Concord Biotech Limited Walk-in Interview 2026 | Production, ADL, Regulatory & QC Jobs in Ahmedabad

Concord Biotech Limited is hiring experienced professionals for Production, Analytical Development Laboratory (OSD & Injectable), and Regulatory Affairs roles at Unit-II Valthera. Don’t miss this walk-in interview on 9th May 2026 for multiple pharma jobs in Ahmedabad. Excellent opportunity for B.Pharm, M.Pharm, M.Sc professionals seeking growth in pharmaceutical careers in India.

About the Company

Concord Biotech Limited is a leading R&D-driven biopharmaceutical company headquartered in Ahmedabad, Gujarat. Specializing in fermentation-based Active Pharmaceutical Ingredients (APIs) and high-quality finished formulations, the company has established itself as a global player with presence in over 70 countries.

With state-of-the-art manufacturing facilities compliant with USFDA, EU-GMP, and other international standards, Concord Biotech focuses on innovation, quality, and regulatory excellence. The company’s Unit-II at Valthera is a modern OSD and Injectable formulation facility supporting its expansion into complex dosage forms.

Job Details

• Company Name: Concord Biotech Limited (Unit – II Valthera)
• Experience: 2 to 15 years (varies by role)
• Qualification: B.Pharm, M.Pharm, M.Sc, B.Sc
• Location: Valthera / Ahmedabad, Gujarat
• Work Type: On-site

Job Description

Concord Biotech Limited is expanding its teams with multiple openings in Production, Analytical Development, and Regulatory Affairs for its advanced formulation facilities. These roles offer professionals the chance to work on OSD, Injectable, and regulatory projects in a highly compliant, growth-oriented environment.

Manager/Asst Manager/Sr. Executive – Production

• Department: Production
• Role: Shift In Charge for manufacturing operations
• Experience: 10 to 15 years
• Education/Qualification: B.Pharm / M.Pharm

Chemist/Officer/Sr. Officer – QC

• Department: Quality Control
• Role: Analytical testing and stability studies
• Experience: 2 to 4 years
• Education/Qualification: M.Sc / M.Pharm

Executive/Sr. Executive – Analytical Development Laboratory (OSD)

• Department: Analytical Development Laboratory – OSD
• Role: Method development and validation for Topical Semisolid
• Experience: 5 to 10 years
• Education/Qualification: M.Sc / M.Pharm

Officer/Senior Officer – Analytical Development Laboratory (Injectable)

• Department: Analytical Development Laboratory – Injectable
• Role: Analysis and method validation for injectables
• Experience: 4 to 6 years
• Education/Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Executive/Senior Executive – Analytical Development Laboratory (Injectable)

• Department: Analytical Development Laboratory – Injectable
• Role: Method validation, transfer, and team mentoring
• Experience: 6 years
• Education/Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Executive/Sr. Executive/Asst. Manager/Deputy Manager/Manager/Sr. Manager – Regulatory Affairs

• Department: Regulatory Affairs
• Role: Dossier preparation and regulatory compliance
• Experience: 5 to 10 years
• Education/Qualification: M.Sc / B.Pharm / M.Pharm

Skills/Qualifications

• Strong experience in cGMP, GLP, and GDP practices
• Hands-on expertise with HPLC, GC, UV, Dissolution, Particle Size, ICP-MS/OES
• Knowledge of analytical method development, validation, and transfer
• Regulatory dossier preparation and query response skills
• Experience in OSD, Topical Semisolid, and Injectable formulations
• Team leadership and cross-functional coordination abilities
• Proficiency in documentation, stability studies, and compliance

Key Responsibilities

• Manage daily manufacturing operations and batch records
• Perform analytical testing of raw materials and finished products
• Develop and validate analytical methods for OSD and Injectables
• Prepare high-quality regulatory dossiers and respond to queries
• Conduct stability studies and support formulation development
• Ensure equipment calibration and compliance with regulatory standards
• Mentor juniors and support investigations and change controls

Benefits/Perks

• Career growth in a fast-expanding biopharma company
• Exposure to USFDA and EU-GMP compliant facilities
• Learning opportunities in advanced analytical and regulatory domains
• Competitive salary with performance incentives
• Professional work culture focused on innovation
• Long-term stability with global project exposure

How to Apply

Interested candidates can attend the walk-in interview with updated CV, current salary proof, and passport-size photographs. Those unable to attend may email their applications to careerfdf@concordbiotech.com with the position applied for clearly mentioned in the subject line.

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Apply today and take your career to the next level with Concord Biotech!

Walk-in Interview Details

• Date: 09th May 2026 (Saturday)
• Time: 10:00 AM to 2:00 PM
• Venue: B1601-1602, B-Wing, Mondeal Heights, Iscon Cross Road, S.G. Highway, Ahmedabad
• Contact/Email: careerfdf@concordbiotech.com

Why You Should Join

Concord Biotech offers a dynamic environment where innovation meets regulatory excellence. As a publicly listed company with strong global presence, it provides long-term career stability, recognition for performance, and opportunities to work on cutting-edge fermentation-based APIs and complex formulations. Join a team committed to quality, sustainability, and delivering life-changing pharmaceutical solutions.

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