Biophore India Pharmaceuticals Pvt. Ltd Walk In Interview 2023. Biophore India Pharmaceuticals Pvt. Ltd Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue. Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry.
Vacancy details:
- Department: AR&D / AQA-Research Analyst/Jr Research Analyst/Jr.Executive / Executive
- Qualification: M.sc (Organic Chemistry)/M.Pharmacy (Pharmaceutical Analysis)/B.Pharmacy
- Experienced:0 to 5 years
- Preferable: Male Candidate’s .
- Skills Required for Freshers : Good Academic results & Good Communication skills.
- Openings:25
Job Description: Greeting from Biophore India Pharmaceuticals Pvt. Ltd !!!!
Important Details :
- Location: Hyderabad/Secunderabad
- Post of date:21/03/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Time and Venue
Date of interview: 24 & 25th of March
Time: 10:00AM to 3:00PM.
Venue: Biophore India Pharmaceuticals Pvt Ltd. Plot# 231, IDA Phase -II, Pashamylaram, Biophore Road, Patancheru (M), Hyderabad. Sangareddy District Telangana – 502307 (view on Map)
if you have any queries please reach me on M-9100033356
We are conducting walk In Interviews for ARD Method Validation Department and Quality Assurance Department .
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.
We are conducting Walk In Interviews on 24th March (Friday )& 25th March (Saturday ) .Please go through the JD .
1. Responsible for Document issue, control, distribution and archival of total documentation system.
2. Responsible for review of analytical documents like pH solubility Data, Hygroscopic Studies Data, Method Feasibility Reports, Batch analysis study Reports, RLD samples reports and Analysts Qualification data.
3. Responsible for Review of Analytical Method Validation Documents Like Protocol, Raw Data and Reports of HPLC, GC, TLC, Auto titrator, UV and PSD instruments etc.
4. Responsible for review Calibration Records of Analytical like HPLC, GC, IR, Auto titrator, Analytical Balance, LCMS, GCMS, ICP MS, IC, CE, UV etc.
5. Responsible for review of review of Analytical Method Transfer data.
6. Attending to all training Programs (internal and external).
