Day-to-Day Responsibilities
Sample and test raw materials, such as active ingredients and excipients, against pharmacopoeia and approved specifications.
Run in-process checks on tablets, capsules, syrups and injectables while production is underway.
Carry out physical, chemical and microbiological tests on finished products before batches are released.
Operate and calibrate lab instruments such as HPLC systems, UV-visible spectrophotometers and dissolution testers.
Record results accurately in logbooks and electronic lab systems, following data integrity rules.
Investigate out-of-specification (OOS) results and report them to the quality assurance team.
Prepare reagents, reference standards and test reports, and follow good manufacturing practice (GMP) procedures at all times.


