Regulatory Affairs Associate

Select how often (in days) to receive an alert: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...

Role OverviewWe are seeking a highly skilled Regulatory Affairs Associate to join our central team at Perrigo, supporting life cycle maintenance activities in medicinal portfolios across the EU. This role involves ensuring compliance with legislative frameworks and internal policies, working collaboratively with international regulatory authorities.As a...

Perrigo is proud to be included in the Forbes list of 'America's Best Employers by State 2024'. We are committed to fostering an inclusive, collaborative culture where each person can experience a sense of belonging.About the RoleAs a Regulatory Affairs Associate, you will support life cycle maintenance activities in medicinal portfolios across the EU,...

Indero, a contract research organization specialized in dermatology and rheumatology, is seeking a highly skilled Regulatory Affairs Specialist. As a key member of our team, you will be responsible for ensuring the quality and compliance of regulatory documents and submissions. This role requires strong knowledge of EU regional regulatory guidelines and...

At TN Poland, we are seeking a seasoned Regulatory Affairs Specialist to join our team. As a key member of our regulatory department, you will play a critical role in ensuring compliance with complex regulatory issues and projects.Responsibilities:Provide consulting and advisory services for regulatory matters.Author and maintain documentation to sustain...

**About the Role:**We are seeking a highly skilled Regulatory Affairs Expert to join our team. As a key member of our regulatory department, you will play a crucial role in ensuring compliance with all applicable regulations and guidelines.In this position, you will be responsible for the preparation and submission of clinical trial applications (CTAs)...

Colgate-Palmolive is a leading consumer products company with a rich history dating back to 1806. We operate in over 200 countries, offering a diverse range of brands and products across four core businesses: Oral Care, Personal Care, Home Care, and Pet Nutrition.We are committed to creating a healthier and more enjoyable life for our consumers through our...

IQVIA is a leading healthcare technology and consulting company, focused on using data and science to drive healthcare forward. Our lifecycle management team is seeking an experienced Regulatory Affairs Manager to support activities on the Russian market.This individual contributor role requires native/fluent Russian language knowledge and solid experience...

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Senior / Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD...

Social network you want to login/join with:Specialist, Regulatory Affairs (Poland), WarsawClient:InderoLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:0b22dd25b017Job Views:3Posted:21.03.2025Expiry Date:05.05.2025Job Description:Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In...

EU Medicines RegulationWe are seeking a highly skilled Regulatory Affairs Associate to join our Central Regulatory Affairs medicines team. The successful candidate will be responsible for managing projects, preparing and submitting product license variations and post-authorisation applications, and supporting various regulatory and quality areas.As a...

IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare...

Our Client, a leading pharmaceutical company, is seeking a talented and motivated Senior Regulatory Affairs Specialist to join their CMC team. As a key member of the team, you will be responsible for supporting global CMC regulatory strategies and documentation.The ideal candidate will have first-hand experience in CMC, regulatory affairs, or a related...

Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under internationally recognized brand names such as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci...

Job SummaryPfizer seeks a Regulatory Data and Conformance Manager to oversee regulatory compliance efforts. The successful candidate will have extensive experience in regulatory affairs, compliance, and project management.This role involves interpreting federal, state, and international regulations, investigating and resolving compliance problems, designing...

We are seeking a highly skilled Regulatory CMC Manager to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products. In this position, you will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development. This...

Role SummaryThe Senior Manager, Global Labelling will lead the development and implementation of labelling strategies for our pharmaceutical products.This role requires a strong understanding of regulatory requirements and the ability to collaborate effectively with cross-functional teams.You will be responsible for managing the labelling process, including...

At J&J Family of Companies, we are dedicated to building a world where complex diseases are prevented, treated, and cured. Our strength in healthcare innovation empowers us to deliver sustainable solutions and support stakeholder needs. We are recruiting for a Manager Regulatory Affairs Process Support, Data Integrity and Compliance with focus on EU.This...

About This Role:GSK is seeking a highly skilled Project Lead - Regulatory Planning and Resource Management to join our team. As a key member of our regulatory affairs team, you will be responsible for developing and implementing effective regulatory strategies to drive business growth and success. This role requires strong project management skills, with the...

We believe our people are our greatest asset at Perrigo. 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.We pride ourselves on fostering an inclusive, collaborative culture where each person...