Quality Assurance Executive
Sleepiz AG
Pune, Maharashtra, IN
4d ago
source : Instahyre

Responsibilities :

  • Act as a Quality Assurance subject matter expert to the Product Development team and apply QA principles throughout the product life cycle to identify defect and design flaws.
  • Support Product Development team as SQA for the automated testing using tools and conduct integration testing and systems testing before the implementation of tested product modules.
  • Ensure continuous improvement and gives input related to testing strategy for product changes.
  • Ensure internal testing documentation and processes meet applicable regulatory compliance.
  • Work with software engineering & device manufacturing teams to develop robust verification test strategies to ensure product safety, reliability etc.
  • To work on Sleepiz QMS framework adapting to ever changing regulatory and compliance environment and documenting, implementing, supporting and continuously improving products.
  • Building a world class product in Healthcare Industry and Medical Devices.
  • Collaborate with stakeholders and team members.
  • Requirements :

  • Must have 3+ years of experience in testing and certifying modules in a complex web / mobile / IoT based SaaS products.
  • Atleast 2+years of experience in automated testing using Selenium or Cypress.Also, must have similar experience in developing and executing manual test cases.
  • Must have experience in test case planning, black-box testing, white box testing and API testing
  • Hands on experience with a SQL based database such as MySQL and NoSQL database like Casandra.
  • Must have hands-on experience in using code versioning software like GitHub or BitBucket along with knowledge of CI tools like Jenkins, Chef.
  • Must have thorough understanding of the Product Development Lifecycle and worked with ALM tools like Tuleap, codeBeamer etc.
  • ISTQB Certification and Experience in Load / Stress testing will be added advantage.
  • Experience in IoT device testing in a regulated Medical Device Quality Assurance environment will be added advantage.
  • Knowledge of ISO 20000, ISO 27001, ISO 14971, ISO 13485, ISO 62304, CE Class certification and FDA certification process will be helpful.
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