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Sr Process Engineer

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San Francisco, California • Today

Full-time

Senior Process Engineer

Worley Alaska

Martinez, California • Today

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USD 133,850.00 - 196,838.00 per year

Sr. Process Engineer

E Ink

Fremont, California • Today

Full-time

USD 158,000.00 - 230,000.00 per year

Sr. Process Engineer

Element Solutions

Fremont, California • Today

Full-time

USD 109,341.00 - 164,011.00 per year

Sr. Process Engineer - Water Treatment

Veolia Environnement SA

Remote or Trevose, Pennsylvania • Today

Full-time

USD 115,000.00 - 135,000.00 per year

Senior Laser Process Engineer

Atomic Machines

Emeryville, California • Today

Full-time

USD 190,000.00 - 230,000.00 per year

Sr. Staff Process Engineer

Bloom Energy

Fremont, California • Today

Full-time

USD 134,500.00 - 193,500.00 per year

Senior/Staff Materials Process Engineer

Mainspring Energy

Menlo Park, California • Today

Full-time

USD 126,000.00 - 178,000.00 per year

Sr. Process & Operations Engineer - Menlo Park, CA

Hims and Hers Health, Inc.

Menlo Park, California • Today

Full-time

USD 130,000.00 - 170,000.00 per year

Sr. Process Engineer - Semi Conductor (Remote with travel)

Parsons Services Company

Remote or Boise, Idaho • Today

Full-time

USD 88,400.00 - 154,700.00 per year

Senior Logistics Process Engineer

Milestone Technologies, Inc.

Remote or Arizona • Today

Full-time

USD 96,000.00 - 120,000.00 per year

Senior Materials and Process Engineer

Mainspring Energy

Menlo Park, California • Today

Full-time

USD 126,000.00 - 148,000.00 per year

Process Engineer III

UltraClean Technology

Fremont, California • Today

Full-time

Process Reengineering Sr Solution Engineer - Remote

UnitedHealth Group

Remote or Eden Prairie, Minnesota • Today

Full-time

Forward Deployed Process Engineer Lead - R37

Remote • Today

Full-time

USD 152,163.00 - 289,353.75 per year

Energetics Process Engineer

Parsons Services Company

Remote • Today

Full-time

USD 88,400.00 - 154,700.00 per year

Process Engineer III

Element Solutions

Fremont, California • Today

Full-time

USD 95,406.00 - 143,108.00 per year

Sr. Process Engineer - Semi Conductor

Parsons Services Company

Remote or Boise, Idaho • Today

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USD 88,400.00 - 154,700.00 per year

Senior Supervising Process Engineer

Parsons Services Company

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USD 125,100.00 - 225,200.00 per year

Senior Process Engineer, Water

Stantec

Walnut Creek, California • Today

Full-time

USD 190,500.00 - 295,300.00 per year

Senior Process Engineer

Element Solutions

Fremont, California • Today

Full-time

USD 109,341.00 - 164,011.00 per year

Job Details

Skills

Real-time
Dashboard
Resin
Process Control
Lean Manufacturing
Six Sigma
Statistics
Root Cause Analysis
FMEA
Technical Writing
Good Manufacturing Practice
Leadership
Production Planning
Operational Excellence
Mentorship
Training
API
Manufacturing Operations
Management
Process Improvement
ROOT
GMP
Documentation
Risk Assessment
Collaboration
Quality Assurance
Supply Chain Management
Communication
Chemical Engineering
Chemistry
Biochemistry
Pharmaceutics
Science
Biotechnology
Statistical Process Control
Lean Six Sigma
Data Analysis
Minitab
Microsoft Power BI
Microsoft Excel
Advanced Analytics
Startups
Manufacturing

Real-time
Dashboard
Resin
Process Control
Lean Manufacturing
Six Sigma
Statistics
Root Cause Analysis
FMEA
Technical Writing
Good Manufacturing Practice
Leadership
Production Planning
Operational Excellence
Mentorship
Training
API
Manufacturing Operations
Management
Process Improvement
ROOT
GMP
Documentation
Risk Assessment
Collaboration
Quality Assurance
Supply Chain Management
Communication
Chemical Engineering
Chemistry
Biochemistry
Pharmaceutics
Science
Biotechnology
Statistical Process Control
Lean Six Sigma
Data Analysis
Minitab
Microsoft Power BI
Microsoft Excel
Advanced Analytics
Startups
Manufacturing

