ASL is looking for an MEP Projects manager to lead the effort in coordinating, managing, executing and completing the MEP trades in construction projects. The MEP trades are HVAC, Plumbing, Fire Fighting, Electrical and Low Current Systems. The Key responsibility include commitment to ensure timely completion of project within budget and resources without compromising on Quality & Safety.
: • Prepare a plan for schedule, budget and resources of the projects from the initiation phase up until commissioning and handover. • Study and review Contract documents. • Monitor projects budget and schedule and oversee performance to ensure on time, quality and budget project execution. • Coordinate activities with material and equipment procurement as well as resources allocation. • Ensure that the projects comply with contracts, specifications, standards, drawings and BOQ. • Ensure that the health and safety requirements comply with project and authorities requirements. • Prepare and review material submittal, method statements, ITPs and quality plan. • Prepare and review drawings (Design, shop drawings and as built). • Prepare and review project schedule taking into account procurement and resources. • Attend regular meetings with Main Contractor, Consultants and Clients to discuss key issues related to project and take effective corrective actions. • Monitor the installation testing, commissioning and start-up of the MEP systems in coordination with other trades. • Coordinate and manage subcontractors, manpower and material suppliers.
Position Objective: Regulatory Affairs Officer acts as a link between Company and the regulatory authorities, ensuring that the products that are distributed by Maquet Middle East are in compliance with the appropriate legislation. Essential Duties and Responsibilities: - Manage and facilitate all medical devices related registration activities for Middle East and Africa Region. - Complete forms and requests originating from government agencies. - Maintain contact with regulatory authorities and company headquarters in Germany. - Provide the Project teams and Managers with regulatory input in order to obtain timely regulatory approvals for the products (medical devices) as part of the product development planning. - Assure compliance with Export regulation for US manufactured products (OFAC & BIS). - Update licensing and collect information on registration instructions and regulations.
Dubai, United Arab Emirates
Medical/Hospital; Healthcare, Practitioner and Technician; Biotechnology