External Quality Lead (Senior Manager/Associate Director, commensurate with experience)

Responsibilities * Tech Transfer Execution: Collaborate closely with the relevant organization (e.g. R&D or CMO) during any technology transfer to ensure CMOs achieve appropriate readiness to move to commercialization. * Validation & Stability Handoff: Align with R&D and Quality Control on touchpoints for the management of the stability Quality Control program. Review and approve process validation, analytical method transfer, and equipment qualification protocols/reports. * Operational Oversight: Provide operational QA oversight for products manufactured at CMOs or at Menarini manufacturing sites, ensuring they are in full compliance to manufacture, test, and release commercial products. Ensure establishment, maintenance and adherence to appropriate Quality Agreements. * Batch Disposition: Lead the review and approval of Master Production Records (MPRs) and Executed Production Records (EPRs) for Drug Substance and Drug Product to drive final product disposition. * Technical Deviation Management: Review and approve deviations, OOS/OOT results, and CAPAs generated by the CMO. Ensure robust root-cause analysis and the implementation of effective preventive actions. * Operational Change Control: Review and approve all CMO change controls to accommodate process scale-up and ensure Operations teams generate appropriate Change Controls for process-related changes prior to execution. * On-Site Oversight: Provide Quality oversight of GMP compliance at manufacturing, packaging, and testing facilities. Lead or support CMO audits and execute "Person-in-Plant" activities as required. * Support the creation and maintenance of appropriate procedural documentation. * Manage and prioritize workload and projects to ensure effective and efficient completion of tasks, and work independently * Cultivate and maintain effective working relationships with internal teams, senior leadership, and CMO management * Act as a bridge between departmental teams and senior leadership, ensuring alignment with corporate goals * Work with Quality Operations management to support regulatory inspections, FDA, EMA, etc. * Travel to CMOs as needed (~25%)## Qualifications * Bachelors degree, preferably in a scientific discipline, or comparable experience * 68 years of experience in Quality Assurance, with at least 3 years supporting Sterile Manufacturing * Minimum of 3-5 years of pharmaceutical quality operations experience or quality oversight of a CMO * Strong knowledge of cGMP, FDA, and/or EU regulations and requirements * Experience working in a Global capacity (I,e, interacting with international third parties) * Strong interpersonal skills including ability to communicate effectively with people individually and in groups; ability to communicate with technical and non-technical colleagues; experience establishing and maintaining effective relationships with leaders and peers * Ability to lead and participate on teams with shared responsibility for outcomes and decision-making * Experience with cGMP computer system validation (CSV) and electronic data management * Prior experience working within SAP, Veeva, and/or Trackwise would be beneficialPlease note: this position is classified as a corporate office position. In accordance with the New York employer convenience rule, Stemline will withhold New York state income taxes for all corporate office employees, regardless of whether these employees work in New York or remotely. Base Salary Range of $140,000-180,000. Menarini Stemline offers generous compensation and benefits packages, including Short- and Long-Term Incentive Programs, Fidelity 401(k) (with company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre-tax FSA/HSA programs.