Summary

Roles and Responsibilities:

Serve as a technical process owner for peptide manufacturing operations, including SPPS, purification, and lyophilization.
Support manufacturing teams during batch execution and provide real-time technical troubleshooting on the floor.
Monitor critical process parameters and key performance indicators across peptide manufacturing processes.
Collect, analyze, and trend manufacturing data to identify process variability, yield losses, bottlenecks, and improvement opportunities.
Develop and maintain manufacturing dashboards tracking yield, cycle time, solvent usage, throughput, batch success rate, and right-first-time metrics.
Evaluate coupling efficiency, resin performance, deprotection efficiency, impurity formation trends, and other process indicators related to SPPS performance.
Identify and implement improvements to reaction conditions, cycle parameters, manufacturing practices, and process controls.
Lead initiatives to improve product yield, throughput, cycle time, overall equipment effectiveness, and process robustness.
pply Lean Manufacturing, Six Sigma, statistical analysis, and structured root cause analysis tools to reduce waste and process variation.
Lead or support investigations related to process excursions, atypical results, yield losses, manufacturing deviations, and equipment/process issues.
Use tools such as Fishbone Analysis, 5 Why Analysis, FMEA, and Statistical Process Control to identify root cause and drive corrective actions.
uthor and revise SOPs, Master Batch Records, process descriptions, manufacturing instructions, technical reports, and process performance summaries.
Support deviation investigations, CAPAs, change controls, risk assessments, process validation, and continued process verification activities.
Ensure technical documentation is accurate, complete, and compliant with cGMP requirements.
Partner cross-functionally with Operations, Engineering, Quality, Supply Chain, and site leadership to improve manufacturing performance.
Support implementation of new equipment, technologies, and manufacturing systems.
Participate in production planning, operational excellence reviews, and process improvement meetings.
Provide technical mentoring and training to manufacturing personnel on process understanding and best practices.

Education and Experience:

Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field.
3-7 years of experience in pharmaceutical, biotechnology, peptide manufacturing, API manufacturing, or related chemical processing environments.
Hands-on experience supporting GMP manufacturing operations, investigations, and process validation activities.
Direct experience with Solid-Phase Peptide Synthesis.
Experience analyzing manufacturing process data and implementing process improvements.
Strong technical troubleshooting skills with the ability to identify root cause and implement sustainable corrective actions.
Experience authoring or revising GMP documentation, including SOPs, batch records, technical reports, deviation investigations, CAPAs, change controls, or risk assessments.
Strong cross-functional collaboration skills and the ability to work closely with Manufacturing, Quality, Engineering, and Supply Chain teams.
Clear communication skills with the ability to translate technical process observations into actionable recommendations.

Nice to Have:

Master's degree or Ph.D. in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field.
Experience in commercial-scale peptide manufacturing.
Experience with process monitoring, Statistical Process Control, and process capability assessments.
Lean Six Sigma Green Belt or Black Belt certification.
Experience using statistical software and data analysis tools such as Minitab, Power BI, Excel advanced analytics, or similar tools.
Experience in a startup or rapidly growing manufacturing organization.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 4c781d019dfe0abc1f8c9d061670bf9
Posted 30+ days ago

Fitment

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Job Details

Skills

Real-time
Dashboard
Resin
Process Control
Lean Manufacturing
Six Sigma
Statistics
Root Cause Analysis
FMEA
Technical Writing
Good Manufacturing Practice
Leadership
Production Planning
Operational Excellence
Mentorship
Training
API
Manufacturing Operations
Management
Process Improvement
ROOT
GMP
Documentation
Risk Assessment
Collaboration
Quality Assurance
Supply Chain Management
Communication
Chemical Engineering
Chemistry
Biochemistry
Pharmaceutics
Science
Biotechnology
Statistical Process Control
Lean Six Sigma
Data Analysis
Minitab
Microsoft Power BI
Microsoft Excel
Advanced Analytics
Startups
Manufacturing

