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Tier-1 brand and product role but niche Loftware requirement limits candidate pool.
Requires regulated-medtech experience and Loftware expertise, limiting cross-industry transferability.
Explicit 10–12 years plus mandatory Loftware and regulated-industry experience increases screening strictness.
Own the end-to-end lifecycle of global enterprise labeling capabilities, including design, approval, content management, and printing within regulated manufacturing and distribution.
Define and execute product vision, strategy, and roadmap aligned with business, regulatory, and manufacturing needs while managing backlog and prioritization.
Lead integrations with enterprise systems (ERP, PLM, MES, WMS), ensure compliance with global standards, and drive stakeholder engagement for adoption and business value realization.
Bachelor's degree in Computer Science, Engineering, Information Systems, or related field; Master's preferred.
10–12+ years experience in product management or enterprise application delivery within regulated industries.
Proven expertise with Loftware Cloud and/or Loftware Cloud Clinical Trials platforms.
Deep knowledge of regulated environment requirements including GxP, UDI, MDR, validation, traceability, audit readiness, and electronic records/signatures.
Experienced in managing complex regulated product platforms in life sciences or MedTech industries, familiar with enterprise labeling ecosystems.
Skilled at cross-functional collaboration and influencing in global matrix organizations with strong stakeholder management.
Data-driven and accountable mindset focused on strategic product ownership, operational excellence, and delivering measurable outcomes in compliance contexts.