Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

QA Lead

Expired Job

Syser Inc Cincinnati , OH 45202

Posted 2 months ago

The QA Lead is responsible for quality and test related process execution with high impact to the business. This includes providing feedback on artifacts developed during requirements and analysis phase within client projects; authoring test plans and test cases; and performing / leading test execution for both project and support related activities.
The QA lead is responsible for leading and supporting testers in an agile environment that may be located locally or remotely in the US or India. The QA lead is responsible for coordinating providing guidance and oversight on testing standards and processes, including assisting with code reviews. Testing can be manual or automated (Selenium Web Driver will utilized for automation). The QA lead must be familiar with the Agile Methodology as well demonstrate hands on experience with Selenium automation concepts and tools.
5+ years of QA Lead experience
3+ years of experience writing Selenium tests in Java
2+ years of experience with test runners (Junit, TestNG, Mocha, Jasmine)
2+ years of experience with CI tools (Jenkins, TeamCity, GitLab)
1+ years of experience with Selenium Grid
1+ years of experience testing web services (manual or automation)
1+ years of working in an Agile/Scrum methodology
1+ years of using Jira for defect tracking
Very strong communication and collaboration skills
Strong experience leading the automation of regression test suites
Prefer candidates with Green Cards or US citizenship
Provide leadership to quality engineers, with complete responsibility and accountability for delivery of project tasks assigned to the QA team.
Ensure Test Case reviews with stakeholders are being held as appropriate
Conduct Defect Triage meetings as appropriate.
Conduct Root Cause Analysis and identify and implement process improvements.
Assess quality and test process maturity level and assist in defining strategy to implement best practices.
Ensure that projects follow prescribed software development life cycle standards.
Understand and utilize risk based testing techniques
Effectively communicate to management and business partners
Effectively determine when test cases are good candidates to be automated

Junit, TestNG, Mocha, Jasmine, Jenkins, TeamCity, GitLab, Agile/Scrum methodology, Selenium tests in Java

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
QA Clinical Research Specialist

Cincinnati Children's Hospital Medical Center

Posted 2 days ago

VIEW JOBS 11/16/2018 12:00:00 AM 2019-02-14T00:00 POSITION TITLE: Specialist - Clinical Research Quality Assurance DEPARTMENT: Pathology SUPERVISOR'S TITLE: Manager TITLES SUPERVISED: Not applicable TOTAL NUMBER OF FTEs DIRECTLY SUPERVISED: 0 TOTAL NUMBER OF FTEs INDIRECTLY SUPERVISED: 0 PURPOSE OF POSITION: To ensure quality, human subject safety and data integrity of clinical trials conducted within the assigned department. Responsibilities * Quality Assurance Monitoring: Develop comprehensive quality assurance plans for all clinical trial activities within the assigned department to ensure that trials are conducted in compliance with the protocol, SOPs, ICH GCP, federal, state, and local regulatory requirements. Prepare and execute quality assurance plans both internally and at affiliate sites, including site visits to ensure protocol and regulatory compliance; data management tasks to ensure study data integrity; verify essential documents are accurate, complete, and maintained; and coordination of applicable follow-up activities. Assist in the development and implementation of action plans for external monitoring/audit follow-up. Assist in preparation and conduct of audits/surveys/inspections by FDA, DHHS, institutional, and accreditation agencies. Develop improvement plans using quality improvement methods (process improvement, continuous improvement, total quality management, etc.). * Training Develop and provide quality assurance training and consultation for faculty, staff, and affiliate sites. Provide regulatory training (ICH GCP, FDA, DHHS, state, local, and institutional) and/or other training initiatives to faculty and staff, as assigned. * Clinical Trial Protocol Development and Implementation: Provide input into the development of new protocols and plans for implementing new trials as requested by Principal Investigators/Managers. Coordinate the development of regulatory sections of investigator-led protocols, e.g., data safety monitoring plans. Develop and maintain SOPs for clinical trials. Act as a primary resource on an ongoing basis for clinical trials staff, responding to questions and issues pertaining to study documentation, GCP, or other issues as requested. * Data and Documentation: Review and analyze quality assurance-related data (internal and external). Provide guidance to clinical faculty and staff in clinical research documentation for patients enrolled in clinical trials. Assist in development and monitoring of clinical trial indicators of quality, reliability, and adherence to SOPs. Develop and communicate outcome measures. Skills & Competencies * Problem Solving: Excellent problem-solving, interpersonal, written and organizational skills required. * Professional Knowledge: Knowledge of clinical settings, medical terminology and anatomy * Clinical Knowledge: Knowledge of clinical trials data management systems. * Professionalism: Strong organizational skills and attention to detail, communication and interpersonal skills, and professionalism required. * Technical Knowledge: Computer literacy in MS Word, Excel, and PowerPoint. Knowledge of electronic data capture/clinical study tracking systems. Experience in clinical research quality assurance or in clinical research monitoring and/or auditing. Required: * Bachelor's degree in a science or healthcare field AND 3 years of experience in clinical research work OR * Master's degree (MPH/Science) AND Quality/Process Improvement Studies AND 2 years experience in clinical research work * Assoc of Clinical Research OR Cert Clinical Research Coord OR Cert Clinical Research Prof OR Registered Quality Assurance Professional OR Attain within 18 months of hire Preferred: Cincinnati Children's Hospital Medical Center Cincinnati OH

QA Lead

Expired Job

Syser Inc