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Chemical Risk Assessment Jobs in California (NOW HIRING)

Danos, LLC

Shelf - Operator Senior

Santa Barbara, CA

Chemical treating and handling * Facilitate maintenance operations by applying/removing isolations as required. * Operation under PTW system, Toolbox Talk and Risk Assessments. * Advise maintenance ...

Hologic Inc.

Quality Engineer 3

San Diego, CA · On-site

$76K - $98K/yr

Perform risk assessments for process-related nonconformances, planned deviations, change controls ... What We Expect * Bachelor's degree in Science, Chemical Engineering, Biology, Chemistry ...

jobr.pro

Director, Pharmaceutical Development

Brisbane, CA · On-site

$218 - $260/hr

Conduct systematic risk assessments to identify Critical Material Attributes (CMAs) and Critical ... Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, Chemistry, or a closely ...

MiniMed

EHS Program Manager

Northridge, CA · On-site

$89K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead risk assessments, Job Hazard Analyses (JHAs), ergonomic evaluations, and safety reviews for ... Hazard Communication and Chemical Safety * Contractor Safety Program * Lead environmental ...

MiniMed

EHS Program Manager

Los Angeles, CA · On-site

$89K - $121K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead risk assessments, Job Hazard Analyses (JHAs), ergonomic evaluations, and safety reviews for ... Hazard Communication and Chemical Safety * Contractor Safety Program * Lead environmental ...

Archer

Safety Engineer

San Jose, CA

$104K - $135K/yr

What you'll do * Conduct risk assessments and safety analyses (e.g., FMEA, HAZOP, FTA) on ... including chemical handling and hazardous materials * Certification as a Certified Safety ...

Mizkan

Environmental, Health & Safety Technician

Rancho Cucamonga, CA · On-site

$70K - $74K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Risk Assessment Training and be able to complete Risk Assessments as needed when new equipment is ... Annually participates in a chemical inventory activity. • Participates in all plant audits. • ...

Artiva Biotherapeutics, Inc.

Senior Manager, MSAT

San Diego, CA · On-site

$150K - $165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Writes Master Batch Records, SOPs, deviation reports and technical risk assessment with a strong ... Bachelor's, Master's or PhD degree in biotechnology, chemical engineering or related disciplines.

Artiva Biotherapeutics

Senior Manager, MSAT

San Diego, CA · On-site

$165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Writes Master Batch Records, SOPs, deviation reports and technical risk assessment with a strong ... Bachelor's, Master's or PhD degree in biotechnology, chemical engineering or related disciplines.

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Showing results 41-60

All JobsChemical Risk Assessment JobsChemical Risk Assessment Jobs in California

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 California?

For Chemical Risk Assessment jobs in California, the most frequently searched job titles are:

What job categories do people searching Chemical Risk Assessment jobs in California look for?

The top searched job categories for Chemical Risk Assessment jobs in California are:

What cities in California are hiring for Chemical Risk Assessment jobs?

Cities in California with the most Chemical Risk Assessment job openings:

Chemical Risk Assessment jobs near you
Infographic showing various Chemical Risk Assessment job openings in California as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, 2% Temporary, and 2% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution.

Director, Pharmaceutical Development

Nurix

Brisbane, CA • On-site

Full-time

Re-posted 6 days ago

Job description

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Position:
Nurix Therapeutics, Inc. is seeking a highly experienced Director of Pharmaceutical Development. The role leads small molecule drug product development focused on oral and topical dosage forms. Responsibilities span QbD-based formulation and process development from early phase through commercial launch. The position requires strong cross-functional collaboration and hands-on CDMO management.
Responsibilities:
Formulation & Process Development
  • Lead QbD-based formulation and process development for small molecule drug programs with a focus on oral and topical dosage forms across all development phases.
  • Apply expertise in BCS Class II/IV compound development and enabling formulation technologies, including amorphous solid dispersions (spray-dried dispersions, hot-melt extrusion), lipid-based drug delivery systems (SMEDDS, SEDDS, lipid suspensions), and nano-formulations to address solubility and bioavailability challenges.
  • Define and document the Quality Target Product Profile (QTPP) and identify Critical Quality Attributes (CQAs) to guide formulation strategy.
  • Conduct systematic risk assessments to identify Critical Material Attributes (CMAs) and Critical Process Parameters (CPPs) using FMEA and other risk assessment tools.
  • Develop and optimize manufacturing processes appropriate to the dosage form, ensuring scalability and process robustness.

