OverviewJoin to apply for the Senior Director, New Product & Technology Integration role at Jazz Pharmaceuticals.If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.ResponsibilitiesReporting to the Head, New Product & Technology Integration, manage Technical Operations’ due diligence assessments of new product candidates and coordinate with Corporate Development to align progress with deal requirements.Coordinate Technical Operations planning for the integration process post-deal and for the implementation of that plan after closure; serve as a critical liaison between Corporate Development, Technical Operations, and potential partners/licensors.Evaluate new technologies with potential to support Technical Operations’ development/manufacturing programs or life cycle management (LCM) of Jazz products; design and implement studies for proof of concept (POC) assessments when warranted.Lead and coordinate with external resources (contractors and consultants) and collaborate with Technical Operations, Regulatory CMC, Commercial, Legal (IP and Contracts), and Finance in a matrix environment; provide leadership and drive accountability for technical assessment and integration decisions.Develop and maintain assessment documents, CMC knowledge, checklists, playbooks, templates, and tools to standardize diligence and integration processes.Required Knowledge, Skills, and AbilitiesExperience in drug substance/drug product process development from Discovery/Phase 1 to post-approval; knowledge of global regulatory requirements desirable.Experience with development of both large and small molecules and related regulatory processes; ability to manage cross-functional inputs and lead technical assessments outside a single background.Proven ability to manage diligence processes and integration programs; strong technical writing and oral communication skills; ability to work in cross-functional teams and in a matrix environment.Leadership, project management, and adaptability to different cultures; mentoring/influencing across levels of the organization.Ability to engage with potential/actual partners and maintain effective working relationships irrespective of size or background.Required/Preferred Education and LicensesBachelors of Science, Master’s or Ph.D. in Pharmaceutical Sciences, Chemical/Biomedical Engineering, or related field.At least 15 years of hands-on experience in drug development and validation, including experience in program outsourcing and management of CMOs/CROs.Experience from early feasibility to post-commercialization with deep technical knowledge in one or more areas.Description of Physical DemandsOccasional mobility within office environment; routinely sitting for extended periods; extensive computer use.Description of Work EnvironmentIndoor office environment with regular computer use; some travel expected; may require work outside normal hours to meet business demands.Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.The successful candidate will be eligible to participate in benefits including medical, dental, and vision insurance, retirement savings, and flexible paid vacation. For more information on benefits please visit: https://careers.jazzpharma.com/benefits.html. #J-18808-Ljbffr