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Fda Jobs in Arizona (NOW HIRING)

Pinnaql

Quality Director

Tempe, AZ · On-site

Ensure compliance with FDA cGMP requirements, applicable provisions of the Federal Food, Drug, and Cosmetic Act, USP standards, and state pharmacy regulations. * Serve as the primary Quality ...

Pinnaql

Quality Director

Tempe, AZ · On-site

Ensure compliance with FDA cGMP requirements, applicable provisions of the Federal Food, Drug, and Cosmetic Act, USP standards, and state pharmacy regulations. * Serve as the primary Quality ...

Pinnaql, Inc.

Quality Director

Tempe, AZ · On-site

$200 - $250/hr

Ensure compliance with FDA cGMP requirements, applicable provisions of the Federal Food, Drug, and Cosmetic Act, USP standards, and state pharmacy regulations. * Serve as the primary Quality ...

BEPC INC

Be Seen First

Regulatory Affairs Manager - PHCS - 30522

Tucson, AZ · On-site

$45 - $55/hr

Interpret FDA and international regulatory expectations and translate requirements into actionable strategies for cross-functional teams. * Risk Management: Proactively identify regulatory risks ...

Pinnaql

Quality Director

Tempe, AZ

Ensure compliance with FDA cGMP requirements, applicable provisions of the Federal Food, Drug, and Cosmetic Act, USP standards, and state pharmacy regulations. * Serve as the primary Quality ...

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How much do fda jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for fda in Arizona is $38.20, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $47.61 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

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

The most popular types of Fda jobs in Arizona are:

What are popular job titles related to Fda jobs in Arizona?

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

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

The top searched job categories for Fda jobs in Arizona are:

What cities in Arizona are hiring for Fda jobs?

Cities in Arizona with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in Arizona as of August 2026, with employment types broken down into 77% Full Time, 11% Part Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $79,460 per year, or $38.2 per hour.

Pharmacist (Part Time)

Tailstorm Health Inc

Chandler, AZ • On-site

Part-time

Posted 5 days ago

Key responsibilities

  • Oversee sterile compounding and aseptic filling operations to ensure compliance with USP <797>, USP <800>, and cGMP requirements.

  • Review and approve batch production records, labels, and associated manufacturing documentation.

  • Support internal audits, customer audits, and regulatory inspections.

Job description

Position Summary

The Pharmacist is responsible for supporting Medivant Healthcare's sterile injectable manufacturing operations while ensuring compliance with FDA regulations, USP <797>, USP <800>, cGMP requirements, and internal quality standards. This role provides oversight of sterile compounding activities, batch record review, labeling verification, cleanroom operations, regulatory compliance, and quality documentation.

The Pharmacist will work closely with Production, Quality Assurance, and Regulatory teams to maintain product quality, manufacturing compliance, and operational excellence. The ideal candidate is a licensed pharmacist with experience in sterile compounding, pharmaceutical manufacturing, or 503B outsourcing facilities and possesses a strong understanding of sterile operations and regulatory requirements.

Key ResponsibilitiesSterile Compounding & Manufacturing Oversight
  • Oversee sterile compounding and aseptic filling operations to ensure compliance with USP <797>, USP <800>, and cGMP requirements.
  • Monitor cleanroom operations, gowning practices, environmental controls, and aseptic techniques.
  • Verify formulation calculations and compounding accuracy.
  • Ensure adherence to established manufacturing procedures and standard operating procedures.
  • Provide guidance and support to technicians and manufacturing personnel on sterile compounding best practices.
Batch Record Review & Documentation Compliance
  • Review and approve batch production records, labels, and associated manufacturing documentation.
  • Ensure accurate completion and maintenance of production and quality records.
  • Verify product labeling and documentation accuracy prior to release activities.
  • Maintain documentation in accordance with regulatory and company requirements.
  • Support data integrity and documentation compliance initiatives.
Quality & Regulatory Compliance
  • Ensure compliance with FDA regulations, DEA requirements, USP standards, state pharmacy board regulations, and internal quality systems.
  • Support internal audits, customer audits, and regulatory inspections.
  • Participate in investigations, deviations, CAPA activities, and corrective action implementation.
  • Assist with validation, qualification, and continuous improvement initiatives.
  • Collaborate with Quality Assurance to maintain inspection readiness and regulatory compliance.
Cross-Functional Collaboration
  • Partner with Production, Quality Assurance, Validation, and Regulatory Affairs teams to support manufacturing operations.
  • Support process improvements that enhance product quality, compliance, and operational efficiency.
  • Provide technical expertise related to sterile manufacturing and pharmacy regulations.
  • Assist in evaluating operational risks and identifying compliance improvement opportunities.
QualificationsRequired:
  • Active Pharmacist License in the State of Arizona in good standing.
  • Minimum 2 years of experience in sterile compounding, pharmaceutical manufacturing, hospital pharmacy, or a 503B outsourcing facility.
  • Strong knowledge of USP <797>, USP <800>, cGMP requirements, and FDA regulations.
  • Experience reviewing manufacturing documentation and batch production records.
  • Strong analytical, problem-solving, and attention-to-detail skills.
  • Excellent verbal and written communication abilities.
  • Ability to work effectively in a regulated pharmaceutical manufacturing environment.
Preferred:
  • Experience in sterile injectable pharmaceutical manufacturing.
  • Experience supporting FDA inspections and regulatory audits.
  • Familiarity with LIMS, ERP, electronic batch record systems, or quality management systems.
  • Previous experience within a 503B outsourcing facility.
  • Experience with validation, deviation investigations, and CAPA processes.
Key Competencies
  • Sterile Compounding & Aseptic Processing
  • USP <797> & USP <800> Compliance
  • Pharmaceutical Manufacturing Operations
  • cGMP Compliance
  • Batch Record Review & Documentation Control
  • Quality Assurance & Regulatory Compliance
  • FDA & DEA Regulatory Knowledge
  • Investigation & CAPA Management
  • Attention to Detail
  • Risk Assessment & Problem Solving
  • Cross-Functional Collaboration
  • Process Improvement
  • Technical Leadership
  • Communication & Documentation Skills
What Success Looks Like
  • Maintain full compliance with USP, FDA, DEA, and company quality requirements.
  • Ensure accurate review and approval of batch documentation and manufacturing records.
  • Support successful regulatory inspections and internal audit outcomes.
  • Maintain high standards for sterile compounding and aseptic manufacturing practices.
  • Contribute to continuous improvement initiatives that enhance compliance, efficiency, and product quality.
  • Serve as a trusted technical resource for pharmacy, manufacturing, and quality teams.
  • Support Medivant Healthcare's mission of providing high-quality, affordable sterile injectable medications to healthcare providers nationwide.
Schedule: Morning 04-05 Hours.





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