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<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
AbbVie Biologics Analytical Research &amp; Development (Biologics Analytical R&amp;D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products.&nbsp; Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologic medicines and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to commercial labs to support product launch.&nbsp; We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines.&nbsp; Careers in AbbVie Biologics Analytical R&amp;D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.&nbsp;
The biologics early analytical development group develops state-of-the-art analytical techniques for analysis of therapeutic proteins and other novel biologic molecules using separation science and other biophysical techniques. We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&amp;D team and can offer exciting and rewarding career opportunities for these candidates.
The candidate will focus on development and implementation of analytical assays for the analysis of complex biologics including antibodies, antibody drug conjugates, and new modalities. The candidate will use and develop a variety of analytical techniques including chromatography, electrophoresis, spectroscopy, and automated methods. The successful candidate will contribute to the development and testing of complex and automated assays and will contribute to the continuous improvement and innovation within the group.
Responsibilities
<ul>
<li>Effectively function as a scientist, generating original technical ideas and research or development strategies.</li>
<li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li>
<li>Independently responsible for project science within his/her area of expertise on one or more project teams leading the method development and validation for complex biologic therapeutics.</li>
<li>Proactively seek out new information in the literature and incorporate this into individual projects as well as the overall program.</li>
<li>Work in partnership with colleagues from Discovery, Process Chemistry/Engineering Formulation Development, and Characterization departments, among others.</li>
</ul>
Qualifications 
<ul>
<li>Compensation/leveling will be commensurate to experience.</li>
<li>
<ul>
<li>Required Qualification for Senior Scientist I: Ph.D. with 0-4 years of relevant experience is required or MS with 8+ years of experience, highly preferred. Bachelor’s Degree with 10+ years of relevant experience.</li>
<li>Required Qualification for Senior Scientist II: Ph.D. with 4+ years of relevant experience is required or MS with 10+ years of experience, highly preferred. Bachelor’s Degree with 12+ years of relevant experience.</li>
</ul>
</li>
<li>Practical experience and strong knowledge in one or more of the following areas: protein/oligonucleotide HPLC, capillary electrophoresis, MALS, automation and/or spectroscopy for biologics.</li>
<li>Previous cGMP or GLP experience and attention to detail in documentation.</li>
<li>Demonstrated record of independent thought, creativity and scientific accomplishment (e.g. peer reviewed journal publications, patents).</li>
<li>Must have a solid understanding of protein/oligonucleotide chemistry and biochemistry, particularly as related to biologics drug development.</li>
<li>Strong data and time organization/management skills coupled with strong interpersonal and effective communication skills for facilitating collaborations with a demonstrated ability to lead cross functional process development teams.</li>
<li>Effective writer and communication of research or other regulatory materials.</li>
<li>Experience with analytical Multivariate Analytical Procedures development and/or validation a plus.</li>
</ul>
Leveling will be commensurate to experience.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;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&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;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>

Senior Scientist I/II, Biologics ARD

<h3>Job Description</h3>
Job Description
Job Title: Analytical Chemist 
Job Description
We are seeking a passionate and skilled Analytical Chemist to join our Analytical Science Hub's Small Molecules Division. This role involves performing qualitative and quantitative analyses of diverse organic compounds to support the research and development pipeline and product portfolio in agrochemical formulations. The ideal candidate will possess strong communication skills, creativity under tight deadlines, and the ability to work independently with limited supervision.
Responsibilities
<ul>
<li>Perform routine and non-routine analyses of active ingredients in liquid and solid formulations using techniques such as HPLC, UPLC, LCMS, and GC.</li>
<li>Conduct physical-chemical characterization techniques, including density, particle size analysis, viscosity, surface tension, contact angle, thermal analysis by DSC/TGA, optical/electron microscopy, and FTIR/NIR/UV-Vis spectroscopy.</li>
<li>Develop and optimize methods for determining chemical compositions of agrochemical formulations and related sample matrices.</li>
<li>Maintain and troubleshoot laboratory instrumentation.</li>
<li>Communicate effectively with diverse and demanding customers and stakeholders across R&amp;D, manufacturing, and product supply.</li>
<li>Prepare complex liquid and solid matrices for qualitative and quantitative analyses.</li>
<li>Respond promptly to collaborator/partner inquiries and analytical/data troubleshooting/reporting requests.</li>
<li>Write reports and interpret analytical results for diverse stakeholders representing early R&amp;D to manufacturing and product supply.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Analytical Chemistry or a closely related field.</li>
<li>Hands-on experience with HPLC, UPLC, LCMS, GC, and physical-chemical techniques.</li>
<li>Experience in maintaining and troubleshooting analytical instrumentation.</li>
<li>Proficiency in sample preparation and method development for chemical samples.</li>
<li>Detail-oriented and highly organized with a commitment to teamwork.</li>
<li>Strong oral and written communication skills.</li>
<li>Self-motivated and able to adapt to rapidly changing analytical/scientific situations.</li>
<li>Ability to multitask in a fast-paced dynamic laboratory environment.</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Chesterfield, MO.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/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 Chesterfield,MO.
Application Deadline
This position is anticipated to close on Jan 27, 2026.
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.

