What Jobs are available for Safety Standards in Las Vegas?

Our client is seeking an experienced Industrial Hygiene and Safety Manager to oversee operations in **Las Vegas, Nevada, US**. This critical role is responsible for developing, implementing, and managing comprehensive safety programs to ensure a safe and healthy work environment for all employees. You will conduct risk assessments, identify potential hazards, and develop and enforce safety policies and procedures in compliance with all relevant local, state, and federal regulations. Key responsibilities include overseeing all aspects of occupational health and safety, conducting regular safety inspections and audits, and investigating incidents and near misses to determine root causes and implement corrective actions. The ideal candidate will possess a Bachelor's degree in Occupational Health and Safety, Environmental Science, or a related field, along with relevant professional certifications such as CIH or CSP. A minimum of 5-7 years of experience in industrial hygiene and safety management is required, preferably within a manufacturing or hospitality environment. Strong knowledge of OSHA regulations, hazard communication, lockout/tagout procedures, confined space entry, and emergency response planning is essential. You will be responsible for training employees on safety procedures, promoting a strong safety culture, and managing the company's safety management system. Excellent communication, leadership, and problem-solving skills are crucial for success in this position. The ability to effectively collaborate with employees at all levels of the organization and drive continuous improvement in safety performance is paramount. Join our client and play a vital role in maintaining a safe and compliant workplace in the vibrant city of Las Vegas.

Our client is looking for a highly experienced and dedicated Senior Industrial Hygienist to lead safety initiatives within their extensive facilities. This hybrid role offers a unique opportunity to blend hands-on site assessments with strategic planning and policy development. You will be responsible for identifying, evaluating, and controlling workplace hazards to ensure a safe and healthy environment for all employees. This position requires a proactive approach to risk management, a thorough understanding of regulatory compliance, and exceptional leadership skills. You will play a critical role in fostering a robust safety culture and minimizing occupational health risks.

Responsibilities:

• Conduct comprehensive industrial hygiene surveys, risk assessments, and exposure monitoring for chemical, physical, and biological agents.
• Develop and implement effective control strategies, including engineering controls, administrative controls, and personal protective equipment (PPE) programs.
• Investigate incidents, near misses, and employee complaints related to workplace hazards, recommending corrective actions.
• Ensure compliance with all relevant local, state, and federal health and safety regulations (e.g., OSHA, EPA).
• Develop, review, and update safety policies, procedures, and training materials.
• Provide expert consultation and technical support to management, employees, and safety committees.
• Manage and maintain industrial hygiene databases, records, and monitoring equipment.
• Lead and mentor junior industrial hygienist and safety personnel.
• Collaborate with environmental, health, and safety (EHS) teams to integrate industrial hygiene principles into broader EHS programs.
• Stay current with industry best practices, emerging hazards, and regulatory changes.

Qualifications:

• Master's degree in Industrial Hygiene, Environmental Health, or a closely related field.
• Certified Industrial Hygienist (CIH) designation required.
• Minimum of 8 years of progressive experience in industrial hygiene and occupational safety, preferably in large-scale manufacturing or complex facility environments.
• Extensive knowledge of industrial hygiene principles, exposure assessment methodologies, and control technologies.
• Proven experience with regulatory compliance (OSHA, EPA, etc.).
• Strong analytical, problem-solving, and decision-making skills.
• Excellent written and verbal communication skills, with the ability to effectively train and influence stakeholders at all levels.
• Demonstrated leadership and project management abilities.
• Proficiency in data analysis and reporting software.
• Ability to travel to various sites as needed, balancing remote work with on-site responsibilities.

This pivotal role, located in Las Vegas, Nevada, US , demands a blend of on-site presence and strategic remote oversight, making it a true hybrid opportunity.

