FDC Limited, a well-established name in the Indian pharmaceutical sector with decades of expertise in manufacturing quality medicines, is actively seeking talented professionals for its state-of-the-art facility in Baddi, Himachal Pradesh. The company is inviting applications from experienced candidates with hands-on knowledge in Oral Solid Dosage (OSD) forms, specifically capsule manufacturing, and strong exposure to international regulatory standards.
This is a rare opportunity for professionals passionate about maintaining high-quality production standards in a cGMP-compliant environment. As an Approved Manufacturing Chemist (Capsule), you will play a pivotal role in overseeing capsule production operations while ensuring full compliance with global regulatory requirements.
Position Overview
- Designation: Officer / Senior Officer – Capsule Manufacturing (Approved Manufacturing Chemist – Capsule)
- Department: Production (Manufacturing)
- Location: Baddi, Himachal Pradesh
- Experience: 5 to 8 years in capsule manufacturing and regulatory environments
- Qualification: B.Pharm / M.Pharm
- Positions: 1 (Male candidates only)
- Eligibility: Only candidates with Himachali domicile will be considered
FDC Limited prioritizes immediate joiners who bring proven regulatory exposure and a commitment to excellence in pharmaceutical manufacturing.
Roles & Responsibilities
In this critical hands-on role, you will be responsible for:
- Leading and executing capsule manufacturing processes as per approved Batch Manufacturing Records (BMR) and Batch Processing Records (BPR)
- Ensuring strict adherence to cGMP guidelines, Standard Operating Procedures (SOPs), and site-specific quality systems
- Overseeing key operations including dispensing, blending, encapsulation, polishing, and packing
- Performing line clearance activities before and after each batch to maintain compliance
- Managing deviations, Out of Specification (OOS), Out of Trend (OOT) results, and contributing to root cause investigations
- Supporting essential validation activities such as process validation, cleaning validation, and scale-up studies
- Maintaining accurate documentation to ensure audit readiness at all times
Regulatory Exposure & Compliance Focus
Candidates must demonstrate solid experience in regulated pharmaceutical environments, including:
- Familiarity with WHO-GMP, USFDA, EU-GMP, MHRA, and TGA guidelines
- Handling CAPA (Corrective and Preventive Actions), Change Control, and Risk Assessment procedures
- Knowledge of regulatory expectations specific to Oral Solid Dosage Forms, particularly capsules
- Active participation and support during internal, customer, and regulatory authority audits
This position is ideal for professionals who thrive in high-compliance settings and contribute to maintaining FDC’s reputation for quality and reliability.
Salary & Benefits
Competitive salary package commensurate with experience (realistic range: ₹4.5 – 7.5 LPA INR, based on industry standards for similar roles in Himachal Pradesh pharma manufacturing). Additional benefits include performance incentives, health insurance, and other statutory perks as per company policy.
How to Apply – Walk-In Interview Details
Interested and eligible candidates are invited to attend the walk-in interview:
- Interview Dates: 05 February 2026 to 07 February 2026
- Time: 10:00 AM – 01:00 PM
- Venue: FDC Limited, Baddi, Himachal Pradesh
- Contact: Call 9736880100 (between 9:00 AM – 5:30 PM) or email sushil.kumar@fdcindia.com for any queries
Important Instructions:
- Only Himachali candidates need apply
- Carry an updated resume, educational certificates, experience letters, and other relevant documents
- Immediate joiners with strong regulatory background will be preferred
Don’t miss this chance to advance your career with a respected pharmaceutical leader like FDC Limited. Prepare your documents and attend the walk-in to explore this rewarding opportunity in capsule manufacturing.
