Principal Regulatory Affairs Consultant

We expect the Manager, Regulatory Affairs CMC to join a growing team and provide support to interpret the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. In this role, a typical day might include the following: Contributes to the management of the regulatory submission form process,...

When our values align, there's no limit to what we can achieve.   We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies...

Description Director, Global Regulatory Affairs, Pediatrics Dublin, Ireland At Gilead we believe every employee deserves a great leader. As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth and retention of talent, and empower...

Who we are looking for Purpose Join regulatory affairs in Rare Diseases Area! Be part of a dynamic, impactful field where every decision brings life-changing therapies closer to patients in need Main Responsibilities Under guidance of the regional Head, prepares, compiles, and maintains regulatory documents to support a broad...

When our values align, there's no limit to what we can achieve.   We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets. This is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country...

McDermott Laboratories Limited At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high quality trusted medicines...

The Opportunity The Regulatory Affairs Specialist, Artwork Labelling  is responsible for supporting product commercialization, for GPN owned and contract brands, for all activities involving regulatory compliance from concept to launch. This role will play a critical role in delivery of the growth objectives of the EMEA region.  Ensuring Product...

Why OutForm?     We are a dynamic consulting team, focused on delivering business transformation programmes, sustainable results and creating an environment for our team and our clients to flourish. We are passionate about building long-lasting relationships with our clients and team. What makes our team unique is that we truly collaborate...

The Position We wish to appoint a highly experienced . The ideal candidate will have a risk, compliance, internal audit, accountancy or similar background and at least 10 years’ experience. As an experienced member of the consulting team, you will have the opportunity to lead or support the delivery of a range of projects of a recurring and...

Our Opportunity We are currently seeking a REACH Regulatory Project Manager to operate within our Industrial Chemicals group for our Chemical Regulation and Food Safety Practice to provide leadership and support project teams working on regulatory submissions for the registration of industrial chemicals in the EU and UK. The role could be based from...

If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million...

SUMMARY: The Manager, Regulatory Submission Project Management will be responsible for leading strategic planning and execution of regulatory milestones from IND Project Approval (IPA) to postmarketing. The incumbent will report to the Sr Mgr Regulatory Submission Project Management and serve as the Reg PM lead for assigned therapeutic area (TA) and...

Regeneron is seeking a Manager to join the Regulatory Intelligence Group! In this role, a typical day might include: The Regulatory Intelligence Manager performs proactive global monitoring and surveillance of changes in the regulatory landscape focused on the drug development lifecycle, i.e., preclinical through commercialization, as well as...

Manager, Scientific Affairs- Test Validation ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Manager, Scientific Affairs- Test Validation-...

Our client is based in Dublin 24 and is currently recruiting for an experienced Regulatory Affairs Administrator to join their busy team. This is a six month contract initially, which may go permanent for the right candidate. Salary is €35 - €40k pa plus great benefits packet should role become permanent. This position offers hybrid working. This role...

Job DescriptionDue to growing demand for our consultancy services we are seeking to hire a Principal Consultant with database development, database management, process & data mapping and data analysis skillsets to join our specialist Turner & Townsend Technology consulting team.The role involves supporting a wide range of projects of all sizes and...

This is a remote position. Principal Software Engineer - Fully Remote in Ireland, Europe or United Kingdom A growing technology company who develop AI B2B solutions across multi-sectors globally have an interesting opportunity for a Principal Software Engineer. You will play a key role building AI solutions & services which are customised and...

Company Description At Turner & Townsend we’re passionate about making the difference. That means delivering better outcomes for our clients, helping our people to realize their potential, and doing our part to create a prosperous society.  Every day we help our major global clients deliver ambitious and highly technical projects, in over 130...

Job Description This is a remote position. Principal Software Engineer - Fully Remote in Ireland, Europe or United Kingdom A growing technology company who develop AI B2B solutions across multi-sectors globally have an interesting opportunity for a Principal Software Engineer. You will play a key role building AI solutions & services which are...

Körber Pharma Software, an industry-leading software firm within the pharmaceutical and biotech industry, has an outstanding career opportunity available for a Principal Consultant MES to join our team. As a Principal Consultant MES you will establish high-level business relations and generate new business ideas, revise strategies and methodologies to...