mechanical Engineering/ Materials Engineering/ Biology or equivalent Technical Requirements Profile:3+ years of relevant work experience required. Preferably in the development of medical device disposable products. Good knowledge in the fields of mechanics, sterility, biocompatibility. Experience in [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 77008646 [. .. ]
Job am 09.01.2026 bei Neuvoo gefunden
Novanta
• Berlin
[. .. ] between the individual departments Technical management of the technical project components and content-related support for the associated work packages (target definition, Do D) together with the project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manager and the specialist departments Creation and maintenance of the technical documentation together with the project manager Responsible for product-specific risk management in collaboration with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of the device and hose set constructions (Alpha, Beta, Vali) Transfer (design transfer) of the products to production Responsible for the review and approval of assembly instructions Transfer (design transfer) of the products to production Responsible for the review and approval of assembly [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 74301752 [. .. ]
Job am 09.01.2026 bei Neuvoo gefunden
Novanta
Senior Regulatory Affairs Specialist Medical Devices (m/f/d)
• Berlin
[. .. ] and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Senior Regulatory Affairs Specialist, youll be working to obtain government approval for new products. Your responsibilities will include analyzing compliance regulations and ensuring product and process compliance. Additionally, youll carry out compliance and inspection activities, report on findings, and make recommendations. Primary Responsibilities Medical device approval: Self-responsible compilation of registration-relevant documents on [. .. ] file as part of the design steering process. Review/approval of regulatory documents in the context of design governance, in particular: Risk Analysis/ Risk Management, Clinical Evaluation, Design Validation/ Design Verification Plans and Protocols, Software Documentation, Instructions for Use and Product Labels. Processing of change processes and checking for relevance to approval General inquiries regarding RA and contact person for interpretation of standard requirements e. g. for steri-validation, biocompatibility, electrical safety etc. Customers and externals: Interface to the RA departments [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 74302515 [. .. ]
Job am 09.01.2026 bei Neuvoo gefunden
Novanta
• Berlin
[. .. ] doctors, and technical experts, our teams continuously search for new ways to innovate. As Design Assurance Engineer you are responsible for creation of an overall quality plan, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review of design verification and validation specifications, test specifications and reports for medical devices (devices and consumables) , review of Design Control documents according to GDP, MDR 2017/ CFR820 and leading/ contributing to risk management, FMEA and other quality (assurance) related tasks within product development. Primary Responsibilities Within the framework of design control: Support [. .. ] improvement of processes Failure analysis for field returns and during development Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions by quality/ environmental officers and the specialist for occupational safety Required Experience, Education, Skills and Competencies Completed technical and/or physical studies At least 2 years of professional experience Experience with product quality in a highly regulated industry (medical device, automotive, aviation etc. ) Experience in theory and application of quality methods and techniques English fluency, Germany [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 74303579 [. .. ]
Job am 18.11.2025 bei Neuvoo gefunden
Novanta
• Berlin
Führungs-/ Leitungspositionen
[. .. ] turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Position Details Summary The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Lead Regulatory Affairs Specialist ensures that: medical devices and the steps involved in developing, testing, and marketing them meet all applicable regulatory requirements, and regulatory submissions and approvals for initial placing and maintaining the devices on the market are timely performed. To make this happen the employee anticipates and plans appropriate tasks and coordinates [. .. ] usability file Control and sole responsibility for reviewing/ releasing approval-relevant documents as part of the design control process, in particular Risk analysis/ risk management, clinical evaluation, design validation/ design verification plans and protocols, software documentation, instructions for use and product labeling Management of/responsible for the regulatory evaluation of change orders and checking for approval relevance Management of/responsible for processing RA-related general inquiries Subject Mater Expert for the interpretation of standard requirements, e. g. for clinical evaluation, biocompatibility, [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 69945889 [. .. ]
Job am 14.11.2025 bei Neuvoo gefunden
Novanta
• Berlin
[. .. ] between the individual departments Technical management of the technical project components and content-related support for the associated work packages (target definition, Do D) together with the project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manager and the specialist departments Creation and maintenance of the technical documentation together with the project manager Responsible for product-specific risk management in collaboration with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of the device constructions (Alpha, Beta, Vali) Responsible for the review and approval of assembly instructions, Transfer (design transfer) of the products to production Responsible for the standard tests of the device Support of the production processes up to the pilot series (NPI) [. .. ] is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy) , sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process. 69535719 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Identity Verification Specialist pro Jahr?
Als Identity Verification Specialist verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Identity Verification Specialist Jobs in Berlin bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Identity Verification Specialist Jobs in Berlin.
Zu welchem Berufsfeld gehören Identity Verification Specialist Jobs in Berlin?
Identity Verification Specialist Jobs in Berlin gehören zum Berufsfeld Netzwerke.
