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BioMatrix Healthcare Announces Walk-in Interviews in Vadodara for Multiple Departments
BioMatrix Healthcare Pvt. Ltd., a pharmaceutical manufacturing company with EU-GMP and Health Canada certifications, is conducting walk-in interviews on Sunday, 2nd November, 2025, at their Vadodara facility. The recruitment drive aims to fill positions across Production, EHS (Environment, Health & Safety), and Warehouse departments.
Event Details
Date: November 2, 2025 (Sunday)
Time: 9:30 AM to 12:00 PM
Venue:
Baroda Productivity Council, 2nd Floor, Productivity House, Productivity Road, Alkapuri, Vadodara – 390007
About BioMatrix Healthcare
BioMatrix Healthcare Pvt. Ltd. has established a new API (Active Pharmaceutical Ingredient) manufacturing facility in Baroda, targeting regulatory markets including WHO, EU, US, South Africa, and ROW (Rest of World). The company is supported by Aamyo Laboratories Pvt. Ltd., which provides a state-of-the-art cGMP plant, in-house R&D, analytical laboratories, and quality control backed by a highly qualified team.
The company focuses on essential medicines across therapeutic areas including anticancer, antidepressants, antidiabetics, antihypertensive, antiplatelet, antifungals, and anticoagulants.
Open Positions
Production Department
Position 1:
Education: B.Sc/M.Sc/B.Pharm/Diploma in Chemical Engineering
Experience: 2-6 years
Designation: Officer/Sr. Officer/Sr. Executive
Position 2:
Education: B.E/B.Tech/M.Sc in Chemical/Pharma Engineering
Experience: 8-15 years
Designation: Assistant Manager/Manager
EHS (Environment, Health & Safety) Department
Position 1:
Education: B.Sc/M.Sc (Chemistry/Environment) or Diploma/B.Tech in Safety/Environmental Engineering
Experience: 3-8 years
Designation: Officer/Sr. Officer/Executive/Sr. Executive
Position 2:
Education: B.E/M.Tech/M.Sc with Diploma in Industrial Safety
Experience: 10-18 years
Designation: Assistant Manager/Manager
Position 3:
Education: ITI/Diploma (Industrial Safety preferred)
Experience: 2-5 years
Designation: Operator
Warehouse Department
Position 1:
Education: B.Sc/B.Com/B.Pharm/MBA
Experience: 3-8 years
Designation: Officer/Sr. Officer/Executive/Sr. Executive
Position 2:
Education: Graduate/PG (Science/Commerce/Pharma)
Experience: 8-15 years
Designation: Assistant Manager/Manager
Position 3:
Education: 10th/12th/ITI
Experience: 2-5 years
Designation: Operator
Industry Preference
BioMatrix Healthcare specializes in API/Chemical/Pharmaceutical Manufacturing.
Plant Location
The manufacturing facility is located at Survey No. 241/1, Samlaya Sherpura Road, Pratap Nagar, Savli 391520, Vadodara, Gujarat.
How to Apply?
Interested candidates are requested to bring their updated CV to the walk-in interview. For advance applications, candidates can also email their resumes to hr@aamyolabs.com or contact via WhatsApp at 9723750054.
FAQ:
1. What are the key parameters monitored during API manufacturing in the production area?
Answer:
Key process parameters include:
Reaction parameters: Temperature, pH, pressure, agitation speed, and reaction time.
Material transfer: Charging sequence, solvent ratios, and addition rates.
Crystallization & Filtration: Cooling rate, seed addition, and slurry handling.
Drying: Inlet/outlet temperature, vacuum level, and moisture content (LOD).
Documentation: BMR/BPR entries, process deviation reporting, and batch traceability.
2. What are the major EHS (Environment, Health & Safety) requirements in a pharmaceutical API plant?
Answer:
EHS requirements include:
Handling of hazardous chemicals as per MSDS and PPE compliance.
Implementation of risk assessments (HAZOP/JSA).
Control of VOC and solvent emissions through scrubbers.
Waste management: Segregation of hazardous and non-hazardous waste.
Emergency preparedness: Mock drills, fire extinguisher training, and spill response.
Permit-to-work system: For confined space, hot work, and height work.
3. How do you ensure cGMP compliance in production activities?
Answer:
Follow SOPs and approved batch records strictly.
Maintain cleanliness and line clearance before batch start-up.
Record in-process checks (pH, yield, assay, etc.) in real-time.
Use calibrated instruments and equipment only.
Ensure material traceability through status labeling (RM, PM, WIP, FG).
Immediately report deviations or breakdowns to QA/Engineering.
4. What are the important aspects of Warehouse management in a regulated pharma environment?
Answer:
Material receipt and quarantine as per SOP.
Segregation: RM, PM, intermediates, and finished goods stored separately.
Environmental monitoring: Temperature and humidity control with log records.
FIFO/FEFO system for inventory management.
Material dispensing under supervision with cross-verification.
Compliance with GDP (Good Distribution Practices).
5. What safety precautions are followed during solvent handling and storage?
Answer:
Use flame-proof (FLP) equipment and intrinsically safe electrical fittings.
Store solvents in earthing and bonding-protected tanks/drums to prevent static charge.
Maintain ventilation and LEL (Lower Explosive Limit) monitoring.
Ensure spill kits, fire extinguishers, and PPEs are readily available.
Follow SOP for solvent transfer and recovery using closed systems.
Maintain MSDS accessibility and training for all operators.
