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IMP Quality Project Manager
Eingestellt von Randstad (Schweiz) AG
Gesuchte Skills: Engineering, Catalyst
Projektbeschreibung
IMP QUALITY PROJECT MANAGER
Randstad Professionals are one of the leading recruitment companies in Switzerland and with a dedicated IT contracting team in Zurich. We are excited to help you in your search. We focus on finding the best contracts for the best contractors.
Currently we are looking for an IMP Quality Project Manager to join our client's team in Basel.
The IMP Quality Project Manager will be responsible for providing Quality Project Management support on IMP (investigational medical product) for Planning, Scheduling and Reporting. He/she will partner with IMP Quality Product Leaders (IMP QPL) to help team to deliver successfully on the objectives agreed upon within their IMP Quality Subteam. The candidate will work closely with the QPLs to manage the timeline, resources, risks, escalate issues and prepare meeting agendas, minutes, reports, and presentations. He/she will ensure product information flows between the quality team members to ensure transparency, informed decision making, and optimal alignment of all quality deliverables within the quality sub-team members. He/she will provide input for staff activities and issues. This position requires excellent communication, collaboration, negotiating, influencing and strategic thinking.
MAJOR RESPONSIBILITIES
Manage IMP Quality Activities for Planning, Scheduling, and Reporting applying project manager knowledge and processes to different technical platforms such as large molecule, device, small molecule
Applies project management expertise including planning, tracking and facilitating Quality meetings and documenting decisions, risks and actions
Monitor critical path timelines and resources for assigned IMPs, using project manager tools, principles and practices to deliver successfully on time
Provide timely presentations and/or reports to Quality Management and information for reporting to appropriate governance committees, Monthly Project Reporting, and Plan Source activities etc.
Proactively communicate issues and concerns providing transparency with key customers and stakeholders in a global setting. Ensure sound decision making principles and agreements and actions are followed up
As a member of the IMP Quality organization, participate in staff meetings and department initiatives
Must be able to independently manage priorities and assignments across multiple projects simultaneously
Act as catalyst and primary contact for multiple functional areas across quality teams, ensuring team dynamics are collaborative
Serve as advocate and role model for integrating change into organization
QUALIFICATIONS
Bachelor's degree in science or engineering required. PMP Certification a plus
3-15 years+ experience of relevant Work in project management within biotech or the pharmaceutical industry with a sound knowledge of drug development processes
Must work well in a collaborative team environment and communicate effectively with all levels of the organization
Ability to create and manage timelines, resources and accommodate multiple priorities
Strong influence and interpersonal skills, and the ability to work well with others in a proactive, positive and constructive manner
Have excellent written and verbal communication skills (German and English)
Strong knowledge of manufacturing or technical development processes, cGMP's and compliance experience preferred
Previous experience with project management software applications and tools a plus
Whether this role is the right fit or you would like to see if there are others that do, our dedicated and expert team is looking forward to hearing from you.
Good to know you!
Randstad Professionals are one of the leading recruitment companies in Switzerland and with a dedicated IT contracting team in Zurich. We are excited to help you in your search. We focus on finding the best contracts for the best contractors.
Currently we are looking for an IMP Quality Project Manager to join our client's team in Basel.
The IMP Quality Project Manager will be responsible for providing Quality Project Management support on IMP (investigational medical product) for Planning, Scheduling and Reporting. He/she will partner with IMP Quality Product Leaders (IMP QPL) to help team to deliver successfully on the objectives agreed upon within their IMP Quality Subteam. The candidate will work closely with the QPLs to manage the timeline, resources, risks, escalate issues and prepare meeting agendas, minutes, reports, and presentations. He/she will ensure product information flows between the quality team members to ensure transparency, informed decision making, and optimal alignment of all quality deliverables within the quality sub-team members. He/she will provide input for staff activities and issues. This position requires excellent communication, collaboration, negotiating, influencing and strategic thinking.
MAJOR RESPONSIBILITIES
Manage IMP Quality Activities for Planning, Scheduling, and Reporting applying project manager knowledge and processes to different technical platforms such as large molecule, device, small molecule
Applies project management expertise including planning, tracking and facilitating Quality meetings and documenting decisions, risks and actions
Monitor critical path timelines and resources for assigned IMPs, using project manager tools, principles and practices to deliver successfully on time
Provide timely presentations and/or reports to Quality Management and information for reporting to appropriate governance committees, Monthly Project Reporting, and Plan Source activities etc.
Proactively communicate issues and concerns providing transparency with key customers and stakeholders in a global setting. Ensure sound decision making principles and agreements and actions are followed up
As a member of the IMP Quality organization, participate in staff meetings and department initiatives
Must be able to independently manage priorities and assignments across multiple projects simultaneously
Act as catalyst and primary contact for multiple functional areas across quality teams, ensuring team dynamics are collaborative
Serve as advocate and role model for integrating change into organization
QUALIFICATIONS
Bachelor's degree in science or engineering required. PMP Certification a plus
3-15 years+ experience of relevant Work in project management within biotech or the pharmaceutical industry with a sound knowledge of drug development processes
Must work well in a collaborative team environment and communicate effectively with all levels of the organization
Ability to create and manage timelines, resources and accommodate multiple priorities
Strong influence and interpersonal skills, and the ability to work well with others in a proactive, positive and constructive manner
Have excellent written and verbal communication skills (German and English)
Strong knowledge of manufacturing or technical development processes, cGMP's and compliance experience preferred
Previous experience with project management software applications and tools a plus
Whether this role is the right fit or you would like to see if there are others that do, our dedicated and expert team is looking forward to hearing from you.
Good to know you!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik