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Chemical Risk Assessment Jobs in Arizona (NOW HIRING)

PRN ASSESSMENT INTAKE COORDINATION (MA/MSW)

Tucson, AZ · On-site

$32K - $37K/yr

The Counselor provides telephonic risk assessment and in-person clinical assessment. The Counselor ... chemical dependency. PVBH has an excellent reputation as an innovative hospital with caring ...

Quality Engineer

Nogales, AZ · On-site

$64K - $83K/yr

The Quality Engineer is responsible for risk assessment of activities stated within the Quality ... Engineering Degree in Mechanical/Industrial/Chemical Engineer or equivalent experience. • ...

Quality Engineer

Nogales, AZ

$64K - $83K/yr

The Quality Engineer is responsible for risk assessment of activities stated within the Quality ... Engineering Degree in Mechanical/Industrial/Chemical Engineer or equivalent experience. • ...

... database chemical lists. (Safety Data Sheets). * Assists in the execution of enforcement of ... Performs on-scene assessments, gathers statements, photographs, and evidence, and ensures accurate ...

EH&S Engineer 2

Phoenix, AZ · On-site

$72K - $95K/yr

... chemical/toxic/pyrophoric gases, and SIMOPs (simultaneous operations). Conduct daily walkthroughs and JHA/JSA risk assessments; support after-hours/holiday critical tasks on site or remotely as ...

Conduct hazard assessments, PSM audits, and risk assessments to identify safety and integrity ... Bachelor's degree in environmental engineering, Chemical Engineering, or related discipline. * 5 ...

Perform systems assessments, develop and implement improvement roadmap via capital and expense ... Work to integrate reliability focus and risk analysis into Systems Engineering job scope, which ...

... quality risk evaluations and assessments by conducting extensive research and data collection on chemical, physical, and biological hazards and exposures, indoor air quality issues, and other ...

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Chemical Risk Assessment information

What is chemical risk assessment?

Chemical risk assessment is the process of evaluating the potential adverse health and environmental effects caused by exposure to chemicals. This involves identifying hazards, assessing how and where people or the environment may be exposed, determining the level of risk, and recommending ways to manage or mitigate those risks. Chemical risk assessment is crucial in regulatory decision-making, workplace safety, and environmental protection. Professionals in this field use scientific data, exposure models, and toxicological information to inform policy and safeguard public health.

What are some typical challenges faced by professionals in Chemical Risk Assessment roles, and how can they be addressed?

Professionals in Chemical Risk Assessment often encounter challenges such as interpreting complex toxicological data, keeping up with evolving regulatory requirements, and effectively communicating risks to both technical and non-technical stakeholders. Addressing these challenges involves continuous learning, close collaboration with regulatory experts and scientists, and developing strong communication skills to present findings clearly. Working in multidisciplinary teams also helps ensure that assessments are comprehensive and aligned with organizational and legal standards.

What are the key skills and qualifications needed to thrive as a Chemical Risk Assessor, and why are they important?

To thrive as a Chemical Risk Assessor, you need a solid background in chemistry, toxicology, and environmental science, typically supported by a relevant degree. Familiarity with risk assessment models, regulatory databases, and statistical analysis software such as EPA’s EPI Suite or OECD tools is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital for interpreting data and conveying complex findings to stakeholders. These skills are crucial to ensure the accurate evaluation of chemical hazards and compliance with safety regulations, ultimately protecting public health and the environment.

What is the difference between Chemical Risk Assessment vs Chemical Safety Specialist?

AspectChemical Risk AssessmentChemical Safety Specialist
Primary FocusEvaluating chemical hazards and risks to health and environmentImplementing safety protocols and ensuring compliance in chemical handling
Required CredentialsDegree in chemistry, toxicology, or related field; risk assessment certificationsSimilar credentials; safety certifications like OSHA or HAZWOPER
Work EnvironmentLaboratories, risk assessment teams, regulatory agenciesIndustrial sites, manufacturing plants, safety departments
Industry UsageRegulatory compliance, environmental agencies, consultingIndustrial companies, chemical plants, safety consulting

While both roles involve chemical safety, Chemical Risk Assessment focuses on analyzing hazards and determining risks, whereas Chemical Safety Specialist emphasizes implementing safety measures and ensuring compliance in workplaces.

