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Biotech Operations Manager Jobs in Seattle, WA (NOW HIRING)

Amgen

Imaging Specialist Manager

Seattle, WA · On-site +1

It is key to our becoming one of the world's leading biotechnology companies. We are global ... You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation ...

Echodyne Corp

Facilities Manager

Kirkland, WA

The Facilities Manager leads day-to-day facilities operations, develops maintenance and capital ... semiconductor, electronics, biotechnology, or similarly complex technical environments.

Echodyne Corp

Facilities Manager

Kirkland, WA · On-site

Oversee operation and maintenance of HVAC, electrical distribution, plumbing, fire protection ... semiconductor, electronics, biotechnology, or similarly complex technical environments.

GenScript/ProBio

Manager of Quality Assurance

Redmond, WA · On-site

$100K - $120K/yr

... operational management of the site's ISO 9001-certified Quality Management System (QMS). The QA ... A/QC experience in a biotech production environment, including substantial management ...

Zymeworks

Senior Program Manager (Clinical)

Bellevue, WA · On-site

$105K - $161K/yr

Company Description Zymeworks is a global biotechnology company managing a portfolio of licensed ... We are a global company headquartered in Vancouver BC, with operations in Bellevue WA, Dublin IRE ...

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Showing results 41-60

All JobsBiotech Operations JobsBiotech Operations Manager JobsBiotech Operations Manager Jobs in Seattle, WA

Biotech Operations Manager information

See Seattle, WA salary details

$35.3K

$72.2K

$134.9K

How much do biotech operations manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for biotech operations manager in Seattle, WA is $72,214.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,700.00 and $88,200.00 per year, depending on experience, location, and employer.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.

What are the key skills and qualifications needed to thrive as a Biotech Operations Manager, and why are they important?

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

What are popular job titles related to Biotech Operations Manager jobs in Seattle, WA?

For Biotech Operations Manager jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biotech Operations Manager jobs in Seattle, WA look for?

The top searched job categories for Biotech Operations Manager jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Biotech Operations Manager jobs?

Cities near Seattle, WA with the most Biotech Operations Manager job openings:

Biotech Operations Manager jobs near you
Infographic showing various Biotech Operations Manager job openings in Seattle, WA as of August 2026, with employment types broken down into 83% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $72,214 per year, or $34.7 per hour.

Senior Project Manager

SystImmune, Inc

Redmond, WA • On-site

$60K - $85K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 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.
We are seeking a Senior Project Manager, R&D to support cross-functional planning and execution for oncology biologics programs from early discovery through IND-enabling activities and support of IND submission. This role will partner closely with Research, Translational Sciences, Nonclinical, Regulatory, Clinical Pharmacology, and external partners to drive integrated development strategy, stage-appropriate planning, risk management, and operational execution.
The ideal candidate brings strong biotech or biopharma drug development experience, excellent cross-functional leadership skills, and a deep understanding of the milestones, dependencies, and decision points required to advance innovative biologics programs into the clinic. This individual will serve as a strategic and operational hub for assigned programs, ensuring alignment, accountability, and timely progress across the portfolio. A key aspect of this role is the effective use of meeting management to strengthen stakeholder integration, communication, decision-making, and execution across internal and external teams.
Key Responsibilities
  • Lead cross-functional project planning and execution for oncology biologics programs spanning target/lead discovery, candidate selection, IND-enabling studies, CMC development, and IND submission
  • Build, maintain, and drive integrated project plans, timelines, milestones, scenarios, and critical path analyses across multiple functional areas
  • Partner with program leaders and functional heads to define development strategy, key objectives, deliverables, governance milestones, and resource assumptions
  • Facilitate cross-functional team meetings, sub-team meetings, and governance reviews; document decisions, action items, risks, and next steps
  • Identify interdependencies, operational risks, and potential bottlenecks early; drive mitigation plans and escalate issues appropriately
  • Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational, Quality, and partner organizations
  • Drive program team preparedness for major stage gates, including candidate nomination, development candidate selection, IND-enabling study initiation, and IND submission
  • Support budget planning, resource tracking, and external partner/CRO coordination as needed
  • Develop concise and decision-oriented communications for senior leadership, governance bodies, and key stakeholders
  • Track progress against program goals and proactively highlight deviations, tradeoffs, and decision needs
  • Promote disciplined program management practices, clear accountability, and efficient team operations
  • Contribute to portfolio planning and cross-program prioritization discussions where appropriate
  • Help apply and improve R&D project management tools, templates, dashboards, and best practices
  • Drive scalable adoption of AI-enabled and digital program management practices, including automation, dashboards, AI-assisted synthesis, standardized workflows, and data-driven reporting, to improve planning, meeting effectiveness, action tracking, knowledge management, risk identification, portfolio governance, and cross-functional execution while ensuring human oversight, data integrity, and compliance.

Required Qualifications
  • Bachelor's degree in life sciences, biomedical sciences, chemistry, engineering, or related field
  • 8+ years of relevant experience in biotech, biopharma, or related life sciences industry
  • 5+ years of project or program management experience supporting drug discovery and/or development programs
  • Demonstrated experience managing biologics programs in oncology or closely related therapeutic areas
  • Strong understanding of drug development from discovery through IND, including:
    • discovery research and candidate selection
    • IND-enabling toxicology and pharmacology
    • CMC and analytical development for biologics
    • regulatory documentation and IND submission processes
  • Proven ability to lead highly matrixed, cross-functional teams without direct authority
  • Excellent communication, facilitation, organizational, and stakeholder management skills
  • Strong problem-solving abilities with demonstrated experience managing complex timelines, dependencies, and risks
  • Experience preparing executive-level presentations, status reports, and governance materials
Preferred Qualifications
  • Advanced degree (MS, PhD, PharmD, or MBA) in a relevant scientific or business discipline
  • Experience with monoclonal antibodies, bispecifics, ADCs, or other complex biologic modalities in oncology
  • Mandarin-English Bilingual Ability
  • PMP or related project management certification is a plus and biotherapeutics life cycles
  • Experience in a fast-paced, innovation-driven biotech environment
Core Competencies
  • Strategic thinking with strong operational execution
  • Cross-functional leadership and influence
  • Decision facilitation and issue resolution
  • Planning discipline and attention to detail
  • Agility in a dynamic R&D environment
  • Strong sense of ownership and accountability
Success in this role will be defined by the ability to:
  • keep complex oncology biologics programs aligned and moving forward from discovery to IND
  • create clarity across scientific and development teams around priorities, timelines, and decisions
  • anticipate risks and dependencies before they become delays
  • enable efficient governance and high-quality decision-making
  • build trust across functions as a strategic and operational partner
Position Type/Expected Hours of Work
  • May need to work outside of standard working hours at times
  • This role is currently working onsite and is expected to work onsite for working hours, with flexibility to work start time. The work location for this role is in Redmond, WA.

Compensation and Benefits:
The expected base salary range for this position is $100,000 - $160,000 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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