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For Employers

Executive

sun pharma industries

0 - 1 years

6 - 12 Lacs

vadodara

Posted:1 day ago| Platform:

Apply

Skills Required

method validation compliance senior executive study director pharma standard operating procedures director principal principal investigator glp chromatography

Work Mode

Work from Office

Job Type

Full Time

Job Description

At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own SunshineAs you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys.

To Access Study Plan and Standard Operating Procedures and to comply with
instructions given in Study Plan and Standard Operating Procedures.
To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw data and are responsible for the quality of their data.
Operation Maintenance and Calibration of Liquid Chromatography and Tandem Mass Spectrometer (LC/MS/MS).
To perform the method Development, method validation and study sample analysis (non-clinical) for GLP Studies.
Preparation of ATP (Method SOP), SOPs, Template for GLP Studies.
Sample preparation for MD, MV and study analysis as per GLP guidelines.
Pipette Maintenance and calibration assigned to the group.
Other job responsibilities assigned by reporting authority.
Preparation of method validation/partial method validation reports and bioanalytical study reports for GLP studies in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP.
Documentation of any type of Deviation in GLP study report communicated directly to the Study Director and/or if appropriate, the Principal Investigator.
Responding to QA observations for bioanalytical reports in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP.

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Executive