Brillio
over-10k employees
About Brillio
Brillio, a global technology consulting and business solutions company, enables the successful digital transformation of businesses by utilizing disruptive technologies to create new customer experiences, achieve cost efficiencies, and gain competitive advantage with speed and agility. This, along with its key technology partnerships and investments in areas such as big data analytics, security, cloud, mobile, and machine learning, delivers innovative processes and solutions that result in significant business impact. Brillio brings business expertise to clients in the Banking and Finance, Utilities, CPG, Retail, Technology, Media and Entertainment industries and is proud to serve leaders in Fortune 500 from these industries.
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Description
- Brillio is a rapidly growing digital technology service provider, partnering with Fortune 1000 companies to drive digital transformation.
- The Product Manager/Owner will contribute to strategic planning and day-to-day execution of digital products in the life sciences sector, including regulated manufacturing and quality platforms.
- Responsibilities include gathering requirements, writing user stories, managing backlogs, supporting UAT, and developing product roadmaps.
- The role requires experience in life sciences domains such as R&D digitization, regulatory systems, digital manufacturing, and clinical platforms.
- The ideal candidate will have 3-6 years of experience in product management within regulated environments, familiarity with agile tools like Jira, and understanding of GxP, 21 CFR Part 11, and data integrity principles.
- The position offers a salary range of $120,000 - $140,000 annually and can be remote or hybrid in NY/NJ.
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Requirements
- 3–6 years of experience in product management, business analysis, or digital solution delivery in LS GMP, regulations
- Experience with requirement gathering, user story writing, Jira, and agile delivery
- Exposure to life sciences domains such as R&D digitization (LIMS, ELN, SDMS)
- Experience with regulatory systems (Veeva Vault, structured content, submissions)
- Experience with digital manufacturing (MES, SCADA, validation)
- Experience with clinical or commercial platforms
- Understanding of regulatory contexts like GxP, 21 CFR Part 11, data integrity (ALCOA+)
- Strong analytical and communication skills, with ability to simplify complex domain concepts
- Comfortable communicating with engineers, SMEs, and executive stakeholders
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Benefits
- Competitive salary
- Remote work options
- Opportunity to work in regulated life sciences environments
- Collaborative and innovative work culture
- Growth and development opportunities