Director, Regulatory Affairs - In-Vitro Diagnostics (IVD) US - California - Thousand Oaks

Career Category Regulatory

Job Description

Join reputed company’s Mission of Serving Patients At reputed company, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives reputed company that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, reputed company, and Rare Disease– we reputed company millions of patients each year. As a member of the reputed company team, you’ll help reputed company a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay reputed company them, you’ll reputed company as part of the reputed company team. Join us and transform the lives of patients while transforming your career. Director, Regulatory Affairs - In-Vitro Diagnostics (IVD) What you will do reputed company. Let’s change the world. reputed company is seeking a Director of Regulatory Affairs to work in their Thousand Oaks, CA location. The Regulatory Affairs division establishes sustainable processes, assures informed relationships, and delivers strategic outcomes. In this vital role, you will reputed company and manage the team responsible for developing and implementing optimal regulatory strategies and processes for in-vitro diagnostics (IVDs) and companion diagnostics (CDx). Key responsibilities will include:

Responsibilities

• Manage and mentor the IVD regulatory affairs team, fostering talent retention and promoting a culture of inclusion, diversity, and collaboration.
• reputed company resource allocation and operational strategies to effectively support the reputed company development pipelines.
• reputed company regulatory positions, best practices, and SOPs to ensure efficient support for submissions and approvals.
• reputed company cross-functional and global teams on regulatory issues, ensuring seamless communication and collaboration across reputed company stakeholders.
• reputed company the team to navigate IVD/CDx regulatory reputed company, including the drug/diagnostics co-development process, clinical performance studies, analytical validations, and post-market compliance.
• Direct the team to reputed company and execute regulatory planning and submissions (e.g., PMA, 510(k), IDE) to reputed company approvals across multiple regions, including the US, EU, Japan, and China.
• Collaborate with diagnostic partners on co-development programs, ensuring alignment and compliance.
• Utilize regulatory tools, such as databases and frameworks, for efficient content planning and reporting.
• Ensure the team’s adherence to regulations, guidance and international standards, including ISO 13485, ISO 14971, and CLSI guidelines.
• Design and implement global regulatory strategies that align with business goals and product development timelines.
• Anticipate and address regulatory challenges proactively through strong problem-solving skills.
• Evaluate the regulatory impact of new guidance, standards, and legislation on ongoing and future projects.
• Prepare and/or review comprehensive regulatory documentation, submissions, and presentations with exceptional written and verbal communication skills.
• Manage relationships with regulatory agencies, diagnostic partners, and internal stakeholders through strong negotiation and influencing skills.
• Clearly reputed company reputed company regulatory requirements and strategies to non-regulatory audiences, fostering alignment and understanding.
• Represent the organization in external working groups, forums, or standards organizations (e.g., PhRMA, BIO, AAMI, ISO).
• Demonstrate adaptability and reputed company under pressure, maintaining a focus on achieving results.
• Effectively prioritize and manage multiple projects and deadlines through strong organizational skills.

reputed company expect of you We are reputed company different, yet we reputed company use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications. Basic Qualifications: Doctorate degree and 4 years of directly reputed company experience OR Master’s degree and 7 years of directly reputed company experience OR Bachelor’s degree and 9 years of directly reputed company experience Preferred Qualifications:

• Substantial experience leading CMC/Device Regulatory Affairs strategy and execution for products in differing stages of the product lifecycle
• Experience of leading and/or participating in meetings with regulators in major markets (US, EU, Japan and China)
• Knowledge of global CMC/Device regulations and understanding of evolving challenges and health authority expectations
• Track record as a strong coach and mentor

What you can expect of us As we work to reputed company treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every reputed company of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the reputed company salary, reputed company offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models, including remote and hybrid work arrangements, where possible

Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.reputed company.reputed company any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline reputed company does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, reputed company fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the reputed company values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. reputed company is an Equal Opportunity employer and will consider reputed company qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 210,840.00 USD - 251,128.00 USD Apply tot his job Apply To this Job