Detail of Job Responsibility: -

1. To plan and execute for the daily sampling and testing of material as per the production

schedule,
1. To ensure for manufacture of quality products.
2. To ensure for high productivity of the employees.
3. To trained & motivate chemists to take more responsibilities.
4. Preparation, up gradation and review of Standard Operating Procedure.
5. Daily report and monthly report submission to Management.
6. Maintain sequential logbook of all critical equipments.
7. Preparation & implementation of Calibration & validation schedule of equipments.
8. Keeping the records of reference standards and working standards.

10.P.V.,AMV,CV of the product to plain & execute
1. Control of retains samples and periodical physical observation.
2. Control of all records.
3. Carry out the stabilities studies as per SOP and maintain records.
4. Planning and execution of cleaning and sanitization of quality Control Department and

Maintaining necessary records as per FDA rules and regulations.
1.



Coordination with quality assurance/production / stores/ finished goods stores/ purchase for

day today operation on raising advance requisition for the requirements.
1. Maintenance of discipline in the department.
2. Completion of necessary records on day to day basis
3. Keep the department clean and provide hygienic workplace to the employees
4. To maintain GLP in Q.C.
5. Inspection of venders.(If required)
6. To face the out of specification for raw material, finished product, packing material and

stability samples.  Authority:-
1. To accept or reject the starting material, in process material and finished goods tested

materials.
1. Development of manpower to achieve targets
2. Appraisal of employees and training of men power
3. Appraisal of venders.

 Key Result Area:-
1. Execution of testing as per production schedule.
2. Selection and training of chemist
3. To implement and adhere to GMP & GLP

Work Location: In person

📌 QC Manager (Bavla)
🏢 ZENON
📍 Bavla