Elton Rodrigues

I am a pharma professional with around 10 years experience in Quality Assurance.I have worked in various roles for companies such as Sanofi, Teva and now currently for FDC India Limited.

I have a wide exposure in Quality Management Systems (Deviation handling, CAPA ,Change control , APQRs and Self Inspections).

I have exposure to SAP, LIMS ,Trackwise , Document management System, Glorya  and eQMS ample logic System.

I am looking for opportunities in Ireland in the pharma Field.

I am having around 10 years experience in quality Assurance .

• Currently working at FDC Pharma, Verna Goa  from March 2021 onwards.(2 years 2 months)
• 6.5 years experience in Quality Assurance department in Tevapharm India Pvt. Ltd from October 2014 to March 2021.
• One year experience in quality assurance department  at Sanofi India Limited Verna-Goa from August 2013 to  August 2014.

Job Responsibility in current role includes

- Investigation of Deviations , non-conformance  ,OOS and OOTs. 

-Investigation of  Market complaints.

-Assessment of change controls. 

-Review of APQRs. 

-CAPA review and its effectiveness 

-Participation in Self Inspections 

-Trending of Deviations and complaints.

Previous responsibility in Teva and Sanofi Include:

- In charge of PQR preparation and review at Teva Goa 

-Batch documentation review and Batch release

- Executing process validation at manufacturing stage as per protocol

-Performing Cleaning Validation as per protocol.

-Executing pack validation as per protocol.

-Self inspection coordinator of Internal Audits at site

-Handling of Global Notification to Management and performing the risk assessment.

-Execution, review of Process performance qualification/Process Validation reports

-Preparation and review of Hold time Summary Reports. 

- Review of executed Batch Manufacturing Records, Batch Packing Records .

-Handling of Change controls, participation in deviation investigation. .

-Line clearances in granulation, compression, coating, tablet inspection and packing    areas.

-In process control checks in manufacturing as well as packing lines

-AQL checks of tablets.

-Sampling at various stages of manufacturing

-Issuance of Batch Manufacturing Records, Batch Packing Records .

I have completed my Masters in Pharmacy from Goa University (India).