Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Experience in regulatory affairs within the pharmaceutical or medical device industry., Strong understanding of EU regulations and guidelines., Excellent communication and analytical skills..

Key responsibilities:

Prepare and submit regulatory documents to health authorities.

Ensure compliance with regulatory requirements for product approvals.

Collaborate with cross-functional teams to support product development.

Monitor changes in regulations and advise on their impact.

As the world’s largest food and beverage company we are driven by a simple aim: unlocking the power of food to enhance quality of life for everyone, today and for generations to come. To deliver on this, we serve with passion, with a spirit of excellence, offering products and services for all stages of life, every moment of the day, helping people care for themselves and their families. Our culture is based on our values rooted in respect: respect for ourselves, respect for others, respect for diversity and respect for the future. We can trace our origin back to 1866, when the first European condensed milk factory was opened in Cham, Switzerland, by the Anglo-Swiss Condensed Milk Company. One year later, Henri Nestlé, a trained pharmacist, launched one of the world’s first prepared infant cereals ‘Farine lactée’ in Vevey, Switzerland. Today, we employ around 273,000 people and have factories or operations in almost every country in the world. With our headquarters still based in the Swiss town of Vevey, we had sales of CHF 84.3 billion in 2020. Our portfolio covers almost every food and beverage category –offering products and services for all stages of life, every moment of the day, helping people care for themselves and their families. House rules: https://nes.tl/HouseRules

Required profile