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Hourly Msat Process Engineer Jobs (NOW HIRING)

Syner-G

Sr. Process Engineer

Newark, DE · On-site

$101K - $131K/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 · On-site

$101K - $131K/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

$101K - $131K/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 ...

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 ...

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 ...

DivIHN

Process Engineer Pharmaceuticals I

NC · On-site

Process Engineer Pharmaceuticals I Duration: 7+ Months Location: Research Triangle Park, NC Only W2 ... and MSAT staff. The contractor will contribute to the timely completion of manufacturing and ...

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All JobsHourly Msat Process Engineer Jobs

Hourly Msat Process Engineer information

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$49.5K

$92K

$142.5K

How much do hourly msat process engineer jobs pay per year?

As of Jun 12, 2026, the average yearly pay for hourly 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 are the key skills and qualifications needed to thrive as an Hourly MSAT Process Engineer, and why are they important?

To thrive as an Hourly MSAT Process Engineer, you need a strong background in chemical or biochemical engineering, process troubleshooting, and operational support, usually backed by a relevant engineering degree. Familiarity with process control systems, data analysis tools, and GMP (Good Manufacturing Practice) regulations is typically required. Excellent problem-solving, communication, and teamwork skills set standout professionals apart in this role. These capabilities are crucial for ensuring efficient, compliant manufacturing and driving continuous process improvements in a dynamic environment.

What is the difference between Hourly Msat Process Engineer vs Msat Process Technician?

AspectHourly Msat Process EngineerMsat Process Technician
CredentialsTypically requires a bachelor's degree in engineering or related fieldOften requires technical diploma or associate degree
Work EnvironmentDesign, optimize, and oversee manufacturing processes in cleanroom settingsOperate and maintain equipment, perform routine process tasks
Employer & Industry UsageUsed in semiconductor manufacturing companies, especially in solar and electronics sectorsCommonly employed in similar manufacturing environments for process support

The Hourly Msat Process Engineer focuses on process development and optimization, often requiring higher education, while the Msat Process Technician handles routine operations and equipment maintenance. Both roles are essential in solar cell manufacturing, but they differ in responsibilities and qualifications.

What is an Hourly Msat Process Engineer?

An Hourly Msat Process Engineer is a technical professional responsible for monitoring, optimizing, and troubleshooting manufacturing processes, typically in the pharmaceutical or biotechnology industry. 'MSAT' stands for Manufacturing Science and Technology, a field focused on bridging the gap between research and manufacturing to ensure consistent product quality and regulatory compliance. Hourly MSAT process engineers often work directly on the production floor, supporting day-to-day operations and implementing process improvements. Their duties may include data analysis, process validation, and ensuring adherence to safety and quality standards. This role requires strong analytical skills, attention to detail, and knowledge of Good Manufacturing Practices (GMP).

What are some of the day-to-day challenges faced by an Hourly Msat Process Engineer, and how can new hires prepare for them?

Hourly Msat Process Engineers often encounter challenges related to maintaining process consistency, troubleshooting equipment issues, and ensuring product quality within strict timeframes. New hires should be ready to quickly adapt to changing production schedules and work collaboratively with both operations and quality assurance teams. Familiarity with data analysis tools and a proactive approach to problem-solving are essential for success in this dynamic environment. Gaining hands-on experience with manufacturing processes and developing strong communication skills will help new engineers excel in this role.
More about Hourly Msat Process Engineer jobs
What cities are hiring for Hourly Msat Process Engineer jobs? Cities with the most Hourly 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 Hourly Msat Process Engineer jobs? States with the most job openings for Hourly Msat Process Engineer jobs include:
What job categories do people searching Hourly Msat Process Engineer jobs look for? The top searched job categories for Hourly Msat Process Engineer jobs are:
Hourly Msat Process Engineer jobs near you
Infographic showing various Hourly Msat Process Engineer job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, and 99% Full Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Principal Engineer - Global MSAT, Site based, Redmond, WA

