Administration and Staff Positions
The Accounting Manager will perform and manage sponsored programs accounting functions involving complex grants and funds and will maintain accounting records for WFIRM intellectual property expenses including accounts payable and accounts receivable functions. A Bachelor's degree, with an accounting concentration preferred, and three years in public accounting or equivalent experience are required.
Assistant Directors, Clinical Manufacturing Center
The Clinical Manufacturing Center is a state-of-the-art GMP- and GTP-compliant, controlled clean room facility that produces novel tissue-engineered/regenerative medicine products. The following assistant directors are sought. To apply, send cover letter detailing interest, a current CV and three letters of recommendation to firstname.lastname@example.org. A background check is required for employment
1. Assistant Director for Process Development, Clinical Manufacturing Center
RESPONSIBILITIES: Responsible for day-to-day process developmental activities. Oversees and conducts project related activities for process development of clinical materials. Performs a variety of moderately complex and generally standardized physical, chemical, or biological operations using equipment and procedures. Provides direction and guidance to lower level personnel.
2. Assistant Director for Manufacturing, Clinical Manufacturing Center
RESPONSIBILITIES: Responsible for the planning and timely execution of manufacturing projects associated with the Clinical Manufacturing Center (CMC). The Assistant Director will be the "upstream" customer of a technology transfer process, bringing in mature, but still experimental processes from research investigators and assisting with translating these processes into reproducible and controlled standard procedures that are compliant with relevant GMP, GTP, medical device Quality Systems regulation, pharmacopeial and institutional requirements.
3. Assistant Director for Regulatory Affairs, Clinical Manufacturing Center
RESPONSIBILITIES: Charged with training, monitoring and leading the organization through the FDA process of approval for projects. The position requires a minimum of eight years' experience in the fields of pharmaceutical, medical device, biotechnology or cellular therapy. It also requires a thorough understanding of GCP and GMP compliance. Must have documented experience in bringing projects successfully through the FDA process using GCP, GTP and GMP. M.S. or Ph.D. preferred.
Other Positions: Clinical Manufacturing Center
Various Technicians within the RMCC will perform experiments relating to specific projects using various techniques. A Bachelor’s or Master’s degree and relevant research experience are required.