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

Menarini Group•, NY

6d•$140,000 - $180,000•Remote

About The Position

The External Quality Lead (EQL) provides the tactical, "day-to-day" Quality oversight of our external manufacturing partners (CMOs) within Menarini Stemline's virtual operating model. In addition to managing commercial batch disposition, this role, working with the Product Quality Lead, ensures quality oversight for all product phases (clinical to commercial) and is critical for compliance with cGMP regulations and Menarini Stemline's quality systems. Key responsibilities include ensuring adherence to cGMP in processes such as batch production, product release, laboratory testing, investigations/CAPA, Change Control, Annual Product Reviews, and Product Quality Complaint handling.

Requirements

Bachelor’s degree, preferably in a scientific discipline, or comparable experience
6–8 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

Nice To Haves

Prior experience working within SAP, Veeva, and/or Trackwise would be beneficial

Responsibilities

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.
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.
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.
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.
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.
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.
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%)