Senior MSAT Engineer: Process Improvement & Scale-Up

Corden Pharma - A Full-Service CDMO; Boulder (CO); On-site; USD 130,000 - 180,000; Full time

Benefits offered by this job

401(k) matching

Dental Insurance

Disability Insurance

Health Insurance PPO/HSA

Wellness Program

Vacation - Three Weeks 1st Year

Job summary

Corden Pharma Colorado (CPC) seeks a Sr. MSAT Development Engineer to lead technical efforts for commercial processes, improve robustness, safety, and cost. The role covers lab-to-plant scale-up, troubleshooting, and implementing new technologies across peptides, small molecules, and APIs.

You will contribute to project data for budgeting, perform root cause analyses, and drive process analytics technology (PAT) to strengthen control strategies within a cGMP framework.

Qualifications

• BS in Chemical Engineering with Master’s or Ph.D. preferred; 5 years in process engineering or process chemistry in pharma/fine chemicals.
• Experience with scale-up engineering, PAT, and process transfer is valued.
• Familiarity with cGMP and regulatory expectations is required.

Responsibilities

• Act as technical lead/SME during lab or plant operations for technology transfer and implementation.
• Provide day-to-day support to manufacturing and process development; troubleshoot and improve processes.
• Develop scalable process improvements and document results for budgeting and transfer.
• Perform root cause analysis of process-related issues and define corrective actions.
• Lead or support PAT strategies to enhance process understanding and control.

Education

BS in Chemical Engineering; Masters or PhD preferred

5 years of demonstrated success in Process Engineering or Process Chemistry in Pharma/Fine Chemicals

Tools

LabVantage LIMS

SAP

Job description

Corden Pharma Colorado (CPC) seeks a Sr. MSAT Development Engineer to lead technical efforts for commercial processes, improve robustness, safety, and cost. The role covers lab-to-plant scale-up, troubleshooting, and implementing new technologies across peptides, small molecules, and APIs.

You will contribute to project data for budgeting, perform root cause analyses, and drive process analytics technology (PAT) to strengthen control strategies within a cGMP framework.