Regulatory Affairs Manager CDx Systems & Software at Roche

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.The PositionA healthier future. Its what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. Thats what makes us Roche.At Roche Global Regulatory Affairs we strive to be the worlds best Regulatory organization championing patient access to the worlds best diagnostics. Our team is tasked with regulatory projects as well as overarching regulatory topics with specific focus in Companion Diagnostics. You can expect an open-minded work environment where you will be working closely with colleagues in other departments and other counties.As a Regulatory Affairs Manager focused on Companion Diagnostics (CDx) with specific focus on systems and software you will be the key strategic partner driving market access for our life-changing IVD products in major global markets primarily the US and Europe.The OpportunityYou oversee regulatory document and submission compilation which includes the development of submission/product registration dossiers of more complex products/programs. You develop and manage parts of comprehensive global regulatory submissions and registration plans.For this specific role you ensure that Roche IVD products systems and software particularly Companion Diagnostics receive timely regulatory clearance/approval in your areas of responsibility (focusing on the US and Europe) by working in close cooperation with other regulatory units.You interface with external management. You understand the structure key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders. You build effective and enduring external relationships and apply effective stakeholder management practices. You contribute to audits by supporting preparation execution and follow up.You lead the organization to adapt to the evolving regulatory environment and requirements. You have an understanding of external environmental changes precedents to navigate complex situations and influence strategies and decision making. You have the ability to interpret and apply understanding of the regulators thinking to projects and apply strategies to the different needs of different regions without significant guidance. You proactively create unique/innovative regulatory strategies and influencing approaches to avoid regulatory obstacles and accelerate worldwide approvals.You effectively partner with external and internal stakeholders to understand and provide best solutions. You take initiative to address problems or opportunities and involve collaborators for best solutions. You develop relationships that significantly influence the current and future direction for Roche and our products.You have courage to make decisions even outside of scope/comfort zone and proactively initiate activities independently. You embrace good decision making principles.You model VAAC Leadership and agility. You identify opportunities to develop VACC competency. You act with integrity courage passion and honor commitments and contribute to an inclusive environment.You are able to pull people together around a common goal and seek to understand and build on different perspectives to enhance outcomes. You address and resolve conflict by creating an atmosphere of openness and trust. You bring out the best in people and teams.Who you areYou have a Bachelors / Master degree in Life Science Data Science or related subject or equivalent experience. Advanced degree preferred.You have 3-5 years experience with PhD degree 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent.You have demonstrated experience and knowledge of Daily Management and Continuous Improvement best practices.You have knowledge of the European US China and other international regulations and demonstrated ability to adequately interpret and implement quality standards considered an advantage.You have demonstrated the ability to manage more complex work and/or at parts of global projects.Experience in Companion Diagnostics is required.Experience with Systems Instruments or Software is required.LocationsYou are local to Tucson Indianapolis Branchburg or Penzberg.No relocation benefits are available for this position.The expected salary range for this position based on the primary location of Tucson Arizona is $103900 and $193000. Actual pay will be determined based on experience qualifications geographic location and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.BenefitsWho we areA healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.Lets build a healthier future together.Roche is an equal opportunity employer. It is our policy and practice to employ promote and otherwise treat any and all employees and applicants on the basis of merit qualifications and competence. The companys policy prohibits unlawful discrimination including but not limited to discrimination on the basis of Protected Veteran status individuals with disabilities status and consistent with all federal state or local laws.If you have a disability and need an accommodation in relation to the online application process please contact us by completing this form Accommodations for Applicants.Required Experience:Manager Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Employment Type : Full-Time Experience: years Vacancy: 1 Monthly Salary Salary: 103900 - 193000