**Job Description**
Mission Support and Test Services, LLC (MSTS) manages and operates the Nevada National Security Site (NNSS) for the U.S. National Nuclear Security Administration (NNSA). Our MISSION is to help ensure the security of the United States and its allies by providing high-hazard experimentation and incident response capabilities through operations, engineering, education, field, and integration services and by acting as environmental stewards to the Site's Cold War legacy. Our VISION is to be the user site of choice for large-scale, high-hazard, national security experimentation, with premier facilities and capabilities below ground, on the ground, and in the air. (See NNSS.gov for our unique capabilities.) Our 2,750+ professional, craft, and support employees are called upon to innovate, collaborate, and deliver on some of the more difficult nuclear security challenges facing the world today.
+ MSTS offers our full-time employees highly competitive salaries and benefits packages including medical, dental, and vision; both a pension and a 401k; paid time off and 96 hours of paid holidays; relocation (if located more than 75 miles from work location); tuition assistance and reimbursement; and more.
+ MSTS is a limited liability company consisting of Honeywell International Inc. (Honeywell), Jacobs Engineering Group Inc. (Jacobs), and HII Nuclear Inc.
**Responsiblities**
The Materials Testing Lab located at the Nevada National Security Site has an opening for an experienced Quality Control Inspector to support ongoing projects.
**Key Responsibilities**
+ Perform independent quality control inspections and verifications, of items, systems, components, or products that are fabricated or installed by other workers for new or existing facilities and infrastructures.
+ Exhibit a high degree of technical knowledge and skills to execute applicable national consensus codes and standards in order to inspect, examine, or test items or products to ensure they meet design requirement.
+ Maintain qualification and or certification to perform Quality Control inspection activities based on education, training, experience in one or more of the inspection disciplines (e.g. welding, nondestructive examination/testing, boilers and pressure systems, geometric dimensioning and tolerancing, materials testing and verification, Concrete, soils, anchoring, etc.).
+ Make autonomous judgment during inspections activities to determine whether items, systems, components, or products are acceptable for use, or not, based on design requirements.
+ Generate nonconformance reports that document the objective evidence where items or products do not meet design requirements.
+ Authority to identify nonconforming conditions or defects and prevent items or products from being released for use until nonconforming conditions are resolved.
+ Interface with internal line personnel (engineering, construction, facility, project, operations, work control, procurement, maintenance, quality assurance, etc.), and external MSTS customers to analyze and correct the production problems.
+ Document the results of inspections or tests in accordance with national consensus standards and codes, procedures, engineering requirements, and/or industry practices as defined in written procedures.
+ Perform other duties as needed, assigned by management.
**Qualifications**
+ Bachelor's degree related field, or equivalent training and experience, and at least 2 years' relevant experience.
+ Must show knowledge, skill, and ability in the field of quality control inspection discipline by passing an oral and written examination, as well as demonstration of proficiency.
+ Must have commensurate experience in interpreting national consensus codes and standards, in the applicable field of inspection (welding, pressure safety, materials testing, geometric dimensioning and tolerancing, etc.) and preparing inspection plans, tests, check lists, establishing inspection set ups and techniques, and determining equipment to use; supervision or surveillance over inspections and tests; providing technical supervision and certifying lower-level personnel; and evaluating the validity and acceptability of inspection and test results.
+ Must possess knowledge of industry and quality program accepted calibration methods, procedures, documentation, and maintenance of instrument standards used for inspection activities. Close attention to detail, and high degree of accuracy is required in inspecting and testing items, systems, structures, components, and products to exact specifications and maintaining a safe work environment.
+ Must possess excellent oral/written communication skills.
+ Must be able to record data accurately, understand technical journals, manuals, regulations, and procedures, and handle questions.
+ Must be able to work independently, make decisions, and prioritize. Must possess good problem-solving skills, integrity, and ability to apply knowledge and experience to determine best course of action.
+ Must possess excellent interpersonal skills to communicate with customers, coworkers, management, and other personnel at all levels in a professional and efficient manner.
+ Computer skills including word processing and spreadsheet software desirable
+ The primary work location will be at the Nevada National Security Site (located approximately 65 miles northwest of Las Vegas, NV.)
+ The work schedule is Monday - Thursday (4/10s), (subject to change).
+ Pre-placement physical examination, which includes a drug screen, is required. MSTS maintains a substance abuse policy that includes random drug testing.
+ Must possess a valid driver's license.
MSTS is required by DOE directive to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants offered employment with MSTS are also subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause a clearance to be denied or terminated by DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment. In addition, Applicants for employment must be able to obtain and maintain a DOE Q-level security clearance, which requires U.S. citizenship, at least 18 years of age. Reference DOE Order 472.2 ( , "Personnel Security". If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted.
**Department of Energy Q Clearance** (position will be cleared to this level). Reviews and tests for the absence of any illegal drug as defined in 10 CFR Part 707.4 ( , "Workplace Substance Abuse Programs at DOE Sites," will be conducted. Applicant selected will be subject to a Federal background investigation, required to participate in subsequent reinvestigations, and must meet the eligibility requirements for access to classified matter. Successful completion of a counterintelligence evaluation, which may include a counterintelligence-scope polygraph examination, may also be required. Reference 10 CFR Part 709 ( , "Counterintelligence Evaluation Program."
MSTS is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, veteran status or other characteristics protected by law. MSTS is a background screening, drug-free workplace.
Annual salary range for this position is: $79,206.40 - $118,809.60.
Starting salary is determined based on the position market value, the individual candidate education and experience and internal equity.

