Process Engineer
South San Francisco, CA · On-site
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
Process Engineer
South San Francisco, CA · On-site
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Quick apply
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Process Engineer
Union City, CA · On-site
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Process Engineer
Union City, CA · On-site
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Process Engineer
South San Francisco, CA · On-site
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
Quick apply
Process Engineer
South San Francisco, CA · On-site
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Process Engineer to join the MSAT team who will contribute significantly to the development of our advanced cell therapy ...
Process Engineer
$95K - $130K/yr
... Process/quality issues and implement corrective actions. * Collaborate with QE/TE/PM to ensure alignment of quality objectives and priorities. * Qualifications: * Bachelor's Degree in an Engineering ...
Process Engineer
$95K - $130K/yr
... Process/quality issues and implement corrective actions. * Collaborate with QE/TE/PM to ensure alignment of quality objectives and priorities. * Qualifications: * Bachelor's Degree in an Engineering ...
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Quick apply
US Pipe is currently seeking a Process Engineer to join our team. Responsibilities will include developing systems and processes that reduce costs, enhance employee safety, improving product quality ...
Process Engineer
San Francisco, CA · On-site
... Packaging Engineer to drive the development of innovative module packaging solutions for new consumer products. In this role, you will own the process development of New Product Introduction ...
Process Engineer
San Francisco, CA · On-site
... Packaging Engineer to drive the development of innovative module packaging solutions for new consumer products. In this role, you will own the process development of New Product Introduction ...
Process Engineer 4
Fremont, CA · On-site
Key Responsibilities: • Design experiments, collect data, analyze data and compile reports on process engineering experiments • Perform root cause analysis, troubleshoot problems and resolve ...
Process Engineer 4
Fremont, CA · On-site
Key Responsibilities: • Design experiments, collect data, analyze data and compile reports on process engineering experiments • Perform root cause analysis, troubleshoot problems and resolve ...
Process Engineer 4
Fremont, CA · On-site
Design experiments, collect data, analyze data and compile reports on process engineering experiments Perform root cause analysis, troubleshoot problems and resolve difficult process engineering ...
Process Engineer 4
Fremont, CA · On-site
Design experiments, collect data, analyze data and compile reports on process engineering experiments Perform root cause analysis, troubleshoot problems and resolve difficult process engineering ...
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
Quick apply
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
PCBA Process Engineer
Milpitas, CA · On-site
$167K - $230K/yr
This position will support process engineering activities across new product introduction, equipment implementation, process optimization, troubleshooting, and continuous improvement in a high ...
PCBA Process Engineer
Milpitas, CA · On-site
$167K - $230K/yr
This position will support process engineering activities across new product introduction, equipment implementation, process optimization, troubleshooting, and continuous improvement in a high ...
The Advanced Process Engineer - Automation & Manufacturing Systems is the technical lead for manufacturing process development and automation within Third-Party Manufacturer (TPM) Operations. This ...
New
The Advanced Process Engineer - Automation & Manufacturing Systems is the technical lead for manufacturing process development and automation within Third-Party Manufacturer (TPM) Operations. This ...
New
Senior Process Engineer
Fremont, CA · On-site
$90 - $120/hr
* Responsible for Process Engineering activities in fuel cell stack and column manufacturing. * Analyze operational metrics, inline process performance, and define reaction plans. * Define preventive ...
New
Senior Process Engineer
Fremont, CA · On-site
$90 - $120/hr
* Responsible for Process Engineering activities in fuel cell stack and column manufacturing. * Analyze operational metrics, inline process performance, and define reaction plans. * Define preventive ...
New
Senior Process Engineer
$98K - $141K/yr
We are looking for a Senior Process Engineer to join our team in one of today's most exciting technologies. This role will report to the Senior Manager, Process Engineering and will be based in ...
Senior Process Engineer
$98K - $141K/yr
We are looking for a Senior Process Engineer to join our team in one of today's most exciting technologies. This role will report to the Senior Manager, Process Engineering and will be based in ...
