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Contract Biotech Jobs in Renton, WA (NOW HIRING)

InduPro Therapeutics

Project Manager-ADC

Seattle, WA

$96.15 - $105.77/hr

The Opportunity We are seeking an enthusiastic and highly-motivated Contract Project Manager to ... Familiarity working in a fast-paced startup biotech environment strongly preferred * 5-10+ years of ...

InduPro Therapeutics

Project Manager-ADC

Seattle, WA · On-site +1

$96.15 - $105.77/hr

The Opportunity We are seeking an enthusiastic and highly-motivated Contract Project Manager to ... Familiarity working in a fast-paced startup biotech environment strongly preferred * 5-10+ years of ...

Anthropic

Commercial Counsel, SPARC

Seattle, WA

Help build and maintain commercial legal infrastructure, including contract templates, playbooks ... Experience with biotech, clinical research, or other life sciences transactions * Familiarity with ...

Omeros

Research Associate I

Seattle, WA

Omeros is an innovative biotechnology company that discovers and develops first-in-class protein ... and external contract organizations * Strong scientific judgment and ability to make sound ...

New

Omeros Corp.

Research Associate I

Seattle, WA · On-site

Omeros is an innovative biotechnology company that discovers and develops first-in-class protein ... and external contract organizations * Strong scientific judgment and ability to make sound ...

New

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All JobsContract Biotech JobsContract Biotech Jobs in Renton, WA

Contract Biotech information

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How much do contract biotech jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for contract biotech in Renton, WA is $40.88, according to ZipRecruiter salary data. Most workers in this role earn between $29.76 and $49.23 per hour, depending on experience, location, and employer.

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

To thrive as a Contract Biotech professional, you need a strong background in biological sciences, laboratory techniques, and data analysis, usually supported by a relevant degree in biotechnology or a related field. Familiarity with lab information management systems (LIMS), molecular biology tools, and compliance regulations like GLP or GMP is typically required. Strong problem-solving, attention to detail, and effective communication skills are essential for collaborating with clients and team members. These competencies ensure accurate project delivery, adherence to regulatory standards, and successful client relationships in a dynamic biotech environment.

What is the difference between Contract Biotech vs Contract Research Associate?

AspectContract BiotechContract Research Associate
CredentialsBachelor's or Master's in Life Sciences, relevant experienceBachelor's or Master's in Life Sciences, laboratory skills
Work EnvironmentBiotech companies, labs, manufacturing facilitiesResearch labs, clinical trial sites, biotech firms
Employer & Industry UsageBiotech firms, pharmaceutical companies, contract research organizationsResearch organizations, biotech companies, clinical research settings

Contract Biotech roles typically involve working on product development, manufacturing, or process optimization within biotech companies, often requiring technical expertise. Contract Research Associates focus on supporting clinical trials and research studies, performing experiments, and data collection. While both roles are contract-based and in the biotech industry, Contract Biotech positions emphasize technical and manufacturing skills, whereas Contract Research Associate roles center on research and clinical support.

What are some common challenges faced by contract biotech professionals, and how can they be addressed?

Contract biotech professionals often encounter challenges related to adapting quickly to new organizational cultures and workflows, as they may work with multiple clients or projects in short timeframes. Balancing the expectations of different stakeholders while ensuring compliance with regulatory standards can also be demanding. To address these challenges, it's important to develop strong communication skills, be proactive in understanding project goals, and stay current with industry regulations. Building a network within the biotech community can also help with knowledge-sharing and support.

What is a Contract Biotech and what do they do?

