Posted:8 months ago|
Platform:
Work from Office
Full Time
a. To approve or reject, starting materials, packaging materials, intermediate, bulk, and finished products.
b. To ensure that all necessary testing is carried out and the associated records evaluated.
c. The approval and monitoring of suppliers of materials.
d. To approve specifications, sampling instructions, test methods, and other Quality Control procedures.
e. To approve and monitor any contract laboratories.
f. To ensure the qualification and maintenance of premises and equipment.
g. To ensure that the appropriate validations are done.
h. To ensure that the required initial and continuing training of his department personnel is carried out and adapted according to need.
The maintenance of the quality management system. These include:
a. The authorization of written procedures and other documents, including amendments.
b. The monitoring and control of the manufacturing environment and trends.
c. Plant hygiene.
d. The retention of records.
e. The inspection, investigation, and taking of samples, in order to monitor factors which may affect product quality.
f. The monitoring of compliance with the requirements of EU/US/WHO/Indian Good Manufacturing Practice in Production, warehouse, QC and QA, and Indian Good Laboratory Practice in QC.
g. control of packaging material.
h. Ensuring that a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management.
Zenzi Pharmaceutical Industries
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