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Full Time Msat Process Engineer Jobs in New York

Jj

Senior Cryopreservation Process Engineer

Raritan, NJ · On-site

Process Engineering Job Category: Scientific/Technology All Job Posting Locations: Raritan, New ... By collaborating with various other functions (MSAT, R&D, Engineering, quality assurance, quality ...

David Protein

Process Engineer

New York, NY · On-site

Role Overview: Provide process and engineering support across all business units and brands ... Benefits Practicalities: * Full-time, in-office role based in New York City. We work onsite five ...

AVTC Group

Manufacturing Process Engineer

Riverdale, NJ · On-site +1

$73K - $98K/yr

Manufacturing Process Engineer All Qualified candidates will be responded to in 24 hours or less ... Six Sigma certification a plus (Green belt or Black belt preferred) Employment type: Full Time - ...

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Full Time Msat Process Engineer information

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.

What is a full time Msat process engineer?

A full-time MSAT (Manufacturing Science and Technology) process engineer is responsible for developing, optimizing, and maintaining manufacturing processes for semiconductor or pharmaceutical products. They analyze process data, troubleshoot issues, and implement improvements to ensure product quality and efficiency, often using tools like statistical analysis and process control. This role typically requires a strong background in engineering, chemistry, or related fields, and may involve working in cleanroom environments or manufacturing facilities.

What are the most commonly searched types of Msat Process Engineer jobs in New York?

The most popular types of Msat Process Engineer jobs in New York are:

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For Full Time Msat Process Engineer jobs in New York, the most frequently searched job titles are:

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Full Time Msat Process Engineer jobs near you
Infographic showing various Full Time Msat Process Engineer job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Senior Manager/Associate Director, MSAT/Process Characterization and Validation Readiness (AAV)

Lexeo Therapeutics

New York, NY • Hybrid

$158K - $205K/yr

Full-time

Re-posted 15 days ago

Job description

Role Summary  

The Senior Manager/Associate Director, MSAT/Process Characterization and Validation Readiness will lead AAV process characterization, technology transfer, control strategy development, and PPQ readiness activities across Sf9/baculovirus and HEK-based manufacturing platforms. This role will partner closely with internal CMC functions and CDMOs to ensure late-stage manufacturing processes are robust, well characterized, and ready for clinical and commercial execution. 

Primary Responsibilities
  • Lead risk-based process characterization strategies and studies for AAV manufacturing processes using Sf9/baculovirus and HEK-based platforms
  • Evaluate process robustness, critical process parameters, process performance, and product quality attributes to support control strategy development
  • Translate development, engineering, and manufacturing data into technical conclusions that support validation readiness, PPQ planning, and regulatory documentation
  • Partner with Process Development, Analytical Development, Manufacturing, Quality, Regulatory, and CDMO teams to align study design, execution, documentation, and deliverables
  • Support technology transfer, manufacturing readiness, FMEA activities, comparability assessments, and process validation planning
  • Author and review protocols, reports, technical summaries, regulatory sections, batch record inputs, and manufacturing support documents
  • Lead technical troubleshooting and continuous improvement activities as appropriate
Required Skills & Qualifications
  • Advanced degree in biochemical engineering, bioprocess engineering, molecular biology, cell biology, biotechnology, or related discipline; Master's with a minimum of 7 years relevant experience or PhD with a minimum of 5 years relevant experience
  • Experience in viral vector, gene therapy, biologics, or advanced therapy process development required; AAV experience strongly preferred
  • Demonstrated experience with process characterization, process optimization, scale-up, scale-down models, technology transfer, and validation-readiness activities
  • Working knowledge of upstream and/or downstream AAV manufacturing processes, including Sf9/baculovirus, HEK-based production, bioreactor operations, TFF, chromatography, or formulation preferred
  • Understanding of DoE, Stage 1 Process Design, Stage 2 Process Qualification, PPQ, CPV, validation strategy, and BLA/PAI readiness preferred
  • Strong understanding of process parameters, CQAs, control strategy development, risk assessments, and late-stage CMC decision-making
  • Experience authoring and reviewing technical protocols, reports, regulatory documentation, and manufacturing support documents
  • Demonstrated ability to lead cross-functional work, manage priorities, communicate clearly, and collaborate effectively with internal teams and CDMOs. 
$158,400 - $205,000 a year
Compensation is dependent on qualifications and experience

About LEXEO  

Lexeo Therapeutics is a clinical-stage genetic medicine company headquartered in New York City, pioneering cardiac genetic medicine candidates to treat the root causes of inherited cardiovascular diseases. Our lead program, LX2006, targets cardiomyopathy associated with Friedreich's Ataxia and anchors a broader pipeline addressing genetically defined conditions such as hypertrophic and arrhythmogenic cardiomyopathies. Backed by a strong financial foundation, Lexeo is positioned to translate groundbreaking science into durable clinical impact.  

Our work culture is a hybrid model with 2 days in the New York City office and 3 days working from home.   

LEXEO Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment. 

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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