Project Leader
GE Healthcare Bio-Sciences AB / Kemiingenjörsjobb / Uppsala
2016-01-15
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As a Project Manager (PM) you will lead global and cross-functional activities and projects to ensure that all LS products will comply with applicable regulations.
As a PM you will be responsible for effective team execution with a holistic view as well as communicating project status to the LS leadership and escalating issues when appropriate to facilitate transparency.
Essential Responsibilities
The mission of product stewardship is to keep the Life Science legacy products compliant and to help NPI projects to meet regulatory requirements. The work is performed in project teams driving change together with R&D, RA and QA. The results of the work are updated compliant products, updated product documentation, new processes and procedures and modified IT systems.
Duties include (but are not limited to):
Leading global, cross-functional product compliance projects and programs for new upcoming regulations or requirements across the Life Sciences business.
Managing projects and programs to ensure no stop shipments due to product compliance reasons.
Working closely with all cross-functional groups in delivering effective processes and ways of working to comply with directives, legislations and compliance requirements.
Accountable for achieving quality objectives, reach agreed objectives for specification, time and cost as well as simplifies ways of working.
Continuously seek and implement improvements in processes and the project execution model.
Report status, progress and issues to stake holder committees in a clear way and by the company set standard.
Managing projects and programs with a risk based approach and making decisions based on business objectives.
Responsible for cost and budget for the projects and programs including estimating budgets, forecasting and reporting.
Interfacing with Regulatory Affairs, Legal and other internal organizations to understand the strategy for achieving product compliance in all areas of the Life Sciences business.
Work closely with GE Healthcare and other businesses for knowledge sharing, ideas of simplification and ways of working.
Aware of and comply with the GEHC Quality Manual, Quality Management System and applicable laws and regulations as they apply to this job type/position.
Identify and report any quality or compliance concerns and take immediate corrective action as required.
Lead continuous improvement activities by driving the implementation of process and product quality improvement initiatives.
Qualifications/Requirements
BS Degree in Biotechnology or Mechanical, Electrical engineering or equivalent experience.
Demonstrated leadership of cross-functional projects or programs and ability to drive project activities to completion.
Experience with work in a global environment with English as the primary language.
Experience from working with product compliance, EU Directives and other regulatory standards.
Proven ability to be a driven finisher, a doer, with flexibility to switch between different projects and tasks.
Knowledge around LS Hardware portfolio
Strong written and verbal communication skills
Desired Characteristics
Experience in leading global crossfunctional projects
Ability to identify and present the key message in a condensed and structured way
Ability to prioritize and drive multiple projects and large programs without losing deadlines or quality
Please apply no later than January 30th.
Varaktighet, arbetstid
Tillsvidare
Heltid
Publiceringsdatum2016-01-15ErsättningFast månads- vecko- eller timlön
Så ansöker duSista dag att ansöka är 2016-01-30
Ange följande referens när du ansöker: 2454972
FöretagGE Healthcare Bio-Sciences AB
AdressGE Healthcare Bio-Sciences AB
Björkgatan 30
75184 Uppsala
KontorsadressBjörkgatan 30
Uppsala
Övriga kontaktuppgifterTelefonnummer: 018-6120000
Jobbnummer 2619772
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