Indoco Remedies Limited Walk-In Interviews for Multiple Positions on 12th Sep 2026

Indoco Remedies Limited is conducting a Walk-In Interview for multiple Quality Control positions at its Unit-III manufacturing facility in Katha, Baddi, Himachal Pradesh. The company is looking for experienced professionals for Quality Control – GLP, Quality Control – Reviewer, and Quality Control – HPLC/GLP/RM roles, with experience requirements ranging from 3 to 10 years depending on the position. Candidates with B.Sc. or M.Sc. qualifications are eligible. The openings are focused on GLP laboratory management, QC data review, QMS activities, analytical testing and HPLC operations, with responsibilities covering calibration and preventive maintenance planning, OOS/OOT and deviation handling, change controls, CAPA, online and offline review of QC instrumental and chemical analytical data, and analytical instrument troubleshooting. Candidates for the HPLC/GLP/RM position should have hands-on experience with Waters and Agilent HPLCs and Empower 3.7 software. The company is conducting the walk-in interview on 12 September 2026, from 9:00 AM to 2:00 PM, at Indoco Remedies Limited, Unit-III, Katha, Baddi, Himachal Pradesh. Interested candidates may also submit their updated CV by email.

📌 Open Positions

1. Senior Executive / Executive – Quality Control (GLP)

• Experience: 7–10 Years
• Qualification: B.Sc. / M.Sc.
• Department: Quality Control – GLP

Key Responsibilities:

• Independently manage the GLP section.
• Plan daily calibration and preventive maintenance activities.
• Handle GLP documentation and related activities.
• Manage Quality Management System (QMS) activities.
• Handle:
  • OOS
  • OOT
  • Incidents
  • Deviations
  • Change Controls
  • CAPA
• Maintain related documentation and records.
• Work with software such as:
  • Caliber LIMS
  • DMS
  • Trackwise
  • SAP
  • Empower 3.7
  • LabSolutions
  • Tiamo
• Ensure appropriate audit-trail controls.
• Good communication skills are required.

2. Executive / Senior Officer – Quality Control (Reviewer)

• Experience: 6–10 Years
• Qualification: B.Sc. / M.Sc.
• Department: Quality Control – Reviewer

Key Responsibilities:

• Handle QMS activities, including:
  • OOS
  • OOT
  • Incidents
  • Deviations
  • Change Controls
  • CAPA
• Conduct online and offline review of QC instrumental and chemical analytical data.
• Review analytical data generated during QC testing.
• Work with Caliber LIMS, Trackwise, Empower 3.7, LabSolutions and Tiamo.
• Maintain and review audit trails.
• Support documentation and quality compliance activities.
• Good communication skills are required.

3. Senior Officer / Officer – Quality Control (HPLC / GLP / RM)

• Experience: 3–7 Years
• Qualification: B.Sc. / M.Sc.
• Department: Quality Control – HPLC / GLP / RM

Key Responsibilities:

• Perform hands-on analysis using Waters and Agilent HPLC systems.
• Work with Empower 3.7 software.
• Perform instrument troubleshooting.
• Support QC laboratory activities related to HPLC, GLP and Raw Material (RM) analysis.
• Ensure analytical activities are performed according to established procedures and quality requirements.

🧪 Key Skills Required

Depending on the position, candidates should have experience in:

• HPLC analysis
• QC instrumental analysis
• Chemical analytical data review
• GLP laboratory operations
• OOS / OOT investigations
• Deviation handling
• Change Control
• CAPA
• QMS
• Calibration and preventive maintenance
• Audit-trail review
• QC documentation
• Empower 3.7
• Caliber LIMS
• Trackwise
• LabSolutions
• Tiamo
• Instrument troubleshooting

📅 Walk-In Interview Details

Date: 12 September 2026
Time: 9:00 AM – 2:00 PM

📍 Interview Venue

Indoco Remedies Limited – Unit III
Katha,
Baddi, Himachal Pradesh.

📧 CV Submission

Candidates who are interested can also send their updated CV to:

avinash.kumar@indoco.com

🎯 Who Can Apply?

This opportunity is suitable for B.Sc./M.Sc. professionals with 3–10 years of pharmaceutical Quality Control experience, depending on the role. Candidates with strong experience in GLP, QMS, analytical data review, HPLC analysis, Empower 3.7, OOS/OOT, CAPA, deviations and QC documentation will be particularly relevant. Professionals experienced with Waters/Agilent HPLC systems and regulated pharmaceutical QC laboratories should consider attending the walk-in interview.