Regulatory Affairs Job at Alcon | Apply Now
Looking for a regulatory affairs job in a global healthcare company? Alcon Careers offers an exciting opportunity for a Regulatory Affairs Associate in Poland. This role is perfect for life science graduates and professionals aiming to build a career in regulatory compliance, medical devices, and global product approvals in a dynamic international environment.
Job Details
- Job Position: Regulatory Affairs Associate
- Location: Warszawa, Poland (Hybrid Work Model)
- Job ID: R-2026-45783
About the Company
Alcon Careers offers opportunities in a global leader dedicated to enhancing sight and improving eye health worldwide. With over 25,000 associates, Alcon focuses on innovation, inclusivity, and delivering impactful healthcare solutions. The company provides an excellent platform for professionals seeking life science jobs in Poland within a fast-paced and collaborative international environment.
Job Description
This regulatory affairs job is part of Alcon’s Global Regulatory Affairs function, ensuring that products comply with global, local, and internal regulations. The role focuses on supporting regulatory strategies, preparing submissions, managing product lifecycle activities, and maintaining compliance for medical devices developed by Alcon.
Qualifications
This Regulatory Affairs Job role requires:
- University degree in Life Sciences or a related technical field
- Knowledge of regulatory affairs principles and submission processes
- Ideally 2 years of experience in Regulatory Affairs (freshers with strong interest can apply)
- Very good command of English (written and spoken)
- Strong communication and collaboration skills
- Excellent planning, organization, and multitasking abilities
- Action-oriented mindset with a strong sense of urgency
Key Responsibilities
This Regulatory Affairs Job role responsibilities include:
- Support and/or prepare device regulatory filings for worldwide registration of medical devices
- Assist in preparing and submitting regulatory documents in compliance with guidelines
- Support response preparation for regulatory requests across the organization
- Develop clear, concise, and complete documentation for approvals
- Ensure timely communication with internal stakeholders regarding project status
- Maintain regulatory data in Alcon systems and approval tracking lists
- Verify registration data to facilitate approvals
- Follow established procedures with decision-making authority within assigned tasks
- Demonstrate attention to detail and strong understanding of regulatory processes
- Adhere to GxP regulations, SOPs, and quality control standards
- Complete required training and contribute to compliance and continuous improvement
Why Join Alcon?
- Opportunity to work in a leading medical devices organization
- Exposure to global regulatory processes
- Work in a high-paced, agile, and international environment
- Collaboration with global teams and stakeholders
- Attractive benefits package with competitive salary and bonus
- Flexible working hours and hybrid work model
- Modern office facilities in Warsaw
