ZipRecruiter

Log In

1

Msat Engineer Jobs in California (NOW HIRING)

Vaxcyte

Staff Engineer, Process Systems

San Carlos, CA · On-site

The Staff Engineer, Process Systems will work closely with Process Development, MSAT, Supply Chain, Quality, Project Management, Business Development, and Regulatory functions, as well as CDMOs. This ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

... engineering run strategies, and regulatory submission readiness. * Drive cross-functional alignment across SynBio, PD, AD, MSAT, QC, and GMP Manufacturing to ensure process consistency, data ...

GeneFab

Program Manager, CRDMO

Alameda, CA

$140K - $200K/yr

... engineering run strategies, and regulatory submission readiness. * Drive cross-functional alignment across SynBio, PD, AD, MSAT, QC, and GMP Manufacturing to ensure process consistency, data ...

Viltis

Be Seen First

Staff Engineer, Downstream Process Development & Manufacturing

San Carlos, CA · On-site

$186K - $218K/yr

Staff Engineer, Downstream Process Development and Manufacturing Location: San Carlos, California ... Associate Director, MSAT - Protein Process Development and Manufacturing, Downstream The ...

Vaxcyte

Staff Engineer, Process Systems

San Carlos, CA · On-site

The Staff Engineer, Process Systems will work closely with Process Development, MSAT, Supply Chain, Quality, Project Management, Business Development, and Regulatory functions, as well as CDMOs. This ...

Bayer

$22 - $24.50/hr

... MSAT) for new product introductions and ensure platform alignment; In this role, you act as the ... Bachelor's degree in a relevant life science or engineering discipline (e.g., Biotechnology, Cell ...

Bayer

$22 - $24.50/hr

... MSAT) for new product introductions and ensure platform alignment; In this role, you act as the ... Bachelor's degree in a relevant life science or engineering discipline (e.g., Biotechnology, Cell ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

... engineering run strategies, and regulatory submission readiness. * Drive cross-functional alignment across SynBio, PD, AD, MSAT, QC, and GMP Manufacturing to ensure process consistency, data ...

previous page

Showing results 41-60

All JobsMsat Engineer JobsMsat Engineer Jobs in California

Msat Engineer information

See California salary details

$58.7K

$110.2K

$200.3K

How much do msat engineer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for msat engineer in California is $110,170.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,400.00 and $130,800.00 per year, depending on experience, location, and employer.

What is an MSAT engineer?

An MSAT (Manufacturing Science and Technology) Engineer focuses on optimizing manufacturing processes in industries like pharmaceuticals, biotech, and chemicals. They work to ensure product quality, scale-up processes, and technology transfers while troubleshooting production issues. MSAT Engineers collaborate with R&D, production, and quality teams to enhance efficiency, compliance, and cost-effectiveness. Their role is critical in maintaining seamless transitions from development to full-scale manufacturing.

What does an MSAT engineer do?

As an MSAT Engineer, your daily tasks may include monitoring ongoing production processes, analyzing data to troubleshoot deviations, and implementing improvements to enhance product yield or quality. You'll regularly collaborate with cross-functional teams—such as QA, R&D, and production—to ensure seamless technology transfer and compliance with regulatory standards. Additionally, you may prepare reports, support validation activities, and contribute to process scale-up or optimization projects. The role offers a dynamic environment with opportunities to drive impactful process improvements and build expertise across multiple areas of the manufacturing process.

What are the key skills and qualifications needed to thrive as an MSAT engineer?

To excel as an MSAT (Manufacturing Science and Technology) Engineer, a strong background in chemical engineering, biotechnology, or a related field is required, often with experience in process development or manufacturing support. Proficiency with process analytical technology (PAT), statistical analysis software (such as JMP or Minitab), and knowledge of GMP regulations and validation procedures are commonly expected. Excellent problem-solving, communication, and team collaboration skills set top candidates apart in this role. These competencies are crucial for ensuring robust process performance, smooth technology transfers, and continuous improvement within pharmaceutical or biomanufacturing environments.

Which engineering job is high in salary?

Among engineering roles, petroleum engineers and computer hardware engineers tend to have the highest salaries, often due to specialized skills and high demand. Senior positions in aerospace, software, and nuclear engineering also offer high compensation, especially with advanced certifications and experience.

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 are popular job titles related to Msat Engineer jobs in California?

For Msat Engineer jobs in California, the most frequently searched job titles are:

What job categories do people searching Msat Engineer jobs in California look for?

The top searched job categories for Msat Engineer jobs in California are:

What cities in California are hiring for Msat Engineer jobs?

