Unichem Laboratories Ltd., one of India’s well-established pharmaceutical companies, has announced a Walk-In Interview Drive on 14 June 2026 (Sunday) for multiple positions across Production, Quality Control, and Materials departments. This recruitment initiative offers an excellent opportunity for both experienced professionals and fresh candidates seeking to build a career in the pharmaceutical manufacturing industry.

With a reputation for quality, reliability, and innovation, Unichem continues to strengthen its workforce by attracting talented professionals committed to maintaining high standards in pharmaceutical operations.

Walk-In Interview Details

Particulars Details

Company

Unichem Laboratories Ltd.

Interview Date

14 June 2026 (Sunday)

Time

10:00 AM to 4:00 PM

Venue

The Verna Classic, Near Titan Gate, Verna IDC, Verna, Goa

Industry

Pharmaceutical Manufacturing

Open Positions

1. Technician – Production Department

Qualification: ITI / 12th Pass

Experience: 1–3 Years

2. Sr. Officer / Officer – Production Department

Qualification: B.Pharm / M.Pharm

Experience: 1–3 Years

3. Sr. Officer / Officer – Quality Control Department

Qualification: B.Sc / M.Sc

Experience: 1–3 Years

4. Apprentice – Technician (Production)

Qualification: ITI / 12th Pass

Experience: Freshers Eligible

5. Sr. Officer / Officer – Materials Department

Qualification: B.Sc / B.Com

Experience: 1–3 Years

Why Join Unichem Laboratories?

Unichem Laboratories is recognized for its commitment to pharmaceutical excellence and employee development. Key benefits include:

Strong presence in the pharmaceutical sector

Modern manufacturing and quality facilities

Career growth and learning opportunities

Focus on quality, compliance, and innovation

Employee safety and well-being initiatives

Exposure to regulated manufacturing environments

Skills Expected from Candidates

Depending on the role, candidates should possess knowledge of:

Production

Good Manufacturing Practices (GMP)

SOP compliance

Batch manufacturing processes

Equipment operation and maintenance

Documentation practices

Quality Control

Analytical testing techniques

Laboratory instruments such as HPLC, GC, UV-Visible Spectrophotometer

Data integrity practices

OOS/OOT investigations

Regulatory compliance

Materials Department

Inventory management

Warehouse operations

SAP/ERP systems

Material reconciliation

Supply chain coordination

Documents to Carry

Candidates attending the walk-in interview should bring:

Updated Resume/CV

Passport-size photographs

Educational certificates

Experience certificates

Salary documents (if applicable)

Government-issued ID proof

Career Outlook

The pharmaceutical industry continues to expand due to increasing healthcare demands and global market opportunities. Professionals in Production, Quality Control, and Materials Management play a crucial role in ensuring product quality, regulatory compliance, and efficient manufacturing operations. Joining a reputed organization like Unichem can provide valuable industry exposure and long-term career growth.

Technical FAQs

1. What is the significance of GMP in pharmaceutical production?

Answer: GMP (Good Manufacturing Practices) ensures pharmaceutical products are consistently produced and controlled according to quality standards. It minimizes risks such as contamination, mix-ups, and errors during manufacturing.

2. Why is HPLC widely used in Quality Control laboratories?

Answer: High-Performance Liquid Chromatography (HPLC) is used for the identification, quantification, and purity assessment of pharmaceutical compounds. It provides high accuracy, sensitivity, and reproducibility.

3. What is an OOS result in pharmaceutical analysis?

Answer: OOS (Out of Specification) refers to a test result that falls outside predefined acceptance criteria. Such results require a structured investigation to identify root causes and ensure product quality.

4. What is batch manufacturing documentation and why is it important?

Answer: Batch manufacturing records document every stage of production, including materials used, process parameters, and operator activities. They provide traceability and support regulatory compliance.

5. How does inventory control impact pharmaceutical manufacturing?

Answer: Effective inventory control ensures the availability of raw materials, prevents stock shortages, reduces wastage, supports batch traceability, and improves overall operational efficiency.

Disclaimer: Candidates are advised to verify all recruitment details directly with Unichem Laboratories Ltd. before attending the walk-in interview.