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How much do regulatory science jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for regulatory science in Arizona is $46.65, according to ZipRecruiter salary data. Most workers in this role earn between $32.50 and $48.37 per hour, depending on experience, location, and employer.

What is regulatory science?

A Regulatory Science job involves evaluating and developing scientific methods to assess the safety, efficacy, and quality of medical products, food, and other regulated items. Professionals in this field work at the intersection of science, policy, and regulation to ensure compliance with government standards. They may collaborate with regulatory agencies, industry stakeholders, and researchers to facilitate product approvals and post-market surveillance.

What are the typical responsibilities of a regulatory science professional?

Regulatory Science professionals are responsible for ensuring that products comply with regulations throughout all development and commercialization stages. Their daily activities may include preparing and submitting regulatory documents, collaborating with R&D, quality assurance, and legal teams, and interpreting updates to regulations or guidelines that affect product approval. They may also interact directly with regulatory agencies and participate in strategic meetings to help guide product development decisions. Working in Regulatory Science often means being a key liaison between internal teams and regulatory authorities to facilitate smooth approvals and ongoing compliance.

What are the key skills and qualifications needed to thrive in regulatory science?

To thrive in Regulatory Science, you need a solid background in life sciences or a related field, strong analytical and research skills, and familiarity with regulatory frameworks. Experience with regulatory submission systems (like eCTD), knowledge of global regulations, and certifications such as RAC (Regulatory Affairs Certification) can be highly advantageous. Excellent attention to detail, problem-solving abilities, and strong cross-functional communication are critical for success in this field. These competencies ensure regulatory compliance and efficient product development while minimizing delays and risks for organizations bringing products to market.

What can you do with a regulatory science degree?

A regulatory science degree prepares individuals for roles in regulatory affairs, compliance, and policy within industries such as pharmaceuticals, biotechnology, and medical devices. Graduates can work as regulatory specialists, managers, or consultants, often utilizing knowledge of regulations, safety standards, and documentation processes to ensure products meet legal requirements and facilitate approval processes.

What does a regulatory scientist do?

A regulatory scientist evaluates and ensures that products such as pharmaceuticals, medical devices, or food meet government regulations and safety standards. They analyze data, prepare documentation for regulatory submissions, and stay informed about evolving policies, often using scientific and regulatory tools to support product approval and compliance.

What are the most commonly searched types of Regulatory Science jobs in Arizona?

The most popular types of Regulatory Science jobs in Arizona are:

What are popular job titles related to Regulatory Science jobs in Arizona?

For Regulatory Science jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Regulatory Science jobs in Arizona look for?

The top searched job categories for Regulatory Science jobs in Arizona are:

What cities in Arizona are hiring for Regulatory Science jobs?

Cities in Arizona with the most Regulatory Science job openings:

Regulatory Science jobs near you
Infographic showing various Regulatory Science job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 21% Part Time, and 2% Contract. Highlights an 76% Physical, 3% Hybrid, and 21% Remote job distribution, with an average salary of $97,033 per year, or $46.7 per hour.

Sr. Regulatory Affairs Specialist - Relocation Assistance Provided

Innovative Health LLC

Scottsdale, AZ • On-site

Full-time

Re-posted 11 days ago

Job description

The Sr. Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for the submission of FDA 510(k)s, periodic updates, Canadian applications and registrations to regulatory agencies.
  • Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially distribute product.
  • Responsible for preparing Canadian applications to obtain approval to commercially distribute product.
  • Review and approve test protocols/reports and other documentation/information for regulatory submissions from various functional areas and check for errors, legibility, and missing information.
  • Prepare routine regulatory correspondence and assure submission to government agencies in support of marketed products.
  • Participate in project development teams and review plans, reports, risk management, and design reviews associated with product and process projects.
  • Assess necessity for submitting a 510(k) application by preparing regulatory assessments for manufacturing, line extensions, design changes, and validation activities. Prepare internal letter to File (US) for changes that do not require a 510(k) submission, and assess also for Canadian impact (i.e. application amendments).
  • Maintain and disseminate current knowledge base of existing regulations, standards, or guidance documents and proactively seek and find information to help resolve questions related to assigned projects.
  • Develop and maintain regulatory procedures and policies to ensure compliance to applicable regulations.
  • Reviews complaints/adverse events for submission of MDRs and Vigilance Reports.
  • Review and approve advertising/marketing material, and product labeling to ensure compliance with applicable regulatory requirements.
  • Participates in internal/external audits and responses to support audit findings or other respective actions related to such audits.
  • Conduct regulatory review and approval of engineering change orders, CAPA/nonconformance, and related project documentation.
  • Coordinate product correction and removals (recalls, market withdrawals, and stock retrievals) per procedures and applicable regulations.
  • Maintain Unique Device Identifier (UDI) activities for implementation/compliance.
  • Maintain regulatory registrations and product listings.
  • Assist in negotiations with the FDA or other regulatory agencies.
  • All other reasonable duties, as assigned.

Qualifications and Experience:
  • Bachelor's Degree in Life Science is preferred with a minimum of 8 years Regulatory experience in the Medical Device industry; or equivalent combination of education and experience;
  • Expert level knowledge of FDA 21 CFR Part 820 and 510(k) submission requirements;
  • Authoring of 510(k) submissions;
  • Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
  • Experience with ToC format for Canadian applications, preferred;
  • Ability to work in a fast paced, collaborative team environment
  • Ability to handle multiple projects and coordinate with cross functional teams;
  • Ability to comfortably and effectively confront difficult situations and issues in a timely and appropriate manner while providing a solution;
  • Ability to recommend technical solutions;
  • Ability to specify regulatory requirements for products;
  • General proficiency in Microsoft Word and other applications (Excel, PowerPoint, Adobe Acrobat, and Visio).
  • Ability to work independently under general guidelines and supervision from the RA Manager.
  • Self-starter and highly motivated.

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