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Manager, Pharmacovigilance Processes, AstraZeneca Gothenburg

  • Övrigt

Mölndal

Job description Working with the PV Processes leads and Process Principals, supporting tasks related to management of Astra Zeneca projects, processes including implementation, communication, quality, compliance, tracking, performance and inspection readiness. Accountable to develop relationships across Patient Safety and other relevant areas of AZ to execute the delivery of the assigned tasks in relation to processes strategy, priorities, alongside governance and management of the current procedural documents. This is a consulting assignment at Astra Zeneca in Gothenburg. Responsibilities Collaborate with PV Process Leads and Principals with support the enhancement of existing processes Working with the Process leads and Principals, and Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting. Support PS Process owners with guidance, advice and support on PD process. Author and collaborate with SMEs to deliver assigned Toolkit documents and templates. Maintain and continuously improve key customer facing service solutions for Process guidance and document access (R&D Process Portal, Lollipop, PSDM SPOL, Q&A ticket portal etc). Coordinate specific tasks related to procedural document management to provide oversight to the Pharmacovigilance (and PS) process team Using understanding of PV and Regulatory processes and regulations to provide support to regulatory process team Promote a culture of continuous improvement, high performance, flexibility and quality emphasising a “can do” attitude and innovative approaches. Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions and drive to implementation. Support and improve reporting tools and analysis processes and process metric /KPI data. Performing the monitoring, analysis and trending of data in own area of work. Identify issues and risks in own area of work and propose options to mitigate them. Ensure that appropriate, up-to-date records are maintained for compliance support activities for GVP, GCP, GRP and GMP audits/inspections Support Delivery of improvement project assignments supporting the business, Provide process training to relevant functional groups or support preparation of training material. Seek personal and professional development opportunities, and share knowledge gained in open forums Contribute to communication and change management activities associated with process initiatives. Building relationships with stakeholders and customers to support pharmacovigilance and regulatory activities and responsibilities including successful partnerships Working collaboratively to provide expertise and sharing best practices across all regions and in all partnerships Qualifications A science/pharmacy/nursing degree, Experience in working cross-functionally Administrative skills including Sharepoint online expertise Project Management skills Good attention to detail Excellent written and verbal communication skills Proven ability to work across cultures For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity. Application 2021-05-05, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible. For more information: Birgitta Nyström +46733434153 About the company Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus!

Randstad AB

Villkor

  • Antal platser: 1
  • Timmar per vecka: 32 - 40 timmar
Sista ansökningsdag: 2021-05-07
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