Process Engineer, Chemical
Livermore, CA · On-site
$105K - $130K/yr
Responsible for all chemical process engineering with a focus on chemical clean processes. * Responsible for ultrasonic cleaning process engineering. * Develop/maintain detailed process routings ...
Process Engineer, Chemical
Livermore, CA · On-site
$105K - $130K/yr
Responsible for all chemical process engineering with a focus on chemical clean processes. * Responsible for ultrasonic cleaning process engineering. * Develop/maintain detailed process routings ...
PCBA Process Engineer
Milpitas, CA · On-site
$167K - $230K/yr
This position will support process engineering activities across new product introduction, equipment implementation, process optimization, troubleshooting, and continuous improvement in a high ...
PCBA Process Engineer
Milpitas, CA · On-site
$167K - $230K/yr
This position will support process engineering activities across new product introduction, equipment implementation, process optimization, troubleshooting, and continuous improvement in a high ...
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
Senior Process Engineer
San Jose, CA · On-site
$121K - $157K/yr
As a key member of our engineering team, you will own process engineering deliverables for industrial-scale systems, including heat and mass balances, process flow diagrams, piping and ...
Process Engineer Process Engineer information
See San Leandro, CA salary details
$56K - $65.5K
2% of jobs
$65.5K - $75.1K
9% of jobs
$83.8K is the 25th percentile. Wages below this are outliers.
$75.1K - $84.6K
15% of jobs
$84.6K - $94.2K
18% of jobs
The median wage is $97.5K / yr.
$94.2K - $103.7K
17% of jobs
$103.7K - $113.3K
14% of jobs
$113.5K is the 75th percentile. Wages above this are outliers.
$113.3K - $122.8K
11% of jobs
$122.8K - $132.4K
6% of jobs
$132.4K - $142K
4% of jobs
$142K - $151.5K
3% of jobs
$151.5K - $161.1K
1% of jobs
$56K
$104K
$161.1K
How much do process engineer process engineer jobs pay per year?
As of Aug 20, 2026, the average yearly pay for process engineer process engineer in San Leandro, CA is $104,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,200.00 and $116,400.00 per year, depending on experience, location, and employer.
What is the difference between Process Engineer Process Engineer vs Process Engineer?
| Aspect | Process Engineer | Process Engineer |
|---|---|---|
| Credentials | Bachelor's in Engineering or related field, certifications like Six Sigma often preferred | Bachelor's degree in Chemical, Mechanical, or Industrial Engineering; certifications like Six Sigma are common |
| Work Environment | Manufacturing plants, chemical facilities, or production lines | Industrial settings, plant floors, or process development departments |
| Industry Usage | Manufacturing, chemical, oil & gas, pharmaceuticals | Similar industries, often overlapping in chemical, manufacturing, and energy sectors |
Both roles focus on optimizing manufacturing processes, ensuring safety, and improving efficiency. They often share similar qualifications and work environments, making them closely related in the industry.
What are popular job titles related to Process Engineer Process Engineer jobs in San Leandro, CA?
For Process Engineer Process Engineer jobs in San Leandro, CA, the most frequently searched job titles are:
What job categories do people searching Process Engineer Process Engineer jobs in San Leandro, CA look for?
The top searched job categories for Process Engineer Process Engineer jobs in San Leandro, CA are:
What cities near San Leandro, CA are hiring for Process Engineer Process Engineer jobs?
Cities near San Leandro, CA with the most Process Engineer Process Engineer job openings:
Full-time
Medical, Dental, Vision, Retirement
Re-posted 5 days ago
Job description
Position Summary
We are seeking an innovative and highly motivated 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, from South San Francisco to other Cellares sites, 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
Requirements
$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.
We are seeking an innovative and highly motivated 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, from South San Francisco to other Cellares sites, 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 MSAT Process Engineer on internal or client projects
- Responsible for technology transfer activities at the site level (within, inbound, and outbound), including any scale-up or other process adaptations
- Execute on 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
- Ownership of 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
- Ownership of 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 3+ 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.
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