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Biotech Manufacturing Jobs in Bothell, WA (NOW HIRING)

Intellectt INC

Validation Engineer II

Bothell, WA · On-site

... biotech environments. This role focuses on executing equipment qualification and supporting ... Collaborate with engineering, manufacturing, and quality teams * Support deviations, CAPAs, and ...

GenScript/ProBio

Production Lead- LNP

Redmond, WA · On-site

$75K - $90K/yr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Redmond, WA Reports to: Sr. Production Manager, Product Development and Manufacturing, Life Science ...

GenScript/ProBio

Production Lead- LNP

Redmond, WA · On-site

$75K - $90K/yr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Redmond, WA Reports to: Sr. Production Manager, Product Development and Manufacturing, Life Science ...

Lundbeck

Downstream Development Associate II

Bothell, WA · On-site

$38 - $45/hr

... manufacturing processes. Join us on our journey to advance brain health and transform lives ... Accredited bachelor's degree and a minimum of 2+ years of biotechnology/pharmaceutical industry ...

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All JobsBiotech Manufacturing JobsBiotech Manufacturing Jobs in Bothell, WA

Biotech Manufacturing information

See Bothell, WA salary details

$13

$23

$37

How much do biotech manufacturing jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for biotech manufacturing in Bothell, WA is $23.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $26.39 per hour, depending on experience, location, and employer.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.
What are the most commonly searched types of Biotech Manufacturing jobs in Bothell, WA? The most popular types of Biotech Manufacturing jobs in Bothell, WA are:
What job categories do people searching Biotech Manufacturing jobs in Bothell, WA look for? The top searched job categories for Biotech Manufacturing jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Manufacturing jobs? Cities near Bothell, WA with the most Biotech Manufacturing job openings:
Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in Bothell, WA as of July 2026, with employment types broken down into 1% As Needed, 85% Full Time, 9% Part Time, 1% Temporary, and 4% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $49,099 per year, or $23.6 per hour.
Senior Manager / Associate Director, External Manufacturing Operations

Senior Manager / Associate Director, External Manufacturing Operations

Immunome, Inc.

Bothell, WA • On-site

Other

Re-posted 24 days ago

Job description

Position Overview 

The Senior Manager / Associate Director, External Manufacturing Operations is responsible for meeting Immunome's supply requirements by enabling and overseeing operations performed at Contract Development and Manufacturing Organizations (CDMOs). This role focuses on biologics manufacturing but will support additional modalities as needed. 

Responsibilities 

  • Serve as the Supplier Relationship Manager (SRM) for specified CDMOs and primary liaison between the CDMO and Immunome.   
  • Collaborate closely with Legal to support the development and negotiation of service agreements, supply contracts, and statements of work across development and commercial phases.   
  • Lead one or more Virtual Management Teams (VMTs) comprising Quality, Product Supply, Technical Development, and other cross-functional stakeholders as necessary. Ensure Immunome's project deliverables stay on track. Align priorities and key communications with the CDMO.    
  • Conduct well-organized and documented project team meetings with CDMOs. Ensure CDMO progress is tracking to plan (e.g., campaign preparation, manufacturing operations, release activities, logistics, etc.). Proactively address delays to avoid impact on supply or regulatory milestones.     
  • Develop a thorough understanding of Immunome's drug product manufacturing processes. Support technical reviews of master and executed batch records, specifications, investigations, and change requests, as required.  
  • Monitor CDMO performance through Key Performance Indicators (KPIs) and drive improvements aligned with Immunome's expectations. Lead or participate in periodic Business Review Meetings.   
  • Work closely with department management and finance team to provide timely progress updates. Ensure that unexpected cost variances are communicated quickly.     
  • Maintain comprehensive knowledge of the CDMO's systems, capabilities, capacities, requirements, and business practices.   
  • Monitor spending against budget. Ensure CDMO invoicing is accurate and aligned with contractual terms.   

Other Responsibilities and Projects

  • Assist with technology transfers as needed, change implementation, and regulatory submission reviews.   
  • Support Technical Operations sourcing efforts and the qualification of new CDMOs.    
  • Support risk assessment development, and implementation of manufacturing network strategies.  
  • This is an individual contributor role. Depending on the business needs and organizational considerations, this role may include staff supervisory responsibly as the product portfolio and manufacturing network expand.    

Qualifications 

  • Bachelor's or advanced degree in biotechnology, biology, chemistry, chemical engineering, or related field.  
  • Minimum of 10 years of biopharmaceutical industry experience, and direct responsibility overseeing third parties performing cGMP manufacturing, or equivalent experience.  
  • Ability to travel (domestic and international) up to 25%, with occasional evening and/or weekend commitment.   

Knowledge and Skills 

  • Strong organizational, communication, and collaboration skills.  
  • Strong technical background in biotechnology/pharmaceutical manufacturing or process development.    
  • Hands-on expertise in drug product process development or cGMP drug product manufacturing. Experience with highly potent products is desired.   
  • Prior success in overseeing external manufacturing operations is required, either as an SRM or Subject Matter Expert (SME). Experience with both clinical and commercial manufacturing is desired.  
  • Well-versed in Quality systems and experienced with deviation investigations, change controls, and corrective actions.  
  • Possess strong negotiation skills and be versed in general contractual terms.   
  • Comfortable with ambiguity and uncertainty; adapt swiftly with focus on delivering to the business needs as priorities change.   

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