BDR Walk-In QA QC Production

BDR Pharma Walk-In 2026 | QA QC Production Jobs

BDR Pharmaceuticals hiring for QA, QC, Production, Engineering & API/OSD roles in Vadodara. B.Pharm, M.Pharm, BSc eligible.

BDR Pharmaceuticals International Pvt. Ltd. has announced a major walk-in drive for multiple pharmaceutical manufacturing and quality operations roles at its Luna Plant near Vadodara, Gujarat. The company is inviting experienced pharma professionals and fresh talent for Production, Quality Control, Quality Assurance, Analytical Method Validation, Micro QC, Engineering, API Manufacturing, and OSD Manufacturing departments.

This walk-in interview is scheduled for 23 May 2026 and offers opportunities for candidates with qualifications including B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, M.Tech, ITI, Diploma, and Microbiology backgrounds.

Professionals looking for pharma jobs in Gujarat, USFDA plant vacancies, API production jobs, OSD manufacturing careers, quality assurance jobs, analytical development roles, pharmaceutical engineering jobs, and regulated market pharma opportunities can apply for these openings.

BDR Pharmaceuticals is particularly seeking candidates with exposure to regulated market products and experience in USFDA-approved pharmaceutical plants.

Company Overview

BDR Pharmaceuticals International Pvt. Ltd. is a well-known pharmaceutical company engaged in manufacturing and development operations across API and formulation businesses.

The organization has built a strong presence in regulated pharmaceutical markets and continues to expand its operations through advanced manufacturing systems, quality-focused production, and compliance-driven pharmaceutical practices.

The Luna manufacturing facility near Vadodara supports multiple pharmaceutical operations including:

• API manufacturing
• OSD manufacturing
• Pharmaceutical packing
• Granulation
• Quality assurance
• Quality control
• Analytical method validation
• Engineering support
• Microbiology quality operations

The company’s hiring focus on regulated market exposure and USFDA-approved plant experience reflects its commitment to global pharmaceutical quality standards.

Professionals working in regulated pharmaceutical plants gain exposure to:

• cGMP compliance
• USFDA documentation standards
• Pharmaceutical validation systems
• Data integrity practices
• Analytical laboratory operations
• Pharmaceutical engineering systems
• Quality management systems
• Manufacturing process optimization

These capabilities are highly valuable in the pharmaceutical and healthcare manufacturing industry.

Job Role & Responsibilities

BDR Pharmaceuticals is hiring for multiple departments and roles across API and OSD divisions.

Production – API / SPD

Candidates working in API production operations will be responsible for:

• Monitoring API manufacturing processes
• Following batch manufacturing procedures
• Handling regulated manufacturing operations
• Maintaining GMP compliance
• Process documentation and batch records
• Coordinating production activities
• Equipment operation and troubleshooting
• Maintaining safety and quality standards

Production – OSD (Packing & Granulation)

OSD manufacturing professionals may handle:

• Granulation activities
• Tablet and capsule manufacturing operations
• Packing line supervision
• Secondary and primary packing activities
• Machine operation and maintenance coordination
• Packaging documentation
• Line clearance activities
• Batch execution processes

Analytical Method Validation & Development – API/OSD

Analytical professionals will be expected to:

• Perform analytical method validation
• Conduct analytical method development activities
• Handle pharmaceutical analytical instruments
• Review analytical documentation
• Maintain regulatory compliance
• Perform stability and analytical studies
• Support quality investigations

Quality Control – OSD

Quality Control candidates may perform:

• Finished product testing
• Stability sample analysis
• Raw material analysis
• Instrument calibration support
• Analytical data review
• GLP documentation maintenance
• Laboratory compliance activities

Micro QC

Microbiology quality professionals may handle:

• Microbial testing activities
• Environmental monitoring
• Sterility-related testing
• Laboratory documentation
• Media preparation and microbiological analysis
• GMP and GLP compliance

Quality Assurance – API/OSD

Quality Assurance professionals will support:

• Batch document review
• Deviation management
• Change control systems
• CAPA activities
• Investigation handling
• Compliance monitoring
• Audit preparation
• Quality management systems

AQA & Issuance

Candidates may handle:

• Documentation issuance
• Controlled document management
• Compliance tracking
• Pharmaceutical documentation systems
• SOP management

Engineering – Electrical & Mechanical

Engineering professionals will support:

• Preventive maintenance
• Electrical maintenance
• Mechanical troubleshooting
• Utility systems maintenance
• Pharmaceutical equipment support
• HVAC and plant maintenance systems
• Engineering documentation

Eligibility / Qualifications

Educational Qualification

Candidates with the following qualifications can apply:

• B.Pharm
• M.Pharm
• B.Sc
• M.Sc
• B.Tech
• M.Tech
• ITI
• Diploma
• Microbiology

