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Senior Specialist Patient Safety

AstraZeneca -
Baar, ZG

Jetzt bewerben

Details zur Stelle

vor 1 Tag

Qualifikationen

Englisch
Projektmanagement
Bachelor
Erfahrung in der IT
Kommunikationsfähigkeit
Deutsch

Vollständige Stellenbeschreibung

Location Baar, Canton of Zug, Switzerland Job ID R-253639 Date posted 04/06/2026

Senior Specialist Patient Safety

Location : Baar , Switzerland

Do you have expertise in, and passion for, Patient Safety? Would you like to apply your expertise in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases.

Come and join our AZ team where you will play a pivotal role in this exciting period of development!

This role will provide a high quality, comprehensive, technical, and scientific pharmacovigilance service in the management and day-to-day processing of pharmacovigilance activities. In addition to this, it will also provide knowledge and expertise to internal and external customers on all aspects of Patient Safety relating to AstraZeneca Portugal activities and fully comply with Good Pharmacovigilance Practice (GVP) requirements and all other AZ policies and Standards.

Main Accountabilities:

The role broadly includes the following key components:

Maintain oversight of all safety-related processes, including processing, quality control, and timely submission of ICSRs and periodic safety reports (PBRERs, DSURs, RMPs) to local health authorities.
Deputy of the PSM, acting as local PV contact point in Switzerland

Responsible for handling pharmacovigilance tasks for the AZ product portfolio And AZ Group of companies (including Alexion)
in the country in alignment with applicable regulations and AstraZeneca Standard Operational Procedures and act as the deputy of responsible person for pharmacovigilance in Switzerland
Responsible for applying the GVP rules on the QMS for AZ Switzerland PS activities
Participate in the implementation of local risk minimization activities and direct healthcare professional communication.

Review Market Research activities and Patient Support programs.
Contribute to the setting up of Safety Agreements with collaborative partners.
Support organization of PV awareness training for internal employees and vendors.
Ensures a local Business Continuity Process (BCP) for Patient Safety is in place and tested at least annually.
Participate and support at Audits and inspections.

Essential for the role

University degree in pharmacy, medicine, life sciences or related field.
Experience in GVP of at least three years and documented education in the field of pharmacovigilance
Demonstrated ability to work independently and in project settings to deliver objectives.
Communication and influencing skills.
Project management
Team work cross functionally in an international environment.
Excellent knowledge of English and German language, both spoken and written

Desirable for the role

Business understanding and customer focus
Timeliness, accountability, and delivery of reliable results
Strong team player
Autonomy work

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We’re on an exciting journey to pioneer the future of healthcare.

Date Posted

05-Jun-2026

Closing Date

11-Jun-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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