Alcon MX
Director, Regulatory Affairs Operations page is loaded## Director, Regulatory Affairs Operationslocations:
Fort Worth, Texastime type:
Full timeposted on:
Posted 12 Days Agotime left to apply:
End Date: January 16, 2026 (18 days left to apply)job requisition id:
R-2025-43246The Director, Regulatory Affairs Operations (Management Path) is primarily responsible for directing product/process registration submissions and providing strategic product direction to teams. You will build effective relationships with regulatory agencies to expedite approvals and address inquiries. Specifics include:* Lead and mentor teams in dossier preparation, Clinical Trial Disclosure, submission management, and submission publishing.* Maintain and drive continuous improvement initiatives for the Veeva RIM Suite and facilitate its rollout to cross-functional teams.* Create job aids detailing document approval processes, workflows, and submission tracking.* Provide user requirements and recommendations for Veeva auto releases and configurations and update associated Standard Operating Procedures (SOPs) in line with process improvements and auto releases.* Foster strong relationships with regulatory staff and cross-functional teams to prioritize compliant submissions.* Maintain oversight of the product support request tool and ensure all requests for documentation in support of marketing applications are fulfilled in a timely manner.* Develop and implement strategies to ensure departmental success and alignment with company goals.* Make key decisions impacting department performance and success.* Ensure timely and accurate submission of regulatory documents.* Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, and ensuring rigorous quality control.* Complete all required training and contribute to the overall compliance of the organization by committing to continuous improvement and adherence to regulatory requirements. All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.* The Director, Regulatory Affairs Operations will support the medical device portfolio of products across the Surgical and Vision Care Franchises.**What You'll Bring to Alcon*** Bachelor’s Degree or Equivalent years of directly related experience (or high school +18 yrs; Assoc.+14 yrs; M.S.+7 yrs; PhD+6 yrs)* The ability to fluently read, write, understand and communicate in English* 10 Years of Relevant Experience* 6 Years of Demonstrated Leadership* Travel: 10-20% Domestic* Work Location: Onsite – Fort Worth, TX (This role may be based at other Alcon locations, subject to business needs)* Relocation: Yes**How you can thrive at Alcon:*** Work together with colleagues to share standard methodologies and discoveries as work progresses.* Discover your career in a fresh way through specific growth and development possibilities.* Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!* Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!Alcon CareersSee your impact at**ATTENTION: Current Alcon Employee/Contingent Worker**If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.***ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY****Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to **alcon.recruitment@alcon.com** and let us know the nature of your request and your contact information.*locations:
Fort Worth, Texastime type:
Full timeposted on:
Posted 27 Days Agotime left to apply:
End Date: January 1, 2026 (3 days left to apply) #J-18808-Ljbffr
Fort Worth, Texastime type:
Full timeposted on:
Posted 12 Days Agotime left to apply:
End Date: January 16, 2026 (18 days left to apply)job requisition id:
R-2025-43246The Director, Regulatory Affairs Operations (Management Path) is primarily responsible for directing product/process registration submissions and providing strategic product direction to teams. You will build effective relationships with regulatory agencies to expedite approvals and address inquiries. Specifics include:* Lead and mentor teams in dossier preparation, Clinical Trial Disclosure, submission management, and submission publishing.* Maintain and drive continuous improvement initiatives for the Veeva RIM Suite and facilitate its rollout to cross-functional teams.* Create job aids detailing document approval processes, workflows, and submission tracking.* Provide user requirements and recommendations for Veeva auto releases and configurations and update associated Standard Operating Procedures (SOPs) in line with process improvements and auto releases.* Foster strong relationships with regulatory staff and cross-functional teams to prioritize compliant submissions.* Maintain oversight of the product support request tool and ensure all requests for documentation in support of marketing applications are fulfilled in a timely manner.* Develop and implement strategies to ensure departmental success and alignment with company goals.* Make key decisions impacting department performance and success.* Ensure timely and accurate submission of regulatory documents.* Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, and ensuring rigorous quality control.* Complete all required training and contribute to the overall compliance of the organization by committing to continuous improvement and adherence to regulatory requirements. All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.* The Director, Regulatory Affairs Operations will support the medical device portfolio of products across the Surgical and Vision Care Franchises.**What You'll Bring to Alcon*** Bachelor’s Degree or Equivalent years of directly related experience (or high school +18 yrs; Assoc.+14 yrs; M.S.+7 yrs; PhD+6 yrs)* The ability to fluently read, write, understand and communicate in English* 10 Years of Relevant Experience* 6 Years of Demonstrated Leadership* Travel: 10-20% Domestic* Work Location: Onsite – Fort Worth, TX (This role may be based at other Alcon locations, subject to business needs)* Relocation: Yes**How you can thrive at Alcon:*** Work together with colleagues to share standard methodologies and discoveries as work progresses.* Discover your career in a fresh way through specific growth and development possibilities.* Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!* Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!Alcon CareersSee your impact at**ATTENTION: Current Alcon Employee/Contingent Worker**If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.***ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY****Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to **alcon.recruitment@alcon.com** and let us know the nature of your request and your contact information.*locations:
Fort Worth, Texastime type:
Full timeposted on:
Posted 27 Days Agotime left to apply:
End Date: January 1, 2026 (3 days left to apply) #J-18808-Ljbffr