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Director Aggregate Jobs in Seattle, WA (NOW HIRING)

Director, Commercial Distribution

Bothell, WA · On-site

$221.55 - $258.54/hr

The director will be a proven leader, willing to accept new challenges and increased ... aggregator(s), data warehouse, and analytics/BI tools--to integrate and govern channel data (3PL ...

Director, Software Engineering

Seattle, WA · Hybrid

$287K/yr

  • Medical

  • Life

  • Retirement

  • PTO

This positon is a apeople manager role reporting to the Senior Director, Software Engineering ... alert aggregation * Bridge the gap between robust backend infrastructure and applied machine ...

Director, Software Engineering

Seattle, WA · On-site

$287K/yr

  • Medical

  • Life

  • Retirement

  • PTO

This positon is a apeople manager role reporting to the Senior Director, Software Engineering ... alert aggregation * Bridge the gap between robust backend infrastructure and applied machine ...

Engineering Technician

Seattle, WA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Direct Hire Compensation: Work Model: Hybrid - onsite and remote Hours: 40.0 Security Clearance ... Perform field testing of soils, concrete, asphalt, and aggregate in accordance with ASTM, AASHTO ...

... aggregation or other methods * Data transformation: Apply quasi-experimental designs (e.g ... Practical working understanding of data-analytics tools, and direct experience managing, analyzing ...

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Showing results 1-20

Director Aggregate information

See Seattle, WA salary details

$35.3K

$142.9K

$243K

How much do director aggregate jobs pay per year?

As of Aug 12, 2026, the average yearly pay for director aggregate in Seattle, WA is $142,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,600.00 and $171,800.00 per year, depending on experience, location, and employer.

What is the difference between Director Aggregate vs Data Analyst?

AspectDirector AggregateData Analyst
Required CredentialsBachelor's or Master's in Business, Finance, or related fields; often with leadership experienceBachelor's in Statistics, Data Science, or related fields; certifications like SQL, Python often preferred
Work EnvironmentLeadership roles in corporate or organizational settings, overseeing teams and strategiesAnalytical roles in various industries, focusing on data collection, analysis, and reporting
Employer & Industry UsageUsed in finance, consulting, and large corporations for strategic oversightCommon in tech, marketing, finance, and healthcare for data-driven decision making

The main difference between a Director Aggregate and a Data Analyst lies in their scope and responsibilities. The Director Aggregate typically holds a leadership position, overseeing data teams and strategic initiatives, requiring advanced credentials and experience. In contrast, a Data Analyst focuses on analyzing data sets to generate insights, often with technical skills and less managerial responsibility. Both roles are essential in data-driven industries but serve different functions within organizations.

What are some common challenges faced by a director aggregate, and how can they be addressed?

A Director of Aggregate often encounters challenges related to balancing production efficiency with safety and environmental regulations. Managing multiple sites, coordinating logistics, and ensuring the consistent quality of materials can also be demanding. Success in this role typically requires strong leadership, excellent communication skills, and the ability to implement process improvements while fostering a culture of safety and compliance. Building strong relationships with both field teams and executive leadership is crucial for effectively addressing these challenges and driving operational excellence.

What does a director aggregate do?

A Director Aggregate is a senior management professional responsible for overseeing the operations and performance of aggregate production or supply businesses, such as those involved in mining, quarrying, or construction materials. Their duties often include managing teams, ensuring compliance with safety and environmental regulations, optimizing production processes, and developing business strategies to improve profitability. They also work closely with other executives and stakeholders to achieve organizational goals, maintain quality standards, and drive growth within the aggregate sector.

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

To thrive as a Director, Aggregate, you need extensive experience in aggregate production, operations management, and a solid understanding of industry regulations, typically supported by a degree in engineering, geology, or business. Proficiency in quarry management systems, safety compliance tools, and financial planning software is often required. Strong leadership, problem-solving abilities, and effective communication are crucial for managing teams and coordinating with stakeholders. These skills ensure efficient operations, regulatory compliance, and the achievement of business goals in a competitive industry.
What are the most commonly searched types of Aggregate jobs in Seattle, WA? The most popular types of Aggregate jobs in Seattle, WA are:
What are popular job titles related to Director Aggregate jobs in Seattle, WA? For Director Aggregate jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Director Aggregate jobs in Seattle, WA look for? The top searched job categories for Director Aggregate jobs in Seattle, WA are:
Infographic showing various Director Aggregate job openings in Seattle, WA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $142,937 per year, or $68.7 per hour.

