Bafna Pharmaceuticals Ltd. has announced a Walk-In Interview for experienced pharmaceutical professionals at its MHRA-approved Formulation Plant in Chennai. The company is hiring for multiple departments including Production, Operators, Quality Control (QC), Quality Assurance (QA), Stores, and Maintenance.

Candidates with qualifications such as B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, Diploma, or Any Degree are invited to attend the interview based on the eligibility criteria mentioned below.

Walk-In Interview Details

Company: Bafna Pharmaceuticals Ltd.

Plant: Formulation Plant (MHRA Approved)

Interview Type: Walk-In Interview

Walk-In Date: 05 July 2026

Time: 09:00 AM to 01:00 PM

Job Location: Chennai, Tamil Nadu

Available Job Positions

1. Production Executive

Qualification:

B.Pharm / M.Pharm

Experience:

4–5 Years

Area of Exposure:

Packing

Manufacturing

2. Operators

Qualification:

ITI

Diploma

Any Degree

Experience:

4–5 Years

Area of Exposure:

Primary Packing

BQS

Granulation

Compression

3. Quality Control Executive

Qualification:

B.Sc (Chemistry)

M.Sc (Chemistry)

B.Pharm

M.Pharm

Experience:

2–6 Years

Technical Skills:

HPLC

GC

LIMS

4. Stores Executive

Qualification:

ITI

Diploma

Any Degree

Experience:

3–5 Years

Area of Exposure:

RM Dispensing

5. Maintenance

Qualification:

ITI / Diploma

Experience:

5–8 Years

Area of Exposure:

Process Maintenance

6. Quality Assurance (QA)

Qualification:

B.Pharm / M.Pharm

Experience:

5–6 Years

Area of Exposure:

QMS

Validation

Interview Venue

Bafna Pharmaceuticals Ltd.

#147, Madhavaram Redhills High Road,

Grantlyon Village, Redhills,

Chennai – 600052, Tamil Nadu.

Documents to Carry

Updated Resume

Recent Passport Size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slips

Government ID Proof (Aadhaar/PAN)

Passport (if available)

Why Join Bafna Pharmaceuticals?

MHRA-approved formulation manufacturing facility.

Opportunity to work with experienced pharmaceutical professionals.

Career growth in Production, QA, QC, Maintenance, and Stores.

Exposure to international quality standards.

Stable career opportunities in the pharmaceutical manufacturing industry.

5 Technical FAQs

1. What is HPLC and why is it important in Quality Control?

Answer: High Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, separate, and quantify pharmaceutical compounds. It ensures products meet quality specifications before release.

2. What is the role of QMS in Quality Assurance?

Answer: A Quality Management System (QMS) ensures pharmaceutical products are consistently manufactured according to GMP guidelines through documentation, deviation handling, CAPA, change control, and audits.

3. What is RM Dispensing in pharmaceutical manufacturing?

Answer: RM (Raw Material) Dispensing is the controlled process of accurately weighing and issuing raw materials according to the approved Batch Manufacturing Record (BMR) while maintaining traceability and compliance.

4. What is process validation?

Answer: Process validation is the documented evidence that a manufacturing process consistently produces products meeting predetermined quality standards, ensuring product safety, efficacy, and regulatory compliance.

5. What are the key responsibilities of a Production Executive?

Answer: A Production Executive supervises manufacturing operations, ensures GMP compliance, maintains batch documentation, monitors equipment performance, coordinates with QA/QC teams, and ensures production targets are achieved safely and efficiently