Experience as QC senior Executive

• Employer

• From

  01 January 2015

• To

• Detail

  Presently working.
  
  
  Planning of daily activities and ensure completion of work within stipulated time.
  To ensure that Good Lab practices are followed in the QC Lab.
  Performing Analysis of Samples in Stability, Raw materials, In-process and finished products.
  Reporting and posting the results into the LIMS after completion of Task.
  Performing Analysis of Dissolution, Assay, Related Substances, Content Uniformity.
  Take part of writing protocols, reports and standard operating procedures.
  Maintaining the Protocol, Records & Log books. Alloting the Analytical Register number sequentially in Register.
  Calibrating analytical equipment, as and when required.
  Monitoring the conditions (temperature/humidity)of stability chambers and updates the stability chamber records.
  Reporting the results of OOS & OOT to the supervisor for the Investigation and take part of it.
  Following the procedure as per the requirements for releasing and rejecting of Materials or Products.
  Supporting all QC activities and Ensuring that procedures are carried out carefully and accurately to eliminate errors.
  Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
  Being the responsible person to follow the internal SOP’s, ICH guidelines, GDP, GLP, RFT, cGMP requirements.
  Observing and complying with company Health and Safety policies.