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Senior Manager, Acquisitions, Divestitures and Remediation, Technology Quality

Job in New Brunswick, Middlesex County, New Jersey, 08933, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-25
Job specializations:
  • IT/Tech
    IT Business Analyst, Cybersecurity, IT Project Manager
Salary/Wage Range or Industry Benchmark: 120000 - 160000 USD Yearly USD 120000.00 160000.00 YEAR
Job Description & How to Apply Below

Senior Manager, Acquisitions, Divestitures and Remediation, Technology Quality Responsibilities

  • Define and manage the Acquisitions, Divestitures and Remediation operating model.
  • Execute TQ assessments for IT systems conveyed from acquisitions/divestitures (infrastructure, applications, healthcare technology systems).
  • Oversee qualification/validation reviews for conveyed IT GxP systems (Manufacturing, Lab, R&D, Infrastructure, IT tools, websites, mobile apps, SAMD, Supply Chain).
  • Provide strategic/operational support to project teams; ensure early TQ & C involvement for preventive/automated controls.
  • Manage end-to-end quality processes; implement/manage TQ metrics and reporting for A&D assessments, integration/separation, and remediation.
  • Lead inspection/audit readiness; participate in audits and approve NC action plans and closure.
  • Perform validation deliverable review/approval (e.g., compliance plans, requirements/user stories, tests, traceability matrices, compliance reports).
  • Lead risk management and provide compliance guidance (NC/CAPA, due diligence, mitigations/workarounds).
  • Manage scope/schedule, resources, intake/budgeting as Power User; track outcomes; identify automation opportunities (AI/RPA).
Qualifications/Requirements
  • Bachelor’s degree (Computer Science/IS/Business or related); advanced degree preferred.
  • 8–10+ years in pharma/med device/biotech with direct CSV experience, especially acquisitions/divestitures.
  • Strong matrix leadership, stakeholder communication, analytical/problem‑solving, and executive presence.
  • Working knowledge of cGMP/CSV including 21 CFR Part 11, 210, 211, 820, Annex 11; PMO/SDLC/GAMP 5/ITIL; global GxP regs; tech risk assessments.
Preferred skills
  • Compliance Management
  • Controls Compliance
  • Digital Assurance/Governance
  • Fact‑Based Decision Making
  • Quality Management Systems (QMS)
  • Quality Validation
  • Regulatory Compliance
  • Stakeholder Engagement
  • SOP
  • Technical Credibility
Benefits (time off per policy)

Vacation (120 hrs/yr), Sick time (40 hrs/yr; CO 48; WA 56), Holiday pay (13 days/yr), Work/Personal/Family Time (up to 40 hrs/yr), Parental Leave (480 hrs/yr).

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Position Requirements
10+ Years work experience
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