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Full Time Msat Engineer Jobs in California (NOW HIRING)

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$117K - $152K/yr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Provide technical mentorship and guidance to junior MSAT engineers and manufacturing specialists ...

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$117K - $152K/yr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Provide technical mentorship and guidance to junior MSAT engineers and manufacturing specialists ...

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$72 - $89/hr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Provide technical mentorship and guidance to junior MSAT engineers and manufacturing specialists ...

Avid Bioservices

Engineer, MSAT Upstream

Tustin, CA · On-site

$95K - $119K/yr

As an Engineer, MSAT Upstream at Avid Bio, you will be the main point of contact for clients and ... This role is a full-time position. Days of work are Monday through Friday. The employee must also ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA · On-site

$103K - $141K/yr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Partner with MSAT to define data extraction and aggregation workflows from EBR, LIMS, and historian ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA · On-site

$72 - $86/hr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Partner with MSAT to define data extraction and aggregation workflows from EBR, LIMS, and historian ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA

$103K - $141K/yr

This position is offered as a contract engagement with eligibility for conversion to full-time ... Partner with MSAT to define data extraction and aggregation workflows from EBR, LIMS, and historian ...

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All JobsMsat Engineer JobsFull Time Msat Engineer JobsFull Time Msat Engineer Jobs in California

Full Time Msat Engineer information

What is a full time MSAT engineer?

A Full Time MSAT (Manufacturing Science and Technology) Engineer is a professional responsible for supporting manufacturing processes by applying scientific and engineering principles to improve product quality, efficiency, and compliance. They work closely with production, quality assurance, and research teams to optimize manufacturing workflows, troubleshoot issues, and implement process improvements. The role often involves data analysis, process validation, technology transfer, and ensuring that manufacturing operations adhere to regulatory standards. MSAT Engineers play a crucial role in industries such as pharmaceuticals, biotechnology, and chemicals, where maintaining high standards in production is essential.

What are some common challenges a full time MSAT engineer faces when working with satellite communication systems?

As a Full Time Msat Engineer, one of the main challenges is ensuring reliable connectivity in diverse and sometimes harsh environments. Engineers must frequently troubleshoot hardware and software issues, manage signal interference, and adapt to evolving satellite technologies. Collaboration with cross-functional teams such as network operations, field technicians, and system architects is essential to address these challenges efficiently. Additionally, staying updated on regulatory changes and industry standards is crucial for maintaining system compliance and performance.

What are the key skills and qualifications needed to thrive as a full time MSAT engineer, and why are they important?

To thrive as a Full Time MSAT (Manufacturing Science and Technology) Engineer, you need a solid background in chemical engineering, biotechnology, or a related field, typically with a relevant degree and experience in process development or manufacturing. Familiarity with process analytical technology (PAT), data analysis tools, and quality management systems is commonly required, along with knowledge of GMP regulations. Strong problem-solving skills, communication abilities, and teamwork are vital soft skills that set top performers apart in this role. These skills and qualifications are crucial for ensuring efficient technology transfer, process optimization, and compliance in pharmaceutical manufacturing environments.

What is the difference between Full Time Msat Engineer vs RF Engineer?

AspectFull Time Msat EngineerRF Engineer
CredentialsBachelor's in Electrical Engineering or related; certifications like RF or microwave certificationsBachelor's in Electrical Engineering or related; certifications in RF or wireless technologies
Work EnvironmentDesign, testing, and deployment of satellite communication systemsDesign, testing, and optimization of radio frequency systems and wireless networks
Industry UsageSatellite communication, aerospace, defenseTelecommunications, wireless service providers, electronics manufacturing

Full Time Msat Engineers focus on satellite communication systems, while RF Engineers work on radio frequency systems across various wireless technologies. Both roles require similar technical credentials and often operate in overlapping industries, but their specific applications and systems differ.

What are the most commonly searched types of Msat Engineer jobs in California?

The most popular types of Msat Engineer jobs in California are:

What cities in California are hiring for Full Time Msat Engineer jobs?

Cities in California with the most Full Time Msat Engineer job openings:

Full Time Msat Engineer jobs near you

Senior Process Engineer, MSAT

GeneFab

Alameda, CA • On-site

$117K - $152K/yr

Full-time

Re-posted 29 days ago

Job description

GeneFab is seeking a highly motivated and technically accomplished Senior Process Engineer, MSAT to serve as a critical technical authority within our Cell and Gene Therapy CDMO. This individual will drive the establishment and maturation of GMP-ready platform processes that form the foundation of our internal manufacturing capabilities, operating with a high degree of autonomy across complex, cross-functional initiatives spanning process development, technology transfer, CMC strategy, and capability buildout.

