Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical 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. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit and on Twitter.
The Senior Manager, Pharmacovigilance Compliance, Aggregate Safety Reporting and Labeling is responsible for executing PV Compliance activities based on relevant regulations, procedures, and contractual requirements. Through implementation of quality and compliance tracking tools/reports, oversight strategy and relationship management, this role will support the development and management continuous improvements across the pharmacovigilance system, including the implementation, tracking, maintenance, and effectiveness checking of activities supporting the Medical Safety and Labeling sub-functions within GPV&L.
Define, develop, and deliver strategy for trending and reporting on aggregate safety report (ASR) quality reviews and health authority feedback
Partner with the GPV&L sub-functions to enhance the ASR quality review process
Perform quality review of ASRs and provide feedback to authors and leadership
Collect, verify, and distribute metrics for monitoring compliance with signal management processes and timelines
Support the development, implementation, and execution of Labeling quality and compliance KPIs/KQPIs
Lead or support (as determined by line management) PV process improvements including authoring/updating controlled procedures as it relates to compliance activities
Maintain documentation and reports for compliance continuous improvement activities
Applies in-depth knowledge to effectively assist in inspection related activities, (pre-, peri- and post-inspection)
Remain current with global pharmacovigilance regulations and requirements, evaluate legislative changes affecting PV, and develop strategies to support the patient safety at the local level
Required Knowledge, Skills, and Abilities
Minimum 5+ years business, pharmaceutical, or biotechnology industry experience
Strong Good Pharmacovigilance Practices (GVP) is required with specific knowledge of GVP Modules I, II, V, VII, IX
Demonstrated ability to review complex documents and perform trending analysis
Demonstrated ability to lead multi-disciplinary projects
Excellent written and verbal communications skills
Ability to work in an entrepreneurial and fast-paced culture
Self-directed and ability to take action as needed with limited oversight
Ability to influence or gain acceptance from others in sensitive situations
Ability to collaborate and partner with various internal and external business partners.
Ability to work in a team environment and support stakeholders
Ability to work across geographical boundaries
Disciplined, detail oriented, and strong time management skills
Required/Preferred Education and Licenses
Bachelor's degree in business or life sciences required
Lean Sigma certification, or equivalent certification, preferred but not required
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.