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About Indoco Remedies Ltd

Indoco Remedies Ltd., a USD 166 million fully integrated, research-driven pharmaceutical company with seven decades of excellence, invites dynamic professionals to be part of its journey. With a presence in over 55 countries and a team of 6,000+ professionals including 300+ scientists, we offer unparalleled opportunities for growth and learning in a regulated, global environment.

📍 Walk-in Interview Details

Dates: 31st July 2025 to 3rd August 2025
Time:

2:00 PM to 5:00 PM (31st July – 2nd August)
9:00 AM to 5:00 PM (3rd August – Sunday)
Venue:
Indoco Remedies Ltd. – Goa Plant I
L-14, Verna Industrial Area, Verna, Salcete, Goa – 403722

Current Openings (Tablet Formulation Division)

🔬 Quality Control Analysts (HPLC / GC)

Experience: 4 to 6 years
Qualification: M.Sc. / B.Sc.

Key Responsibilities:

Hands-on experience with Empower software
Strong understanding of chromatographic practices
3+ years handling HPLC/GC instruments
Instrument troubleshooting expertise

🏭 Production – Tablet Formulation

Position: Officer / Sr. Officer / Executive
Experience: 1 to 5 years
Qualification: B.Pharm / M.Pharm

Areas: Granulation, Compression, Capsule, Coating
Preferred Skills:

Experience with FETTE, Sejong, Cadmach (compression)
FBD, FBE & RMG (granulation)
FDA approval preferred

📦 Production – Packing (Tablet Formulation)

Position: Officer / Sr. Officer
Experience: 1 to 4 years
Qualification: B.Pharm / M.Pharm

Job Profile:

Experience with high-speed blister/bottle lines
Handling Track & Trace systems
Batch reconciliation and shift coordination

🔧 Production – Packing / Production Operators

Position: Associate / Technician / Operator
Experience: 1 to 4 years
Qualification: DME / DEE / D.Pharm

Job Profile:

Operation of machines for granulation, compression, coating, blister packaging, cartoning, and bottle packing

🛡 Quality Assurance (Tablet Formulation)

QA – QMS

Experience: 5 to 6 years
Qualification: B.Pharm / M.Pharm

Key Tasks:

Change control, deviation management, CAPA, risk assessment
SOPs, training coordination
Regulatory plant experience essential

QA – IPQA

Experience: 7 to 9 years
Qualification: B.Pharm / M.Pharm

Key Responsibilities:

Line clearance, in-process checks, QA rounds
Swab sampling, batch release, material verification
Use of IPQC instruments

QA – Validation

Experience: 8 to 10 years
Qualification: B.Pharm / M.Pharm