Operator Granulation

Himalaya Wellness Europe; Dubai; On-site; AED 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company in Dubai is seeking an Operator - Granulation to perform granulation processes in compliance with cGMP guidelines. The ideal candidate has 3-5 years of experience within the pharmaceutical industry and strong knowledge of granulation equipment and regulatory standards. Responsibilities include operating equipment, maintaining production logs, and ensuring quality and safety standards are met. This is a full-time role offering an opportunity to work in a dynamic environment.

Qualifications

• 3-5 years of experience in granulation within the pharmaceutical industry.
• Experience in a cGMP-compliant facility is preferred.

Responsibilities

• Operate granulation equipment according to production schedules.
• Ensure adherence to cGMP, WHO, US FDA, EMA, and UAE guidelines.
• Perform in-process quality checks to meet product specifications.
• Collaborate with QA to address deviations and implement corrective actions.
• Maintain accurate production logs and BMRs.

Skills

In-depth knowledge of granulation processes

Familiarity with regulatory standards

Strong technical and operational skills

Education

Diploma or certification in Pharmaceutical Manufacturing or Chemical Engineering

Job description

Job Title: Operator - Granulation

Location: Dubai Industrial City, Dubai

Employment Type: Full-Time

Reports To: Department Leads

Position Summary

The Operator - Granulation will be responsible for performing granulation processes in compliance with cGMP guidelines, SOPs, and UAE regulatory requirements. The role involves operating, monitoring, and maintaining granulation equipment to ensure efficient production of high-quality pharmaceutical products. The operator will report directly to the Executive - Tablet and Liquid Manufacturing and collaborate with cross-functional teams to achieve operational excellence.

Key Responsibilities

• Operate granulation equipment, including high‑shear mixers, fluid bed dryers, and mills, according to production schedules and approved protocols.
• Accurately follow batch manufacturing records (BMR) and SOPs during granulation processes.
• Ensure adherence to cGMP, WHO, US FDA, EMA, and UAE Ministry of Health guidelines during all operations.
• Perform in‑process quality checks, including granule size, moisture content, and blending uniformity, to meet product specifications.
• Collaborate with the QA team to address deviations and implement corrective actions.
• Perform routine cleaning, setup, and maintenance of granulation equipment.
• Report equipment malfunctions and assist the engineering team in troubleshooting.
• Maintain accurate production logs, equipment usage records, and BMRs.
• Assist in preparing reports for internal audits and regulatory inspections.
• Identify opportunities to improve granulation efficiency, reduce waste, and enhance product quality.
• Support process validation and scale‑up activities as required.
• Adhere to safety protocols and ensure a clean and safe working environment.
• Participate in regular safety training sessions and implement best practices.

Candidate Specification

Experience + Exposure + Education

• Diploma or certification in Pharmaceutical Manufacturing, Chemical Engineering, or a related field.
• 3‑5 years of experience in granulation within the pharmaceutical industry, preferably in a cGMP‑compliant facility.

Key Skills

• In-depth knowledge of granulation processes, equipment, and troubleshooting.
• Familiarity with regulatory standards (UAE Ministry of Health, WHO, US FDA, EMA).
• Strong technical and operational skills, with a focus on quality and efficiency.

Key Competencies

• Attention to detail and ability to follow processes accurately.
• Effective communication and teamwork skills to coordinate with cross‑functional teams.
• Proactive approach to identifying and resolving production challenges.