Real-time
Dashboard
Resin
Process Control
Lean Manufacturing
Six Sigma
Statistics
Root Cause Analysis
FMEA
Technical Writing
Good Manufacturing Practice
Leadership
Production Planning
Operational Excellence
Mentorship
Training
API
Manufacturing Operations
Management
Process Improvement
ROOT
GMP
Documentation
Risk Assessment
Collaboration
Quality Assurance
Supply Chain Management
Communication
Chemical Engineering
Chemistry
Biochemistry
Pharmaceutics
Science
Biotechnology
Statistical Process Control
Lean Six Sigma
Data Analysis
Minitab
Microsoft Power BI
Microsoft Excel
Advanced Analytics
Startups
Manufacturing

Summary

Roles and Responsibilities:

Serve as a technical process owner for peptide manufacturing operations, including SPPS, purification, and lyophilization.
Support manufacturing teams during batch execution and provide real-time technical troubleshooting on the floor.
Monitor critical process parameters and key performance indicators across peptide manufacturing processes.
Collect, analyze, and trend manufacturing data to identify process variability, yield losses, bottlenecks, and improvement opportunities.
Develop and maintain manufacturing dashboards tracking yield, cycle time, solvent usage, throughput, batch success rate, and right-first-time metrics.
Evaluate coupling efficiency, resin performance, deprotection efficiency, impurity formation trends, and other process indicators related to SPPS performance.
Identify and implement improvements to reaction conditions, cycle parameters, manufacturing practices, and process controls.
Lead initiatives to improve product yield, throughput, cycle time, overall equipment effectiveness, and process robustness.
pply Lean Manufacturing, Six Sigma, statistical analysis, and structured root cause analysis tools to reduce waste and process variation.
Lead or support investigations related to process excursions, atypical results, yield losses, manufacturing deviations, and equipment/process issues.
Use tools such as Fishbone Analysis, 5 Why Analysis, FMEA, and Statistical Process Control to identify root cause and drive corrective actions.
uthor and revise SOPs, Master Batch Records, process descriptions, manufacturing instructions, technical reports, and process performance summaries.
Support deviation investigations, CAPAs, change controls, risk assessments, process validation, and continued process verification activities.
Ensure technical documentation is accurate, complete, and compliant with cGMP requirements.
Partner cross-functionally with Operations, Engineering, Quality, Supply Chain, and site leadership to improve manufacturing performance.
Support implementation of new equipment, technologies, and manufacturing systems.
Participate in production planning, operational excellence reviews, and process improvement meetings.
Provide technical mentoring and training to manufacturing personnel on process understanding and best practices.

Education and Experience:

Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field.
3-7 years of experience in pharmaceutical, biotechnology, peptide manufacturing, API manufacturing, or related chemical processing environments.
Hands-on experience supporting GMP manufacturing operations, investigations, and process validation activities.
Direct experience with Solid-Phase Peptide Synthesis.
Experience analyzing manufacturing process data and implementing process improvements.
Strong technical troubleshooting skills with the ability to identify root cause and implement sustainable corrective actions.
Experience authoring or revising GMP documentation, including SOPs, batch records, technical reports, deviation investigations, CAPAs, change controls, or risk assessments.
Strong cross-functional collaboration skills and the ability to work closely with Manufacturing, Quality, Engineering, and Supply Chain teams.
Clear communication skills with the ability to translate technical process observations into actionable recommendations.

Nice to Have:

Master's degree or Ph.D. in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field.
Experience in commercial-scale peptide manufacturing.
Experience with process monitoring, Statistical Process Control, and process capability assessments.
Lean Six Sigma Green Belt or Black Belt certification.
Experience using statistical software and data analysis tools such as Minitab, Power BI, Excel advanced analytics, or similar tools.
Experience in a startup or rapidly growing manufacturing organization.

Dice Id: 91116760
Position Id: 4c781d019dfe0abc1f8c9d061670bf9
Posted 30+ days ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

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