Jobs in the United States

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Added 1 min ago
Software Engineer, Assistant Vice President
MUFG Bank, Ltd.
Jersey City, NJ
This role involves contributing to the architecture, design, development, integration, and modernization of enterprise systems across various Transaction Banking initiatives. The successful…
Added 1 min ago
Associate Director, Injectable Drug Product Technology Transfer
AstraZeneca
New Haven, CT · New Haven
Lead cross-functional teams in the design, execution, and oversight of injectable drug product technology transfers to internal and external GMP manufacturing sites.
Added 1 min ago
O
Lead Principal Application Software Engineer- Forward Deployed Engineer
Oracle
Oklahoma City, OK
- $104,600 to $264,100 USD / year
Oracle Customer Success Services (CSS) is seeking a Senior Principal Forward Deployed Engineer to lead the delivery of strategic AI and data transformation programs for Oracle's largest…
Added 1 min ago
Specialist, Product Management (MTSS)
Pearson
Oklahoma City, OK
…builds assessment experiences that help schools put multi-tiered systems of support (MTSS) into…
Added 1 min ago
Lead Product Owner - Edge
Lumen
Oklahoma City, OK
Lumen is seeking a highly experienced Lead Technical Product Owner to own the vision, roadmap, and prioritized backlog for strategic Edge Fabric and Edge Infrastructure capabilities across…
Added 1 min ago
Lead Product Manager, Value realization
Humana
Oklahoma City, OK
To help deliver on this mission, we are seeking an experienced Lead Product Manager to own the strategy and delivery of the measurement and reporting product for Next Best Action (NBA).…
Added 1 min ago
Lead Product Manager, Next Best Action Use Case Management
Humana
Oklahoma City, OK
To help deliver on this mission, we are seeking an experienced Lead Product Manager to own the end-to-end product for Next Best Action (NBA). This is a “builder” role responsible for…
Added 1 min ago
HI
HVAC Tech II
Hospira, Inc.
NC
- $28.76 to $47.93 USD / hour
…improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to…
Added 1 min ago
PI
Medical Analytics Impact & Outcomes Data Analyst
Pfizer Inc
NY · MA · CT · PA
- $124,400 to $207,400 USD / year
Oversee data systems holding in close collaboration with data mgmt. lead and ensure appropriate collection, storage, and processing of data within team
Added 1 min ago
PI
Sr. Associate - Solutions Engineer
Pfizer Inc
NY · PA
- $79,400 to $132,400 USD / year
Design, build, configure, integrate, extend, test, and maintain responsive web, mobile, application, and internal productivity solutions.
Added 1 min ago
Q3-NAMORC-Anaplan-LCON-Capital Group-Irvine CA
Infosys
United States
In the assigned Job Role of Package Project Lead 1, your Area Of Responsibility will be as below:
Added 3 mins ago
Team Lead
EssilorLuxottica Group
Newport Beach, CA
The Team Lead creates exceptional value in the lives of customers & patients by delivering exceptional customer service. Ensures customers & patients are always delighted. Assists in the…
Added 3 mins ago
Licensed Optician - Team Lead
EssilorLuxottica Group
Raleigh, NC
The Licensed Team Lead creates exceptional value in the lives of customers & patients by delivering exceptional customer service. Ensures customers & patients are always delighted. Assists…
Added 3 mins ago
Director, M&A Separation & Carve-Out Execution
Stefanini Group
Deerfield, IL
Lead operational separation planning for divestitures, carve-outs, asset sales and other portfolio transactions from pre-sign through close and post-close.
Added 3 mins ago
JC
Senior Project Manager
JRM Construction Management, LLC
Los Angeles, CA · Costa Mesa, CA
- $200,000 to $225,000 USD / year
Serve as the primary point of accountability for the overall success of assigned projects, acting as the lead liaison between the client, design team, consultants, and subcontractors from…
Added 3 mins ago
Sr. Process Engineer, HRG Engineering Research
Asphalt Materials, Inc.
Indianapolis, IN
Required Bachelor's Degree - Lead process engineering projects, including feasibility studies and remedial designs.- Design and optimize manufacturing processes to enhance efficiency and…
Added 3 mins ago
Product Strategy Sr Manager
ServiceNow
San Diego, CA
…execution at scale. You will partner across product, engineering, design, customer operations, and communications to turn complex inputs into aligned plans, decision-ready insights, and…
Added 3 mins ago
Engineering Manager – Design & Configuration
Jabil Inc.
Austin, TX
Jabil is seeking a collaborative and technically experienced Engineering Manager – Design & Configuration to lead a multidisciplinary team supporting the design, release, configuration and…
Added 4 mins ago
Senior Data Scientist - Enterprise Credit
Bank of America, National Association
United States
Ability to lead and influence stakeholders across multiple levels and organizations, aligning technical teams and business stakeholders to deliver actionable insights.
Added 4 mins ago
Infrastructure Engineer
Default - MMO
Cleveland, OH · Dublin, OH
…(including off hours on-call support). He/she will also assist with design and implementation of new technologies to replace legacy systems and…
Added 4 mins ago
Project Engineer IV
TRC Companies, Inc.
San Francisco, CA
TRC, Member of WSP, is a global consulting environmental and engineering firm and one of the top design firms in the energy sector. Together, TRC and WSP’s 83,000 experts create positive,…
Added 5 mins ago
S
Senior RF Communications Engineer
Secmation
Huntsville, AL
- $140,000 to $225,000 USD / year
…and RF sensing technologies while contributing directly to systems from design through integration, testing, and field…
Added 5 mins ago
Global Vice President, HR Business Partnering
Clinigen
Remote, United States
Lead organization design, strategic workforce planning and organizational effectiveness initiatives.
Added 5 mins ago
Director, Organizational Effectiveness & Culture Transformation
Clinigen
Remote, United States
Design and lead leadership sessions that move teams from discussion to clear decisions, accountable owners and committed action.
Added 5 mins ago
Human Factors Engineer II
Nemera
Chicago, IL
…of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices,…

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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