Pharmacovigilance Specialist Stellenangebote


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10 Jobs für Pharmacovigilance Specialist


Stellenangebote Pharmacovigilance Specialist Jobs


Job vor 5 Tagen bei StepStone gefunden Bausch + Lomb

Technical Responsible Person (FvP) / Senior Quality Assurance Specialist (m/f/d)

• Zug Beratungs-/ Consultingtätigkeiten [. .. ] Maintain the Quality Management System (QMS) and conduct internal audits and training management activities. Communicate with Swiss health authorities, manage regulatory activities in Switzerland, and maintain product [...]
MEHR INFOS ZUM STELLENANGEBOT[...] registrations/ licenses. Support pharmacovigilance and materiovigilance activities for the Swiss market, by handling routine activities (including literature research, reporting obligations, managing adverse event reports and participation in product recalls) . Regularly report and monitor Quality Performance Indicators (QPIs) . Qualify suppliers, service providers, and customers. Organize and conduct audits to ensure quality and compliance. [. .. ] a parental leave replacement. We look forward to receiving your detailed online application JBRT1DE. Bausch + Lomb sucht in Zug eine/n Technical Responsible Person (Fv P) / Senior Quality Assurance Specialist (m/f/d) (ID-Nummer: 14502008) 03250423 [. .. ]

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Neu Job vor 2 Std. bei Neuvoo.com gefunden The BIG Jobsite Technical Responsible Person (FvP) / Senior Quality Assurance Specialist (m/f/d) • Saxony Zug [. .. ] Maintain the Quality Management System (QMS) and conduct internal audits and training management activities. Communicate with Swiss health authorities, manage regulatory activities in Switzerland, and maintain product [...]
MEHR INFOS ZUM STELLENANGEBOT[...] registrations/ licenses. Support pharmacovigilance and materiovigilance activities for the Swiss market, by handling routine activities (including literature research, reporting obligations, managing adverse event reports and participation in product recalls) . Regularly report and monitor Quality Performance Indicators (QPIs) . Qualify suppliers, service providers, and customers. Organize and conduct audits to ensure quality and compliance. [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Planet Pharma

Associate Director Biostatistics

• AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire [...]
MEHR INFOS ZUM STELLENANGEBOT[...] recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. J-18808-Ljbffr 03446195 [. .. ]

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Job vor 8 Tagen bei Mindmatch.ai gefunden Gouya Insights

Clinical Project Manager

• AT- 9 Wien [. .. ] medical device companies. As Clinical Project Manager, you will take operational ownership of early-phase clinical studies and development projects, working at the interface between our clients, clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sites, CROs, specialist vendors, and internal clinical development experts. You will translate clinical development strategies into operational execution, coordinate cross-functional project teams, and ensure timely delivery of projects within budget constraints, maintaining high quality and GCP standards. This role suits a proactive leader who enjoys taking ownership, working in a dynamic early-[. .. ] and crossfunctional experts. Track criticalpath activities and proactively identify, elevate, and resolve operational risks, issues, and dependencies. Coordinate crossfunctional activities with Medical Experts and Medical Writers, Clinical Data Management, Biostatistics, Pharmacovigilance, and Quality. Maintain effective project governance, including project, risk, and action trackers, status reporting, and project meetings. Support clinical trial budget management, forecasting, accruals, and change control. Lead the selection, coordination, and oversight of CROs and specialist clinical trial vendors and support their contracting and qualification. Review scopes of work, [. .. ]

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Job gestern bei Jobleads gefunden

Specialist Regulatory Affairs DACH (m/f/d)

• Neuss, Nordrhein- Westfalen Abgeschlossenes Studium Specialist Regulatory Affairs (m/f/d) Zur Verstärkung unseres Regulatory Affairs DACH Teams suchen wir ab sofort für unseren Standort Neuss einen Specialist Regulatory Affairs DACH (m/w/d) In dieser Rolle werden Sie [...]
MEHR INFOS ZUM STELLENANGEBOT[...] direkt an den Head of Regulatory Affairs DACH berichten. Sie werden für die DACH Region (Deutschland, Österreich, [. .. ] von Zulassungsstrategien für z. B. Entwicklungsprojekte und kompetitive Claims Koordination bzw. Durchführung von Zulassungsverfahren (DCP, MRP, national) Mitarbeit in regulatorischen und funktionsübergreifenden Projektteams (Marketing, Medical Affairs, R D, Commercial Quality, Pharmacovigilance, Supply Chain) Organisation und Koordination von wissenschaftlichen Beratungsgesprächen Beobachtung des nationalen und europäischen regulatorischen Umfeldes Qualifikationen Abgeschlossenes Studium einer naturwissenschaftlichen Fachrichtung (z. B. Biologie, Pharmazie, Chemie oder Lebensmittelchemie) / Absolventen oder Teilnehmer des Lehrganges Master of Drug Regulatory Affairs Idealerweise mehrere Jahre Berufserfahrung im Bereich Regulatory Affairs Arzneimittel bzw. im [. .. ]

