Scrum Master

1 month ago

Santa Clara, United States Motion Recruitment Full time

Title: Scrum Master

Location: Santa Clara, CA

Duration: 6+ months of contract with possible extension

*W2 Candidates Only*

About Client:

A prominent force in the realm of pharmaceuticals and diagnostics, this global innovator stands at the forefront of scientific advancement dedicated to enhancing human well-being. With a unique synergy between pharmaceuticals and diagnostics, it has pioneered personalized healthcare, tailoring treatments to individual patients with precision. Renowned for its groundbreaking contributions, this entity boasts the largest portfolio in biotechnology, encompassing transformative medications spanning oncology, immunology, infectious diseases, ophthalmology, and disorders of the central nervous system. Additionally, it leads the world in in vitro diagnostics and tissue-based cancer diagnostics, while also spearheading advancements in diabetes management.

Description:

As a part of this role, you will be acting as Scrum Master and supporting a highly talented software engineering team for a SaaS Next Generation Sequencing (NGS) data analysis platform targeting the healthcare industry. You will work with the cross-functional teams and help to decide priorities and delivery of the tasks/objectives.

Overview:

Led the scrum team in using Scaled Agile Framework methodology and scrum practices Helping the product owner and development team to achieve the project goals Led the scrum and development teams in self-organization Remove impediments and coach the scrum team in removing impediments Help the scrum and development teams to identify and fill in blanks in the Agile framework Resolve conflicts and issues that occur Help the scrum team achieve higher levels of scrum maturity and project execution efficiency Feel and be accountable for the software deliverables (including supporting creation of formal documentation). Escalate delays and issues and provide mitigation plans to address them.

Nice to have:

Guide the software team in navigating and applying the Design Control processes to be compliant with medical device guidelines (such as IEC 62304 FDA 21 CFR 820, etc)

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