Oversee successful transfer and implementation of new projects, successful delivery of commercialization of existing projects, drive harmonization of industry best practices, assist with corporate projects and lead site-related deviations/issue resolution
Job Summary
Oversee successful transfer and implementation of new projects, successful delivery of commercialization of existing projects, drive harmonization of industry best practices, assist with corporate projects and lead site-related deviations/issue resolution.
Lead hands on troubleshooting efforts and root cause investigations to resolve deviations related to the equipment, process or product.
Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.
Matching Summary
Oversee successful transfer and implementation of new projects, successful delivery of commercialization of existing projects, drive harmonization of industry best practices, assist with corporate projects and lead site-related deviations/issue resolution.
Skills & Requirements
Must-have
Biopharmaceutical GMP manufacturing
Downstream purification unit operations
Single-use equipment
Automated process equipment
Process Control Strategy (PCS)
Process risk assessments
Validation Protocols/Reports
Nice-to-have
Collaborative colleagues
Fast-paced project execution
Continuous improvement initiatives
Client Communication experience
Key Requirements
Tertiary degree in Engineering
3+ years of experience
Knowledge of process development, scale-up and cGMP manufacturing
Expertise in scale up of downstream purification unit operations