Responsibilities: As the selected candidate, you will have the opportunity to: - Perform scientific review, interpretation, and documentation of product manufacturing data to evaluate the safety and quality of cell therapy products (e.g., stem cells, cancer vaccines, cellular immunotherapies, engineered tissue, medical devices) in regulatory submissions to FDA.
- Contribute to guidance and policy development activities relevant to cell therapy.
Basic Qualifications: Ph.D. or equivalent advanced degree with a strong research background in cell therapy, cell and stem cell biology, microbiology, cellular immunology, cancer biology, regenerative medicine, and/or biomedical engineering. Occupational series which may be considered include General Natural Resources Management and Biological Sciences (0401), Microbiology (0403), and Biomedical Engineering (0858). Please refer to the link for each occupational series for more information regarding specific education requirements. Additional Qualifications: Candidates are expected to be proficient in applying relevant scientific knowledge and research experience to support multi-disciplinary scientific and review of regulatory submissions. In addition, the candidate must have strong collaborative skills, excellent written and oral communication skills, and evidence of leadership potential. Preferred Specialized Experience: Postdoctoral experience is highly preferred. Also, knowledge of federal regulations applicable to drugs, biologics, and medical devices is helpful but not a requirement for consideration. Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. For further information, visit the U.S. Department of Education website for Foreign Education Evaluation. Salary: Salary is commensurate with education/experience. Location: FDA White Oak Campus in Silver Spring, MD Conditions of Employment: This position will be filled through the Service Fellowship program. The appointment provides up to (4) years with opportunities for renewal. Applications will ONLY be accepted from U.S. citizens and/or permanent residents (green card). No previous Federal experience is required. Appointment does not confer any entitlement to a position in the competitive service, and there is no entitlement to Merit Systems Protection Board (MSPB) appeals rights. - One-year probationary period may be required.
- Official Transcripts required
- Background and/or Security investigation required.
- Prohibited financial interest restrictions may apply. For additional information on the prohibited financial interests, please visit the FDA Ethics and Integrity Office website at FDA Ethics and Integrity Office.
How to Apply: If you’re seeking a challenging and rewarding career opportunity, we invite you to apply today by completing the following step: - Submit a statement of interest, resume or curriculum vitae (CV) detailing relevant experience, transcripts, names/contact information for three references, proof of U.S. citizenship or lawful permanent residency status, and other supporting documentations to Melanie Eacho at melanie.eacho@fda.hhs.gov. Applications will be accepted through January 31, 2021. However, candidates will be considered as received. For best consideration, please submit your application as soon as possible. Please reference Job Code: OTAT-21-02-BES.
HHS/FDA is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. |