Scale-Up & Technology Transfer
  • Lead manufacturing scale-up activities from laboratory to pilot and commercial scale, ensuring robust and reproducible processes.
  • Troubleshoot manufacturing deviations, out-of-specification results, and process failures; drive root cause analysis and implement corrective actions.

Late-Stage Development & Regulatory
  • Drive late-stage development activities (Phase 2b through commercial launch) including clinical supply manufacturing, process performance qualification (PPQ), and continued process verification (CPV).
  • Author and review CMC sections of regulatory submissions including INDs, NDAs, and MAAs.
  • Ensure all development activities comply with current GMP regulations and internal quality standards.

CDMO Management & Cross-Functional Leadership
  • Manage external CDMO partnerships, including vendor qualification, technical oversight, and performance governance to ensure project timelines, quality standards, and budget commitments are met.
  • Serve as the primary technical point of contact between pharmaceutical development and cross-functional teams including Analytical Development, Clinical Operations, Regulatory Affairs, Quality, Supply Chain, and Commercial.
  • Provide scientific leadership and mentorship to junior scientists, associates, and project team members.

Requirements
  • Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, Chemistry, or a closely related discipline strongly preferred with 12 years of industry experience.
  • 12+ years of progressive pharmaceutical development experience in an industry setting (biotechnology, pharmaceutical, or CDMO).
  • Deep expertise in small molecule drug product development with a focus on oral and topical dosage forms, especially enabled formulation development (e.g., amorphous solid dispersions, lipid-based systems, nano-formulations).
  • Comprehensive hands-on experience with QbD methodologies: QTPP definition, CQA identification, CMA/CPP risk assessment, DoE, design space development, and control strategy establishment.
  • Significant late-stage development experience (Phase 2b/3 and NDA/MAA submission) is required.
  • Proven track record of authoring and/or reviewing CMC regulatory submissions (INDs, NDAs, CTDs) and successfully responding to agency queries.
  • Direct CDMO management experience, including technical oversight, project governance, and relationship management.
  • Knowledge of lifecycle management, post-approval changes, and SUPAC guidance.
  • For the Director level: demonstrated people management experience leading a team of scientists/managers, department-level strategic planning, and budget/resource ownership across multiple concurrent programs.
  • Primarily office and laboratory environment; occasional GMP manufacturing facility access required.
  • Approximately 25% travel required, including domestic and international trips to CDMO sites, clinical manufacturing sites, regulatory agency meetings, and scientific conferences.
  • Must be able to gown for cleanroom/GMP environments

Core Competencies
  • Scientific Leadership - Recognized internal and external thought leader in pharmaceutical development; drives scientific innovation and excellence.
  • Strategic Thinking - Ability to anticipate technical and regulatory risks and develop proactive mitigation strategies that protect project timelines.
  • Cross-Functional Collaboration - Demonstrated ability to build strong working relationships and influence without authority across diverse internal and external stakeholders.
  • Project Management - Experienced in managing multiple complex projects simultaneously in a fast-paced, deadline-driven environment.
  • Communication - Exceptional written and verbal communication skills; able to present complex scientific data clearly to both technical and non-technical audiences, including senior leadership and regulatory agencies.
  • People Development - Commitment to mentoring and developing scientific talent within the organization.

Salary Range: $218,000 - 260,000
Location: This position is on site in the Brisbane, CA office.
Fit with Nurix Culture and Values:
  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view

Apply