Jobs in the United States

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Added 2 mins ago
Senior Mechanical Design Engineer
Andromeda Systems Incorporated
Lexington Park, MD
ASI is seeking a highly skilled Senior Mechanical Design Engineer to support complex aircraft modification, prototyping, and integration projects within the Aircraft Prototype Systems…
Added 6 mins ago
Test Engineer II | Engines - VEEx | Van Horn, TX
Blue Origin Personnel, LLC
Van Horn, TX
…plethora of development and flight rated hardware. As a test engineer at the Vacuum Engine Experiment (VEEx) test stand, you will take on a critical role by contributing to test operations…
Added 6 mins ago
Prototype Engineer - SWORD
Blue Origin Personnel, LLC
Space Coast, FL
Broad experience in manufacturing: welding, assembly, integration, instrumentation, cleaning, non-destructive testing, leak testing, fabrication, machining, etc.
Added 6 mins ago
Mechanical Engineer II - New Glenn Umbilicals
Blue Origin Personnel, LLC
Space Coast, FL
Provide technical guidance and on-site support for manufacturing, production, integration, and test activities
Added 11 mins ago
HI
Senior Validation Engineer
Hospira, Inc.
KS
- $82,700 to $137,900 USD / year
Comprehensive understanding of {Current} Good Manufacturing Practices {part of GxP} guidelines outlined in Code of Federal Regulations.
Added 13 mins ago
Principal BIOS Design Engineer
Jabil Inc.
Austin, TX
The BIOS Developer is responsible for leading BIOS/UEFI development and platform integration activities across complex hardware programs. This role provides technical ownership for firmware…
Added 17 mins ago
Business Continuity Engineer
Samsung Austin Semiconductor, LLC.
1530 FM 973 Taylor, TX
Reporting to the Director of Innovation, the Business Continuity Engineer will spearhead the enhancement of Samsung Austin Semiconductor’s Business Continuity Program (BCP) across both the…
Added 21 mins ago
Test and Launch Operations Engineer I
Rocket Lab Corporation
Wallops Island, VA
Test and Launch Operations Engineers are responsible for taking years of design and manufacturing to flight in the operation of launch vehicles. As a member of Rocket Lab's Test & Launch…
Added 22 mins ago
Process Engineer III – (E3)
Applied Materials
Santa Clara, CA · Santa Clara
As a Process Engineer, you'll play a crucial role in designing and optimizing manufacturing processes for display and semiconductor manufacturing technologies. You will collect and analyze…
Added 24 mins ago
Embedded SDE, Payload Radio Gateway
Amazon Kuiper Manufacturing Enterprises LLC
Sunnyvale, CA · Redmond, WA · San Diego, CA
Own unique embedded software functions through design, implementation (in C, C++, RUST or other), test, and integration in an embedded Linux or real-time operating system (RTOS) environment.
Added 24 mins ago
Embedded Software Engineer, Leo Payload Radio
Amazon Kuiper Manufacturing Enterprises LLC
Sunnyvale, CA · Redmond, WA · San Diego, CA
…through design, implementation (in C, C++ or other), test, and integration in an embedded Linux…
Added 26 mins ago
Controls Engineer II
Barry-Wehmiller
Denver, CO
BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals…
Added 26 mins ago
Superintendent, Construction
Barry-Wehmiller
Pasadena, CA · Phoenix, AZ · Sacramento, CA
BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals…
Added 29 mins ago
Senior Quality Engineer Electro-Mechanical Assembly
Neros Technologies
Torrance, CA
As a Senior Quality Engineer at Neros, you'll own electro-mechanical build quality across the factory as we scale production, from motors, harnesses, and mechanisms through the finished…
Added 33 mins ago
Manufacturing Project Engineer
Textron Systems
Slidell, LA
…internal development initiatives and our contract programs. The Manufacturing Project Engineer/Manager will work primarily with the Manufacturing and Program teams to plan and execute ARV…
Added 36 mins ago
Sr Quality Engineer I
Kite Pharma, Inc.
CA
Support implementation and deployment of manufacturing automation systems, including integration with enterprise and supporting systems.
Added 36 mins ago
Mechatronics Engineer I
Ginkgo Bioworks Inc.
Boston, MA
Ginkgo is hiring a Mechatronics Engineer I to join our in-house automation and integration team. This team is responsible for designing, developing, and deploying automation solutions to…
Added 41 mins ago
Controls Engineer
Burford Corp
Maysville, OK
…Burford is a long-standing, respected brand known worldwide for manufacturing quality custom products through innovative baking solutions. Products include the famous twist tie machine,…
Added 43 mins ago
Software Sales Associate Director - Procurement Software/Tech
Accenture LLP Company
NY
Experience selling into at least one target industry vertical at enterprise scale (CPG, Life Sciences, Financial services, manufacturing, energy) and deep relationships across domains.
Added 43 mins ago
A
Electrical Engineer
Actalent
Sunnyvale, CA
- $105 USD / hour
Job Title: Electrical EngineerJob DescriptionThe Electrical Engineer designs, develops, tests, and oversees the manufacturing and installation of electrical equipment, components, and…
Added 44 mins ago
AVD Steering Design Release Engineer
General Motors LLC
Warren, MI
…organization (CAE, Vehicle Architecture, Cost Estimating, Performance Integration, Manufacturing, Service Engineering, other commodities (Body, HVAC, Powertrain, etc.) to creatively and…
Added 44 mins ago
Compartment Integration Design Engineer – 2D/3D Math and VR/MR
General Motors LLC
Warren, MI
General Motors is seeking a Compartment Integration Design Engineer (CIDE) to support General Arrangement / vehicle packaging, 3D part creation for physical buck development, and Virtual…
Added 44 mins ago
Senior Studio Design Quality Engineering
General Motors LLC
Warren, MI
The Studio Design Quality Engineer serves as the craftsmanship-quality representative for interior and exterior vehicle integration. This customer-facing surface integration role partners…
Added 45 mins ago
Senior AI Engineer, Forward Deployed Engineering
NVIDIA USA
CA
…our supply chain on Palantir Foundry and AIP. As a Senior AI Engineer and Forward Deployed Engineer, you will work directly with planners and supply-chain experts to turn their decision…
Added 49 mins ago
Instrumentation & Control Systems Engineer
Fortera Corporation
San Jose, CA
The Controls System Engineer will contribute to successful design and operation of control system hardware and software for all Fortera processes including mineral grinding, kiln…