Analytical Chemist

<h3>Job Description</h3>
Job Description
Molecular Biologist
Job Description
The biologist in this role will utilize molecular cloning, transient plant transformation, DNA extraction, DNA sample cleanup, and basic sequence analysis to test recombinase variants for activity and specificity. Candidates should possess hands-on experience in a molecular biology laboratory environment and preferably with plant tissue culture.
Responsibilities
<ul>
<li>Perform molecular cloning using techniques such as restriction/ligation and assembly.</li>
<li>Conduct DNA extraction and purification.</li>
<li>Execute PCR and qPCR procedures.</li>
<li>Analyze sequences using basic bioinformatics tools like BLAST, SnapGene, and Geneious.</li>
<li>Carry out transient plant transformation, for example, Agrobacterium-mediated methods.</li>
<li>Engage in plant tissue culture, if preferred.</li>
<li>Understand site-specific recombination systems including Cre/lox and FLP/FRT.</li>
<li>Evaluate the activity and specificity of recombinase variants.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in molecular cloning techniques.</li>
<li>Experience in DNA extraction and purification.</li>
<li>Ability to perform PCR and qPCR.</li>
<li>Competence in sequence analysis with bioinformatics tools.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Microbiology, Molecular Biology, Plant Biology, or a related field.</li>
<li>Hands-on experience in a molecular biology lab, either academic or industry.</li>
<li>Familiarity with plant systems is a strong advantage.</li>
<li>Experience with DNA cleanup kits and protocol troubleshooting.</li>
</ul>
Work Environment
The role involves working in a molecular biology laboratory setting, requiring attention to detail in experimental design and data recording. The candidate must be able to work independently as well as collaboratively within a team. The work environment supports strong problem-solving and troubleshooting skills, fostering a culture of continuous learning and scientific exploration.
Job Type &amp; Location
This is a Contract position based out of Chesterfield, MO.
Pay and Benefits
The pay range for this position is $28.00 - $35.00/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 Chesterfield,MO.
Application Deadline
This position is anticipated to close on Jan 27, 2026.
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.

Molecular Biologist

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>Competitive salary</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Opportunity for advancement</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
 Reports To: President of R&amp;D Position Summary: We are seeking an inventive and highly strategic Director of R&amp;D Color Cosmetics to lead our formulation lab in the development of high-performance, clean, and on-trend color products. This role requires a rare blend of scientific depth and creative experimentation to deliver the next generation of beauty innovations for our clients. Key Responsibilities: 
<ul>
<li>Lead the formulation and technical development of color cosmetics (lip, eye, face, and complexion).</li>
<li>Manage a team of chemists and technicians in a collaborative, innovation-first culture.</li>
<li>Translate trend insights, client briefs, and consumer needs into innovative, scalable formulas.</li>
<li>Partner cross-functionally to ensure smooth handoff from concept to commercialization.</li>
<li>Drive a strong innovation pipeline using new raw materials, textures, and technologies.</li>
<li>Ensure products meet all regulatory, safety, and quality standards globally.</li>
<li>Contribute to IP development, technical claims, and prototype presentation.</li>
<li>Foster a culture of curiosity, exploration, and excellence in formulation science.</li>
</ul>
Qualifications: 
<ul>
<li>810 years of formulation experience in the color cosmetics industry.</li>
<li>Expertise in emulsion, anhydrous, pigment dispersion, and pressed powder technologies.</li>
<li>Strong understanding of ingredient trends (e.g. clean, vegan, long-wear, multifunctional).</li>
<li>Proven leadership of R&amp;D teams and complex product portfolios.</li>
<li>Passion for innovation, formulation science, and working at the cutting edge of beauty.</li>
</ul>

