-
Implementing good manufacturing practice, good laboratory practice and good documentation practice regulations related to the QC department.
-
Analyzing raw materials, packaging materials, intermediate, bulk and finished products.
-
Preparing specifications, sampling instructions, test methods and other QC procedures.
-
Ensuring all necessary testing is carried out.
-
Checking the maintenance of the QC department, premises and equipment.
-
Revising and writing standard QC operating procedures.
-
Ensuring lab cleanliness and safety standards are maintained.
-
Conducting routine and non-routine analysis for in-process materials, raw materials, environmental samples, finished goods and stability samples.
-
Compiling laboratory test data and performing appropriate analysis.
-
Calibrating, validating and maintaining laboratory equipment.
-
Completing the documentation needed to support the testing procedures including data capture forms, equipment logbooks and inventory forms.
-
Monitoring the testing procedures to ensure that all tests are performed according to the established item specifications, standard test methods and protocols.
-
Ensuring that lab cleanliness and safety standards are maintained.
-
Conducting new vendor qualification testing.
-
Participating in the investigation for the complaints related to the quality of products.
-
Calibrating and maintaining laboratory instruments/equipment.
PREREQUSITE PROFILE
Education:
Bachelor’s degree in pharmacy/ chemistry/ Biochemistry/ any relevant field.
Experience:
1 – 2+ years’ experience in similar field.