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Msat Engineer Jobs (NOW HIRING)

Engineer 3, DPFG MSAT

Holly Springs, NC · On-site

$63K - $81K/yr

The Engineer 3, MSAT DPFG provides technical oversight for routine manufacturing operations, including on-floor support, deviation and root-cause investigations, change control, risk assessments, and ...

Engineer 3, DPFG MSAT

Holly Springs, NC · On-site

$63K - $81K/yr

The Engineer 3, MSAT DPFG provides technical oversight for routine manufacturing operations, including on-floor support, deviation and root-cause investigations, change control, risk assessments, and ...

Engineer 3, DPFG MSAT

Holly Springs, NC · On-site

$63K - $81K/yr

The Engineer 3, MSAT DPFG provides technical oversight for routine manufacturing operations, including on-floor support, deviation and root-cause investigations, change control, risk assessments, and ...

Engineer 3, DPFG MSAT

Holly Springs, NC · On-site

$63K - $81K/yr

The Manufacturing Science and Technology (MSAT) Engineer 3 provides technical leadership across current good manufacturing practice (cGMP) manufacturing, delivering end-to-end support for scale-up ...

Senior Process Engineer, MSAT

Alameda, CA · On-site

$117K - $152K/yr

GeneFab is seeking a highly motivated and technically accomplished Senior Process Engineer, MSAT to serve as a critical technical authority within our Cell and Gene Therapy CDMO. This individual will ...

Senior Process Engineer, MSAT

Alameda, CA

$117K - $152K/yr

GeneFab is seeking a highly motivated and technically accomplished Senior Process Engineer, MSAT to serve as a critical technical authority within our Cell and Gene Therapy CDMO. This individual will ...

GeneFab is seeking a highly motivated and technically accomplished Senior Process Engineer, MSAT to serve as a critical technical authority within our Cell and Gene Therapy CDMO. This individual will ...

This position will serve as a mid-level engineer focused on drug product and process development in the Manufacturing Sciences and Technology (MSAT) department. This engineer will join a team in the ...

For more information, please visit www.resilience.com The Process Engineer III, MSAT independently owns all technical aspects of assigned technology transfers from feasibility through PPQ completion ...

Process Engineer, MSAT

Bedford, MA · On-site

$94K - $125K/yr

This position will serve as a mid-level engineer focused on drug product and process development in the Manufacturing Sciences and Technology (MSAT) department. This engineer will join a team in the ...

Director, MSAT

Walkersville, MD · On-site +1

$205K - $239K/yr

The Director will work closely with Engineering, Manufacturing, Quality, Automation, EHS, and ... Lead the MSAT workstream for an assigned U.S. growth investment project, ensuring successful ...

MSAT Process Engineer

Portsmouth, NH · On-site

$106K - $137K/yr

Summary Lonza is searching for a dynamic Sr. Process Engineer for our Manufacturing Sciences and Technology Department (MSAT) at our Portsmouth, NH facilities. This challenging position is available ...

Director, MSAT

Walkersville, MD · On-site +1

$205K - $239K/yr

The Director will work closely with Engineering, Manufacturing, Quality, Automation, EHS, and ... Lead the MSAT workstream for an assigned U.S. growth investment project, ensuring successful ...

Showing results 21-40

Msat Engineer information

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$59.5K

$111.6K

$203K

How much do msat engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for msat engineer in the United States is $111,632.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $132,500.00 per year, depending on experience, location, and employer.

What is an MSAT engineer?

An MSAT (Manufacturing Science and Technology) Engineer focuses on optimizing manufacturing processes in industries like pharmaceuticals, biotech, and chemicals. They work to ensure product quality, scale-up processes, and technology transfers while troubleshooting production issues. MSAT Engineers collaborate with R&D, production, and quality teams to enhance efficiency, compliance, and cost-effectiveness. Their role is critical in maintaining seamless transitions from development to full-scale manufacturing.

What does an MSAT engineer do?

As an MSAT Engineer, your daily tasks may include monitoring ongoing production processes, analyzing data to troubleshoot deviations, and implementing improvements to enhance product yield or quality. You'll regularly collaborate with cross-functional teams—such as QA, R&D, and production—to ensure seamless technology transfer and compliance with regulatory standards. Additionally, you may prepare reports, support validation activities, and contribute to process scale-up or optimization projects. The role offers a dynamic environment with opportunities to drive impactful process improvements and build expertise across multiple areas of the manufacturing process.

