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Unichem Laboratories is Hiring for Production, QC, QA, and Engineering roles

Career Opportunity: Walk-In Interview at Unichem Laboratories Ltd.

Job Summary:
Unichem Laboratories Ltd., a leading name in the pharmaceutical industry, is hosting a walk-in interview drive for talented professionals to join our facility in Baddi, Himachal Pradesh. We are looking for skilled individuals to fill multiple openings across our Production, Quality Control, Quality Assurance, and Engineering departments. This is an excellent opportunity for candidates with OSD (Oral Solid Dosage) experience to advance their careers within a reputable organization committed to excellence and innovation.


Available Positions

We are hiring for the following roles. Candidates must possess relevant OSD experience:

1. Production Department

  • Role: Technician
  • Focus Area: Compression (Sejong/Fette) / Granulation
  • Requirements: ITI qualification with 2–5 years of experience in an OSD environment.

2. Quality Control (QC)

  • Role: Officer / Analyst
  • Requirements: B.Pharm or B.Sc degree with 2–3 years of experience in OSD.

3. Engineering

  • Role: Officer
  • Focus Area: Process / HVAC / Water System
  • Requirements: Diploma, BE, or B.Tech degree with 2–5 years of experience in an OSD environment.

4. Quality Assurance (QA)

  • Role: Officer
  • Focus Area: IPQA / Documentation / Validation
  • Requirements: B.Pharm degree with 2–3 years of experience in OSD.

Responsibilities

  • Production: Operate compression and granulation machinery, ensure batch manufacturing adheres strictly to Standard Operating Procedures (SOPs), and maintain accurate production records.
  • Quality Control: Analyze raw materials and finished products, document test results systematically, and ensure the proper calibration and maintenance of laboratory instrumentation.
  • Engineering: Oversee HVAC, water systems, and general plant utilities. Conduct preventive and breakdown maintenance while ensuring full compliance with GMP (Good Manufacturing Practice) standards.
  • Quality Assurance: Execute IPQA activities and in-process quality checks, manage documentation and validation protocols, and ensure all processes meet regulatory requirements.

Requirements

  • Educational Qualifications: ITI, Diploma, B.Sc, B.Pharm, BE, or B.Tech (depending on the specific role).
  • Experience: Proven, relevant experience in Oral Solid Dosage (OSD) manufacturing.
  • Core Skills: Strong understanding of GMP guidelines, pharmaceutical manufacturing processes, and safety protocols.
  • Personal Attributes: Ability to work in a regulated environment, attention to detail, and a commitment to quality and safety.

Salary & Benefits

  • Compensation: Competitive salary range of ₹2.5 LPA – ₹5.5 LPA, commensurate with experience and the specific role.
  • Professional Development: Gain invaluable exposure to a highly regulated pharmaceutical manufacturing environment.
  • Growth: Excellent prospects for internal career progression within a stable and well-established global organization.

Walk-In Interview Details

Interested candidates are invited to attend the interview in person. No prior appointment is required, but please ensure you are prepared for a technical discussion.

  • Date: 2nd April 2026 (Thursday)
  • Time: 09:00 AM to 05:30 PM
  • Venue: VPO Batholi Kalan, Baddi – 173205, Himachal Pradesh
  • Inquiries: For any questions, you may contact: +91 9971322100 or +91 9805533243

How to Apply

To be considered for these positions, please bring the following documentation to the interview venue:

  1. A printed, updated copy of your Curriculum Vitae (CV).
  2. Details of your current salary structure (CTC breakup).
  3. Copies of your academic mark sheets and previous experience certificates.

We look forward to meeting candidates who are driven by quality and eager to contribute to our mission of providing high-quality healthcare solutions. Please ensure you arrive promptly and are prepared to discuss your technical expertise in detail.