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Pharmaceutical Research Unit (PRU) or Arab Pharmaceutical Industry Consulting (APIC) is a leading clinical research organization (CRO) that was established in Jordan in 1993. At PRU/APIC we offer clinical development solutions that aim to transform drug development & health industries worldwide. We are the largest CRO in the MENA region – capacity wise- & we pride ourselves on providing a comprehensive list of services to pharmaceutical & healthcare companies at the highest principles of personal & professional conduct.
We have an exciting opportunity for Validation & Maintenance Engineer in QA Department to support us in our continuous growth.
Responsibilities:
Manage all documents of software or/and instrument qualification.
Review and approve validation master plan, qualification protocols and final report
Ensure the proper implementation and management of the maintenance system
Communicate and coordinate the maintenance and preventive maintenance carried out by external parties
Follow of operating procedures related to maintenance and preventive maintenance.
Prepare and execute the annual schedule of calibration and preventative maintenance.
Qualification and controlling of thermal devises such as freezers and refrigerators.
Follow up and maintain the EM alarms.
Receive the maintenance requests and handle the instrument failures and maintenance
Follow-up of pest control process internally and with external agent
Follow-up waste destruction process internally and with external agent
Follow-up of safety measures internally and with external agent
Must-Haves:
B.Sc. Mechanical engineering, Mechatronics; or any related qualifications.
Years of experience at least two years.
Communicator with a positive attitude towards work.
Presentable, well read, and well-spoken with good public relations abilities.
People oriented with good communication and negotiating skills.
Excellent command of Arabic and English languages both spoken and written.
Strong organizational skills, attention to detail, and demonstrated ability to identify quality and compliance issues.
Proven validation experience, with ability to multi-task, follow-up on assignments, and display effective use of time management.
Proficiency with the use of project, spreadsheet, and word processing software (Microsoft Professional)
If your qualifications meet our criteria, please submit your resume at: