Details: Do you have regulatory affairs project management experience within the pharmaceutical industry? Are you looking for a new opportunity and a new challenge? If so, we may have the perfect opportunity for you.Kelly Scientific Resources is recruiting for a Regulatory Affairs Project Manager, to work for a leading pharmaceutical company, in the St. Louis, Missouri area. This is a contract opportunity that is available immediately. This position will have responsibility for the following:• Maintenance of regulatory project timelines• Coordination of US and International regulatory affairs• Directing sub-teams within regulatory labeling groupsThe qualified candidate will have the following experience:• BS/BA in Science• Project management software experience• 5 + years of Regulatory Affairs experience, preferably within the pharmaceutical industry• cGMP experience • Prior knowledge of product labeling, compliance requirements, US and international labeling• Knowledge of drug submissions requirementsOur recruiters are actively reviewing resumes received through the online application process. To be considered for this position, as well as future positions, please apply online. We regret that visa sponsorship is not available for this opportunity. Kelly Scientific Resources ® has grown into a $270 million global business as the scientific division of Kelly Services. Our staff of scientists provides scientific staffing to a broad spectrum of industries including: chemical, cosmetics, food, pharmaceutical, biomedical, consumer products, environmental, medical device, medical laboratory, petrochemical, and clinical research. We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide: www.kellyscientific.com. Kelly Services is an Equal Opportunity Employer.
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