Sr. Global Quality Auditor at Alexion

Position SummaryThe Senior Quality Auditor at Alexion Rare Disease Unit (ARDU) has key responsibilities for auditing a variety of GMP/GDP sites (internal and external suppliers) used for commercial and development projects. The manufacturing sites audited range from biotechnology combination products medical devices raw material to fill finish facilities. Laboratory and distributor facilities are also audited.The auditor will assess the internal network and suppliers of ARDU by supporting the end-to-end audit process including planning leading reporting and closure of audits in accordance with ARDUs Quality Management System regulations and industry best practices.This role supports compliance and process improvement projects within ARDU and provides support to internal and external key-stakeholders by providing quality and compliance guidance.Principal ResponsibilitiesEnsures compliance with regulatory and internal requirements by leading and supporting the complete audit lifecycle inclusive of planning execution reporting review and acceptance of responses and audit closure for complex audits of ARDU sites and suppliers of biologics active pharmaceutical ingredients finished drug products and contracted services.Maintaining supporting and adhering to the global audit schedule and generating periodic metric reports suitable for viewing by and presentation to Management/ leadership/ External parties (e.g. regulators).Conducting independent appraisals of quality and compliance systems within technically advanced manufacturing settings.Initiating and maintaining close contacts with regulatory agencies and/or industry/ professional organizations to maintain knowledge of trends and initiatives in quality assurance compliance and inspections.Partnering with ARDU stakeholders for the effective execution of audits.Building and maintaining strong customer relationships with other functions whose activities overlap influence or affect compliance.Support and lead key and senior conversations with key stakeholders on all audit related topics such as metrics/queries/actions as required.Providing leadership to the Audit team.Working closely with other QA colleagues to assure common understanding of developing interpretations of cGMP/GDP.Developing solutions to a diverse range of problems that require complex judgements using highly developed levels of conceptual thought and analysis.Driving role modelling and supporting a strong lean culture that promotes standardization simplification and continuous improvement in Audit Performance.Supports inspection readiness activities for the function as required.60% travel required (mostly regional/locally America regions).Commutable to site at the ARDU New Haven CT and Boston MA facilities.Qualifications12 years experience in a GMP/GDP/Medical Device or related industry in a quality/compliance function is required with strong Quality Management Systems knowledge.5 years GMP/GDP QA experience supporting or conducting audits (preferred). Audit experience preferably within the biologics area.Thorough knowledge of applicable international GxP regulations and standards (e.g. GMP GDP Medical Device etc.) inclusive of FDA and EU regulations.Ability to navigate and be successful in a fast-paced cross-functional work environment.Excellent written and verbal communication skills.Strong attention to details skills with an ability to think strategically.Strong organizational skillsTechnical writing/ reporting skillsAbility to multi-task and prioritize work effectively.Team-oriented approach to project management and problem resolution.The duties of this role are generally conducted in an audit environment. The Auditor must be proficient in the use of complex electronic systems and a quick learner of new applications and be able to engage in communications via phone video and electronic messaging; engage with auditees efficiently and effectively so as to maximize audit performance.The Auditor must be able to collaborate with auditees and colleagues respectfully and maintain general availability during standard business hours.EducationBachelors Degree required preferably at Masters level within the life science area.Lead auditor training certification (preferred).Date Posted09-Dec-2025Closing Date29-Dec-2025Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.Required Experience:Senior IC Key Skills Quality Assurance,Quality Inspection,Calipers,ISO 9001,Quality Audits,Process Mapping,Fair Housing Regulations,Quality Control,Underwriting,cGMP,As9100,Manufacturing Employment Type : Full-Time Experience: years Vacancy: 1