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Metro product owner with a generalist title attracts moderate competition; smaller employer reduces density.
Pharma QC lab and CSV/CSA expertise limits transferability across industries.
Requires Empower CDS, CSV/CSA validation and lab integration expertise, increasing shortlisting strictness.
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Own and manage the Empower CDS platform product lifecycle across QC and analytical labs, including roadmap prioritization and version upgrades such as Empower 3 FR.
Serve as the single accountable liaison between QC lab leads, Quality, IT, and validation teams, overseeing validated state, change control, impact assessments, and CSV/CSA deliverables for each release.
Lead requirement gathering with laboratory stakeholders to map data workflows and automate processes; track and report project milestones, dependencies, and risks in the integration stream.
Experience Required: Not explicitly mentioned in the JD.
Knowledge of CSV/CSA validation processes and change control management mandatory.
Experience coordinating with QC labs, Quality, IT, and validation teams explicitly required.
Notice Period: Not explicitly mentioned in the JD.
Experienced in owning and managing complex laboratory data systems or software platforms with strong product ownership skills.
Proficient in stakeholder management across multiple technical and quality functions within pharmaceutical or laboratory environments.
Skilled at translating laboratory process needs into governed backlogs and requirements, with familiarity in validated software environments and regulatory compliance.