Senior Regulatory Specialist

UL
Northbrook, IL
Full-time

Responsibilities

The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data and regulations in order to prepare documents for government agencies, curate lists and / or develop Environment, Health, Safety, and Transportation (EHS&T) information for the control and use of chemicals in the market place.

The Senior Regulatory Specialist responsible for Canadian legislation provides subject matter expertise to clients when requested which involves local, regional, national or international knowledge of industrial or consumer sectors.

The Senior Regulatory Specialist utilizes relevant software and can contribute to troubleshooting and enhancement of these software products.

Mentors and trains Regulatory Specialists. Interfaces with all levels of management to provide consultation on regulatory requirements.

  • Uses relevant software to meet client EHS&T needs.
  • Uses regulatory knowledge to provide subject matter expertise to clients and management for efficient EHS&T services when applicable.
  • Monitors applicable regulations relevant to specific job duties while maintaining a broad understanding of current regulatory landscape so that appropriate actions can be identified.
  • Collaborates with or leads multi-functional teams to improve and assist with testing of software and provides feedback to improve software products where applicable.
  • Provides expert regulatory knowledge to support the Marketing and Sales teams as is necessary.
  • Presents expert regulatory knowledge via Webinars and conferences to audiences to showcase UL's expertise.
  • Takes on additional responsibility as required to support business operations.
  • Read and follow the Underwriters Laboratories Code of Conduct, and follow all physical and digital security practices.
  • Performs other duties as directed.

LI-Hybrid

LI-MB1

Qualifications

University Degree (Equivalent to Bachelor's degree) in Chemistry, Biology, Environmental Sciences, Toxicology, or a related discipline with 5 years minimum relevant Canadian EHS&T experience.

Higher / advanced degree equivalent to a Master's degree in science-related field and 3 years minimum relevant Canadian EHS&T experience is preferred.

  • Aligns with UL values of integrity, competitiveness and collaboration.
  • Demonstrated effective time management to handle and prioritize multiple projects or streams of work to ensure timely and accurate completion of assigned work.
  • Ability to effectively communicate with both internal and external customers, peers and manager.
  • Bilingual in French a plus.
  • Proficient user of Microsoft Office applications such as Word, Outlook, PowerPoint, and Excel. Experience with chemical SDS authoring or supply chain network software preferred.

What you will experience working at UL :

  • Mission : For UL, corporate and social responsibility isn't new. Making the world a safer, more secure and sustainable place has been our business model for the last 130 years and is deeply engrained in everything we do.
  • People : Ask any UL employee what they love most about working here, and you'll almost always hear, "the people." Going beyond what is possible is the standard at UL.

We're able to deliver the best because we employ the best.

  • Diversity & inclusion : UL is committed to celebrating acceptance, equity and inclusion of all people. We believe our diverse views when combined bring a greater representation of the world and a better representation of our customers.
  • Interesting Work : Every day is different for us here as we eagerly anticipate the next innovation that our customers' create.

We're inspired to take on the challenge that will transform how people live, work and play. And as a global company, in many roles, you will get international experience working with colleagues around the world.

Grow & Achieve : We learn, work and grow together with targeted development, reward and recognition programs as well as our very own UL University that offers extensive training programs for employees at all stages, including a technical training track for applicable roles.

All employees at UL Solutions are eligible for annual bonus compensation. The target for this position is 10% of the base salary offered.

Employees are eligible for health benefits such as medical, dental and vision; wellness benefits such as mental & financial health;

and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country, for the relevant position level.

We also provide employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

Internal applicants with questions related to the Total Rewards for this position should submit a ticket via askHR for more insights.

Working at UL is an exciting journey that twists and turns daily. We thrive in the twists and revel in the turns. This is our every day. This is our normal.

2 hours ago
Related jobs
Promoted
Baxter
Deerfield, Illinois
Remote

Compile regulatory documents for FDA submission (eCTD experience preferred), including: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulato...

Promoted
UL, LLC
Northbrook, Illinois

The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data, and regulations in order to prepare documents for government agencies, curate lists, and develop Environment, Health, Safety, and Transportation (EHS&T) informa...

Promoted
baxter healthcare
Deerfield, Illinois
Remote

Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...

Baxter
Deerfield, Illinois

Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...

Katalyst HealthCares & Life Sciences
North Chicago, Illinois

Handling data management and retrieval of regulatory documents. Preparing and submitting US regulatory filings on time and in compliance. Staying current with regulations and providing expertise in regulatory affairs. Training team members and ensuring regulatory compliance. ...

Abbott
Green Oaks, Illinois

Senior Regulatory Affairs Specialist. Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. Work with Regulatory and CFT to improve efficiency in regulatory deliverables. Understand, investigate and evaluate regulatory history/backg...

Mediabistro
Deerfield, Illinois
Remote

Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...

Promoted
Sysmex America, Inc
Lincolnshire, Illinois

The Senior Manager Regulatory Affairs is the regulatory expert and is responsible for leading the preparation, documentation and submission of regulatory applications for Sysmex products. The Senior Manager position in Regulatory Affairs leads the regulatory strategy for new and modified Sysmex medi...

Promoted
AbbVie
North Chicago, Illinois

Global Regulatory Affairs Strategy roles (U. Responsible for supporting teams & efforts around major filing activities & Regulatory Health Authority (RHA) interactions & meetings, attending & providing regulatory support to other departments, project teams & committees. Assist Re...

Promoted
Brooksource
Mundelein, Illinois

We are seeking an experienced SAP Cutover Project Manager to join the SAP Unify Program for a leading healthcare manufacturer client. Minimum of 8+ years of SAP project management experience, ideally 10+ years of project management experience (PMP Preferred). Oversee the full lifecycle of SAP S/4HAN...