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Alcon

Eye care products and vision solutions

Director, Regulatory Affairs Operations

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time$199.8k - $258.5k /yr

About the Job

Requirements

  • A bachelor's degree or equivalent years of directly related experience is required; alternatively, high school plus 18 years of experience, an associate degree plus 14 years, a master's degree plus 7 years, or a PhD plus 6 years is accepted.
  • Fluency in reading, writing, understanding, and communicating in English is required.
  • 10 years of relevant experience is required.
  • 6 years of demonstrated leadership is required.

Responsibilities

  • Direct product and process registration submissions and provide strategic product direction to teams.
  • Build effective relationships with regulatory agencies to expedite approvals and address inquiries.
  • Lead and mentor teams in dossier preparation, Clinical Trial Disclosure, submission management, submission publishing, licensing, and labeling.
  • 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 in line with process improvements and auto releases.
  • Foster relationships with regulatory staff and cross-functional teams to prioritize compliant submissions.
  • Maintain oversight of the product support request tool and ensure requests for documentation supporting 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.
  • Follow Good Practice regulations and Standard Operating Procedures, maintain accurate and complete documentation, ensure rigorous quality control, complete required training, and support continuous improvement and organizational compliance.
  • Support the medical device portfolio across the Surgical and Vision Care Franchises.

About the Company

Alcon

Eye care products and vision solutions

Alcon provides eye care products and vision solutions to improve how people see. It develops and manufactures devices and consumables for eye health, including cataract surgery equipment and intraocular lenses, retinal health therapies, and contact lenses, distributed through eye care professionals, hospitals, and consumers. The products work by supporting eye surgery, protecting and restoring vision, or correcting vision with lens-based options, backed by research and development and a global distribution network. Alcon differentiates itself with a broad, end-to-end portfolio across the eye care continuum, a strong emphasis on research and development, strategic partnerships with healthcare providers, and a commitment to diversity and inclusion. Its goal is to enhance vision and quality of life by delivering reliable, high-quality eye care solutions and advancing the science of eye health.

Company size
10,001+
Company stage
IPO
Headquarters
Geneva, Switzerland
Founded
1945

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