Qppv Qualified Person Responsible for Pharmacovigilance Stellenangebote

QPPV / Qualified Person Responsible for Pharmacovigilance (m/f/x) Heidenheim an der Brenz Vollzeit THE FORCE CT GmbH … with a passion in the field of medical sciences, medical affairs, or pharmacovigilance. WHAT MAKES YOU FIT RIGHT IN? You have a medical degree and a keen … you and we are aiming for. But above all, we are interested in you as a person and focus on your specific talents. We are looking for that certain …Responsible StellenangeboteHead QPPV & PRRC Office (f/m/d) Wehr Vollzeit Novartis 384853BR Head QPPV & PRRC Office (f/m/d) Germany About the role The Head QPPV & PRRC Office … has the dual accountability of (1) acting as the EU Qualified Person for Pharmacovigilance (QPPV) and UK QPPV including the responsibility for the global Novartis … QPPV & PRRC Office has the dual accountability of (1) acting as the EU Qualified Person for Pharmacovigilance (QPPV) and UK QPPV including the …Qualified Responsible PharmacovigilanceDeputy EU QPPV Deutschland Vollzeit BeiGene … passionate interest in fighting cancer. General Description: The Deputy EU QPPV together with the EU QPPV is responsible for maintaining, overseeing and … EU QPPV is responsible for maintaining, overseeing and promoting BeiGene’s pharmacovigilance system and overseeing the benefit-risk profile of BeiGene’s medicinal … language an advantage) Essential Functions of the job: Supports the EU Qualified Person responsible for PV (EU QPPV) in the establishment and maintenance …Qualified Person Responsible for

EU-QPPV & Head QPPV Office (d/f/m) Holzkirchen Vollzeit Sandoz … oversight of PV operations in Europe/EEA and non-EU/EEA countries, with QPPV requirements together with PV, Safety Operations & Compliance, Medical … countries with local QPPV requirements together with GDD and Regional Pharmacovigilance/Quality Head. To contribute (as a member) to the Medical Safety Review … information about all suspected adverse actions which are reported to the person of the Marketing Authorization Holders (MAHs), and its medical …Qppv Qualified Responsible PharmacovigilanceGlobal Safety Manager (m/w/d) Freiburg Vollzeit Dr. Falk Pharma GmbH … studienspezifischer Dokumente Unterstützung des Head Global Safety / EU-QPPV / Stufenplanbeauftragten bei der Erfüllung der … Erstellung und Pflege der Pharmakovigilanz-Stammdokumentation (Pharmacovigilance System Master File, PSMF) Sicherstellen der erforderlichen Qualität der … und finanzieller Unabhängigkeit Für Fragen stehen wir Ihnen unter personal@drfalkpharma.de oder unter der Telefonnummer + 49 761 1514-102 gerne …Qppv Qualified Responsible for StellenangebotePharmacovigilance Associate Deutschland Vollzeit knoell Germany GmbH … to oversee routine pharmacovigilance activities under the guidance of our QPPV, ensuring adherence to high-quality standards and providing valuable … YOUR TASKS We are seeking a dedicated professional to oversee routine pharmacovigilance activities under the guidance of our QPPV, ensuring adherence to … a biological science to join our team. The candidate does not need to be a qualified veterinarian but will work closely with veterinarians from the clinical …Qppv Qualified Person Responsible for PharmacovigilanceExpert* Pharmacovigilance & Scientific Information Münster Teilzeit Diapharm GmbH & Co. KG … medizinischer Informationen. Consulting / Beratung Funktion als EU-QPPV, Stufenplanbeauftragter und / oder Informationsbeauftragter Erfassung und … sicher - in Deutsch & Englisch Diapharm lebt eine Kultur, die Entwicklung fördert und Engagement belohnt! Sie können uns helfen? Dann rufen Sie an! Ich …Person for Stellenangebote(Junior) Pharmacovigilance Officer (w/f/d) Global Drug Safety Frankfurt am Main Vollzeit Merz Therapeutics … channels, responsibilities, and work processes in collaboration with the QPPV and the German "Stufenplanbeauftragte". Tracking and analysis of updates … Temporary Position for 18 months YOUR CONTRIBUTION Join our Pharmacovigilance Group within Global Product Safety and grow with new challenges. Your …Qppv Responsible for Pharmacovigilance StellenangeboteMedical / Clinical Advisor (all genders) Wiesbaden Vollzeit AbbVie … your mark: The purpose of this role is to support the International/EU QPPV in meeting their regulatory PV obligations, ensuring oversight of AbbVie’s … science, healthcare discipline (medicine, pharmacy or nursing) or pharmacovigilance. At least 5 years in regulated pharmaceutical industry; must have … legislation. As part of the Office of the QPPV, the incumbent will also be responsible for sharing relevant product safety, risk management and PV policy …Person Responsible for PharmacovigilancePharmacovigilance Officer/ EU-QPPV* (Reporting to the Chief Medical Officer) Deutschland Vollzeit AiCuris GmbH & Co. KG … well as the primary contact for PV inspections in Europe Taking over EU-QPPV responsibility as well as the Graduated Plan Officer … Your mission At AiCuris, the role of the Pharmacovigilance Officer is of the highest importance. Bringing broad knowledge to the drug … accommodations we enable our people to integrate business into their personal life. Benefits: Employer-funded pension comes along with an attractive …Qualified Responsible Pharmacovigilance Stellenangebote Patient Safety Europe Lead Deutschland Vollzeit BeiGene … maintain and improve the international PV operations, as well as the QPPV Office and GPS Quality Management Operations to provide an overview of the … Representatives (LSRs) in each European country ensures that all local pharmacovigilance (PV) activities are performed as required by European and local … operations in Europe or a major European country or as National PV Contact Person (per GVP) Fluent in written and spoken English, second European language …Qppv Qualified Responsible for Stellenangebote Vigilance Specialist 790 Deutschland Vollzeit ProductLife Group … PV department as soon as possible. Responsibilites Ability to support the QPPV Ability to support in PV audit Ability to take on GPO (graduated plan … or medical degree is a plus) 1-6 years of experience as a drug safety or Pharmacovigilance department/industry German Speaker Agility and analytical Proficiency in … in PV audit Ability to take on GPO (graduated plan officer) or local PV person responsibilities Experience in case management or medical information and …Person for Pharmacovigilance Stellenangebote