Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role:

As the Site Regulatory Compliance Lead, you will be instrumental in ensuring regulatory adherence across our multidisciplinary projects, including product launches and technical changes. Acting as the primary regulatory contact, you will collaborate closely with various internal departments, such as MSAT, Production, QA, QC, and Engineering. Your responsibilities will include evaluating site change controls and ensuring timely communication with the Swiss Authority, which is crucial for the submission of regulatory documentation. This role is vital for fostering compliance and facilitating effective communication across diverse regulatory landscapes. You will track amendments and regulatory assessments, coordinate the writing of registration dossiers, and manage deadlines to ensure timely regulatory submissions. Additionally, you will serve as a key point of contact for health authorities, providing necessary data and responses to inquiries. You will actively participate in the preparation for inspections and audits, ensuring our readiness and compliance. By leading internal audits and contributing to corporate and continuous improvement projects, you will help shape our regulatory landscape.

Who you are:

• You hold a degree in Pharmacy or Life Science, Biotech, Medical, PharmD, or a related discipline (minimum M. Pharm or MSc or equivalent degree); a higher degree (e.g., PhD) is preferable.
• You have at least 7 years of experience in Regulatory Affairs, focusing on medicines (new, generic, similar, and biological).
• You are fluent in both English and French.
• You possess strong analytical, strategic, and conceptual thinking skills.
• You are an influential and proactive individual with excellent interpersonal relationship skills.
• You have experience with regulatory systems such as Veeva Vault.
• You can manage multiple projects and meet tight deadlines effectively.
• Your communication skills, both written and verbal, are exceptional.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Notice on Fraudulent Job Offers

Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information here.

Applicant Profile
Along with our brand-new career site, we've also revamped our application process. If you've applied for a position before April 16th 2025, you can log into your old profile to see the status of past applications. For the application you’ve will completed, and any in the future, you can create a new profile to check in on your status.

WHAT WE OFFER

Money makes the world go round. But at Merck there’s more than just financial rewards. We offer a range of attractive benefits to help you work your magic.

Financial & Protection

These core benefits help to provide long-term financial stability for you and your family.

Health and Wellbeing

This pillar is important to us. Therefore, our health benefits are designed to support employees physical and mental wellbeing, e.g. health checkups or medical insurance.

Family

From our Fertility Benefit, to helping support your family life through all its different stages.

Time Away

Time to recharge and specific Leaves to support life events and choices

Life-style

Such as flexible working, gyms, car benefits, shopping discounts.

OuR RECRUITING PROCESS

Depending on the position (level, functional area, country) the process can vary slightly.

You apply

Complete your online application for your preferred role(s) that match your interests and qualification. If you cannot find a suitable role please join our Talent Zone and stay connected for your next career opportunity.

We screen

We review your application and if we determine that you are a good fit we will move you to the selection process.

We assess

You are interviewed by phone, via video and/or face to face.

Mutual agreement

Ideally you are the perfect match for us! We hope you consider us as your new employer.

Work your magic!

To guarantee you a smooth start our onboarding preparation begins.