My TOD

11/24/2021

"Giving Liberates The Soul"- such an incredible and truthful statement! loved serving together this morning!

11/24/2021

Meet the myTOD team!

The people who are building our organization are a strong representation of our values and commitment to making a positive impact in the lives of those we connect with. We are so thankful that you are on this amazing journey with us.

11/24/2021

At myTOD we offer an ALTERNATIVE way of supporting your In-house Talent Acquisition Team initiatives and goals. We are here for you when you need us; we tackle the world of hiring together! Please check out this introductory video:

In this video, we explain how recruiting as a service works.

11/24/2021

Our values help us connect your business with talent that matches your ambitions, culture, and goals!

11/24/2021

Here's why you'll love this job:

• You enjoy working in a fast-paced, deadline-driven work environment where accountability is a core value!
• You will be working in a dynamic, never-boring company with a rapidly growing product portfolio!
• You have a passion for learning new things and bringing ideas and strategies to the table.
• You like to make smart decisions on your own.
• You are a creative problem-solver with a keen eye for detail who loves a challenge!

Here's what you'll be doing:

• Manage multiple applications simultaneously and interface directly with regulatory bodies, agencies, distributors, and other stakeholders to resolve application issues.
• Work on cross functional teams and communicate complex regulatory requirements and technical data in an understandable way for any audience to bring exciting new products to the market.
• Author and compile technical documentation for submissions, licensing and re-licensing, and change reporting.
• Research and report relevant regulations and conduct impact/gap analyses to ensure smooth implementations in assigned markets.
• Support local partners on regulatory documentation for both compliance and importation where needed.

Here's what you'll bring to the role:

• 5+ years of Regulatory Affairs Experience at a Medical Device Company and/or Cosmetics Company
• Working Knowledge of International Regulations and standards such as CFR 820, EU MDD/MDR, IEC, ISO, etc.
• Keen communication skills including technical writing for global submission files
• Ability to work independently and with minimal supervision
• Ability to work in a face paced environment and manage multiple projects simultaneously
• Familiarity with Document Control Systems, MS Office