This role is pivotal in shaping GeneFab's ability to deliver scalable, regulatory-compliant manufacturing platforms that clients can leverage directly in their IND filings and beyond. The Senior Process Engineer will translate scientific insight into robust manufacturing processes while building the infrastructure, capability, and frameworks necessary to support GMP operations at scale. The ideal candidate thrives in a fast-paced, entrepreneurial environment, is energized by building capabilities from the ground up, and brings the independent judgment to drive programs forward.

This position is offered as a contract engagement with eligibility for conversion to full-time employment based on performance, business needs, and mutual alignment. GeneFab is committed to investing in high-performing contributors and views this role as a long-term addition to the organization.

Requirements
  • Lead the GMP implementation of internal platform processes for cell and gene therapy modalities, including upstream and downstream unit operations.
  • Collaborate closely with Process Development to evaluate platform candidates, align on scalable manufacturing approaches, and ensure all platforms are structured to support CMC regulatory expectations for regulatory filings.
  • Serve as a technical lead for technology transfer, validation, and lifecycle management initiatives.
  • Contribute to CMC regulatory submissions by authoring and reviewing CMC module 3 sections, development summaries, and supporting data packages for applicable regulatory filings.
  • Apply deep CMC knowledge to ensure internal platform processes align with current regulatory guidance (FDA, EMA, ICH Q8/Q9/Q10/Q11/Q12) and support the development of CMC content strategies.
  • Serve as an MSAT lead for advanced technology transfer activities, including transfers from external clients and inbound transfers from internal process development groups.
  • Develop and execute comprehensive tech transfer plans including process descriptions, batch records, comparability strategies, and acceptance criteria.
  • Lead the identification, evaluation, procurement, and implementation of GMP manufacturing equipment required to enable platform capabilities and enhance existing capabilities.
  • Author, review, and approve SOPs, work instructions, master batch records, and other GMP-controlled documents for processes and associated equipment.
  • Provide technical oversight during engineering and GMP manufacturing runs to evaluate process reproducibility, identify performance gaps, and drive data-driven continuous improvement initiatives.
  • Function as the MSAT subject matter expert (SME) across cross-functional teams spanning Process Development, Quality, Regulatory and Manufacturing.
  • Provide technical mentorship and guidance to junior MSAT engineers and manufacturing specialists; develop and deliver training materials for platform processes, equipment, necessary systems.
  • Own, drive, and support quality management records, including but not limited to deviations, CAPAs, change controls, SCARs and effectiveness checks.
Qualifications
  • Bachelor's degree in Chemical Engineering, Biochemical Engineering, Bioprocess Engineering, or a closely related life sciences field required; advanced degree (M.S. or Ph.D.) strongly preferred.
  • Minimum 6-8+ years of progressive experience in bioprocess development, MSAT, or GMP manufacturing within the biopharmaceutical or cell and gene therapy industry, commensurate with degree level.
  • Demonstrated expertise in advanced technology transfer, including hands-on leadership of complex tech transfer programs from process development through GMP manufacturing; CDMO or CMO experience highly preferred.
  • Experience in cell therapy (CAR-T, TIL, NK, or similar), gene therapy (AAV, lentiviral, or other viral vectors), or adjacent CGT modalities is highly preferred.
  • Experience supporting IND, IMPD, or BLA filings with the ability to author and critically review CMC sections of regulatory submissions, working knowledge of ICH Q8, Q9, Q10, Q11, and Q12 guidelines.
  • Deep understanding of GMP regulations (21 CFR Parts 210/211/600/610, EU GMP Annex 1/15) as applied to advanced therapy manufacturing; strong command of GMP documentation practices including SOP authorship, batch record design, deviation management, and CAPA.
  • Working knowledge of process characterization, design of experiments (DoE), and data-driven process optimization methodologies; familiarity with analytical methods used to characterize cell and gene therapy products (i.e. identity, potency, purity, safety testing).
  • Demonstrated ability to operate with a high degree of independence, define scope, manage competing priorities, and deliver results in a fast-paced, dynamic environment.
  • Strong technical writing capability with experience authoring SOPs, batch records, validation protocols, deviation reports, and regulatory submission content; excellent cross-functional communication and collaboration skills.
$72 - $89 an hour
About GeneFab 
GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.

We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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