Project Manager / Release Manager (m/f/d) - Sterile Products

Feldkirchen

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We at Getinge believe in self-organized and cross-functional teams, adopting lean and agile methods in product development and project management to successfully realize medical technology in a fast changing and complex environment. With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Aufgaben

Define, plan and set-up product releases together with the Value Creation Teams
Manage product releases through all project phases from ideation/initiation to release to market including design transfer to contract manufacturers
Establish project schedules/timelines including budget calculations and investment requests.
Stabilize and lead cross-functional cooperation (e.g. with product management, marketing, supply chain management, purchasing, regulatory affairs, quality and external partners such as test laboratories, service providers and suppliers)
Define and manage key project constraints such as scope, schedule, budget, resources and risks.
Ensure release plans and deliverables are compliant with appropriate design control procedures and any other applicable procedure and/or regulations
Head interdisciplinary agile Value Creation Teams in delivering on time and quality
Coach agile Teams and their Scrum Masters in agile methodologies to establish a common mindset and facilitate continuous improvement of their agile way of working. Close collaboration with other Release Managers to develop best practices across the R&D organization.
Prepare reports, as needed and present to management on the status of product releases
Moderation and documentation of complex decision-making processes
Drive the definition of ways of working to increase clarity and efficiency in the R&D organization.

Profil

University degree (Bachelor, Master, Diploma) in Medical, Biomedical, Plastics, Mechatronic or Mechanical Engineering, or closely related disciplines
Minimum of 3 years hands-on engineering experience in the medical device industrie or other regulated businesses
Fluency in English (written and spoken) and basic German language skills (willingness to advance)
Proficiency in agile development environments, with the ability to work in sprints and manage backlogs
Familiarity with contract manufacturing
Experience with outsourced development and external partners incl. contract management, ensuring quality standards and project management
Broad understanding of the (medical) device development process and its interfaces with the companie's internal support functions
Backround in managing geographically dispersed and hybrid teams
Acumen in developing sterile products in a regulated environment
Strong competence in cross-functional collaborations
Excellent communication and presentation skills
Analytical mind set and well-organized working style
Cross-cultural intelligence
On-site work for at least 2 days per week is expected. Hence, residing in the greater metropolitan area of Munich is advantageous.