Publish Date: 27th April 2015
Published By: TestingQ.com
Company Name: ClinAsia Labs Private Limited
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Published By: TestingQ.com
Company Name: ClinAsia Labs Private Limited
Location: Hyderabad
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Job Description:
Job Description:
- Review User/Business Requirements, create and execute manual test cases in test management tool.
- Perform Smoke, functional, system and regression testing for every new build.
- Able to create test suite/test bed which includes test data, data mapping, positive and negative test scenarios.
- Execute test cases and capture test results and test execution reports.
- Track and manage defects in defect tracking tool.
- Able to create test deliverable documents like test plan, RTM, test summary report and SQA signoff report.
- Identify reusable test cases and prepare automation test bed.
- Able to work in flexible timings and strict time lines.
- Maintain and utilize automation suite for complete regression testing.
- Execute automation regression test scripts, capture test reports and log any identified defects
About Company:
ClinAsia Labs Private Limited
ClinAsia Labs Pvt.Ltd is the closely-held affiliation of MaxisIT Inc. (NJ, USA organization). MaxisIT has been in business for over 11 years serving primarily to Pharmaceutical and Life Sciences industry companies in the areas of clinical trial management, clinical data management, biostatistics, regulatory documents and submission management and Pharmacovigilance utilizing its organically grown integrated suite of software . ClinAsia Labs Pvt. Ltd. was established 8 year's back in India with an objective of building a global full service contract research organization offering integrated software platform based clinical research and allied services to global organizations, combining extreme focus on software-driven consistent Quality and built-in process level Compliance to global regulatory standard (including ICHGCP, ICMR, EMEA and FDA Standards). ClinAsia has wide range of experience working with top pharmaceutical companies located across different geographic regions of the world on therapeutic areas of Infectious diseases, Neurology, Diabetes, Oncology, Gynecology, Endocrinology, Respiratory, Rheumatology, Dermatology, Immunology and Vaccines. ClinAsia has it's headquarter offices at India and United States and satellite offices at Canada, Europe and Singapore. ClinAsia, with its globally integrated clinical research platform based services based in emerging region, brings Asian advantage and global reach to the table. ClinAsia is uniquely positioned as an electronic clinical research organization that provides full scale of clinical research and allied services to Pharma, Biotech, Medical devices companies as well as other CROs globally via its completely integrated clinical development infrastructure that is technology enabled and guarantees efficiency, consistent quality, regulatory compliance, global reach, and of course the cost arbitrage of low-cost delivery region. We are ISO 9001:2008 certified, ensuring the quality standards of Documentation and Training in the organization, ISO 27001 and ISO 20000 in terms of security and services respectively. All our products are 21 CFR Part11 regulatory complaint and all our projects are executed as per ICH-GCP guidelines
ClinAsia Labs Pvt.Ltd is the closely-held affiliation of MaxisIT Inc. (NJ, USA organization). MaxisIT has been in business for over 11 years serving primarily to Pharmaceutical and Life Sciences industry companies in the areas of clinical trial management, clinical data management, biostatistics, regulatory documents and submission management and Pharmacovigilance utilizing its organically grown integrated suite of software . ClinAsia Labs Pvt. Ltd. was established 8 year's back in India with an objective of building a global full service contract research organization offering integrated software platform based clinical research and allied services to global organizations, combining extreme focus on software-driven consistent Quality and built-in process level Compliance to global regulatory standard (including ICHGCP, ICMR, EMEA and FDA Standards). ClinAsia has wide range of experience working with top pharmaceutical companies located across different geographic regions of the world on therapeutic areas of Infectious diseases, Neurology, Diabetes, Oncology, Gynecology, Endocrinology, Respiratory, Rheumatology, Dermatology, Immunology and Vaccines. ClinAsia has it's headquarter offices at India and United States and satellite offices at Canada, Europe and Singapore. ClinAsia, with its globally integrated clinical research platform based services based in emerging region, brings Asian advantage and global reach to the table. ClinAsia is uniquely positioned as an electronic clinical research organization that provides full scale of clinical research and allied services to Pharma, Biotech, Medical devices companies as well as other CROs globally via its completely integrated clinical development infrastructure that is technology enabled and guarantees efficiency, consistent quality, regulatory compliance, global reach, and of course the cost arbitrage of low-cost delivery region. We are ISO 9001:2008 certified, ensuring the quality standards of Documentation and Training in the organization, ISO 27001 and ISO 20000 in terms of security and services respectively. All our products are 21 CFR Part11 regulatory complaint and all our projects are executed as per ICH-GCP guidelines
