Jobs in the United States

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Project Manager 2
Fort Mill, SC
…teams for the purpose of delivering safe, cost-effective, and quality execution of small to medium scale electric substation, transmission, distribution and communications projects and/or…
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Advanced Product Quality Engineer
USA 3M Company
MN
As an Advanced Product Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here,…
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Maintenance Supervisor (Tonawanda, NY)
USA 3M Company
NY
As a Manufacturing Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact…
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Reliability Engineer
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Collegedale, TN
…products, and Drake’s Cakes®, McKee Foods Corporation is seeking an engineer to join our Plant Engineering team as a Reliability Engineer. This position will support a broad range of…
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Electrical Test Technician LV 1
INTERMOUNTAIN ELECTRONICS INC
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Construction Quality Engineer - CSLA (Data Centers)
Legacy Professional Services
Lebanon, IN
Legacy Professional Services is seeking a Construction Quality Engineer - CSLA to provide field-based quality assurance and quality control support for Civil, Structural, Landscape, and…
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Mechanical Engineer
Harmattan AI
Austin, Texas, TX
As a Mechanical Engineer on Harmattan AI’s Airframe team, you will design UAV platforms and subsystems in an autonomous, fast-paced environment. You will take ownership of projects from…
Added 1 min ago
Mechanical Engineer - Proliant Dairy Ingredients
Proliant Dairy Ingredients
St. Johns, MI
The Mechanical Engineer will apply engineering principles to design, improve, and develop facilities, equipment, machinery, testing systems, and manufacturing processes across Proliant…
Added 1 min ago
Technical Writer T3
CACI
Sterling, VA · Sarasota, FL · Sterling · Sarasota
Work closely with the Responsible Engineer for each project to complete the System Installation Standards technical volumes; this requires gathering detailed information from our…
Added 1 min ago
Senior Project Manager - Industrial Capital Projects
ITAC
Waco, TX
Ensure quality standards are met across all deliverables and services.
Added 1 min ago
Project Manager - Industrial Capital Projects
ITAC
Waco, TX
Ensure quality standards are met across all deliverables and services.
Added 2 mins ago
Industrial Engineering Lead - Toledo, OH
Military Spouse Jobs & VetJobs
United States
The main purpose of the Lead Industrial Engineer is to work to eliminate waste of time,
Added 2 mins ago
Systems Engineer - Oak Ridge, TN
Military Spouse Jobs & VetJobs
United States
Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting…
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Engineer (Hotel Maintenance)
AC Miami Wynwood
Miami, FL
Perform preventative and repair maintenance work to ensure the hotel is maintained according to established quality and sustainability standards while treating guests in a warm and friendly…
Added 3 mins ago
Chemical Coating Operator
Dayton Granger, Inc.
Fort Lauderdale, FL
…metal parts. You will follow work instructions, check parts for quality, and safely handle chemicals. The ideal candidate has experience working in manufacturing, handling industrial…
Added 3 mins ago
Product Design Engineer
Micro Matic
Brooksville, FL
Collaboration with Quality in identifying on the specification the critical characteristics/features that are essential to the function of the product.
Added 3 mins ago
Lead Software Engineer - Java/Microservices/AWS
JPMC page
Wilmington, DE
As a Lead Software Engineer - Java/Microservices/AWS at JPMorganChase within the Consumer and Community Banking team, you are an integral part of an agile team that works to enhance, build,…
Added 4 mins ago
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Senior Scientist I, Lentiviral Engineering & In Vitro Assay Development
AbbVie
South San Francisco, CA
- $96,500 to $183,500 USD / year
Design and engineer lentiviral vectors and fusion protein receptors, and oversee lentiviral production by leveraging internal capabilities and external CRO partnerships.
Added 4 mins ago
VP of Product
Leena AI
New York, NY
…and the ability to explain a wrong answer - not just model…
Added 4 mins ago
Packaging Engineer
QCS Staffing
Michigan
Packaging Engineer – Kalamazoo Michigan, US – Initial 12-Month Contract – Life Sciences Are you based in Kalamazoo, Michigan and looking for your next pharmaceutical contract role? Our…
Added 4 mins ago
Electrical Technician Senior
ROUSH
Allen Park, MI
…diagrams (P&ID). The role will follow procedures to set up and run quality checks on various wiring harnesses. The Electrical Technician Senior will mentor and oversee team member’s…
Added 5 mins ago
Engineering and Maintenance Manager
TerraPower LLC.
Kemmerer, WY
…partners closely with operations, Equipment Qualification, EHS, quality, and Natrium program teams to drive equipment reliability, configuration control, and continuous…
Added 5 mins ago
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Senior Software Engineer (Evergreen)
Vynca
IL · UT · NC · TX · AZ · FL · NV · CO · GA · CA · OR · WA
- $160,000 to $180,000 USD / year
At Vynca, our mission is to provide comprehensive care for more quality days at home.
Added 5 mins ago
R
Software Engineer, Comms Platform
Ramp
Remote, United States
- $172,000 to $280,000 USD / year
We're looking for a backend engineer to own a core part of that platform. You'll take responsibility for an area such as message delivery and channel integrations, communication…
Added 6 mins ago
Product Quality Engineer
US Conec, Ltd.
Fort Worth, TX
US Conec is seeking a detail-driven Product Quality Engineer to champion product excellence across the lifecycle of precision-engineered components and assemblies. In this role, you’ll…