What are the key skills and qualifications needed to thrive as an MSAT engineer?

To excel as an MSAT (Manufacturing Science and Technology) Engineer, a strong background in chemical engineering, biotechnology, or a related field is required, often with experience in process development or manufacturing support. Proficiency with process analytical technology (PAT), statistical analysis software (such as JMP or Minitab), and knowledge of GMP regulations and validation procedures are commonly expected. Excellent problem-solving, communication, and team collaboration skills set top candidates apart in this role. These competencies are crucial for ensuring robust process performance, smooth technology transfers, and continuous improvement within pharmaceutical or biomanufacturing environments.

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Infographic showing various Msat Engineer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $111,632 per year, or $53.7 per hour.

Engineer 3, DPFG MSAT

Fujifilm

Holly Springs, NC • On-site

$63K - $81K/yr

Other

Re-posted yesterday


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 68 frontline employees who took The Breakroom Quiz

50th of 540 rated manufacturers


Job description

Position Overview
The Manufacturing Science and Technology (MSAT) Engineer 3 provides technical leadership across current good manufacturing practice (cGMP) manufacturing, delivering end-to-end support for scale-up, process validation, continued process verification, and continuous improvement. This role drives technology transfer (TT) of new and existing drug product processes into and between sites, ensuring robust process fit, compliant documentation, and readiness through close collaboration with Process Engineering, Quality Assurance (QA), Quality Control (QC), Supply Chain, and Manufacturing. The Engineer 3, MSAT DPFG provides technical oversight for routine manufacturing operations, including on-floor support, deviation and root-cause investigations, change control, risk assessments, and data-driven performance monitoring, ensuring product quality, compliance, and reliable supply.
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: ;br>
Job Description
What You'll Do:
  • Conducts lab and pilot plant experiments
  • Generates and coordinates execution sampling protocols
  • Serves as subject matter expert (SME), leading and conducting troubleshooting, processing impact assessments, and executing root cause analysis (RCA) and corrective and preventive action (CAPA) in response to deviations
  • Executes and analyzes lab and pilot plant work aimed at solving complex manufacturing problems
  • Leads and supports technology transfer (TT) across multiple unit operations
  • Coordinates, plans, and executes manufacturing process validation runs
  • Supports design and leads generation of sampling plans for process validation reports (PVRs) and investigations
  • Writes and reviews master batch records (MBRs) and standard operating procedures (SOPs), as needed
  • Generates and executes process training and consults on topics related to manufacturing and process
  • Leads technical risk assessments for new manufacturing processes
  • Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis aimed at both process monitoring and continued process verification
  • Writes documentation for internal and external use, such as manufacturing campaigns summary reports, process performance qualification (PPQ) protocol and reports, impact assessments etc.
  • Leads training of manufacturing staff and process sciences group on new processes, procedures, and use of equipment in the lab
  • Interprets and utilizes new knowledge to promptly drive data-based decisions
  • Collaborates with the manufacturing department to support commercial and clinical manufacturing campaigns, including on-floor support
  • Leads continuous improvement projects within unit operations, in partnership with manufacturing when applicable, to improve manufacturability, reliability, yield and cost
  • Supports supplier technical evaluations, risk assessments, and raw material evaluation and qualification
  • Performs other duties, as assigned

Minimum Requirements:
  • Associate's degree in Engineering, Life Science or Chemical Engineering with 7 years of applicable industry experience OR
  • Bachelor's degree in Engineering, Life Science or Chemical Engineering with 5 years of applicable industry experience OR
  • Master's degree with 3 years of applicable industry experience
    OR
  • PhD with no prior experience
  • Experience using quality systems (e.g., deviation management system, change control, CAPA, document management system)
  • Experience using risk management and RCA tools

Preferred Requirements:
  • Experience working in a Good Manufacturing Practices (GMP) environment
  • Strong knowledge of regulatory standards and guidance documents for sterile medicinal products
  • Prior Drug Product and manufacturing experience, including process development, validation, and transfer
  • Experience with drug product formulation, sterile filtration including filter validation, isolator filling equipment, single-use systems, qualifying visual inspection including manual and automated, and validating CCIT methods

EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ().

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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