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Chemical Process Engineer
Corden Pharma - A Full-Service CDMO. Perform research and development activities to transfer and design or improve processes and technologies .
Posted 10/22/2026full-timeBoulder • Colorado • United StatesMid-LevelSenior💰 $91,000 - $114,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Process Engineering, focusing on Chemical Manufacturing and Pharmaceutical Bulk API Production. Proficient in process development, troubleshooting, and compliance with regulatory standards such as cGMP and Process Safety Management.
Highest-signal resume keywords
Process Engineering FundamentalsChemical Manufacturing ExperienceProcess Safety Management (PSM)Process Modeling Software ProficiencyRegulatory Compliance Knowledge
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Process DevelopmentTroubleshootingData AnalysisTechnical EvaluationsScale-Up TechniquesBatch Record AuthoringProcess ValidationRoot-Cause AnalysisMathematical AnalysisQuality Standards Compliance
Soft Skills
Clear Written CommunicationEffective Presentation SkillsCross-Functional Team CollaborationProblem-SolvingCustomer Interaction
Tools & Technologies
Microsoft OfficeMinitabJMPProcess Modeling Software
Industry Keywords
CGMPFDAICH Q7Pharmaceutical ManufacturingBulk API ProductionProcess SafetyQuality AssuranceQuality ControlEnvironmental Health and Safety (EHS)Hazard Analysis
About the role
Key responsibilities & impact- Perform research and development activities to transfer and design or improve processes and technologies
- Provide process engineering support for manufacturing processes through continuous improvements and troubleshooting of production methods and equipment
- Provide day-to-day support for 24/7 manufacturing, including manufacturing-floor support and attention outside normal work hours when needed
- Evaluate new process fit into manufacturing, considering safety, cost, equipment, chemistry, and unit-operation technology needs
- Perform process development using process modeling or laboratory-scale testing, focusing on scale-up from kilo-scale to full production scale
- Maintain accurate documentation, follow laboratory safety procedures, and ensure compliance with quality standards and Good Laboratory Practices
- Support technology transfer between manufacturing sites by assembling transfer packages, developing success plans, and implementing processes
- Analyze data to improve yields, cycle times, product quality, safety, environmental risks, downtime, consistency, and process robustness
- Conduct process troubleshooting and root-cause analyses; support deviation closure and CAPA development
- Author and maintain master batch records
- Author process-training documentation and train operators
- Support process validation by authoring protocols and reports, participating in execution, and analyzing validation data
- Monitor manufacturing operations, collect production data, identify anomalies, resolve real-time issues, evaluate process performance, and author campaign summary reports
- Support Process Safety Management through hazard analyses, risk assessments, safety reviews, mass and energy balances, and engineering data
- Support change-control activities for process, equipment, and procedural changes
- Collaborate with Manufacturing, Quality Assurance, Quality Control, Validation, Engineering, Maintenance, and EHS personnel
- Address Process Engineering requirements for assigned projects as part of a cross-functional team
- Follow cGMP, FDA, ICH Q7, and other applicable global regulatory requirements
- Pursue professional development through on-the-job training, lectures, professional organizations, formal training, and conferences
Requirements
What you’ll need- Bachelor’s Degree in Chemical Engineering or a related technical field
- Demonstrated knowledge of Process Engineering fundamentals
- Experience in Chemical Manufacturing, especially Pharmaceutical Bulk API Production, is preferred
- Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents
- Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community
- Ability to write speeches and articles for publication that conform to prescribed style and format
- Ability to effectively present information to top management, public groups, and/or boards of directors
- Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
- Ability to apply mathematical operations to frequency distribution, test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
- Ability to define problems, collect data, establish facts, and draw valid conclusions
- Ability to interpret extensive technical instructions in mathematical or diagram form and deal with abstract and concrete variables
- Ability to occasionally lift and/or move up to 50 pounds
- Working knowledge of applicable regulatory and compliance requirements, including cGMP, Process Safety Management (PSM), OSHA, EPA, and company quality systems
- Proficiency with Microsoft Office applications, process modeling software, and statistical analysis programs such as Minitab and JMP
- Knowledge of plant-scale unit operations, scale-up, process safety, and bulk API manufacturing operations
- Ability to analyze process performance, interpret data, support troubleshooting, perform technical and economic evaluations, and develop practical engineering solutions
- Ability to participate in PHAs, incident reporting and investigations, deviations, and CAPAs
- Clear, concise written communication skills for technical reports, investigations, procedures, validation documentation, and campaign reports
- Ability to communicate technical information through presentations, discussions, and cross-functional interactions
- Ability to work effectively in cross-functional teams
- Certificates, licenses, registrations: None
Benefits
Comp & perks- 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
- Accident Plan
- Critical Illness Insurance
- Dental Insurance
- Disability Insurance
- Employee Assistance Program
- Flexible Spending Account
- Health Insurance PPO/HSA
- Hospital Indemnity Plan
- ID Theft Protection
- Life Insurance
- Paid Parental Leave
- Tuition Reimbursement
- Wellness Program
- Vacation – Three Weeks 1st Year
- Vision Insurance