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QA Engineer

1 month ago

As a QA Engineer, you’ll work with world-class engineers on our data platform and APIs that process and deliver biomedical information to scientists and operations personnel at biotech and pharmaceutical companies Join a NY-based software company remotely.

The product is used by the biopharma industry to analyze sensitive genomic data collected from patients on oncology clinical trials.

pythonQA

Responsibilities

  • Support Quality Assurance activities and training
  • Develop and modify automated test suites and validation protocols
  • Execute validation protocol procedures as part of the software release cycle
  • Develop Standard Operating Procedures and documentation
  • Communicate with Management re: status of quality, compliance, and security of ongoing projects
  • Update and review specification and design documents and provide feedback as-needed
  • Create tools to automate testing and validation activities
  • Creating detailed, comprehensive and well-structured test plans and test cases
  • Estimating, prioritizing, planning and coordinating quality testing activities
  • Identify, record, document thoroughly and track bugs

Requirements

  • 3-5 years of experience in software Quality Assurance testing
  • Expertise in best-practice testing methodologies, experience with standard QA and development tools for Python
  • Understanding how all elements of software ecosystems work together, including cloud-based systems, and developing QA approaches that fit the overall strategy
  • Adaptability and attention to finalizing testing details and duties, even when requirements or implementation details change
  • Proven track record of taking full ownership of end-user quality and usability
  • Experience with growing a team from its early stages and identifying, developing, and implementing scalable software tools and test infrastructure
  • Excellent communication skills
  • Bachelor’s degree in Computer Science, Computer Engineering, or equivalent

Other things we look for:

  • Experience with validation of regulatory-compliant systems
  • Expertise in GxP Validated Systems and Quality Management Systems
  • Familiarity with ISO 27001 Information Security Management System, ISO 14971:2007 – Medical Devices

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