Unison Pharmaceuticals Walk-In-Interview For BSc/ MSc/ B.Pharm/ M.Pharm

Walk In Interview for Quality Control (HPLC & GLP) analyst at Unison Pharmaceuticals

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

1. 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 the 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

2. GLP Operation (Analyst) – QC Instrument Calibration & Qualification

Responsible for handling of instruments like HPLC, Dissolution Test Apparatus, UV Spectro Photometer, Disintegration Apparatus and Other Physico Chemical instruments.

Responsible for perform the Calibration of all Analytical Instruments/Equipment lying at Quality control laboratory.

Responsible to perform Equipment/ Instruments Calibration/ Verification. In-case of OOC results 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 Raw 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.

Interested candidates may Walk-in-interview for an interview along-with their updated CVs, Salary Slip and relevant documents as per below schedule:

Date: Saturday, 28th May, 2022

Timings: 10.00 a.m. – 4.00 p.m.

Venue: Unison Pharmaceuticals Pvt. Ltd.

Unit III, C 7,8,9, Steel Town,

Opp. CIL Nova Petro, Behind HOF,

Moraiya, Taluka : Sanand,

Ahmedabad 38 22 13.

Contact Person: Manisha Rajput

Interested candidates may also email their resume to carreer@unisonpharmaceuticals.com

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