CURIA

Validation Engineer IV

Albuquerque, NM, United States

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Job details

Posting language: English
Posted: Nov 2, 2026

Original job description

Validation Engineer IV (NPI) in Albuquerque, NM Build your future at Curia, where our work has the power to save lives 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!

As a member of the NPI Tech Transfer Team, this position is responsible for supporting New Product Introduction (NPI) and technology transfer activities within their assigned functional area (e.g., Quality, Technical Operations, Validation, Microbiology, Analytical Sciences, Manufacturing, etc.). This role serves as the primary Subject Matter Expert (SME) for the functional area throughout the NPI lifecycle, providing technical leadership, risk assessment, planning, execution support, and operational readiness to ensure successful transfer and efficient commercialization of new products. Working as a core member of the NPI Tech Transfer Team, the SME collaborates closely with Program Management, Operations, Quality, Regulatory, as a member of the customer-facing team, working to drive project execution through Tech Transfer stage gates, facilitate knowledge transfer, identify and mitigate risks, and ensure compliance with site procedures, regulatory requirements, and customer expectations. The position is dedicated to NPI activities and serves as the functional customer-facing point of contact for multiple concurrent tech transfer programs.

The Validation Engineer IV is a senior-level professional responsible for leading the development, review, and execution of complex validation protocols supporting manufacturing, quality, and regulatory compliance. This role provides advanced technical expertise and strategic guidance on equipment, process, system, and computer system validations in accordance with cGMP, FDA regulations, and industry standards such as GAMP. The Validation Engineer IV leads cross-functional validation projects, coordinates validation activities across multiple departments, and ensures seamless integration with production and quality timelines. This role authors and approves comprehensive validation master plans, protocols, and technical reports while driving continuous improvement initiatives to optimize validation processes. Additionally, the Validation Engineer IV mentor’s junior validation staff, supports regulatory inspections and audits, manages validation-related investigations and deviations, and collaborates with external vendors and regulatory bodies. This position plays a key role in shaping validation strategies and ensuring organizational readiness for new product introductions and regulatory submissions. The role also includes providing technical support for new product introductions, equipment, re-qualification schedules, and ensuring plant readiness post-shutdowns.

