Urgent Openings in Production & QC Departments @ Symbiotec Pharmalab Pvt. Ltd - PHARMA WISDOM

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Sunday, 1 December 2019

Urgent Openings in Production & QC Departments @ Symbiotec Pharmalab Pvt. Ltd


Openings in Production & QC Departments @ Symbiotec Pharmalab Pvt. Ltd
1.Quality control:-
Designation- Officer
Exp-2-5 Years
Qualification:- B.Sc / M.Sc / B.Pharm
Job Description:
1.To perform calibration records of Gas chromatography in QC lab and to maintain record for the same.
2.To initiate and completion of analytical record for Gas chromatography.
3.To carry out the GC analysis of raw materials, finish products and intermediates as required.
4.To perform and achieve departmental objectives.
5.To follow the guidelines of GLP and cGMP requirements.
6.To carry out GC analysis of stability samples.
7.To maintain GC columns records and to maintain GC columns un good working condition.
8. To follow good laboratory practices as laid down in the Quality Control procedures.
9. Check of test results against standards and confirmation of doubtful results before
submission of reports to the next level.
10. Execution of special assignments given by the Department Head.
11. Upkeep of laboratory working area to prevent any contamination/ cross contamination.
12. To ensure adequate identification and segregation of test samples to avoid mix up and cross
Contamination.
13. Timely reporting of results of testing to facilitate the achievement of production schedules.
14. Discussion of out of specification laboratory results with the manager, initiation of investigation of such results and submission of additional results.
HPLC-
1.To perform and maintain calibration records of HPLC in QC lab.
2.To ensure proper and regular servicing of all the analytical instruments.
3.To ensure updation of all HPLC log books.
4.To initiate and completion of analytical record for HPLC.
5.To carry out HPLC analysis of Raw-materials, finish products, intermediates and working standards.
6.To perform and achieve departmental objectives.
7.To follow the guidelines of GLP and cGMP requirements.
8.To carry out instrumental analysis of stability samples
9.To maintain HPLC columns records.
10.To carry out chemical analysis of raw materials, finish products, intermediates and working standards.
2. API -Production:
Position- Chemist/ Officer/ Sr. Officer
Experience- 3-8 Years
Qualification-B.Sc/M.Sc/ BE
Job Description:
1. To perform and control the manufacturing activities in shift.
2. To maintain batch manufacturing records for the batch manufactured and check that all the BMR's are adequately filled.
3. To maintain all related documents for production.
4. To co-ordinate with engineering and maintenance department for routine activities.
5. To co-ordinate for the raw materials from stores.
6. To perform in safe work environment.
7. To allocate manpower for shift activities.
8. To monitor and maintain good housekeeping in respective areas.
9. To perform and achieve department objectives.

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