Skip to content

ALKEM Laboratories – Walk-Ins for Production / QA / QC Departments on 29th Mar’ 2026

Job Opportunity: Hiring for Multiple Roles in Formulation Manufacturing at Alkem Laboratories Ltd.

Job Summary:
Alkem Laboratories Ltd., a premier pharmaceutical leader in India, is hosting a Walk-in Interview for its manufacturing facility in Baddi, Himachal Pradesh. We are looking for skilled professionals and technicians with 2 to 10 years of experience to join our Production, Quality Control (QC), and Quality Assurance (QA) teams. This is a significant opportunity to contribute to high-quality drug formulation and API manufacturing within a global, innovation-driven environment.


Company Overview

Alkem Laboratories Limited is a renowned pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality formulations and APIs. With a massive presence in both domestic and international markets, we are committed to healthcare innovation, stringent regulatory compliance, and excellence in manufacturing standards. Our Baddi facility serves as a critical hub for our formulation production operations.


Walk-in Interview Details

We invite interested and eligible candidates to attend our upcoming recruitment drive:

  • Date: 29 March 2026 (Sunday)
  • Time: 09:00 AM – 03:00 PM
  • Venue: Alkem Laboratories Ltd., Baddi, District Solan, Himachal Pradesh.
  • Contact Information: 01795-668999 (Ext. 207) or 9857417569
  • Email: [email protected]

Department-wise Openings

Department Qualification Role & Experience Key Expertise Required
Production B.Pharm / M.Pharm Senior Officer / Executive (2–7 yrs) Manufacturing, Production, & Packing
Production ITI / Diploma Operator / Technician (2–10 yrs) Granulation (FBD/RMG), Compression (Korsch/Sejong), Coating, Packing (CVC/Auto Cartonator)
Quality Control B.Pharm / M.Sc (Chem) Senior Officer / Executive (2–7 yrs) HPLC, KF, Stability Studies, RM Testing, GLP
Quality Assurance B.Pharm Senior Officer / Executive (2–7 yrs) IPQA, Regulatory Compliance, Documentation

Key Responsibilities

  • Production: Manage large-scale manufacturing operations, supervise packing lines, and ensure efficient handling of high-end machinery.
  • Quality Control: Perform rigorous analytical testing, stability studies, and lab documentation adhering to GLP standards.
  • Quality Assurance: Oversee In-Process Quality Assurance (IPQA), maintain comprehensive documentation, and ensure site-wide regulatory compliance.
  • General Operations: Uphold Good Manufacturing Practices (GMP) and optimize production efficiency to meet corporate targets.

Required Skills & Qualifications

  • Technical Proficiency: Expertise in HPLC, IPQA, and pharmaceutical production equipment.
  • Regulatory Knowledge: Strong working knowledge of GMP, GLP, and industry-standard regulatory compliance.
  • Operational Skills: Proven ability in troubleshooting and managing complex manufacturing processes.
  • Soft Skills: Strong teamwork, high attention to detail, and professional communication.
  • Educational Background:
    • Pharma Roles: B.Pharm / M.Pharm / M.Sc.
    • Technical Roles: ITI / Diploma.

Documents Required for Interview

Please carry the following documents for the verification process:

  1. Updated Resume / Curriculum Vitae.
  2. Current Salary Breakup and/or latest Increment Letter.
  3. Passport-sized photographs.
  4. Photocopies of Aadhaar and PAN Card.

Important Notes

  • This drive is strictly for candidates with relevant experience in the pharmaceutical manufacturing sector.
  • We welcome applications from both male and female candidates, especially for our specialized packing roles.
  • Candidates must ensure they bring all original documents for verification at the venue.

Why Build a Career at Alkem?

Joining Alkem Laboratories offers you a platform to work with one of the most respected names in the Indian pharmaceutical industry. You will gain invaluable exposure to cutting-edge manufacturing and QC technologies. We provide a robust learning environment where you can master the complexities of a regulated pharmaceutical ecosystem (GMP/GLP), ensuring long-term career growth in the domains of production, QA, and QC.

We look forward to meeting you at the walk-in interview!