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Process Development Associate Jobs in Lansdale, PA

LEAPSTARR PRODUCTIONS

Client Development Associate

NJ · On-site

Candidates will also be expected to assist the Director of Client Development in daily business ... Must possess the willingness and ability to learn our Company's systems and processes. Additional ...

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Process Development Associate information

See Lansdale, PA salary details

$18

$32

$47

How much do process development associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for process development associate in Lansdale, PA is $32.61, according to ZipRecruiter salary data. Most workers in this role earn between $26.78 and $40.05 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.
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Process Development Associate jobs near you
Infographic showing various Process Development Associate job openings in Lansdale, PA as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 21% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $67,824 per year, or $32.6 per hour.

Process & Analytical Development Specialist

Verismo Therapeutics

Philadelphia, PA • On-site

Full-time

Re-posted 8 hours ago

Job description

Process & Analytical Development Specialist
Full-Time position
Level: Specialist
Location: On-site in Philadelphia PA
Start date: Open
Why Join Verismo?
Our team is small but driven, with the single focus of bringing life-changing cell therapies to patients with cancer. With a solid pipeline built around a novel KIR-CAR platform, our technology has found a way to circumvent the barriers in solid cancer where other CAR therapies have limited success. KIR-CARs eliminate the artificial chimeric constructs within T cells and instead use a natural NK-cell derived signaling system. This system is potent against both hematologic and solid tumors, and in preclinical models is superior to current CAR-T in conferring long-term sustained anti-tumor function to overcome the challenges posed in solid cancer. We have a strong team for CMC, clinical product manufacture, and clinical investigators already established and moving fast to bring KIR-CARs to patients in need.
Our company is comprised of individuals who each bring something unique to the table and are valued for their contributions. Our culture is based on the concept of 'love what you do' and the dedication that builds a team where people do their best and support one another. Because we believe our people are our greatest asset, career development is an important aspect of our investment in our team and we encourage work/life balance.
About the Position:
We are seeking a passionate and skilled Process & Analytical Development Specialist to join our growing CMC team. In this role, you will play a pivotal role in advancing Verismo's cell therapy products by supporting process and analytical development activities. Reporting directly to the Senior Manager of Process Development, you will contribute hands-on expertise to scale up processes, analyze data, and support tech transfers to external manufacturing partners.
Essential Duties & Responsibilities:
  • Contribute to the setup and organization of Verismo Therapeutics' process and analytical development capabilities.
  • Execute complex development studies (with multiple experiment sets) related to process development and scale-up, ensuring studies balance time and resources.
  • Apply Quality by Design (QBD) principals to process development, characterization, establish process parameters, and contribute to CMC regulatory filings.
  • Support next generation manufacturing processes and analytics for cell therapy and lentiviral vector
  • Author technical and scientific documents including but not limited to SOPs, Master Batch Records, study protocols and reports.
  • Ensure all documentation and reports are accurate, complete, and suitable for support of development, characterization, and regulatory approval of products.
Preferred Experience & Abilities:
  • Experience in a cGMP manufacturing and/or QC setting or process and/or analytical development laboratory
  • Background in cell processing, scale up and tech transfer
  • Working knowledge of analytical tools commonly utilized in cell therapy manufacturing
  • Familiarity with quality by design (QbD) approaches and design of experiment (DoE) based studies
  • Ability to function in a dynamic environment.
  • Knowledge of GMP regulations as it pertains to best practices in cGMP manufacturing
  • Experience with Good Documentation Practices (GDP)
Qualification Requirements:
Bachelor's degree in a scientific field with at least 2 years of relevant experience.

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