Senior Software QA, Information Systems Cord Blood Registry
THIS JOB HAS EXPIRED Are you someone who is willing to spend 40 hours a week doing something you're passionate about? So are we!
As our company continues to grow, so does our CBR family of employees; and we want employees who are truly passionate about their jobs, their co-workers and what we do at CBR. We encourage innovation and leadership and provide the resource and support that enable our employees to succeed. Joining the CBR Family means becoming an integral part of our culture, The CBR Way.
Cbr Systems is the largest and most experienced stem cell bank in the world.
We are a privately held, financially stable company.
We receive umbilical cord blood and cord tissue from families all over the world and we process and store it in our laboratory in Tucson, Arizona.
We offer competitive salaries and benefits including medical, dental, vision, and 401K.
We encourage professional growth and opportunity for our team members.
We maintain a rigorous quality system, which allows us to offer our families the highest quality stem cell product available.
A Senior Software QA, Information Systems is responsible for evaluating existing and new software systems according to pre-determined specifications and standards. Additional responsibilities include the review of test results, risk management, defect analysis, and training. Strict adherence to application development methodology and support processes is required.
Lead testing efforts for functional areas depending on need
Create test cases and test data
Execute test scripts using testing software programs
Coordinate testing by users and third parties
Review output from other QA team members to ensure quality and completeness
Work closely with Product and Engineering staff to ensure test cases are valid
Document, track, and communicate test plans, test results, analysis, and unresolved problems.
Install, maintain, and use testing software programs
Contribute to establishment of standards and procedures for program design and testing.
Respond to inquiries from users and technical support regarding functions and operations of software programs
Recommend program improvements/revisions
Identify program variances from standards and suggest modifications to conform
Establish benchmarks for program efficiency in operating and response times
Program Performance Monitoring
Defect Analysis and Tracking - Identify, analyze, and document defects, questionable functions, errors, and inconsistencies in software program functions, outputs, online screens, and content
Document writing and review
Interface with team members and department leads who work at different physical sites (i.e. San Bruno, CA and Tucson, AZ)
Participate in development projects/agile teams from origination to completion
Education & Training
BA/BS in Computer Science or equivalent experience
5+ years related experience and/or training
Management/Team Leadership experience
Experience and proficiency in black box and white box testing methods
Experience with database querying
Experience using formal defect tracking systems
Working knowledge of software engineering and quality assurance processes
Excellent oral and written communication skills
Excellent listening skills
Strong teamwork, analytical, and organization skills
Familiar with standard concepts, practices and procedures within the areas of data analysis and statistical analysis
Ability to effectively interface with technologists, business owners, and end-users
Ability to work creatively and analytically in a problem-solving environment
Ability to handle multiple tasks under tight deadlines
Ability to manage multiple ongoing projects/tasks simultaneously
Criminal background screening is a condition of employment
Working knowledge in FileMaker Pro, Siebel, .NET, Oracle Business Intelligence, Target Process, and Quality Center
Experience with FDA Software Validation Principles (CFR Part 11, CFR Part 361, CFR Part 351, GMP)
||1200 Bayhill Drive |
San Bruno, CA 94066
THIS JOB HAS EXPIRED