Senior Project Engineer
3 weeks ago
We are looking for a knowledgeable Engineering resource to join our Life Sciences team in support of a pharmaceutical project in the Indianapolis area. Ideal candidates should have a strong understanding of capital project engineering lifecycle and experience providing Project Engineering support in highly regulated or pharmaceutical/biotech facilities.
AMTS has opportunities throughout the country and overseas supporting multiple locations in MA, NH, RI, NC, Europe, and other locations.
Responsibilities:
· Provide engineering and technical support related to operation, maintenance, design, installation, start-up/commissioning, testing and qualification of product and infrastructure equipment and systems.
· Systems may include production equipment such as bioreactors, fermenters, centrifuges, UFDF, Chromatography, CIP skids, and other support equipment such WFI, CS, Process Gases, HVAC, and Core Building Utility Systems.
· Support the design and qualification of improvements, changes or upgrades to the equipment and startup and validation documents.
· Lead projects of various complexities to support departmental initiatives and participate in various cross-functional teams to support process improvements.
· Identify and schedule project events around manufacturing operations.
· Identify materials required to support project execution work.
· Communicate project requirements to vendors to obtain proposals for equipment and piping changes.
· Provide project design and cost estimates.
· Manage project implementation including oversight of selected vendors.
· Redline drawings to prepare the As-Built set and maintain the site master drawing.
· Report project status and progress to Senior Project management.
Education and Experience:
· Bachelor’s degree in Mechanical or Chemical Engineering.
· Minimum 3+ years’ experience providing Project Engineering support.
· Candidate must be able to work across functional areas such as operations, maintenance, quality and validation.
· Proficiency in the arena of process, utility and building engineering in cGMP environment within a biopharma facility.
· Working knowledge of documents such as P&IDs, URS, FRS, and qualification documents.
· Effective verbal and written communication skills.
· Excellent interpersonal, teamwork, and leadership skills required.
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