Join Indoco Remedies for exciting pharma jobs in Goa! Walk-in on September 28, 2025, for QC, QA, and production roles at our USFDA-approved tablet facility.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 3.1 Quality Control Analysts (Tablet Formulation)
- 3.2 Production Officer/Sr. Officer/Executive (Tablet Formulation)
- 3.3 Packing Officer/Sr. Officer (Tablet Formulation)
- 3.4 Associate/Technician/Operator (Packing/Production)
- 3.5 QA-QMS (Tablet Formulation)
- 3.6 QA-IPQA (Tablet Formulation)
- 3.7 IPQA Section Head (Tablet Formulation)
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Walk-in Interview Details
- 9 Why You Should Join
- 10 FAQs
About the Company
Indoco Remedies Limited, a leading pharmaceutical company, boasts a robust global presence with regulatory approvals from USFDA and UKMHRA. Operating a state-of-the-art tablet manufacturing facility in Goa, Indoco excels in producing high-quality formulations for regulated markets.
With over 78 years of industry expertise, the company employs advanced technologies and adheres to stringent quality standards, fostering innovation and growth. Indoco is a trusted name in pharmaceutical careers, offering stable, rewarding opportunities for professionals in India.
Job Details
- Company Name: Indoco Remedies Limited
- Experience: 1–15 years
- Qualification: B.Sc., M.Sc., B.Pharm, M.Pharm, DME, DEE, D.Pharma
- Location: L-14, Verna Industrial Area, Verna, Goa
- Work Type: On-site, Full-time (all shifts) in tablet formulation
Job Description
Indoco Remedies is hiring for multiple roles in quality control, quality assurance, and production at its USFDA-approved tablet manufacturing facility in Goa. These pharma jobs cater to professionals with expertise in HPLC/GC, granulation, packing, and QA processes, offering dynamic career paths in a regulatory-compliant environment.
Quality Control Analysts (Tablet Formulation)
- Department: Quality Control
- Role: Analysts for HPLC/GC
- Experience: 4–6 years
- Education/Qualification: B.Sc./M.Sc.
Production Officer/Sr. Officer/Executive (Tablet Formulation)
- Department: Production
- Role: Officer/Sr. Officer/Executive Production
- Experience: 1–5 years
- Education/Qualification: B.Pharm/M.Pharm
Packing Officer/Sr. Officer (Tablet Formulation)
- Department: Packing
- Role: Officer/Sr. Officer – Packing
- Experience: 1–4 years
- Education/Qualification: B.Pharm/M.Pharm
Associate/Technician/Operator (Packing/Production)
- Department: Packing/Production
- Role: Associate/Technician/Operator
- Experience: 5–6 years
- Education/Qualification: DME/DEE/D.Pharm
QA-QMS (Tablet Formulation)
- Department: Quality Assurance
- Role: QA-QMS
- Experience: 7–9 years
- Education/Qualification: B.Pharm/M.Pharm
QA-IPQA (Tablet Formulation)
- Department: Quality Assurance
- Role: QA-IPQA
- Experience: 7–9 years
- Education/Qualification: B.Pharm/M.Pharm
IPQA Section Head (Tablet Formulation)
- Department: Quality Assurance
- Role: IPQA Section Head
- Experience: 10–15 years
- Education/Qualification: B.Pharm/M.Pharm
Skills/Qualifications
- Proficiency in HPLC/GC operations with Chromeleon/Empower software (QC roles)
- Expertise in granulation, compression, coating, and oral liquid manufacturing (Production)
- Experience with high-speed blister packaging, cartonator, and Track and Trace systems (Packing)
- Knowledge of QMS, change controls, deviations, CAPA, and SOP preparation (QA-QMS)
- Skills in IPQA activities like line clearance, sampling, and batch record review (QA-IPQA)
- Leadership in IPQA operations and audit compliance (IPQA Section Head)
- Relevant qualifications: B.Sc./M.Sc., B.Pharm/M.Pharm, DME/DEE/D.Pharm
- 1–15 years in USFDA/UKMHRA-regulated tablet manufacturing environments
Key Responsibilities
- Operate and troubleshoot HPLC/GC instruments for quality control analysis
- Manage granulation, compression, capsule filling, and coating processes
- Oversee high-speed blister packing, bottle packing, and batch reconciliation
- Handle QMS tasks like change controls, deviations, and quality risk management
- Conduct IPQA activities including line clearance, in-process checks, and swab sampling
- Lead IPQA teams, perform batch releases, and ensure audit compliance
- Ensure adherence to USFDA/UKMHRA standards and GMP practices
Benefits/Perks
- Competitive salaries aligned with industry standards for pharma jobs in India
- Career advancement in a globally recognized, USFDA-approved facility
- Comprehensive training in regulatory compliance and advanced technologies
- Collaborative work culture promoting innovation and professional growth
- Health insurance, on-site facilities, and employee wellness programs
- Preference for Goan candidates, fostering local talent development
How to Apply
Email your resume to hrdl@indoco.com with the subject “Application for [Role Name] – Goa”.
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Walk-in Interview Details
- Date: September 28, 2025 (Sunday)
- Time: 9:00 AM to 5:00 PM
- Venue: Indoco Remedies Limited, L-14, Verna Industrial Area, Verna, Goa
- Contact/Email: Ms. Deepika Gayak – HR, hrdl@indoco.com, 08326624109
Why You Should Join
Indoco Remedies offers a gateway to thriving pharmaceutical careers in a USFDA and UKMHRA-approved tablet manufacturing facility. With a legacy of excellence, you’ll work with cutting-edge technology, contribute to global markets, and grow in a supportive environment.
Ideal for Goan candidates, these roles ensure long-term stability and skill development in a high-compliance setting. Join Indoco to make a lasting impact in the pharma industry.
FAQs
What qualifications are needed for Indoco’s pharma jobs in Goa?
Roles require B.Sc./M.Sc., B.Pharm/M.Pharm, or DME/DEE/D.Pharm with 1–15 years in regulatory plants.
Is experience in regulatory plants mandatory?
Yes, candidates must have experience in USFDA/UKMHRA-regulated tablet manufacturing environments.
What should I bring to the walk-in interview?
Bring your updated resume, educational certificates, ID proof, and experience letters for screening.
How can I learn more about salaries and benefits?
Discuss salary details during the interview. Explore more at Pharma Recruiter.