Process Engineer II

Overview In this role you support vaccine, biologic and sterile manufacturing processes through data analysis, troubleshooting and reporting. You’ll help implement change control, write and improve procedures, and contribute to safety reviews while learning new processes. You’ll work across shifts and partner with cross-functional teams to resolve issues and drive process improvements in a cGMP environment. This is a hands-on, impact-focused opportunity in pharmaceutical manufacturing. ResponsibilitiesCreate and maintain highly detailed spreadsheetsProvide technical support for vaccine, biologic, and sterile manufacturing via data analysis, troubleshooting and report writingSupport change control implementationLearn new processes and proceduresRecommend, create and write process control and automation instructionsPerform shift work as neededConduct technical investigations and analysesRecommend and implement corrective and preventive actions and lead reduction of atypical eventsWrite, review and improve procedures for operation of equipment and processesContribute to process and equipment safety reviews Key requirementsExperience in a cGMP environmentWork, co-op, or internship experience in industryExcellent academic recordStrong verbal and written communication skillsStrong problem solving skills with a hands-on, field-based approachAbility to examine issues from diverse perspectives (safety, compliance, maintenance, automation, equipment, process, people)Enthusiasm, initiative and continuous learning mindsetLeadership, judgment, organization and project management abilitiesIndependent decision making and coordination of activitiesAttention to detail and follow-up skillsstrong verbal and written communicationteam skillsethicsdata analysistroubleshootingreport writing