Operator at Hikma Pharmaceuticals PLC

Al Salt, Balqa, Jordan -

Full Time

Start Date

Immediate

Expiry Date

04 Jul, 26

Salary

0.0

Posted On

05 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Equipment setup, Machine operation, cGMP compliance, FDA regulations, Documentation, Inventory management, Production line maintenance, Quality control, Safety compliance, Data capture, Cleaning procedures, Process improvement

Industry

Description

Policies, Processes & Procedures : Follows all relevant departmental policies, processes, standard operating procedures and instructions so that work is carried out in a controlled and consistent manner. Day-to-day Operations : Follows the day-to-day operations related to own job to ensure continuity of work. Job Specific Accountabilities : 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. Continuous Improvement : 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. Reporting : Assists in the preparation of timely and accurate reports of the Manufacturing department to meet company and department requirements, policies and standards. Safety, Quality & Environment : Complies with all relevant safety, quality and environmental management policies, procedures and controls to ensure a healthy and safe work environment. Related Assignments : Performs other related duties or assignments as directed. QUALIFICATIONS, EXPERIENCE, & SKILLS : Minimum Qualifications: Bachelors’ in Manufacturing or related field OR High School Diploma Minimum Experience: 0-2 years relevant experience in a cGMP/Manufacturing facility

Responsibilities

The operator is responsible for performing equipment setup, cleaning, and changeover activities while ensuring compliance with cGMP and FDA regulations. They must also maintain accurate production documentation, logbooks, and inventory records to support manufacturing processes.