ZipRecruiter

Log In

1

Msat Engineer Jobs in Washington (NOW HIRING)

Medallia

Medallia Strategy Analytics, Analyst

Mclean, VA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Role As an MSAT Analyst / Senior Analyst, you will apply statistical and analytical ... Collaborate cross-functionally with Sales, Professional Services, Product, and Engineering teams to ...

Valspec

Process Validation Engineer

Rockville, MD · On-site

$70 - $80/hr

This person will partner closely with Manufacturing, Manufacturing Sciences (MSAT), Automation, and ... Provide engineering technical support for assigned process area, specifying equipment and process ...

next page

Showing results 1-20

All JobsMsat Engineer JobsMsat Engineer Jobs in Washington

Msat Engineer information

See Washington salary details

$67.4K

$126.4K

$229.9K

How much do msat engineer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for msat engineer in Washington is $126,434.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,200.00 and $150,100.00 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.

What are popular job titles related to Msat Engineer jobs in Washington?

For Msat Engineer jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Msat Engineer jobs in Washington look for?

The top searched job categories for Msat Engineer jobs in Washington are:

Msat Engineer jobs near you
Infographic showing various Msat Engineer job openings in Washington as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $126,434 per year, or $60.8 per hour.

Senior Process Engineer, Global Manufacturing Science and Technology, Cell Therapy Technical Op[...]

Socket.dev

Gaithersburg, MD • On-site

$96.20 - $144.29/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Job description

ResponsibilitiesDevelopment and Manufacturing Interface
  • Represent Global MSAT in the technology transfer and process characterization teams to ensure successful commercialization of cell therapy products.
  • Communicate Manufacturing Operations needs to the CMC team, ensuring high-quality and timely program deliverables (comparability and validation study completion, etc).
  • Develop PPQ readiness and PPQ execution technical framework for the site MSAT team and oversee execution at the manufacturing sites.
  • Implement proactive process analysis and Continued Process Verification (CPV) strategies across manufacturing sites to ensure continued process understanding and control across all sites.
Lifecycle Management
  • Provide technical oversight across cell therapy manufacturing lifecycle — from pivotal manufacturing technology transfer, process validation, commercialization, and post‑approval.
  • Identify and implement process improvements that increase robustness, cost of goods, plant throughput, and supply continuity.
  • Contribute to post‑approval process optimization initiatives, comparability strategies, ensuring scientific rigor and managing regulatory risks.
  • Proactively identify and mitigate technical and operational risks; ensure standardization across sites and teams.
Regulatory & Quality Support
  • Lead global Change Controls and ensure timely implementation and compliance.
  • Contribute to authoring CMC sections of regulatory submissions — Pivotal INDa, BLA, MAA, and supplements — with high efficiency and optimal content.
  • Partner with quality and regulatory to maintain full compliance with cGMP, ICH guidelines, and global regulatory expectations.
  • Develop and defend sound scientific justifications for the integrated control strategy and lifecycle changes.
Cross‑Functional Partnerships
  • Late‑Stage Process Development – provide MSAT input for process definition, improvements, and process characterization.
  • Site MS&T – partner to ensure timely implementation of process changes and improvements at the sites.
  • Quality – ensure process compliance and product quality standards.
  • Supply Chain – inform long‑range supply planning and risk mitigation.
Qualifications
  • Education: B.S. or M.S. or Ph.D. in Chemical/Biochemical/Biomedical Engineering, Bioengineering, Biochemistry, Biotechnology, Cell Biology, or a closely related discipline. Advanced degree preferred.
  • Experience: Ph.D. with 1+ years; OR M.S. with 5+ years, OR B.S. with 7+ years of relevant cell therapy/biologics/vaccines industry experience in technical development, MS&T, or CMO management areas.
  • Technical and hands‑on expertise in cell therapy manufacturing processes and technologies is highly desirable. Experience in viral vectors, vaccines, or biologics will be considered.
  • Background in GMP manufacturing operations and technology transfer.
  • Experience in process validation and CPV desired.
  • Experience in authoring CMC sections for major regulatory filings (INDa, BLA, MAA) and regulatory inspections.
  • High standards of quality, accountability, and urgency — with the resilience to thrive in a fast‑paced cell & gene therapy field.
Benefits

The annual base pay for this position ranges from $96,196.80 - $144,295.20. Our positions offer eligibility for various incentives—an opportunity to receive short‑term incentive bonuses, equity‑based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Equal Employment Opportunity

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics.

#J-18808-Ljbffr

Apply