*PhD or Master in Life Science (e.g. Immunology, Biochemistry, Biotechnology, Biology) or equivalent
*Minimum of 10 -15 years in the pharmaceutical industry, with a minimum of 8 years CMC regulatory (biologics preferred) experience.
*Cell therapy experience with global CMC regulations and regulatory submissions strongly preferred.
*Excellent working knowledge/experience in regulatory submission and approval processes for cell and gene therapies and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements
*Proficient with other international regulations, including ICH guidelines
*Excellent communication and writing skills
To apply, please visit the following URL:http://jobviewtrack.com/en-us/job-124a416e60274f3c4213550f091501151c0030011b16495f525f2f370a004e1b52432c081c0206541b1a6b214f4c48414c10001c5e54632e2b633c02025518091d1c58521d6944160a0d531b52612c081c0206541b1a493067683c1e1457/e15871e3e108c4d54dbd1c9bab88bf6e.html→