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Msat Biotech Jobs (NOW HIRING)

Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for ... The MSAT Engineer will be an integral part of Denali's growing GMP manufacturing site in Salt Lake ...

Provide MSAT support across biologics manufacturing processes , spanning development, technology ... biotechnology) or equivalent; advanced degree preferred. * Experience supporting latestage and/or ...

Position Summary You will lead the MSAT Technical Execution team in the United States. You will ... Advanced degree in engineering, biotechnology or related field. * Experience with technical ...

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Msat Biotech information

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$15

$47

$91

How much do msat biotech jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for msat biotech in the United States is $47.72, according to ZipRecruiter salary data. Most workers in this role earn between $27.40 and $60.58 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an MSAT Biotech professional, and why are they important?

To thrive as an MSAT (Manufacturing Science and Technology) Biotech professional, you need a strong background in biotechnology, bioprocess engineering, or related fields, often supported by a relevant degree. Familiarity with bioprocessing equipment, process analytical technologies (PAT), and regulatory compliance systems such as GMP is crucial. Strong problem-solving skills, attention to detail, and effective cross-functional communication are valuable soft skills in this role. These competencies ensure robust process optimization, regulatory compliance, and successful technology transfer in biotech manufacturing environments.

What are some common challenges faced by professionals in an MSAT (Manufacturing Science and Technology) Biotech role, and how can they be addressed?

Professionals in MSAT Biotech roles often encounter challenges related to process scale-up, technology transfer, and troubleshooting complex manufacturing issues. These challenges require strong problem-solving skills, close collaboration with cross-functional teams such as R&D, Quality, and Manufacturing, and adaptability to evolving technologies. To address these challenges, staying updated on the latest industry best practices, maintaining clear communication channels, and proactively participating in process optimization initiatives are highly beneficial. Building strong relationships across departments also helps in efficiently resolving technical issues and ensuring seamless product delivery.

What is the difference between Msat Biotech vs Clinical Research Associate?

AspectMsat BiotechClinical Research Associate
Required CredentialsBachelor's in Life Sciences, relevant certificationsBachelor's in Life Sciences, clinical research certifications often preferred
Work EnvironmentLaboratories, biotech companiesClinical sites, hospitals, research organizations
Employer & Industry UsageBiotech firms, pharmaceutical companiesContract research organizations, hospitals
Common Search & ComparisonJob roles, responsibilities, qualifications

Msat Biotech and Clinical Research Associate roles share similar educational backgrounds and work environments, but Msat Biotech focuses more on laboratory research and biotech development, while Clinical Research Associates primarily oversee clinical trials at research sites. Understanding these differences helps job seekers find roles aligned with their skills and career goals.

What are MSAT Biotech roles?

MSAT (Manufacturing Science and Technology) Biotech roles focus on supporting and optimizing the manufacturing processes of biotechnological products, such as biologic drugs or vaccines. Professionals in these positions bridge the gap between research/development and large-scale manufacturing, ensuring that processes are efficient, compliant, and scalable. Their responsibilities often include process validation, troubleshooting, technology transfer, and continuous improvement to ensure product quality and regulatory compliance. MSAT teams work closely with engineering, quality assurance, and production departments to resolve technical issues and implement new technologies. These roles are essential for maintaining high standards in biopharmaceutical production.
More about Msat Biotech jobs
What cities are hiring for Msat Biotech jobs? Cities with the most Msat Biotech job openings:
What states have the most Msat Biotech jobs? States with the most job openings for Msat Biotech jobs include:
Infographic showing various Msat Biotech job openings in the United States as of June 2026, with employment types broken down into 2% Internship, 5% As Needed, 77% Full Time, 12% Temporary, 2% Contract, and 2% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $99,248 per year, or $47.7 per hour.
MSAT Engineer

MSAT Engineer

Denali Therapeutics

Salt Lake City, UT โ€ข On-site

Full-time

Medical, Retirement

Posted 27 days ago


Job description

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

The MSAT Engineer will be an integral part of Denali's growing GMP manufacturing site in Salt Lake City, Utah. You will support currently manufactured products and technology transfers of future products in Denali's rapidly expanding large molecule pipeline. The MSAT Engineer will foster an environment that encourages Denali's Core Values, innovation, and continuous improvement.

Key Accountabilities/Core Job Responsibilities:

  • Support recipe authoring and technical content development for GMP manufacturing processes, procedures and reports

  • Assist in technical transfers to enable production of new clinical processes, translating process requirements into the ability to successfully execute manufacturing.

  • Function as a process and technology subject matter expert providing on-the-floor technical support

  • Analyze data to monitor manufacturing in real time, support investigations, perform process monitoring, and optimization

  • Serve as a subject matter expert on process and technology related topics during regulatory inspections

  • Partner with Quality to assess deviations, perform product impact analysis, determine root cause and execute preventive and corrective actions

  • Ability to work intermittent, on-call schedules as needed to support manufacturing

  • Draft, revise and maintain SOPs, protocols and reports that accurately reflect process conditions, equipment configurations and regulatory compliance

  • Execute validation and process improvement studies coordinating execution, process monitoring, sampling, and in-process data collection

  • Coordinate and perform sample preparation, chain of custody, labeling and timely transfer to QC or analytical laboratories

  • Execution of laboratory scale cell culture and purification operations

Qualifications/Skills:

  • Typically requires a Bachelor's degree in Chemical, Mechanical or Biomedical Engineering or a related discipline and 5+ years of engineering-related experience (or a Master's Degree and 3+ years of experience)

  • Ability to travel up to 20% by air and road

  • Physical - must be able to put on specialized gowning, lift and manipulate items over 25 lbs, climb ladders, stand for multiple hours at a time

  • Experience in product/process support within a GMP manufacturing setting

  • Builds trustful and effective relationships with authenticity and humility

  • Confidence to lead through uncertainty in a rapidly changing environment

  • The ability to contribute to a team where employees have a shared purpose and vision; foster a "One Denali" environment

  • Strong self-awareness of the impact communication and working style has on others

  • Proficient oral presentation and written communication skills

Preferred Qualifications

  • BioPharma Industry experience related to protein therapeutics

  • Experience in design and operation of bio-processing technologies (cell culture and purification), with experience with single use technologies

  • Experience in scale-up and tech transfer of bio-processes

  • Direct knowledge of FDA cGMP regulations/requirements for manufacturing clinical biopharmaceuticals

  • Experience with GXP system implementation, procedures, and documentation

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more athttps://www.denalitherapeutics.com/careers

Thiscompensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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