Director, Pharmacovigilance

Umoja Biopharma

Seattle, WA

Full-time

Re-posted 12 days ago


Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.

Umoja Biopharma – Your Body. Your Hope. Your Cure.

POSITION SUMMARY:

The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma's global safety strategy across clinical-stage programs. This individual will be responsible for day-to-day pharmacovigilance operations, ensuring high-quality safety data management, regulatory compliance, and effective signal detection.

Working cross-functionally with Clinical Development, Regulatory, and external partners, the Director will help build and optimize scalable PV processes to support Umoja's advancing pipeline, with an emphasis on operational excellence and inspection readiness.

This role will operate as an Individual Contributor and manage PV relationships with vendors and CROs to start. This person may be responsible for building the Pharmacovigilance team and organization in Umoja in the near future.

This position will ideally be based out of our Seattle, WA office and work onsite at least 2 days/week. This position may have the ability to be remote in the US based on candidate experience.

CORE ACCOUNTABILITIES:

Pharmacovigilance Operations

  • Oversee case processing activities, including intake, triage, medical review support, and expedited reporting
  • Ensure compliance with global safety reporting requirements (FDA, EMA, ICH guidelines)
  • Manage relationships with PV vendors/CROs, ensuring service quality, timeliness, and data integrity
  • Support maintenance of safety databases and related systems (e.g., Argus, ArisGlobal)
  • Coordinate with Clinical Development to drive internal cross-functional pharmacovigilance activities

Aggregate Reporting & Regulatory Support

  • Lead or contribute to preparation of DSURs, PSURs/PBRERs, and IND safety reports
  • Support safety sections of regulatory submissions and responses to health authority queries
  • Contribute to development and maintenance of SOPs and Pharmacovigilance System Master File (PSMF)

Signal Detection & Risk Management

  • Support signal detection activities, including data review, trend analysis, and documentation
  • Participate in safety review meetings and cross-functional risk discussions
  • Assist in development and implementation of Risk Management Plans (RMPs)

Cross-Functional Collaboration

  • Partner with Clinical Development on protocol safety design, adverse event monitoring, and investigator communications
  • Collaborate with Regulatory Affairs to ensure alignment on safety reporting strategy
  • Support Medical Affairs in communicating safety information as needed

Inspection Readiness & Quality

  • Ensure PV processes are audit- and inspection-ready
  • Participate in internal audits, vendor audits, and regulatory inspections
  • Drive continuous improvement initiatives across PV operations

The successful candidate will have:

Education & Experience

  • Advanced degree (PharmD, PhD, MD, or MS) or health-related degree/certification (PA, RN, NP)) with at least 10 years of pharmacovigilance experience in biotech or pharmaceutical industry is required
  • Experience supporting clinical-stage programs and working with outsourced PV models
  • Exposure to regulatory submissions and inspections preferred

Technical Expertise

  • Strong working knowledge of global pharmacovigilance regulations (FDA, EMA, ICH)
  • Experience with safety databases and case processing workflows
  • Familiarity with aggregate reporting and signal detection processes
  • Experience in oncology, cell therapy, or gene therapy preferred

Leadership & Operating Style

  • Strong execution focus with attention to detail and quality
  • Ability to manage external partners and influence cross-functional teams
  • Comfortable operating in a fast-paced, evolving biotech environment
  • Proactive problem-solver with sound judgment

Physical Requirements:

  • The ideal candidate will be able to work onsite based out of our Seattle, WA office at least 2 days/week. There may be the ability to work remotely within the US and travel to Seattle, WA at least 5 days/month.
  • Ability to travel as needed
  • Ability to sit for prolonged periods of time

Salary Range: $204,000 - $305,000

Benefits Offerings

Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.