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<h3>Job Description</h3>
Job DescriptionQuality ChemistPosition Summary
The&nbsp;Quality Chemist I&nbsp;is responsible for performing analytical testing to assess the quality of bulk chemicals, pharmaceutical compounds, and environmental samples. This entry-level role requires a foundational understanding of chemistry or microbiology and laboratory techniques. The position involves solving moderately complex technical problems under close supervision and contributes to maintaining high standards of product quality and regulatory compliance.
Key Responsibilities
<ul>
<li>Conduct analytical testing of bulk chemicals, pharmaceutical compounds, and environmental monitoring samples using appropriate laboratory techniques.</li>
<li>Maintain a clean and organized laboratory environment, including restocking reagents and consumables.</li>
<li>Review peer data from routine analyses to ensure accuracy and consistency.</li>
<li>Maintain detailed and accurate laboratory notebooks in accordance with documentation standards.</li>
<li>Compile, analyze, and report test data to relevant departments.</li>
<li>Communicate testing status and timelines to internal stakeholders as needed.</li>
<li>Participate in investigations of non-conforming samples and assist in identifying corrective and preventive actions (CAPA).</li>
</ul>
Qualifications
Education &amp; Experience
<ul>
<li>Bachelor’s degree in Chemistry, Microbiology, or a related scientific field required.</li>
<li>0–1 years of relevant laboratory experience, or an equivalent combination of education and experience.</li>
</ul>
Skills &amp; Competencies
<ul>
<li>Strong attention to detail and commitment to laboratory safety.</li>
<li>Effective verbal and written communication skills.</li>
<li>Ability to work collaboratively in a team-oriented environment.</li>
<li>Sound judgment and basic understanding of chemical principles and laboratory practices.</li>
<li>Proficiency in Microsoft Office and basic computer skills.</li>
</ul>
Working Conditions &amp; Physical Requirements
<ul>
<li>Standard laboratory environment.</li>
<li>Must be able to stand or walk for extended periods.</li>
<li>May require lifting up to 30 pounds and performing repetitive motions.</li>
</ul>
Pay and Benefits
The pay range for this position is $28.00 - $33.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Rancho Cordova,CA.
Application Deadline
This position is anticipated to close on Aug 18, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom Technician
Pay: $17/hr 
Job Description
As a Cleanroom Technician, you will work in a quiet, clean, and air-conditioned environment, wearing appropriate attire such as headphones and a hair net. You will perform light assembly tasks involving gluing tubes or connectors using small equipment. This hand assembly work is performed on a tabletop and requires exceptional attention to detail, as the parts assembled are used in detailed cardiac surgeries.
Responsibilities
<ul>
<li>Perform light assembly tasks involving gluing tubes or connectors.</li>
<li>Work with components for detailed surgeries, ensuring precision and accuracy.</li>
<li>Handle cardiac surgery devices ranging from 10-12 inches long.</li>
<li>Package, seal, and label components, ranging from 1 to 25 items per package.</li>
<li>Ensure repetitive tasks are completed with high attention to detail.</li>
<li>Undergo thorough training for approximately one month.</li>
</ul>
Essential Skills
<ul>
<li>Detail-oriented mindset.</li>
<li>1-2 years of light assembly experience.</li>
<li>Proficiency in hand assembly and mechanical assembly.</li>
<li>Ability to read and understand blueprints.</li>
<li>Familiarity with cleanroom and medical device assembly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with production tasks.</li>
<li>General labor proficiency.</li>
</ul>
Why Work Here?
Join a team that values precision and attention to detail, offering a quiet and clean working environment. Benefit from thorough training and the opportunity to work with components that make a difference in cardiac surgeries. Enjoy a merit-based yearly increase and flexible working hours.
Work Environment
You will work the first shift from 6:00 AM to 6:30 PM on Friday, Saturday, and Sunday, with the option to work additional hours during the week to complete a full 40-hour work week. The cleanroom is air-conditioned and requires specific attire, ensuring comfort and focus while performing your duties.
Job Type &amp; Location
This is a Contract to Hire position based out of Grand Rapids, Michigan.
