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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Warren, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Sterling Heights, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Lansing, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Ann Arbor, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Automations Engineer
GPAC
El Dorado, AR
This privately-owned company is rapidly growing and seeking an Automations Controls Engineer to design clear, complete and accurately working products and systems using CAD, rough or…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Livonia, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Dearborn, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Clinton Township, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
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Civil Design Engineer | Land Development (EIT or PE)
GPAC
Canton, MI
- $80,000 to $100,000 USD / year
Our company is seeking a Civil Design Engineer with land development experience to design and deliver residential, commercial, and mixed-use site projects. You'll handle site layout,…
Added 2 mins ago
Lead Night Shift Field Engineer
Bechtel Corporation
Houston, TX
Performs night shift field engineering planning, work package development, and daily coordination with the Project Field Engineer, supervision, and job-site operating sections.
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Facilities Technician - 2nd Shift
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Devens, MA
Are you someone that likes to get your hands dirty, get so involved with a project that you cannot believe the workday is over? Do you want to have a sense of accomplishment at the end of…
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Maintenance Repair and Overhaul Engineer (Onsite) P2
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…technologies for these products. Technical disciplines in CSE include Project Engineering, Mechanical Design, Structural Analysis, and Product…
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Principal Mechanical Design Engineer IV(Onsite)
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A Principal Mechanical Engineer will be working in a focused, cross-functional team of engineers developing highly reliable products which meet customer specified requirements/expectations…
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Senior Mechanical Design Engineer(Onsite)
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The Auxiliary Power System (APS) Project Engineering (PE) will support specific APU model in support of the respective Model Program Chief Engineer (MPCE). The PE will be an integral member…
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Auxiliary Power Systems Sr. Engineer (Onsite)
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The Senior Engineer, Project Engineering will be responsible for overseeing and improving designs, manufacturing, and engine test processes for legacy and new production Military APU…
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Senior Sustaining Project Engineer (Onsite)
RTX
United States
Coordinate among manufacturing sites, customers, and suppliers to develop project plans for product or process changes.
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Production Engineer
ASML US, LP. (US20)
Wilton, CT
As a Production Engineer at ASML in Wilton, Connecticut, you will help turn advanced engineering designs into reliable manufacturing processes. Your work will directly support the…
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Customer Program Manager
AEye, Inc
Pleasanton, CA
4+ years of program or project management experience in a hardware, technology, or engineering-driven environment.
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Project Engineer-Electrical
McKim & Creed, Inc.
Pittsburgh, PA · Berkeley Lake, GA · Atlanta, GA
Communicates and coordinates with the Project Manager, Sr. Electrical Engineer and other design team members to complete work efficiently.
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Engineering Academy Associate Engineer
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Lincolnshire, IL
The Engineering Academy Associate Engineer is an entry-level engineering position designed for recent graduates participating in the Engineering Academy, a structured two-year development…
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Advanced Mfg Engineer Sr Adv
Aerospace
Torrance, CA
As an Advanced Manufacturing Engineer Senior Advanced here at Honeywell Aerospace, you will drive advanced manufacturing strategies, optimize processes, and implement cutting-edge…
Added 5 mins ago
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Advanced Mfg Engineer Sr
Aerospace
Torrance, CA
- $119,000 to $148,000 USD / year
As an Advanced Manufacturing Engineer Sr here at Honeywell Aerospace, you will play a pivotal role in optimizing and advancing our manufacturing processes to ensure high-quality production…
Added 6 mins ago
Staff Software Engineer, AI/ML
Google
Mountain View, CA · New York, NY
…mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google’s needs with opportunities to switch teams and projects as…
Added 6 mins ago
Senior Software Engineer, AI/ML, ML Training
Google
Sunnyvale, CA · Kirkland, WA
…mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google’s needs with opportunities to switch teams and projects as…

CURIA

Principal Engineer

United States

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Job details

Experience: Experience: Minimum 10+ years of pharmaceutical engineering experience in sterile drug product manufacturing or CDMO technical operations
Posting language: English
Posted: Nov 4, 2026

Original job description

Principal Engineer – Filling & Lyophilization – United States Build your future at Curia, where our work has the power to save lives. The Principal Engineer will lead equipment engineering for large capital projects in sterile filling and lyophilization to support Curia’s strategic growth. This includes leading network-wide capital execution to expand, modernize, and standardize manufacturing infrastructure. The incumbent will direct the specification, procurement, installation, commissioning, and qualification of advanced aseptic technologies to increase capacity, efficiency, and compliance for drug product programs. This position interfaces with Curia’s network manufacturing sites, client technical teams, and global leadership. The role provides technical oversight, mentorship, and engineering guidance across site-based teams and major capital project teams. 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. We proudly offer

Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!

