Job Description Process Engineer for Bulk Sterile Antibiotic facility Startup Team
Job Responsibilities:
• Serve on a startup team to demonstrate operation of a bulk sterile antibiotic manufacturing facility operate, troubleshoot, and solve problems related to equipment and process
• Investigate manufacturing deviations and atypical events write investigation reports
• Work collaborative as part of a team of technical professionals
• Collect process data and perform trending and analysis
• Review, analyze, and improve process documentation
• Train operating staff
• Shift work is required
Required Qualifications and Experience:
• B.S. or M.S. degree in scientific or engineering field relevant to sterile processing (such as mechanical, chemical or biomedical engineering)
• Demonstrated strong written and verbal communication skills
• Demonstrated strong interpersonal skills including collaboration, teamwork, and flexibility
• Proven analytical abilities and ability to solve technical problems
• Desire to work in a hands-on, manufacturing environment
Preferred Qualifications and Experience:
• Pharmaceutical processing experience
• Experience with DeltaV manufacturing controls system
• Experience with SAP enterprise management system
• Experience in a GMP or regulated environment
• Experiences requiring problem solving to meet customer or production needs
• Industry experience in sterile processing, manufacturing, or process development
Job Responsibilities:
• Serve on a startup team to demonstrate operation of a bulk sterile antibiotic manufacturing facility operate, troubleshoot, and solve problems related to equipment and process
• Investigate manufacturing deviations and atypical events write investigation reports
• Work collaborative as part of a team of technical professionals
• Collect process data and perform trending and analysis
• Review, analyze, and improve process documentation
• Train operating staff
• Shift work is required
Required Qualifications and Experience:
• B.S. or M.S. degree in scientific or engineering field relevant to sterile processing (such as mechanical, chemical or biomedical engineering)
• Demonstrated strong written and verbal communication skills
• Demonstrated strong interpersonal skills including collaboration, teamwork, and flexibility
• Proven analytical abilities and ability to solve technical problems
• Desire to work in a hands-on, manufacturing environment
Preferred Qualifications and Experience:
• Pharmaceutical processing experience
• Experience with DeltaV manufacturing controls system
• Experience with SAP enterprise management system
• Experience in a GMP or regulated environment
• Experiences requiring problem solving to meet customer or production needs
• Industry experience in sterile processing, manufacturing, or process development