Pay and Benefits
The pay range for this position is $17.00 - $17.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Aug 16, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit <a href="https://global.allerganaesthetics.com/" target="_blank">https://global.allerganaesthetics.com/</a>. Follow Allergan Aesthetics on LinkedIn.
Job Description 
The Neurotoxin Research Group at Allergan/AbbVie is seeking a highly motivated and independent Associate Scientist II to join our Toxin Innovation Pharmacology Group. This individual will execute in vivo neuromuscular and sensory pharmacology studies, contributing to the design, execution, and communication of novel research in our highly collaborative neurotoxin discovery and innovation program.
The successful candidate for this position will contribute to projects aimed at in vivo pharmacological characterization of biotherapeutics. He/she/they will be required to work on a variety of in vivo pharmacology models to help characterize and evaluate biological compounds. The successful candidate will organize, analyze, and interpret results, come forward with recommendations, and present the findings to senior personnel or in team meetings. Experience with rodent models is required. A background in neurobiology is highly desirable but not required.
Key Responsibilities
<ul>
<li>Design, execute, and analyze in vivo assays to answer scientific questions and contribute to conceptual and experimental protocols</li>
<li>Work with cross-functional team members to accomplish the goals and requirements of the organization, including excellence in execution, and workload prioritization</li>
<li>Hands-on experimentalist: perform small animal handling, dosing of molecules through a variety of delivery routes, conduct behavioral studies, and post-mortem tissue harvest</li>
<li>Demonstrate critical thinking to troubleshoot and provide creative solutions to address experimental challenges</li>
<li>Effectively organize and present scientific plans and data to functional leaders</li>
<li>Demonstrate flexibility and a commitment to scientific excellence</li>
<li>Meet experimental timelines and impact projects through lab-based contributions</li>
<li>Understand and adhere to corporate standards regarding conduct, safety, material handling, CDC compliance, and animal care</li>
<li>Learn, understand, and become proficient at new experimental techniques</li>
</ul>
<ul>
<li>Effectively prepare and communicate presentations to multidisciplinary teams</li>
</ul>
Qualifications 
Minimum Education and Experience:
<ul>
<li>Bachelor’s Degree with&nbsp;3+ years of experience OR Master’s Degree&nbsp;</li>
<li>Experience with small animal/rodent handling is required</li>
<li>Experience with behavioral assays (sensory or motor)</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with small animal dosing and post-mortem tissue harvest is highly desirable.</li>
<li>Familiarity with in vivo behavioral or pharmacological assays is highly desirable.</li>
<li>Working knowledge of neuroscience and animal anatomy is a plus</li>
<li>Experience with histological techniques, including immunohistochemistry, microscopy, and other laboratory techniques, is a plus.</li>
<li>Experience with in vitro assays including cell culture techniques is a plus.</li>
<li>Knowledge of graphing software (e.g., GraphPad prism) and basic understanding of statistical analyses is a plus.</li>
</ul>
Other Required Skills:
<ul>
<li>Exhibit flexibility and a commitment to scientific excellence</li>
<li>Highly motivated, hands-on experimentalist who thrives in a collaborative, multidisciplinary environment</li>
<li>Willing and able to conduct various in vivo behavioral and pharmacological assays in small animals</li>
<li>Independently design and conduct critical experiments that advance project goals in a timely manner</li>
<li>Proactively seek advice from others when developing new models or when troubleshooting</li>
<li>Possess strong interpersonal skills and able to collaborate with diverse groups within the organization.</li>
<li>Meticulous attention to detail and diligence in record keeping</li>
<li>Interpret results and draw conclusions from own multistage experiments</li>
<li>Note significant deviations and suggest, design, and pursue relevant experiments</li>
<li>Present findings in team meetings and to senior personnel using precise written and oral communication</li>
<li>Possess basic understanding of standard statistical analysis of scientific data</li>
<li>Excellent writing and communication skills.</li>
<li>Computer skills: working knowledge of MS-Office (Excel, Word, PowerPoint) is required.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist II - In Vivo Pharmacology

<h3>Job Description</h3>
Job Description
When you join Groundwater &amp; Environmental Services, Inc. (GES), you are not a number – you become the reason for our success. You’ll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world’s leading organizations solve their most complex environmental challenges.