Actalent

Validation Engineer

Baltimore, MD, United States

$55 to $65 USD / hour

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Job details

Pay: $55 to $65 USD / hour
Experience: Minimum of 5 years of experience in a biopharmaceutical or related environment in the area of system qualification or validation.
Posting language: English
Posted: Nov 9, 2026

Original job description

Job Title: Validation EngineerJob DescriptionThe Validation Engineer manages and prioritizes all phases of assigned validation projects from concept through performance qualification and ongoing support of cGMP operations. This role ensures cGMP regulatory compliance by adhering to site and corporate validation plans, policies, and procedures. The engineer contributes at a high level to Commissioning and Qualification as well as Computer Systems Validation, supporting complex biopharmaceutical manufacturing operations and driving continuous improvement in validation practices.Responsibilities

Manage and prioritize all phases of assigned validation projects from initial concept through performance qualification and ongoing support of cGMP operations.
Ensure cGMP regulatory compliance by following site and corporate validation plans, policies, procedures, and applicable GxP requirements.
Apply strong knowledge of validation and related practices, including governmental regulations associated with equipment, utility, and facility validations, as well as computer system validations.
Review and approve validation-related system lifecycle design documentation, including user requirements, functional specifications, design specifications, commissioning protocols, qualification protocols, protocol deviations, and validation reports.
Review data generated by validation personnel for temperature mapping studies and ensure the accuracy, completeness, and compliance of results.
Contribute subject matter expertise in Commissioning and Qualification (C&Q) activities, including IQ/OQ execution and documentation for equipment and utilities.
Lead or support Computer Systems Validation (CSV) and software validation efforts, ensuring systems such as DeltaV, LIMS, and MES meet regulatory and internal quality requirements.
Write, review, and execute validation protocols for equipment validation, process validation, and validation testing in a biopharmaceutical or biotech environment.
Support validation activities associated with manufacturing bulk drug substance in a single-use facility, ensuring systems and processes perform as intended.
Collaborate with cross-functional teams, including MSAT and bioprocessing groups, to improve processes and enhance validation strategies.
Effectively prioritize and coordinate multiple validation activities and projects at varying levels of complexity to meet program goals and timelines.
Use strong problem-solving and critical thinking skills to troubleshoot validation issues, propose solutions, and implement corrective and preventive actions.
Prepare clear, concise technical documentation and communicate validation findings and recommendations to stakeholders through verbal and written communication.
Utilize validation-specific software and Microsoft Office applications to manage documentation, track project progress, and maintain accurate records.
Maintain up-to-date knowledge of current validation best practices, industry standards, and regulatory expectations, and apply them to ongoing validation programs.

Essential Skills

Minimum of 5 years of experience in a biopharmaceutical or related environment in the area of system qualification or validation.
Bachelors degree (BS) in Engineering, Science, or Project/Program Management.
Experience validating equipment associated with manufacturing bulk drug substance in a single-use facility.
Strong knowledge of validation practices and governmental regulations associated with equipment, utility, and facility validations, as well as computer system validations.
Subject matter expertise in Commissioning and Qualification (C&Q) and Computer Systems Validation (CSV).
Proven ability to write and execute validation protocols for equipment validation, process validation, and validation testing.
Hands-on experience with cGMP operations and a solid understanding of GxP requirements.
Highly effective verbal and written communication skills for technical and cross-functional collaboration.
Demonstrated ability to effectively prioritize and coordinate multiple activities and projects.
Proficiency in Microsoft Office applications and validation-specific software programs.
Strong problem-solving and critical thinking skills with the ability to conduct technical programs and achieve program goals.
Strong organizational skills to handle and delegate multiple projects at differing levels of complexity.
Knowledge of current validation best practices and regulatory expectations in biopharmaceutical, pharmaceutical, biotech, and bioprocess environments.

Additional Skills & Qualifications

Experience in biotechnology, biologics, or biopharmaceutical manufacturing environments.
Experience in validation within CDMO or contract development and manufacturing settings.
Familiarity with process improvement initiatives in MSAT or related technical support functions.
Experience with IQ/OQ activities and documentation for equipment and utilities.
Experience in process validation and validation testing for bioprocess operations.
Experience with Computer Systems Validation (CSV) and software validation, including systems such as DeltaV, LIMS, and MES.
Exposure to or understanding of LIMS and MES systems in a regulated environment.
Comfort working across pharmaceutical, biotech, and related life sciences industries.
Ability to think and act both strategically and tactically in a fast-paced, growth-oriented environment.

Work EnvironmentThe role operates primarily on the manufacturing floor and in laboratory environments within a cGMP biopharmaceutical facility. You will work closely with manufacturing, MSAT, and quality teams in areas where bulk drug substance is produced using single-use technologies. The environment is highly regulated and safety-focused, with strict adherence to safety guidelines, procedures, and standard operating procedures. Work may involve time in cleanroom or controlled areas, around complex process equipment, utilities, and computer-based control systems such as DeltaV, LIMS, and MES. The culture emphasizes scientific excellence, collaboration, and innovation, with a strong focus on helping clients solve technical challenges, improve R&D productivity, and accelerate time to market while maintaining high standards of compliance and quality. Job Type & LocationThis is a Contract position based out of Baltimore, MD. Pay and BenefitsThe pay range for this position is $55.00 - $65.00/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 Baltimore, MD. Application DeadlineThis position is anticipated to close on Nov 23, 2026. Workplace TypeThis is a fully onsite position in Baltimore,MD.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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