ZipRecruiter

Log In

1

Biotech Scientist Jobs in Bothell, WA (NOW HIRING)

Pfizer

Head of AI Clinical Excellence

Bothell, WA

$89K - $121K/yr

PhD in Life Sciences, Clinical Research, Data Science, Biostatistics, Computer Science, Engineering, or related field and 5+ years of relevant experience within pharmaceutical, biotechnology, CRO ...

SystImmune, Inc

Scientist, Immuno-Oncology

Redmond, WA · On-site

$90K - $110K/yr

We are seeking a highly motivated Scientist with a strong experimental background in cellular and ... SystImmune is a leading and well-funded biotech company with a bright future. We offer an ...

Systimmune

Scientist, Immuno-Oncology

Redmond, WA · On-site

$90K - $110K/yr

We are seeking a highly motivated Scientist with a strong experimental background in cellular and ... SystImmune is a leading and well-funded biotech company with a bright future. We offer an ...

previous page

Showing results 41-60

All JobsBiotech Scientist JobsBiotech Scientist Jobs in Bothell, WA

Biotech Scientist information

See Bothell, WA salary details

$47.5K

$105.5K

$171K

How much do biotech scientist jobs pay per year?

As of Aug 12, 2026, the average yearly pay for biotech scientist in Bothell, WA is $105,550.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $133,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a biotech scientist?

To thrive as a Biotech Scientist, you need a strong background in molecular biology, biochemistry, and data analysis, usually supported by at least a bachelor's or master's degree in a life science field. Familiarity with laboratory techniques like PCR, cell culture, and the use of bioinformatics tools and laboratory information management systems (LIMS) is essential. Critical thinking, attention to detail, and effective teamwork are standout soft skills in this position. These capabilities are crucial for ensuring scientific rigor, driving innovation, and delivering reliable results in a collaborative research environment.

What is the difference between Biotech Scientist vs Microbiologist?

AspectBiotech ScientistMicrobiologist
Required CredentialsBachelor's or Master's in Biotechnology, Biology, or related fieldBachelor's or Master's in Microbiology, Biology, or related field
Work EnvironmentLaboratories, biotech companies, research institutionsLaboratories, healthcare facilities, research institutions
Industry UsageBiotechnology, pharmaceuticals, agricultureHealthcare, environmental, food safety
Common Search/ComparisonYesYes

Biotech Scientists and Microbiologists both work in laboratory settings and require similar educational backgrounds. However, Biotech Scientists focus on developing biotechnological applications and products, while Microbiologists study microorganisms and their impacts. Both roles are vital in research and industry, often overlapping but with distinct specializations.

What opportunities exist for career growth as a biotech scientist within a research organization?

As a Biotech Scientist, career advancement typically involves progressing from bench-level research roles to positions such as Senior Scientist, Principal Investigator, or Project Lead. Many organizations offer professional development through mentorship, cross-disciplinary projects, and leadership training. Collaboration with multidisciplinary teams and publication of research results can also enhance your visibility and open doors to new responsibilities. Demonstrating initiative and staying updated on emerging technologies are key factors in moving up within the field.
What are popular job titles related to Biotech Scientist jobs in Bothell, WA? For Biotech Scientist jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Biotech Scientist jobs in Bothell, WA look for? The top searched job categories for Biotech Scientist jobs in Bothell, WA are:
Biotech Scientist jobs near you
Infographic showing various Biotech Scientist job openings in Bothell, WA as of August 2026, with employment types broken down into 70% Full Time, 15% Temporary, and 15% Contract. Highlights an 100% In-person job distribution, with an average salary of $105,550 per year, or $50.7 per hour.

Senior Scientist, Purification Process Development

Zymeworks

Bellevue, WA • On-site

$116K - $178K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago

Job description

Company Description
Zymeworks is a global biotechnology company managing a portfolio of licensed healthcare assets and developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases, including cancer, inflammation, and autoimmune disease. The Company's asset and royalty aggregation strategy focuses on optimizing positive future cash flows from an emerging portfolio of licensed products such as Ziihera® (zanidatamab-hrii) and other licensed products and product candidates such as pasritamig. In addition, Zymeworks is also building a portfolio of healthcare assets that can generate strong cash flows, while supporting the early-stage development of innovative medicines. We are a global company headquartered in Vancouver BC, with operations in Bellevue WA, Dublin IRE, and Singapore.
Why Work With Us
Nothing is more critical to our success than the quality of our team. The work we do is meaningful and impactful - we care about each other as well as the patients we serve. We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.
This role will be located in Bellevue, WA and is hybrid with a minimum of 3 days per week onsite.
What You'll Do
  • Responsible for developing a robust early phase process specifically related to all purification operations.
  • Develop scalable purification processes suitable for GMP manufacturing.
  • Coordinate with research group on upcoming projects and evaluate manufacturability.
  • Collaborate with analytical development to establish critical quality attributes (CQAs) and monitor process performance.
  • Maintain downstream database for purification development data, reports, purification related raw materials, equipment, and process history, and analyze downstream data using statistical analysis or other methods.
  • Author and review process development reports, technical protocols, batch records, SOPs, risk assessments, and technology transfer documentation.
  • Serve as subject matter expert to plan, review, approve, monitor, and analyze process development experiments, GMP manufacturing and investigations.
  • Responsible for late-stage purification process characterization; performing risk analysis, defining control strategy and process qualification.
  • Collaboration with external CDMO partners to ensure successful scale-up and technology transfer to GMP facility.
  • Review executed batch documentation in support of batch release.
  • Author relevant sections of regulatory filings, including IND, IMPD and sections of BLA, and provide responses to health authorities as required.
  • Provide technical oversight and support of GMP manufacturing operations.
  • Effectively communicate with managers, peers, and external partners, to comprehend downstream progress, present process data and trending results, and update manufacturing performance.
  • Establish and maintain positive working relationships with peers, management and external partners.
  • Works closely with all internal and external resources to ensure DS supply availability.

What You'll Bring
  • A PhD, MSc, or BSc, in Chemical/Biochemical Engineering, Biological Sciences or related disciplines with at least 8 years (5+ years for PhD) of industrial experience in downstream process development with some GMP manufacturing experience.
  • Experienced in downstream process development, characterization, scale-up and manufacturing in the cGMP environment.
  • Experience working with contract manufacturing organizations.
  • Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Ability to establish and maintain effective working relationships.
  • Excellent organizational skills and the ability to work effectively in a high paced, fast changing environment.
  • Excellent oral and written communication skills, including the ability to integrate complex data to produce clear and accurate reports and presentations.
  • Strong background in the regulatory compliance requirements for the cGMP production of biologicals for clinical and commercial use.
  • Working knowledge of regulatory guidelines and expertise in CMC, PK or toxicology for the advancement of therapeutics through different phases of development.
  • Proficiency with cGMP and ICH guidelines.
  • Familiarity with QbD and Control Strategy Development or multivariate analysis and DoE approaches to process development a plus.
  • Experience working in a GMP manufacturing environment a plus.

Total Rewards
We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.
The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate's location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).
Our total rewards package that includes:
  • Industry leading vacation and paid time off
  • Exceptional medical, dental and vision benefits by country
  • Zymelife health and wellness benefits
  • Matching RRSP / 401K / Pension program
  • Employee Share Purchase Program
  • Employee Equity Program
  • Paid time off to volunteer in your community

This role is not eligible for relocation or immigration support.
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.
NOTE TO AGENCIES: Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract.
The pay range for this role is:
116,250 - 178,250 USD per year (US)

Apply