We work hard, and we have a lot of fun while we’re at it. Our core values are centered on doing what’s right – for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. 
Groundwater &amp; Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks an experienced Geologist or Environmental Scientist to support environmental remediation project activities in Southern California. 
<ul>
<li>Under general supervision, provides project management support including client involvement, work plan and proposal preparation, project scheduling and deadline tracking, budget evaluation and analysis, and technical editing and report finalization. </li>
<li>Must be a detail-oriented team player able to multi-task, and possess strong communication, analytical, organizational, problem-solving, planning, technical writing, delegation, mentoring, and time management skills. </li>
<li>Executes, supervises, and documents field aspects of environmental site assessment and remediation activities using standard operating procedures (SOPs). Conducts compliance assessment (e.g., facility response plan compliance), remedial testing, operation, maintenance, and monitoring (OM&amp;M), short-term remedial events (e.g., chemical injection, groundwater and vapor extraction), and other project-support field activities.</li>
<li>Self-performs or directs junior staff in the installation of soil borings, monitoring wells, remediation activities, waste management and disposal, and other field requirements using standard operating procedures (SOPs). Self-performs and may direct junior staff in the performance of engineering design, permitting, OM&amp;M, remedy process optimization, and environmental compliance.</li>
<li>Acts as the primary author for site work plans and proposals for routine scopes of work on low/medium priority projects, and co-author for complex scopes of work including comprehensive site characterizations and remedial actions. Co-authors comprehensive site characterizations and remedial action plans. These reports contain multiple level and interrelated interpretations and conclusions as well as provide recommendations based upon conclusions with focus on conceptual site model development.</li>
<li>May manage various level priority projects by providing technical, regulatory, and financial project support. Technical responsibilities may include monitoring contaminant concentrations, fate and transport analysis, QA/QC of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Provides technical, regulatory, and financial project support for O&amp;M sites. Technical responsibilities may include monitoring contaminant concentrations, site remediation activities, quality of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Knowledgeable of pertinent regulations and their application to the compliance and progression of the projects. </li>
<li>Performs hydrogeological assessments regarding groundwater flows to identify contamination impact and related concerns. </li>
<li>Researches information relating to identifying geological formations and soil delineation studies and prepares reports and geological maps based on the findings.</li>
<li>Participates in the identification of viable remedial solutions consistent with all federal, state, and local regulations </li>
<li>Procures and manages subcontractors and vendors for completion of project tasks (e.g., trenching and excavation, system construction, and electrical work), including supplier bid package development.</li>
</ul>
Skills &amp; Requirements:
<ul>
<li>A Bachelor's degree or higher in geology, environmental science, engineering or related scientific discipline.</li>
<li>4+ years of related experience.</li>
<li>GIT or EIT a plus</li>
<li>Must be detail-oriented, and a team player with good communication, analytical, organization, and time management skills.</li>
</ul>
Our comprehensive benefits include: medical, dental, vision, prescription, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Continuing Education/Training Course Assistance, Bonus Plan, and more.
