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Senior Manager, Acquisitions, Divestitures and Remediation, Technology Quality
Job in
New Brunswick, Middlesex County, New Jersey, 08933, USA
Listed on 2026-06-25
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-06-25
Job specializations:
-
IT/Tech
IT Business Analyst, Cybersecurity, IT Project Manager
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).
- 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.
- Compliance Management
- Controls Compliance
- Digital Assurance/Governance
- Fact‑Based Decision Making
- Quality Management Systems (QMS)
- Quality Validation
- Regulatory Compliance
- Stakeholder Engagement
- SOP
- Technical Credibility
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).
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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