QA Analyst Level II
Company Name:-
Anju Software
Job Location:-
Bengaluru, Karnataka
Job Summary:-
Come join us!
At Anju Software, we are looking for team members that share the passion and commitment to create the best product solutions available within the Life Sciences Software Sector.
If you enjoy a fast-paced collaborative work environment.
Please send a cover letter and resume to Careers and specify the desired open position and include the code following the position title.
POSITION:
QA Analyst Level II (Bengaluru or Pune, INDIA)
Position Summary
Anju Software, Inc.
specializes in delivering advanced solutions specifically designed for healthcare.
Anju provides a comprehensive suite of clinical trial capabilities that can be mixed and matched to build a solid foundation for each trial environment.
The Quality Assurance Analyst II (QA II) is responsible for implementing Quality Assurance Software Change Control policies and programs.
The QA Analyst will execute the quality assurance and software change disciplines as directed by the Director Quality Assurance.
The QA Analyst II will work as a member of a cross functional team including clinical staff, product analysts, software engineers, and QA analysts, so effective communication, collaboration, and team work is essential for success.
Personal Qualities
Professional; adaptability; possess strong teamwork building capabilities; excellent time management skills; strong communication skills to articulate complex technical issues; self-starter with ability to work within a large team environment.
Responsibilities
Responsible for providing leadership in all activities related to the quality and releasing of software testing.
Manage several QA testing and assurance plans on multiple projects.
Develop program test plans for developed systems and subsystems.
Perform testing of developed and co-developed systems and subsystems.
Ensure that full project tests are conducted at regular intervals throughout a project.
Ensure that related test plans are run for all changes made to the system.
Responsible for ensuring the software complies with the requirements set forth in the FDA guideline 21 CFR Part 11.
Assist in the identification and resolution of program, system and subsystem deficiencies.
Enter into, maintain and close software related issues in t
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