Naveen Kumar

Experience

• 

  Surya Pharmaceutical Limited

  Feb 2008 - Oct 2010

  Chemist

   Issuance of raw materials from warehouse and preparing the lot of raw materials as per processrequirement and dispense the raw material with proper label. Batch charging as per Batch Production Record (B.P.R), following the production Schedule. To operate the process activities as per Sop’s and in case of any breakdown bring to theknowledge of in charge and get it attended promptly. To look out all powder processing activities i.e. milling, blending, sifting and packing of finishedGoods as per Batch Production Record (B.P.R) and following the concern SOP. In case in process analysis to be done by QC Chemist, Coordinate with QC chemist for samplingand result. To maintain the plant machines and surrounding area clean and tidy always. To follow the cGMP norms lay down by Company. To follow all safety rules and use various safety application provided by the company i.e. To working in manner that complies with the company EHS policies as informed by concernedarea in charge. To working in a manner that prevents injury to self and to others To follow established plant safe work practices. To be notify area in charge about incidents/ accident. To attend the training program for cGMP and safety as per the company policy. To fill the BPR online and to get check the critical process parameter from shift in charge. To share any problem in process & plant with superiors Show less

• 

  Teva Active Pharmaceutical Ingredients

  Oct 2010 - Jul 2021

   Tunfa manager Handing Lims & Trackwise. Preparing process validation protocol and report, monitoring validation activity. Preparing cleaning validation protocol and report, monitoring validation activity. Investigating manufacturing deviations, OOS & OOT. Manufacturing Change control. Strictly following cGMP with the guidelines of ICH. Participating in internal audit programs conducted by the production department. Product quality review and evaluation (APQR). Continued process verification (CVP). Product Quality Risk assessment . Show less  Handling of ERP system. Planning, organizing and monitoring day to day activities. Raw material arrangement for the production as per the process order. Entering the batch details raw materials, batch starting and batch closing in SAP. Preparing process validation protocol and report, monitoring validation activity. Preparing cleaning validation protocol and report, monitoring validation activity. Preparing BPR and ECR. Strictly following cGMP with the guidelines of ICH. Strictly following the SAFETY as per EHS. Participating in internal audit programs conducted by the production department Show less

  • Quality Assurance Specialist

    Jan 2020 - Jul 2021

  • Officer

    Aug 2018 - Jul 2021

  • Officer

    Apr 2016 - Jul 2018

  • Sr. chemist

    Oct 2010 - Mar 2016
• 

  Teva Pharmaceuticals

  Jul 2021 - Mar 2023

  Quality Assurance Analyst
• 

  Teva Active Pharmaceutical Ingredients

  Apr 2023 - now

  Deputy Manager Quality Compliance (Quality Analyst-II)