Regulatory Affairs Manager - Oeiras

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. · ...

Experience HELM as a unique family business and an attractive employer. Through a constant exchange of ideas, our ultimate goal is to offer our customers future-oriented solutions within our global network. · You take responsibility for preparing and managing registration proced ...

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. · ...

We're Hiring: Senior Regulatory Affairs Manager – Biological Products (EU Market) · Are you a strategic Regulatory Affairs professional with strong expertise in biologicals and bioinputs within the European market? This is an opportunity to play a key role in shaping regulatory s ...

Regulatory Affairs Manager (m/f/d) · Maser's degree in Lifescience. · Three to five years' experience in regulatory affairs for European and national procedures or other highly regulated markets. · ...

We are seeking a passionate and visionary Medical Affairs professional to join our team and drive a fundamental shift in the Portuguese healthcare system—from reactive to proactive, · Actively engage with clinical societies and Key Opinion Leaders (KOLs) to embed our high-value d ...

We are seeking a passionate and visionary Medical Affairs professional to join our team... · ...

We are seeking a passionate and visionary Medical Affairs professional to join our team and drive a fundamental shift in the Portuguese healthcare system—from reactive to proactive. · ...

This is an excellent opportunity to join an international pharmaceutical company seeking a Regulatory Affairs Manager to support its global regulatory operations. · ...

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. · Bachelor's or Master's degree in Life Sciences or related fieldEight or more years in Regulatory Affairs ...

We are looking for a Regulatory Affairs Manager to support the compliance registration and certification of our medical devices across multiple markets. · Excellent understanding of medical devices to ensure our products fulfil all regulatory directives; · Compile review submit a ...

+This is a great opportunity to join a global consultancy with a strong track record of advising clients in the chemical sector, with a focus on agrochemicals, biocides and REACH, to help them navigate the complexities of the EU regulatory environment. · +The Regulatory Affairs P ...

This Regulatory Affairs Officer will drive regulatory strategy and delivery across complex projects, lead cross-functional workstreams, prepare submission materials, act as a subject-matter expert throughout clinical trials. · ...

This position will be responsible for developing and executing medical affairs plans related to the assigned ophthalmology therapy area across the cluster. · Lead the planning and implementation of cluster-level medical activities in ophthalmology across PASEBA. · ...

At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech-tailored delivery model, we accelerate clinical development from early phase through global registrational st ...

An amazing opportunity has arisen for a Therapy Area Lead (TAL) in Ophthalmology within the PASEBA Cluster. · Lead the planning and implementation of cluster-level medical activities in ophthalmology across PASEBA, · Build and maintain strong scientific engagement with the ophtha ...

An amazing opportunity has arisen for a Therapy Area Lead (TAL) in Ophthalmology within the PASEBA Cluster. · ...

An amazing opportunity has arisen for a Therapy Area Lead (TAL) in Ophthalmology within the PASEBA Cluster. · Lead the planning and implementation of cluster-level medical activities in ophthalmology across PASEBA... · ...

You'll serve as a senior subject-matter expert on Third-Party Management Program and will be involved in the risk assessments across Anti-Corruption, Antitrust, and Anti-Money Laundering. · ...

Experienced Regulatory Affairs Professional – C‑ROSS Lifecycle Submissions (LS) · ...