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Mid-level product owner title, metro location, and likely 3–6 year expectation increases competition.
Role requires domain-specific lab, validation, and Empower CDS knowledge, limiting industry transferability.
Regulated validation (CSV/CSA) and niche Empower CDS experience make screening highly selective.
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Own and manage the Empower CDS platform product for QC and analytical labs, including roadmap prioritization and version upgrades (e.g., Empower 3 FR upgrade).
Serve as the single point of accountability coordinating between QC lab leads, Quality, IT, and validation teams, and maintain the validated state by overseeing change control, impact assessments, and CSVCSA deliverables.
Lead requirement gathering and stakeholder management activities to translate lab needs into a governed backlog and support integration stream project tracking and risk management.
Experience in product ownership or management of laboratory software platforms like Empower CDS: Not explicitly mentioned in the JD.
Familiarity with Compliance Standards Validation (CSV) and CSV Compliance Standards and Assessments (CSVCSA).
Work Experience Required: Not explicitly mentioned in the JD.
Not explicitly mentioned notice period or educational qualifications.
Has strong cross-functional coordination experience between QC labs, quality assurance, IT, and validation teams within regulated environments.
Capable of leading detailed requirement gathering workshops and translating complex laboratory workflows into technical backlogs.
Experienced in managing software lifecycle for validated systems including change control and compliance deliverables in the pharmaceutical or analytical lab domain.