Our client is seeking a highly experienced and detail-oriented Senior Quality Control Manager to lead their quality assurance efforts. This hybrid role, based in Las Vegas, Nevada , offers a balance of in-office responsibilities and remote work flexibility. You will be responsible for developing, implementing, and maintaining comprehensive quality control systems and procedures across all manufacturing processes. This includes establishing quality standards, conducting regular inspections and audits, and analyzing production data to identify and resolve defects. Your role will involve leading a team of quality control technicians, providing training, and ensuring adherence to regulatory requirements and company policies. The ideal candidate will have a strong understanding of statistical process control (SPC), root cause analysis, and quality management methodologies (e.g., Six Sigma, ISO 9001). Excellent analytical, problem-solving, and leadership skills are essential. You will work collaboratively with production, engineering, and supply chain teams to foster a culture of quality throughout the organization. This position requires meticulous attention to detail, strong organizational abilities, and the capacity to manage multiple priorities effectively. Your insights will be crucial in driving continuous improvement initiatives and ensuring that all products meet the highest standards of quality and customer satisfaction. We are looking for a proactive and results-driven individual who can significantly contribute to maintaining and enhancing our client's reputation for excellence. This is a key leadership position with the opportunity to make a substantial impact on product integrity and customer trust.

Job Description

Job Description

JOB SUMMARY

The Chemist II, under minimal supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Has demonstrated competence in conducting all types of physical and chemical analyses (including complex analyses) using all equipment. Detects, conducts, and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. Participates in troubleshooting analyses and instrumentation. Trains less senior staff.

All incumbents are responsible for following applicable Division & Company policies and procedures.

KEY ACCOUNTABILITIES

Analysis & Testing

• Conducts laboratory analyses according to approved test methods: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.
• Uses laboratory software for analyses
• Reviews and approves laboratory test data and documentation for completeness and compliance
• Is alert to and detects abnormalities during performances of tests and reviews. Elevates abnormalities to Supervisor
• Performs lab methods transfer and participate in method validation/verification studies

Lab Equipment

• Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping
• Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals
• Troubleshoots instrument/chromatography problems and identifies improvements/CAPAs

Investigations

• Detects, conducts and reports on OOS/OOT/NOE and other investigations
• Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action
• Writes, edits and reviews SOPs and laboratory investigations

Training

• Maintains assigned training records current and in-compliance
• Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures

Compliance

• Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting
• Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs
• Follows internal processes related to controlled substances

Safety

• Follows EH&S procedures to ensure a safe work environment
• Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS

QUALIFICATIONS

Education & Experience

• Bachelor of Science Degree in chemistry, chemical engineering or related field with 4+ years’ relevant analytical laboratory experience OR
• Master’s Degree in above disciplines with 2+ years’ relevant analytical lab experience

Knowledge

• Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports
• Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.
• Thorough knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS
• Has demonstrated competence in conducting chemical analyses
• Strong knowledge of wet chemistry techniques
• Competency in Microsoft Office Suite

Skills & Abilities

• Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information, reporting to management
• Ability to display and analyze data in a logical manner
• Ability to critically review, analyze data, interpret information, and draw conclusions from relevant or missing information
• Ability to display and analyze data in a logical manner
• Strong verbal and written communication skills as well as good computer skills
• Strong attention to details and accurate record keeping
• Establish and maintain cooperative working relationships with others
• Solid organizational skills
• Ability to coach less senior staff and develop laboratory skills and ability
• Ability to take initiative, set priorities and follow through on assignments

