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Added 2 mins ago
Distinguished Hardware Engineer
Cisco Systems, Inc.
San Jose, CA
Advanced Packaging: Architect next Generation 2.5D/3D heterogeneous integration strategies, resolving complex thermal, power, delivery, and signal integrity challenges for large sale AI and…
Added 8 mins ago
Process Engineer, Gold-To-Gold Interconnect & Flip Chip Assembly (Starlink/Akoustis)
SpaceX
Bastrop, TX
We are looking for a hands-on Process Engineer to develop, optimize, qualify, and implement advanced IC assembly processes, with a focus on Gold-to-Gold Interconnect (GGI) and thermosonic…
Added 10 mins ago
Control Systems Engineer (Instrumentation & Controls)
HDR
Folsom, CA · Walnut Creek, CA
…environment. This isn’t just a job, it’s a chance to lead innovation, engineer impact, and build a legacy of…
Added 22 mins ago
Advanced Package Development Engineer
Apple
CA
- Define specs, drive process windows, and establish advanced packaging solutions (2.5D/3D, hybrid bonding, high-density wafer-level interconnects).
Added 23 mins ago
Control Systems Engineer (Instrumentation & Controls)
HDR
Folsom, CA · Walnut Creek, CA
…environment. This isn’t just a job, it’s a chance to lead innovation, engineer impact, and build a legacy of…
Added 23 mins ago
Epitaxy/CVD Process Development Engineer (SM1)
Texas Instruments
Sherman, TX
…precision: adding exactly the right material, at exactly the right process parameters, without disturbing localized films and area. At SMFAB in Sherman, these processes don’t yet exist in…
Added 24 mins ago
Control Systems Engineer (Instrumentation & Controls)
HDR
Folsom, CA · Walnut Creek, CA
…environment. This isn’t just a job, it’s a chance to lead innovation, engineer impact, and build a legacy of…
Added 33 mins ago
F
Build Your Robotics Career. Explore the Country as a Robotics Field Service Engineer or Technician
Formic
United States
- $25 to $32 USD / hour
…experienced technician ready for bigger challenges or an accomplished engineer looking for your next chapter, you'll work with cutting-edge robotics, solve meaningful technical problems,…
Added 43 mins ago
Application Engineer IV (E4)
Applied Materials, Inc
Santa Clara, CA
Minimum 3+ years of proven industry experience in wafer inspection, or advanced packaging process, with demonstrated hands-on experience supporting manufacturing and customer applications.
Added 55 mins ago
R
Staff Electronic Design Engineer
Rivian
Palo Alto, CA
- $186,000 to $232,000 USD / year
Added 1 hour ago
Application Engineer IV (E4)
Applied Materials
Santa Clara, CA · Santa Clara
Minimum 3+ years of proven industry experience in wafer inspection, or advanced packaging process, with demonstrated hands-on experience supporting manufacturing and customer applications.
Added 1 hour ago
Distinguished Hardware Engineer
Cisco
San Jose, CA
Advanced Packaging: Architect next Generation 2.5D/3D heterogeneous integration strategies, resolving complex thermal, power, delivery, and signal integrity challenges for large sale AI and…
Added 1 hour ago
KC
Computational Physics Algorithm Engineer
KLA Corporation
Milpitas, CA
- $136,300 to $231,700 USD / year
…and memory chips, specialty semiconductors, wafers, reticles, advanced packaging, process equipment and materials. We also develop technologies for specialty processes, IC substrates, and…
Added 1 hour ago
Software Engineering Intern
KLA Corporation
Austin, TX
…and memory chips, specialty semiconductors, wafers, reticles, advanced packaging, process equipment and materials. We also develop technologies for specialty processes, IC substrates, and…
Added 1 hour ago
KC
Software Engineer
KLA Corporation
Milpitas, CA
- $114,800 to $195,200 USD / year
…and memory chips, specialty semiconductors, wafers, reticles, advanced packaging, process equipment and materials. We also develop technologies for specialty processes, IC substrates, and…
Added 1 hour ago
IC
Senior Product Failure Analysis Engineer
