Sr. Manager Labeling

Overview: Jazz Pharmaceuticals is a global biopharmaceutical company dedicated to developing life-changing medicines for people with serious diseases - often with limited or no options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in key therapeutic areas. Our focus is in neuroscience, including sleep medicine and movement disorders, and in oncology, including hematologic and solid tumors. We actively explore new options for patients including novel compounds, small molecule advancements, biologics and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in more than 90 countries.We are looking for the best and brightest talent to join our team. If you're looking to be a part of a company with an unwavering commitment to improving patients' lives and being a great place to work, we hope you'll explore our career openings and get to know Jazz Pharmaceuticals. Responsibilities: The Senior Manager, Global Labeling (Neuro) will be responsible for regulatory support in the area of product labelling for Jazz Pharmaceuticals. This position reports to the Director, Global Labeling and will be will be responsible for key functions including creating, updating and maintaining labeling documents throughout the product lifecycle, with primary focus on Company Core Data Sheets and regional/local labels for products marketed globally. This position will help maintain controlled records for historical labeling changes, and communicate labeling changes to stakeholders at the time of implementation. As needed, this position will also support the implementation of process improvement changes to increase the efficiency and effectiveness of labeling processes. This position will interact with Regulatory Affairs colleagues and interact cross-functionally with members of the Clinical, Medical, Legal, Safety, Commercial, Quality and Supply Chain organizations.Essential Functions

• Maintain expertise regarding key labeling requirements worldwide and stay current with labelling regulations and guidance as they pertain to the development/maintenance of labeling; and advise key stakeholders on the application of these labeling principles.
• Provide project management to the Labeling Team throughout the entire process, from the decision to update a CCDS/USPI/SmPC or other labeling document (including patient information labelling such as Med Guides, IFUs, PIL), to ensure that labeling documents are produced in a timely manner according to internal SOPs and external regulatory requirements.
• Responsible for proofreading and departmental QC work.
• When developing new labels, research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities.
• Schedule, coordinate and lead LC meetings, and coordinate endorsement.
• Maintain controlled records for historical, current and proposed labeling changes, including labelling compliance activities (management of product information on corporate labeling webpages, as well as participating in audit and inspections as required).
• Communicate labeling changes to stakeholders at the time of implementation, including PRA and Medical Information colleagues.
• Maintain awareness of regulatory legislation pertaining to labeling; assessing and communicating the impact on Jazz business and products.
• Manage quality control over entire labeling process and management of revisions, including assigning, tracking projects, workflow execution, and issue resolution.
• Assist in implementing process improvements to increase the efficiency and effectiveness of the label review process.
• Lead and manage more junior labeling roles as required.

• Minimum of 7 years' experience in the pharmaceutical industry, with 4 as direct experience in Global Labeling or 3 in other regulatory affairs function(s).
• Proven experience in regulatory affairs with particular focus on labeling
• Experience associated with global product labeling regulations strongly desired
• Strong judgment and decision-making skills
• Excellent verbal and written communication skills and collaborative interpersonal skills.
• Ability to review regulatory labeling documents for accuracy and adherence to regulatory requirements, noting deficiencies and inconsistencies
• Must be able to work successfully within a team/partnership environment and as an individual contributor, with a high level of professionalism
• Ability to travel occasionally - approximately 10-20% regional and/or international travel
• Responsibilities may require working outside of "normal" hours, in order to meet business demands.

• Bachelor's degree required (Scientific discipline preferred) (or equivalent in industry related experience)