🔶 Symbiotec Pharma Lab Indore jobs for Production QC Microbiology Instrumentation apply now
🔶Openings for Chemist / Officer / Sr. Officer / Executive- QC / Micro / API Production/ Engineering @ SYMBIOTEC PHARMALAB PVT. LTD
Openings: 25
Location: Indore
Quality Control
Position- Chemist/ Officer/ Sr. Officer
Experience- 2-6 Years
Qualification-B.Sc/M.Sc
Job Description:
HPLC-
To perform and maintain calibration records of HPLC in QC lab.
To ensure proper and regular servicing of all the analytical instruments.
To ensure updation of all HPLC log books.
To initiate and completion of analytical record for HPLC.
To carry out HPLC analysis of Raw-materials, finish products, intermediates and working standards.
To perform and achieve departmental objectives.
To follow the guidelines of GLP and cGMP requirements.
To carry out instrumental analysis of stability samples
To maintain HPLC columns records.
To carry out chemical analysis of raw materials, finish products, intermediates and working standards.
Wet Lab:
To carry out the analysis of raw materials, in- process, intermediates, packaging materials, finish products, water & working standards.
To updation of log books of raw materials, in process, packaging materials and finish products.
To updation of log books and preparation of test solution and volumetric solution.
To maintain all calibration records.
To perform sampling of water, raw materials, packaging materials, intermediates and finish products.
Temperature monitoring of QC lab.
To follow the guidelines of GLP and cGMP requirements.
To perform calibration of instruments like pH meter, conductivity meter, Karl – Fischer, Analytical Balance, LOD oven, vacuum oven and UV analysis.
To carry out chemical analysis of raw materials, finish products, intermediates and working standards.
Upkeep of samples under analysis and retain samples.
Upkeep of laboratory working area.
Destruction of expired samples timely.
To ensure adequate identification and segregation of test samples to avoid mix up and cross contamination.
Timely reporting of results of testing to facilitate the achievement of production schedules.
Discussion of out of specification laboratory results with the manager, initiation of investigation of such results and submission of additional results.
To check report from the analyst against standards and submission of inspected reports for review.
To ensure that the records, which are made of the results of inspection and testing of materials, intermediates and finished products are formally assessed against specification.
GC:
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.
To follow good laboratory practices as laid down in the Quality Control procedures.
Check of test results against standards and confirmation of doubtful results before
submission of reports to the next level.
Execution of special assignments given by the Department Head.
Upkeep of laboratory working area to prevent any contamination/ cross contamination.
To ensure adequate identification and segregation of test samples to avoid mix up and cross
Contamination.
Timely reporting of results of testing to facilitate the achievement of production schedules.
Discussion of out of specification laboratory results with the manager, initiation of investigation of such results and submission of additional results.
Microbiology:
To monitor qualification of instrument.
To ensure collect the samples of potable water, purified water, finished products per procedure.
Monitoring manufacturing clean area and microbiology department.
To ensure carry out microbiology test and BET test as per procedure.
Calibration of all analytical instruments of microbiology section.
To ensure the guideline of cGLP & cGMP requirements.
To coordinate with outside party for Annual Maintenance Contract (AMC) for Microbiology Instrument.
API Production:
Position- Chemist/Officer/Sr. Officer
Experience- 2-8 Years
Qualification-B.Sc/M.Sc/BE
Job Description:
Preparation of documents for production.
To co-ordinate with Production people and control manufacturing activities.
To co-ordinate with other departments like maintenance, QC, warehouse and QA etc. for smooth production.
To review production documents and check that are filled adequately and signed.
To ensure that correct raw materials are issued for respective batch.
To check status on materials during all stages of operation.
To co-ordinate in reviewing the non-conformance of the product.
To ensure congenial and safe work environment.
To monitor production activities to meet the products requirements.
To perform and achieve department objectives.
Engineering- Instrumentation:
Position-Sr. Executive
Experience- 5-9 Years
Qualification-BE (Instrumentation)
Job Description:
Preparation and execution of Preventive maintenance as per Plan for Instruments and Control systems.
Supervision of the breakdown of all Process and Utility instruments.
Execution of Modification works related to plant and utilities.
Maintaining of inventory for Engineering Spares and consumables related to Instruments and Control system.
Ensuring for Execution of activities as per EHS requirement
Compliance to cGMP practices and Compliance to relevant SOPs.
To handle and perform all routine activities related to DCS.
To perform and achieve departmental objectives.
To monitor the equipments and check their status.
Ensure that all instruments are in within calibration and co-ordination within Engineering.
Identification and implementation of the Energy Conservation ideas to save Energy.
Interested candidates please mail your CVs at ruchi.kashyap@symbiotec.in
Reference - Industrial Guide [Naitik Patel]
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