Qa Functional Tester
this is pranesh from orgspire inc. We have an immediate opening with one of our client. Kindly confirm your interest by replying to this email with your updated resume and convenient time/number to discuss further.
title: qa functional tester
location: glendale, ca
duration: 9 months with possibility of extension
interview process: phone and then in person interview is required
performs complex testing functions and tasks
performs analysis of requirements, test coverage and impact of proposed requirements changes
ensure that testing activities allow applications to meet business requirements and identify existing or potential issues
create and maintain testing deliverables based on user requirements and technical specifications
tests software in accordance with established quality standards prior to implementation to ensure proper operation and freedom from critical defects
analyze test results in order to report any defects, bugs, errors or configuration issues.
Communicate testing progress, test results, and other relevant information to management.
Cultivate and disseminate knowledge of quality assurance best practices.
minimum of 4 years into quality assurance – desktop and mobile application testing
experienced in designing , writing and executing manual test cases
strong knowledge of sql queries experience in web services testing highly desired
automation scripting using qtp or selenium preferred
preferred experience in usability testing
bachelor's degree in business, computer science or information systems or equivalent business experience
effective oral, written, and interpersonal communication skills
thanks & regards
pranesh+5 Other Responses
Currently looking for a qa expert for a project in emeryville ca
one qa automation expert who can provide guidance on the increasing automation (suggest tools, process changes, etc.), especially on the server side. The server side of qa has more potential for automation as it does not need devices for testing. The duration and the skill set will be same as #1
this is a 5 weeks to start than extend to 4 to 6 months. Someone that can give assessment and make recommendations.+3 Other Responses
Quality Assurance Service
this is mafas we have an immediate opening with one of our client. Kindly confirm your interest by replying to this email with your updated resume and convenient time/number to discuss further.
In case if you are not currently available or not interested in the below position, i apologize for the inconvenience and request you to forward my mail to your friends or colleagues whom you feel would excel this opportunity
job title: qa- quality assurance
location: pleasanton, ca
terms: contract to hire
summary of experience :
· good experience in a linux and db2 (or similar sql) environment.
· automation tool soap ui, java not required but a plus.
· any deployment with anthil or jenkins a plus.
· experience with transaction processing, particularly financial – also a plus
thanks & regards
mafas+5 Other Responses
Quality Assurance Development In California
This is a sr. Director of quality assurance,development full time position opportunity in california.
this position will have oversight and leadership of developmental quality assurance programs to meet phase appropriate compliance, validation, and gxp quality assurance requirements.
-establish and maintain a robust quality program that will effectively support the various phases of drug development – preclinical through phase 3, plus product/process improvements.
-employ the principles of ich q8 (pharmaceutical development) and q9 (risk management) to the development of manufacturing processes.
-ensure a systematic approach to development is employed that begins with pre-defined objectives and emphasizes product and process understanding and process control based on sound science and quality risk management.
-provide leadership and managerial oversight to the quality department responsible for development qa.
-establish and maintain a phase appropriate approach to product/process development qa.
-as project team member, represent qa on product development teams including pre-clinical, phase 1, 2, and 3 development studies, and manufacturing improvement teams.
-responsible for document review and qa release of ds/dp to be used in phase 1, 2, and 3 clinical studies.
-responsible for phase appropriate quality systems implementation for ds/dp manufactured for use in phase 1, 2, and 3 clinical studies.
-acts as technical advisor to vp global quality on topics related to development and commercial quality.
-develop and implement effective development qa programs aligned with corporate strategic initiatives and business goals.
-interpret regulatory authority regulations, guidelines and policies. Utilize internal audits and quality compliance assessments programs to evaluate processes and procedures as they pertain to product development activities.
-must be able to maintain a “big picture” perspective without losing site of the details necessary to meet deliverables and deadlines.
-supervise and develop quality personnel.
-direct the review and approval of the applicable sops, batch records, test methods, raw material specifications.
-provide quality expertise as needed for deviations reports and out-of-specification reports.
-ensure that manufacturing processes, equipment, facilities meet phase appropriate gmp requirements.
-ensure that suppliers and contract manufacturers associated with product/process development are operating in compliance with state, federal, and international gxp regulations and guidelines as necessary through an external audit program.
-hire and/or develop the team to establish and maintain efficient and effective quality systems and programs as they relate to product/process development.
-develop operational budgets, cost controls, cost estimates, capacity and resource plans to support corporate strategic business objectives.
-ba/bs in a relevant scientific discipline and a minimum of 15 years industry experience with 7+ years of management experience providing both strategic and leadership guidance to an organization in quality assurance. For senior director level consideration, the ideal candidate must have at least 2 years’ experience at the director level.
-must have a development quality background from the biotechnology/pharmaceutical industry.
-experience in quality management and compliance systems.
-in-depth knowledge development qa and experience implementing phase appropriate quality systems to achieve gxp compliance.
Contact us here on zintro for further details.+13 Other Responses