Regulatory Affairs Manager Jobs

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Senior Regulatory & Scientific Affairs Specialist - Nutrition

Nestle USA

On-site in Arlington, Virginia, USA

Full-time

As the world leader in nutrition, health and wellness for children from birth to preschool, Gerber Products Company is committed to creating a strong future. We joined the Nestl Nutrition family in 2007, and have been a partner in parenthood ever since. Our Anything for Baby team works closely with experts to create products that enrich and establish healthy habits for children, and are good for the planet as well. A career at Gerber provides meaningful opportunities to develop professionally, a

Regulatory & Medical Affairs - Project Manager

HonorVet Technologies

On-site in Lawrence Township, New Jersey, USA

Contract

Position: - Regulatory & Medical Affairs - Project Manager Location: - Lawrence Township, NJ 08648 Duration: -6 months 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 knowledge management experts, data scientists, analysts and data visualization specialists work on multiple projects simultaneously, ranging from pi

Regulatory & Medical Affairs - Project Manager

Sunrise Systems, Inc.

On-site in 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

Regulatory and Medical Affairs - Project Manager

Net2Source Inc.

On-site in 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 Princeton Pike

Regulatory Affairs Senior Manager

Software Guidance & Assistance

On-site in Hawthorne, New York, USA

Full-time

Software Guidance & Assistance, Inc., (SGA), is searching for a Regulatory Affairs Senior Manager for a FULL TIME assignment with one of our premier Pharmaceutical Services clients in Hawthorne, NY. Responsibilities: US Agent for all Firm's products, responsible for communication between the FDA and manufacturing sites. Communicate and follow-up status with FDA for any Chemistry, Bioequivalence and Patents issues and correspondences on both pending and approved applications Lead, guide and t

Regulatory Affairs Specialist for Chemical Industry

Infojini

On-site in Stamford, Connecticut, USA

Contract

Regulatory Affairs Specialist Location - Stamford, CT 06901 Duration - 12 months Requirements: Bachelor's degree in a relevant field (e.g., Chemistry, Environmental Science, Regulatory Affairs, Biology, Computer Science, etc.). 2-3 years of experience in regulatory affairs, specifically in SDS authoring, GHS classifications, or related compliance work within the consumer products industry. Proficiency in SAP systems for data management and report generating. Advanced skills in Microsoft Office

Regulatory Affairs Project Leader

Intellectt INC

On-site in Plymouth, Minnesota, USA

Contract

Hello, This is Venkat from Intellectt Inc. Please find the below position and let me know your response. Title: Regulatory Affairs Project Leader Location: Plymouth, MN Duration: 12+ Months Job Description: This individual will support global Regulatory changes with responsibility for monitoring, analyzing, interpreting, and communicating medical device regulations to a broad audience. Daily, this individual will work with regional experts to understand the regulation change and determine