Intel Corporation
OR
- $140,830 to $198,820 USD / year
Intel Foundry is building the future of semiconductor manufacturing by delivering process technology, advanced packaging, and manufacturing solutions for customers around the world. As a…
Added 2 hours ago
P
Senior Endpoint Engineer
Procom
Remote, United States
- $110,000 USD / year
Senior Endpoint Engineer: On behalf of our technology client, Procom is searching for a Senior Endpoint Engineer for a permanent role. This position is a remote position and the client is…
Added 2 hours ago
A
Application Engineer
Actalent
Greenville, SC
- $43.7 to $48.7 USD / hour
Job Title: Application Engineer Windows Virtual Desktop (VDI)Job DescriptionThis role serves as the primary technical owner of the Windows Virtual Desktop Infrastructure (VDI) for an…
Added 2 hours ago
Product Development Engineer
Pregis LLC
Grand Rapids, MI
We're Not Just in the Packaging Business–We're in the "Wow" Business
Added 2 hours ago
Externals Design Engineer Intern (Summer 2027) (Onsite)
RTX
United States
…analysis; oil and thermal management systems; engine externals packaging and architecture; and nacelles for both commercial and military engine models. Key technical disciplines include…
Added 2 hours ago
Manager, DRAM Product Planning
Samsung Semiconductor
San Jose, CA
Semiconductor Fundamentals: Familiarity with fab processes, semiconductor manufacturing, and advanced packaging.
Added 2 hours ago
SS
Production Operator, Module Operations
Silfab Solar
Fort Mill, SC
- Up to $18 USD / hour
Our state-of-the art facilities in the US and Canada engineer and design the latest generation of solar products and utilize advanced manufacturing technology to produce high-efficiency PV…
Added 2 hours ago
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Application Engineer
Actalent
Greenville, SC
- $43.7 to $48.7 USD / hour
Job Title: Application Engineer Windows Virtual Desktop (VDI)Job DescriptionThis role serves as the primary technical owner of the Windows Virtual Desktop Infrastructure (VDI) for an…
Added 2 hours ago
Validation Engineer IV
CURIA
Albuquerque, NM
The Validation Engineer IV is a senior-level professional responsible for leading the development, review, and execution of complex validation protocols supporting manufacturing, quality,…
Added 3 hours ago
PAS - Microsoft 365 AI Solution Architect- Consulting - Senior - Multiple Locations
EY
Sacramento, CA · Jericho, NY · Oklahoma City, OK · San Antonio, TX · Stamford, CT · Indianapolis, IN · Denver, CO · Salt Lake City, UT · Irvine, CA · Hartford, CT · Boca Raton, FL · Phoenix, AZ · Charlotte, NC · Chattanooga, TN · Southfield, MI · Charleston, WV · Detroit, MI · Tucson, AZ · Cleveland, OH · Las Vegas, NV · Raleigh, NC · Wichita, KS · Baltimore, MD · Rochester, NY · Milwaukee, WI · Pittsburgh, PA · Rogers, AR · Secaucus, NJ · Grandview Heights, OH · Nashville, TN · Hoboken, NJ · St. Louis, MO · Orlando, FL · Akron, OH · Westlake Village, CA · San Francisco, CA · New Brunswick, NJ · Birmingham, AL · Toledo, OH · Iselin, NJ · Greenville, SC · Seattle, WA · Cincinnati, OH · Minneapolis, MN · New Orleans, LA · Buffalo, NY · Arlington, VA · Memphis, TN · Portland, OR · Los Angeles, CA · Houston, TX · Philadelphia, PA · Providence, RI · Dallas, TX · Grand Rapids, MI · San Jose, CA · Baton Rouge, LA · Albany, NY · Louisville, KY · New York, NY · Jacksonville, FL · Tulsa, OK · Miami, FL · Austin, TX · Chantilly, VA · Palo Alto, CA · Alpharetta, GA · San Diego, CA · San Mateo, CA · Tallahassee, FL · Atlanta, GA · Washington, DC · McLean, VA · Huntsville, AL · Des Moines, IA · Kansas City, MO · Fort Worth, TX · Richmond, VA · Boston, MA · Tampa, FL · Chicago, IL
As an M365 SharePoint Engineer, you will have in-depth knowledge of Microsoft Dynamics 365 Finance and Supply Chain Management which enable you lead and participate in enterprise solution…

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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