Gallery
Experience
Pharmaceutical Lab Head
Drafting of ISO17025:2017 documents.
Implementation of GLP as per WHO guidelines and ISO 17025 requirements.
Responsible for receipt of analysis samples in the laboratory.
Validation and verification of analytical methods.
Verification and approval of analysis raw data and reports.
Ensure all the test items received in the laboratory are uniquely and unambiguously
identified.
Preparation of appropriate standard operation procedures.
Maintenance of the laboratory stock registers for the equipment and consumables.
Training and evaluation of laboratory personnel to develop competency.
Clean, maintain and keep records of equipment and apparatus as guided by the quality
manual.
Clean, maintain and keep records of equipment and apparatus as guided by the quality
manual.
Ensuring that the tests are performed to acceptable timescales and to the required
quality standards
Participate in internal and third party audits and implement resultant corrective,
preventive and improvement actions.
Snr Quality Control Analyst
Sampling of all received starting materials in consultation with warehouse manager.
Carrying out physical/chemical tests on raw materials, intermediate, finished products and stability studies products.
Handling, operating and calibrating sophisticated instruments like HPLC, UV, IR Spectrophotometer, and other QC instruments.
Ensuring that approved and rejected records of starting materials are maintained properly.
Preparation of Standard Testing Procedures (STPs).
Carrying out analytical method validations, process validation and cleaning validation.
Reporting and investigating Out Of Trend (OOT) and Out of Specification (OOS).
Reporting any accident or injury that arises in the course or in connection with my work.
Quality Control Analyst
Receiving, sampling and analysis of raw materials, packaging materials, intermediate and finished products.
Providing accurate information/analytical results leading to sound decisions on the approval or rejection of raw materials, packaging materials, intermediate, bulk or finished products.
Carrying out environmental controls and keeping records.
Preparation and standardization of reagents and volumetric solutions.
Implementing all the aspects of Quality control systems and associated documentations with regard to cGMP, cGLP and approved pharmacopoeias.
Quality Control Analyst
Was introduced to Quality Control work.
