Unison Pharmaceuticals Pvt. Ltd-Walk-In Interview for Quality Control On 28th May’ 2022
Job Description
Walk-In Interview for Quality Control (HPLC & GLP) Analyst @ Unison Pharmaceuticals Pvt. Ltd
An opportunity for B.Sc/ M.Sc/ B.Pharm/ M.Pharm qualified candidates to join EU GMP Approved our State-of -Art Manufacturing Sites (OSD) for the position of Officer/ Sr. Officer/ Executive
- Quality Control (HPLC)
- M.Pharm/ M.Sc/ B.Pharm with 3 to 6 years hands-on experience of HPLC handling of Raw Material, Packing Material, In Process Quality Control and Finished Product in OSD forms
Job Description
HPLC Operation (Analyst-Assay/ Dissolution/ RS/ CU/BU
- 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.
- Perform analysis as per the criteria mentioned in worksheet.
- 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 standard formula mentioned in worksheet and match the result with worksheet range.
- Quality Control (GLP)
- M.Pharm/ M.Sc/ B.Pharm with 3 to 5 years hands-on experience of GLP section like Calibration of Instruments, Working Standard and Qualification activities in OSD forms.
GLP Operation (Analyst) QC Instrument Calibration & Qualification
- Responsible for handling of instrument like HPLC, Dissolution Test Apparatus, UV Spectro Photometer, Disintegration Apparatus and other Physico Chemical instruments.
- Responsible for perform the Calibration of all Analytical Instrument/Equipment lying at Quality Control laboratory.
- Responsible to perform Equipment/ Instruments Calibration/ Verification. In-case of OOC result inform to superior immediately and follow respective SOP.
- Responsible for maintain the Inventory, log record of HPLC columns as per respective Column management SOP.
- Execution of Calibration and Preventive Maintenance of QC instruments as per predefined schedule.
- Working Standard, Reference Standard and Chemical/Reagent management.
- Daily/ weekly monitoring of Temperature/ Humidity of QC laboratory.
- Responsible for preparation of Analytical documents like Specification, Method of Analysis and Worksheet for Active Material, Inactive Raw Material, Finished Product, Finished Product Strip/Blister, Semi Finished Product, Granules, and Packing Material and for Working standard qualification.
For the positions, Candidates should also have sound knowledge cGMP documentation and must be familiar with cGMP requirements.
Date : 28th May’ 2022
Time: 10:00 AM to 04:00 PM
Venue: Unison Pharmaceuticals Pvt. Ltd, Unit -III, C 7,8,9, Steel Town, Opp. CIL Nova Petro, Behind HOF, Moraiya, Taluka: Sanand, Ahmedabad 382213
- Contact Person: Manisha Rajput
- Interested Candidate may also email their resume to carreer@unisonpharmaceuticals.com
Unison Pharmaceuticals Pvt. Ltd-Walk-In Interview for Quality Control On 28th May’ 2022
