Biophore India Pharmaceuticals Pvt. Ltd. has announced a Walk-In Interview for experienced professionals in the AR&D (Analytical Research & Development) – GCMS Department. Candidates with experience in GC-MS/MS method development, validation, genotoxic impurity analysis, and nitrosamine impurity testing are invited to attend the interview at the Biophore R&D Centre, Hyderabad.

This is an excellent opportunity for professionals looking to build a career in pharmaceutical research and analytical development.

Biophore Walk-In Interview Details

Particulars Details

Company Name

Biophore India Pharmaceuticals Pvt. Ltd.

Department

AR&D – GCMS

Position

Jr. Research Analyst / Research Analyst

Qualification

M.Sc / B.Pharmacy / M.Pharmacy (Analysis)

Experience

2 to 5 Years

Gender

Only Male Candidates

Interview Date

8th August 2026 (Saturday)

Interview Time

10:00 AM to 03:00 PM

Work Location

Biophore R&D Centre, Pashamylaram, Hyderabad

About the Opportunity

Biophore is seeking talented analytical professionals with hands-on experience in GC-MS/MS technology and impurity profiling. The selected candidates will work on advanced pharmaceutical research projects involving genotoxic impurities, nitrosamine impurities, and unknown impurity identification.

Candidates with strong analytical skills and regulatory knowledge related to pharmaceutical products and active pharmaceutical ingredients (APIs) will be preferred.

Key Responsibilities

Selected candidates will be responsible for:

Method development and validation of Genotoxic Impurities (GTIs).

Analysis of Nitrosamine Impurities in pharmaceutical products and substances.

Performing studies using GC-MS/MS instrumentation.

Development of analytical methods for identification of unknown impurities.

Conducting impurity screening studies.

Data interpretation, documentation, and compliance with regulatory requirements.

Supporting analytical research activities within the AR&D department.

Eligibility Criteria

Educational Qualification

M.Sc

B.Pharmacy

M.Pharmacy (Analysis)

Experience Required

2 to 5 years of relevant experience in GCMS analytical research.

Preferred Skills

GC-MS/MS operation and troubleshooting.

Method development and validation.

Nitrosamine impurity analysis.

Genotoxic impurity testing.

Pharmaceutical analytical documentation.

Regulatory compliance knowledge.

Documents Required

Candidates should carry:

Updated Resume/CV

PAN Card Copy

Aadhaar Card Copy

Last 3 Months Salary Slips or

Last 6 Months Bank Statements

How to Apply?

Interested candidates can directly attend the walk-in interview on the scheduled date.

Candidates who are unable to attend the interview may share their updated profile through the company’s recruitment email:

Email: recruitments@biophore.com

Why Join Biophore?

Opportunity to work in a reputed pharmaceutical R&D organization.

Exposure to advanced analytical technologies.

Experience in impurity profiling and regulatory projects.

Career growth in Analytical Research & Development.

Collaborative and innovation-driven work environment.

Technical FAQs

1. What is GC-MS/MS and why is it used in pharmaceutical analysis?

GC-MS/MS (Gas Chromatography-Tandem Mass Spectrometry) is an advanced analytical technique used to separate, identify, and quantify trace-level compounds, impurities, and contaminants in pharmaceutical products with high sensitivity and accuracy.

2. What are genotoxic impurities (GTIs)?

Genotoxic impurities are chemical substances that can damage DNA and potentially cause genetic mutations or cancer. Regulatory agencies require strict monitoring and control of GTIs in pharmaceutical products.

3. What are nitrosamine impurities?

Nitrosamines are potentially carcinogenic compounds that may form during API synthesis or product manufacturing. Regulatory authorities worldwide mandate rigorous testing and control of nitrosamine levels.

4. What is analytical method validation?

Method validation is the process of proving that an analytical method consistently produces reliable, accurate, precise, and reproducible results according to ICH and regulatory guidelines.

5. How are unknown impurities identified using GC-MS/MS?

Unknown impurities are identified by analyzing mass spectral data, fragmentation patterns, retention times, and library matching techniques. GC-MS/MS helps determine the molecular structure and origin of impurities in pharmaceutical products.