Project Engineer II

curiate.co

Springfield, MO

JOB DETAILS
SKILLS
3D Modeling, Analysis Skills, AutoCAD, Biotech and Pharmaceutical, Budgeting, Building Permits, CAD (Computer-Aided Design) Software, Capital Project, Change Control, Construction Industry Software, Continuous Improvement, Contract Manufacturing, Cost Control, Cost Engineering, Cost Estimates, Current Good Manufacturing Practice (cGMP), Documentation, Documentation Standards, Drug Manufacturing, Electrical Engineering, Engineering, Engineering Consulting, Environmental Health, Facilities Management, GMP (Good Manufacturing Practices), Heat Transfer, Identify Issues, Interpersonal Skills, Manufacturing, Mechanical Engineering, Microsoft Project, Negotiation Skills, Occupational Health, On Site Support, Operations Processes, Patient Care, Plant Layout and Design, Procedure Development, Process Improvement, Process Validation, Project Control, Project Engineering, Project Estimates, Project Lifecycle, Project Management Professional (PMP), Project Schedule, Project/Program Management, Quality Assurance, Regulations, Reimbursement, Reliability Engineering, Requirements Management, SAP, Safety Standards, Safety/Work Safety, SolidWorks, Spreadsheets, Standard Operating Procedures (SOP), Technical Operations, Technical Support, Technical/Engineering Design, Validation Plan, Vendor/Supplier Management, Word Processing
LOCATION
Springfield, MO
POSTED
1 day ago

Project Engineer II – Springfield, MOBuild your future at Curia, where our work has the power to save lives.The Project Engineer provides technical engineering support and project management expertise to the pharmaceutical production facility. Acting as a critical link between operational needs and engineering execution, this role advances the Curia Way by driving continuous improvement, delivering reliable results, and partnering closely with production, quality, and operations teams to build a safer, more efficient facility.Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.BenefitsGenerous benefit options (eligible first day of employment)Paid training, vacation and holidays (vacation accrual begins on first day of employment)Career advancement opportunitiesEducation reimbursement401K program with matching contributionsLearning platformAnd more!ResponsibilitiesProject Development & ExecutionDefine project scopes, develop detailed designs, and prepare technical specifications for process and equipment initiatives.Build project budgets and schedules, including cost estimation, vendor price negotiation, and delivery coordination; manage capital projects typically ranging from $100K to $1.2M.Design plant and facility improvements; oversee the design process when consulting engineers are engaged.Supervise and inspect project work in progress at the plant site and at fabricator facilities.Manage equipment start‑ups, troubleshooting efforts, and operator/supervisor technical support in the field.Continuous Improvement & Technical ExcellenceApply unit operations principles (heat and mass transfer, etc.) to design and implement optimization programs that reduce costs and cycle times.Support and champion Continuous Improvement activities across the site.Provide project cost control throughout the full project lifecycle.Prepare PSM analysis and documentation; write operating procedures as required.Compliance & DocumentationSupport Quality Assurance and Good Manufacturing Practices by preparing and executing validation protocols.Prepare permit applications for construction and provide technical data for environmental permit applications.Maintain thorough engineering administration and project documentation standards.QualityQuality is something we take pride in together. You'll perform your work in alignment with cGMP requirements and Curia's standards, which means:Perform all documentation in compliance with ALCOA++ principles and site SOPs.Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms.Keep all required cGMP training current and elevate quality concerns along with proposed solutions to the Quality department.QualificationsB.S. in Engineering (Electrical or Mechanical Engineering preferred).3-5 years of relevant engineering experience in a manufacturing environment.Demonstrated project management skills, including interpersonal, negotiation, and vendor management abilities.Proficiency with SAP, MS Project, and standard office productivity software (word processing, spreadsheets, databases, presentations).Working knowledge of GMP regulations, process validation strategies, and environmental, health, and safety standards.Other QualificationsMust pass a background check.Must pass a drug screen.May be required to pass Occupational Health Screening.PreferredExperience in pharmaceutical manufacturing is strongly preferred.PMP Certification.Experience developing User Requirement Specifications (URS) with project owners.Proficiency with CAD software such as AutoCAD, SolidWorks, or equivalent 2D/3D modeling tools.Equal OpportunityCuria is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E‑Verify employer.#J-18808-Ljbffr

About the Company

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curiate.co