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Process Analytical Technology Scientist Jobs in Raleigh, NC

Pwc

FP&A Tech, Anaplan Director

Raleigh, NC · On-site

$155K - $410K/yr

... making processes. You will analyze financial data, develop performance metrics, and design ... Accounting, Analytics/Data Science, Business Administration/Management, Computer Science ...

Fidelity Investments

Director, Data Science

Durham, NC · On-site

... processing; aggregating time series and transaction tables; creating appropriate features for ... DE analyzing technology solutions for supporting model deployment and integration in Cloud and on ...

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How much do process analytical technology scientist jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for process analytical technology scientist in Raleigh, NC is $40.90, according to ZipRecruiter salary data. Most workers in this role earn between $30.62 and $47.21 per hour, depending on experience, location, and employer.

What are some typical challenges faced by Process Analytical Technology (PAT) Scientists in implementing new analytical tools within manufacturing environments?

Process Analytical Technology Scientists often encounter challenges such as integrating new analytical tools with existing manufacturing systems, ensuring data integrity, and managing cross-functional collaboration between engineering, quality, and production teams. They must also address regulatory requirements and validate new technologies to meet compliance standards. Staying updated on emerging technologies and training staff effectively are crucial for successful implementation and ongoing process optimization.

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

To thrive as a Process Analytical Technology Scientist, you need a strong background in chemistry, chemical engineering, or a related field, often supported by an advanced degree and experience in process development. Familiarity with analytical instrumentation (such as NIR, FTIR, Raman spectroscopy), data analysis tools, and regulatory frameworks like FDA's PAT guidance is crucial. Strong problem-solving, collaboration, and communication skills help bridge the gap between R&D, manufacturing, and quality teams. These abilities ensure that processes are robust, efficient, and compliant, leading to higher product quality and regulatory success.

What does a Process Analytical Technology (PAT) Scientist do?

A Process Analytical Technology (PAT) Scientist is responsible for developing and implementing analytical tools and techniques to monitor and control manufacturing processes, particularly in the pharmaceutical, biotechnology, and chemical industries. Their main goal is to ensure product quality, consistency, and efficiency by collecting real-time data during production. PAT Scientists work closely with engineers, quality assurance teams, and manufacturing staff to optimize processes, troubleshoot issues, and comply with regulatory standards. They also help integrate advanced technologies like spectroscopy, chromatography, and chemometrics into production environments.

What is the difference between Process Analytical Technology Scientist vs Quality Control Analyst?

AspectProcess Analytical Technology ScientistQuality Control Analyst
Required CredentialsBachelor's or Master's in Chemistry, Chemical Engineering, or related field; knowledge of PAT toolsBachelor's in Chemistry, Biology, or related field; focus on testing and analysis
Work EnvironmentPharmaceutical or biotech manufacturing, R&D labs, process developmentQuality control labs, manufacturing facilities, testing environments
Industry UsageUsed in process optimization, real-time monitoring, and process validationUsed for product testing, quality assurance, and compliance

The Process Analytical Technology Scientist focuses on implementing real-time analytical tools to optimize manufacturing processes, while the Quality Control Analyst primarily conducts testing to ensure product quality. Both roles require chemistry-related credentials and work within manufacturing or lab environments, but their core responsibilities differ in scope and purpose.

What are popular job titles related to Process Analytical Technology Scientist jobs in Raleigh, NC? For Process Analytical Technology Scientist jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Process Analytical Technology Scientist jobs in Raleigh, NC look for? The top searched job categories for Process Analytical Technology Scientist jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Process Analytical Technology Scientist jobs? Cities near Raleigh, NC with the most Process Analytical Technology Scientist job openings:
Process Analytical Technology Scientist jobs near you
Infographic showing various Process Analytical Technology Scientist job openings in Raleigh, NC as of June 2026, with employment types broken down into 3% Internship, 3% As Needed, 88% Full Time, 3% Part Time, and 3% Contract. Highlights an 84% In-person, 3% Hybrid, and 13% Remote job distribution, with an average salary of $85,075 per year, or $40.9 per hour.
In Process Research Associate

In Process Research Associate

KBI Biopharma, Inc.

Durham, NC • On-site

$19.23/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position Summary:
We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally.
The In-Process Support Associate will be trained to execute analytical test methods and their corresponding analytical techniques. The In-Process Support Associate will complete data analysis and/or perform data integrity review of STAT samples, which support manufacturing operations. Additionally, when time permits, QC testing will be executed for Release and in-process samples.
*This position will primarily work 1st shift hours, but night/weekend/holiday work will sometimes be required. Off-shift coverage is assigned to team members as-needed on a rotating basis.
Position Responsibilities:
  • Performs testing on in-process or drug substance/drug product using bio-analytical techniques such as (but not limited to) HPLC, UV-Vis and simple compendial testing. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals
  • Makes detailed observations and carries out elementary data analysis
  • Understand experiments, conducts troubleshooting analysis, and maintains knowledge of instrumentation
  • Documentation (i.e. Notebook and Worksheet) upkeep and writing skills
  • Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature
  • Assures proper labeling, handling, and storage of all chemicals used in the area, assures proper labeling and disposition of hazardous waste in satellite area; adheres to all safety requirements and follows safety procedures, and attends all required safety and health training, including handling hazardous waste
  • Reacts to change productively and handles other essential tasks as assigned

Position Requirements:
  • BS in scientific discipline or equivalent
  • Experience in QC analysis of proteins, antibodies, peptides, or vaccines a plus, but not required
  • Excellent verbal and written communication skills.
  • Experience working in a cGMP environment preferred.

Pay Range: $19.23/hour - 26.44/hour
Pay range provided per current averages and expectations. The pay rate and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting upon hire and employee recognition programs.
About KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com.
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.
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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