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Indoco Remedies Walk-in Interview for Pharma Jobs in QC, QA, and Production Roles on 28th September

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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.

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.

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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
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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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Indoco Remedies Walk-in Interview for Pharma Jobs in QC, QA, and Production Roles on 28th September

For more pharma job resources, visit Pharma Recruiter. Apply now to join Indoco’s dynamic team!

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.

How can I learn more about salaries and benefits?

Discuss salary details during the interview. Explore more at Pharma Recruiter.

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