Sr. Associate II, Regulatory Affairs Strategy

Alcon Research•Fort Worth, TX

8d•Onsite

About The Position

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us? Alcon is looking to hire a Sr. Associate II, Regulatory Affairs Strategy, this role is part of Alcon’s Quality & Regulatory Affairs function—a critical organization responsible for ensuring our products meet global regulatory requirements and the highest standards of safety, quality, and performance. As a Sr. Associate II, regulatory compliance and strategy activities for Alcon’s Intraocular Device portfolio, including intraocular lenses (IOLs), implantable glaucoma devices and associated delivery systems. This onsite position is based in Fort Worth, Texas (other on-site locations available) and plays a key role in enabling compliant, timely access to innovative devices across global markets. Through your work, you will help strengthen regulatory excellence, support business objectives, and uphold Alcon’s commitment to quality, compliance, and patient safety.

Requirements

Bachelor’s Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs).
The ability to fluently read, write, understand and communicate in English
2 Years of Relevant Experience

Responsibilities

Perform specialized tasks and conduct independent research within the Regulatory Affairs Strategy team to optimize outcomes and contribute to project goals.
Coordinate product submissions, renewals, and updates by liaising with plants, agents, and authorities to ensure timely submissions and approvals.
Provide regulatory strategies for new product introductions and changes, maintaining compliance to drive competitive advantage.
Support products in the medical device families, ensuring adherence to relevant regulations.
Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining documentation, ensuring quality control, and completing required training.
Commit to continuous improvement in operations and contribute to the organization's overall compliance.