Processes Principal, Regulatory Processes
Hays Specialist Recruitment AB / Biomedicinjobb / Mölndal
Observera att sista ansökningsdag har passerat.
Visa alla biomedicinjobb i Mölndal,
Göteborg,
Partille,
Härryda,
Kungsbacka eller i
hela Sverige Visa alla jobb hos Hays Specialist Recruitment AB i Mölndal,
Göteborg,
Jönköping,
Helsingborg,
Lund eller i
hela Sverige Regulatory Process and Compliance Team
Hays Life Sciences is now looking to recruit a Process Principal in the Regulatory Process and Compliance Team for a 6-month contact assignment at AstraZeneca in Gothenburg or work remotely.
Do you have expertise in regulatory issues and are looking for new ways to develop? Are you highly collaborative and like to take the lead in driving process improvements? This opportunity as Processes Principal in the Regulatory Process and Compliance team might be the right opportunity for you.
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.
Global Regulatory Excellence's vision is to Leading enterprise wide regulatory strategies, policy and delivery - so that no patient waits. In the Regulatory Process and Compliance team we network collaboratively to enable our customer groups to operate efficient processes in a compliant manner.
What you'll do
As a Processes Principal in the Regulatory Process and Compliance team you will be working with the Processes Leads and taking responsibility for the management of assigned AstraZeneca projects-processes including implementation, communication, compliance, performance and inspection readiness. Act as technical writers and project management support to ongoing procedural document update program, including communication and training activities.
You will be accountable to execute the delivery of the process's strategy, priorities, alongside governance, authoring and lifecycle management current procedural documents. We hope that you have the drive to establish a culture of continuous improvement, high performance, flexibility and quality, emphasizing a "can do" attitude and innovative approach.
Other key responsibilities in this position:
* Identify opportunities for and drives the enhancement of existing processes through knowledge of internal and external environment.
* Using deep understanding of regulatory processes and regulations provide process support to regulatory teams and submissions.
* Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions and drive to implementation.
* Identify and promote innovation and new ways of working to drive efficiency and improved deliverables in all processes
* Identify issues and risks and propose options to mitigate them
* Provide process training to relevant functional groups.
* Serve as the delegate, where appropriate, for the Process Leads
* Contribute to communication and change management activities associated with process initiatives.
* Working collaboratively to provide expertise and sharing best practices across all regions and in all partnerships
Essential for the role
* A science/pharmacy/nursing degree, with 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
* Good attention to detail
* Excellent written and verbal communication skills
* Proven ability to work across cultures
Desirable for the role
* MSC/PhD in scientific discipline
* Knowledge of new and developing regulatory and pharmacovigilance expectations
* Knowledge of existing AstraZeneca external alliances and collaborative projects
* Knowledge of Regulatory operating model and organisation
* Experience of working in a global organisation, preferably within the pharmaceuticals industry, and of the drug development life cycle and commercial aspects of the industry
Varaktighet, arbetstid
Heltid Contract
Publiceringsdatum2022-03-01ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2022-03-11
FöretagHays Specialist Recruitment AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "899865".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Hays Specialist Recruitment AB (org.nr 556640-6103)
Ansökan E-post:
Hays.48730.3101@haysse.aplitrak.com Arbetsplats Hays Specialist Recruitment
Kontakt Jay Mistry
matus@hays.pl +46736425550 Jobbnummer 6390281
Observera att sista ansökningsdag har passerat.