Cyprotex

Redmond, WA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

Job Title: Principal Process Engineer - Global MSAT
About Us: this is who we are
At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated.
Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge, ...in our journey
We're looking for a passionate and curious Principal Process Engineer to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.
As a Principal Process Engineer at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team.
Just is seeking a highly motivated Principal Process Engineer in Global MSAT team that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to provide project leadership for late-stage molecule process transfer / tech transfer for clinical and commercial biologics manufacturing, including the support for development and maintenance of technical documentation for process control and validation strategies.
The selected candidate as part of the Global MSAT Tech Transfer team is responsible for supporting the implementation of network alignment strategy and creation of global templates/documentation for Tech transfer/New Product introduction across JUST Evotec Manufacturing network. The team member will also provide onsite support for new facility or client startup engineering runs and performance qualification runs, assist in generation of relevant regulatory submissions, and provide support for regulatory and site inspections. This role may also include direct reports/management of junior process engineers.
What You'll Do:
  • Project Lead for technology transfer of a Late-Stage molecule/ commercial manufacturing and/or PPQ campaign support.
  • Lead site to site Tech Transfer activities
  • Lead technology transfer activities ensuring gap analysis/risks assessments are performed and mitigation plans are in place and ensuring design spaces (PAR & NOR ranges) are built for critical process parameters for validation and support of late stage/commercial manufacturing operations.
  • Support development, review and approval of technical documentation including global protocols for performance qualifications, batch records, and reports related to engineering, GMP and PPQ runs.
  • Lead the development and implementation templates for Process Validations and Continued Process Verification strategies.
  • Lead the analysis of process data including annual periodic reviews across the network of Manufacturing sites.
  • Develop Process transfer document and or Process Control strategy for phase III and commercial programs for receiving sites across the MFG network.

Who You Are:
  • Bachelor's degree in engineering science or related program with 12+ years relevant experience or 8+ years of relevant experience with an MS.
  • Considered a subject matter expert in cell culture biopharmaceutical manufacturing and or development of cell culture processes including perfusion technologies, single use bioreactor operations, and scale-up strategies (Upstream)
  • Considered a subject matter expert in downstream processing, including downstream process chromatography and specifically continuous chromatography, large scale column packing, viral filtration, and tangential flow filtration, but also knowledgeable in single-use bioreactors and perfusion technology. (Downstream)
  • Experienced in leading technology transfer and process validation activities for late-stage clinical manufacturing and commercial qualification PPQ campaigns/ commercial campaign support.
  • Understanding of GMP concepts and quality systems necessary to execute process transfer and process validation activities.
  • Experience developing and providing oversight to continuous process monitoring strategies and process validation status throughout commercial lifecycle.
  • Apply manufacturing process lifecycle management principles for establishment and continuous improvement of process control strategy.
  • Experience authoring regulatory CMC documents, coordinating responses to health authority questions, and providing inspection support.
  • Solid background in statistical analysis
  • Significant experience with process risk assessment tools (e.g. FMEA), and facilitating risk assessments.
  • Working knowledge of manufacturing process equipment, DeltaV automation systems, and Manufacturing Execution Systems
  • Candidate must possess strong focus on quality and attention to detail as well as effective task/ time management organizational skills
  • Strategic mindset, ability to organize, analyze/interpret, and effectively translate upstream expertise into global procedures/templates
  • Demonstrated skill managing and mentoring direct reports.

Additional Preferred Qualifications:
  • Recognized technical mastery of either upstream or downstream operations and continuous processing bench-scale through commercial manufacturing scale.
  • Knowledge and expertise to solve complex technical problems; may apply novel approaches that provides significant technology advancement.
  • Experience leading technical projects with external collaborators and vendors
  • Ability to navigate global regulatory CMC documents.
  • High level of demonstrated initiative, exhibit flexibility in work approach, and demonstrate strong follow through and accountability.

Why Join Us:
  • Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow.
  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This role is site based.
  • Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged.
  • Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
  • A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them.

Are You Still Curious?
If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you-and how it will shape the future of Just Evotec Biologics.
Let your curiosity guide your career-#BeCurious and explore the endless possibilities at Just Evotec Biologics!
The base pay range for this position at commencement of employment is expected to be $155,000 to $172,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

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