Systems Designer
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Key skills for this role
About the Role
Zimmer Biomet is seeking a Systems Designer to analyze business needs, define software system specifications, and participate in all stages of the software development lifecycle. The role requires experience in Agile development, software design, and validation, with a focus on medical device systems.
Key Skills for This Role
Responsibilities
- Analyze business needs and define software system specifications considering technical and functional requirements
- Write high quality design and product development documentation ensuring compliance with applicable standards and procedures
- Participate in planning, coordinating, and supporting execution of verification and validation of the software product
- Interact with different teams to validate new technologies implementation and maintain innovation
- Participate in implementation of systems as well as training and customer support
- Participate in maintenance of existing products by carrying out preventive and corrective actions
Requirements
- Experience in software development or software design in an Agile environment
- Experience as a software verification/validation specialist in an Agile environment
- Experience with Agile practices Scrum and Scaled (SAFe)
- Knowledge of regulations 21 CFR Part 11, 21 CFR 820
- University degree in engineering (computer, software, biomedical or equivalent)
- At least 3 years of experience in product development (business analyst) or validation, ideally in software systems or highly regulated domain (medical, aeronautical, pharmaceutical)
- Bilingual (French and English), both oral and written
Full Job Posting
How You'll Create Impact
- We are looking for an enthusiastic individual, with great interpersonal skills to facilitate the numerous collaborations with teams and clients.
- As Systems Designer/business analyst, you will actively participate as part of the product development team in all stages of the software development process, including analysis, design, implementation, and release.
Specifically, In This Role You Will
- Analyze business needs and define software system specifications, while considering technical and functional requirements.
- Write high quality design and product development documentation and ensure compliance with all applicable standards and procedures, in order to guarantee the quality and security of the system.
- Participate in planning, coordinating, and supporting the execution of the verification and validation of the software product, including the documentation of the tests for each of the components and their execution.
- Interact with different teams to validate new technologies implementation and maintain innovation.
- Participate in implementation of systems as well as training and customer support for our system.
- Participate in maintenance of existing products by carrying out preventive and corrective actions.
Your Background
- Experience in software development or software design in an Agile environment
- Experience as a software verification/validation specialist in an Agile environment
- Experience with Agile practices Scrum and Scaled (SAFe) (certification and experience as Scrum Master, an asset)
- Knowledge of regulations 21 CFR Part 11, 21 CFR 820
- University degree in engineering (computer, software, biomedical or equivalent)
- At least 3 years of experience in product development (business analyst) or validation, ideally in software systems or highly regulated domain (medical, aeronautical, pharmaceutical)
What Will Make You Stand Out
- Ease in interacting with internal and external collaborators, understanding and simplifying complex technical subjects
- Excellent analytical skills and ability to manage priorities and deadlines
- Bilingual (French and English), both oral and written
- Interest in the medical field
- Creativity and problem solving inclination
- Autonomy, interpersonal skills, and ability to work in a team
- Excellent oral and written communication skills
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