Concord Biotech Walk-In Interview Drive for Production and Quality Control Departments
Pharm'Up 
Concord Biotech Limited, a leading biopharmaceutical company specializing in fermentation-based APIs and high-quality formulations, has announced a walk-in interview drive for its manufacturing facility located in Ahmedabad, Gujarat.
Walk-In Interview Details
- Date: October 2, 2026
- Time: 10:00 AM to 2:00 PM
- Venue: 297-298/2P, At: Valthera, Taluka Dholka, Dist. Ahmedabad 382225, Gujarat, India.
- Email for Applications (if unable to attend): careerfdf@concordbiotech.com (mentioning the applied position in the subject line).
Department-Wise Vacancies & Requirements
1. Production Department
- Asst. Manager / Sr. Executive / Executive
- Experience: 05 to 10 years
- Qualifications: M.Sc / B.Pharm / M.Pharm
- Key Responsibilities: Manage daily manufacturing operations as a shift in-charge while ensuring cGMP, safety, and regulatory compliance; handle production planning, batch records, and qualification documents (IQ/OQ/PQ); coordinate with QC and Warehouse; oversee equipment maintenance, calibration tracking, and team training.
- Supervisor / Officer
- Experience: 03 to 05 years
- Qualifications: B.Pharm / M.Pharm
- Key Responsibilities: Handle manufacturing processes including Granulation, Coating, and Capsule Filling Machine operations.
- Granulation / Coating / Capsule Operator
- Experience: 03 to 07 years
- Qualifications: ITI / Diploma
- Key Responsibilities: Operate FBP (Top Spray Granulation), Coating, and Capsule filling machines.
2. Quality Control (QC) Department
- HPLC Analyst
- Experience: 06 to 08 years
- Qualifications: B.Sc / M.Sc / B.Pharm
- Key Responsibilities: Perform analysis on HPLC instruments for raw materials, finished products, and in-process samples.
- Dissolution and Chemical Analyst
- Experience: 02 to 05 years
- Qualifications: B.Sc / M.Sc / B.Pharm
- Key Responsibilities: Handle Dissolution Test apparatus, Karl Fischer apparatus, Auto Titrator, UV Instrument, ICP-OES/MS, and perform other chemical analyses.
- QC Reviewer
- Experience: 08 to 10 years
- Qualifications: B.Sc / M.Sc / B.Pharm
- Key Responsibilities: Review GMP documents, conduct data review for raw material and finished product analysis, and troubleshoot analytical instruments.
Documents Required
- Updated CV
- Current salary proof
- Passport size photograph
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