Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or related field.
3-7 years of experience in pharmaceutical, biotechnology, or peptide manufacturing environments.
Hands-on experience in GMP manufacturing operations and process validation.
Direct experience with Solid-Phase Peptide Synthesis (SPPS).
Proven ability to analyze manufacturing data and implement improvements.
Strong troubleshooting skills for identifying and resolving technical issues.
Experience in authoring GMP documentation such as SOPs and technical reports.
Responsibilities
Serve as the technical process owner for peptide manufacturing operations, including SPPS and purification.
Support manufacturing teams during batch execution with real-time technical troubleshooting.
Monitor key performance indicators and critical process parameters for manufacturing processes.
Analyze manufacturing data to identify process variability and improvement opportunities.
Develop and maintain dashboards tracking manufacturing metrics such as yield and throughput.
Identify and implement improvements in reaction conditions and manufacturing practices.
Lead initiatives focused on improving product yield, process robustness, and overall efficiency.
Benefits
Opportunities for technical training and career development.
Cross-functional collaboration with Operations, Quality, and Engineering teams.
Involvement in cutting-edge peptide manufacturing technologies.
The chance to contribute to process improvement initiatives.
Supportive work environment focused on operational excellence.
Full Job Description
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.