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Job gestern bei Jobleads gefunden

Director, Global Medical Safety Lead

• Genf Führungs-/ Leitungspositionen [. .. ] Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role. Key Responsibilities: Act as the medical safety lead for assigned [...]
MEHR INFOS ZUM STELLENANGEBOT[...] products, providing strategic pharmacovigilance and benefit-risk expertise across clinical, regulatory and cross-functional teams. Lead safety signal detection, evaluation and risk assessment activities, ensuring emerging safety data is reviewed and interpreted effectively. Chair or contribute to cross-functional safety review meetings and drive evidence-based decision making regarding product safety profiles. Support the [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden Associate Director Biostatistics • Lavamünd, Kärnten Lavamuend Führungs-/ Leitungspositionen [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire [...]
MEHR INFOS ZUM STELLENANGEBOT[...] recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 03438143 [. .. ]

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Job vor 14 Tagen bei Jobleads gefunden

Medical Science Liaison, Cardiovascular Surgery (m/w/d)

• Mannheim, Baden- Württemberg [. .. ] adoption of innovative products designed to support cardiac surgical procedures across the DACH region. The MSL will work closely with cardiac surgeons, surgical teams, anesthesiologists, perfusionists, hospital [...]
MEHR INFOS ZUM STELLENANGEBOT[...] pharmacists, and other specialist healthcare professionals. The successful candidate will act as a trusted scientific partner in the field, supporting clinical education, scientific exchange, launch readiness, and the collection of meaningful medical insights. Location: Southern Germany Territory: DACH region Key responsibilities Build and maintain peer-to-peer scientific relationships with key external experts, surgical [. .. ] correct medical information process. Ensure all adverse events, special situations, product quality complaints, and safety-relevant observations are reported within required timelines. Work closely with internal medical, market access, commercial, pharmacovigilance, medical information, and clinical operations colleagues while maintaining clear medical and commercial boundaries. Experience and qualifications Previous industry experience working as an MSL or closely related scientific role is essential Strong background in cardiology, cardiovascular medicine, cardiac surgery, perfusion, anaesthesiology, or a closely related hospital specialty. Pharm D, Ph D, MD, MSc, [. .. ]

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Job am 18.08.2026 bei Jobleads gefunden

Clinical Quality Manager (m/f/d)

• Frankfurt, Hesse [. .. ] and perform various clinical vendors audits against Gx P and local regulatory requirements. You contribute to training for selected functional groups related to Good Clinical Practice, Good [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Clinical Laboratory Practice, Good Pharmacovigilance Practice (pre-marketing related) , and clinical trials regulations. You host the local and international Notified Body and authorities inspection/ External Audits. You manage CAPA of the RA inspections/ External Audits as well as support inspection readiness/ regulatory compliance status at R D. What we expect from you: You ideally [. .. ] training : Your personal and professional development is the key to success for us. To foster this, we conduct regular development discussions and facilitate a wide range of management and specialist training courses, soft skills courses, e-learning courses, language courses and coaching sessions. Find out more about our benefits at https:/ / careers. merz-aesthetics. com. #J-18808-Ljbffr 01527501 [. .. ]

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Job am 05.09.2026 bei Neuvoo.com gefunden Planet Pharma

Medical Doctor

• Hamburg [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire [...]
MEHR INFOS ZUM STELLENANGEBOT[...] recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. Please click apply or contact Theresa Ayebaare (Recruitment I) [. .. ]

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Jobs



Häufig gestellte Fragen

Wieviel verdient man als Pharmacovigilance Specialist pro Jahr?

Als Pharmacovigilance Specialist verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Pharmacovigilance Specialist Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 10 offene Stellenanzeigen für Pharmacovigilance Specialist Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Specialist Jobs?

Aktuell suchen 5 Unternehmen nach Bewerbern für Pharmacovigilance Specialist Jobs.


Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Specialist Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Specialist Stellenangebote:


  • Planet Pharma (2 Jobs)
  • The BIG Jobsite (1 Job)
  • Gouya Insights (1 Job)


In welchen Bundesländern werden die meisten Pharmacovigilance Specialist Jobs angeboten?

Die meisten Stellenanzeigen für Pharmacovigilance Specialist Jobs werden derzeit in Baden-Württemberg (1 Jobs), Sachsen (1 Jobs) und Hamburg (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Pharmacovigilance Specialist Jobs?

Pharmacovigilance Specialist Jobs gehören zum Berufsfeld Pharmazie.


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