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Validation Lead Jobs (NOW HIRING)

Compli

CSV Lead/ Computer System Validation Lead

Marietta, PA · On-site

$96K - $127K/yr

CSV Lead/ Computer System Validation Lead Location : Marietta, PA Compli, LLC was founded in 2001 to provide Commissioning, Validation and Regulatory Support Services to the Life Sciences industry.

JPI

Milestone & Validation Specialist

Coppell, TX · On-site

The position will report to the Milestone-Validation Lead. Essential Functions & Responsibilities Responsible for Overseas validation of Open space captures, and drone deploy captures * Ensure Open ...

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How much do validation lead jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for validation lead in the United States is $28.64, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $34.62 per hour, depending on experience, location, and employer.

What are Validation Leads?

Validation Leads are professionals responsible for overseeing and managing the validation process in industries such as pharmaceuticals, biotechnology, and manufacturing. They ensure that systems, equipment, and processes meet regulatory standards and function as intended. Their duties include planning validation activities, coordinating with cross-functional teams, reviewing documentation, and troubleshooting issues during validation. Validation Leads also play a key role in maintaining compliance with industry regulations and ensuring product quality and safety.

What are the typical challenges a Validation Lead faces when coordinating cross-functional teams during validation projects?

As a Validation Lead, one common challenge is ensuring effective communication and alignment among cross-functional teams such as quality assurance, engineering, production, and regulatory affairs. Each team may have different priorities and perspectives, which can create delays or misunderstandings if not managed proactively. Successful Validation Leads facilitate regular meetings, clarify project goals, and address issues promptly to keep validation activities on track. Being adaptable and fostering collaboration are key to overcoming these challenges and delivering compliant, on-time results.

What is the difference between Validation Lead vs Validation Specialist?

AspectValidation LeadValidation Specialist
CredentialsTypically requires a degree in life sciences or engineering, with experience in validation processesSimilar credentials, often with less managerial experience
Work EnvironmentLeads validation projects, manages teams, and oversees validation activitiesPerforms validation tasks, executes protocols, and documents results
Industry UsageCommonly found in pharmaceutical, biotech, and medical device industriesUsed across similar industries, often reporting to Validation Leads

The Validation Lead is responsible for overseeing validation projects and managing teams, while the Validation Specialist executes validation tasks and documents results. Both roles require similar credentials and are integral to quality assurance in regulated industries. The Lead has a broader scope, including project management, whereas the Specialist focuses on technical validation activities.

What are the key skills and qualifications needed to thrive as a Validation Lead, and why are they important?

To thrive as a Validation Lead, you need expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and a background in science or engineering, often supported by a relevant degree. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and standards like GAMP 5 is typically required. Strong leadership, attention to detail, and effective communication help coordinate cross-functional teams and ensure documentation accuracy. These skills are crucial for maintaining product quality, meeting regulatory standards, and ensuring successful project delivery in regulated industries.
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Validation Lead jobs near you
Infographic showing various Validation Lead job openings in the United States as of May 2026, with employment types broken down into 97% Full Time, and 3% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $59,575 per year, or $28.6 per hour.
CSV Lead/ Computer System Validation Lead

CSV Lead/ Computer System Validation Lead

GBA Companies

Philadelphia, PA • On-site

$103K - $136K/yr

Other

Posted 29 days ago

Job description

Job: CSV Lead/ Computer System Validation Lead

Location: Marietta, PA

Compli, LLC was founded in 2001 to provide Commissioning, Validation and Regulatory Support Services to the Life Sciences industry.

We serve pharmaceutical companies across the United States, offering a vast array of services that assist companies with exceeding their goals and objectives. In todays world, its never been more important to understand regulations and quality assurance activities as they relate to operations, vendors, engineering, construction and contractors. In 2020, Compli, LLC became a wholly owned subsidiary of George Butler Associates, Inc. This acquisition allowed Compli, LLC to become part of an integrated network of services where clients have more options to engage an impressive suite of in-house services.

What You'll Do:
  • Supporting Validation of Computer systems in support of a newly constructed drug manufacturing facility.
  • Position will serve a key role in delivery to accommodate the exit of the existing facility.
  • Lead the development and execution of CSV documents
  • Provide project / process engineering support for capital project delivery projects.
  • Ensure planned progress with respect to the engineering deliverables for projects, process engineering planning & scheduling, preparation of progress reports, manpower & resource forecasts, and utilize resources effectively & efficiently.
  • Provide process design & detailed engineering including performing process simulations, design calculations, process optimization, sizing & selection of equipment for projects.
  • Prepare various engineering deliverables (drawings & documents) such as process flow diagrams, P & I diagram, process datasheets, equipment specifications, cause & effect diagrams, control philosophies, shutdown philosophies, and HAZOP studies & reports.
  • Facilitates and executes engineering change control documentation.
  • Provide the necessary process engineering inputs for capex projects to the other disciplines and other departments.
  • Prepare and issue RFIs, evaluate vendors quotations, clarifications, and perform technical bid analysis. Review vendors documents, drawings, datasheets, specifications and calculations.
  • Supports construction and trade groups with site safety programs and assist in safety documentation.
  • Other duties as assigned.
What You'll Bring:
  • BS in related engineering field (Chemical / Mechanical / Architectural / Electrical) (required).
  • 10 to 15 years of experience in support of project or production, processes and process optimization (required) // process engineering including process design (if possible).
  • Prepare process engineering deliverables for investment projects (e.g., PFDs, Equipment Specifications), experience is preferred but not required.
  • Act in assigned roles within capital investment projects (e.g., Project /Process Engineer), experience is preferred but not required
  • Kneat experience preferred.
  • Prior experience in a pharmaceutical / biotech manufacturing environment
  • Prior experience with Current Good Manufacturing Practices and other applicable regulations
  • Excellent client-facing relationship building skills.
  • Excellent written and verbal communication skills.
  • Excellent math and problem-solving skills.
  • Ability to work independently or in collaboration with others.
  • Solid organizational skills including attention to detail and multitasking skills.
  • Proficient in MS Excel, MS Word, MS Project, MS PowerPoint, MS Access

Travel: Local to the Marietta, PA Metropolitan area. No per diem or travel assistance currently offered.

*This role is not open to C2C staffing.

Its more than just a job

At Compli, we are about innovative and intelligent people who want to solve problems. Were known for our technical excellence, but we bring so much more to the table. We strive to create remarkable solutions for a higher quality of life. And we are changing the industry by integrating the design and construction process with use of new technology.

At Compli, we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law.

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