Regulatory Affairs Analyst Jobs in Arizona
Regulatory affairs analyst jobs in Arizona are concentrated in pharmaceuticals, medical devices, and biotechnology, with the market anchored by a strong cluster of life sciences employers across the Phoenix metro and Tucson. Companies such as Honeywell, Banner Health, and Microchip Technology have lasting regulatory functions in the state, and demand runs from entry-level coordinators to senior regulatory strategy roles. Submissions management, FDA compliance, and quality systems are the most consistently requested specialties in Arizona postings. See the openings below and apply to the ones that match your experience.
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The Position
This is an exciting opportunity to help shape the future of pathology within a market-leading organization with a strong pipeline of innovative instruments, software, and digital solutions. As a Senior Regulatory Affairs Manager, you will be a strategic regulatory partner to cross-functional teams, influencing key decisions from early development through global market access and lifecycle management. You will have the opportunity to navigate complex and evolving regulatory areas—including integrated instrument systems, software, cybersecurity, automation, connectivity, and digital technologies—while helping translate innovation into regulatory strategies that enable successful product development and commercialization. This role offers significant visibility, autonomy, and opportunity to influence, making it ideal for an experienced regulatory professional who enjoys solving complex problems, shaping strategy, and seeing their work directly contribute to the future of pathology and patient care.
The Opportunity
- Regulatory document and submission compilation: Oversees the development of submission/product registration dossiers of the most complex products/programs. Develops and manages comprehensive global regulatory submissions and registration plans. Mentors more junior team members in this area.
- External interface management: Leads external complex initiatives including the collaboration with key stakeholders. Cultivates and utilizes external relationships that significantly influence the current and future direction for Roche and our products. Challenges and resolves complex issues and overcomes organizational barriers. Develops/maintains health authority relationships and actively shapes the regulatory environment. Has the ability to represent Roche in audits and other complex stakeholder negotiations.
- Regulatory knowledge and strategy: Lead the organization adapt to evolving regulatory environment and requirements. Experience in solving complex, critical health authority issues or equivalent understanding of external environmental changes, precedents, to navigate complex situations and influence strategies and decision making. 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. Proactively creates unique/innovative regulatory strategies and influencing approaches to avoid regulatory obstacles and accelerate world wide approvals.
- Stakeholder management and influencing: Leads complex initiatives including collaboration with key stakeholders. Cultivates and utilizes relationships that significantly influence the current and future direction for Roche and our products. Challenges and resolves complex issues and overcomes organizational barriers.Ability to shift the perspectives of key stakeholders to achieve a specified goal. Builds common ground and alignment even if initial positions were far apart. Negotiates to maximize value for Roche and stakeholders so we have biggest impact for customers and patients.
- Decision making: Has courage to make decisions even outside of scope/comfort zone. Proactively initiates activities independently and initiates interactions across departments as applicable. Embrace the good decision making principles. Pushes decision making to the lowest appropriate level. Commits to decisions that have been made. Shows good judgment in decision making. Makes good decisions without necessarily having all the information in a timely manner.
- Innovation and problem solving: A mindset of creativity and experimentation - a true trailblazer and support radical simplification as well as continuous innovation. Challenges the organization to be curious, question the status quo and adopt new approaches. Fosters a culture that leverages unique perspectives. Has vision; often brings up ideas about potentials and possibilities for the future. Actively drives new ideas/ approaches into the business.Able to troubleshoot issues as they arise, independently develop and implement cost effective and non-complex actions solutions to ensure that daily work is completed without jeopardizing compliance. Identifies problems before they occur and actively drives mitigation strategies to avoid them. Leads others in problem-solvingactivities.
- VAAC Leadership and agility: Role model forwe all lead. Actively develops VACC competencies and deploys them in our daily work. Fosters an inclusive environment. Shows dedication to advancement of others. Demonstrates commitment to identify, solicit and provide growth opportunities for others. Demonstrates outstanding achievement in areas of technical expertise, leading innovation and/or mobilizing the organization.Change ambassador for their environment and actively develops their agile mindsets and behaviors and encourages others to do so as well. Identifies and acts on opportunities for improvement within and across Q - embraces new technologies and other means to simplify and increase productivity
- Teamwork and communication: Is able to pull people together around a common goal. Seeks to understand and build on different perspectives to enhance outcomes. Addresses and resolves conflict by creating an atmosphere of openness and trust. Brings out the best in people and teams.Establishes an environment for open, honest communication for everyone and ensures that people feel that they are truly heard. Clearly articulates even the most complex concepts. Encourages direct and open discussions about important issues and can be depended on to tell the truth regardless of the circumstances. Courageously speaks the truth regardless hierarchy and creates an environment where people are appreciated and recognized for their contributions.