Responsibilities

Capital Project Execution: Lead filling and lyophilization equipment engineering for major capital projects ($10M–$50M+) from conceptual design through Commissioning, Qualification, and Validation (CQV)
Technical Transfer & Client Support: Drive robust, on-time technical transfers of API and Drug Product (DP) programs, partnering with the Global Program Management Office and site technical operation teams to satisfy client expectations
Equipment Specification & Procurement: Author User Requirement Specifications (URS), drive vendor selection, conduct capital cost estimation, and lead Factory/Site Acceptance Testing (FAT/SAT) for primary equipment (fill lines, isolators, lyos, VHP, capping)
Network Capability & Talent Development: Mentor site-based engineering teams across the Curia network, sharing best practices, upgrading skill sets, and driving technical standardization
Operational Excellence & Continuous Improvement: Partner with sites to troubleshoot complex equipment deviations, increase OEE, reduce cycle times, and execute cost-improvement programs
Vendor & Engineering Firm Management: Oversee external engineering design firms, equipment vendors, and field contractors for filling and lyophilization installations
Regulatory Compliance: Ensure all equipment and system designs comply with cGMP, EU Annex 1 (Contamination Control Strategy), FDA guidance, and global regulatory standards
This job has no direct supervisory responsibilities; serves as a technical lead and matrix manager for project teams and site engineering resources
Travel Requirement: Up to 40% travel, including international travel to plant sites and vendor facilities Education and Experience
Education: BS in Mechanical, Chemical, Electrical, or Biomedical Engineering (or related discipline)
Experience: Minimum 10+ years of pharmaceutical engineering experience in sterile drug product manufacturing or CDMO technical operations
Capital Projects: Proven track record leading major capital equipment execution projects exceeding $10M Technical Expertise: Advanced expertise in
Aseptic processing, high-speed sterile filling (vials, syringes, cartridges), and barrier technology (Isolators/RABS)
Lyophilization processes and automated loading/unloading systems (ALUS)
Decontamination systems (VHP / Hydrogen Peroxide Vapor)
Sterilization processes (SIP, Autoclaves, Depyrogenation Tunnels)
Critical Utilities (WFI, Clean Steam, Clean Compressed Air, Process Gases, Cleanrooms, and HVAC)
Commissioning, Qualification, and Validation (CQV / ISPE Baseline Guide approach)
Regulatory & Quality Knowledge: Deep understanding of global pharmaceutical regulations (FDA cGMP, EMA, EU Annex 1, PIC/S) Skills & Capabilities
Analytical & Problem Solving: Demonstrated root-cause analysis skills (e.g., FMEA, 6-Sigma) to address complex process and equipment deviations
Communication & Stakeholder Management: Excellent verbal and written communication skills with experience presenting technical concepts to executive leadership, site teams, and external clients
Computer & Software Skills: Proficient in project management software, CAD systems, CMMS, Trackwise/QMS systems, MS Office Suite (Word, Excel, PowerPoint), and process automation systems (PLC/SCADA/DCS) Other Qualifications & Requirements
Must pass a background check and drug screen
Ability to work in cleanroom environments (Gowning required) Physical Demands & Work Environment
Physical Demands: Regularly required to talk, hear, sit, stand, walk, reach, and lift up to 25–50 lbs
Work Environment: Mix of office environment, active construction sites, and cGMP cleanrooms. Moderate noise level with exposure to moving mechanical parts and industrial chemical/utility systems This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbents will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. This document does not create an employment contract, implied or otherwise, other than an “at will” relationship.

Salary range:$120,200-$144,100/year 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. Curia 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.

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More about this job

Skills

Procurement
Regulatory compliance
Program management
Microsoft Office
Estimating
Process improvement
Troubleshoot
Biomedical engineering
Pharmaceutical technology
SIP
HVAC
Pharmaceutical legislation
Problem solving
Root cause analysis
Communication skills
Stakeholder management
Project management
CMMS
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
PLC
SCADA
DCS
Heavy lifting

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