Global Quality Template Lead - Clinical/R&D; Hybrid
Listed on 2026-10-17
-
Research/Development
Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Johnson & Johnson Innovative Medicine is seeking a Global Template Owner for Quality Management focused on Clinical/R&D. This hybrid role will be based in Titusville, NJ with alternate sites.
You will consolidate Clinical/R&D Quality processes, align with the Transcend roadmap, and drive standardization across regions, supported by SAP S/4
HANA. Travel up to 30% may be required; on-site three days a week with two remote days; you will collaborate with global teams to ensure regulatory compliance
This is a genuine opportunity to take on the Global Quality Template Lead
- Clinical/R&D (Hybrid) role at Johnson & Johnson Innovative Medicine.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Quality Template Lead
- Clinical/R&D (Hybrid) role in the description above.
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