Virtual interview At Ajanta Pharma Ltd – Submit Resume

Ajanta Pharma Ltd Released Job Openings On 06-09-2021.Ajanta Pharma is a specialty pharmaceutical company engaged in development, manufacturing and marketing of quality finished dosages. Committed to ‘Serve Health Care Needs Worldwide’, we produce a comprehensive range of specialty products targeting different therapeutic segments for treatment of patients, customised to each market we are present in.

Vacancy Details:

Ajanta Pharma Ltd Recruiting B.Pharm. / M.Sc. Candidates with 05+ Years of Experience for Quality Assurance Dept-Officer or Sr. Officer – QA (Male candidate) Position.Complete Details for the Quality Assurance Dept-Officer or Sr. Officer – QA (Male candidate) as follows.

Important Details :

• Location :Paithan MIDC, Paithan Dist – Aurangabad (Maharashtra)
• No of Vacancies:Not Disclosed by Recruiter
• Details of Salary: Not Disclosed by Recruiter
• Opening date for online Application: 06/09/2021
• Mode of application :Online
• Email id:rahul.bhat@ajantapharma.com ,manish.datta@ajantapharma.com

Job Description/Skills Required

1. Responsible for fulfilment of regulatory requirements of Drug Regulatory Affairs (DRA) department.
2. Review and online maintenance of cGMP and analytical documents of quality control.
3. Document control (Issuance, retrieval, storage and destruction).
4. Review and investigation of Out of Specification (OOS) investigation.
5. Review of specification, Standard Test Procedure (STP) & General Test Procedure (GTP).
6. Review and maintenance of deviation, incidence, corrective and preventive actions, non-  conformance and change control.
7. In process checking in the quality control department i.e. verification of calibration report of instruments and equipments, analytical report, reference standard, working standard, instrument usage and column logbook, recording of temperature and humidity, electronic reconciliation, stability sample tracking, charging and withdrawal records etc.
8. To ensure the integrity of data.
9. Review of analytical method validation / verification of documents.
10. Review of cleaning validation documents.
11. Review of technology transfer documents.
12. To review and initiate change control, incident and Corrective Action and Preventive Action (CAPA) in Quality Management System (QMS).
13. Placing of portable data logger in to the consignment, preparation of report and trending.
14. The candidate should have exposure of Quality Control department.This communication is valid upto Sep 20, 2021.

CV can be sent at:
rahul.bhat@ajantapharma.com
manish.datta@ajantapharma.com