Looking for pharma jobs, walk-in interviews, QA jobs, QC jobs, or regulatory affairs jobs? Concord Biotech is hiring experienced professionals for Regulatory Affairs, Analytical Development Laboratory (OSD), and Quality Assurance roles in Ahmedabad.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 3.1 Regulatory Affairs Executive / Senior Executive / Assistant Manager / Deputy Manager / Manager / Senior Manager
- 3.2 Analytical Development Laboratory (OSD) – Chemist / Officer / Senior Officer
- 3.3 Analytical Development Laboratory (OSD) – Executive / Senior Executive
- 3.4 Quality Assurance Officer / Senior Officer
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Walk-in Interview Details
- 9 Why You Should Join Concord Biotech?
- 10 FAQs
About the Company
Concord Biotech is one of India’s leading biotechnology and pharmaceutical companies, known for its strong expertise in fermentation-based APIs and finished formulations.
The company has built a strong reputation for innovation, regulatory compliance, and global market presence. Concord Biotech serves multiple international pharmaceutical markets with a focus on quality, research, and advanced manufacturing.
With a mission toward building a healthier tomorrow, the company offers excellent opportunities for pharmaceutical professionals to grow in a compliance-driven environment.
Job Details
- Company Name: Concord Biotech
- Experience: 2–12 Years
- Qualification: M.Sc, B.Pharm, M.Pharm
- Location: Valthera, Dholka, Ahmedabad, Gujarat
- Work Type: On-site
- Industry: Biotechnology / Pharmaceutical Manufacturing
- Interview Type: Walk-In
Job Description
Concord Biotech is conducting a walk-in interview for experienced candidates across Regulatory Affairs, Analytical Development Laboratory (OSD), and Quality Assurance departments.
This recruitment drive offers excellent opportunities for candidates with strong expertise in dossier preparation, analytical development, and stability management.
Regulatory Affairs Executive / Senior Executive / Assistant Manager / Deputy Manager / Manager / Senior Manager
- Department: Regulatory Affairs
- Market: Global & Domestic Regulatory
- Role: Dossier Preparation & Compliance Management
- Experience: 6–12 Years
- Education/Qualification: M.Sc / B.Pharm / M.Pharm
Analytical Development Laboratory (OSD) – Chemist / Officer / Senior Officer
- Department: Analytical Development Laboratory (OSD)
- Market: Formulation Development
- Role: Raw Material & Drug Product Analysis
- Experience: 2–4 Years
- Education/Qualification: M.Sc / M.Pharm
Analytical Development Laboratory (OSD) – Executive / Senior Executive
- Department: Analytical Development Laboratory (OSD)
- Market: Method Development & Validation
- Role: Analytical Development
- Experience: 5–10 Years
- Education/Qualification: M.Sc / M.Pharm
Quality Assurance Officer / Senior Officer
- Department: Quality Assurance
- Market: Stability Management
- Role: Stability Sample Management & Documentation
- Experience: 5–8 Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Dossier preparation expertise
- Regulatory compliance knowledge
- CDSCO and SUGAM portal experience
- Product permission handling
- COPP documentation
- HPLC and GC operation
- UV and dissolution testing
- ICP-OES analysis
- Stability study management
- GLP and GDP knowledge
Key Responsibilities
- Prepare regulatory dossiers
- Handle CDSCO approvals
- Perform analytical method development
- Conduct routine testing
- Support formulation development
- Manage stability samples
- Prepare stability protocols
- Maintain retain samples
- Handle documentation compliance
- Support audits and inspections
Benefits/Perks
- Career growth opportunities
- Exposure to global regulatory markets
- Learning and development support
- Competitive salary package
- Advanced analytical experience
- Strong compliance environment
- Professional development
- Long-term career stability
- Work with experienced pharma teams
How to Apply
Interested candidates can directly attend the walk-in interview with their updated CV, current salary proof, and passport-size photograph.
Candidates unable to attend can email their resumes to:
Email: careerfdf@concordbiotech.com
Please mention the applied position clearly in the subject line.
For latest pharma jobs and walk-in interview updates, visit Pharma Recruiter.
Apply now and become part of Concord Biotech’s mission toward a healthier tomorrow.
Walk-in Interview Details
- Date: 13th June 2026
- Time: 10:00 AM to 02:00 PM
- Venue: 297-298/2P, At: Valthera, Taluka Dholka, Dist. Ahmedabad – 382225, Gujarat, India
- Contact/Email: careerfdf@concordbiotech.com
Why You Should Join Concord Biotech?
Concord Biotech offers a strong platform for pharmaceutical professionals to work in regulatory, analytical, and quality-focused roles. The company has a strong reputation in biotechnology innovation and compliance.
Employees gain valuable experience in international regulatory markets, analytical development, and quality systems. This provides excellent long-term growth and professional development.
Its focus on quality, innovation, and global standards makes Concord Biotech a preferred employer in the pharma industry.
FAQs
Who can apply for this walk-in interview?
Candidates with relevant qualifications and 2–12 years of experience can apply.
Can I apply by email if I cannot attend?
Yes, candidates can send their resumes to careerfdf@concordbiotech.com.
What documents should I carry?
Carry updated CV, current salary proof, and passport-size photo.
Is regulatory affairs experience mandatory?
Yes, for Regulatory Affairs roles, prior dossier and compliance experience is required.
