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Director Fda Tobacco Inspector Jobs in Bothell, WA

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This is a senior individual contributor QA leadership role with no direct reports. This position is ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...

Systimmune

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This is a senior individual contributor QA leadership role with no direct reports. This position is ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

The Director will provide leadership for internal and external data management teams, ensure high ... FDA, EMA, and other applicable regulatory requirements, while maintaining inspection readiness.

Omeros Corp.

Director, Quality Control

Seattle, WA · On-site

... FDA-approved for the treatment of hematopoietic stem cell transplant-associated thrombotic ... Experience with regulatory authority meetings and GMP site inspections * Extensive experience with ...

Omeros

Director, Quality Control

Seattle, WA

... FDA-approved for the treatment of hematopoietic stem cell transplant-associated thrombotic ... Experience with regulatory authority meetings and GMP site inspections * Extensive experience with ...

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Showing results 21-40

All JobsFda Tobacco Inspector JobsDirector Fda Tobacco Inspector JobsDirector Fda Tobacco Inspector Jobs in Bothell, WA

Director Fda Tobacco Inspector information

See Bothell, WA salary details

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How much do director fda tobacco inspector jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for director fda tobacco inspector in Bothell, WA is $30.58, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $35.19 per hour, depending on experience, location, and employer.

What is the difference between Director Fda Tobacco Inspector vs Tobacco Inspector?

AspectDirector Fda Tobacco InspectorTobacco Inspector
CertificationsFDA certifications, compliance trainingBasic inspection certifications, industry-specific training
Work EnvironmentRegulatory agencies, corporate compliance departmentsManufacturing plants, quality control labs
Employer & IndustryFDA, government agencies, tobacco companiesTobacco manufacturing, quality assurance firms

The main difference is that a Director Fda Tobacco Inspector oversees regulatory compliance at a higher level, often managing teams and policies, while a Tobacco Inspector conducts on-the-ground inspections of tobacco products and facilities. The Director role involves strategic oversight, whereas the Inspector focuses on detailed product and process checks.

How do you become a Director FDA Tobacco Inspector?

To become a Director FDA Tobacco Inspector, candidates typically need a background in public health, regulatory compliance, or law enforcement, along with experience in tobacco product regulation. Advancement often requires progressing through inspector roles, gaining specialized knowledge, and demonstrating leadership skills, with some positions requiring federal employment exams or certifications. Strong analytical, communication, and inspection skills are essential for this role.

What job categories do people searching Director Fda Tobacco Inspector jobs in Bothell, WA look for?

The top searched job categories for Director Fda Tobacco Inspector jobs in Bothell, WA are:

What cities near Bothell, WA are hiring for Director Fda Tobacco Inspector jobs?

Cities near Bothell, WA with the most Director Fda Tobacco Inspector job openings:

Director Fda Tobacco Inspector jobs near you
Infographic showing various Director Fda Tobacco Inspector job openings in Bothell, WA as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 18% Part Time, 1% Temporary, and 3% Contract. Highlights an 89% Physical, 5% Hybrid, and 6% Remote job distribution, with an average salary of $63,613 per year, or $30.6 per hour.

Associate Director/Director, Bioanalytical Laboratory

Systimmune

Redmond, WA • On-site

$150K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 26 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is seeking an experienced and visionary Associate Director/Director of Bioanalytical Laboratories to lead, expand, and inspire our bioanalytical capabilities supporting preclinical and clinical programs in biologics and ADC development.
 

This role combines scientific depth, operational excellence, and people leadership. The Director will oversee assay development, validation, and execution for pharmacokinetic (PK) and anti-drug antibody (ADA) analyses supporting ADCs and other biologics, while building a high-performing team and fostering a culture of scientific rigor and continuous learning. This is a hands-on, high-impact role for a leader who thrives at the intersection of science, strategy, and mentorship.

The position is full-time onsite and based in Redmond, WA.
ResponsibilitiesStrategic & Scientific Leadership
  • Define and execute bioanalytical strategies supporting discovery, preclinical, and clinical development of biologics and ADCs.
  • Lead the design, development, validation, and troubleshooting of PK, ADA, and biomarker assays using ligand-binding, ELISA, ECLIA, LC-MS/MS, and hybrid methods.
  • Serve as the bioanalytical lead in cross-functional project teams and regulatory interactions.
  • Anticipate and adapt to evolving regulatory expectations and scientific advances to ensure SystImmune remains at the forefront of bioanalytical science.
Operational & Laboratory Management
  • Oversee day-to-day laboratory operations to ensure compliance with GLP, GCP, ICH, and 21 CFR Part 11 standards.
  • Direct equipment qualification, calibration, and maintenance programs.
  • Establish and maintain SOPs, safety protocols, data integrity systems, and quality management processes.
  • Partner with Quality Assurance to prepare for audits and regulatory inspections, maintaining a state of perpetual readiness.
Team Leadership & Talent Development
  • Build, inspire, and empower a team of exceptional scientists and analysts.
  • Foster a culture that emphasizes mentorship, growth, and scientific curiosity, helping staff expand their technical expertise and leadership potential.
  • Create individualized development plans and cross-training opportunities to strengthen technical depth and career progression.
  • Promote open communication, shared accountability, and recognition of high performance.
Cross-Functional & Global Collaboration
  • Collaborate closely with Translational Sciences, Clinical Pharmacology, Regulatory Affairs, and Quality to ensure alignment on analytical strategy and regulatory submissions.
  • Partner with global bioanalytical and translational teams to harmonize methods, data standards, and reporting practices.
  • Represent SystImmune’s bioanalytical expertise in internal governance forums and external scientific networks.

Qualifications

  • Ph.D. in Pharmacology, Biochemistry, Analytical Chemistry, Immunology, or related discipline (M.S. with significant experience considered).
  • 10+ years of industry experience in bioanalytical sciences supporting biologics or ADC programs, including 5+ years in a leadership role.
  • Demonstrated expertise in assay development, validation, and regulatory submission for PK/ADA/biomarker methods.
  • Proven success managing GLP/GCP-compliant lab operations and preparing for health authority inspections.
  • Strong understanding of global regulatory requirements (FDA, EMA, NMPA, ICH M10, E6).
  • Exceptional leadership and people management skills with a record of developing scientific talent and fostering high-performance teams.
  • Effective communicator who can translate complex data into strategic decisions.
  • Experience managing CROs or global lab partnerships a plus.

Compensation and Benefits:
The expected base salary range for this position is $150,000 - $230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
 
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
 
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
 
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
 

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