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Sr. Associate I, Regulatory Affairs Strategy

Alcon
Saudi Arabia, KSA
Mid-Senior
1 months ago
AffairsAssociateRegulatoryStrategy
Free

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Overview

  • At Alcon, we are driven by the meaningful work we do to help people see brilliantly.
  • We innovate boldly, champion progress, and act with speed as the global leader in eye care.
  • Here, you’ll be recognized for your commitment and contributions and see your career like never before.
  • Together, we go above and beyond to make an impact in the lives of our patients and customers.
  • We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
  • As a Senior Associate Regulatory Affairs supporting the EMEA Regulatory Operations team, you will be trusted to work on regulatory compliance, dossier development, and product registration activities across a diverse portfolio in Riyadh.
  • _Please note that for this position Saudi nationals are preferred._
  • In this role, a typical day will include:
  • Collaborating with regional affiliates and cross-functional teams to address regulatory requirements and health authority inquiries across the Middle East and EMEA region
  • Preparing and managing regulatory dossiers, submissions, licensing activities, and labeling documentation for pharmaceuticals, medical devices, cosmetics, and food supplements
  • Maintaining accurate and up-to-date submission databases, ensuring timely approvals and compliance tracking
  • Supporting clinical trial disclosure and submission publishing activities with high attention to quality and regulatory standards
  • Ensuring full adherence to GxP requirements, SOPs, and documentation standards to maintain audit readiness and regulatory compliance

WHAT YOU’LL BRING TO ALCON

  • Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, or a related field
  • Minimum 3 years of experience in Regulatory Affairs within the Middle East region in a multinational medical or pharmaceutical company
  • Strong knowledge of regulatory frameworks in the Middle East; understanding of EU regulations is highly desirable
  • Proven ability to manage regulatory submissions, dossier preparation, and compliance documentation
  • Excellent collaboration, communication, and influencing skills within matrix organizations
  • Fluency in English and Arabic (written and spoken)
  • High level of organization, adaptability, and a proactive, solution-oriented mindset

How You Can Thrive At Alcon

  • Work in a dynamic, international environment with exposure to diverse product categories and regulatory landscapes
  • Take ownership of meaningful projects that directly impact patient safety and product accessibility across markets
  • Collaborate with a highly skilled, supportive team where innovation, continuous improvement, and personal growth are encouraged

Alcon Careers

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