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How much do process development associate jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for process development associate in Redmond, WA is $37.72, according to ZipRecruiter salary data. Most workers in this role earn between $30.96 and $46.30 per hour, depending on experience, location, and employer.

What is the role of a process associate?

A process development associate is responsible for designing, testing, and optimizing manufacturing or operational processes to improve efficiency, quality, and safety. They often analyze data, collaborate with cross-functional teams, and use tools like process mapping and statistical analysis to implement improvements.

What is the difference between Process Development Associate vs Process Engineer?

AspectProcess Development AssociateProcess Engineer
Required CredentialsBachelor's in Chemistry, Chemical Engineering, or related field; often some experience in process developmentBachelor's or Master's in Chemical Engineering or related; more emphasis on engineering principles
Work EnvironmentLaboratory and pilot plant settings, focused on process research and developmentManufacturing plants, production lines, and process optimization environments
Employer & Industry UsagePharmaceutical, biotech, and chemical industries; entry to mid-level rolesChemical, manufacturing, and process industries; more senior roles in process optimization

The Process Development Associate primarily focuses on developing and optimizing new processes in lab and pilot settings, often working closely with R&D teams. In contrast, the Process Engineer applies engineering principles to scale up processes, improve manufacturing efficiency, and troubleshoot production issues. While both roles require a background in chemical or process engineering, the Process Development Associate is more research-oriented, whereas the Process Engineer emphasizes process implementation and optimization in production environments.

What jobs in the US pay 300,000 a year?

In the US, high-paying roles such as senior-level physicians, specialized surgeons, corporate executives, investment bankers, and certain technology executives can earn $300,000 or more annually. Process Development Associates typically do not reach this salary level unless they advance to senior management or specialized roles with significant experience and responsibilities.

What are the key skills and qualifications needed to thrive as a Process Development Associate, and why are they important?

To thrive as a Process Development Associate, you need a strong background in biochemistry, chemical engineering, or a related field, often supported by a bachelor’s or master’s degree. Experience with laboratory instrumentation, process optimization tools, and familiarity with regulatory standards such as GMP are typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills for excelling in this role. These competencies are crucial for ensuring efficient process design, regulatory compliance, and successful scale-up in manufacturing environments.

What is the highest paying job in manufacturing?

In manufacturing, senior roles such as Manufacturing Director, Plant Manager, or Engineering Manager tend to be the highest paying positions, often earning six-figure salaries. These roles typically require extensive experience, leadership skills, and knowledge of production processes and safety standards.

What is a process development associate?

A process development associate is a professional responsible for designing, testing, and optimizing manufacturing or operational processes to improve efficiency, quality, and cost-effectiveness. They often work with cross-functional teams, utilize data analysis tools, and may require knowledge of regulatory standards and process validation techniques.

What are the primary challenges faced by a Process Development Associate when scaling up laboratory processes to manufacturing scale?

A Process Development Associate often encounters challenges in translating small-scale laboratory protocols into large-scale manufacturing processes. Variations in equipment, raw material quality, and environmental conditions can impact reproducibility and efficiency. Addressing these issues requires strong troubleshooting skills, attention to detail, and close collaboration with cross-functional teams such as manufacturing, quality assurance, and engineering to ensure smooth technology transfer and consistent product quality.
What job categories do people searching Process Development Associate jobs in Redmond, WA look for? The top searched job categories for Process Development Associate jobs in Redmond, WA are:
What cities near Redmond, WA are hiring for Process Development Associate jobs? Cities near Redmond, WA with the most Process Development Associate job openings:
Process Development Associate jobs near you
Senior Manager / Associate Director, External Manufacturing Operations

Senior Manager / Associate Director, External Manufacturing Operations

Immunome, Inc.

Bothell, WA

Other

Posted 11 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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