Junior Software Quality Assurance Analyst (offline)
Job Description
Required:
2 years+ of industry experience (BSA, QA Engineer or similar),
Strong analytical skills and knowledge of SDLC,
Ability to analyze and interpret complex and complicated documents (software requirements and design specifications, standards and regulations),
Strong knowledge and understanding of software quality assurance concepts and practices,
Strong team player,
Ability to do multiple tasks with competing deadlines,
Upper-intermediate English (fluent English); the ability to understand and talk to native speakers is a must.
Desired:
Fundamentals of Quality Management Systems (ISO13485, IEΠ‘62304),
Knowledge of Software Testing Foundations (ISTQB),
Risk analysis techniques (FTA, FMEA) knowledge,
Job Responsibilities
Analyzing established processes and defining areas of improvement
Reviewing and approving project documentation (such as development reports, verification test plans and reports, etc.)
Analyzing software requirements
Control of software verification activities
Communicating with a customer on quality assurance topics
Software product risk management
Assessing project activities against established procedures, standards, and regulations (QMS for medical device software development)
Department/Project Description
Medical software device of class C.
Required:
2 years+ of industry experience (BSA, QA Engineer or similar),
Strong analytical skills and knowledge of SDLC,
Ability to analyze and interpret complex and complicated documents (software requirements and design specifications, standards and regulations),
Strong knowledge and understanding of software quality assurance concepts and practices,
Strong team player,
Ability to do multiple tasks with competing deadlines,
Upper-intermediate English (fluent English); the ability to understand and talk to native speakers is a must.
Desired:
Fundamentals of Quality Management Systems (ISO13485, IEΠ‘62304),
Knowledge of Software Testing Foundations (ISTQB),
Risk analysis techniques (FTA, FMEA) knowledge,
Job Responsibilities
Analyzing established processes and defining areas of improvement
Reviewing and approving project documentation (such as development reports, verification test plans and reports, etc.)
Analyzing software requirements
Control of software verification activities
Communicating with a customer on quality assurance topics
Software product risk management
Assessing project activities against established procedures, standards, and regulations (QMS for medical device software development)
Department/Project Description
Medical software device of class C.
About GlobalLogic
GlobalLogic, a Hitachi Group Company, is a leader in digital engineering. We put people first. As part of our team, you will grow, be challenged, and expand your skill set working alongside highly experienced and talented people.In Ukraine, GlobalLogic is:
- one of the TOP-3 largest IT companies
- 6,000+ professionals
- 90%+ of our projects involve complex R&D
- fully autonomous offices are located in Kyiv, Kharkiv, Lviv, and Mykolaiv, along with 10 temporary mini-offices across Ukraine
What is GlobalLogic in numbers:
- 29,000+ engineers
- 20+ countries
- 500+ active clients
- 50+ product engineering centers
- Headquartered in Silicon Valley
Company website:
https://bit.ly/GlobalLogic-Ukraine
DOU company page:
https://jobs.dou.ua/companies/globallogic/
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