Assoc Princ Specialist PS Enablement
Qrios Minds AB / Biomedicinjobb / Göteborg
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hela Sverige Visa alla jobb hos Qrios Minds AB i Göteborg,
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hela Sverige Do you have knowledge in regulatory/pharmacovigilance and partnership issues ? Do you have a "can do" attitude and an innovative approach and want to contribute to ensure good relationships across Patient Safety and related functions within Astra Zeneca and Alexion? Then this unique role with a broad spectrum of responsibilities might be the one for you!
About the position
At AstraZeneca, we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Ensuring AstraZeneca comply with Pharmacovigilance regulations is key and in our team we make sure to make this a reality. To meet our business priorities and address resource demands, we are now looking for you who wants to join our Global Patient Safety Process & Partnership team.
We are responsible for the management of assigned AstraZeneca projects, processes and partnerships including implementation, communication, compliance, performance, vendor oversight and inspection readiness within the ICSR area. We ensure good relationships across Patient Safety in CMO and other relevant areas of AZ to execute the delivery of the processes and partnership strategy, priorities, alongside governance and management of the current procedural documents and partnerships
Responsibilities
As an Associate Director you will be working with Directors and Associate Directors in PV Processes, Partnerships and Contracts area, taking responsibility for the management of ICSR process and vendor oversight in AstraZeneca/Alexion, covering processes and partnerships including implementation, communication, compliance, performance and inspection readiness. You will be accountable to develop relationships across Patient Safety in CMO and other relevant areas of AZ to execute the delivery of the processes and partnership strategy, priorities, alongside governance and management of the current procedural documents and partnerships.
Here you will have a great opportunity to use your deep understanding of regulatory and pharmacovigilance processes and regulations providing process or compliance support to safety and regulatory teams and submissions as well as to develop and maintain a vision and strategy for nominated pharmacovigilance or regulatory processes. In addition you will:
• Identify opportunities for and drives the enhancement of existing processes and partnerships through knowledge of internal and external environment
• Working with the PV Process, Partnership and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting
• Utilise safety and regulatory knowledge to maintain and support the global inspection readiness strategy
• Manages relationships/partnerships/alliances external to the AZ CMO function that are essential to delivering AstraZeneca's pharmacovigilance and regulatory LTO responsibilities
• Identify opportunities for and drives the enhancement of existing processes and partnerships through knowledge of internal and external environment
• Working with the PV Process, Partnership and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting.
• Utilise safety and regulatory knowledge to maintain and support the global inspection readiness strategy.
• Manages relationships/partnerships/alliances external to the AZ CMO function that are essential to delivering AstraZeneca's pharmacovigilance and regulatory LTO responsibilities
• Provide support and oversight to the outsourcing partner(s) to facilitate compliance with regulatory and legal requirements and maintaining inspection
With this in mind, we are looking for you that have a proven ability to work across cultures using your strong negotiation, conflict management and interpersonal skills to influence whilst maintaining independent and objective view.
Your profile
Essential for the role
• A science/pharmacy/nursing degree, with at least 5 years relevant experience (pharmaceutical, regulatory, safety and partnership)
• Experience in working cross-functionally
• Leadership skills, including proven leadership of project teams experience
• Thorough scientific knowledge sufficient to understand all aspects of regulatory/pharmacovigilance and partnership issues
• Thorough knowledge of the drug development process
Desirable for the role
• Knowledge of new and developing regulatory and pharmacovigilance expectations
• Knowledge of existing AstraZeneca external alliances and collaborative projects
• Experience of working with third party suppliers
• Experience in safety database functionalities
About the organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year. During this time you will be hired by us at QRIOS.
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden's leading pharmaceutical and life science companies. So whether you're interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.
About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world's leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
Ersättning Fast lön
Så ansöker du Sista dag att ansöka är 2023-04-21
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "792".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Qrios Minds AB (org.nr 556599-5999),
http://www.qrios.se/ Arbetsplats Qrios Life Science & Engineering AB
Kontakt Alma Foric
alma.foric@qrios.se 073-850 49 73 Jobbnummer 7641072
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