Cities in California with the most Msat Engineer job openings:

Msat Engineer jobs near you
Infographic showing various Msat Engineer job openings in California as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $110,170 per year, or $53 per hour.

Associate Director, Process Validation

Vaxcyte

San Carlos, CA • On-site

Full-time

Re-posted 8 days ago

Job description

Join our Mission to Protect Humankind!
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.
WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values:
*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.
*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.
*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.
*MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.
Summary:
The Associate Director, Process Validation and Risk Management will lead and facilitate commercial process validation and risk management activities across Vaxcyte's end-to-end manufacturing processes. This role focuses on technical strategy, execution, and cross-functional coordination to support commercial readiness, regulatory compliance, and lifecycle management.
The incumbent will provide leadership to ensure the organization is equipped to effectively design, execute, and communicate process validation and risk management strategies to internal stakeholders, external partners, and regulatory agencies.
This position will report to the Sr. Director of Process Validation within the Global MSAT organization and will collaborate on overall validation strategy, with primary responsibility for process validation execution and risk management frameworks supporting commercial manufacturing.
Essential Functions:
Process Validation Leadership
  • Provide strategic and scientific leadership for process validation (PPQ, CPV, lifecycle validation) across commercial programs.
  • Lead and facilitate execution of validation strategies to support technology transfer, site readiness, and product launch.
  • Ensure alignment of validation activities with regulatory expectations and lifecycle management plans.

Risk Management
  • Develop and implement risk management frameworks, tools, and processes in collaboration with Quality.
  • Lead cross-functional risk assessments to identify, evaluate, and mitigate operational, technical, and regulatory risks.
  • Monitor and communicate risk trends and key risk indicators to stakeholders.

Commercialization & Lifecycle Support
  • Support commercial manufacturing operations by ensuring processes remain in a validated and controlled state.
  • Contribute to lifecycle management activities, including process improvements and continued process verification.

Cross-functional Interface
  • Collaborate with Regulatory, CMC, Quality, Supply Chain, Procurement, and Engineering to support commercialization and supply continuity.
  • Partner with internal teams and external CMOs to ensure alignment on validation and risk strategies.

Technical Oversight
  • Provide guidance for validation of processes, systems, facilities, and methods within the commercial organization.
  • Support deviation investigations, ensuring timely resolution and sustained compliance.

Regulatory
  • Contribute to authoring and reviewing regulatory filings and responses to health authorities.
  • Effectively communicate the scientific and commercial rationale for validation and risk management strategies.

Process Validation & Comparability
  • Provide leadership for execution of process validation and comparabilityactivities, ensuring data integrity and compliance.

Raw Material & Network Support
  • Provide guidance on raw material qualification strategies to ensure supply reliability.
  • Support validation activities across internal and external manufacturing networks.

Communication & Leadership
  • Communicate process validation performance and risk insights to key stakeholders.
  • Build strong working relationships and influence across a matrixed organization.
  • Contribute as a key member of the Global MSAT organization to enable successful commercialization.
  • Travel - 10-30% domestic and international travel required.
Requirements:
  • Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 9+ years of relevant experience for Ph.D., 11+ years for M.S./M.A., or 14+ years for B.S./B.A.
  • Strong experience in biologics/vaccine manufacturing, including:
    • Process validation (PPQ/CPV)
    • MSAT, technical operations, or late-stage development
  • Technology transfer and commercialization
  • Experience in quality risk management (ICH Q9) and regulatory expectations
  • Demonstrated leadership in matrixed or cross-functional team environments
  • Ability to apply deep technical knowledge to develop strategies and drive execution
  • Strong problem-solving, organizational, and strategic planning skills
  • Excellent communication and stakeholder engagement skills
  • Ability to analyze data and align stakeholders with organizational strategy
  • Innovative and entrepreneurial mindset to drive continuous improvement
  • An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.

Reports to: Senior Director, Process Validation
Location: San Carlos, CA or North Carolina
Compensation:
The compensation package will be competitive and includes comprehensive benefits and an equity component.
Salary Range: $174,000 - $203,000 (SF Bay Area). Salary ranges for non-California locations may vary.
Equal Opportunity
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
Recruitment Fraud Notice
Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent Vaxcyte in recruitment activities. Vaxcyte has an established recruitment process for all positions prior to issuing an offer for employment and we will never extend unsolicited employment offers or ask candidates to provide financial or sensitive personal information as part of the application process. All legitimate communication from Vaxcyte will come from an official @vaxcyte.com email address. Qualified and interested candidates should apply to current openings at vaxcyte.com/careers.
Vaxcyte logo

About Vaxcyte

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

San Carlos, CA, US

Year founded

2013

View All Vaxcyte Jobs

Apply