Regulatory Affairs Project Manager

Perrigo Company; Oost-Vlaanderen; Hybrid; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Perrigo is seeking an experienced Regulatory Affairs Project Manager to reinforce regulatory activity for new products and the maintenance of existing dossiers. You will advise internal teams and external stakeholders to achieve registrations, market access, and compliant promotions.

In this role you will contribute to lifecycle management, labeling, packaging approvals, and submissions across EU Benelux regions. Fluency in Dutch and English is required; French/German an asset.

Qualifications

• Master’s degree in Life Sciences, Foods, Pharmacy, or related field.
• ≥4 years Regulatory Affairs experience.
• Fluent Dutch and English; French and/or German a plus.
• Strong knowledge of EU and Benelux regulations.

Responsibilities

• Assist regulatory activities to meet submission, approval and launch goals.
• Oversee lifecycle management including NPD, launches, and maintenance.
• Maintain labeling and packaging in compliance with EU laws.
• Prepare and manage regulatory submissions and authority communications.
• Collaborate with marketing, sales, and other regulatory and quality functions.
• Support change management and SOP-compliant documentation.

Skills

Regulatory affairs

Project management

Communication

Autonomy

Cross-cultural collaboration

Education

Master’s degree in Life Sciences, Foods, Pharmacy, or related field

Job description

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Description Overview

Are you an experienced Regulatory Affairs Project Manager with business acumen and a keen eye for detail?

We are looking for a new colleague to reinforce the regulatory activity required to submit, approve and launch new products and the maintenance of existing commercialized products and dossiers. In this role, you will be a key advisor to internal teams and external stakeholders, contributing to successful product registrations and market access projects, promotional campaigns, and protection of existing products in a fast changing regulatory environment.

Scope of the Role

• Assist in execution of regulatory activities per the project plan to assure new products meet submission, approval and commercial launch goals.
• Highly involved in the products’ lifecycle, including New Product Development (NPD) and launches, lifecycle maintenance and promotional activities.
• Support manufacturing and procurement in the management of change to existing commercial products.
• Maintain product labeling in compliance with local and EU laws and regulations; develop and approve label specifications in compliance with SOPs.
• Support the development and approval of packaging materials in a timely manner.
• Process change requests in compliance with GMPs and regulations.
• Maintain regulatory files and data systems in compliance with SOPs.
• Ensure timely and effective communication and collaboration with other departments including marketing, CS&I (trade marketing), sales and corporate regulatory and innovation.
• Review technical documentation and manage regulatory submissions in a timely manner.
• Process feedback from regulatory authorities and notified bodies.
• Support the development and clearance of promotional materials.
• Provide input for analysis of data and/or management review, if required.
• Assist in the process of reporting and investigating critical non-conformities and opportunities for improvement.

Experience Required

Master’s degree in Life Sciences, Foods, Pharmacy, or a related field

• At least 4 years of experience in Regulatory Affairs
• In-depth knowledge of local and EU regulations; at least in one of the countries of the Benelux and one or more of the following regulatory frameworks: medicines, medical devices, food supplements, biocides, general health products or cosmetic products.
• Strong communication and project management skills
• The ability to work both autonomously in local and international teams
• Strong communication, persuasion and problem-solving skills, with the ability to translate regulatory complexity to non-regulatory employees
• Curiosity - An eager and quick learner willing to develop and improve
• Fluent in Dutch and English is a must; knowledge of French and German is an asset

Benefits

We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

Hybrid Working Approach

We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo