Are you ready for a new step in your career?

Mead Johnson Nutrition is a long-standing multinational brand specializing in infant and child nutrition. Our company vision is to become the world's leading provider of scientifically backed child nutrition and specialized food products and services. At Mead Johnson Nutrition, we are deeply committed to creating nutritional brands and products that give babies and children the best start in life. With over 450 employees, our Nijmegen factory produces super-premium child nutrition for the largest market in the world, Greater China. Quality, reliability, innovation, and ethics are core values at Mead Johnson.

Join our dynamic team as we strive to excel in regulatory affairs within a leading company known for innovation, quality, and ethics. We are seeking a proactive and detail-oriented Regulatory Affairs Manager to lead impactful change and ensure the highest standards of compliance and operational excellence. This pivotal role offers you the chance to work in a fast-paced environment and make a significant difference.

What will you do?

• Develop and implement regulatory strategies that align with business objectives and ensure compliance with global and local regulations.
• Collaborate with cross-functional teams to oversee product registration processes and maintain compliance throughout the product lifecycle.
• Ensure timely submission and approval of registration dossiers to regulatory bodies.
• Monitor and interpret regulatory changes, assessing their impact on company operations and advising stakeholders accordingly.
• Prepare and review documentation required for regulatory submissions, ensuring accuracy and completeness.
• Act as the point of contact for regulatory inquiries and audits, providing necessary support and documentation.
• Lead continuous improvement initiatives to enhance the efficiency of regulatory processes.

Who are you?

• Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field.
• A minimum of 5 years of experience in regulatory affairs, preferably within the pharmaceutical industry.
• In-depth knowledge of current regulatory guidelines and industry practices.
• Experience in managing and submitting regulatory documents and interactions with health authorities.
• Strong analytical and problem-solving skills with attention to detail.
• Excellent communication and interpersonal skills, with proficiency in English; additional language skills are an advantage.
• Ability to work independently and collaboratively within a team-oriented environment.

What We Offer

An inspiring and collaborative work environment where you will have the opportunity to advance your career in regulatory affairs. We offer flexible working hours, a comprehensive pension plan, health insurance options, continuous professional development opportunities, and a supportive team atmosphere.

How to Apply

If you are passionate about regulatory affairs and eager to contribute to our mission of excellence, we would love to connect with you. Please send your CV and a cover letter through the 'Apply Now' button. For further information about this opportunity, please contact us via email at steven.vanharen@mjngc.com. Note that VOG screening may be part of our recruitment process.