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Bio Manufacturing Jobs in Bothell, WA (NOW HIRING)

Microsoft

Senior Software Engineer

Redmond, WA · On-site

$160K - $261K/yr

... manufacturing, and pharmaceuticals, showcasing its potential to solve real-world challenges through ... Familiarity with widely used scientific tools in chemistry, physics and bio sciences. * Proficiency ...

HOK

Architecture - Lab Planner

Seattle, WA · On-site

$100K - $120K/yr

... bio-containment, research, teaching (science), pharmaceutical, public health, clinical, process and manufacturing facilities. * Architecture license preferred. * LEED accreditation or Green Associate ...

Microsoft

Software Engineer II

Redmond, WA · On-site

$133K - $219K/yr

... manufacturing, and pharmaceuticals, showcasing its potential to solve real-world challenges through ... Familiarity with widely used scientific tools in chemistry, physics and bio sciences. * Proficiency ...

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All JobsBio Manufacturing JobsBio Manufacturing Jobs in Bothell, WA

Bio Manufacturing information

See Bothell, WA salary details

$39.7K

$89.3K

$125.8K

How much do bio manufacturing jobs pay per year?

As of Jul 14, 2026, the average yearly pay for bio manufacturing in Bothell, WA is $89,258.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,400.00 and $99,500.00 per year, depending on experience, location, and employer.

What is the job of a biotechnician?

A biotechnician assists in laboratory and manufacturing processes related to biotechnology, including preparing samples, operating equipment, and maintaining lab environments. They often follow strict safety protocols and may need technical certifications or training in biotechnology techniques.

What biology jobs pay over $100k?

In the field of bio manufacturing, roles such as senior bioprocess engineers, regulatory affairs managers, and research directors often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, specialized skills in bioprocessing or quality assurance, and experience managing large-scale production or research projects.

What are the key skills and qualifications needed to thrive in Bio Manufacturing, and why are they important?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What is bio manufacturing?

Bio manufacturing, also known as biomanufacturing, is the process of using biological systems like cells or enzymes to produce commercial products such as medicines, vaccines, biofuels, and food ingredients. This field combines biology, engineering, and technology to create products in a controlled and scalable way, often using fermentation or cell culture techniques. Biomanufacturing plays a critical role in the pharmaceutical, biotechnology, and food industries, enabling the production of complex molecules that are difficult to synthesize chemically. Professionals in this field work on developing, optimizing, and scaling up these biological processes to ensure high-quality and cost-effective product output.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

Is biotech a high paying job?

Bio manufacturing jobs in the biotech industry often offer competitive salaries, especially for roles requiring specialized skills or advanced education. Entry-level positions may have moderate pay, but experienced professionals with certifications or technical expertise can earn higher wages. Overall, biotech careers can be financially rewarding compared to many other manufacturing or laboratory roles.

How much does biomanufacturing pay?

Biomanufacturing technicians and specialists typically earn between $50,000 and $80,000 annually, depending on experience, education, and location. Entry-level roles may start around $40,000, while experienced professionals or those with advanced certifications can earn over $100,000. The field often requires knowledge of GMP standards, bioprocessing equipment, and quality control procedures.
What job categories do people searching Bio Manufacturing jobs in Bothell, WA look for? The top searched job categories for Bio Manufacturing jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Bio Manufacturing jobs? Cities near Bothell, WA with the most Bio Manufacturing job openings:
Bio Manufacturing jobs near you
Director/Senior Director of Analytical

Director/Senior Director of Analytical

SystImmune, Inc

Redmond, WA • On-site

$190K - $280K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Located in Redmond WA, SystImmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic multi-specific antibodies, as well as antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor.
The Director/ Senior Director of Analytical will lead the Analytical teams, working collaboratively with the Director of Process Development, Head of Cell Science in Redmond, WA and CMC leads in Chengdu. This role is responsible for driving analytical strategy, method development, and release assay designs to support early-stage biologics development and GMP manufacturing. The role is responsible for integration of analytical workflows with upstream and downstream processes and is accountable for analytical method transfer to the company's GMP manufacturing site in China.
Key Responsibilities
  1. Leadership & Strategy:
    • Manage and mentor Analytical teams.
    • Develop strategies for analytical method development, validation, and tech transfer.
    • Drive innovation in integrated discovery and manufacturability for novel biologics.
  2. Analytical Strategy Development:
    • Develop and implement analytical strategies to support antibody and ADC development, including phase-appropriate analytical development, characterization, and release strategies.
    • Collaborate with cross-functional teams to establish critical quality attributes (CQAs) and specifications.
    • Oversee analytical development, release, and stability testing at external partners.
    • Ensure the integrity, organization, and integration of analytical datasets, supporting development and regulatory submissions.
    • Support regulatory filings (e.g., IND, BLA) with robust analytical data and interpretation.
    • Partner with QC teams in Chengdu to ensure successful product release, characterization, and scaling.
  3. Collaboration & Integration:
    • Partner closely with the Director of Process Development for PAT workflows.
    • Participate in cross-functional PD/CMC working groups to meet project milestones.
    • Work closely with the manufacturing facility and R&D center in Chengdu to ensure alignment in process development, scale-up, and manufacturing activities.
    • Facilitate technology transfer and ensure consistency between sites, maintaining high-quality standards and regulatory compliance.
    • Identify and manage processes, and ensure successful technology transfer for scale-up and GMP manufacturing, particularly between the U.S. and China.

Qualifications
  • Advanced degree (PhD preferred) in Analytical Chemistry, Biochemistry, or related field.
  • At least 10+ years of laboratory experience in an industrial setting. Extensive experience in analytical development for biologics, including method validation and tech transfer.
  • Proven experience supporting co-development alliances and global technology transfers.
  • Strong leadership skills with a proven track record of managing multidisciplinary teams.
  • Knowledge of GMP regulations and global regulatory expectations.

Experience:
  • Extensive experience antibody or ADC drug development.
  • Deep understanding of the design, development, optimization, and tech transfer of antibody or ADC manufacturing processes.
  • Expertise in developing, optimizing, troubleshooting, and tech transferring analytical methods for antibodies or ADCs.
  • Proficient in analyzing and interpreting complex datasets from multiple methodologies..
  • Expertise in method robustness assessment, validation, and testing.
  • Demonstrated experience in cross-functional and functional leadership roles with strong collaboration and stakeholder relationship management skills.
  • Proficient in drafting, reviewing, approving, and supporting regulatory filings and responses.
  • Comprehensive knowledge of ICH and FDA regulations and guidance for biologics and ADCs.
  • Language Skills: Proficiency in reading and writing Mandarin Chinese is required to effectively collaborate with the Chengdu facility and global partners.

The expected base salary range for this position is $190,000 - $280,000 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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