A Contract Biotech refers to a company or professional that provides biotechnology research, development, and manufacturing services to other organizations on a contractual basis. These services can include laboratory research, drug development, clinical trials, and production of biological products. Contract Biotech organizations help pharmaceutical companies, academic institutions, and startups accelerate their projects without needing to build extensive in-house capabilities. This allows clients to access specialized expertise and facilities, manage costs, and bring products to market more efficiently.
What are the most commonly searched types of Biotech jobs in Renton, WA? The most popular types of Biotech jobs in Renton, WA are:
What cities near Renton, WA are hiring for Contract Biotech jobs? Cities near Renton, WA with the most Contract Biotech job openings:
Contract Biotech jobs near you

Project Manager-ADC

InduPro Therapeutics

Seattle, WA

$96.15 - $105.77/hr

Contractor

Re-posted 13 days ago

Job description

About InduPro
InduPro develops life-changing therapies using a proprietary cell-surface labeling platform that leverages spatial proximity within microenvironments to enable the discovery of novel multispecific biologics. This approach has generated a growing pipeline of candidates advancing into clinical development across oncology and autoimmune diseases. InduPro fosters a culture of innovation at every level.

The Opportunity

We are seeking an enthusiastic and highly-motivated Contract Project Manager to help advance our emerging pipeline from development candidate selection through IND-enabling studies and beyond.  

Key Responsibilities:
  • Drive integrated program plans spanning development candidate (DC) selection through IND-enabling activities
  • Facilitate core team and sub-team meetings; ensure alignment on objectives, deliverables, and timelines
  • Identify critical path, key risks, and decision points; proactively manage trade-offs to maintain timelines
  • Work with external partners and collaborators to ensure adherence to timelines, budgets and deliverables
  • Maintain clear communication of program status, risks, and mitigation plans to stakeholders and governance bodies
  • Track progress against milestones including DC nomination, GLP tox initiation/completion, CMC readiness, and IND submission
  • Ensure dependencies across functions are identified and managed effectively
  • Proven ability to manage complex, cross-functional projects with competing priorities
  • Partner with project leaders to charter teams, develop core documents, establish timelines and budgets, and align project tactics with project strategy
Other Skills & Abilities:
  • Comprehensive understanding of drug development process, with working experience across product life cycle (early development products to mid-clinical stage products), including biologics and antibody-drug conjugates for cancer, autoimmune disease, nonclinical, CMC, and regulatory requirements
  • Experience managing CROs for IND-enabling activities 
  • Proficiency with project management tools (e.g., MS Project, Smartsheet) and budgeting/resource planning
  • Strong competencies in planning, project management, and organization with the ability to lead multiple activities in parallel while maintaining a focus on quality
  • Exceptional interpersonal skills to effectively work in a team or matrix environment, to collaborate and coordinate with internal and external department staff at various levels, and to influence others effectively; able to build and collaborate with a cross-functional network
  • Self-directed quick learner who is proactive and takes initiative, with the ability to adapt to a dynamic environment and a demonstrated ability to grasp general knowledge of multiple fields
  • Creative and critical problem-solving skills with high comfort in ambiguous situations
Education & Experience:
  • BS, Masters or PharmD in oncology, cell biology or related field
  • Experience with antibody drug conjugates strongly preferred
  • Demonstrated experience managing oncology biologics program from development candidate to IND stage and/or beyond in biotech or pharma environment
  • Familiarity working in a fast-paced startup biotech environment strongly preferred
  • 5-10+ years of research experience in either Oncology or Inflammation disease areas
  • 5-10+ years of demonstrated project management experience supporting research programs in the biopharmaceutical or biotech industry
  • 2+ years of managerial experience directly handling people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
Physical Work Requirements:
  • Prolonged periods sitting at a desk and working on a computer
Travel Requirements:

This position does not generally require travel.

Physical presence at the InduPro worksite, or in the field, is required for this role. At InduPro we believe that physical presence helps enhance collaboration, innovation, productivity, employee well-being, employee engagement, and Company culture.

$96.15 - $105.77 an hour
At InduPro we believe that being face to face helps enhance collaboration, innovation, productivity, employee well-being, employee engagement, and Company culture. 
 
InduPro, Inc. is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability, or any other status protected by federal, state, or local law.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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