Regulatory Affairs Associate (Hybrid)

Benjamin Moore & Co
Montvale, New Jersey, USA
Full-time

Regulatory Affairs Associate (Hybrid)

ID 2024-1727

Category Product Stewardship

Position Type Salaried

Remote No

Shift Time 40

Overview

At Benjamin Moore, we empower our team members to achieve their goals and make a positive impact in our communities. We offer a rewarding and inspiring work environment that fosters creativity, collaboration, and a strong sense of camaraderie.

Our culture of excellence and transparency encourages our colleagues to bring their authentic selves and unique perspectives / ideas every day.

With 140 years of rich history behind our brand, we know that our people are the driving force behind our success. We believe in investing in our colleagues by offering work-life balance, competitive / benefits, ongoing learning / continuing education, and skill development.

Through a positive and engaging workplace, we facilitate growth, development, and fulfillment for all.

Join us and be a part of a brand that inspires creativity, innovation, and passion in support of locally-owned stores around the world.

Click here to see how you can paint your future!

Responsible for data gathering and collating information for global product regulation and compliance issues. Duties may include new product and raw material evaluation, health and safety compliance with all applicable regulations, labeling, Safety Data Sheet creation, chemical and product registrations, and any other related support.

This person will assist with the development of efficient processes to ensure compliance with applicable global regulations.

In addition, actively participate in the enhancement of the Product Stewardship team.

Responsibilities

Functional Capabilities and Essential job Tasks :

  • Understanding, communicating, and general awareness of applicable legislation, regulatory procedures.
  • Assist in the creation of regionally compliant Safety Data Sheet's and Label text.
  • Learn and understand compliance software.
  • Supports Product Specialists in collecting and analyzing data.
  • Prioritize daily tasks.
  • Read, understand, and follow Product Stewardship Standard Operating Procedures.

Qualifications

  • Bachelor's degree in environmental or chemical engineering, chemistry, environmental Science or a related field is required.
  • 1+ years of professional experience.
  • General awareness of domestic and international product regulations is desirable.
  • Strong interpersonal and verbal communication skills are required.
  • Basic knowledge chemical processing is desirable.
  • Experience in a team environment is desirable.
  • Ability to adapt to a quickly changing environment.
  • Attention to details.
  • Motivated, conscientious and self-development oriented.
  • Proficient in typical office software is desirable.
  • 4 days ago
Related jobs
Promoted
Benjamin Moore & Co
Montvale, New Jersey

Regulatory Affairs Associate (Hybrid). Understanding, communicating, and general awareness of applicable legislation, regulatory procedures. ...

Promoted
Sun Pharmaceutical Industries, Inc.
Northvale, New Jersey

In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...

Benjamin Moore & Co
Montvale, New Jersey

Regulatory Affairs Associate (Hybrid). Understanding, communicating, and general awareness of applicable legislation, regulatory procedures. ...

Promoted
Sun Pharmaceutical Industries, Inc.
Rockleigh, New Jersey

In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...

Phibro Animal Health Corporation
Teaneck, New Jersey

The Senior Regulatory Affairs Associate/Manager plays a key role in ensuring compliance with regulatory requirements that govern the development, registration and commercialization of livestock and poultry products (primarily medicated feed additives and water-soluble products) while also providing ...

Cornerstone Search Group
NJ, United States

This hybrid role will lead US and Global regulatory activities in their Oncology therapeutic area on a potential first-in-class asset, serve as the regulatory expert on cross-functional product development teams globally on unpartnered assets and work with other pharmas on their partnered assets, an...

PHIBRO ANIMAL HEALTH CORP
Teaneck, New Jersey

The Associate Director Regulatory Affairs is an integral part of our Regulatory Affairs team based out of our US - Teaneck, NJ site. The Associate Director/Director plays a key role in developing and executing regulatory strategies and ensuring compliance with regulatory requirements that govern the...

Hays
NJ, United States

Responsible for assisting the Regulatory Team with the processes of maintenance and registration of new products and state wholesaler licenses as required from the FDA (Food and Drug Administration) and other regulatory agencies. At least 5 years of experience in the pharmaceutical industry includin...

Phibro Animal Health Corporation
Teaneck, New Jersey

The Associate Director/Director plays a key role in developing and executing regulatory strategies and ensuring compliance with regulatory requirements that govern the development, registration and commercialization of livestock and poultry products (primarily medicated feed additives and water-solu...

On-Board Companies
Somerset, NJ

On-Board Scientific is hiring a Regulatory Affairs Assistant!. The Regulatory Assistant needs to exhibit working knowledge of pharmaceutical operations. The Regulatory Assistant will need to utilize scientific and technical information to ensure that documents produced are consistently accurate and ...