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Remote Msat Jobs (NOW HIRING)

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Senior Engineer, Process Validation

Dallas, TX · On-site +1

$100K - $130K/yr

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Senior Engineer, Process Validation

Dallas, TX · On-site +1

$100K - $130K/yr

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

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Showing results 1-20

Remote Msat information

See salary details

$83.5K

$127K

$171K

How much do remote msat jobs pay per year?

As of Jul 21, 2026, the average yearly pay for remote msat in the United States is $127,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $143,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Msat vs Remote Msa?

AspectRemote MsatRemote Msa
Required CredentialsCertifications in medical billing, coding, or related fieldsCertifications in medical billing, coding, or related fields
Work EnvironmentRemote, often from home, with flexible hoursRemote, often from home, with flexible hours
Industry UsageHealthcare, medical billing, and coding companiesHealthcare, medical billing, and coding companies
Common Search/ComparisonRemote MsatRemote Msa

Remote Msat and Remote Msa are similar roles in healthcare billing, both requiring certifications in medical billing or coding. They are typically performed remotely from home and are used within healthcare organizations and billing companies. The main difference lies in the specific job functions: Msat often focuses on insurance claims processing, while Msa may involve more administrative or support tasks. Both roles are in high demand for remote healthcare billing professionals.

What are the key skills and qualifications needed to thrive as a Remote Manufacturing Science and Technology (MSAT) Specialist, and why are they important?

To thrive as a Remote MSAT Specialist, you need a strong background in chemical engineering, biotechnology, or a related field, with experience in process development and manufacturing support. Familiarity with process analytical technology, data analysis tools (like JMP or Minitab), and knowledge of regulatory systems (such as GMP) are typically required. Excellent problem-solving abilities, clear written and verbal communication, and the capacity to collaborate across remote teams are vital soft skills. These competencies enable effective troubleshooting, ensure process compliance, and drive continuous improvement in a virtual manufacturing environment.

What are some common challenges faced by Remote MSAT professionals, and how can they be addressed?

Remote MSAT (Manufacturing Science and Technology) professionals often encounter challenges such as limited on-site access to manufacturing facilities, which can make troubleshooting and process optimization more complex. Effective communication and collaboration with on-site teams are crucial to bridge this gap. Utilizing digital tools for virtual monitoring and regular video meetings helps maintain strong team dynamics and ensures timely support for manufacturing operations. Proactively seeking feedback and maintaining clear documentation also contribute to overcoming remote work obstacles in this highly collaborative environment.

What are Remote MSAT jobs?

Remote MSAT jobs refer to positions in Manufacturing Science and Technology (MSAT) that can be performed remotely, outside of a traditional office or laboratory setting. MSAT professionals typically focus on improving manufacturing processes, ensuring product quality, and supporting technology transfer in biopharmaceutical or pharmaceutical production. Remote MSAT roles often involve data analysis, process optimization, troubleshooting, and collaboration with onsite teams using digital tools. These roles are ideal for professionals who have strong technical backgrounds and are comfortable working independently while staying connected with remote teams. While some onsite presence may be required for specific tasks, many MSAT functions can be effectively managed from a remote location.
More about Remote Msat jobs
What cities are hiring for Remote Msat jobs? Cities with the most Remote Msat job openings:
What are the most commonly searched types of Msat jobs? The most popular types of Msat jobs are:
What states have the most Remote Msat jobs? States with the most job openings for Remote Msat jobs include:
Infographic showing various Remote Msat job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $127,031 per year, or $61.1 per hour.
Senior Engineer, Process Validation

Senior Engineer, Process Validation

Danaher

Houston, TX • On-site, Remote

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 29 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time.

Learn about the Danaher Business System which makes everything possible.

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines.

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote.

In this role, you will have the opportunity to:

  • Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
  • Lead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping.
  • Drive risk-based approaches using tools such as pFMEA, risk ranking, and criticality assessments and apply statistical tools to evaluate process performance, including but not limited to process capability, trend analysis and control charts and DOE) interpretation.
  • Serve as a technical SME for process validation with external clients, across internal teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.
  • Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design

The essential requirements of the job include:

  • Bachelor or master degree in engineering and 5+ years of experience
  • Prior experience in leading process development, engineering, and deliverables across all three stages of process validation in biologics/small and large molecules manufacturing train using statistical analysis, risk assessment, and process improvement tools required.
  • Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
  • Proficiency in technical writing with deviation investigations, root cause analysis, and risk assessments.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 15% to site to support validation project executions, routine inspections, audits, and client visits.

It would be a plus if you also possess previous experience in:

  • Packaging and shipping validation of final product container closure configurations.
  • Client facing roles such as prior experience in a CDMO environment

Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Aldevron we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Aldevron can provide.

The annual salary range for this role is $100,000 to $130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

#LI-PF1

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984