ZipRecruiter

Log In

1

Chemical Risk Assessment Jobs in Baltimore, MD (NOW HIRING)

Salas O'Brien

Federal Process Engineer

Baltimore, MD · On-site

Evaluate production, manufacturing, utility, chemical, and industrial processes to improve safety ... Experience performing process safety analyses and risk assessments. * Proficiency with Microsoft ...

next page

Showing results 1-20

All JobsChemical Risk Assessment JobsChemical Risk Assessment Jobs in Baltimore, MD

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 Baltimore, MD?

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

What job categories do people searching Chemical Risk Assessment jobs in Baltimore, MD look for?

The top searched job categories for Chemical Risk Assessment jobs in Baltimore, MD are:

Chemical Risk Assessment jobs near you

Technical Product / Tech Transfer Lead

Workforce Genetics

Baltimore, MD

Contractor

Re-posted 18 days ago

Job description

TECHNICAL PRODUCT/TECH TRANSFER LEAD (6mo. Contract-to-Hire)


Department: MS&T

Location: Baltimore, MD


Company

Join a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art sterile manufacturing footprint in Baltimore. This organization is a strategic partner to leading pharmaceutical and biotech companies, specializing in the end-to-end development and commercialization of complex injectable products. With a reputation for scientific excellence and a commitment to Quality by Design, they offer a dynamic, client-facing environment where technical experts lead the transition of life-saving therapies from the lab to commercial scale.


Job Summary

The role is responsible for providing technical leadership across process development, technology transfer, and manufacturing support within the Manufacturing Sciences & Technology (MS&T) organization. This role serves as the primary technical subject matter expert (SME) for client products and processes, overseeing development, scale-up, process validation, transfer to manufacturing, and lifecycle management.


The position combines scientific expertise with client-facing involvement, ensuring robust process design, successful commercialization, and continuous improvement of pharmaceutical products. The role also acts as the primary point of contact for technical matters with clients and internal personnel.


Key Responsibilities:

Technical Leadership & Process Development

  • Lead process development activities including formulation, process optimization, scale-up, technology transfer, and troubleshooting.
  • Design and oversee studies to evaluate process robustness and establish validation strategies.
  • Serve as SME for manufacturing processes, equipment, and product lifecycle management.
  • Analyze process data to identify critical process parameters (CPPs) and ensure consistent product performance.
  • Apply Quality by Design (QbD), risk assessment, and statistical tools to support process characterization.


Technology Transfer & Commercial Support

  • Lead and coordinate technology transfer from development to commercial manufacturing.
  • Provide ongoing technical support for commercial operations including deviations, investigations, and continuous process verification.
  • Own technical documentation, including protocols, reports, risk assessments, and SOPs.


Client & Stakeholder Engagement

  • Act as the primary technical point of contact (PoC) for client programs and internal stakeholders.
  • Lead technical discussions with clients, providing strategic guidance and resolving complex problems.
  • Collaborate cross-functionally with manufacturing, QA, QC, and engineering, validation, and project management teams.


Continuous Improvement & Operations

  • Drive process improvements, troubleshooting, and root cause investigations.
  • Lead lifecycle management activities, including process monitoring and optimization.
  • Support media fill programs, validation strategies, and regulatory submissions as needed
  • Maintain and improve laboratory and manufacturing capabilities, including equipment oversight.


Leadership & Project Management

  • Manage multiple cross-functional projects and ensure timely delivery of milestones.
  • Provide technical guidance and mentorship to junior staff.
  • Influence stakeholders and drive alignment across teams and organizations.
  • Foster a culture of collaboration, innovation, and accountability. [Technical...den


Eduction & Experience

  • Bachelor’s degree with 8+ years, Master’s degree with 5–7 years, or PhD with ~5 years of relevant experience.
  • Degree in Chemical Engineering, Pharmaceutical Sciences, or related field.
  • Experience in process development, tech transfer, and commercial manufacturing support.


Required Skills & Competencies

  • Strong expertise in pharmaceutical process development, formulation, and manufacturing technologies
  • Knowledge of sterile processing, lyophilization, and analytical characterization techniques.
  • Experience with QbD, Risk Assessment tools, and statistical analysis methods.
  • Strong understanding of cGMP, regulatory requirements, and validation principles.
  • Excellent leadership, communication, and stakeholder management skills.
  • Ability to manage complex projects in a fast-paced environment.


Physical & Work Environment

  • Office, laboratory, and manufacturing environment with cross-functional interaction.
  • Ability to analyze data, communicate technical information, and manage multiple priorities.
  • Occasional travel may be required (Rare).