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Flagship Biotech International Pvt. Ltd - Walk-In Interviews for Production, QC, QA on 13th & 14th December 2019
Greetings from Flagship Biotech International Pvt. Ltd!!
Please find below the company and Job details and interview details:
Job Location: Baroda, Gujarat
Profile: Production Officer
Experience: 1-3 years
Job details-
1. To monitor the daily activities in Production area as per the GMP guidelines.
(Washing area, manufacturing area, filling area etc.)
2. To handle the men power in production area.
3. To handle the visual inspection department.
4. To check preparatory work for Manufacturing batches and its documentation.
5. To do in process checking in production area.
6. To fill the BMRs and other daily formats.
7. To check the quantity of primary packing materials as per the requisition.
8. To fill the daily activity/manpower reports for production department.
9. To update the status board in production area.
10. To take entry of daily production batches in computer from BMR register.
11. To be responsible for doing the documentation in production area as per the GDP.
Profile : QA/QC Officer
Experience: 1 to 3 Years
Job Description for QA Officer
1. Line Clearance & In-process checks in dispensing & Manufacturing area.
2. Line Clearance & In-process checks in aseptic area for unloading, filtration,
Transfer & Filling Activities in Aseptic Area.
3. Line Clearance & In-Process checks for filling line & Its documentation.
4. Line clearance and monitoring of Washing and Sterilization area.
5. Line clearance in visual inspection and visual release of product for labeling and packing.
6. Verification of production log books, environment monitoring record & Calibration records for the aseptic area.
Job Description for QC Officer
1. To be Responsible for Chemical & Instrumental Analysis of Raw material, Intermediate & Finished product samples as per the laid down procedure.
2. To Prepare & Review of the Standard testing procedure, Specifications, Standard testing procedure.
3. To be Responsible for preparation and standardization of Reagent and solution for physicochemical Analysis.
4. To be Responsible for preparation of standard reagents & volumetric solution with its standardization as per SOP.
5. To be Responsible for periodical calibration of Quality control Instruments like Spectrophotometer, HPLC etc.
6. To handle and perform the analysis on HPLC.
Date & Time: 13th & 14th December, 2019 at 10 AM onwards
Venue:
Divine Laboratories Pvt. Ltd. (WHO - cGMP Company)
24 / B. Sahajanand Indl. Estate,
Mujmahuda,
Vadodara - 390 020
Gujarat, India. Tel. : 0265 - 2351855 / 2354853
Contact - Vinayak Pandey (6351149095)