06 Aug
|
Vitely Bio
|
Ahmedabad
06 Aug
Vitely Bio
Ahmedabad
">
1. Checking of Method development, method validation Study data.
2. Responsible for checking of Calibration of all instruments in Operation department.
3. Ensure completeness of document related to project and qualification activity
4. On-line and retrospective checking of log books of Operation department.
5. Perform Quality control (QC) checks on report to identify inconsistencies, errors, and deviations from standard practices.
6. Ensure lab cleanliness and safety standards in analytical laboratory.
7. Review Scientific and technical reports, including study reports and method validation reports
8. Ensure clarity, accuracy and compliance of reports with regulatory requirements and positive clinical practice (GCP) and good laboratory practice (GLP).
9. Work Closely with Scientist, analysts,
statisticians and quality assurance team to interpret data and ensure accurate presentation of study results.
10. Ensure GLP and GDP practices in analytical activities.
11. To review environmental monitoring data of controlled area and instruments.
12. Any Additional responsibilities or activity assigned by Head of Department/ Management.
Required Skills
basic understanding of analytical services Quality Documentation Data Review Officer-Operation Report / Protocol Preparation Data Review as Quality Control
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
📌 Jr. Research Associate (Ahmedabad)
🏢 Vitely Bio
📍 Ahmedabad