Relevant Courses

Bachelor of Pharmacy, Master of Pharmacy, Pharmaceutical Sciences, Chemistry, Analytical Chemistry, Microbiology, Biotechnology, Chemical Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering, Diploma in Mechanical Engineering, Diploma in Electrical Engineering, Life Sciences

Experience Required

Different departments require different experience levels:

• 0 to 12 years depending on role
• Apprentice to Executive-level openings available
• Freshers and experienced professionals can apply for selected positions

Preferred Candidate Profile

BDR Pharmaceuticals prefers:

• Candidates with regulated market exposure
• Professionals from USFDA-approved plants
• Candidates familiar with GMP documentation
• Individuals with pharmaceutical manufacturing experience
• Professionals with analytical and compliance exposure

Why Pharma Professionals Prefer Regulated Market Companies

Working in regulated pharmaceutical facilities provides strong long-term career growth opportunities.

Professionals in regulated market plants gain exposure to:

• USFDA compliance systems
• MHRA standards
• Pharmaceutical quality systems
• Data integrity practices
• International manufacturing standards
• Validation and qualification procedures
• Pharmaceutical regulatory frameworks

These skills improve career growth prospects in:

• Pharmaceutical manufacturing
• Regulatory affairs
• Validation
• Quality operations
• Analytical research
• Global pharmaceutical companies
• Contract manufacturing organizations

Candidates with regulated market exposure often receive better opportunities and higher salary growth within the pharmaceutical sector.

Location & Salary

Job Location

Luna, Padra, Vadodara, Gujarat

Approximate Salary

Based on pharmaceutical industry standards and experience level, expected salary ranges may include:

• Freshers & Apprentices: ₹2.2 LPA to ₹3.5 LPA
• Officers & Executives: ₹3.5 LPA to ₹8 LPA
• Senior Executives & Assistant Managers: ₹8 LPA to ₹14 LPA

Salary depends on:

• Experience level
• Technical skills
• Regulatory market exposure
• Current CTC
• Department specialization

Candidates with USFDA plant experience and strong pharmaceutical compliance knowledge may receive higher compensation packages.

Application Process

Interested candidates can attend the walk-in interview directly.

Walk-In Interview Details

• Date: 23 May 2026
• Time: 10:00 AM to 04:00 PM

Venue

BDR Pharmaceuticals International Private Limited 578 & 579, Near Effluent Channel Road, Village Luna, Taluka Padra, District Vadodara – 391440

Important Note

The walk-in drive is only for the mentioned openings.

Candidates interested in other positions can visit the BDR career portal:

https://bdrhrcareers.peoplestrong.com/job/joblist

Contact Details

API Division

• Kush Dave – kush.dave@bdrpharma.com
• Vidhi Machhi – vidhi.machhi@bdrpharma.com
• Mrunali Uttekar – mrunali.uttekar@bdrpharma.com

OSD Division

• Pritam Singha – pritam.singha@bdrpharma.com

Documents to Carry

Candidates should carry:

• Updated Resume
• Educational Certificates
• Experience Documents
• Salary Slips
• Government ID Proof
• Passport Size Photographs

Career Growth Opportunities in Pharma Manufacturing

The pharmaceutical manufacturing sector in India continues to generate strong hiring demand across:

• API manufacturing
• OSD manufacturing
• Quality assurance
• Quality control
• Analytical research
• Engineering services
• Regulatory affairs
• Validation operations

Professionals with experience in regulated market plants often transition into senior roles such as:

• Production Manager
• QA Manager
• QC Lead
• Validation Specialist
• Compliance Manager
• Analytical Scientist
• Engineering Head
• Plant Operations Manager

India remains one of the largest pharmaceutical manufacturing hubs globally, making regulated pharmaceutical experience highly valuable.

FAQs

1. Which company is conducting this walk-in drive?

BDR Pharmaceuticals International Pvt. Ltd. is conducting the walk-in drive for multiple pharmaceutical roles.

2. Which departments are hiring?

Departments include Production, Quality Control, QA, Engineering, Micro QC, Analytical Method Validation, API, and OSD Manufacturing.

3. What qualifications are eligible?

Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, M.Tech, ITI, Diploma, and Microbiology qualifications can apply.

4. Is regulated market experience preferred?

Yes, candidates with regulated market exposure and USFDA-approved plant experience are preferred.

5. Where is the job location?

The work location is Luna, Padra, Vadodara, Gujarat.

6. What is the walk-in interview date?

The walk-in drive will be conducted on 23 May 2026.

Summary Table

Company	BDR Pharmaceuticals International Pvt. Ltd.
Department Vacancies	Production, QA, QC, API, OSD, Engineering, Micro QC, AMV
Qualification	B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, M.Tech, ITI, Diploma
Experience	0–12 Years
Location	Vadodara