Unison Pharmaceuticals hiring for Quality Control department

Unison Pharmaceuticals hiring for Quality Control department

Greetings from Unison Pharmaceuticals..!!!

Opening for Quality Control – HPLC
Position:

  1. HPLC Operation (Analyst)- Dissolution
  2. HPLC Operation (Analyst)- Assay
  3. HPLC Operation (Analyst)- Others

Experience: 2 – 7 years
Location: Ahmedabad(Moraiya)
Job Purpose:
The QC analyst performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. He / She conducts and validates various biological and chemical quality control Assay, RS, Dissolution, CU, BU, Swab etc. He / She compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. He / She is also responsible for establishing specifications for conducting various analyses.
Key Accountabilities/ Responsibilities
1. HPLC Operation (Analyst)- Assay

  • Collect worksheet and sample for analysis as per plan
  • Check the instrument calibration details
  • Purging the interior part of the instrument
  • Take the columns as per worksheet and put in instrument
  • Initiate solution preparation for analysis as per worksheet which majorly includes; Mobile Phase, Standard and sample
  • Prepare HPLC sequence for analysis and get it review by reviewer
  • As per the sequence initiate the analysis and online verify SSC criteria as per worksheet
  • Post completion of the analysis perform documentation and send to reviewer
  • Calculate final analysis result as per the standard formula mentioned in worksheet and match the result with worksheet range

2. HPLC Operation (Analyst)- Dissolution

  • Collect worksheet and sample for analysis as per plan
  • Check the instrument calibration details
  • Purging the interior part of the instrument
  • Take the columns as per worksheet and put in instrument
  • Initiate dissolution solution preparation for analysis as per worksheet and also prepare dissolution medium
  • Perform dissolution analysis as per the criteria mentioned in worksheet
  • Post completion of the analysis perform documentation and send to reviewer
  • Calculate final analysis result as per the standard formula mentioned in worksheet and match the result with worksheet range
  1. HPLC Operation (Analyst)- Others
  • RM- Assay, RS, IR
  • In process- Assay by UV and HPLC
  • PV Sample- Assay by UV and HPLC, Dissolution
  • FP- Assay, Dissolution, RS, DT, Average weight, hardness, Friability, IR
  • Cleaning validation

Candidates should also have sound knowledge cGMP documentation and must be familiar with cGMP requirements.

Interested candidates may also email their resume to [email protected]

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