|Req ID: 5615
Find Similar Jobs
NEW YORK NY US
|Minimum Years Experience:|
|Job Type:||Full Time|
Direct, coordinate, and exercise functional authority for the planning, organization, control, integration, and completion of pharmaceutical construction projects.
|Essential Duties and Responsibilities|
Direct, coordinate, and exercise functional authority for the planning, organization, control, integration, and completion of pharmaceutical construction projects. Prepare outline plans on front-end design packages for the pharmaceutical industry. Prepare outline process flow diagrams for pharmaceutical processes and pharmaceutical equipment flows. Lead Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) for pharmaceutical equipment. Lead commissioning and validation for utilities and pharmaceutical process equipment. Meet federal regulatory compliance for pharmaceutical cGMP utilities and cGMP equipment. Procure, install and commission equipment required for bio-pharmaceutical manufacturing plants and oral dosage plants including fermentation, purification, final-fill, tableting, coating, inspection, packaging and lyopholization. Plan and formulate engineering programs. Organize project staff according to project requirements. Assign project personnel to specific phases or aspects of projects, such as technical studies, design, preparation of specifications and technical plans, and testing, in accordance with engineering disciplines of staff. Review pharmaceutical construction plans for compliance with engineering principles, company standards, customer contract requirements, and related specifications. Evaluate and approve design changes, specifications, and drawing releases. Control expenditures within limitations of project budget. Analyze technology, resource needs, and market demand to plan and assess the feasibility of projects. Participate as necessary in pre-construction services. Conduct thorough construction reviews. Prepare a contract items list. Develop trade requisitions for bid packages and major material/equipment purchases. Assist in the purchasing process. Implement mock-ups and associated testing, review, and approval. Implement engineering management/document control systems. Manage project close out, including securing warranties, guarantees, and acceptance of work, sub-contract and vendor close, final payment, and records retention. Maintain responsibility for the procurement, expediting, verification, and commissioning of all processes required for the following systems as part of the construction process of pharmaceutical projects: United States Pharmacopeia water (USP), Reverse Osmosis (RO), Water for injection (WFI), clean steam, chilled water, plant steam, compressed air, building management systems (BMS), heating/ventilation/air conditioning (HVAC) and other cGMP equipment and utilities. Use AutoCAD, 3-D AutoCAD scheduling tools, and Microsoft Office tools in connection with above duties.
The Project Engineer position requires four years of experience in job offered or four years of experience preparing outline plans on front-end design packages for the pharmaceutical industry; preparing outline process flow diagrams for pharmaceutical processes and pharmaceutical equipment flows; led FAT and SAT for pharmaceutical equipment; leading commissioning and validation for utilities and pharmaceutical process equipment; meeting federal regulatory compliance for pharmaceutical cGMP utilities and cGMP equipment, utilizing AutoCAD, 3-D AutoCAD scheduling tools and MicroSoft tools; and performing installation and start up of biopharmaceutical manufacturing plants and oral solid dosage plants including packaging and Lyopholization.
Significant travel required.
Reference # 10809278.
Work Location: New York, NY.
Position is part of company employee referral program.
|Physical Demands and Work Environment:|
BrowseView All Jobs
View your Equal Employment Opportunity rights under the law"EEO is the Law" poster