What are popular job titles related to Chemical Risk Assessment jobs in Arizona? For Chemical Risk Assessment jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Chemical Risk Assessment jobs in Arizona look for? The top searched job categories for Chemical Risk Assessment jobs in Arizona are:
Infographic showing various Chemical Risk Assessment job openings in Arizona as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Staff Quality Engineer - Product Development, Tempe, AZ - (IK)

Staff Quality Engineer - Product Development, Tempe, AZ - (IK)

Central Business Solutions

Tempe, AZ • On-site

$110K - $115K/yr

Full-time

Posted 2 days ago


Job description

Job Responsibilities:
  • Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance) and chemical and pharmaceutical operations (e.g., drug product manufacturing, analytical testing, process development and quality assurance)
  • Ability to create, support, review, and investigate analytical test methods used to support pharmaceutical combination devices.
  • The ability to create, support, review chemistry, manufacturing, and controls device submissions
  • Participates as team leader or as an active member of the team to meet company objectives and ensure department responsibilities are completed
  • Leads development of risk assessments and test method activities (e.g., development and validation for physical and analytical test methods)
  • Leads component qualifications, design validation, design verification, drug stability and process validation
  • Leads product investigations
  • Ability to make and present risked based decisions
  • Assess product changes against product design
  • Supports translation of design inputs into manufacturing control plans
  • Develop and implement procedures to comply with corporate and industry standards.
  • Coordinates and/or directs all aspects of product development activity related to a product line
  • Leads development of risk assessments and test methods
  • Quality engineering representation on Product Development and Design Review teams
  • Prepare and present project updates and technical discussions
  • Participate in project planning, budgeting, scheduling, and tracking
  • Support internal and external supplier audits
  • Provide support to the regulatory department in writing technical submissions
  • Complies with company procedures and policies, government regulations
  • Actively participates in training and providing input to training of employees on division procedures and policies
  • Ability to travel for business, project, and issues approximately up to 25% of time.
  • Other duties and projects, as assigned

Required Education and Experience:
  • BS in Engineering, Biological Science, or a related engineering field (Masters or Ph.D preferred). Fields of study include Chemical Engineering, Bioengineering, Pharmacy, or Biochemistry
  • Minimum of eight years of experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry
  • Extensive proven understanding of design controls in development stage
  • Pharmaceutical or combination product experience

Required Qualifications:
  • Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)
  • Ability to lead creation of risk management files
  • Ability to develop solutions with business impact
  • Advanced statistical and risk assessment techniques
  • Working knowledge of test method (development and validation), equipment qualifications, process and design validation, risk assessment techniques, and component qualification methodologies
  • Ability to make and present risk-based decisions
  • Strong interpersonal skills
  • Ability to analyze and optimize manufacturing and quality systems
  • Product, design & prototyping
  • Ability to create and provide training
  • Problem solving ability
  • Ability to create, review and coordinate test protocols and reports
  • Ability to generate engineering proposals
  • Oral and written presentation skills
  • Ability to lead cross functional teams
  • Understanding of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 210/211/820 , ICH Guidelines

Skills and Certifications
Drug Device delivery combination products
Compensation
Base Salary - USD $110,000 to $115,000
Full-time
Benefits - Full
Relocation Assistance Available - Possible for ideal candidate
Candidate Details
8+ to 10 years experience
Seniority Level - Mid-Senior
Minimum Education - Bachelor's Degree
Willingness to Travel - Occasionally
Ideal Candidate
8+ years experience in New Product Development of combination devices