Regulatory Affairs Associate Jobs in 08869

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Global Regulatory lead - Associate Director

Dizer Corp

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Millburn, New Jersey, USA

Contract, Third Party

Title - Global Regulatory Lead - Associate Director Location - Short Hills, NJ Develop global regulatory strategy for Oncology products in development and through life cycle management taking into account all relevant guidance, commercial needs, and company objectives. Responsibilities: Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic dir
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Posted 2 days ago | Updated 2 days ago

Regulatory & Medical Affairs - Project Manager

Sunrise Systems, Inc.

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Lawrence Township, New Jersey, USA

Contract

Job Title: Regulatory & Medical Affairs - Project Manager Job ID: 24-01565 Location: Lawrence Township, NJ, 08648 Duration: 06 Months contract on W2 Onsite full time at Princeton Pike. Innovation and Digital Health, Project Manager - Digital Optimization Initiatives Position Summary The Innovation Lab team partners with R&D stakeholders to design and deliver innovative analytics solutions that help them make better decisions, reduce costs and/or drive efficiencies. Our diverse analytics team of
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Posted 43 days ago | Updated 20 hours ago

Regulatory & Medical Affairs - Project Manager

Net2Source Inc.

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Lawrence Township, New Jersey, USA

Contract

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants.Job Description: Onsite full time at Princet
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Posted 43 days ago | Updated 9 hours ago

Senior Regulatory Affairs Specialist (Medical Devices)

ApTask

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Remote

Contract

Job Title: Senior Regulatory Affairs Specialist (Medical Devices) Location: Remote Duration: Long term contract Job Description: -Subject Matter Expert for Class II and Class 510(K) submission. -Hands on experience with 510(k) authoring, submissions, and communicating with the FDA. -Hands on experience with software as a Medical Device (SaMD) and validation requirements and applicable consensus standards. Key Responsibilities: -Authoring US FDA 510(k) submission using eSTAR submission tool.
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Posted 1 day ago | Updated 19 hours ago

Regulatory Affairs Specialist, Cell & Gene Therapy

Zachary Piper Solutions, LLC

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Remote

Full-time

Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for a remote based opportunity to join an innovative biotechnology company creating life-saving cell therapies. Responsibilities of the Regulatory Affairs Specialist, Cell & Gene Therapy Coordinate and manage timing for regulatory submissions, collaborating with internal teams and stakeholders. Oversee external publishing coordination for IND/CTA submissions and related documents. Support document workf