Key Responsibilities include:

·Initiate, author, review, and approve change control, specifications, risk assessments, work orders, standard operating procedures (SOPs), capital project approvals (CPAs), purchase requisitions/orders, factory/site acceptance tests (FAT/SAT), corrective actions, and associated interim/final reports and other paperwork in compliance with Company policy.

Ensure all quality systems and operations are maintained
Ensure operations have fully functioning systems with the appropriate back-up systems in place
Provides day-to-day maintenance support, both scheduled and unscheduled or emergency, for assigned area.
Participates in internal or external facility audits and inspections.
Utilizes Lean Manufacturing and Six Sigma principals to solve problems, eliminate waste, and effectively organize maintenance work.
Ensure maintenance, calibration, and work order programs are running smoothly
Assist in Safety, Health, and Environmental related activities and maintain compliances
Develop and train team members
Qualification :

Master/ Bachelor of Engineering

Min. 7 years in Pharmaceutical industry and 2 years in the same position.

Working knowledge of cGMPs and of regulatory requirements as they apply to the pharmaceutical industry
Strong communication (written/verbal), and multi-tasking abilities

Experience in Microsoft Office, projects Management and Auto Cad.

Please send updated CV with recent Photo to : recruitment@fas-tech.com
mentioning Job Title in the Subject

Preferable resident in Saudi Arabia with transferable Iqama.