Groundwater &amp; Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

Mid-Level Environmental Scientist, Geologist, or Engineer

<h3>Job Description</h3>
Job DescriptionGeotechnical Engineer
Job Title: Geotechnical Engineer Job Location: Duquesne, PA Salary: $75K-125K Requirements: 5+ years of civil engineering/geotechnical engineering required. Experienced with Retaining wall and slope stability design also required. Position Overview: We are seeking a skilled Geotechnical Engineer to join our team. The ideal candidate will be responsible for conducting geotechnical investigations, analyzing data, and designing foundations, retaining walls, and other structures. This position plays a crucial role in ensuring the stability and safety of construction projects. Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations and soil testing to assess site conditions</li>
<li>Analyze data and prepare geotechnical reports for projects</li>
<li>Design foundations, retaining walls, and other earth structures</li>
<li>Evaluate slope stability and provide recommendations for land development</li>
<li>Collaborate with civil engineering teams to integrate geotechnical solutions into overall project design</li>
<li>Ensure compliance with relevant codes and regulations</li>
<li>Provide technical support during construction and monitor site conditions</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree in Geotechnical Engineering or Civil Engineering</li>
<li>E.I.T. (Engineer in Training) certification or P.E. (Professional Engineer) certification preferred</li>
<li>5+ years of experience in geotechnical engineering/civil engineering</li>
<li>Strong knowledge of soil mechanics and foundation design</li>
<li>Experience with retaining wall and slope stability design</li>
<li>Proficiency in geotechnical software and data analysis tools</li>
</ul>
Benefits
<ul>
<li>Medical</li>
<li>Vision</li>
<li>Dental</li>
<li>401(K) Match</li>
<li>Bonus</li>
<li>Generous PTO</li>
<li>And More!&nbsp;</li>
</ul>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. This job was first posted by CyberCoders on 06/05/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please contact a member of our Human Resources team to make arrangements.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
&nbsp;Celebrating our 90th year, Daubert Chemical Company is a profitable, family-owned specialty chemical manufacturer and a market leader in the brands that we sell to our end users and distributors, including products such as corrosion preventive coatings, industrial greases and adhesives. We are seeking an experienced&nbsp;R&amp;D Formulation Chemist&nbsp;for the coatings products in&nbsp;our R&amp;D Lab; this role is onsite at our chemical manufacturing plant near Midway Airport.&nbsp;This is an advanced level Chemist role requiring extensive R&amp;D laboratory and formulation experience, including scale up from lab to production. The successful candidate will conduct extensive research, analysis, and experimentation on substances to resolve quality problems, improve the marketability or profitability of current products, and develop new products with minimal supervision. A high degree of creativity and latitude is required as work is generally independent yet collaborative. This role does not have direct reports, but may be a project-specific leader and mentor Chemist I and II and Lab Technician roles.
ESSENTIAL DUTIES AND RESPONSIBILITIES, include but not limited to:&nbsp;&nbsp;
<ul>
<li>Develops formulations for new products and/or existing product modifications based on project outline delegated by management. Researches materials, ingredients, and processes to develop bench-scale batches. Performs stability, performance and data required for generating a Safety Data Sheet (SDS).&nbsp;&nbsp;</li>
<li>Develop, write and present technical reports for new products and modifications of existing products to executive management for evaluation of critical business solutions.&nbsp;&nbsp;</li>
<li>Identifying and resolving formulation-related issues during development and production.&nbsp;</li>
<li>
Provide technical service support as assigned and direct dialogue with customer and sales with minimal supervision once competency is established.&nbsp;&nbsp;
</li>
<li>
Prepare samples and test reports; follow through with Sales and customers until project is complete; this includes understanding and meeting or exceeding customer specifications, batch-ups, QA testing, audit preparation of documentation, etc.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Thorough understanding of Daubert’s manufacturing processes (tanks, engineering capabilities), GMP and capabilities. Advanced knowledge of quality, manufacturing, engineering and sales within the company to be able to answer other’s questions.&nbsp;
</li>
</ul>
<ul>
<li>
Maintaining accurate and detailed records of formulation development, testing plans, materials, methodology and results.&nbsp;
</li>
</ul>
<ul>
<li>
Generates lab reports, formulations, and cost sheets for appropriate team members.&nbsp;
</li>
</ul>
<ul>
<li>
