SYMBIOTEC PHARMALAB PVT. LTD – Urgent Vacancy in Quality Control/ Quality Assurance/ API Production/ Biotech

SYMBIOTEC PHARMALAB PVT. LTD - Urgent Vacancy in Quality Control/ Quality Assurance/ API Production/ Biotech

Greetings from SYMBIOTEC PHARMALAB PVT. LTD..!!!
We are hiring following positions. Please find the details attached below.

Department: Quality Control
Position: Chemist/ Officer/ Sr. Officer
Experience: 2-6 Years
Qualification: BSc/ 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.

Department: API Production
Position: Chemist/Officer/Sr. Officer
Experience: 2-8 Years
Qualification: B.Sc/M.Sc/B.E
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.

Department: Quality Assurance – QMS
Position: Officer/ Sr. Officer/ Executive
Experience: 3-8 yeara
Qualification: B.Sc/ M.Sc/ B.Pharm/ M.Pharm
Job Description:

  • To issue correct version of BMR/BPR/PCOCR/MCVR and other documents.
  • To review filled Batch manufacturing record and analytical record.
  • To prepare the department SOP as and when required.
  • To maintain the records for FP/Intermediate batch release documents.
  • To prepare and review of the APQR.
  • To exercise document and data control whichever required.
  • To prepare and review of process validation and cleaning validation protocols and reports.
  • To prepare and review of audit compliance.
  • To participate in self inspection / internal audit program.
  • To initiate, wherever essential and to handle change control, deviations and incidents, CAPA, OOS, Market complaint.
  • To maintain the storage of master copies of all controlled documents.
  • To perform the work assigned by Manager-QA/Head-Quality.

Department: IPQA
Job Description:

  • To issue correct version of BMR/BPR/PCOCR/MCVR and other documents.
  • To review filled Batch manufacturing record and analytical record.
  • Verification of work in progress of manufacturing plant in accordance to approved BMR/BPR and SOPs.
  • To verify the equipment/shop floor cleaning and shall check the results of cleaning samples analysis during changeover of product.
  • To perform dispatch related activity.
  • To verify packing activities of finished product for dispatch as per OIS & SOP.
  • To verify line clearance for next product.
  • To verify the calibration and verification of weighing balance.
  • To review filled Batch manufacturing record and analytical record.
  • To prepare the department SOP as and when required.
  • To exercise document and data control whichever required.
  • To issue and retrieval controlled copies of logbooks and monthly formats of all department.
  • To initiate, wherever essential and to handle change control, deviations and incidents, CAPA.
  • To maintain the storage of master copies of all controlled documents.
  • To verify dispensing activities of raw material required for production of API.


Department: Biotech- Inoculum
Position: Jr. Executive
Experience: 1-3 Years
Qualification: M.Sc. (Biochemistry OR Biotechnology OR Microbiology OR Life Sciences)
Job Description:

  • To follow the SOPs of Inoculum lab and maintain the training record.
  • To monitor the lab equipments and record their status.
  • To perform verification and calibration of lab instruments.
  • To prepare the batch media and fill the batch manufacturing record.
  • To prepare culture media and sterility media.
  • To perform the sterility test.
  • To perform and record isolation and propagation and maintenance of microbial culture
  • To perform the productivity test.
  • To follow the production planning.
  • To coordinate with QA department for issuance and submission of lab records and for calibration and validation of lab equipments.
  • To coordinate with QC and Micro department for analysis, microbial monitoring and GPT of media.
  • To coordinate with ware house department for issuance of batch media.
  • To coordinate with maintenance department for calibration and validation of lab equipments.
  • To follow the GMP and GDP procedures in Inoculum lab.
  • To perform and achieve departmental objectives.

Department: Biotech – Fermentation
Position: Jr. Executive
Experience: 1-3 Years
Qualification: M.Sc. (Biotechnology / Microbiology) OR B.Tech / M.Tech. (Biotechnology)
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.

Interested candidates please share cv on ruchi.kashyap@symbiotec.in

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