Sr. Associate, Regulatory Affairs Strategy

Posted 4 Days Ago
Be an Early Applicant
Warszawa, Mazowieckie, POL
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Support regulatory strategies, submissions, product and establishment licenses, regulatory records, health authority interactions, labeling reviews, market actions, and compliance activities for medical device and pharmaceutical products. Monitor regulatory changes, assess impacts and gaps, respond to stakeholder queries, and contribute to operational excellence while collaborating with global and cross-functional teams.
Summary Generated by Built In

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?

Sr. Associate, Regulatory Affairs Strategy

In this role, a typical day will include:

· Support the development and execution of regulatory strategies and plans for new and marketed products, ensuring timely submissions, approvals, and lifecycle compliance in collaboration with Global Regulatory Affairs and cross-functional stakeholders.

· Prepare and support submission of regulatory dossiers (as required) tailored to local requirements to facilitate efficient health authority review and approval.

· Maintain all product and establishment licenses (e.g., marketing authorizations, import licenses) to ensure uninterrupted business continuity.

· Maintain accurate regulatory records and databases (e.g., Veeva RIM), ensuring all product information and submission statuses are current and audit-ready.

· Monitor regulatory changes, conduct regulatory impact assessments and gap assessments as needed, and support updates to internal policies, procedures, and documentation.

· Engage with internal stakeholders and support interactions with Health Authorities to enable effective regulatory execution and alignment with business objectives.

· Perform review and approval (as applicable) of local labeling, advertising, and promotional materials in compliance with applicable regulations and company standards.

· Provide regulatory support for market actions (e.g., FSCAs, recalls) and related health authority communications.

· Support initiatives to drive performance improvements and contribute to achieving performance targets and operational excellence.

· Deliver timely responses to regulatory queries from stakeholders across the organization

· Perform additional duties as required by the regional or affiliate QRA function.

WHAT YOU’LL BRING TO ALCON:

· BSc Degree in a Scientific or Engineering discipline or related field

· Proven experience (at least 2 years) in Regulatory Affairs function in the medical device or pharmaceutical industry, including comprehensive knowledge of ISO13485 and/or similar

· Very good command of English (written and spoken), Nordic language is considered a strong advantage

· Experience working in an international environment

· Excellent communication and interpersonal skills

· Strong stakeholder management skills, with the ability to build effective relationships across different functions and levels of the organization

HOW YOU CAN THRIVE AT ALCON:

  • Collaborate with teammates to share standard processes and learnings as work evolves!
  • Attractive benefits package (private medical care, group insurance, lunch card, transportation allowance, pension plan, Multisport/cultural card, Alcon products for you and your significant other)
  • Employment contract, full‑time position
  • ON - SITE WORK
  • Modern office with many facilities inside located at NewCity building, 15 Marynarska Street, Warsaw

Alcon Careers
See your impact at alcon.com/careers

  

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.

Find Jobs for Employees

Find Jobs for Contingent Worker

Skills Required

  • Bachelor of Science degree in a scientific, engineering, or related field
  • At least 2 years of experience in Regulatory Affairs within the medical device or pharmaceutical industry
  • Comprehensive knowledge of ISO 13485 or similar standards
  • Very good written and spoken English
  • Experience working in an international environment
  • Excellent communication and interpersonal skills
  • Strong stakeholder management and relationship-building skills
  • Nordic language proficiency

Alcon Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Alcon and has not been reviewed or approved by Alcon.

  • Retirement Support — Retirement benefits are framed as unusually strong, pairing a 401(k) match with an additional employer-funded retirement plan contribution. Stock purchase access and performance bonuses are also positioned as meaningful components of total rewards.
  • Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, life, disability, and mental health support. Distinctive vision-related perks, including free contact lenses in some cases, reinforce the perceived strength of the health-and-wellness offering.
  • Leave & Time Off Breadth — Time-off offerings are characterized as robust, including paid holidays, PTO/vacation, paid sick time, and parental leave. Flexible time off for certain exempt roles and reported year-end shutdown periods further strengthen perceived coverage.

Alcon Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Geneva
20,962 Employees
Year Founded: 1945

What We Do

Alcon helps people see brilliantly. As the global leader in eye care with a heritage spanning more than seven decades, we offer the broadest portfolio of products to enhance sight and improve people’s lives. Our Surgical and Vision Care products touch the lives of more than 260 million people in over 140 countries each year living with conditions like cataracts, glaucoma, retinal diseases and refractive errors. Our more than 20,000 associates are enhancing the quality of life through innovative products, partnerships with eye care professionals and programs that advance access to quality eye care.

Similar Jobs

Pfizer Logo Pfizer

Principal Engineer

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Remote or Hybrid
31 Locations
121990 Employees
177K-294K Annually

CrowdStrike Logo CrowdStrike

Sales Engineer

Cloud • Computer Vision • Information Technology • Sales • Security • Cybersecurity
Remote or Hybrid
3 Locations
11000 Employees

Capco Logo Capco

Consultant

Fintech • Professional Services • Consulting • Energy • Financial Services • Cybersecurity • Generative AI
Remote or Hybrid
Poland
6000 Employees

Capco Logo Capco

Consultant

Fintech • Professional Services • Consulting • Energy • Financial Services • Cybersecurity • Generative AI
Remote or Hybrid
Poland
6000 Employees

Similar Companies Hiring

Granted Thumbnail
Artificial Intelligence • Healthtech • Insurance • Mobile • Financial Services
New York, New York
23 Employees
OneImaging Thumbnail
Healthtech
Miami, FL
62 Employees
Vitalize Thumbnail
Artificial Intelligence • Healthtech • Software
US
50 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account