Project Manager Validation
Company Name:
Regeneron
Summary:
Responsible for planning, coordinating and facilitating validation activities required for the development and commercialization of Regenerons drug candidates.
Essential Duties and Responsibilities include, but are not limited to, the following:
Lead cross-functional teams to plan and facilitate validation activities required for drug development throughout the clinical phases and into commercial approval and launch.
Develop reports and metrics to measure progress and performance. Provide regular updates on progress as requested by Senior Management.
Track team activities and timelines to ensure that the deliverables within the project plan are met and are on-time.
Serve as liaison between the IOPS site and all Tarrytown located departments.
Coordinate all IOPS communications to and from collaborative partners.
Coordinate the validation activities required for submission of license applications, INDs, and other regulatory documents to government agencies.
Manage and set priorities for specific projects/programs.
Lead special projects in validation as needed, including resource planning and estimation, budget tracking and issue resolution.
Experience and Required Skills:
Education and
Experience:
Requires BS/BA in a scientific discipline with at least 4
years of progressive related experience in a cGMP environment (Assoc level); or 6
years related experience within the field of Biotech Process sciences, Validation, Manufacturing for Project Manager level.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regenerons unwavering commitment to combining good science & good business.
Apply online at:
http://careers.regeneron.com/united-states/industrial-operations-%EF%B9%A0-product-supply/jobid5589162-project-manager-validation-jobsEstimated Salary: $20 to $28 per hour based on qualifications.
Regeneron
Summary:
Responsible for planning, coordinating and facilitating validation activities required for the development and commercialization of Regenerons drug candidates.
Essential Duties and Responsibilities include, but are not limited to, the following:
Lead cross-functional teams to plan and facilitate validation activities required for drug development throughout the clinical phases and into commercial approval and launch.
Develop reports and metrics to measure progress and performance. Provide regular updates on progress as requested by Senior Management.
Track team activities and timelines to ensure that the deliverables within the project plan are met and are on-time.
Serve as liaison between the IOPS site and all Tarrytown located departments.
Coordinate all IOPS communications to and from collaborative partners.
Coordinate the validation activities required for submission of license applications, INDs, and other regulatory documents to government agencies.
Manage and set priorities for specific projects/programs.
Lead special projects in validation as needed, including resource planning and estimation, budget tracking and issue resolution.
Experience and Required Skills:
Education and
Experience:
Requires BS/BA in a scientific discipline with at least 4
years of progressive related experience in a cGMP environment (Assoc level); or 6
years related experience within the field of Biotech Process sciences, Validation, Manufacturing for Project Manager level.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regenerons unwavering commitment to combining good science & good business.
Apply online at:
http://careers.regeneron.com/united-states/industrial-operations-%EF%B9%A0-product-supply/jobid5589162-project-manager-validation-jobsEstimated Salary: $20 to $28 per hour based on qualifications.
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