Pharmacovigilance & QA - Barcelona

Oxford Global Resources is looking for a Pharmacovigilance & Quality Assurance Consultant to support our client's Global Quality & Compliance team within Veterinary Medicine R&D (VMRD). · ...

5+ years of experience in IT roles within the Life Sciences industry. At least 3 years in a Technical Owner, Application Manager, or Technical Lead role for Regulatory Affairs or Pharmacovigilance systems. · ...

5+ years of experience in IT roles within the Life Sciences industry. · At least 3 years in a Technical Owner Application Manager or Technical Lead role for Regulatory Affairs or Pharmacovigilance systems. · ...

The role is responsible for ensuring commercial distribution activities are conducted in full compliance with EU Good Distribution Practice (GDP) and EU Good Pharmacovigilance Practice (GVP), while supporting business growth through pragmatic risk-based governance in the Southern ...

We are seeking a dynamic and experienced Regulatory Affairs professional to join our team asap. As an RA Project Manager, you will be responsible for a wide range of regulatory activities to support our company's third-party activities. · ...

We have established a Global Capability Center in Barcelona to support Galderma's growth trajectory and our global commercial and functional teams. Located in the upscale Eixample district in the heart of the city, it offers the possibility for professional career development thr ...

As the Opella Health and Science Global function within the Digital Division our mission is clear we are dedicated to revolutionizing healthcare. · Bachelor's degree in a relevant field Master's degree preferred. · Proven extensive experience in digital leadership roles within th ...

We are dedicated to making self-care as simple as it should be. That starts with our culture. · ...

+We look for people who focus on getting results, embrace learning and bring a positive energy. · ++Propose and recommend measures aiming at minimizing risks during clinical development; release and update the Development Risk Management Plans (DRMPs) · + · Partner with internal ...

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an enviro ...

This position involves writing and/or editing high-quality clinical and safety documents for submission to regulatory authorities. The ideal candidate will have experience in regulatory writing for the pharmaceuticals/healthcare industry and excellent communication skills. · ...

The company is looking for a Senior Quality Assurance Lead to oversee all aspects of the Quality Management System (QMS) to ensure compliance with regulatory requirements and internal standards. · Improve and maintain the Quality Management System (QMS) · Develop, implement and m ...

Expert Medical Regulatory Writer writes and/or edits under guidance high-quality clinical and safety documents for submission to regulatory authorities to support marketing authorization applications renewals and maintenance activities including complex Clinical Study Reports CSR ...

The PVA Data Surveillance will assume activities required to meet vigilance needs for products within the Rx, Ax, and Cx portfolios for post-marketing surveillance activities, · and regulatory submissions.Routine PV activities to ensure compliance with global vigilance requiremen ...

The Risk Management Manager leads activities and initiatives designed to identify and categorize risks that potentially impact the vigilance system and the broader Patient Safety & Pharmacovigilance organization. · ...

Technical owner with experience in IT roles within the Life Sciences industry required. At least 3 years of experience as Technical Owner, Application Manager or Technical Lead. · ...

Sanofi Global Hub is an internal Sanofi resource organization based in India. · Main responsibilities: · ...

We are seeking a Principal Medical Regulatory Writer to join our team at Sanofi Global Hub in Barcelona. · ...

The Lead Commercial Quality South ensures that commercial distribution activities are conducted in full compliance with EU Good Distribution Practice (GDP) and EU Good Pharmacovigilance Practice (GVP), while supporting business growth through pragmatic, risk-based governance in t ...

The Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products. · ...