Jobs in the United States

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Added 18 mins ago
Process Engineer
Roche
Branchburg, NJ
As the Process Engineer, you will ensure robust automation, clean utility, and manufacturing processes by providing technical support to multiple Reagent Manufacturing laboratories and Site…
Added 40 mins ago
UX/UI Design Engineer (5816)
SMX
United States
SMX is seeking a creative and technically skilled UX/UI Design Engineer to join our innovative Solutions team. The successful candidate will design and build intuitive user experiences for…
Added 3 hours ago
Process Engineer
Roche Molecular Systems, Inc.
United States
As the Process Engineer, you will ensure robust automation, clean utility, and manufacturing processes by providing technical support to multiple Reagent Manufacturing laboratories and Site…
Added 4 hours ago
INGENYX - Quality Engineer 3 (Hybrid)
Teleflex
Trenton, GA
…include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and…
Added 6 hours ago
A
Validation Engineer
Actalent
Clayton, NC
- $60 to $90 USD / hour
Job Title: Validation EngineerJob DescriptionThe Validation Engineer leads validation activities for assigned projects across the full lifecycle, from requirements definition through…
Added 13 hours ago
Senior Machine Learning Engineer
Treasure AI
Remote, United States
● Experience in applying scientific method: hypothesis formulation and testing, exploratory
Added 15 hours ago
S
R&D Project Engineer
SprintRay
Huntington Beach
- $80,000 to $95,000 USD / year
The R&D Project Engineer is a hybrid role that combines program leadership with hands-on laboratory work. Approximately half of the role (~50%) is dedicated to planning and driving…
Added 1 day ago
C
Process Engineering Assistant (Intern)
Catalent
San Diego, CA
- $20 USD / hour
Assist in experimentation and development activities under the supervision of a full-time pharmaceutical process engineer or chemist.
Added 1 day ago
EI
Senior Engineer, Materials Quality Engineering
Entegris, Inc.
Colorado Springs, CO
- $31,533 USD / year
Drive supplier performance improvement, including corrective actions, audits, process capability reviews, andpolymerizationprocess/formulation assessments (raw material handling,…
Added 2 days ago
J
IT DevOps Engineer
Jobot
Montebello, CA
- $80,000 to $95,000 USD / year
If you are an IT DevOps Engineer and want to join a growing, tech-savvy E-Commerce company with a dynamic team then apply now!
Added 2 days ago
Manager, Materials Process Engineer
L3Harris
Camden, AR
Job Title: Manager, Materials Process Engineering
Added 2 days ago
PA
Industrial Engineer (Job Code: 176007)
Piston Automotive LLC
North Kansas City, MO
- $87,116 USD / year
Responsible for the supervision, formulation, administration and coordination of industrial engineering policies designed to improve operating performance, reduce waste and delays and…
Added 2 days ago
Supervisory Healthcare Engineer (Deputy)
Veterans Affairs, Veterans Health Administration
Long Beach, CA
Added 2 days ago
Senior Data Engineer
Walmart
BENTONVILLE, AR
…of current data science and analytics trends. Tech. Problem Formulation: Translates/co-owns business problems within one's discipline to data related or mathematical solutions. Identifies…
Added 2 days ago
Senior Materials Engineer
US0767 Prysmian Cables and Systems Usa LLC
Indianapolis, IN
…in a manufacturing or industrial R&D environment, including formulation optimization, compounding, and process…
Added 2 days ago
Engineer I-III (SCADA Engineer)
TXNM Energy
Albuquerque, NM
The position will be filled at the Engineer I, II, or III level based on the selected candidate¿s qualifications and experience. Assignments, independence, and technical responsibility will…
Added 2 days ago
Engineer I-III (OMS Analyst)
TXNM Energy
Albuquerque, NM
The position will be filled at the Engineer I, II, or III level based on the selected candidate¿s qualifications and experience. Assignments, independence, and technical responsibility will…
Added 2 days ago
Senior Decision Intelligence Engineer
Humana
Boston, MA
The Senior Machine Learning Engineer, Decision Intelligence is a hands-on individual contributor responsible for building, deploying, and operating ML and decisioning pipelines for the NBA…
Added 2 days ago
Senior Principal Engineer, Late Stage LNP Process Development
Lilly
Boston, MA
We are seeking an experienced LNP Process Development Engineer to join the Late Stage LNP Process Development team within Verve. You will be joining a team that is focused on the…
Added 2 days ago
Senior R&D Materials Engineer
US0767 Prysmian Cables and Systems Usa LLC
Taunton, MA
We are seeking an R&D Materials Senior Engineer to lead specialty compound development and formulation at our Taunton, MA site. This is a highly hands‑on, formulation‑focused role-not a…
Added 2 days ago
Senior Decision Intelligence Engineer
Humana
Cheyenne, WY
The Senior Machine Learning Engineer, Decision Intelligence is a hands-on individual contributor responsible for building, deploying, and operating ML and decisioning pipelines for the NBA…
Added 2 days ago
Senior Decision Intelligence Engineer
Humana
Providence, RI
The Senior Machine Learning Engineer, Decision Intelligence is a hands-on individual contributor responsible for building, deploying, and operating ML and decisioning pipelines for the NBA…
Added 2 days ago
Senior Decision Intelligence Engineer
Humana
Frankfort, KY
The Senior Machine Learning Engineer, Decision Intelligence is a hands-on individual contributor responsible for building, deploying, and operating ML and decisioning pipelines for the NBA…
Added 2 days ago
Senior Decision Intelligence Engineer
Humana
Bismarck, ND
The Senior Machine Learning Engineer, Decision Intelligence is a hands-on individual contributor responsible for building, deploying, and operating ML and decisioning pipelines for the NBA…
Added 2 days ago
Process Engineer/Senior Process Engineer
Kymanox
Morrisville, NC
The Process Engineer / Senior Process Engineer will join our Technical Services team as a full-time Drug Product/Fill Finish Subject Matter Expert (SME), serving as a Functional Lead and…

