New

Associate Director, Regulatory Affairs (Remote)

Jazz Pharmaceuticals
$152,000.00 - $228,000.00
vision insurance, 401(k)
United States, California, Palo Alto
Nov 06, 2025
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. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. 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. The Associate Director, Regulatory Affairs will be a key stakeholder in the company's regulatory activities and initiatives to ensure the quality of the company's records, products, and processes. He/she/they will support Jazz Pharmaceuticals' efforts to obtain worldwide approvals to market our products. An Associate Director, Regulatory Affairs within the Regulatory Strategy group will manage worldwide interactions and negotiations with regulatory agencies and marketing partners in support of investigational studies, product registrations, and commercial products. An Associate Director, Regulatory Affairs will be a key member of project teams and teams responsible for evaluation of product concepts. Essential Functions/Responsibilities Develop and implement regulatory strategies to facilitate the progress of programs in all phases of development Serve as the Regulatory Affairs representative on project teams; assure the progress of projects by providing direction, solutions, and feedback to the teams Lead regulatory interactions with health authorities, marketing partners, and vendors for their products/projects Support the company's commercial products Review and approve labeling for the company's products Ensure the timely submission of INDs, NDAs, amendments, and supplements for their products/projects Maintain awareness of and communicate changing regulatory agency requirements; provide training and regulatory intelligence to the organization Required Knowledge, Skills, and Abilities A minimum of 8 years in roles of increasingly responsible in regulatory affairs or related areas in pharmaceutical drug development Deep and broad knowledge of regulatory affairs; direct experience with pharmaceutical regulatory submissions and product approvals Proven track record of effective collaboration with regulatory agencies, including FDA, EMA, and PMDA Demonstrated leadership success in management of regulatory activities Excellent verbal and written communication skills Evaluative, analytical and interpretative skills enabling review and synthesis of reports and other documents used in regulatory planning and submissions Ability to work with limited supervision, to set priorities to meet timelines and to motivate and influence others Required/Preferred Education and Licenses Masters or advanced degree in a scientific discipline preferred 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. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $152,000.00 - $228,000.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.