Job Description
To ensure 21 CFR Part 11 Compliance in Manufacturing and QC of Troikaa Pharmaceuticals Ltd.
To perform and evaluate the adequacy of Computerized System Validation across all sites of Troikaa Pharmaceuticals Ltd.
To prepare, review and implementation of Corporate Policies and Standard Operating Procedures for Computerized Systems.
To perform CSV compliance audit as a part of self-inspection and gap assessment across all sites of Troikaa Pharmaceuticals Ltd.
Handling of QMS w.r.t Computerized System Validation.
To create awareness regarding Data Integrity / Reliability across all sites.
To provide support across all sites during regulatory audit w.r.t. CSV
To impart training to employees w.r.t Computerized System Validation.
To assist in Validation and Qualification activities of various equipments and instruments
Any other responsibility assigned by Management.