Enters new product entries and implements and follows up on engineering change orders.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Research and orders new lab equipment with approval; implements into processes and trains others; utilizes and maintains lab equipment and bench space on a regular basis.&nbsp;
</li>
</ul>
<ul>
<li>
Perform 5S in the lab.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Log in SDS, check in raw materials, calibrate equipment.&nbsp;
</li>
</ul>
<ul>
<li>
Maintains a safe and clean working environment, i.e. office space, lab equipment, and lab space.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
All duties must be performed in a safe manner following OSHA’s Laboratory Standard (29 CFR 1910.1450) and Daubert Chemical Company’s training, instructions and procedures including proper wearing of required PPE.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Continuous learning mindset; pursue education opportunities and skills improvement.&nbsp;&nbsp;&nbsp;
</li>
</ul>
Your Qualifications:&nbsp;
<ul>
<li>B.S. in Chemistry from an accredited institution is the minimum requirement; a Master's or PhD is highly preferred ; minimum of 7&nbsp;years related experience, preferably in an industrial chemical environment. &nbsp;</li>
<li>&nbsp;History of innovative product development.&nbsp;&nbsp;</li>
<li>Ability to read,&nbsp;write and speak English; prepare advanced reports and correspondence and speak confidently when presenting information both inside and outside of the Company. Ability to discuss problems and solutions professionally and effectively with customers, suppliers, and company employees</li>
<li>Undergraduate research is a plus.&nbsp;&nbsp;</li>
<li>Interpret documents presented in writing, such as safety rules, operating and maintenance instructions, and procedure manuals.&nbsp; </li>
<li>Possess advanced ability to choose the right mathematical methods or formulas to solve a problem.&nbsp;&nbsp;</li>
<li>Interpret a variety of instructions furnished in written, oral, diagram, or schedule form; identify gaps in data and conduct further experimentation to generate needed information.&nbsp;</li>
<li>Demonstrate ability in defining and solving problems.</li>
<li>Support and practice a culture of safety; follows all workplace health and safety procedures. Responsible for safety performance in respective area and ensures that injury prevention efforts are a strong focus.&nbsp;&nbsp;</li>
<li>&nbsp;PC proficiency in Microsoft programs such as Outlook, Office (Excel, Word &amp; PowerPoint). Advanced Excel is required for formulations and cost sheets. Advanced PowerPoint. Apply these skills in report writing, graphs and charts to represent solutions and conclusions to customers, suppliers, and management. Intermediate photo taking and editing skills.</li>
</ul>
&nbsp;Benefits &amp; Compensation:
<ul>
<li>The level III offers a range of $90,000 to $126,000 annually.&nbsp;Actual compensation will be based on qualifications such as experience, education, and skills.&nbsp;</li>
<li>BCBS of Illinois Medical &amp;&nbsp;Dental, plus Vision Service Plan.&nbsp;</li>
<li>401(k) Savings Plan + generous Company match</li>
<li>Paid time off, plus&nbsp;11 annual Holidays&nbsp;</li>
<li>Disability, Family, &amp; Military Leave</li>
<li>Term Life Insurance, Identity Protection and more!</li>
</ul>
Relocation assistance is not available. Must be authorized to work in the U.S.
Equal Opportunity Employer: Disability/Veteran
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R&D Chemist III

<h3>Job Description</h3>
Job Description
We are currently seeking a Microbiology Lab Technician for a prominent Pharmaceutical client of ours. This position is in Social Circle, GA. Details for the position are as follows:
<ul>
<li>Pay: 23.00-33.00/hr.</li>
<li>Length of Assignment: 11.5 months to start with potential for extension or conversion.</li>
<li>Shift: Thursday- Sunday, 6am-4:30pm or 1:30pm-12:00am est.</li>
<li>Conducts and performs a wide range of biological, chemical, and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and may include environmental monitoring programs.</li>
<li>Environment monitoring, critical utility sampling, endotoxin testing, bioburden for raw materials and in process, process samples, microbial identification and final product sterility testing is nice to have but not required.</li>
<li>Position may be applicable to QC Analytical or Microbiological testing, Compliance, QCMIS, or Laboratory Operations.</li>
<li>Collect samples from manufacturing areas to evaluate environmental classification or critical utility integrity.</li>
<li>Conduct critical biological, chemical and physical analyses such as raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at the company manufacturing facilities, etc.</li>
<li>Use sophisticated laboratory instrumentation and computer systems to collect and record data (such as LIMS system). Perform assays requiring precise analytical skills and understanding of biology and chemistry principles.</li>
</ul>
Company DescriptionThe Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort. Browse our website below for additional information on our company. The Fountain Group “We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.” 
