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Full Time Msat Process Engineer Jobs (NOW HIRING)

Abzena Inc.

Process Engineer II/Sr

Bristol, PA · On-site

$101K - $131K/yr

Partner with Manufacturing and MSAT teams to improve process robustness, throughput, yield ... Lead or serve as the Process Engineering technical lead for technology transfer activities from ...

ElevateBio

Engineer I, MSAT

Pittsburgh, PA · On-site

The Role As a Process Engineer for Manufacturing Science and Technology (MSAT), you will provide process science support for GMP manufacturing, technology transfers, development studies ...

Evotecgroup

Principal Process Engineer

Seattle, WA · On-site

Job title: Principal Process Engineer Location: Redmond, WA Reports to: Director, Technical ... Partner with Site MSAT Manufacturing Technology & Science teams on global and site objectives.

Evotec

Principal Process Engineer

Redmond, WA

Job title: Principal Process Engineer Location: Redmond, WA Reports to: Director, Technical ... Partner with Site MSAT Manufacturing Technology & Science teams on global and site objectives.

Evotec

Principal Process Engineer

Redmond, WA · On-site

Job title: Principal Process Engineer Location: Redmond, WA Reports to: Director, Technical ... Partner with Site MSAT Manufacturing Technology & Science teams on global and site objectives.

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Full Time Msat Process Engineer information

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

As of Sep 12, 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.

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.
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Full Time Msat Process Engineer jobs near you
Infographic showing various Full Time Msat Process Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Process Engineer II/Sr

Bristol, PA • On-site

Abzena Inc.
Manufacturing • 51 - 200 employees
Learn more about Abzena Inc.external

$101K - $131K/yr

Full-time

Posted 15 days ago

Key responsibilities

  • Provide advanced process engineering support for GMP manufacturing operations, including troubleshooting and issue resolution.

  • Lead or support technology transfer activities, process scale-up assessments, and manufacturing readiness planning.

  • Serve as a senior technical resource and mentor to process engineers and manufacturing personnel.

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Senior Process Engineer provides advanced process engineering support and technical leadership for GMP manufacturing operations at the Bristol, PA site. Responsibilities include technical leadership of manufacturing campaigns, complex process troubleshooting, technology transfer, process optimization, scale-up, engineering studies, and operational readiness activities.
Reporting to the Director, Process Engineering, the Senior Process Engineer works cross-functionally with Manufacturing, MSAT, Quality, Facilities & Engineering, Supply Chain, and Program Management to support safe, compliant, reliable, and effective manufacturing operations. The role serves as a senior technical subject matter expert, independently leads complex engineering activities, provides technical guidance and mentorship to less experienced engineers, and drives improvements in process performance and reliability within bioconjugation and biologics manufacturing operations.
Responsibilities
Process Engineering & Manufacturing Support
  • Provide advanced process engineering support for GMP manufacturing operations including bioconjugation, chromatography, filtration, formulation, and single-use processing systems.
  • Provide on-floor technical leadership during manufacturing campaigns, including complex troubleshooting, technical decision support, and issue resolution.
  • Partner with Manufacturing and MSAT teams to improve process robustness, throughput, yield, scalability, and execution efficiency.
  • Lead technical investigations related to process deviations, operational issues, and adverse process performance trends, including root cause analysis and corrective action development.
  • Develop and implement process improvements and engineering solutions that enhance operational reliability and reduce recurring manufacturing risk.

Technology Transfer & Scale-Up
  • Lead or serve as the Process Engineering technical lead for technology transfer activities from Process Development into GMP Manufacturing.
  • Lead process scale-up assessments, equipment fit evaluations, engineering studies, and manufacturing readiness planning.
  • Review and provide technical approval or input for manufacturing records, protocols, technical documents, and process instructions to ensure readiness and technical accuracy.
  • Lead or provide technical oversight for process validation, PPQ activities, engineering runs, and process characterization studies.

Technical Leadership & Team Contribution
  • Serve as a senior technical resource and mentor to Process Engineers and manufacturing personnel.
  • Coach less experienced engineers in troubleshooting, technical writing, investigation methodology, and GMP engineering practices.
  • Promote accountability, collaboration, GMP compliance, technical rigor, and continuous improvement across engineering activities.
  • Independently prioritize complex engineering work and support the Senior Manager in coordinating technical activities aligned with manufacturing schedules and site objectives.

Quality & Compliance
  • Ensure assigned engineering activities are executed in compliance with cGMP regulations, internal procedures, and Abzena quality standards.
  • Lead or provide senior technical support for deviations, CAPAs, investigations, change controls, and risk assessments related to process engineering.
  • Participate in regulatory inspections and client audits as a technical SME and support preparation of technical responses.
  • Drive improvements that reduce repeat deviations, strengthen process consistency, and improve technical control of manufacturing processes.

Operational Excellence
  • Analyze process performance metrics, equipment utilization, manufacturing trends, and process capability to identify improvement opportunities.
  • Lead Lean and continuous improvement initiatives focused on process efficiency, waste reduction, throughput, and manufacturing effectiveness.
  • Develop and implement standardized engineering practices, technical tools, and operational improvements across manufacturing operations.
  • Collaborate with Operations leadership to improve schedule adherence, campaign execution reliability, and technical readiness.

Cross-Functional Collaboration
  • Partner closely with Manufacturing, MSAT, Quality, Supply Chain, Facilities & Engineering, and Program Management teams.
  • Support and, when appropriate, lead client-facing technical discussions related to manufacturing execution, investigations, process performance, and improvement plans.
  • Provide technical leadership in campaign planning, operational readiness reviews, and production support activities.
  • Identify and escalate significant technical risks, operational constraints, and process concerns to the Senior Manager, Process Engineering with recommended actions.

Qualifications
  • Bachelor's degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, Biotechnology, or related scientific discipline required.
  • Advanced degree preferred.
  • Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
  • Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
  • Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
  • Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
  • Experience serving as a technical SME during regulatory inspections or client audits preferred.
  • Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
  • Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
  • Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
  • Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
  • Experience serving as a technical SME during regulatory inspections or client audits preferred.

Preferred Qualifications
  • Experience within bioconjugation, ADC, oligonucleotide, or complex biologics manufacturing environments.
  • CDMO experience supporting external clients.
  • Experience supporting startup operations or facility expansions.
  • Lean Six Sigma or continuous improvement experience preferred.

FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

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