Senior Manager, Acquisitions, Divestitures and Remediation, Technology Quality
Job in
Raritan, Somerset County, New Jersey, 08869, USA
Listed on 2026-06-17
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-06-17
Job specializations:
-
IT/Tech
IT Business Analyst, Cybersecurity, IT Consultant, IT Project Manager
Job Description & How to Apply Below
Job Title
Senior Manager, Acquisitions, Divestitures and Remediation, Technology Quality
PurposeTechnology Quality and Compliance (TQ&C) manages Quality and Compliance for IT systems (applications, infrastructure, and digital health solutions). Serves as SME for validation/qualification per J&J SDLC and CSV Framework; ensures enterprise compliance with global regulations; helps close audit/inspection gaps; drives improvements via data-driven independent monitoring.
Responsibilities- Defining and managing the Acquisitions/Divestitures/Remediation operating model
- Executing TQ assessment strategy/framework for IT systems conveyed from acquisitions
- Assessing qualification/validation of conveyed IT GxP systems (Manufacturing, Lab, R&D, Infrastructure, IT tools, websites, mobile apps, SAMD, supply chain)
- Executing divestiture strategy for IT systems in brand/company separations
- Providing strategic direction and operational support to project teams; ensuring early TQ&C involvement to build automated/preventive controls
- Managing end-to-end quality process; implementing/maintaining A&D metrics and reporting
- Translating A&D strategy into operational plans and ensuring global consistency; supporting new/emerging technology qualification/validation strategies
- Ensuring inspection/audit readiness; participating in audits and approving NC action plans/closure
- Supporting incident management/CAPA and NC; reviewing/approving validation deliverables (plans, requirements/user stories, tests, traceability matrices, compliance reports, production release)
- Proactively monitoring compliance with SOPs and best practices; identifying automation opportunities (AI/RPA)
- Stakeholder management, risk management, and project management for A&D initiatives (including due diligence and intake/budget/resource management)
- Bachelor’s degree (Computer Science/IS/Business Adm. or related); advanced degree preferred
- 8–10+ years in pharma/med device/biotech with direct CSV experience, particularly acquisitions/divestitures
- Strong matrix/global collaboration and stakeholder communication/influencing
- People leadership, decision‑making, executive presence, analytical/problem-solving skills
- Working knowledge of cGMP/CSV including 21 CFR Part 11/210/211/820 and Annex 11; PMO, SDLC, GAMP 5, ITIL; security role design/segregation of duties
- Familiarity with cybersecurity/privacy principles; understanding of global/regional GxP regs; experience with technology risk assessments
- Vacation 120 hrs/yr
- Sick time 40 hrs/yr (CO 48; WA 56)
- Holiday/Floating 13 days/yr
- Work/Personal/Family up to 40 hrs/yr
- Parental leave 480 hrs
- Bereavement 240 hrs (immediate) and 40 hrs extended/yr
- Caregiver leave 80 hrs
- Volunteer 32 hrs/yr
- Military spouse time‑off 80 hrs/yr
Position Requirements
10+ Years
work experience
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