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Added 1 min ago
Design Verification Engineer Intern (Summer 2027)
MIPS Holding Inc
TX
MIPS – A GlobalFoundries company is seeking a Design Verification Engineer Intern to join the CPU verification team in Plano, Texas. The intern will gain hands-on experience verifying…
Added 1 min ago
Design Verification Engineer (2027 New College Graduate)
MIPS Holding Inc
TX
MIPS – A GlobalFoundries company is seeking a Design Verification Engineer to join our CPU verification team. The successful candidate will work on verification of processor components,…
Added 5 mins ago
Lead DevOps Engineer St. Louis, USA
London Stock Exchange Group Holdings Inc
St. Loui, MO
…We are dedicated, open-access partners with a commitment to excellence in delivering the services our customers expect from us. With extensive experience, deep knowledge and worldwide…
Added 6 mins ago
Staff QA Engineer
DexCom Inc
San Diego, CA
You drive Quality Management System excellence by identifying systemic weaknesses and leading sustainable improvements to procedures, process controls, validation frameworks, FMEAs, and…
Added 14 mins ago
Senior Product Development Engineer
International Motors, LLC
San Antonio, TX
International Motors is seeking a Senior Product Development Engineer to play a critical role in supporting all stages of a product's lifecycle, including product development,…
Added 16 mins ago
Full Stack Java Developer
USA7 DXC Technology Services LLC
FORT WORTH, TX
…across their entire IT estate. Learn more about how we deliver excellence for our customers and colleagues at…
Added 26 mins ago
Quality Engineer
Conti Electric Inc
Sterling Heights, MI
high-quality products and solutions. We are committed to delivering excellence and innovation
Added 27 mins ago
*Engineering Lead Analyst - CONVERSION*
Citibank, N.A.
United States
…experience. We reimagine client and partner experiences to deliver excellence through secure, reliable, and efficient…
Added 28 mins ago
Site Reliability Engineer III
LexisNexis Risk Solutions Inc. Company
Alpharetta, GA · Boca Raton, FL
The Site Reliability Engineer III is responsible for improving the reliability, scalability, security and operational maturity of cloud-hosted platforms and services. The role combines…
Added 32 mins ago
Lead Process Engineer
Actalent
Springfield, VA
Job Title: Lead Process EngineerJob DescriptionThe Lead Process Engineer oversees the operations and team members of a new polymer facility, ensuring a smooth transition from the existing…
Added 32 mins ago
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Systems Engineer
Actalent
Saint Paul, MN
- $65 to $95 USD / hour
Job Title: Senior Systems Engineer Job DescriptionThe Senior Systems Engineer will provide technical leadership for the design, development, and optimization of advanced hypersonic test…
Added 34 mins ago
Industrial Engineer
Luminator Technology Group
Plano, TX
We’re searching for Industrial Engineer to join our team and play a key role in driving our vision forward. Join a team where your ideas drive results. As an Industrial Engineer, you will…
Added 37 mins ago
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Electronic Systems Engineer
Knorr-Bremse
Westminster, MD
- $89,900 to $134,900 USD / year
The Electronic Systems Engineer is responsible for the design and development of pneumatic and hydraulic brake systems controls, for passenger rail transit vehicles.
Added 38 mins ago
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Mid-Level Structural Engineer - Kiewit Power Engineering
Kiewit
Phoenix, AZ · Tempe, AZ · Detroit, MI · Raleigh, NC · Chattanooga, TN · Houston, TX · Richmond, VA · Lenexa, KS
- $95,000 to $100,000 USD / year
As a Structural Design Engineer, you will be a part of a growing team that supports all aspects of the construction process by performing innovative design engineering through brainstorming…
Added 41 mins ago
Product Quality Engineer
DuPont Electronic Materials International, LLC
Marlborough, MA
Qnity is seeking a Product Quality Engineer to join our ST-Litho Quality Team in Marlborough, MA. This role is focused on driving material quality excellence across key product lines while…
Added 43 mins ago
Operations Manager (Highways & Toll Roads)
CINTRA US SERVICES LLC
Austin, TX
Collaborative excellence: Work alongside talented professionals in a collaborative environment where your ideas and contributions are valued.
Added 43 mins ago
AP
Senior Automation Scientist/Engineer - Biologics Engineering
AstraZeneca Pharmaceuticals LP Company
Gaithersburg, MD
- $124,000 to $171,000 USD / year
…industry-leading biologics discovery platform that unites scientific excellence, automation, and digital…
Added 44 mins ago
JH
Senior Missile Performance & Flight Systems Engineer
Johns Hopkins Applied Physics Laboratory
Laurel, MD
- $100,000 USD / year
Are you an experienced aerospace engineer passionate about solving challenging problems in missile system design, performance analysis, and hypersonic flight?
Added 45 mins ago
Principal Engineer, Identity & Access Management (IAM) - Microsoft Entra ID
Boston Scientific
Arden Hills, MN
Boston Scientific is seeking a Principal Engineer, Identity & Access Management (IAM), specializing in Microsoft Entra ID and cloud identity to provide enterprise-level technical leadership…
Added 46 mins ago
Software Development Engineer, Amazon Customer Service
Amazon.com Services LLC
Austin, TX · Seattle, WA
- Tackle complex technical challenges, create innovative solutions with direct impact on customer trust, and work on systems critical to Amazon's operational excellence.
Added 46 mins ago
Software Development Engineer, Creative Advertiser Experience, CreativeX
Amazon.com Services LLC
Santa Monica, CA
…other employees, supervisors, and staff; adhere to standards of excellence despite stressful conditions; communicate effectively and respectfully with employees, supervisors, and staff to…
Added 46 mins ago
Lead ASIC Modem Design Engineer, Satellite Communication
Amazon Kuiper Manufacturing Enterprises LLC
Sunnyvale, CA · San Diego, CA
Lead ASIC Modem Design Engineer, Satellite Communication role within a high performance ASIC Modem design team. This team is using industry leading methodologies to develop proprietary…
Added 49 mins ago
Project Engineer - Mission Critical
Intermountain Electric Inc
Aurora, CO
Through strategic planning, collaboration, and technical excellence, and guided by our values of Integrity, Safety, Ingenuity, Relationships, Craftsmanship, and Spark, we empower our…
Added 49 mins ago
GVP, Enterprise Verticals Sales US (Manufacturing, Transportation & Energy)
ServiceNow
Vienna, VA
Operational Excellence: Implement best practices for sales operations, including territory planning, quota setting, sales process optimization, and CRM utilization. Ensure data-driven…
Added 49 mins ago
Distinguished Hardware Engineer
Cisco
San Jose, CA
Experience with technical leadership at the Fellow, Distinguished Engineer, or Chief Architect level, with multi-generation tapeout successes on cutting-edge process nodes (sub-5nm, 3nm,…

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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