Essential Duties and Responsibilities:

Act as the designated functional SME for all assigned NPI and technology transfer projects.
Participate in cross-functional Tech Transfer teams from project initiation through commercial launch.
Lead discipline-specific assessments, gap analyses, risk evaluations, and readiness reviews.
Support development and execution of project plans, timelines, and deliverables required for Tech Transfer stage gates.
Provide technical expertise during customer meetings, technical discussions, audits, and governance reviews.
Partner with Program Managers to identify project risks, mitigation plans, and escalation pathways.
Ensure functional deliverables, documentation, and approvals are completed in accordance with established procedures and project timelines.
Drive operational readiness activities necessary to support development, validation, and commercial manufacturing.
Support knowledge transfer activities between sending and receiving organizations, ensuring effective and efficient transfer of process, product, analytical, and operational knowledge.
Participate in Technical Review Boards (TRBs), stage gate reviews, and leadership governance meetings.
Collaborate with cross-functional departments to resolve technical challenges and remove execution barriers.
Contribute to continuous improvement of NPI and Tech Transfer processes, tools, templates, and best practices.
Lead the development, execution, and review of complex validation protocols, including computer system validation, manufacturing equipment qualification, packaging equipment validation, and lyophilizer qualification.
Provide technical leadership for qualification and validation activities such as new product introductions, sterilization systems, computerized systems, cleaning validation, manufacturing / packaging equipment, cleanrooms, aseptic processing operations and critical utilities (water for injection / clean steam).
Provide technical leadership for qualification and validation activities such as new product introductions, sterilization systems, computerized systems, cleaning validation, manufacturing / packaging equipment, cleanrooms, aseptic processing operations and critical utilities (water for injection / clean steam).
Author, maintain, and approve comprehensive validation master plans ensuring full compliance with regulatory requirements and industry standards such as FDA, cGMP, GAMP, and EU GMP Annex 11.
Oversee and conduct validation testing activities, analyze data for accuracy, reliability, and compliance, and prepare detailed final reports with recommendations for adjustments or corrective actions.
Lead cross-functional collaboration to coordinate and integrate validation activities with production and quality teams, ensuring projects meet timelines with minimal disruption.
Provide expert technical guidance and mentorship on new equipment installations, system modifications, and validation best practices to junior and mid-level validation staff.
Manage relationships with external vendors and consultants to support validation projects and ensure adherence to quality and compliance standards.
Support regulatory inspections and audits by preparing documentation, responding to inquiries, and addressing validation-related observations.
Develop and deliver technical training and support to personnel on validation methodologies, regulatory expectations, and quality standards.
Participate in special projects and perform additional duties as assigned by management to support departmental goals and organizational objectives.
Read/interpret SOPs to ensure compliance
Maintain up to date trainings
Other duties as assigned

Education and Experience:

Bachelor’s degree in science, Engineering, or relevant field with a minimum of eight (8) years relevant experience of pharmaceutical validation in an aseptic/sterile product environment OR
Master’s degree in science, Engineering, or relevant field with six (6) years relevant experience of pharmaceutical validation in an aseptic/sterile product environment
Experience with validation tools and processes, including temperature mapping and use of Kaye Validator / Ellab Loggers etc.
Experience with FDA and EU regulations for pharmaceuticals and validation requirements, preferred
Knowledge of regulatory requirements, including FDA regulations, ISO 9000-3, PIC/S guidelines for cGMP, and GAMP 4 and 5 based on the GAMP V-Model Framework, as well as EU GMP Annex 11 for computer systems compliance

Supervisory Responsibilities:

This role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.

Other Skills and Abilities:

Provides guidance and mentorship to team members
Fosters a collaborative and positive work environment
Champions change
Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
Demonstrates strong attention to detail
Proficiency in advanced mathematics (e.g., calculus) and technical writing

Other Qualifications:

Must pass a background check Must pass a drug screen May be required to pass Occupational Health Screening Must obtain and maintain gowning certification May be required to obtain and maintain media qualification May be required to wear a respirator 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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