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Engineering Operations Leader Probes (m/f) Job (Zipf, Austria)

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Job Number: 2611216
Business: GE Healthcare
Business Segment: Healthcare Ultrasound
About Us:
GE Healthcare provides transformational medical technologies and services that are shaping a new age of patient care.

Our broad expertise in medical imaging and information technologies, medical diagnostics, patient monitoring systems, drug discovery, biopharmaceutical manufacturing technologies, performance improvement and performance solutions services help our customers to deliver better care to more people around the world at a lower cost. In addition, we partner with healthcare leaders, striving to leverage the global policy change necessary to implement a successful shift to sustainable healthcare systems.

Our "healthymagination" vision for the future invites the world to join us on our journey as we continuously develop innovations focused on reducing costs, increasing access and improving quality around the world.

The site at Zipf is specialized in diagnostic ultrasound systems and world market leader in 3D/ 4D ultrasound and is global "Center of Excellence" within the GE Healthcare Group.
Posted Position Title: Engineering Operations Leader Probes (m/f)
Career Level: Experienced
Function: Services
Function Segment: Project Management
Location: Austria
U.S. State, China or Canada Provinces:
City: Zipf
Postal Code: 4871
Relocation Assistance: No
Role Summary/Purpose: The Engineering Operations Leader Probes leads a global team of documentation specialists to support new product introduction (NPI) process, engineering documentation in product data management system and ensure that product changes will be processed correctly and support all activities concerning installed base. Engineering Operation Leader Probes works in a cross-functional team and provides global leadership on standardization and simplification for Global Ultrasound Probes.
Essential Responsibilities:
  • Setting direction of the team and driving continuous improvement of processes
  • Leadership of the team, including recruitment, team/talent development, skill set improvement, mentoring and coaching
  • Resource assignment and prioritization
  • Synchronization of activities and priorities with local functions
  • Specialist of local and global change management process, driving continuous improvement and standardization and Support local and global team in execution of changes
  • Coordinate changes for different functions and synchronization of changes with different departments
  • Present changes in local Change Control Board
  • Implementation of new Design Controls requirements including review with Quality, update of local procedures/work instructions or templates and transfer new requirements to affected functions
  • Support program management teams in execution of programs related to quality requirements, timelines and execution
  • Lead, execute and support global or local driven regulatory, service or quality related projects like Product Controllership, Chemical testing, Biocompatibility, Labeling, Packaging, …
  • Reply local or global service, regulatory and quality requests
  • Support and drive local and global End-of-life and portfolio cleanup activities
  • Support any kind of audits
  • Coordinate CAPAs related to Probes, define owners, drive execution on time, support and execute required actions
  • Synchronization of CAPAs with different departments
  • Present progress on CAPAs in local CAPA review board and provide status to globally
Qualifications/Requirements:
  • At least Bachelor’s Degree in operations/industrial Engineering or similar or equivalent professional experience
  • Significant relevant work experience
  • Relevant project management or direct or indirect people leadership experience
  • Experience of product development process and manufacturing cooperation
  • Strong written and verbal communication skills in German and English
The collective agreement provides a minimum gross salary of €
2.700,- / month, salary depends on qualification and experience and might be higher.

Additional Eligibility Qualifications:
Desired Characteristics:
  • Familiarity with ISO, FDA and other regulatory standards
  • Proven ability to work cross-functionally
  • Experience working in global organization and project teams
  • Demonstrated ability to deliver results while working on multiple projects simultaneously, balancing resources, timing and quality of outcomes
  • Demonstrated problem-solving and leadership skills
KARR_AUT

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