BioMatrix Healthcare has announced a Walk-In Interview in Ankleshwar on 28 February 2026 for multiple positions in API Manufacturing, Quality Control, Research & Development, Production, QMS, Process Engineering, and EHS at its Vadodara, Gujarat facility.
This recruitment drive supports the company’s backward integration strategy to strengthen its API manufacturing operations in Vadodara. Candidates with experience in pharmaceutical and API manufacturing are encouraged to attend.
📅 Walk-In Interview Details
- Date: 28 February 2026
- Registration Time: 09:30 AM – 12:30 PM
- Venue: VITS Shalimar Hotel, Near Railway Station, GIDC Reservoir, Valia Road, Ankleshwar – 393002
- Plant Location: Survey No. 241/1, Samlaya Sherpura Road, Pratap Nagar, Savli – 391520, Vadodara, Gujarat
Available Job Openings at BioMatrix Healthcare
BioMatrix Healthcare is hiring experienced professionals in API pharmaceutical manufacturing across the following departments:
🔹 Department: Production
1️⃣ QMS (5–8 Years) – Officer to Sr. Executive
Key Responsibilities:
- Handling CCF, OOS, OOT, deviation & risk assessment reports
- Process validation (PV), cleaning validation (CV)
- Equipment qualification documentation
- Compliance with cGMP & regulatory standards
2️⃣ Process Engineer (8–10 Years) – Officer to Sr. Executive
Key Responsibilities:
- Mass & heat balance preparation
- Utility calculations & product costing
- PFD, P&ID & Design Basis development
- Technology transfer (R&D to Pilot to Commercial plant)
3️⃣ Manufacturing (6–10 Years) – Officer to Sr. Executive
Key Responsibilities:
- Batch production handling
- Cryogenic reaction management
- Regulatory-compliant manufacturing
- Coordination with service departments
🔹 Department: Quality Control
GLP Executive (6–8 Years)
- GLP compliance
- Stability studies & AMV
QC Analyst (2–5 Years) – Officer to Executive
- Instrument calibration & verification
- WS/RS/Column/IMP management
- RM/PM/In-process/FG testing
🔹 Department: Research & Development
Synthesis (3–8 Years) – Officer to Executive
- Literature search & ROS finalization
- Molecule synthesis
- Daily reaction monitoring
ADL (3–8 Years) – Officer to Executive
- Method development & validation
- HPLC, GC, UV, IR, KF, GCMS, LCMS analysis
- Routine API & intermediate testing
🔹 Department: EHS (8–10 Years)
- Monitoring EHS compliance
- CAPA initiation
- ETP & MEE operations at ZLD plant
- Statutory compliance management
Eligibility Criteria
✔ Experience in API / Pharmaceutical Manufacturing Industry
✔ Relevant technical qualification (B.Pharm, M.Pharm, MSc, BE/BTech Chemical, etc.)
✔ Strong knowledge of cGMP & regulatory compliance
✔ Experience as per role requirement
Salary & Benefits
- Estimated Salary Range: ₹3.0 LPA – ₹12.0 LPA (Based on experience & role)
- Opportunity to work in a rapidly expanding API manufacturing company
- Exposure to regulatory-compliant pharmaceutical operations
- Career growth in integrated pharma ecosystem
How to Apply?
Interested candidates can:
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