India's DMPLOI - Jobs & Networking AppBioMatrix Healthcare has announced a Walk-In Interview Drive on 14 June 2026 (Sunday) for multiple positions across Quality Control (QC), Analytical Development Laboratory (ADL), Production, and Engineering departments. The company is inviting qualified and experienced professionals from the pharmaceutical industry to join its growing team.
As a leading manufacturer and exporter of Oral Solid Dosage (OSD), liquid, and dry syrup formulations, BioMatrix Healthcare operates under stringent international quality standards, including EU-GMP, WHO-GMP, and Health Canada approvals. This recruitment drive offers excellent career opportunities for candidates seeking growth in a regulated pharmaceutical manufacturing environment.
About BioMatrix Healthcare
BioMatrix Healthcare is a reputed pharmaceutical company known for its strong research and development capabilities and global presence. The organization specializes in the manufacturing and export of high-quality pharmaceutical formulations while maintaining compliance with international regulatory standards.
Walk-In Interview Details
Interview Date: 14 June 2026 (Sunday)
Registration Time: 09:30 AM to 01:00 PM
Interview Venue:
Corporate Office, 502-B, Times Square Grand,
Sindhu Bhavan Road, Thaltej, Ahmedabad – 380059
Job Location:
Survey No. 624, Sarkhej-Bavla Highway, Vill. Rajoda, Ahmedabad, Gujarat
Open Positions
1. Quality Control (QC) Department
Designation: Officer to Sr. Officer
Experience: 2–6 Years
Qualification: B.Sc, M.Sc, B.Pharm
Key Responsibilities
Analytical testing of raw materials, in-process samples, finished products, and stability samples.
Operation and troubleshooting of HPLC and GC instruments.
Compliance with GMP, GLP, and regulatory requirements.
Documentation and review of analytical records.
2. Analytical Development Laboratory (ADL)
Designation: Officer to Sr. Officer
Experience: 2–6 Years
Qualification: M.Sc, B.Pharm
Key Responsibilities
Method development and validation activities.
Routine analytical testing of OSD products.
Exposure to formulation development and analytical techniques.
Preparation of validation protocols and reports.
3. Production Department
Designation: Officer / Operator
Experience: 2–6 Years
Qualification: ITI, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm
Key Responsibilities
Operation of granulation, compression, coating, and encapsulation equipment.
Monitoring critical process parameters.
Line clearance and equipment cleaning activities.
Maintaining production records as per SOPs and BMRs.
4. Engineering Department
Designation: Officer / Operator
Experience: 2–6 Years
Qualification: ITI, Diploma, BE (Mechanical/Electrical)
Key Responsibilities
Preventive and breakdown maintenance of pharmaceutical equipment.
Calibration and maintenance of instruments and utilities.
Ensuring equipment uptime and reliability.
Compliance with safety and engineering standards.
How to Apply
Candidates unable to attend the walk-in interview can share their updated CVs through:
Email:
career@biomatrixhealthcare.com
hr@biomatrixhealthcare.com
Contact Numbers:
63574 10551
63589 70525
97259 01031
92288 93058
Technical FAQs
1. What is the purpose of system suitability testing in HPLC analysis?
System suitability testing verifies that the HPLC system is performing correctly before sample analysis. Parameters such as theoretical plates, tailing factor, resolution, and %RSD of replicate injections are evaluated to ensure reliable analytical results.
2. Why is method validation important in an ADL laboratory?
Method validation demonstrates that an analytical method is suitable for its intended purpose. Validation parameters include accuracy, precision, specificity, linearity, robustness, LOD, and LOQ as per ICH guidelines.
3. What are critical process parameters (CPPs) in tablet manufacturing?
CPPs are process variables that directly affect product quality. Examples include granulation moisture content, compression force, tablet hardness, coating spray rate, and inlet air temperature.
4. What is preventive maintenance in pharmaceutical engineering?
Preventive maintenance involves scheduled inspection, servicing, calibration, and replacement of equipment components to minimize unexpected breakdowns and ensure continuous production operations.
5. What is the significance of GMP documentation in pharmaceutical manufacturing?
GMP documentation ensures traceability, consistency, and regulatory compliance. Accurate records help demonstrate that products are manufactured and tested according to approved procedures and quality standards.
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