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Process Analytical Technology Jobs in Pennsylvania

Lifesteps Inc

Business Process Analyst

Butler, PA · On-site

$55K - $73K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Associates Degree in Business Administration, Management, Information Technology or related field and three 2 years of experience analyzing business processes * Bachelor's Degree in Business ...

Deckers

Lead Process Analyst

Indiana, PA · On-site +1

$55K - $74K/yr

Perform change impact assessments across people, process, technology, data, and organizational ... Strong analytical, critical thinking, and problem-solving skills with the ability to evaluate ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Process Analytical Technology (PAT), Protein Analysis, Proteomics, R Programming, Secondary Ion Mass Spectrometry (SIMS), Spectrometry, Vaccine DevelopmentPreferred Skills: Current Employees apply ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We believe this future starts with a strong foundation of laboratory tools: innovative robotics, process analytical technology (PAT), high-throughput technologies, data science, integrated ...

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Process Analytical Technology information

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How much do process analytical technology jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for process analytical technology in Pennsylvania is $25.54, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $29.62 per hour, depending on experience, location, and employer.

What is Process Analytical Technology (PAT)?

Process Analytical Technology (PAT) is a system used in the pharmaceutical and biotech industries to design, analyze, and control manufacturing processes through the measurement of critical quality and performance attributes. PAT uses real-time data and analytical tools to monitor and optimize production, ensuring consistent product quality and compliance with regulatory standards. By implementing PAT, companies can improve efficiency, reduce waste, and gain better control over manufacturing processes.

How does a Process Analytical Technology (PAT) professional typically collaborate with production and quality assurance teams in a pharmaceutical setting?

PAT professionals work closely with both production and quality assurance teams to ensure real-time monitoring and control of manufacturing processes. They help implement analytical tools and sensors that collect critical data, which is then shared with production teams to optimize process parameters and with quality assurance to maintain compliance and product quality. Regular meetings, data reviews, and troubleshooting sessions are common, fostering a highly collaborative environment where input from multiple departments drives continuous improvement.

What are the key skills and qualifications needed to thrive as a Process Analytical Technology (PAT) specialist, and why are they important?

To thrive as a Process Analytical Technology (PAT) Specialist, you need a strong background in chemistry, chemical engineering, or related sciences, often with a bachelor's or master's degree and experience in pharmaceutical manufacturing or process engineering. Familiarity with analytical instrumentation (e.g., NIR, Raman spectroscopy), data analysis software, and regulatory standards like FDA guidelines is crucial. Strong problem-solving skills, attention to detail, and effective communication enable collaboration across multidisciplinary teams. These competencies ensure robust process monitoring, regulatory compliance, and enhanced product quality in complex manufacturing environments.

What is the difference between Process Analytical Technology vs Process Control Engineer?

AspectProcess Analytical TechnologyProcess Control Engineer
Primary FocusReal-time analysis and monitoring of manufacturing processesDesign and implementation of control systems to regulate processes
Required CredentialsTypically degrees in chemistry, chemical engineering, or related fieldsDegrees in chemical, electrical, or control engineering
Work EnvironmentPharmaceutical, biotech, or manufacturing facilitiesIndustrial plants, manufacturing facilities, automation environments
Industry UsageUsed to ensure quality and compliance in productionUsed to optimize process efficiency and safety

Process Analytical Technology focuses on real-time process monitoring and quality assurance, while Process Control Engineers develop systems to regulate and optimize manufacturing processes. Both roles are essential in manufacturing industries but serve different functions related to process management and quality control.

What are popular job titles related to Process Analytical Technology jobs in Pennsylvania?

For Process Analytical Technology jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Process Analytical Technology jobs in Pennsylvania look for?

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What cities in Pennsylvania are hiring for Process Analytical Technology jobs?

Cities in Pennsylvania with the most Process Analytical Technology job openings:

Process Analytical Technology jobs near you
Infographic showing various Process Analytical Technology job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $53,114 per year, or $25.5 per hour.

Process & Analytical Development Specialist

Verismo Therapeutics

Philadelphia, PA • On-site

Full-time

Re-posted 12 days 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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