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Chemical Risk Assessment Jobs in Missouri (NOW HIRING)

Conduct inspections, audits, observations, and hazard and risk assessments; maintain practical controls for JSAs/JHAs, LOTO, machine guarding, PPE, chemical safety, ergonomics, and corrective-action ...

Quality Engineer II

Hannibal, MO · On-site

$68K - $87K/yr

Assess risk and make decisions related to food safety and quality for ingredients and finished ... Bachelor's Degree in Food Science, Chemical Engineering, or other related fields with at least 3 ...

Reliability Engineer

Carthage, MO · On-site

$70 - $90/hr

... • Risk Assessment: Assesses potential risks associated with equipment failures and develop ... What you need to succeed:** • Bachelor's degree in mechanical, electrical, chemical engineering ...

Reliability Engineer

Carthage, MO · On-site

$87K - $109K/yr

Risk Assessment: Assesses potential risks associated with equipment failures and develop strategies ... Bachelor's degree in mechanical, electrical, chemical engineering or related field. Master's degree ...

EHS Coordinator

Springfield, MO · On-site

$60 - $80/hr

... chemical inventory * Support waste management processes, including proper handling and storage of ... and risk assessments * Participate in 5S and continuous improvement events from a safety ...

Showing results 21-40

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 Missouri?

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

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

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

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

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

Infographic showing various Chemical Risk Assessment job openings in Missouri as of June 2026, with employment types broken down into 76% Full Time, 11% Temporary, and 13% Contract. Highlights an 89% In-person, and 11% Remote job distribution.

Supervisor, Manufacturing Sciences & Technology

Catalent Pharma Solutions

Kansas City, MO • On-site

$59K - $80K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

62nd of 86 rated pharmaceutical


Job description

Supervisor, Manufacturing Sciences & Technology

Position Summary

  • 100% based on-site in Kansas City

  • Work Schedule: M-F during regular business hours

Catalent's Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions-from science and engineering to operations and logistics.

The Kansas City Clinical Development & Supply Floor Manufacturing Sciences and Technology Supervisor will develop and lead a group, including the transfer between external clients and Manufacturing. The supervisor is responsible for leading the team of strong engineers, scientists, or qualified person to be technology transfer process owner to deliver excellent services to internal and external customers.

The Role

  • Strategic client facing leader of the MS&T team on the behalf of the organization.

  • Works cross functionally with project managers, manufacturing, label design and control, quality assurance, quality control, supply chain, and facilities departments to effectively transfer and maintain processes in the facility.

  • Participates and leads commercial manufacturing transition and support for process development.

  • Enhance productivity by exploring, analyzing, facilitating, and leveraging efficiency initiatives for packaging processes through The Catalent Way.

  • Ensure that changes to existing processes or the introduction of new processes are carried out and documented according to approved change control procedures and in compliance with cGMP requirements.

  • Bridge the focus areas of Project Management, Operations, Quality, EHS, Supply Chain and Engineering to create common understanding and objectives and ensure robust products and flawless packaging.

  • Leads the compilation of process data, including communicating project status, and delivering internal and client presentations.

  • Collects and trend process data for external (Clients) and internal review to ensure process consistency.

  • Provides business case for process improvement projects.

  • Other duties assigned

The Candidate

  • Bachelor's degree in Biotechnology, Chemical or Pharmaceutical Engineering, or related field, OR a HS Diploma/GED and 4+ years of relevant experience required.

  • Experience with Upstream and Downstream processes of cGMP clinical packaging.

  • Project management experience/skills required including method transfers, and risk assessment.

  • Knowledge of regulatory, validation and documentation requirements for product development, commercial production, and site transfers.

  • Experience in investigating and closing out deviations, OOS, CAPAs, and change controls.

  • Experience working on late phase and commercial programs is a plus.

  • Knowledge of thermoforming/cold-forming equipment is required.

  • A good working knowledge of Microsoft Office (Word, PowerPoint, Excel and Visio) and TOPS Pro (Total Optimization Packaging System) or similar software program

  • Ability to learn and use software packages (e.g. TrackWise, ComplianceWire).

  • Demonstrated strong working knowledge of Tech Transfer (Internal and External).

  • Understanding and application of Risk Assessment tools (Hazard Analysis, FMEA, etc.).

Why you should join Catalent

  • Career growthwith a clear path and regular performance reviews

  • Day-one benefits:medical, dental, vision

  • 401(k) match, tuition reimbursement, and wellness perks

  • Paid time off:152 hours + 8 holidays

  • Inclusive culturewith Employee Resource Groups and community initiatives

  • Discountsfrom 900+ merchants via Perkspot

  • A mission-driven workplacewhere your work helps save lives

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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