Senior Project Manager, Csp Applications Development
AptarGroup Inc
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5-7 years product development experience
Bs degree in engineering field required
Iso 9001 and iso 13485 standards knowledge
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AptarGroup Inc is seeking a Senior Project Manager for Csp Applications Development, responsible for driving the commercialization of new medical devices and pharmaceutical products. The ideal candidate will have extensive experience in product development, project management, and cross-functional team leadership, with a strong focus on regulatory compliance and stakeholder communication.
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Job Summary
The role involves defining and communicating a commercialization path for new medical devices or pharmaceutical products from concept through release.
Candidates must lead cross-functional project execution ensuring strict compliance with ISO 9001 and ISO 13485 quality management standards.
The position requires collaborating with R&D, Regulatory, and Operations teams to deliver services related to pre-clinical to Phase II drug development.
Matching Summary
Match Score: 75
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AptarGroup Inc is seeking a Senior Project Manager for Csp Applications Development, responsible for driving the commercialization of new medical devices and pharmaceutical products. The ideal candidate will have extensive experience in product development, project management, and cross-functional team leadership, with a strong focus on regulatory compliance and stakeholder communication.
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Skills & Requirements
Must-have
5-7 years product development experience
BS Degree in Engineering field required
ISO 9001 and ISO 13485 standards knowledge
Cross-functional team leadership skills
Design verification and validation expertise
Nice-to-have
PMP certification preferred
Experience with IND NDA drug development
Knowledge of polymeric materials processing
Sustainability and recyclability initiative experience
Statistical tools and DOE proficiency
Key Requirements
BS Degree in Engineering (Chemical, Electrical, Mechanical, Biomedical)
5-7 years leading product development in Medical Device or Pharma
PMP certification strongly preferred
Familiarity with US, EU, Japan, China regulatory requirements