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Full Time Msat Process Engineer Jobs (NOW HIRING)

Lyell Immunopharma

Director, MSAT

Bothell, WA · On-site

Optimize the MSAT process support model to ensure all Manufacturing operations are supported ... BA/BSc in biochemistry, chemical engineering, bioengineering, or related scientific field with a ...

Syner-G

Sr. Process Engineer

Wilmington, DE · On-site

$100.90K - $130.50K/yr

Acting as a key technical partner to MSAT, Manufacturing, QA, and Engineering, this individual will drive process robustness, efficiency, and compliance across client programs. WORK LOCATION: Travel ...

Syner-G

Sr. Process Engineer

Newark, DE

$101.70K - $131.50K/yr

Acting as a key technical partner to MSAT, Manufacturing, QA, and Engineering, this individual will drive process robustness, efficiency, and compliance across client programs. WORK LOCATION: Travel ...

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Full Time Msat Process Engineer information

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$49.5K

$92K

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How much do full time msat process engineer jobs pay per year?

As of May 28, 2026, the average yearly pay for full time msat process engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Msat Process Engineer vs Full Time Semiconductor Process Engineer?

AspectFull Time Msat Process EngineerFull Time Semiconductor Process Engineer
CredentialsBachelor's in Engineering or related field, certifications in process engineeringBachelor's or higher in Electrical, Chemical, or Materials Engineering, certifications in process or manufacturing
Work EnvironmentCleanroom manufacturing, R&D labs, production facilitiesCleanroom fabs, R&D labs, manufacturing plants
Industry UsagePrimarily in semiconductor manufacturing, especially in MSAT (Manufacturing Science and Technology)Broader semiconductor industry, including fabrication, testing, and assembly

While both roles focus on process optimization within semiconductor manufacturing, the Full Time Msat Process Engineer specializes in manufacturing science and technology processes, often emphasizing process development and troubleshooting. The Full Time Semiconductor Process Engineer has a broader scope, covering various fabrication and process steps across the semiconductor industry. Both roles require similar technical skills and work in cleanroom environments, but their specific focus areas differ slightly.

More about Full Time Msat Process Engineer jobs
What cities are hiring for Full Time Msat Process Engineer jobs? Cities with the most Full Time Msat Process Engineer job openings:
What are the most commonly searched types of Msat Process Engineer jobs? The most popular types of Msat Process Engineer jobs are:
What states have the most Full Time Msat Process Engineer jobs? States with the most job openings for Full Time Msat Process Engineer jobs include:
What job categories do people searching Full Time Msat Process Engineer jobs look for? The top searched job categories for Full Time Msat Process Engineer jobs are:
Full Time Msat Process Engineer jobs near you
Infographic showing various Full Time Msat Process Engineer job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 82% Full Time, and 17% Part Time. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.
Process Engineer, Process Development

Process Engineer, Process Development

Kyverna Therapeutics

Emeryville, CA • On-site

$135K - $150K/yr

Full-time

Posted 24 days ago

Job description

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what's possible.

Position Overview

Kyverna is seeking a hands-on Process Engineer to support process development for autologous CAR T cell products. The role will focus on developing, optimizing, and transferring upstream and downstream processes to GMP.  Process development will focus on closing and automating product formulation and fill/finish steps, and integration with robotics systems. This individual designs experiments supporting these ends and creates objectives to support the company's goals. The role requires strong partnership with functions within technical operations including Analytical Development, Quality, and Manufacturing, and with other internal and external stakeholders. The ideal candidate will leverage their experience in cell therapy process development and partner cross-functionally with MSAT, manufacturing, analytical development, and quality to enable robust, GMP-ready processes.

Department: Technical Development
Location: Emeryville, CA (On-site) 
Reports To: Sr. Director, Process Development

Responsibilities
  • Lead design, optimization and technical execution of process development activities for autologous CAR T cell workflows (cell isolation, activation, transduction/transfection, expansion, harvest, formulation, cryopreservation).
  • Develop and implement automated formulation and fill/finish processes for cell therapy drug product, including closed-system and aseptic considerations.
  • Support the integration and validation of robotics platforms with cell processing steps as process subject matter expert.
  • Design experiments, run bench- and pilot-scale studies, maintain accurate lab notebook entries, analyze data, and generate technical reports.
  • Draft and maintain process documentation including process descriptions, process control strategies, bill of materials, and standard operating procedures.
  • Maintain accurate documentation (protocols, batch records, risk assessments, CAPAs) consistent with regulatory and GMP standards.
  • Support technology transfer to MSAT and manufacturing, including development of manufacturing instructions, equipment requirements, training materials, and execution support.
  • Work with analytical development and quality control to define in-process controls, release testing, and associated acceptance criteria.
  • Support equipment qualification, process validation, and troubleshooting in GMP environments.
  • Participate in cross-functional project teams and present technical updates to stakeholders.
Qualifications
  • BS in Chemical, Biomedical, Biological Engineering, or related field  and 8 years experience in process development for cell therapy products; direct experience with autologous CAR T highly preferred.
  • MS in Chemical, Biomedical, Biological Engineering, or related field (MS preferred) and 6 years experience in process development for cell therapy products; direct experience with autologous CAR T highly preferred..
  • Practical experience designing and executing cell culture/expansion and formulation processes for cell therapy drug products.
  • Hands-on experience with automation of formulation and fill/finish steps; familiarity with closed-system processing and aseptic fill technologies.
  • Knowledge of GMP requirements, technology transfer practices, and manufacturing support (MSAT).
  • Strong data analysis skills and proficiency with experimental design, statistical analysis, and process characterization.
  • Excellent technical writing skills for protocols, reports, and process transfer packages.
  • Experience with specific automated platforms (e.g., CliniMACS Prodigy, CTS Rotea, CTS Compleo, GatheRex, GE WAVE, Dynaselect) or robotic solutions.
  • Experience integrating robotics and automation systems (e.g., liquid handlers, robotic arms, automated incubators/bioreactors) into bioprocess workflows.
  • Strong problem-solving and troubleshooting capability in laboratory and pilot-scale environments.
  • Collaborative team player with demonstrated ability to work cross-functionally with MSAT, manufacturing, analytical, QA, and RegCMC.
  • Effective communicator-able to present complex technical concepts clearly to scientific and non-scientific stakeholders.
  • Organized, detail-oriented, able to manage multiple priorities and project timelines.
  • Comfortable working in dynamic, fast-paced biotech environments.

The salary range for this position is from $135,000. To $150,000. USD annually. This salary range is an estimate of what we reasonably expect to pay for this posted position, and the actual salary may vary based on various factors, including without limitation individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.  This position is also eligible for bonus, benefits, and participation in Company's stock plan.

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