ARCADIS ARE SEEKING A PROJECT ENGINEER FOR A CLIENT-SIDE BIOPHARMA ASSIGNMENT IN MAYO

The Project Engineer is responsible for safely coordinating and leading projects associated with New Product Introductions, Process Improvements, Automation, Aseptic processing, New Processing equipment with some Facility / utilities modifications to incorporate same. The primary responsibility of the role is to ensure that Projects meet agreed goals/targets on time and on budget. The PE will give advice and support to ensure the equipment/facility/utilities design and goals/targets are achieved.

REQUIREMENTS:

• Third level qualification in an Engineering or equivalent discipline/experience.
• Experience of working in Biologics, Pharmaceuticals or Medical device industry.
• Project Management experience with a proven record

• Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. Processing equipment would include e.g., Autoclaves, RABS & Isolator Filling machines, LAF units, Compounding skids, Vessels, Containment booths & Stopper processing eq.
• Writing URS, selecting vendors and completing vendor evaluation matrix.
• Writing RCE’s, placing orders, Project Management & Design review meetings.
• Working to the ASME BPE 2019 Standard and relevant ISPE Guidelines etc.
• Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
• Lead the Project Team participation in FAT program.
• Coordination of all equipment documentation requirements.
• Commissioning of equipment and Engineering support during qualification.
• Handover training, coordination of O&M manuals, Spare parts, & PM schedules
• Contribute to a team environment on specific technical problem-solving forums associated with Product manufacture & Aseptic fill.
• Deliver on Process improvement / cost reduction projects.
• Lead your regular weekly / bi-weekly Project review meetings with your Project team