<h3>Company Description</h3>
The Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort.\r\n\r\nBrowse our website below for additional information on our company.\r\n\r\nThe Fountain Group\r\n\r\n“We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.”

Microbiology Lab Technician

<h3>Job Description</h3>
Job Description
Position Summary
The RWE biostatistician provides statistical expertise for all observational research project sponsored by the US Evidence Based Medicine in protocol development, Statistical Analysis Plan (SAP) preparation and study report. The role needs to ensure that appropriateness of study design, sample size and statistical methodologies are used and adherence to the established standards and SOPs. The role manages the timely execution of statistical and research methodological components of RWE study protocols in order to meet project objectives and has a thorough understanding of current requirements for statistical standards.
Roles/Responsibilities
Utilize statistical knowledge of and expertise to provide statistical support for RWE studies, with a main focus of real-world observational studies, database examples:
1)US medical and pharmacy claims databases (e.g. MarketScan); 2) US medical record databases (e.g. GE Healthcare); 3) US government public use databases (e.g. NHANES, MEPS)
Participate in study concept, protocol and SAP development and ensure appropriateness of study design, sample size and statistical methodologies proposed.
Specify the structure of the datasets that will be delivered for statistical analysis to ensure that the structure follows any existing company standard for databases pooling.
Mock-up, review, and approve tables, listings and graphs specifications.
Actively participate in project/study team meetings
Establish/negotiate timelines for completion of study-related statistical activities. Ensure the study timelines are met.
Conduct observational data analysis, include data management, statistical programming, interpretation of analyses results, and write-up/review the corresponding sections of RWE study report.
Produce analysis datasets, listings, tables, and figures for research projects, according to specifications, while maintaining documentation and complying with pre-defined project / study standards.
Provide oversight of the biostatistics-related activities for RWE studies subcontracted to a CRO:
Oversee the CROs work on the preparation of analysis plans, development and validation of computer algorithms for inferential analyses, statistical writing of study reports, and other outsourced analyses as appropriate.
Perform quality control procedures to ensure that statistical deliverables conform to the requirements outlined in the SAP
Qualifications:
Ph.D. in Statistics or epidemiology with Minimum 1+ year experience in pharmaceutical industry; Strong R programming skills.
Working knowledge and experience with bio statistical analysis and R and/or SAS programming.
Excellent oral and written communication skills in English are a must.
Prior work experience in epidemiology, health economic and outcome research, or clinical research area is a plus.
Specific experience and understanding of outcomes research, drug development is an asset
Familiarity with observational databases desirable; database examples
US medical and pharmacy claims databases (e.g. MarketScan)
US medical record databases (e.g. GE Healthcare)
US government public use databases (e.g. NHANES, MEPS)
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Company Description<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a> 
<h3>Company Description</h3>
<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a>

Sr. Statistician for RWE (Real World Evidence, Remote)

<h3>Job Description</h3>
Compunnel Healthcare is seeking a travel Physicist for a travel job in Mountain View, California.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 09/15/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours</li>
<li>Employment Type: Travel</li>
</ul>
Requirement: •\tFive (5) years medical physics experience. •\tExperience with Stereotactic Radiation Surgery (SRS), Stereotactic Body Radiation Therapy (SBRT), Intensity-Modulated Radiation Therapy (IMRT), High and/or Low Dose Brachytherapy, superficial therapy, and external beam treatment planning. License/Certification/Registration Requirements : •\tBoard Certified American Board of Radiology in Radiation Therapy Physics and /or American Board of Medical Physics in Radiation Oncology Physics preferred. •\tBoard of Licensure for Professional Medical Physicists preferred. •\tValid Radioactive Material License.
Compunnel Healthcare Job ID #11209103. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined.
About Compunnel Healthcare
Compunnel Healthcare is at the forefront of the healthcare staffing industry,
offering personalized and affordable solutions to help you find your ideal job
within local, regional, and national healthcare organizations. We are dedicated
to providing you with the best opportunities that align with your career goals
while also meeting the specific needs of employers.