Director of Research & Development- Color Cosmetics

<h3>Job Description</h3>
Job Description
Analytical Chemist
Job Description
We are seeking an Analytical Chemist to execute analytical testing using GC-FID, GC-MS, and UV-Vis methods. You will collaborate with scientists and engineers to plan experimental designs that address challenging analytical problems in filtration product development. The role involves analyzing and interpreting data, authoring detailed reports and data presentations, and participating in problem-solving to provide recommendations to the project team based on analytical data. Additional assignments, such as standardized testing and EHS initiatives, may also be required.
Responsibilities
<ul>
<li>Execute analytical testing using GC-FID, GC-MS, and UV-Vis methods.</li>
<li>Collaborate with scientists and engineers to plan experimental designs.</li>
<li>Analyze and interpret analytical data.</li>
<li>Author detailed reports and data presentations.</li>
<li>Participate in problem-solving and provide recommendations based on analytical data.</li>
<li>Perform additional assignments such as standardized testing and EHS initiatives.</li>
</ul>
Essential Skills
<ul>
<li>Expertise in hands-on chromatography (e.g., HPLC, SEC, LCMS, GCMS) with ideally 8+ years of experience.</li>
<li>Experience with bioanalytical testing such as CEDEX Testing and Microbial Plate reading.</li>
<li>Strong problem-solving skills with the ability to create test methods dependent on the task.</li>
<li>Minimum Bachelor's Degree in chemistry, biochemistry, materials, or related fields.</li>
<li>5+ years of relevant industrial experience.</li>
<li>5+ years of hands-on experience with gas chromatography.</li>
<li>8+ years in an analytical chemistry lab.</li>
<li>Excellent organizational and communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Proficiency in mass spectrometry and chromatography techniques.</li>
<li>Experience with laboratory and analytical chemistry tools.</li>
</ul>
Work Environment
This position is based in a lab/office setting with 1st shift hours. The role offers an opportunity to work on a unique and critical project with high potential for future business opportunities. The project is focused on sustainability and aims to be safe and cost-effective for consumers and manufacturers. You will be part of a great collaborative team environment.
Job Type &amp; Location
This is a Contract position based out of Minneapolis, MN.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/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 Minneapolis,MN.
Application Deadline
This position is anticipated to close on Jan 27, 2026.
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.

<h3>Job Description</h3>
Job DescriptionActively Screening for Chemist to join health company in Lithia Springs, GA! 
Job Description
This role focuses on our growing monoclonal antibody and vaccine portfolios, working closely with partner groups across the organization.
Responsibilities
<ul>
<li>Conduct laboratory experiments supporting analytical method transfer.</li>
<li>Perform processes and operate equipment required for large-scale monoclonal antibody production.</li>
<li>Utilize various modern analytical tools and technologies such as U/HPLC, ELISA, GC, MS, dissolution, and particle size measurement.</li>
<li>Maintain equipment and troubleshoot as necessary.</li>
<li>Understand, follow, and accurately complete process documentation to ensure high-quality product standards.</li>
<li>Adhere to safety policies and work collaboratively with members from other departments.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Biological Sciences or a related field.</li>
<li>5+ years of experience in chemistry and analytical chemistry.</li>
<li>Proficiency with HPLC, ELISA, Empower Software, and other laboratory technologies.</li>
<li>Strong understanding of quality control, method transfer, method validation, and GDP, GMP, GLP standards.</li>
<li>Excellent documentation and analytical problem-solving skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in large-scale production or laboratory scale.</li>
<li>In-depth knowledge of modern techniques for separation science, including HPLC, NMR, GC, LC/MS, and dissolution.</li>
<li>Understanding of chemistry and formulation processes.</li>
<li>Basic understanding of the pharmaceutical development process.</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Lithia Springs, GA.
Pay and Benefits
The pay range for this position is $33.00 - $55.00/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 Lithia Springs,GA.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
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.

