Production, Quality Control & Quality Assurance

Why This Role Matters

This walk-in opportunity at Unichem Laboratories Ltd. offers candidates a strong entry and growth pathway in the pharmaceutical manufacturing sector, particularly in Oral Solid Dosage (OSD). With multiple openings across Production, Quality Control (QC), Quality Assurance (QA), and Engineering, this drive is ideal for professionals aiming to build expertise in regulated environments. Working in such roles ensures direct contribution to medicine quality, compliance, and patient safety, while also enhancing technical and operational skills aligned with industry standards like GMP.

Job Description

Unichem Laboratories is conducting a walk-in interview to hire skilled professionals for various departments at its Baddi facility. Candidates will be responsible for executing department-specific operations such as manufacturing, analytical testing, quality compliance, and engineering maintenance. The roles require hands-on involvement in OSD processes, documentation, and adherence to regulatory requirements, ensuring smooth and compliant plant operations.

Key Features of the Role:

• Walk-in interview scheduled on 2nd April 2026 (Thursday)
• Multiple openings across Production, QC, QA, and Engineering
• Location: Baddi, Himachal Pradesh
• Exposure to regulated pharmaceutical manufacturing environment
• Opportunity to work with industry-standard equipment and processes
• Roles suitable for ITI, Diploma, B.Sc, B.Pharm, and Engineering graduates

Responsibilities

• Production: Operate compression and granulation machines, execute batch manufacturing, and maintain production records as per SOPs
• Quality Control: Perform analysis of raw materials and finished products, ensure proper documentation, and calibrate lab instruments
• Engineering: Manage HVAC systems, water systems, and utilities, and perform preventive and breakdown maintenance
• Quality Assurance: Conduct IPQA activities, handle documentation and validation processes, and ensure regulatory compliance
• Ensure adherence to GMP guidelines and maintain audit readiness
• Support cross-functional coordination for smooth manufacturing and quality operations

Required Qualifications

• ITI / Diploma / B.Sc / B.Pharm / BE
• Relevant experience in OSD (Oral Solid Dosage) manufacturing

Educational Requirements:

• Technical qualifications (ITI/Diploma) for technician and engineering roles
• Science or pharmacy background (B.Sc/B.Pharm) for QC and QA roles
• Engineering degree/diploma for utility and maintenance functions

Experience and Skills:

• 2–5 years of experience depending on the role
• Hands-on experience in OSD manufacturing is essential
• Strong knowledge of GMP and pharmaceutical processes
• Good documentation and reporting skills
• Familiarity with equipment handling and troubleshooting
• Ability to work in a regulated and compliance-driven environment

Salary Insights

• Estimated salary range: ₹2.5 LPA – ₹5.5 LPA
• Salary depends on role, qualification, and experience
• Additional benefits include career growth, regulated exposure, and competitive compensation

Company Overview

Unichem Laboratories Ltd. is a well-established pharmaceutical organization known for its strong presence in formulation development and manufacturing. The company focuses on quality-driven production and compliance with global regulatory standards. With manufacturing facilities catering to both domestic and international markets, Unichem provides a robust platform for professionals to gain industry-relevant experience and long-term career growth.

FAQs

• Who can attend the walk-in interview?
Candidates with relevant qualifications (ITI/Diploma/B.Sc/B.Pharm/Engineering) and OSD experience can attend

• Is prior pharma experience mandatory?
Yes, relevant OSD experience is required for most roles

• What documents should I carry?
Updated resume, educational certificates, experience letters, and ID proof

• Is this a permanent role?
Yes, these are full-time roles based on department requirements

• What is the work location?
Baddi, Himachal Pradesh

Application Tips

• Reach the venue early between 09:00 AM – 05:30 PM to avoid last-minute rush
• Carry multiple copies of your resume and all supporting documents
• Revise key concepts of GMP, OSD processes, and your domain expertise
• Be prepared to discuss hands-on experience with equipment and procedures
• Dress professionally and be ready for on-the-spot interviews

Walk-In Interview Details
Date: 2nd April 2026 (Thursday)
Time: 09:00 AM to 05:30 PM
Venue: VPO Batholi Kalan, Baddi – 173205, Himachal Pradesh