 
Our approach is centered on creating a mutually beneficial relationship
between job seekers like you and healthcare employers. We strive to ensure
that every placement is a perfect match, adhering to high standards of ethics,
credibility, and quality service. With a deep understanding of what employers
are looking for and what you need to succeed in your career, we tailor our
services to fit your unique specifications and goals.
 
By choosing Compunnel Healthcare, you gain access to a team of experts
who are committed to your professional growth and satisfaction. We work
diligently to place you in roles that enhance your skills and advance your
career.

Travel Physicist

<h3>Job Description</h3>
Job Description
Department:&nbsp;Registration and Collections Management
Reports to:&nbsp;Associate Objects Conservator
Job Type:&nbsp;Regular – Part-time&nbsp;
Job Classification:&nbsp;Hourly (Non-exempt)
Workplace Location:&nbsp;Los Angeles – Academy Museum
Summary/Objective:
The Conservation Technician will support the Museum’s conservators and collections registrars in a range of conservation and preservation tasks. Primary responsibilities include preventive conservation, gallery maintenance, environmental monitoring, pest management, routine dusting of objects on open display, and assisting with installations. Additional tasks include preparing cleaning and adhesive solutions, entering data into the collections database, and assisting with minor conservation treatments.
This position is represented by a union.
Essential Functions of the Job:
<ul>
<li>Assist with downloading environmental dataloggers, preparing reports, and analyzing the data.</li>
<li>Assist with preventive and active pest management, including creating anoxic chambers.</li>
<li>Assist with routine gallery maintenance, including checking light levels and cleaning of open-air displays.</li>
<li>Examine artwork and create written and photographic documentation. Photography instruction will be provided.</li>
<li>Perform minor conservation treatments, including solvent and mechanical surface cleaning.</li>
<li>Assist Textile Conservator with preparing mannequins for exhibition.</li>
<li>Assist with daily conservation laboratory tasks (e.g., keeping SDS information up to date, preparing adhesives and cleaning solutions, and studio maintenance).</li>
<li>Assist with material analysis.</li>
<li>Assist with object handling and moving artwork.</li>
<li>Communicate and maintain effective working relationships with co-workers by contributing to a positive working environment based on mutual respect, collegiality, and collaboration.</li>
<li>Assist registrars with various collection handling and database work.</li>
</ul>
Required Competencies:
<ul>
<li>1+ years of related education, training, and/or experience working with a conservator in an institutional or private practice setting required.</li>
<li>At least one semester of college-level chemistry with an in-person lab.</li>
<li>Knowledge of safe art handling practices and Museum collections care.</li>
<li>Experience writing examination reports for artwork required.</li>
<li>Experience performing minor surface cleaning of artwork, such as with a vacuum and brushes required.</li>
<li>Competency in working with power tools and using basic conservation tools, such as scalpels and handmade cotton swabs.</li>
<li>Ability to read and interpret Safety Data Sheets, laboratory rules, and conservation documentation documents.</li>
<li>Experience using Microsoft Office for generating reports. Experience using iPads is desired.</li>
<li>Ability to multi-task in a fast-paced environment.</li>
<li>A commitment to diversity, equity, accessibility, and inclusion.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to move and transport objects up to 50 pounds.</li>
<li>Ability to climb ladders.</li>
<li>Ability to remain in a stationary position for extended periods.</li>
</ul>
Required Vaccination:&nbsp;Full vaccination against COVID-19 is required, including any booster vaccinations as applicable.&nbsp;Exception:&nbsp;Medical and religious accommodations approved by the Office of People &amp; Culture.
Compensation:&nbsp;The expected salary for this role is $25.00 per hour. The actual base pay offered will be determined by factors such as experience, skills, training, location, certifications, education, and other factors permitted by law. Decisions will be made on a case-by-case basis.)
To Apply:
<ul>
<li>As part of your application, please submit a resume, cover letter, and a minimum of three professional references.</li>
</ul>
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