Project Engineer II

Curia, Inc.

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S. in Engineering, preferably Electrical or Mechanical.
  • 3-5 years of engineering experience in a manufacturing setting.
  • Demonstrated project management, negotiation, and vendor management skills.
  • Proficient in SAP, MS Project, and standard office productivity software.
  • Knowledge of GMP regulations and process validation.

Responsibilities

  • Define project scopes and develop detailed designs with technical specifications.
  • Build budgets and schedules for capital projects ranging from $100K to $1.2M.
  • Oversee design and implementation of plant improvements with consulting engineers.
  • Supervise and inspect project work both on-site and at fabricator locations.
  • Manage equipment start-ups and provide technical support to operators.

Benefits

  • Opportunity to work in a fast-paced pharmaceutical production environment.
  • Engagement in continuous improvement activities that drive efficiency.
  • Ability to influence project outcomes and enhance technical processes.
  • Involvement in compliance-related activities ensuring high quality standards.
Full Job Description
Job Description

Project Engineer II in Springfield, MO

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.

Responsibilities

Project Development & Execution
  • Define 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 Excellence
  • Apply 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 & Documentation
  • Support 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

Good Manufacturing & Documentation Practices

Quality 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 escalate quality concerns along with proposed solutions to the Quality department.

Qualifications
  • B.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 Qualifications
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening

Preferred
  • Experience 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.

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address.

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