Chemist

<h3>Job Description</h3>
Job Description1st shift Assembler $19-20/HR
*If interested, please apply. Then text: Jack @ 513-229-2006+
Job Description
Join a leading company in the commercial van industry, specializing in leasing refrigerated vans for the last mile of distribution. Our clients include well-known companies in various sectors such as edible arrangements, brewing, and hospital equipment.
Responsibilities
<ul>
<li>Assemble and install components in commercial vans using hand and power tools.</li>
<li>Conduct mechanical assembly tasks efficiently and accurately.</li>
<li>Maintain a clean and organized work area.</li>
<li>Collaborate with the team to manage inventory and support shipping activities.</li>
</ul>
Essential Skills
<ul>
<li>Experience in the automotive industry.</li>
<li>Proficiency with hand and power tools.</li>
<li>Mechanical assembly knowledge.</li>
<li>Ability to lift and bend to handle up to 50 lbs.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Mechanical aptitude is essential.</li>
</ul>
Why Work Here?
Be part of a growing company that offers significant opportunities for career advancement.
Work Environment
Work in a non-temperature controlled warehouse setting, where teamwork and productivity are key.
Job Type &amp; Location
This is a Contract to Hire position based out of Sharonville, OH.
Pay and Benefits
The pay range for this position is $19.00 - $20.00/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 Sharonville,OH.
Application Deadline
This position is anticipated to close on Jan 26, 2026.

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.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Job Title: Quality Control Chemist
Job Description
As a Quality Control Chemist, you will be responsible for performing routine analysis of raw materials, in-process, and finished products. This includes conducting tests such as titrations, FTIR, GC, HPLC, Color, and using a viscometer. Your role involves performing calculations for batch tests in a lab environment using instrumentation and physical test methods. You will follow setup procedures and work instructions for laboratory equipment while adhering to customer and company quality standards. Safety is paramount, so you must follow all safety rules and regulations, including the use of appropriate PPE at all times.
Responsibilities
<ul>
<li>Conduct routine analysis of raw materials, in-process, and finished products.</li>
<li>Perform tests including titrations, FTIR, GC, HPLC, Color, and viscometer.</li>
<li>Carry out calculations for batch tests using lab instrumentation and physical test methods.</li>
<li>Set up and operate laboratory equipment according to established procedures.</li>
<li>Ensure compliance with customer and company quality standards.</li>
<li>Follow all safety rules and regulations, using appropriate PPE at all times.</li>
</ul>
Essential Skills
<ul>
<li>Minimum 1 year of industry experience in analytical testing, troubleshooting, and quality assurance.</li>
<li>Proficiency in gas chromatography (GC), high-performance liquid chromatography (HPLC), and FTIR.</li>
<li>Strong understanding of quality control processes in chemical manufacturing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Chemistry or other Sciences preferred; AS in Chemistry is acceptable.</li>
<li>Experience in chemical manufacturing is preferred.</li>
<li>Familiarity with basic laboratory equipment (GC/LC/FTIR) and techniques (titration, liquid-liquid partition).</li>
</ul>
Work Environment
You will work independently on the night shifts in the lab, handling chemical products. The lab is equipped with newer equipment to assist with testing. The role offers opportunities for cross-training and education in certifications, contributing to employee development and career growth.
Job Type &amp; Location
This is a Contract to Hire position based out of High Point, NC.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 High Point,NC.
Application Deadline
This position is anticipated to close on Jan 20, 2026.
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.

Overnight Quality Control Chemist

<h3>Job Description</h3>
Job Description
Quality Control Chemist - 2nd shift (Monday-Thursday, 2pm-1am)
Job Description
The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC.
Responsibilities
<ul>
<li>Follow standard operating procedures to ensure quality control.</li>
<li>Conduct quality testing and document results accurately.</li>
<li>Maintain and calibrate laboratory instruments regularly.</li>
<li>Assist with the transfer of test methods.</li>
<li>Train personnel on equipment usage and testing methods.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's Degree in Chemistry</li>
<li>Minimum of 3 years of laboratory experience</li>
<li>Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in HPLC, GC, and analytical test method development and transfer</li>
<li>Familiarity with microbial testing and procedures</li>
<li>Experience in contract manufacturing and testing</li>
</ul>
Work Environment
The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours.
Job Type &amp; Location
This is a Permanent position based out of Edgerton, WI.
Pay and Benefits
The pay range for this position is $62400.00 - $62400.00/yr.
Medical, dental, vision, 401K
Workplace Type
This is a fully onsite position in Edgerton,WI.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
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.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionSalary: 
At Argenta, were more than a company were a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. 
 
