FDC Limited, one of India’s leading pharmaceutical companies, has announced an Open Interview Drive for experienced candidates at its manufacturing facility located in Baddi, Himachal Pradesh. Candidates from Production, Quality Control, and Quality Assurance departments are invited to attend the walk-in interview scheduled on 10 October 2026.

This recruitment drive offers excellent opportunities for professionals with experience in pharmaceutical manufacturing, quality systems, and analytical testing.

Company Details

• Company Name: FDC Limited
• Location: Village Khol-Bhud, Tehsil Baddi, District Solan, Himachal Pradesh – 173205
• Interview Type: Open Interview
• Interview Date: 10 October 2026

Available Positions

1. Production Supervisor

Department: Production

Skills Required:

• Compression Machine Operation
• Granulation Machine
• Coating Machine
• Dry Syrup Filling Machine

Qualification: 12th Pass with ITI

Vacancies: 4

Experience: 4–6 Years

2. Production Officer

Department: Production

Skills Required:

• Pharmaceutical Manufacturing Operations

Qualification:

• B.Pharm
• M.Pharm

Vacancies: 2

Experience: 2–6 Years

3. Quality Control Officer

Skills Required:

• HPLC Testing
• Stability Studies
• Gas Chromatography (GC)

Qualification:

• B.Pharm
• M.Pharm
• M.Sc Chemistry

Vacancies: 3

Experience: 2–4 Years

4. Quality Assurance Executive / Sr. Executive

Skills Required:

• QMS Documentation
• GMP Compliance
• Deviation Management
• Market Complaints Handling
• Change Control
• CAPA Management
• Risk Assessment
• SOP Review
• Regulatory Audit Exposure

Qualification:

• B.Pharm
• M.Pharm

Vacancies: 1

Experience: 8–10 Years

Documents Required

Candidates are requested to carry:

• Updated Resume/CV
• Latest CTC Annexure
• Educational Certificates
• Experience Certificates
• Government ID Proof
• Recent Passport Size Photographs

Contact Details

Department: Human Resources

Email: sushil.kumar@fdcindia.com

Contact Number: 9736880100

Why Join FDC Limited?

• Reputed pharmaceutical organization
• Modern manufacturing facility
• Career growth opportunities
• Exposure to regulated pharmaceutical environments
• Competitive salary and benefits

Technical FAQs

1. What is HPLC testing in Quality Control?

HPLC (High Performance Liquid Chromatography) is an analytical technique used to identify, quantify, and test the purity of pharmaceutical products and raw materials.

2. What is CAPA in Quality Assurance?

CAPA stands for Corrective and Preventive Action. It is a quality system process used to investigate deviations, identify root causes, and prevent recurrence.

3. What is GMP compliance?

Good Manufacturing Practices (GMP) are regulatory guidelines that ensure medicines are consistently produced and controlled according to quality standards.

4. What is Change Control in pharmaceutical manufacturing?

Change Control is a documented process used to evaluate, approve, implement, and monitor changes that may impact product quality or regulatory compliance.

5. What is Stability Testing?

Stability testing evaluates how a pharmaceutical product maintains its quality, safety, and effectiveness over its shelf life under different environmental conditions.