BDR Pharmaceuticals International Pvt. Ltd., a leading pharmaceutical company specializing in API and formulation manufacturing, has announced a Walk-In Drive on 20 June 2026 for experienced professionals across multiple departments. This recruitment drive offers excellent career opportunities for candidates with experience in Production, Engineering, Quality Control, Quality Assurance, ADL, and Research & Development.

Candidates possessing relevant qualifications and pharmaceutical industry experience are invited to attend the interview at the company’s manufacturing facility in Luna, Padra, Vadodara.

Walk-In Interview Details

Particulars Details

Company Name

BDR Pharmaceuticals International Pvt. Ltd.

Interview Date

20 June 2026

Time

10:00 AM to 04:00 PM

Location

BDR Pharmaceuticals International Private Limited, Luna, Padra, Vadodara, Gujarat

Industry

Pharmaceutical Manufacturing

Experience Required

2 to 10 Years

Hiring Type

Walk-In Interview

Available Job Openings

1. Production Department – API Division

Positions

Officer to Technician

Senior Executive

Experience

Officer to Technician: 2–10 Years

Senior Executive: 8–10 Years

Educational Qualification

B.Sc

M.Sc

B.Tech

M.Tech

ITI

Diploma

Key Responsibilities

Shift handling

Production planning

Documentation management

SAP activities

Manufacturing operations

Mandatory Requirement

English written communication skills

2. Production Department – OSD (Granulation & QMS)

Position

Technician to Executive

Experience

3–8 Years

Qualification

B.Pharm

M.Pharm

ITI

Diploma

Functional Area

Granulation

Quality Management System (QMS)

Oral Solid Dosage manufacturing

3. Engineering Department – API Division

Positions

Technician to Senior Officer

Experience

3–7 Years

Qualification

B.E.

Specializations

Mechanical Engineering

Electrical Engineering

Instrumentation Engineering

Documentation activities

4. Engineering Department – OSD Division

Positions

Junior Officer

Senior Executive

Functional Area

Mechanical Engineering

Requirement

Formulation plant experience is mandatory

5. Quality Control (QC) – API/OSD

Position

Officer to Executive

Experience

2–7 Years

Qualification

B.Sc

M.Sc

B.Pharm

M.Pharm

Responsibilities

Analytical testing

Instrument operation

Laboratory documentation

Quality compliance

6. Microbiology QC (Male Candidates Preferred)

Position

Officer & Senior Officer

Experience

2–5 Years

Qualification

B.Sc Microbiology

M.Sc Microbiology

Responsibilities

Environmental monitoring

Microbial analysis

Sterility testing

Laboratory compliance

7. Quality Assurance (QA) – API IPQA & Issuance (Male Candidates Preferred)

Position

Officer to Senior Officer

Experience

2–5 Years

Qualification

B.Sc

M.Sc

Functional Area

In-Process Quality Assurance (IPQA)

Batch issuance

GMP compliance

Documentation review

8. Analytical Development Laboratory (ADL) – API

Position

Officer to Executive

Experience

2–7 Years

Qualification

M.Sc in Organic Chemistry

Responsibilities

Method development

Analytical validation

Stability studies

API analytical support

9. Research & Development (R&D) – API

Position

Officer to Executive

Experience

2–7 Years

Qualification

M.Sc in Organic Chemistry

Expertise Required

Polymorphism studies

Peptide chemistry

Organic synthesis

Process development

Work Location

BDR Pharmaceuticals International Private Limited

578 & 579, Near Effluent Channel Road,

Village: Luna, Taluka: Padra,

District: Vadodara – 391440, Gujarat

Contact Persons

API Division

Kush Dave

Email: kush.dave@bdrpharma.com

Vidhi Machhi

Email: vidhi.machhi@bdrpharma.com

OSD Division

Pritam Singha

Email: pritam.singha@bdrpharma.com

Documents Required for Interview

Candidates should carry:

Updated Resume/CV

Passport Size Photographs

Educational Certificates

Experience Certificates

Salary Slips

Aadhaar Card/PAN Card

Previous Employment Documents

Why Join BDR Pharmaceuticals?

Leading pharmaceutical organization

Opportunities in API and OSD manufacturing

Exposure to advanced technologies

Career growth opportunities

GMP-compliant manufacturing environment

Learning and development programs

Technical FAQs

1. What is the role of IPQA in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) ensures that manufacturing activities comply with approved procedures, GMP guidelines, and quality standards throughout the production process.

2. What is granulation in OSD manufacturing?

Granulation is a process that improves powder flowability and compressibility by converting fine powders into granules before tablet compression.

3. Why is SAP knowledge important in pharmaceutical production?

SAP helps manage production planning, inventory control, batch records, material tracking, and overall operational efficiency within manufacturing facilities.

4. What are the key responsibilities of an ADL professional?

ADL professionals perform analytical method development, method validation, impurity profiling, stability testing, and support regulatory submissions.

5. What is polymorphism in pharmaceutical R&D?

Polymorphism refers to the ability of a drug substance to exist in different crystal forms, which can significantly impact solubility, stability, bioavailability, and manufacturing performance.

Conclusion

The BDR Pharmaceuticals Walk-In Drive on 20 June 2026 presents an excellent opportunity for experienced pharmaceutical professionals seeking career advancement in Production, Engineering, QC, QA, ADL, and R&D departments. Candidates meeting the eligibility criteria are encouraged to attend the interview with all required documents and explore rewarding career opportunities with one of India’s growing pharmaceutical organizations.