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.
 
Were in a unique position. We are the worlds only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.
Our uniqueness means:
 
We are ambitious, growing and building a one team culture, guided by our values.
<ul>
<li>
<ul>
<li>We are team players;</li>
<li>We are doers;</li>
<li>We are customer-centric;</li>
<li>We are innovators.</li>
</ul>
</li>
</ul>
We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best paw forward we will make the lives of the animals we care for, better.
 
With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Lets Make It Happen, Together.
 
TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.
 
Argenta is currently looking to fill the role of Microbiologist Iat our Shawnee, KS location. Incumbents in this position are responsible for testing of raw materials, intermediates and finished products according to cGMP's in order to ensure satisfactory levels of microbial quality are met. Fundamental microbiological principles are applied in order to interpret test results. Responsibilities also include monitoring of controlled environments to ensure that manufacturing and testing processes occur under appropriate conditions. The incumbent maintains, compiles and reviews laboratory worksheets to assure accuracy of test data.

On a daily basis, the incumbent must plan for and respond to the analytical needs of a laboratory involved in fast turnaround of pharmaceutical analyses to meet manufacturing deadlines. This planning requires good communication, attention to detail, organization skills and the use of the various analytical instrumentation systems and procedures. All incumbents are responsible for following applicable Division &amp; Company policies and procedures.
 
Key Accountabilities
<ul>
<li>Performs testing of raw material, in-process and finished product samples according to approved procedures.</li>
<li>Perform Environmental monitoring of the manufacturing and laboratory facilities including cleanroom environments, personnel, water systems, compressed gases, and laminar flow hoods.</li>
<li>Identify microbial isolates using manual or automated techniques per written procedures in a timeframe that supports customer requirements.</li>
<li>Prepares media, solutions, materials and equipment to support sampling and testing.</li>
<li>Performs growth promotion and quality testing on media used for microbiological testing, and environmental monitoring in the Microbiology QC Department as needed.</li>
<li>Maintain the record storage systems in a manner that ensures quick and reliable retrieval of the data as needed.</li>
<li>Provide support to laboratory projects and assist other team members as needed.</li>
<li>Adhere to the pertinent aspects of compliance and plant safety programs.</li>
<li>Critical understanding of proper and thorough laboratory investigations</li>
<li>Support QA Operations as required for laboratory investigations</li>
<li>Continuous improvement and assessment of laboratory practices to eliminate over-processing of data</li>
<li>Adhere to GMP and/or GLP standards as required for daily operations</li>
<li>Safety first in the laboratories</li>
</ul>
 
Qualifications
<ul>
<li>BA / BS in a related scientific field such as biology, chemistry, microbiology, or biochemistry.</li>
<li>1+ year laboratory experience, which can include academic experience or microbiology laboratory.</li>
<li>The incumbent should have basic background for the understanding, planning, and execution of laboratory Standard Operating Procedures relating to instrument use, sample analysis, document generation and control, personal safety, and environmental safety.</li>
<li>Knowledge of FDA regulations (or similar regulated environment) to include Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)</li>
<li>Basic computer skills are required.</li>
<li>The incumbent must be able to pass a DEA background check.</li>
<li>Proven, effective written and verbal communication skills.</li>
<li>Demonstrated skills in the use of a wide range of microbiology test methods and instrumentation, including the following:
<ul>
<li>Bioburden testing</li>
<li>Endotoxin testing</li>
<li>Aseptic technique</li>
</ul>
</li>
<li>Water quality sampling and testing</li>
<li>Standing and/or moving &gt;50% of the time</li>
</ul>
 
Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth. Argenta is an equal opportunity employer

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