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Process Development Associate Jobs in Durham, NC

IQVIA

Associate Business Development Director

Durham, NC · On-site

$89K - $250K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

KBI Biopharma, Inc.

In Process Research Associate

Durham, NC · On-site

$19.23/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a global leader in biopharmaceutical development and manufacturing, we empower life science ... The In-Process Support Associate will be trained to execute analytical test methods and their ...

IQVIA

Associate Business Development Director

Durham, NC

$89K - $250K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

KBI Biopharma, Inc.

In Process Research Associate

Durham, NC

$19.23/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a global leader in biopharmaceutical development and manufacturing, we empower life science ... The In-Process Support Associate will be trained to execute analytical test methods and their ...

AskBio

Process Engineer II

Durham, NC · On-site

... Associate Director, MSAT. Job Responsibilities * Collaborate with cross-functional teams to transfer small-scale gene therapy processes from Process Development into the MSAT laboratory and ...

AskBio

Process Engineer II

Durham, NC · On-site

... Associate Director, MSAT. Job Responsibilities * Collaborate with cross-functional teams to transfer small-scale gene therapy processes from Process Development into the MSAT laboratory and ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... Mentor junior validation associates in Process Validation, cGMP regulations, and principles of ...

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Process Development Associate information

See Durham, NC salary details

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How much do process development associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for process development associate in Durham, NC is $30.52, according to ZipRecruiter salary data. Most workers in this role earn between $25.05 and $37.45 per hour, depending on experience, location, and employer.

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 are the key skills and qualifications needed to thrive as a process development associate?

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 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 Durham, NC look for? The top searched job categories for Process Development Associate jobs in Durham, NC are:
What cities near Durham, NC are hiring for Process Development Associate jobs? Cities near Durham, NC with the most Process Development Associate job openings:
Process Development Associate jobs near you
Infographic showing various Process Development Associate job openings in Durham, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $63,479 per year, or $30.5 per hour.

Program Integration Associate II

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

Posted 9 days ago

KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Position Summary:
The Program Integration Associate II independently coordinates planning, integration, and execution-readiness activities across process development and CMC programs. The position applies technical and operational knowledge to support facility fit assessments, BOM forecasting, regulatory readiness activities, viral clearance laboratory operations, and external vendor coordination. The Associate II identifies routine risks, coordinates cross-functional deliverables, supports execution of viral clearance studies, and facilitates alignment across stakeholders to ensure successful program execution. Reporting to the Director, Program Integration, this role supports efficient and scalable program execution while independently managing assigned activities and priorities
Position Responsibilities:
  • Coordinate facility fit and cadence assessments by compiling technical and operational inputs, identifying scheduling constraints or resource gaps, and facilitating alignment with functional stakeholders
  • Develop, maintain, and analyze development-stage BOM forecasts to support material planning, identify forecasting gaps, and communicate updates to program stakeholders
  • Coordinate cross-functional deliverables supporting regulatory submissions and program execution activities, ensuring alignment of timelines, priorities, and deliverables
  • Coordinate viral clearance laboratory readiness and study execution activities, including virus spiking, chromatography and viral filtration operations, laboratory scheduling, sample logistics, inventory management, and study documentation
  • Develop and maintain program dashboards, trackers, and metrics used to communicate program status, risks, milestones, and planning activities
  • Coordinate development, review, and maintenance of CMC documentation supporting viral clearance, cell banking, process development, and regulatory submission activities
  • Manage timelines, deliverables, documentation, and communication associated with external viral clearance, MCB, and other development service providers.
  • Maintain and improve standardized templates, repositories, and documentation tools supporting Program Integration and CMC planning activities.
  • Coordinate documentation readiness activities and support responses related to audits, inspections, and regulatory reviews

Minimum Requirements:
  • Bachelor of Science degree in Chemical Engineering, Biochemical Engineering, Biology, Microbiology, Biochemistry, Biotechnology, or related scientific discipline with 2-5 years of relevant experience; or Master's degree with 0-2 years of relevant experience.
  • Working knowledge of biologics development, CMC activities, process development workflows, regulatory submissions, and/or manufacturing operations.
  • Familiarity with GMP, GLP, and regulated documentation environments.
  • Demonstrated ability to coordinate multiple projects, priorities, and deliverables simultaneously with limited supervision.
  • Ability to analyze information, identify risks or gaps, and recommend solutions within established practices.
  • Experience coordinating activities across cross-functional teams.
  • Strong written and verbal communication skills with the ability to effectively communicate technical and operational information.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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