- Bachelor’s / Master degree in Life Science, Data Science or related subject. Advanced degree is considered an advantage.
- Demonstrated experience and knowledge of Daily Management and Continuous Improvement best practices.
- 5-10 years experience with PhD degree, 7-10 with Masters degree and 8-10 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent.
- Knowledge of the European, US, China and International regulations and demonstrated ability to adequately interpret and implement quality standards considered an advantage
- Has demonstrated the ability to manage even the highest complexity of work and/or global projects.
- Preferred - You have experience with complex regulatory product launch strategies encompassing integrated systems/modular systems, change control, cybersecurity, software (SiMDs, SaMDs and AIML) for major global markets not limited to US and EU.
This role can be based in Tucson, Branchburg, Indianapolis, or Carlsbad. This is a primarily onsite role; no remote arrangements are available.
Relocation benefits are not available for this position.
The expected salary range for this position based on the primary location of Arizona is $126,800- $235,000. 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.
Benefits
Who we are
A healthier future drives us to innovate. Together, more than 100’000 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.
Let’s 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 company's 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 formAccommodations for Applicants.
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Where Arizona roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Arizona
A snapshot from current Arizona openings, updated as new roles post.
Who's Hiring



Top Industries Hiring
- Insurance
What Arizona Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Arizona.
- Bachelor's degree in life sciences, engineering, chemistry, or a related technical field
- Working knowledge of FDA regulations including 21 CFR Parts 11, 820, or 211
- Experience preparing and submitting regulatory documents such as 510(k)s or NDAs
- Familiarity with quality management systems and ISO 13485 or ICH guidelines
- Strong technical writing skills for regulatory submissions and SOPs
- Proficiency with document management systems and regulatory information databases
Regulatory Affairs Analyst Jobs in Arizona: Frequently Asked Questions
How do you become a regulatory affairs analyst in Arizona?
Most regulatory affairs analyst positions in Arizona require a bachelor's degree in a life sciences, engineering, or health-related field, and employers in the Phoenix and Tucson markets strongly favor candidates with hands-on experience in FDA-regulated industries. Arizona does not issue a state-specific license for this role, but earning the Regulatory Affairs Certification through the Regulatory Affairs Professionals Society signals credibility and is increasingly preferred by Arizona's medical device and pharmaceutical employers.
Which companies hire regulatory affairs analysts in Arizona?
Companies currently hiring regulatory affairs analysts in Arizona include Roche, Stryker, and Oscar Health, per current listings on Migrate Mate as of September 2026. Arizona's concentration of medical device manufacturers and pharmaceutical operations in the Greater Phoenix corridor means these employers regularly maintain active regulatory teams.
Which Arizona cities have the most regulatory affairs analyst jobs?
The cities with the most regulatory affairs analyst openings in Arizona are Tucson, Scottsdale, and Tempe. The Phoenix metro drives the majority of postings due to its dense cluster of medical device manufacturers, pharmaceutical operations, and large healthcare systems, while Tucson contributes a meaningful share tied to its life sciences research institutions and defense-adjacent technology companies.
Are there remote regulatory affairs analyst jobs in Arizona?
Yes, and more than most fields, because regulatory affairs work is largely document-driven and does not require a physical presence on a production floor. About 0% of regulatory affairs analyst openings tied to Arizona are remote or hybrid as of September 2026, reflecting how well the role translates to distributed work. Submissions management, regulatory writing, and literature review functions tend to be the most frequently offered in remote or hybrid formats.
How can I get hired as a regulatory affairs analyst in Arizona with little or no experience?
The most realistic entry path is moving laterally from a quality assurance, clinical operations, or laboratory role inside an FDA-regulated company, since Arizona's medical device and pharmaceutical employers, including those operating manufacturing sites in the East Valley and Tucson, regularly hire regulatory coordinators from their own quality teams. Pursuing the Regulatory Affairs Certification as a candidate, completing an internship through Arizona State University's biomedical programs, or targeting associate regulatory affairs roles at contract research organizations based in Phoenix are all concrete steps that give first-time applicants a competitive edge.
Where can I find and apply to regulatory affairs analyst jobs in Arizona?
You can find and apply to regulatory affairs analyst jobs in Arizona on Migrate Mate, which lists current Arizona openings from employers across the state. Search the available roles, find the ones that fit your background and location preferences, and apply directly to the positions that match your experience.
See All 6 Regulatory Affairs Analyst Jobs in Arizona
Find roles in Arizona that match your experience and apply in just a few clicks.
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