ProPharma Jobb i Sverige

We are seeking a Regulatory Affairs Manager to join our Nordic Regulatory Affairs team. As a Regulatory Affairs Manager you will lead and contribute to diverse projects for pharmaceutical clients. · ...

We are looking for an experienced · Senior Pharmacovigilance Manager to lead our Benefit-Risk team.In this key leadership position you will manage a team of Managers, Scientists, Coordinators and Subject Matter Experts, · drive high-quality delivery of pharmacovigilance projects ...

The Compliance and Quality Assurance Consultant position is responsible for supporting the management of compliance and quality assurance related projects and providing consulting and contract services to clients to address quality and regulatory / GMP issues, as needed. · ...

We help pharmaceutical companies bring life-changing therapies to market. From early development through clinical approval and commercialization · ...

+The Compliance and Quality Assurance Consultant (CQA) position is responsible for supporting the management of compliance and quality assurance related projects and providing consulting services to clients. · +Represent the company in assigned areas of quality assurance and regu ...

We are seeking a Regulatory Affairs Manager to join our Nordic Regulatory Affairs team. As a key member of the team, you will provide expert regulatory support across the Nordic region (Sweden, Denmark, Norway, Finland, Iceland) and manage submissions including new registrations, ...

We help pharmaceutical biotechnology and medical device companies bring life-changing therapies to market from early development through clinical regulatory approval and commercialization we provide expert guidance to navigate complex challenges and accelerate success · We celebr ...

We are looking for Nurses to support clinical trials sites in Sweden with patient home visits. · ...

We are looking for an experienced and proactive Senior Pharmacovigilance Manager to lead our Benefit-Risk team. · Lead and develop a high-performing team (line management, mentoring, onboarding, training & coaching) · Oversee delivery of aggregate safety reports (PSURs/PBRERs...) ...

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. · ...

ProPharma partners with clients to provide advice and expertise across the product lifecycle. · ...

The Senior Consultant - MedTech Regulatory Sciences is a senior regulatory role within ProPharma's global MedTech team providing expert regulatory support across EU medical device and IVD programs. · This position focuses on regulatory strategy project execution and subject matte ...