A leading biotechnology company, founded in 2000, has established itself as an R&D-centric organization with a strong focus on fermentation, semi-synthetic, and synthesis-based product development. Since its inception, the company has consistently achieved substantial growth, driven by strategic diversification and continuous improvements in its operational processes. The firm operates from a state-of-the-art manufacturing facility, which holds prestigious approvals from both the US FDA and EUGMP, underscoring its commitment to global quality standards.
Recognized internationally, this professionally managed company is a trusted supplier of fermentation-based Active Pharmaceutical Ingredients (APIs) and enzymes. Beyond product manufacturing, it extends its expertise to offer comprehensive biotechnology services, including advanced strain improvement programs and specialized contract fermentation and manufacturing solutions, catering to a broad range of industry needs.
The company is currently seeking talented and experienced professionals to join its dynamic team. Opportunities are available across the Production and Quality Control departments.
Job Roles and Requirements
Production Department:
- Assistant Manager / Senior Executive (Production):
- Qualification: B.Pharm / M.Pharm.
- Experience: 10 to 15 years.
- Key Responsibility: Manage daily manufacturing operations and ensure strict compliance with current Good Manufacturing Practices (cGMP).
- Supervisor / Officer (Production):
- Qualification: M.Sc / B.Pharm / M.Pharm.
- Experience: 3 to 5 years.
- Key Skill: Demonstrated experience in granulation, coating, and capsule filling processes.
- Granulation / Compression / Coating Operator:
- Qualification: ITI / Diploma.
- Experience: 3 to 7 years.
- Key Skill: Proficient in operating Fluid Bed Processing (FBP) machines for top spray granulation or other coating machines.
Quality Control (QC) Department:
- HPLC Analyst (QC):
- Qualification: B.Sc / M.Sc / B.Pharm.
- Experience: 6 to 8 years.
- Key Responsibility: Conduct analysis of raw materials, finished products, and stability samples using High-Performance Liquid Chromatography (HPLC) instruments.
- Dissolution and Chemical Analyst (QC):
- Qualification: B.Sc / M.Sc / B.Pharm.
- Experience: 2 to 5 years.
- Key Skill: Competency in handling dissolution tests, Karl Fisher titration, and Auto Titrator operations.
- GC Analyst (QC):
- Qualification: B.Sc / M.Sc / B.Pharm.
- Experience: 5 to 7 years.
- Key Responsibility: Perform analyses on Gas Chromatography (GC) instruments, including Headspace analysis, for raw materials and finished products.
Walk-In Interview Details:
Interested and eligible candidates are invited to attend a walk-in interview.
- Date: June 27, 2026
- Time: 10:00 A.M. to 02:00 P.M.
- Venue: Survey No 297-298/2P, At: Valthera, Tal Dholka, Dist. Ahmedabad-382225
Candidates attending the interview should bring their updated CVs, current salary proof, and a passport-size photograph.
For those who are unable to participate in the walk-in event, applications can be submitted via email. Please send your detailed resume to careerfdf@concordbiotech.com, ensuring that the specific position you are applying for is clearly mentioned in the subject line of your email.
Documents to Carry for Interview:
To facilitate a smooth interview process, please ensure you bring the following essential documents:
- Your latest passport-size photograph.
- A current and updated resume.
- Xerox copies of all your qualification certificates.
- Proof of current remuneration, which includes your last 3 months’ salary slips, a copy of your current company’s offer letter, or your CTC proof, along with your last 3 months’ bank statements.
