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Contract Pipeline Inspector Jobs in Seattle, WA (NOW HIRING)

... pipeline projects, roadway upgrades, and heavy civil works projects. The construction manager ... contract documents and verifying quality and safety goals are met * Coordinates with inspection ...

Track Engineering Design Lead

Seattle, WA · On-site

$116K - $153K/yr

... contracts, and construction inspections to ensure compliance with FRA, FTA, CPUC, AREMA, and other ... Support long-term strategy, growth, and pipeline development for the transit and rail engineering ...

Track Engineering Design Lead

Seattle, WA · On-site

$174.50 - $259/hr

... contracts, and construction inspections to ensure compliance with FRA, FTA, CPUC, AREMA, and other ... Support long‑term strategy, growth, and pipeline development for the transit and rail engineering ...

Track Engineering Design Lead

Seattle, WA

$116K - $153K/yr

... contracts, and construction inspections to ensure compliance with FRA, FTA, CPUC, AREMA, and other ... Support longterm strategy, growth, and pipeline development for the transit and rail engineering ...

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Contract Pipeline Inspector information

See Seattle, WA salary details

$14

$31

$59

How much do contract pipeline inspector jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for contract pipeline inspector in Seattle, WA is $31.14, according to ZipRecruiter salary data. Most workers in this role earn between $21.06 and $35.82 per hour, depending on experience, location, and employer.

What is a contract pipeline inspector?

Contract Pipeline Inspectors are professionals hired on a contract basis to oversee the construction, maintenance, and safety of pipelines transporting oil, gas, or other substances. They are responsible for ensuring that pipeline projects comply with industry standards, government regulations, and safety protocols. Their duties include inspecting materials, monitoring construction activities, and documenting any issues or violations. Contract Pipeline Inspectors play a critical role in preventing leaks, ensuring environmental protection, and maintaining the integrity of pipeline systems.

What skills and qualifications are needed to be a contract pipeline inspector?

To thrive as a Contract Pipeline Inspector, you need expertise in pipeline construction standards, regulatory compliance, and inspection protocols, typically backed by relevant certifications such as API 1169 or NACE. Familiarity with inspection software, GPS mapping tools, and documentation systems is essential for accurate reporting and data management. Strong attention to detail, effective communication, and problem-solving skills help inspectors identify issues and collaborate with contractors. These skills ensure the safety, integrity, and regulatory compliance of pipeline projects, protecting both the environment and public safety.

What are common challenges faced by contract pipeline inspectors, and how can they be managed?

Contract Pipeline Inspectors often encounter challenges such as working in remote locations, adhering to strict safety regulations, and managing tight project deadlines. Effective communication with construction crews, project managers, and other inspectors is crucial for resolving issues quickly and maintaining compliance. Staying organized, keeping detailed records, and proactively identifying potential problems can help inspectors manage these challenges and ensure the integrity and safety of pipeline installations.

What is the difference between Contract Pipeline Inspector vs Pipeline Quality Control Inspector?

AspectContract Pipeline InspectorPipeline Quality Control Inspector
CertificationsOSHA, API certifications, safety trainingOSHA, API certifications, safety training
Work EnvironmentConstruction sites, field inspections, outdoor environmentsConstruction sites, field inspections, outdoor environments
Employer & Industry UsageOil & gas, pipeline construction companiesOil & gas, pipeline construction companies
Primary FocusInspecting contractual compliance and project progressEnsuring pipeline quality and adherence to standards

Both roles involve field inspections in pipeline projects and require similar certifications. However, Contract Pipeline Inspectors focus on contractual compliance and project progress, while Pipeline Quality Control Inspectors emphasize maintaining pipeline quality and standards. The roles often overlap but serve distinct aspects of pipeline project oversight.

How do I become a contract pipeline inspector?

To become a contract pipeline inspector, candidates typically need a high school diploma or equivalent, along with experience in pipeline construction, maintenance, or inspection. Certifications such as API 570 or API 653 are often required, and knowledge of safety protocols and inspection tools is essential. Some positions may also require a valid driver's license and the ability to work in various environmental conditions.

What are the most commonly searched types of Pipeline Inspector jobs in Seattle, WA?

The most popular types of Pipeline Inspector jobs in Seattle, WA are:

What are popular job titles related to Contract Pipeline Inspector jobs in Seattle, WA?

For Contract Pipeline Inspector jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Contract Pipeline Inspector jobs in Seattle, WA look for?

The top searched job categories for Contract Pipeline Inspector jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Contract Pipeline Inspector jobs?

Cities near Seattle, WA with the most Contract Pipeline Inspector job openings:

Infographic showing various Contract Pipeline Inspector job openings in Seattle, WA as of August 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $64,796 per year, or $31.2 per hour.

