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Msat Process Expert Jobs (NOW HIRING)

Kelly Services

Sr MSAT Engineer

Stafford, TX

$60/hr

Support broader MSAT activities as needed, including process troubleshooting, process assessments ... That means our team of expert Science & Clinical recruiters will have access to your profile ...

ElevateBio

Engineer I, MSAT

Pittsburgh, PA · On-site

$70K - $91K/yr

The primary responsibility is to the be Subject Matter Expert (SME) for manufacturing processes ... Represents MSAT on project teams as technical subject matter expert (SME) for drug product ...

Denali Therapeutics

MSAT Engineer

Salt Lake City, UT · On-site

The MSAT Engineer will be an integral part of Denali's growing GMP manufacturing site in Salt Lake ... Serve as a subject matter expert on process and technology related topics during regulatory ...

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As of Sep 10, 2026, the average hourly pay for msat process expert in the United States is $25.47, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $29.57 per hour, depending on experience, location, and employer.

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Infographic showing various Msat Process Expert 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 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $52,986 per year, or $25.5 per hour.

Sr MSAT Engineer

Stafford, TX

Kelly Services
See more jobs at Kelly Servicesexternal

$60/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 21 days ago

Job description

Senior MSAT Engineer
Kelly® Science & Clinical is seeking a Senior MSAT Engineer for a 12-month contract position at a cutting-edge client in Houston, TX. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay: $60/hour
Schedule: Mon-Fri Day Shift Onsite
Overview
Our client is an industry-leading company at the forefront of cell therapy manufacturing and CMC-GMP operations. This is a unique opportunity to join a cutting-edge organization where you will play a critical role in supporting quality records and PLI inspection readiness within a fast-paced, highly regulated biopharmaceutical environment.
In this role, you will be responsible for owning and driving deviations, investigations, and CAPAs from initiation through closure, while partnering cross-functionally with Manufacturing, QA, and other technical teams. You will apply structured problem-solving methodologies, draft inspection-ready technical documentation, and support broader MSAT activities including process troubleshooting, change controls, and continuous improvement initiatives.
Responsibilities:
  • Own and drive deviations, investigations, and CAPAs from initiation through closure
  • Support execution of PLI-enabling CAPAs and other inspection-readiness quality records
  • Lead root cause analysis, technical impact assessments, and development of corrective actions
  • Draft clear, technically sound, inspection-ready investigation and CAPA documentation
  • Partner with Manufacturing, QA, and other technical functions to drive timely closure of quality records
  • Apply structured problem-solving and risk-assessment methodologies
  • Support broader MSAT activities as needed, including process troubleshooting, process assessments, change controls, manufacturing support, and continuous improvement
Qualifications:
  • Bachelor’s degree in engineering, Life Sciences, or a related technical field
  • 7+ years of relevant biopharmaceutical manufacturing, MSAT, or Process Engineering experience
  • Direct cell therapy manufacturing experience required
  • Strong experience owning deviations, investigations, and CAPAs in a cGMP environment
  • Excellent GMP technical writing and documentation skills
  • Strong root cause analysis and cross-functional problem-solving capability
  • Ability to work independently and manage multiple time-sensitive priorities
Preferred:
  • Autologous cell therapy experience
  • Late-stage, pivotal, or commercial manufacturing/MSAT experience
  • PLI / inspection-readiness experience
  • Veeva or other electronic Quality Management System (eQMS) experience
  • Houston-area based
What happens next:
Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry – even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.