BioMatrix Walk-in API Production, QC & R&D
- Company Overview
- Job Role & Responsibilities
- Production – API Manufacturing
- Quality Control – API Laboratory
- Research & Development – API Development
- Eligibility / Qualifications
- Location & Walk-In Details
- Application Process
- Why API Manufacturing Careers Are High Value
- Career Growth Opportunities
- Frequently Asked Questions (FAQs)
- 1. Where is the actual job location?
- 2. Where is the walk-in interview conducted?
- 3. Is API experience mandatory?
- 4. Are freshers eligible?
- 5. What documents should I carry?
- Walk-In Drive Summary
BSc MPharm API Jobs Ankleshwar Vadodara
BSc/MSc/BPharm API Production, QC & R&D vacancies at BioMatrix API Manufacturing, Vadodara. Walk-in 28 Feb 2026 Ankleshwar.
BioMatrix is conducting walk-in interviews in Ankleshwar for its expanding API manufacturing operations in Vadodara, Gujarat. As part of its strategic backward integration into Active Pharmaceutical Ingredient (API) production, the company is hiring experienced professionals across Production, Quality Control, and Research & Development departments.
If you are looking for API manufacturing jobs in Gujarat, process engineer roles in bulk drug plants, pharmaceutical QC careers, or R&D opportunities in regulated manufacturing environments, this walk-in drive offers direct access to a growing integrated pharmaceutical setup.
Company Overview
BioMatrix is strengthening its presence in the pharmaceutical industry by expanding into API manufacturing as part of a vertically integrated growth strategy. The company’s expansion into bulk drug production supports end-to-end pharmaceutical capabilities, from API development to finished dosage manufacturing.
Integrated pharmaceutical ecosystems are critical in today’s global market. Backward integration into API manufacturing enhances supply chain control, regulatory compliance, cost efficiency, and product quality assurance.
API plants must operate under strict cGMP guidelines, environmental compliance norms, and international regulatory expectations. Professionals working in such facilities gain hands-on exposure to:
- Bulk drug manufacturing processes
- Process engineering and scale-up
- Quality Control laboratory systems
- Research & Development innovation pipelines
- Regulatory audit readiness and documentation systems
The expansion in Vadodara reflects the company’s long-term investment in high-value pharmaceutical manufacturing infrastructure.
Job Role & Responsibilities
BioMatrix is hiring for multiple technical functions in API manufacturing.
Production – API Manufacturing
Role: Production Professionals / Process Engineers
Key Responsibilities:
- Handling bulk drug production processes
- Monitoring reaction parameters and batch manufacturing activities
- Managing reactor charging and mass balance operations
- Ensuring compliance with Batch Manufacturing Records (BMR)
- Maintaining safety and cGMP standards on the shop floor
- Coordinating with Quality Control for in-process testing
Process Engineers will focus on optimizing yield, improving efficiency, and ensuring regulatory compliance during scale-up and commercial production.
Experience in chemical synthesis, reactor operations, and API bulk drug plants is highly preferred.
Quality Control – API Laboratory
Key Responsibilities:
- Performing analytical testing of raw materials, intermediates, and finished APIs
- Operating instruments such as HPLC, GC, and related analytical systems
- Supporting method validation and stability studies
- Handling OOS (Out of Specification) and deviation investigations
- Maintaining documentation in accordance with data integrity principles
Quality Control professionals play a direct role in regulatory submission readiness and batch release compliance.
Research & Development – API Development
Key Responsibilities:
- Supporting API process development activities
- Conducting laboratory-scale trials and optimization studies
- Assisting in scale-up from lab to pilot plant
- Preparing technical documentation for process transfer
- Collaborating with Production and QC teams for validation support
R&D roles contribute to innovation, cost optimization, and development of robust API synthesis pathways.
Eligibility / Qualifications
Educational Qualifications (comma-separated):
B.Sc Chemistry, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, B.Pharm, M.Pharm, B.Tech Chemical Engineering, M.Tech Chemical Engineering
Experience Requirements:
- Relevant experience in API manufacturing or bulk drug production preferred
- Exposure to reactor operations and chemical synthesis (Production roles)
- Analytical instrument handling experience (QC roles)
- Process development exposure (R&D roles)
Core Skills:
- Knowledge of cGMP compliance
- Documentation accuracy and audit readiness
- Understanding of regulatory standards in API manufacturing
- Strong technical and analytical aptitude
Candidates without relevant pharmaceutical manufacturing experience may not meet eligibility criteria.
Location & Walk-In Details
Walk-In Date: 28th February 2026
Registration Time: 09:30 AM – 12:30 PM
Interview Venue:
VITS Shalimar Hotel
Near Railway Station
GIDC Reservoir, Valia Road
Ankleshwar – 393002
Work Location: Vadodara, Gujarat (API Manufacturing Unit)
Vadodara and Ankleshwar are key pharmaceutical manufacturing hubs in Gujarat, offering strong exposure to export-driven API production and regulated market operations.
Salary will depend on experience, technical competency, and prior API exposure.
Application Process
Interested candidates should attend the walk-in interview on the specified date and time.
Steps to Apply:
- Carry updated resume with detailed API manufacturing experience.
- Highlight process engineering, QC instrumentation, or R&D expertise clearly.
- Attend registration between 09:30 AM and 12:30 PM.
- Participate in technical and HR discussion rounds.
Candidates are advised to arrive early to ensure smooth registration.
Why API Manufacturing Careers Are High Value
Active Pharmaceutical Ingredient manufacturing forms the foundation of the pharmaceutical supply chain. Without high-quality APIs, finished formulations cannot meet regulatory approval standards.
Professionals working in API plants develop expertise in:
- Chemical process scale-up
- Industrial reactor management
- Regulatory documentation and compliance
- Quality Control validation systems
- Integrated pharmaceutical manufacturing ecosystems
Global demand for compliant API facilities continues to grow, making API production and R&D careers highly stable and technically rewarding.
Career Growth Opportunities
Selected candidates may progress toward:
- Senior Production Manager – API
- Process Development Lead
- QC Laboratory Manager
- Technical Services Head
- Regulatory Compliance Manager – API Division
Experience in integrated API manufacturing significantly strengthens long-term earning potential in regulated pharmaceutical markets.
Frequently Asked Questions (FAQs)
1. Where is the actual job location?
Vadodara, Gujarat (API Manufacturing Unit).
2. Where is the walk-in interview conducted?
At VITS Shalimar Hotel, Ankleshwar.
3. Is API experience mandatory?
It is strongly preferred, especially for Production and QC roles.
4. Are freshers eligible?
Preference is given to experienced professionals; eligibility depends on department requirements.
5. What documents should I carry?
Updated resume and relevant experience details.
Walk-In Drive Summary
| Company | BioMatrix |
|---|---|
| Vacancies | Production / Process Engineer; Quality Control Executive; Research & Development Professional |
| Required Education | B.Sc/M.Sc Chemistry, B.Pharm, M.Pharm, B.Tech/M.Tech Chemical Engineering |
| Experience | Relevant Experience in API Manufacturing Preferred |
