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Biotech Project Management Jobs in Bothell, WA (NOW HIRING)

PSC Biotech

Business Development Manager

Seattle, WA

$125K - $145K/yr

Direct industry, client-facing experience in an engineering or project management role within pharmaceutical manufacturing and biotechnology is strongly preferred. * Minimum of 5+ years of experience ...

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Biotech Project Management information

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$43K

$114.8K

$181.1K

How much do biotech project management jobs pay per year?

As of May 30, 2026, the average yearly pay for biotech project management in Bothell, WA is $114,787.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,800.00 and $137,500.00 per year, depending on experience, location, and employer.

What is a Biotech Project Management job?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are the key skills and qualifications needed to thrive in the Biotech Project Management position, and why are they important?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in Biotech Project Management roles?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.
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What job categories do people searching Biotech Project Management jobs in Bothell, WA look for? The top searched job categories for Biotech Project Management jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Project Management jobs? Cities near Bothell, WA with the most Biotech Project Management job openings:
Biotech Project Management jobs near you
Infographic showing various Biotech Project Management job openings in Bothell, WA as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $114,787 per year, or $55.2 per hour.
Scientific Project Manager (In Vitro Diagnostics)

Scientific Project Manager (In Vitro Diagnostics)

INBIOS INTERNATIONAL INC

Seattle, WA • On-site

$88K - $125K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago

Job description

Description:

Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.


About Us

InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.

  • Location: Seattle, WA
  • Employment Type: Full-time | On-site (Will consider hybrid work situation once established in position.)
  • Position Salary Range (Annual): $88,000.00 - $125,000.00
    The starting annual salary offered will depend on the selected applicant’s job-related knowledge, skills, and experience and internal equity.
What You’ll Do

We’re looking for a Scientific Project Manager to lead in vitro diagnostic (IVD) development programs in infectious diseases and oncology. The role requires strong technical project management experience across immunodiagnostic and molecular diagnostic platforms, with responsibility for managing government-funded programs from early development through GMP manufacturing, clinical validation, and FDA and CE regulatory submission.


Key Responsibilities
  • Lead end-to-end project management for IVD programs, from proposal development through regulatory clearance.
  • Manage government-funded contracts and grants, ensuring compliance with technical, financial, and reporting requirements.
  • Develop and maintain project timelines, budgets, resources, and risk mitigation plans.
  • Coordinate assay development and validation across immunochemistry platforms (e.g., lateral flow, ELISA) and molecular diagnostics (e.g., PCR, nucleic acid–based methods).
  • Support cGMP manufacturing, technology transfer, and validation activities.
  • Support FDA and CE/IVDR regulatory submissions in collaboration with regulatory and quality teams.
  • Serve as primary liaison with internal teams, CROs, clinical sites, academic collaborators, and government agencies.
  • Oversee preparation of project documentation, protocols, reports, and sponsor communications.
What We’re Looking ForRequired Qualifications
  • MS or PhD in relevant life science, or equivalent experience.
  • Demonstrated experience managing diagnostic development programs in infectious diseases and/or oncology.
  • Proven experience managing federally funded research or product development programs.
  • Working knowledge of immunochemistry-based and molecular diagnostic assay development.
  • Experience in cGMP-regulated environments.
  • Familiarity with FDA regulatory pathways; CE/IVDR experience preferred.
  • Strong organizational, analytical, and communication skills.
Preferred Qualifications
  • Proficiency with project management tools (e.g., Microsoft Project).
  • Experience supporting FDA submissions and/or CE marking for IVDs.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • 2 weeks paid vacation + 11 paid holidays , which includes the annual “winter-break” week (Christmas Day through New Year’s Day).
  • Supportive, mission-driven culture
Apply Today

Be part of a team that’s advancing science and improving lives.

Requirements: