36 results for Global Regulatory Affairs Manager Jobs

HSO way of workingIn fulfilling our roles, we areAccountable for our own capabilities and development.Focused on delivering results without excuses, andAlive to the sensitivities, risk, and impact we have on others and work in a way that helps others do their work effectively.We are looking for peop...

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that se...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment ...

Regulatory Affairs Manager – Clinical Trials📍 London | 💼 Fixed-Term (2–3 Years) | 💷 £52,000–£60,000 | 🕒 Full-timeThe RoleAre you confident navigating complex global clinical trial regulations? Do you bring experience guiding research teams through the challenges of compliance in an evolving regu...

Lexington Medical is a medical device company, developing and manufacturing minimally invasive surgical stapling solutions in the Boston area. With the highest standards in design engineering and smart manufacturing, our team delivers disruptive technology to health care providers which improves sur...

Are you experienced within the Regulatory CMC area taking a strategic perspective in handling CMC documentation for pharmaceutical products? Are you an inspiring leader and a skilled people manager? Join us in making a difference for people living with allergy!The positionRegulatory CMC is an area w...

Summary / purpose of the position As a Senior Manager in Global Regulatory Affairs, you will develop and supervise the implementation of regulatory strategies for all assigned projects, including products in early development and/or the life cycle management of mature products and all of its compone...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine...

MissionTo coordinate regulatory activities triggering successful life-cycle management for Almirall Global products approved worldwide in liaison with local regulatory responsible at market companies, consultants, or partners and in close collaboration with CMC and roll-out regulatory responsible.Ta...

The RoleThe Regulatory Operations Global Publishing Manager is responsible for overseeing the planning, creation, and submission of regulatory submissions. In collaboration with the Regulatory Lead, you will manage and prepare high-quality global submissions, both in-house and via CROs, ensuring tim...