Bharat Parenterals Limited Walk-In Interview – QC, QA & Formulation Development Opportunities

Bharat Parenterals Limited Announces Walk-In Interview Drive

Bharat Parenterals Limited, a well-established pharmaceutical manufacturing company, has announced a Walk-In Interview Drive for experienced and aspiring pharmaceutical professionals. The recruitment drive is scheduled for 17th August and 18th August 2026 (Monday & Tuesday) from 10:00 AM to 04:00 PM at the company’s Vadodara facility in Gujarat.

This hiring initiative focuses on key functions including Quality Control (QC), Quality Assurance (QA), and Formulation & Development (F&D). Candidates with relevant qualifications and pharmaceutical industry experience are encouraged to participate.

Company Overview

Company Name: Bharat Parenterals Limited

Industry: Pharmaceutical Manufacturing

Location: Vadodara, Gujarat

Recruitment Type: Walk-In Interview

Walk-In Interview Details

Interview Dates: 17th August & 18th August 2026

Days: Monday & Tuesday

Time: 10:00 AM to 04:00 PM

Venue

Bharat Parenterals Limited

144-A, Village: Haripura,

Ta: Savli, Jarod Samlaya Road,

Vadodara, Gujarat – 391520

Available Job Openings

1. Quality Control (QC)

Position: Senior Officer

Number of Vacancies: 01

Experience: 03–05 Years

Qualification: B.Sc / M.Sc

Technical Requirement: HPLC, GC Analysis

Key Responsibilities

Operation and calibration of HPLC and GC instruments.

Analysis of raw materials, in-process samples, and finished products.

Documentation as per GMP and regulatory guidelines.

Investigation of laboratory deviations and OOS results.

2. Quality Assurance (QA)

Position: Trainee / Junior Officer

Number of Vacancies: 02

Experience: 01–03 Years

Qualification: B.Pharm / M.Pharm

Technical Requirement: IPQA Activities

Key Responsibilities

In-process quality checks during manufacturing.

Batch record review and documentation.

Monitoring GMP compliance.

Line clearance and process verification.

3. Formulation & Development (F&D)

Position: Research Scientist

Number of Vacancies: 01

Experience: 04–06 Years

Qualification: M.Pharm

Technical Requirement: Solid Oral Formulation Development

Key Responsibilities

Development of solid oral dosage forms.

Scale-up and technology transfer activities.

Stability study evaluation.

Optimization of formulations for commercial production.

Required Documents

Candidates attending the interview should carry:

Updated Resume/CV

Aadhaar Card

Current CTC Breakup

Passport Size Photograph

Educational Certificates

Experience Documents

Important Note

Candidates must be willing to sign a 3-year long-term association agreement with the organization.

Why Join Bharat Parenterals Limited?

Opportunity to work in a reputed pharmaceutical organization.

Exposure to advanced analytical techniques and formulation development.

Career growth in Quality Control, Quality Assurance, and R&D functions.

Professional work environment with regulatory compliance standards.

Technical FAQs

1. What is the role of HPLC and GC in Quality Control?

HPLC (High Performance Liquid Chromatography) and GC (Gas Chromatography) are analytical techniques used for identification, quantification, purity testing, and impurity profiling of pharmaceutical products and raw materials.

2. What are IPQA activities in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) involves monitoring manufacturing processes, performing line clearance, verifying GMP compliance, conducting process checks, and ensuring product quality during production.

3. What is meant by Solid Oral Formulation Development?

Solid oral formulation development involves designing and optimizing tablets, capsules, and other oral dosage forms to achieve desired stability, efficacy, dissolution, and manufacturability.

4. What is an Out of Specification (OOS) result?

An OOS result occurs when a laboratory test result falls outside the predefined acceptance criteria. Such results require investigation to determine root cause and corrective actions.

5. Why is GMP important in the pharmaceutical industry?

Good Manufacturing Practices (GMP) ensure pharmaceutical products are consistently manufactured and controlled according to quality standards, ensuring patient safety and regulatory compliance.

Conclusion

The Bharat Parenterals Limited Walk-In Interview 2026 offers an excellent opportunity for professionals in Quality Control, Quality Assurance, and Formulation Development. Candidates possessing the required qualifications and relevant experience are encouraged to attend the interview on 17th and 18th August 2026 at the Vadodara facility with all necessary documents.

Bharat Parenterals Limited Walk-In Interview – QC, QA & Formulation Development Opportunities
Bharat Parenterals Limited Walk-In Interview – QC, QA & Formulation Development Opportunities

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