Tevapharm India Pvt. Ltd.
ï‚· Conduct in process audit of the Bioanalytical phase of BA/BE studies
ï‚· Ensure loading and disposal of processed samples on to HPLC-audosampler as per
analytical sequence
 Perform ‘Document control and issuance’ activities for SOPs, forms, formats, log
books, study specific protocols, validation protocols, qualification protocols of all
departments of WPPL as and when required.
ï‚· Conduct internal study audit, system audits to ensure compliance with GCP/GLP,
Protocols, SOPs and applicable regulatory requirements.
ï‚· Review of generated raw data and respective clinical study report, abbreviated clinical
study report, CRFs, SERs, eCTD compilation, of clinical study as per the requirement.
ï‚· Prepare audit report to adhere with the guidelines, written procedures and regulatory
inspections.
New Global Technologies
Job Description:-
A QA Engineer, or Software Quality Assurance Engineer, is responsible for ensuring that software meets quality standards and requirements.
Their responsibilities include:
Designing tests: Creating test plans, scenarios, scripts, and procedures to identify bugs and defects
Analyzing results: Analyzing testing results and communicating solutions to developers
Reviewing documentation: Reviewing software documentation to ensure it's accurate, complete, and compliant
Monitoring quality: Monitoring the quality of the software throughout the development process
Collaborating with developers: Collaborating with developers to fix bugs and improve the product
Providing feedback: Providing feedback and recommendations to developers on software usability and functionality
Documenting defects: Using a bug tracking system to document software defects and report them to developers
Reviewing the final product: Reviewing the final product's functionality before it's released