Senior Director of Life Science Business Development

Truveta

Seattle, WA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted yesterday


Job description

Senior Director of Life Science Business Development
Truveta is the world's first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta' s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values.
Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required at least once per year for an onsite meeting.
For overall team productivity, we optimize meeting hours in the pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT, however, ad hoc meetings occur between 8am-6pm Pacific time. #LI-remote
Who We Need
Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you.
This Opportunity
Truveta is seeking a Senior Director of Life Sciences Business Development to accelerate growth within the pharmaceutical and biotechnology sectors. Reporting to the Vice President of Life Sciences Sales, this is a player/coach leadership role responsible for both individual revenue generation and leading a team of business development professionals.
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations while also building, mentoring, and scaling high-performing sales teams.
This leader will carry an individual quota, directly manage a team of business development professionals, and serve as a trusted advisor to pharmaceutical, biotech, clinical development, epidemiology, HEOR, medical affairs, and data science stakeholders.
The successful candidate must be comfortable discussing complex scientific, clinical, and technical topics, including observational research, epidemiology, regulatory-grade evidence generation, AI/ML applications, healthcare data assets, and real-world data methodologies.
Responsibilities
Business Development & Revenue Leadership
    • Achieve and exceed individual revenue targets through direct management of strategic pharmaceutical and biotechnology accounts.
    • Develop executive-level relationships with key stakeholders across clinical development, medical affairs, HEOR, epidemiology, market access, commercial analytics, and data science organizations.
    • Lead complex, multi-stakeholder sales cycles from initial engagement through contract execution.
    • Develop and execute territory and account strategies that drive sustainable revenue growth.
    • Represent Truveta at industry conferences, scientific meetings, and customer events.

Team Leadership & Coaching
    • Lead, coach, and develop a team of business development professionals.
    • Recruit, onboard, and retain top commercial talent.
    • Establish performance expectations and accountability measures that drive consistent attainment.
    • Participate in strategic deal reviews, pipeline inspections, and forecasting activities.
    • Foster a culture of collaboration, continuous learning, and customer-centric execution.

Scientific & Technical Engagement
    • Engage confidently with scientific, clinical, and technical audiences regarding Truveta's data assets, research capabilities, and analytical solutions.
    • Translate complex healthcare data concepts into business value for life sciences customers.
    • Partner closely with Research, Product, Clinical Informatics, and Data Science teams to support customer needs and strategic opportunities.
    • Maintain a deep understanding of industry trends, regulatory changes, competitive offerings, and evolving customer requirements.

Strategic Leadership
    • Contribute to commercial strategy, market expansion initiatives, and product feedback loops.
    • Provide voice-of-customer insights to executive leadership.
    • Help shape go-to-market strategy and future team structure as the business scales.
    • Serve as a leader and mentor across the broader Life Sciences organization.

Key Qualifications
  • 10+ years of experience selling Real-World Data, Real-World Evidence, healthcare analytics, clinical research solutions, or related technology to life sciences organizations.
  • 3+ years of direct people management experience with a demonstrated track record of hiring, coaching, and developing successful sales professionals.
  • Proven history of exceeding revenue targets in enterprise-level life sciences sales environments.
  • Strong network of relationships across pharmaceutical and biotechnology organizations.
  • Demonstrated ability to engage credibly with scientific, clinical, technical, and executive stakeholders.
  • Strong understanding of Real-World Data, Real-World Evidence, observational research methodologies, epidemiology, healthcare data assets, and AI-enabled analytics.
  • Experience leading complex, consultative sales cycles involving multiple stakeholders and functional teams.
  • Excellent communication, executive presentation, and negotiation skills.
  • Willingness to travel as required.

Preferred Qualifications
  • Advanced degree in a scientific, clinical, public health, healthcare, or related discipline (MS, MPH, PharmD, PhD, MD, or equivalent).
  • Experience selling healthcare data, research platforms, clinical analytics, or AI-driven solutions.
  • Experience building and scaling commercial teams in a high-growth environment.
  • Familiarity with regulatory and evidence-generation use cases supporting pharmaceutical and biotechnology organizations.

Why Truveta?
Be a part of building something special. Now is the perfect time to join Truveta. We have strong, established leadership with decades of success. We are well-funded. We are building a culture that prioritizes people and their passions across personal, professional and everything in between. Join us as we build an amazing company together.
We Offer:
  • Interesting and meaningful work for every career stage
  • Great benefits package
  • Comprehensive benefits with strong medical, dental and vision insurance plans
  • 401K plan
  • Professional development & training opportunities for continuous learning
  • Work/life autonomy via flexible work hours and flexible paid time off
  • Generous parental leave
  • Regular team activities (virtual and in-person as soon as we are able)
  • The base pay for this position is $200,000 to $240,000. The pay range reflects the minimum and maximum target. Pay is based on several factors including location and may vary depending on job-related knowledge, skills, and experience. This role is eligible for additional compensation such as incentive pay and stock options.

If you are based in California, we encourage you to read this important information for California residents linked here.
Truveta is committed to creating a diverse, inclusive, and empowering workplace. We believe that having employees, interns, and contractors with diverse backgrounds enables Truveta to better meet our mission and serve patients and health communities around the world. We recognize that opportunities in technology historically excluded and continue to disproportionately exclude Black and Indigenous people, people of color, people from working class backgrounds, people with disabilities, and LGBTQIA+ people. We strongly encourage individuals with these identities to apply even if you don't meet all of the requirements.
Please note that all applicants must be authorized to work in the United States for any employer as we are unable to sponsor work visas or permits (e.g. F-1 OPT, H1-B) at this time. We appreciate your interest in the position and encourage you to explore future opportunities with us.