Regulatory Associate - Stockholm, Stockholm County

We're looking for a talented Licensing & Regulatory Affairs Associate to support our Compliance Team from our Bogotá office. · We're building a world where ambition knows no borders and where financial success follows you wherever life takes you. We've built a mobile banking plat ...

We're looking for a motivated and detail-oriented lawyer eager to grow in our dynamic international environment. · ...

A job to develop and execute the global product compliance strategy in alignment with business goals. · Develop and execute the global product compliance strategy in alignment with business goals · Ensure globally harmonized compliance practices while adapting to regional regulat ...

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. · ...

We're on a mission to empower people with disabilities to do what they once did or never thought possible. · ...

We're seeking a driven and organised Scientific Affairs officer to take responsibility for the daily local regulatory affairs workflow for pre-defined portfolio and support the medical information and pharmacovigilance management in the Scandinavian region. · ...

At Resurs we are strengthening how we work with financial crime prevention to stay ahead in a changing regulatory landscape. · ...

As Associate Director within Project Management you will be responsible for the direction implementation control and completion of CMC projects from early development through launch and beyond while ensuring alignment with company strategy commitments and goals. · ...

We are looking for an Software Verification Engineer to develop and enhance test automation solutions in Python. · ...

We are committed to maintaining the first-class service and high standard of excellence that have defined Morgan Stanley for over 89 years. · ...

We are looking for someone who has experience in leading larger product organisations in medtech, healthtech, or other regulated or technically complex industries. · Has experience delivering products used in European and US healthcare markets · ...

This is the opportunity for you to play a key role in bringing innovative therapies to patients by leading CMC projects. · Lead and execute CMC activities supporting product development regulatory variations approvals and launches across multiple territories · Manage CMC project ...

The Clinical Trial Associate supports clinical study teams by coordinating operational activities and ensuring accurate setup, · maintenance, and closure of the Study Master File in compliance with GCP, · SOPs, · and regulatory requirements. · This role is part of our SRS team, · ...

This role will oversee outsourced pharmaceutical development clinical manufacturing preparations for commercial manufacturing and supply activities performed at CDMOs for designated projects. · You will manage activities performed both internally and through external experts ensu ...

IQVIA is seeking an experienced and passionate pharmaceutical product development strategist to join our team as Therapeutic Strategy VP. · ...

The Clinical Trial Associate supports clinical study teams by coordinating operational activities and ensuring accurate setup, maintenance, and closure of the Study Master File in compliance with GCP, SOPs, and regulatory requirements. · ...

We are seeking a Chief Medical Officer to serve as the senior clinical leader at Getinge. The CMO will guide the medical and scientific strategy of our product portfolio and ensure that all medical device development is grounded in clinical evidence. · ...

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. · ...

The Clinical Trial Associate (CTA) supports clinical study teams by coordinating operational activities and ensuring accurate setup, · maintenance, and closure of the Study Master File in compliance with GCP,v SOPs,and regulatory requirements. · As part of our SRS team,you will w ...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPha ...