Post Your Job Opening (Paid) & Advertise With Us Today
POST NOW

Ipca Laboratories Walk-in Interviews for QA, QC, Production, Engineering & Warehouse Departments on 1st June 2025

Share With Your Friends

Ipca Laboratories Ltd., a globally recognized, USFDA-approved, and WHO-GMP certified pharmaceutical leader, invites talented professionals to join our state-of-the-art Sikkim Formulation Plant.

With over 70 years of excellence, Ipca is renowned for manufacturing over 350 formulations and 80 APIs across various therapeutic segments. We are hosting walk-in interviews on June 1, 2025, in Rangpo, Sikkim, for roles in Quality Control (QC), Production, Quality Assurance (QA), Administration, Engineering, and Warehouse.

Be part of our mission to deliver A Dose of Life through quality healthcare solutions.

Note: Candidates must have relevant experience in pharmaceutical formulations (OSD preferred). API or chemical industry experience is not eligible for these positions.

Interview Details

  • Date: Sunday, June 1, 2025
  • Time: 10:00 AM to 4:00 PM
  • Venue: Hotel Palm Grove Suits Inn & Spa, Majitar, Rangpo, Sikkim
  • Requirements: Bring updated resume, last 3 months’ salary slips, current company appointment letter with CTC structure, educational certificates, and Aadhar/PAN card copies.
  • Unable to Attend? Email your CV to punam.chettri@ipca.com.
  • Contact: +91 9002103678, +91 7479354446, +91 8958793000
  • Website: Ipca Laboratories

Important: Ipca Laboratories does not charge any fees for job applications. Beware of fraudulent invitations requesting payment. Contact hrd@ipca.com for verification.

Available Positions

Quality Control (QC) – HPLC/GLP/FG/Micro

  • Designation: Officer/Sr. Officer
  • Qualification: B.Pharm/M.Pharm/BSc/MSc
  • Experience: 4-8 Years
See also  Mepro Pharmaceuticals – Urgent Hiring for QA, QC, QC-Micro, F&D, and Engineering

Job Responsibilities:

  • Perform analysis using HPLC, GC, UV, IR, and dissolution testing.
  • Conduct GLP, finished goods (FG), and microbiological testing (e.g., EM, MLT, BET).
  • Manage stability studies, QMS, OOS/OOT investigations, and regulatory compliance.

Production – Granulation/Compression/Coating

  • Designation: Executive/Officer/Sr. Officer
  • Qualification: B.Pharm/M.Pharm
  • Experience: 4-8 Years

Job Responsibilities:

  • Operate and supervise granulation, compression, and coating machines (e.g., FBD, RMG, Fette, Sejong).
  • Handle QMS, BMR/BPR documentation, and ensure GMP compliance.
  • Monitor critical process parameters for OSD formulations.

Production – Granulation/Compression

  • Designation: Technician
  • Qualification: ITI/Diploma/12th/10th
  • Experience: 4-8 Years

Job Responsibilities:

  • Operate granulation and compression equipment (e.g., RMG, FBP, Fette, Cadmach).
  • Perform in-process checks and maintain production logs.
  • Ensure adherence to SOPs and safety standards.

Quality Assurance (QA) – IPQA

  • Designation: Asst. Manager/Executive/Officer/Sr. Officer
  • Qualification: B.Pharm/M.Pharm
  • Experience: 6-12 Years

Job Responsibilities:

  • Conduct IPQA activities, line clearance, and in-process quality checks.
  • Review BMR/BPR, handle CAPA, deviations, and market complaints.
  • Support validation, APQR, and QMS compliance.

Administration

  • Designation: Sr. Executive/Asst. Manager
  • Qualification: BBA/MBA
  • Experience: 8-10 Years

Job Responsibilities:

  • Manage administrative operations, facility management, and compliance.
  • Coordinate employee welfare and office logistics.
  • Support HR and documentation processes.

Engineering – Process: Electrical/Instrument

  • Designation: Executive/Officer
  • Qualification: B.Tech/M.Tech
  • Experience: 5-8 Years

Job Responsibilities:

  • Maintain and troubleshoot electrical and instrumentation systems.
  • Support equipment qualification (DQ, IQ, OQ, PQ) and preventive maintenance.
  • Ensure compliance with cGMP and safety standards.

Warehouse – RM/Dispensing/PPIC

  • Designation: Asst. Manager/Executive/Sr. Officer
  • Qualification: BA/B.Com
  • Experience: 5-12 Years

Job Responsibilities:

  • Manage raw material (RM) dispensing and production planning (PPIC).
  • Oversee inventory control, material reconciliation, and documentation.
  • Ensure compliance with GMP and regulatory requirements.
See also  Amico Formulations LLP in Vadodara for QA, QC, Store, Maintenance & Engineering Roles

Why Join Ipca Laboratories?

  • Global Leader: Work with a company recognized by USFDA, UK-MHRA, and WHO, with a presence in over 120 countries.
  • Innovative Environment: Contribute to OSD formulations in a cutting-edge facility.
  • Career Growth: Access training, career advancement, and a collaborative work culture.
  • Benefits: Competitive salary, health insurance, and employee-centric policies.

Learn more about our legacy at Ipca Laboratories and industry standards at USFDA or WHO.

How to Apply

  • Attend the walk-in interview with all required documents.
  • Email your CV to punam.chettri@ipca.com if unable to attend.
  • Follow #PharmaJobs and #SikkimJobs on X.com for the latest pharmaceutical career updates.
Ipca Laboratories Walk-in Interviews for QA, QC, Production, Engineering & Warehouse Departments on 1st June 2025

Join Ipca Laboratories to make a difference in global healthcare!

Share With Your Friends

Connect with Us for Latest Job Alerts!