Analyst

7 days ago

GUJARAT INDIA STAFF AHMEDABAD WEST VIROCHAN NAGAR Troikaa Group Full time

To perform accurate and reliable analysis of Finished Products, In-process samples, stability sample, validation samples (process and cleaning validation) as per method of analysis or protocol.

To perform method transfer, method verification, analytical method validation and protocol base study. 

To record the procedure of the test performed and observations contemporaneously. 

To review the results against specification / acceptance criteria mentioned in the protocol. If any abnormality to be informed immediately to Section head. 

To review the Method of analysis / worksheet prior to analysis and shall inform to the section In charge for the potential failure (if any).

Preparation of Standard Test Procedure, Method of Analysis, Specification and Standard Operating Procedure as and when required

To operate the QC equipment(s).

To prepare, maintain and update the Column list of UHPLC / HPLC 

Sample Receive:

To receive the sample along with Test request slip (TRF) or Goods Receipt Notes (GRN). To verify the physical sample condition and sample label against TRF / GRN.

To allocate the AR. No. in 'Inward register'. 

General :

To verify the sample details (Product Name, Sample Name, Batch No., Station etc.) before perform the analysis. 

To ensure the current version method of analysis and specification available before analysis.

To verify the instrument calibration status before perform the analysis. 

At start of the shift inform to operator/ supervisor for requirement of chemical usage in analysis. 

After completion of analysis to maintain the instrument usage log. 

After completion of analysis enter the results in LIMS software.

Record the analytical document on line (contemporaneously) and submit to reviewer / section head after completion

Work completion status to be updated in work allotment logbook.

To follow good laboratory practices.

To attain the training in LMS software before due date.

Disposal of Residual Sample, Left over material after testing, expired chemicals.

Reporting of all above analytical work to section head / In-charge-QC.

Sample preparation & Related documentation for the sample to be sent to the outside laboratory 

To record the temperature and humidity of quality control area.

To ensure the working condition of safety shower. 

To verify and record the cleaning of quality control area.

To participate in investigations of OOS / laboratory incident / OOT / deviation.

To inform the section In charge for the break-down of equipment. 

Immediately information to the In-charge-QC in case of any abnormal observation found during analysis.

Any data integrity related observation in the department shall be bring to notice of QC-Head

To maintain the discipline in laboratory.

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