Concord Biotech Limited is conducting a walk-in interview on 2 October 2026 for experienced professionals in Production and Quality Control (QC) at its Unit II, Valthera facility in Gujarat. The company is hiring for multiple positions, including Production executives, supervisors, manufacturing operators, HPLC Analysts, Dissolution & Chemical Analysts, and QC Reviewers.
The walk-in interview is scheduled from 10:00 AM to 2:00 PM at Valthera, Taluka Dholka, Ahmedabad, Gujarat.
According to Concord Biotech’s official career information, the company operates across pharmaceutical and biotechnology manufacturing, including API and finished-formulation activities. Its Valthera operations include formulation and injectable manufacturing facilities.
Concord Biotech Walk-In Interview 2026 – Job Details
| Particular | Details |
|---|---|
| Company | Concord Biotech Limited |
| Unit | Unit II, Valthera |
| Departments | Production & Quality Control |
| Interview Date | 2 October 2026 |
| Interview Time | 10:00 AM to 2:00 PM |
| Job Location | Valthera, Dholka, Ahmedabad, Gujarat |
| Experience | 2–10 years depending on position |
| Employment Type | Full-time |
| Salary | Not disclosed by the employer |
| Interview Type | Walk-in Interview |
Vacancies at Concord Biotech
1. Assistant Manager / Senior Executive / Executive – Production
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 5–10 years
The selected candidate will work as an experienced shift in-charge responsible for managing daily manufacturing operations while maintaining cGMP, safety and regulatory compliance.
Key responsibilities include:
- Managing daily manufacturing and shift operations.
- Planning production activities and ensuring execution according to the production plan.
- Preparing and maintaining batch manufacturing records.
- Handling qualification documentation, including IQ/OQ/PQ documentation.
- Coordinating with QC and Warehouse teams for uninterrupted production.
- Monitoring equipment maintenance and calibration schedules.
- Supporting troubleshooting and minimizing manufacturing downtime.
- Leading team training and ensuring adherence to GMP and safety procedures.
- Maintaining consistent quality and production output.
2. Supervisor / Officer – Production
Qualification: B.Pharm / M.Pharm
Experience: 3–5 years
Candidates should have relevant experience in pharmaceutical manufacturing processes.
Preferred manufacturing experience:
- Granulation
- Coating
- Capsule filling
- Pharmaceutical production operations
- Manufacturing documentation and GMP compliance
3. Granulation / Coating / Capsule Operator
Qualification: ITI / Diploma
Experience: 3–7 years
Candidates should have hands-on experience operating pharmaceutical manufacturing equipment.
Relevant experience includes:
- FBP top-spray granulation machines
- Granulation operations
- Coating machines
- Capsule filling/operating machines
- Equipment operation and process monitoring
- Following manufacturing and safety procedures
4. HPLC Analyst – QC
Qualification: B.Sc / M.Sc / B.Pharm
Experience: 6–8 years
The HPLC Analyst will be responsible for analytical testing of pharmaceutical materials and products.
Key responsibilities include:
- Performing HPLC analysis.
- Testing raw materials.
- Analysing finished products.
- Testing in-process samples.
- Maintaining analytical records and documentation.
- Following laboratory procedures and GMP requirements.
- Supporting troubleshooting of analytical issues.
5. Dissolution & Chemical Analyst – QC
Qualification: B.Sc / M.Sc / B.Pharm
Experience: 2–5 years
Candidates should have practical experience handling pharmaceutical analytical instruments.
Relevant analytical experience includes:
- Dissolution testing
- Karl Fischer apparatus
- Auto titrator
- UV instruments
- ICP-OES / ICP-MS
- Other chemical analysis techniques
- Analytical documentation and GMP laboratory practices
6. QC Reviewer
Qualification: B.Sc / M.Sc / B.Pharm
Experience: 8–10 years
The QC Reviewer position is intended for experienced quality control professionals with strong GMP documentation and analytical review experience.
Key responsibilities include:
- Reviewing GMP documents.
- Reviewing raw material analytical data.
- Reviewing finished-product analytical data.
- Identifying discrepancies and documentation issues.
- Supporting troubleshooting of analytical instruments.
- Ensuring laboratory records comply with applicable quality requirements.
Who Can Apply?
The Concord Biotech walk-in recruitment drive is suitable for candidates with qualifications such as:
- B.Pharm
- M.Pharm
- B.Sc
- M.Sc
- ITI
- Diploma
The required experience varies by position from 2 to 10 years. Candidates should apply for positions matching their educational qualification, technical experience and area of expertise.
Documents Required for Walk-In Interview
Candidates attending the Concord Biotech walk-in interview should bring:
- Updated CV / Resume
- Current salary proof
- Passport-size photograph
Candidates should ensure that their resume clearly highlights relevant pharmaceutical manufacturing, production, HPLC, analytical testing, QC documentation or GMP experience, depending on the position applied for.
Concord Biotech Walk-In Interview 2026 – Venue
Concord Biotech Limited – Unit II, Valthera
Address:
297-298/2P, At: Valthera,
Taluka Dholka, Dist. Ahmedabad – 382225,
Gujarat, India
Date: 2 October 2026
Time: 10:00 AM to 2:00 PM
How to Apply
Eligible candidates can attend the Concord Biotech walk-in interview at the above-mentioned venue with their updated CV, current salary proof and passport-size photograph.
Candidates who cannot attend the walk-in interview can send their CV by email to:
