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Full Time Msat Process Engineer Jobs (NOW HIRING)

Evotec

Process Engineer 2

Redmond, WA · On-site

Process Engineer II Location: Redmond, WA Department ... Global MSAT Reports To: Director, GMSAT About Us: this is who we are At Just Evotec Biologics , we ...

Evotec

Process Engineer 2

Redmond, WA · On-site

Process Engineer II Location: Redmond, WA Department ... Global MSAT Reports To: Director, GMSAT About Us: this is who we are At Just Evotec Biologics , we ...

Evotecgroup

Process Engineer 2

Redmond, WA · On-site

Process Engineer II Location: Redmond, WA Department ... Global MSAT Reports To: Director, GMSAT About Us: this is who we are At Just Evotec Biologics , we ...

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

As of Aug 23, 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 August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

MSAT Bioprocess Engineer III / IV

Theradaptive

Frederick, MD • On-site

Full-time

Posted 23 days ago

Job description

Theradaptive is revolutionizing the field of therapeutic delivery with a pipeline of best-in-class products that address multiple global markets. Theradaptive is performing cutting edge science in the area of regenerative medicine, working at the interface of biology and tissue repair.
Our lead therapeutics are in the following indications:
  • Spinal Fusion
  • Long Bone Repair
  • Osteochondral Repair
  • Dental and Facial Bone Repair
  • Immuno-Oncology

We are an innovative, fast-paced team that is advancing a diverse array of cutting-edge translational research projects.
POSITION SUMMARY
Theradaptive is seeking a skilled and driven MSAT Process Engineer III/IV to join our Manufacturing Science and Technology team. This role will provide hands-on technical leadership and manufacturing support for GMP operations, lead deviation investigations and CAPA activities, support process validation and continued process verification (CPV), and partner cross-functionally to advance Theradaptive's combination product pipeline. The successful candidate will bring strong technical judgment, a data-driven approach to problem solving, and the ability to translate process knowledge into robust, compliant, and scalable manufacturing solutions.
Travel requirement: Up to 10%, primarily to support CMO/CDMO technology transfer activities.
RESPONSIBILITIES
GMP Manufacturing Support
  • Serve as the primary technical point of contact for day-to-day GMP manufacturing operations.
  • Monitor real-time manufacturing activities, troubleshoot process issues, and drive timely resolution of technical challenges.
  • Ensure manufacturing processes remain continuously aligned with cGMP requirements and applicable regulatory expectations.

Deviation Management & Investigations
  • Lead and independently author deviation investigations, applying structured root cause analysis (RCA) methodologies (e.g., 5-Why, Fishbone, FTA).
  • Develop and track robust CAPA plans; assess effectiveness and drive closure in a compliant and timely manner.
  • Manage change control activities, evaluating technical impact and ensuring thorough documentation.

Process Validation & Continued Process Verification (CPV)
  • Own and execute process validation activities including Process Performance Qualification (PPQ) protocols and reports.
  • Apply Design of Experiments (DOE) principles to support process characterization, parameter optimization, validation strategy, and establishment of robust process control ranges.
  • Analyze CPV metrics and process datasets to proactively identify trends, risks, and opportunities for improvement.
  • Support product lifecycle management and post-approval change activities.

Technology Transfer
  • Lead or support technology transfer activities between process development, internal GMP manufacturing, and external contract manufacturing organizations (CMOs/CDMOs).
  • Author and review technology transfer plans, batch records, and technical reports to ensure manufacturing readiness.
  • Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations.

GMP Documentation
  • Author, review, and approve GMP documentation including deviations, technical reports, validation protocols/reports, change controls, and SOPs.
  • Maintain high documentation standards consistent with regulatory expectations and internal quality systems.

Cross-Functional Collaboration & Continuous Improvement
  • Partner cross-functionally with Manufacturing, QC, QA, Supply Chain, and Regulatory teams to drive compliant, efficient operations.
  • Champion continuous improvement initiatives and apply process excellence principles to manufacturing performance.
  • Participate in audit and inspection readiness activities, including preparation of technical summaries and subject-matter expert support.

QUALIFICATIONS
  • Bachelor's or master's degree in engineering, Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
  • Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP manufacturing support in biologics or medical devices,
  • Demonstrated ability to independently lead deviation investigations, CAPA development, and change control activities.
  • Hands-on experience with process validation (PV), Process Performance Qualification (PPQ) and CPV programs.
  • Prior involvement in technology transfer activities, including transfers to or from CMO/CDMO partners, preferred.
  • Working knowledge of biologics unit operations, including one or more of the following:
    • Cell culture (mammalian, microbial, or primary cell systems)
    • Downstream purification (chromatography, filtration, centrifugation)
    • Formulation and fill-finish operations
  • Experience with statistical data analysis, SPC charting, and process trending tools.
  • Familiarity with regulatory frameworks including FDA 21 CFR Part 211/600, ICH Q8/Q9/Q10, and ISO standards.
  • Proficiency with GMP documentation systems (electronic or paper-based) and quality management systems (e.g., Track Wise, Master Control).
  • Data-driven problem solver with strong scientific judgment.
  • Clear technical communicator and cross-functional collaborator.
  • Detail-oriented, accountable, adaptable, and improvement-minded.

PHYSICAL DEMANDS
  • Ability to work in classified cleanroom environments and meet all applicable gowning and PPE requirements.
  • Capacity to stand for extended periods and perform repetitive technical tasks in a GMP setting.
  • Ability to lift and handle laboratory equipment and supplies as required.

COMPENSATION RANGE:
$108,000-$139,000 annually, based on qualifications and level.
POSITION LOCATION:
On-site at Theradaptive's corporate headquarters in Frederick, MD.
https://www.theradaptive.com
Theradaptive is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, ethnic or national origin, ancestry, pregnancy (including childbirth or related condition), citizenship, familial status, mental or

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