Concord Biotech Limited, one of India’s leading biotechnology and pharmaceutical companies, has announced a Walk-In Interview for experienced candidates in the Production and Quality Control (QC) departments. This recruitment drive offers excellent career opportunities for professionals with experience in pharmaceutical manufacturing, analytical testing, granulation, coating, and quality control operations.
Candidates meeting the required qualifications and experience criteria are invited to attend the interview and become part of a growing pharmaceutical organization committed to quality, innovation, and regulatory compliance.
Walk-In Interview Details
Particulars Details
Company Name
Concord Biotech Limited
Location
Unit-II, Valthera, Taluka Dholka, Ahmedabad, Gujarat
Interview Date
27th June 2026
Interview Time
10:00 AM to 2:00 PM
Industry
Pharmaceutical / Biotechnology
Job Type
Walk-In Interview
About Concord Biotech Limited
Concord Biotech Limited is a renowned biotechnology company specializing in fermentation-based APIs, formulations, and biotechnology products. The company is known for its commitment to quality manufacturing, regulatory compliance, innovation, and global healthcare solutions.
Working with Concord Biotech offers professionals exposure to advanced pharmaceutical manufacturing technologies, GMP-compliant operations, and opportunities for career growth.
Available Positions
Production Department
1. Assistant Manager / Senior Executive
Qualification:
B.Pharm / M.Pharm
Experience:
10 to 15 Years
Key Responsibilities:
Manage daily manufacturing operations.
Ensure compliance with cGMP, safety, and regulatory requirements.
Production planning and execution.
Preparation of batch manufacturing records.
Handling qualification activities (IQ/OQ/PQ).
Coordination with QC and Warehouse departments.
Equipment maintenance and calibration tracking.
Team management and training activities.
2. Supervisor / Officer
Qualification:
M.Sc / B.Pharm / M.Pharm
Experience:
3 to 5 Years
Key Responsibilities:
Manufacturing process execution.
Granulation operations.
Coating process handling.
Capsule filling machine operations.
Process monitoring and documentation.
3. Granulation / Compression / Coating Operator
Qualification:
ITI / Diploma
Experience:
3 to 7 Years
Key Responsibilities:
Operating FBP (Fluid Bed Processor) for top spray granulation.
Compression machine operation.
Coating machine operation.
Equipment cleaning and maintenance.
GMP documentation compliance.
Quality Control (QC) Department
1. HPLC Analyst
Qualification:
B.Sc / M.Sc / B.Pharm
Experience:
6 to 8 Years
Key Responsibilities:
Analysis of raw materials.
Testing of finished products.
In-process sample analysis.
HPLC instrument operation and troubleshooting.
Documentation and data integrity compliance.
2. Dissolution & Chemical Analyst
Qualification:
B.Sc / M.Sc / B.Pharm
Experience:
2 to 5 Years
Key Responsibilities:
Dissolution testing.
Karl Fischer moisture analysis.
Auto titrator operation.
UV spectroscopy analysis.
ICP-OES/MS testing.
Chemical analysis and documentation.
3. GC Analyst
Qualification:
B.Sc / M.Sc / B.Pharm
Experience:
5 to 7 Years
Key Responsibilities:
Gas Chromatography (GC) analysis.
Headspace GC operation.
Raw material testing.
Finished product analysis.
In-process sample evaluation.
Method execution and reporting.
Documents Required
Candidates attending the walk-in interview should carry:
Updated Resume/CV
Passport Size Photograph
Current Salary Proof
Educational Certificates
Experience Certificates
Identity Proof
Alternative Application Method
Candidates who are unable to attend the walk-in interview can apply through the company’s official recruitment email by clearly mentioning the position applied for in the subject line.
Why Join Concord Biotech?
Strong growth opportunities
Learning and development programs
Safe and compliant work environment
Exposure to advanced pharmaceutical technologies
Collaborative and professional culture
Long-term career development prospects
Technical FAQs
1. What is IQ, OQ, and PQ in pharmaceutical manufacturing?
IQ (Installation Qualification) verifies equipment installation, OQ (Operational Qualification) confirms operational performance, and PQ (Performance Qualification) demonstrates consistent performance under routine manufacturing conditions.
2. What is the purpose of HPLC analysis in QC?
High Performance Liquid Chromatography (HPLC) is used to identify, quantify, and assess the purity of pharmaceutical compounds in raw materials, intermediates, and finished products.
3. What is FBP in granulation processes?
FBP (Fluid Bed Processor) is equipment used for drying, granulation, and coating pharmaceutical products by fluidizing particles with controlled airflow.
4. Why is dissolution testing important?
Dissolution testing measures the rate and extent of drug release from a dosage form, ensuring product performance, bioavailability, and regulatory compliance.
5. What is Headspace GC analysis?
Headspace Gas Chromatography is used to detect and quantify residual solvents and volatile impurities in pharmaceutical products without direct sample injection.
Conclusion
The Concord Biotech Walk-In Interview on 27th June 2026 presents an excellent opportunity for experienced professionals in Production and Quality Control functions. Candidates with expertise in manufacturing operations, granulation, coating, HPLC, GC, dissolution testing, and pharmaceutical quality systems are encouraged to attend and explore rewarding career opportunities with one of India’s leading biotechnology companies.


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