Job Description

About Us

For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.

As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.

To set up, operate and clean equipment in moderately complex production areas as well as ensure products follow appropriate procedures in a clean and safe work environment in order to meet all cGMP, FDA, DEA, OSHA and other applicable regulations.

Key Responsibilities:

• Performs line/equipment setup, cleaning and changeover activities that require the use of hand tools, removing and replacing machine parts, adjusting instrumental devices and cleaning parts in order to ensure compliance with cGMP, FDA, DEA, OSHA and other applicable regulations .
• Completes appropriate documentation to support process and production procedures including data capture, forms, logbooks, and inventory batch records-
• Ensures all finished products from each vendor manufacturing orders are received properly in order to account for any excess materials
• Fills out all necessary department forms, logbooks, and records in order to maintain proper filing of information
• Follows verbal and written procedures in order to correctly operate production equipment and perform processing steps
• Operates one machine or part of the production line under close and direct supervision in order to ensure compliance with set guidelines and meet production targets
• Cleans production area, equipment, tools, etc., following appropriate company and regulatory procedures and guidelines in order to prepare for the next production run.
• Contributes to the identification of opportunities for continuous improvement of processes and practices taking into account ‘international best practice’, improvement of business processes, cost reduction and productivity improvement.

Qualifications

• Minimum Qualifications: Diploma degree in related fields.
• Minimum Experience: 0-3 years relevant experience in a cGMP/Manufacturing facility.