EXPERIENCE / SKILLS / QUALIFICATIONS:

• Minimum 3 years College Diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related.
• Minimum of three (3) years of relevant work experience, or equivalent.
• Preferred Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related) preferred, with a minimum of three (3) years of relevant work experience.
• Proficiency in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP preferred.
• Experience with both Automated and manually operated process equipment.
• Strong understanding of Computerized systems, Data management systems, Quality management systems, SAP, SOPs, automation, and other relevant software/applications.

• Coordinate and schedule the daily and weekly tasks of the technical staff, while also reviewing and verifying the completion and accuracy of all documents, including Records, SOPs, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring charts, in compliance with GMP guidelines.
• Coordinate and support units within department (Downstream) and other outside departments (Maintenance, Automation, QO test labs, etc.) and ensure timely completion of production activities.
• Oversee data management for Influenza manufacturing operations in Downstream and supervise the administration of related manufacturing activities.
• Ensure Health, Safety, and GMP environment maintenance; lead process improvement efforts and prepare trending reports.
• Coordinate technical staff’s schedules for facility, equipment, and process improvement projects with MTech and Engineering & Technical Services.