Biophore- Walk-In on 21st – 22nd April 2023 for Freshers & Experience

Biophore- Walk-In on 21st – 22nd April 2023 for Freshers & Experience

Founded in 2007, Biophore India Pharmaceuticals Pvt. Ltd has established itself as a trusted partner for niche and complex products. With 4 US FDA and EU approved API manufacturing facilities, one dedicated intermediate facility and a world class  R&D lab housing 400 scientists with varied expertise, Biophore has emerged as one of the leading API companies globally. We have consistently been in the Top 10 US DMF filers with the US FDA over the past 5 years and with most of our APIs, we are one of the fastest companies to bring them to the market enabling wider access for patients worldwide

Biophore Walk In

  • Qualification: MS/M.Sc(Science) in Organic Chemistry, Chemistry, /M.Pharma
  • Experience : 00-05+years
  • Job Location: Hyderabad/Secunderabad
  • No. of Openings: 15
  • Experience : 00 – 05 Years
  • Role: Research Analyst/Jr.Research Analyst/Trainee
  • Department : AR&D

Time and Venue

21st April – 22nd April , 9.30 AM – 2.30 PM
Biophore India Pharmaceuticals Pvt Ltd. Plot# 231, IDA Phase -II, Pashamylaram, Biophore Road, Patancheru (M), Hyderabad. Sangareddy District Telangana – 502307

Job description

Greetings from Biophore Inida !!

We are hiring for AR&D Department-API.

Experience :0-6 years

Qualification : M.Sc /M.Pharma

Job Location : R&D Center, Pashmylaram ,Hyderabad

Walk In Interviews : 21st April & 22nd April (Friday & Saturday ).

Time :10:00 AM to 03:00 PM.

Documents need to carry :

Updated CV

Last 03 Months Pay Slips

copy of Educational Documents

Please go through the JD .

1. Perform HPLC Validations and Analysis like Assay by HPLC, RS/Purity by HPLC

2. Perform Assay by HPLC, RS/Purity by HPLC Equivalency studies.

3. Perform Assay by HPLC, Analytical balance and pH instruments calibrations.

4. Perform the Requalification analysis of Impurity standards and Reference/Working standards. (Like HPLC, FTIR, LOD and Water content/Moisture Content).

5. Perform Assay by HPLC and RS by HPLC methods forced degradation studies.

6. Attending on job trainings and cGMP trainings.

7. Perform the method feasibility studies.

8. Perform the method verifications as per Protocols.

9. Maintain online documentation.

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