Project Leader

GE Healthcare Bio-Sciences AB / Maskiningenjörsjobb / Uppsala
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Role Summary/Purpose

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 driven in project teams driving change together with R&D, Sourcing, RA and QA. The results of the work are updated compliant products, updated product documentation, new processes and procedures and modified IT systems.

Essential Responsibilities

As a Global Project Leader you be able to lead global and cross-functional activities and projects to ensure that all LS products will comply with applicable regulations. 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.

Duties include (but are not limited to):

Leading global, cross-functional product compliance projects for new or changed regulations across the Life Sciences business.
Drive Implementation of new processes as a result of the projects
Responsible for cost and budget for the projects including estimating budgets, forecasting and reporting.
Report status, progress and issues to stake holder committees.
Close collaboration with Product Management to set projects scope.
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.
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.
Handle ad-hoc tasks in the compliance area
Aware of and comply with the LS Quality Management System.

For further questions about the position, please contact Carl Lindner, 018-6121679.

Qualifications/Requirements

BS Degree in Biotechnology or Mechanical, Electrical engineering or equivalent experience.
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.
Strong written and verbal communication skills
Experience from Implementing Processes globally.
Fluent in Swedish and English
Experience from Project Management

Desired Characteristics

Experience in leading global cross functional projects
Ability to identify and present the key message in a condensed and structured way
Goal oriented team player and doer
Ability to prioritize and drive multiple projects and large programs without losing deadlines or quality
Strong ability to motivate and inspire people to increase performance
Curious and interested in learning new things
Problem solving capabilities
Experience In Change Management/ conflict resolution
Knowledge around LS hardware product portfolio

We believe that you are flexible, eager to learn, able to make quick decisions, seeing things from a holistic approach, need to be able to plan and work alone but also as a team-member.

Varaktighet, arbetstid
Tillsvidare
Heltid

Publiceringsdatum
2016-05-09

Ersättning
Fast månads- vecko- eller timlön

Så ansöker du
Sista dag att ansöka är 2016-05-23
Klicka på denna länk för att göra din ansökan
Ange följande referens när du ansöker: 2571959

Företag
GE Healthcare Bio-Sciences AB

Adress
GE Healthcare Bio-Sciences AB
Björkgatan 30
75184 Uppsala

Kontorsadress
Björkgatan 30
Uppsala

Övriga kontaktuppgifter
Telefonnummer: 018-6120000

Jobbnummer
2833197

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