Actalent

Validation Engineer

Clayton, NC, United States

$60 to $90 USD / hour

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Job details

Pay: $60 to $90 USD / hour
Posting language: English
Posted: Nov 2, 2026

Original job description

Job Title: Validation EngineerJob DescriptionThe Validation Engineer leads validation activities for assigned projects across the full lifecycle, from requirements definition through decommissioning. This role develops and maintains comprehensive validation documentation, drives protocol authoring and execution, and ensures systems, equipment, and processes comply with applicable regulatory and internal quality standards. The position is fully on-site and offers the opportunity to contribute directly to the manufacture of therapies that improve patient lives, while gaining career-defining experience in a complex, high-performing pharmaceutical environment.

Responsibilities

Lead the validation effort for assigned projects, serving as the primary owner of validation activities from initial requirements through decommissioning.
Develop, revise, and maintain validation documentation in accordance with established procedures, including validation plans and reports, specifications, risk assessments, traceability matrices, and decommissioning plans and reports.
Author, execute, and generate reports for Design Review/Qualification, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Validation activities, as required for each project.
Support commissioning and qualification activities to ensure systems, equipment, and processes are ready for validation execution.
Attend Factory Acceptance Testing (FAT) and other project-related testing events as needed to support validation and qualification activities.
Track all validation documentation associated with assigned projects, ensuring timely completion, accuracy, and proper approvals.
Provide routine project status updates, including progress, risks, and issues, and escalate concerns to project managers when necessary.
Identify, investigate, and document deviations or engineering changes encountered during validation activities, ensuring appropriate follow-up and resolution.
Initiate, author, and support Change Controls, including assessing validation impact for proposed changes and ensuring alignment with quality and regulatory expectations.
Utilize approved electronic systems, such as TIMS (HP ALM) and VeeVa (QualityDocs, VaultQuality), to create, revise, route, and approve validation and change control records.
Ensure all validation deliverables comply with applicable Good Manufacturing Practice (GMP) requirements, FDA regulations, EU Annex 15 guidance, and internal procedures.
Collaborate closely with engineers, validation specialists, quality professionals, and manufacturing teams to support cross-functional project execution and continuous improvement.
Contribute to the upgrade of an existing manufacturing facility by supporting validation activities for equipment, utilities, and processes within the established operation.

Essential Skills

Demonstrated experience in validation within a GMP-regulated pharmaceutical or manufacturing environment.
Hands-on experience with validation of manufacturing equipment and process control systems.
Ability to develop, author, execute, and report on IQ, OQ, PQ, and Process Validation protocols.
Proficiency in creating and maintaining validation documentation, including validation plans, reports, specifications, risk assessments, and traceability matrices.
Experience identifying, documenting, and investigating deviations and engineering changes during validation activities.
Capability to initiate and support Change Controls, including assessing validation impact for proposed changes.
Familiarity with regulatory and guidance requirements such as GMP, FDA expectations, and EU Annex 15.
Ability to use electronic quality and validation systems such as TIMS (HP ALM) and VeeVa (QualityDocs, VaultQuality) for document and record management.
Strong organizational skills to track multiple validation deliverables and provide clear project status updates.
Effective communication skills to collaborate with cross-functional teams and present validation status, risks, and recommendations.

Additional Skills & Qualifications

Experience with aseptic formulation and filling equipment validation.
Background in validation of vision inspection systems used in pharmaceutical manufacturing.
Exposure to assembly processes and related equipment within a regulated manufacturing environment.
Interest in working on complex validation projects involving equipment qualification, utilities, process validation, cleaning validation, computerized systems validation, and commissioning support.
Motivation to contribute to meaningful work that directly supports the manufacture of therapies for patients worldwide.
Desire to work in an industry-leading environment focused on quality, operational excellence, and advanced manufacturing technologies.
Interest in collaborating with high-performing, cross-functional teams of engineers, validation specialists, quality professionals, and manufacturing leaders.
Ambition to build long-term career growth through exposure to future capital projects, operational readiness initiatives, and ongoing manufacturing expansion.

Work EnvironmentThis position is fully on-site at a pharmaceutical manufacturing facility in Clayton, North Carolina, five days per week. The role follows normal business hours, with the flexibility to work occasional overtime, evenings, and weekends, particularly during larger projects or plant shutdowns. The work takes place in an established, older facility undergoing upgrade rather than a new capital project, offering exposure to modernization efforts within an existing operation. The environment is highly regulated and quality-focused, with access to advanced manufacturing technologies and electronic quality systems such as TIMS (HP ALM) and VeeVa (QualityDocs, VaultQuality). You will work closely with experienced engineering, validation, quality, and manufacturing teams in a collaborative, professional setting that emphasizes technical excellence, continuous improvement, and a strong commitment to ensuring safe and reliable product supply. Job Type & LocationThis is a Contract position based out of Clayton, NC. Pay and BenefitsThe pay range for this position is $60.00 - $90.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Clayton, NC. Application DeadlineThis position is anticipated to close on Nov 16, 2026. Workplace TypeThis is a fully onsite position in Clayton,NC.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Documentation
Electronics
Good manufacturing practices
Process improvement
Control engineering
Organizational skills
Communication skills
Inspection
Pharmaceutical processes
Assembly
Cleaning
Apply advanced manufacturing
Quality control systems

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