Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.
What You will do:
Support development and feasibility of new and existing intravascular devices and administration kits
Identify and manage project topics and work with external design companies, consultants, and experts
Liaise with multiple teams, stakeholders both internal (manufacturing, quality assurance, regulatory, product management) and external (clinical leadership and labs), as well as other project managers within the organization to aid the progression of projects in a timely and high-quality manner
Support R&D operations
Ensure that project blockers are identified, remedied and learnings are distilled and implemented in order to prevent re-occurrence
Develop and champion project progress-tracking and reporting tools
Create transparency and driving cross team communication
Plan and prioritize project activities, develop a project schedule and execute project to meet the agreed upon schedule and budget constraints
Provide written and verbal project updates with manager, project sponsors and other stakeholders regarding project status, risks/issues and accomplishments
Identify opportunities to improve the product development process and proactively lead change as directed by manager
Assist in new product development projects and cost-reduction design activities
Find and work with vendors capable of sourcing both off-the-shelf and custom chemical components
Plan and conduct R&D activities to define and develop implantable devices
Quality assurance testing of devices to ensure conformance to design specifications
Write technical documentation including requirements, process descriptions, and test methods
Create and maintain FDA compliant Design History Files (DHF)
Execute process improvements as they relate to quality system compliance with FDA 510(k), QSR and ISO13485
Participate in complaint investigations, and failure analysis of products
Provide root cause analysis support and drive the implementation of corrective action for process-related issues
Perform other duties as assigned or required
What You will have:
Bachelor’s degree; quantitative or life-science focused is preferred, advanced degree strongly preferred
5+ years of working experience in project/program management required, healthcare or academic setting preferred
Training and experience in project management methodologies (e.g., PMP, SCRUM, Agile)
Experience using project management tracking systems (such as JIRA, MS Project, etc.) is required
Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry
Experience working within a company’s Quality System is preferred
Experience with design verification & validation
Professional working experience with Excel and PowerPoint required
Excellent organizational skills and attention to detail
Strong communication skills, both oral and written
A combination of education and experience may be substituted for requirements, we are willing to review candidates with strong and competitive backgrounds that have a passion for science and technology
What will set You apart:
2+ years of cross functional project/program management preferred
Experience in the development of regulated medical devices or combination products is preferred
Experience in medical device development or healthcare focused project management is preferred
#LS-OS1
Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.
How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
To find out more about Siemens Healthineers businesses, please visit our company page here.
The base pay range for this position is:
$104,930 - $144,276Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.
Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.
EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.
Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.
If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at [email protected]. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.
California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here.
Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”
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To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.
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What We Do
At Varian, a Siemens Healthineers company, we envision a world without fear of cancer.
For more than 70 years, we have developed, built and delivered innovative cancer care technologies and solutions for our clinical partners around the globe to help them treat millions of patients each year. With an Intelligent Cancer Care approach, we are harnessing advanced technologies like artificial intelligence, machine learning and data analytics to enhance cancer treatment and expand access to care. Our 10,000 employees across 70 locations keep the patient and our clinical partners at the center of our thinking as we power new victories in cancer care. Because, for cancer patients everywhere, their fight is our fight.
