Auditor, Alexion Operations Audit

Position Summary The Quality Auditor at Alexion Rare Disease Unit (ARDU) has key responsibilities for auditing a variety of GMP/GDP sites (internal and external suppliers) used in 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 ARDU’s 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 Responsibilities Supporting and performing complex and timely audits of ARDU sites and suppliers of biologics, active pharmaceutical ingredients, finished drug products, or contracted services. Adherence to the global audit schedule and global audit metrics. 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. Working closely with other QA colleagues to assure common understanding of developing interpretations of cGMP/GDP. 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. Qualifications 5 years’ experience in a GMP/GDP/Medical Device or related industry in a quality/compliance function is required, with strong Quality Management Systems knowledge. 2 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 skills Technical writing/ reporting skills Ability 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. Education Bachelor’s Degree required, preferably at Master’s level within the life science area. Lead auditor training certification (preferred). Date Posted 24-Nov-2025 Closing Date 14-Dec-2025 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In 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. For over three decades, patients and their caregivers have been at the center of everything we do. Every day, we are inspired to follow the science and think differently to create better outcomes for them and their families. Our mission is driven by understanding who they are as unique individuals, not solely defined by their diseases. We’re a leading rare disease company with a diversified projects. Our pioneering legacy in rare diseases is rooted in being the first to translate the complex biology of the complement system into transformative medicines over the past three decades. Today, we continue to push the boundaries of science and deepen our understanding of rare diseases with patient-centricity at the core. This knowledge allows us to innovate and evolve into new areas where needs are unmet and provide an opportunity to help people fully live their best lives.