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Process Analytical Technology Scientist Jobs in Boca Raton, FL

Open Scientific

Sr Engineer, Process Development

Sunrise, FL · On-site

$99K - $128K/yr

Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Conduct risk analysis including DFMEA, PFMEA and create/maintain necessary documentation. Support ...

Chewy

Senior Data Scientist

Plantation, FL

$109K - $190K/yr

Conduct exploratory data analysis to uncover patterns, trends, behavioral signals, and ... Familiarity with AWS technologies such as SageMaker, Glue, Athena, Redshift, or Bedrock.

ASR Group

NPD Research Scientist

Boca Raton, FL · On-site

Supports development of pilot plant processes, systems, methods and technologies by keeping ... Hands-on experience of analytical and physical testing methodologies within food industry ranging ...

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All JobsProcess Analytical Technology Scientist JobsProcess Analytical Technology Scientist Jobs in Boca Raton, FL

Process Analytical Technology Scientist information

See Boca Raton, FL salary details

$20

$39

$61

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

As of Aug 9, 2026, the average hourly pay for process analytical technology scientist in Boca Raton, FL is $39.93, according to ZipRecruiter salary data. Most workers in this role earn between $29.90 and $46.06 per hour, depending on experience, location, and employer.

What are some typical challenges faced by process analytical technology 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?

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 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 Boca Raton, FL? For Process Analytical Technology Scientist jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Process Analytical Technology Scientist jobs in Boca Raton, FL look for? The top searched job categories for Process Analytical Technology Scientist jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Process Analytical Technology Scientist jobs? Cities near Boca Raton, FL with the most Process Analytical Technology Scientist job openings:
Process Analytical Technology Scientist jobs near you

Associate Director/Director, CMC Analytical Development, Separation

Syncromune

Fort Lauderdale, FL • On-site, Remote

$165K - $200K/yr

Full-time

Re-posted 15 days ago

Job description

The Associate Director/Director of CMC Analytical Development will oversee the execution of the analytical strategy for drug substance and drug product development across all phases of clinical development and commercialization. This role is responsible for overseeing method development, validation, transfer, and lifecycle management to ensure compliance with regulatory requirements and alignment with company objectives.
Principal Duties and Responsibilities include the following:
  • Define and implement analytical development strategies to support CMC programs from early development through commercialization.
  • Provide technical leadership in analytical sciences, including chromatography, spectroscopy, and characterization techniques.
  • Guide analytical development activities at CDMO and CTL, including method development, optimization, transfer, validation, troubleshooting, and lifecycle management for GMP test methods for DS and DP.
  • Guide extended characterizations in support of comparability and regulatory applications.
  • Foster collaboration with cross-functional groups including Process Development, Quality, and Regulatory Affairs.
  • Author and review analytical sections of regulatory submissions (IND, IMPD, NDA, BLA).
  • Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities.
  • Drive continuous improvement and innovation in analytical technologies and processes.
Supervisory Responsibilities:
  • Indirect Reports: supervise CDMO, CTL, and external resources (such as consultants)
Qualification Requirements:
Education:
  • Ph.D. or M.S. degree in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
Experience:
  • Must have 8+ years of pharmaceutical or biotechnology industry experience specializing in analytical development.
  • Must have working knowledge of cGMP, ICH, and regulatory guidelines.
  • Must have hands-on experience managing global CTLs and CDMOs.
  • Must have strong technical expertise in separation science, such as liquid chromatography or mass spectrometry.
  • Must have strong technical experience in at least one of the modalities: monoclonal antibody and/ or oligonucleotide.
  • Must have experience in method development, validation, and lifecycle management for QC methods.
  • Good to have experience in complex drug products, such as co-formulation, multi-components, conjugates, etc.
  • Good to have experience in extended characterization & comparability studies to support BLA submission.
  • Good to have experience in authoring technical and scientific documents for regulatory submissions, including IND and BLA filings.
  • Good to have late phase experience, such as PPQ and commercialization.
  • Candidates proficient in both English and Mandarin are highly encouraged to apply.
  • Ability to work in a fast-paced virtual environment.
  • Flexibility to travel domestically and internationally as required.
  • Excellent communication, leadership, organizational and project management skills.
Working Conditions:
  1. Specify work environment:
  • Work from home.
  • Domestic and international travel up to 25%.
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range for Assoc Director and Director levels: $165-$245K
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
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