Our client, a prominent manufacturer of specialized components, is seeking a detail-oriented Senior Quality Control Inspector for their facility in Las Vegas, Nevada, US . This role is crucial in upholding the exceptional quality standards of the company's products. You will be responsible for performing rigorous inspections and tests on raw materials, in-process components, and finished goods to ensure they meet precise specifications and industry regulations. The ideal candidate will possess a strong understanding of quality control methodologies, measurement tools, and relevant industry standards. You will identify, document, and report non-conformities, working closely with production and engineering teams to implement corrective actions. This position requires meticulous attention to detail, excellent analytical skills, and the ability to interpret technical drawings and specifications. You will play a vital part in maintaining product integrity and driving continuous improvement in manufacturing processes.

Key responsibilities include:

• Conducting comprehensive inspections and tests on incoming raw materials, in-process work, and finished products using various measurement instruments and testing equipment.
• Interpreting technical drawings, blueprints, and specifications to verify product conformity.
• Identifying, documenting, and segregating non-conforming materials or products.
• Performing root cause analysis for quality defects and collaborating with production and engineering to implement corrective and preventive actions.
• Maintaining accurate inspection records, test results, and quality documentation.
• Participating in internal quality audits and supporting external audit preparations.
• Calibrating and maintaining inspection and testing equipment.
• Ensuring adherence to quality control procedures, safety regulations, and industry standards.
• Providing feedback to production and engineering teams on quality issues and improvement opportunities.
• Mentoring and guiding junior quality inspectors as needed.

Qualifications:

• High School Diploma or equivalent; Associate's degree or relevant technical certification preferred.
• Minimum of 5 years of experience in quality control inspection within a manufacturing environment.
• Proficiency in using various precision measurement tools (e.g., calipers, micrometers, CMM).
• Ability to read and interpret complex technical drawings, GD&T, and specifications.
• Strong understanding of quality management systems (e.g., ISO 9001).
• Excellent analytical and problem-solving skills.
• Meticulous attention to detail and accuracy.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team in a production environment.
• Knowledge of statistical process control (SPC) is a plus.

This role is essential for ensuring the reliability and performance of manufactured goods, contributing directly to the company's reputation for quality.

Our client is seeking an experienced Lead Pharmaceutical Quality Control Scientist to oversee and execute critical quality control activities within their state-of-the-art facility in Las Vegas, Nevada, US . This pivotal role demands a deep understanding of pharmaceutical regulations, analytical chemistry, and quality management systems to ensure the safety, efficacy, and purity of our products. You will lead a team of scientists, set standards, and drive the continuous improvement of our quality control processes.

Responsibilities:

• Lead and manage the daily operations of the Quality Control laboratory, including personnel management, workflow optimization, and resource allocation.
• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, ICP-MS, and Karl Fischer titration.
• Ensure all testing is performed in compliance with cGMP, FDA regulations, ICH guidelines, and other relevant regulatory requirements.
• Review and approve analytical test data, reports, and specifications, ensuring accuracy and completeness.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to support product development, process validation, and lifecycle management.
• Manage the qualification and calibration of laboratory equipment and instrumentation.
• Train and mentor QC analysts, fostering a culture of scientific rigor and compliance.
• Contribute to the development and maintenance of the Quality Management System (QMS).
• Participate in internal and external audits as a subject matter expert.
• Stay current with scientific advancements and regulatory changes impacting pharmaceutical quality control.

Qualifications:

• Master's or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a closely related scientific discipline.
• A minimum of 8 years of progressive experience in pharmaceutical quality control or analytical development.
• Demonstrated experience in leading and managing a team of scientists in a QC laboratory setting.
• Expertise in a wide range of analytical techniques relevant to pharmaceutical product testing, with a strong emphasis on chromatographic methods (HPLC, GC).
• Thorough understanding of cGMP, FDA 21 CFR Part 210/211, ICH guidelines (Q2, Q7, Q8), and USP/EP monographs.
• Proven experience with method validation and transfer.
• Strong knowledge of laboratory information management systems (LIMS).
• Excellent documentation, data review, and investigation skills.
• Exceptional problem-solving abilities and a meticulous attention to detail.
• Strong leadership, communication, and interpersonal skills.