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Fulltime Msat Process Engineer Jobs (NOW HIRING)

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

Work as the Senior MSAT Process Engineer on client projects * Responsible for technology transfer activities at the site level (within, inbound, and outbound), including any scale-up or other process ...

Cellares

Senior Process Engineer

South San Francisco, CA

$90K - $210K/yr

Work as the Senior MSAT Process Engineer on client projects * Responsible for technology transfer activities at the site level (within, inbound, and outbound), including any scale-up or other process ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

Work as the Senior MSAT Process Engineer on client projects * Responsible for technology transfer activities at the site level (within, inbound, and outbound), including any scale-up or other process ...

Leiters Inc

MSAT Process SME II

Englewood, CO · On-site

$85K - $105K/yr

... MSAT MBRs * Manage and own Technology Transfer campaigns for new product introductions, and process ... S degree required in Chemical Engineering, Chemistry, Industrial Engineering, Biochemistry or a ...

Evotec

Process Engineer II

Redmond, WA

Process Engineer II Location: Redmond, WA Reports To ... Director, Global MSAT About Us: this is who we are At Just Evotec Biologics, we believe that ...

Evotec

Process Engineer II

Seattle, WA

Process Engineer II Location: Redmond, WA Reports To ... Director, Global MSAT About Us: this is who we are At Just Evotec Biologics, we believe that ...

Takeda

MSAT Systems Business Owner

Boston, MA · On-site

$154K - $242K/yr

... in MSAT and/or process engineering. * Proven experience as abusiness owner, process owner, or ... Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt ...

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Fulltime Msat Process Engineer information

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How much do fulltime msat process engineer jobs pay per year?

As of Jul 17, 2026, the average yearly pay for fulltime msat process engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What engineers make $200,000 a year?

Fulltime MSAT Process Engineers typically do not earn $200,000 annually; such high salaries are more common in senior or specialized engineering roles like software engineers, petroleum engineers, or aerospace engineers with extensive experience, advanced skills, and often in leadership positions. Compensation varies based on industry, location, and level of expertise, with some senior engineers in high-demand fields reaching or exceeding this salary level.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as software engineering, petroleum engineering, and certain aerospace engineering roles can earn $300,000 or more annually, especially with extensive experience, advanced skills, and leadership responsibilities. High compensation often involves working in high-demand industries, holding managerial or executive positions, or possessing rare expertise and certifications.

What does an MSAT engineer do?

An MSAT (Manufacturing Science and Technology) engineer is responsible for supporting the manufacturing process of biopharmaceutical products, ensuring process consistency, troubleshooting issues, and optimizing production methods. They often work with process development, validation, and equipment calibration, using tools like chromatography and bioreactors. The role requires strong technical skills, knowledge of GMP regulations, and collaboration with cross-functional teams.

What engineer makes $500,000 a year?

Fulltime MSAT Process Engineers typically do not earn $500,000 annually; such high salaries are more common in executive or specialized roles within the tech industry. Engineers in high-level management, senior technical leadership, or with extensive experience and unique skills may reach this level, often supplemented by bonuses or stock options.
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Fulltime Msat Process Engineer jobs near you
Senior Process Engineer

Senior Process Engineer

Cellares

South San Francisco, CA • On-site

$125K - $161K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted yesterday

Job description

Position Summary
We are seeking an innovative and highly motivated Senior Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform.
This position is responsible for supporting the activities involved in the development, process transfer, compliance, and scalability for Cellares' manufacturing operations. This individual will focus on technology transfers from Process Development into GMP manufacturing facilities, as well as drive and develop process automation to improve process reliability, safety, cost-effectiveness, scalability, and compliance.
This is a multidisciplinary role requiring the ability to interface with internal and external stakeholders across functional areas to develop the best solutions possible. The successful candidate will be a resident expert in the areas of technology transfer and Manufacturing Science and Technology. It is expected that this individual will work closely with other functional areas and partners to ensure deliverables are met.
Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Own the process knowledge of the product(s) assigned throughout the development lifecycle, work collaboratively for comprehensive process mapping, maintain the oversight on process capability, through data trending and statistical analysis of critical variables, ensuring process(es) are robust, in a continued state of validation and continuously improving
  • Ensure the seamless flow of knowledge and information across functions, and with external stakeholders when applicable, with a focus on the assigned product(s)
  • Work to identify and communicate standards and best practices for process design and manufacturing to ensure consistency across the manufacturing of cell therapies
  • Work as the Senior MSAT Process Engineer on client projects
  • Responsible for technology transfer activities at the site level (within, inbound, and outbound), including any scale-up or other process adaptations
  • Lead technical transfer project team at site and liaises efficiently with involved internal and external functional groups as appropriate
  • Support development of manufacturing operations, including GMP system implementation and tasks related to GMP readiness
  • Support Process Development and process comparability activities on Cellares technology as required
  • Write and review relevant SOPs for manufacturing operations and systems, as well as batch records and BOMs
  • Support labor and equipment capacity modeling and participate in sales and operations planning process (S&OP) for supply review
  • Perform manufacturability assessments for new process introductions
  • Define and provide user requirements for process equipment associated with multiple facilities for the manufacture of cell therapies
  • Support our software team in developing a robust end-user solution for cell therapy manufacturing that integrations with external manufacturing processes and data management software including eBR, MES, QMS, ERP, and LIMS
  • Provide technical leadership to Manufacturing and other departments associated with GMP operations
  • Assess all major deviations including those that impact product quality
  • Own root cause analysis investigations and discussions, including effectively liaising across the appropriate functional teams to drive resolution to major quality events and deviations
  • Propose and implement corrective and preventive actions (CAPAs) as necessary and own respective effectiveness checks to ensure recurrence was prevented
  • Own process-related change controls and change orders, from ideation and change control board review to implementation and effectiveness check
  • Facilitate and/or own the generation of process or operational-related Failure Modes and Effects Analysis (FMEA) and resulting mitigations and actions
  • Develop training and onboarding content and curriculum for new hires and new methods
  • Provide input when troubleshooting processes on the manufacturing floor and during post-operational investigations
  • Maintain and report process run summaries and continued process verification reports
  • Prepare and present data associated with manufacturing processes to internal and external partners, as well as health authority inspectors
  • Support for process qualification and validation preparation, execution, monitoring, and reporting
  • Work with clients on process mapping of the manufacturing processes

Requirements
  • Bachelor's Degree in a scientific or related field is required
  • A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
  • Experience in the Pharma/Biotech industry in technology transfer
  • Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries. Must comply with safety policies of the company and site
  • Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products. All personnel are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, product defects, and related actions
  • Relevant experience bringing biotechnology equipment and processes from design through GMP operational readiness is a plus
  • Must have experience writing and reviewing GMP documentation
  • Strong analytical, problem-solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability
  • Excellent teamwork and interpersonal skills with the ability to influence and build strong working relationships at all levels within the organization
  • Experience with Operational Excellence and/or Lean Manufacturing is a plus
  • Self-motivated and passionate about advancing the field of cell therapy
  • Self-awareness, integrity, authenticity, and a growth mindset
  • Desire to be part of a rapidly evolving organization with compelling technology and taking products and processes to the next level
  • Excellent planning, organization, technical writing, and time-management skills, including the ability to support, problem-solve, and prioritize multiple projects and deadlines

$90,000 - $210,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares
Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.
Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
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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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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