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<h3>Job Description</h3>
Job Description
Research Scientist, AI/ML 
Chicago, IL

The Opportunity
The AI/ML team is funding and building one of the largest computing systems dedicated to nonprofit life sciences research in the world. This new effort will provide the scientific community with access to predictive models of healthy and diseased cells, which will lead to groundbreaking new discoveries that could help researchers cure, prevent, or manage all diseases by the end of this century.
As a Scientist on the AI/ML team, you will apply and optimize state-of-the-art models in artificial intelligence and machine learning to solve important problems in the biomedical sciences aligned with our mission. You will work on a team responsible for developing and deploying ML models that use data developed by our organization and research partners all for the purpose of contributing to greater understanding of human cell function.
This role will be based out of the Chicago location.
What You'll Do
Develop and apply state-of-the-art AI/ML method to model biological sequences and structures.
Design and implement cutting-edge computational methods for modeling 3D structures of Immune protein complexes.
In depth analysis of computational 3D biomolecular models.
Benchmarking structure and sequence based predictive model for downstream tasks.
Coordinate with our lab scientists to design and optimize design and validation strategies.
Contribute to scientific publications and presentations at conferences.What You'll Bring
Essential -
PhD in Computer Science, Computational Biology, Math or a related quantitative field
2 years experience in applying deep learning to model biological sequences and structures
Experience with PyMol or other molecular visualization software
History of writing clean, well-documented, and reproducible code
Excellent problem-solving skills and ability to work independently
Nice to have
Ability to work effectively in teams spanning computational and experimental domains
Prior projects focused on modeling 3D biological structures and protein-protein interactions
Track record of high-impact publications in computational biology or related fields
Familiarity with bioinformatics tools and drug discovery pipelinesCompensation
The Chicago, IL base pay range for a new hire in this role is $143,000 - $181,100. New hires are typically hired into the lower portion of the range, enabling employee growth in the range over time. Actual placement in range is based on job-related skills and experience, as evaluated throughout the interview process.
Benefits for the Whole You
We're thankful to have an incredible team behind our work. To honor their commitment, we offer a wide range of benefits to support the people who make all we do possible.
Provides a generous employer match on employee 401(k) contributions to support planning for the future.
Paid time off to volunteer at an organization of your choice.
Funding for select family-forming benefits.
Relocation support for employees who need assistance moving
If you're interested in a role but your previous experience doesn't perfectly align with each qualification in the job description, we still encourage you to apply as you may be the perfect fit for this or another role.

Research Scientist, AI/ML Chicago, IL

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
As a Research Associate/Sr. Research Associate, you will play a pivotal role in a high-performance, cross-disciplinary team developing molecular and genetic diagnostic tests. This position provides an opportunity to work hands-on in the lab, contributing to the design, execution, and analysis of experiments supporting product development, verification, and validation. Shift: Monday - Friday daytime.

PRIMARY RESPONSIBILITIES:
<ul>
<li>
Execute laboratory experiments using molecular biology and laboratory techniques to prepare samples for Next Generation Sequencing (NGS).
</li>
<li>
For Levels I and II: Follow protocols to run experiments and assist in sample preparation under supervision.
</li>
<li>
For Senior Level: Independently design and execute complex experiments, troubleshoot protocols, and lead project tasks.
</li>
<li>
Analyze data, derive conclusions, and communicate findings with a multidisciplinary team of biologists, bioinformaticians, statisticians, and engineers.
</li>
<li>
Maintain a detailed and organized lab notebook to record processes, results, and insights.
</li>
<li>
Track samples via LIMS, perform database queries, and verify accuracy in sample processing and analysis.
</li>
<li>
Perform standard laboratory procedures, escalating equipment or protocol issues to appropriate personnel when needed.
</li>
<li>
For Senior Level: Write and refine standard operating procedures (SOPs) and other lab documentation.
</li>
<li>
For Level I: Support lab maintenance tasks, manage inventory, and contribute to general organization.
</li>
<li>
Adhere to laboratory safety guidelines and Good Laboratory Practices (GLP).
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
Research Associate I: BS/BA in a biological science or equivalent; laboratory coursework or internship experience is a plus.
</li>
<li>
Research Associate II: BS/BA in a biological science with a minimum of 2 years of molecular biology laboratory experience.
</li>
<li>
Sr. Research Associate: BS/BA or MS in a biological science with at least 4 years of relevant experience or equivalent expertise.
</li>
</ul>

KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>
Hands-on experience with molecular techniques, such as DNA isolation, PCR, qPCR, and DNA quantitation.
</li>
<li>
Familiarity with PCR library preparation for NGS and sequencing platforms (e.g., Illumina NovaSeq).
</li>
<li>
Proficiency in laboratory automation platforms and relevant robotics systems.
</li>
<li>
Strong organizational skills with the ability to manage multiple priorities and tasks.
</li>
<li>
For Senior Level: Effective project management skills to lead small teams or initiatives.
</li>
<li>
Familiarity with Microsoft Office Suite, especially Excel and Word.
</li>
<li>
For Levels II and III: Strong communication skills to interface with suppliers, document protocols, and present findings.
</li>
</ul>

PHYSICAL DEMANDS &amp; WORK ENVIRONMENT:
<ul>
<li>
Primary duties performed in a laboratory setting.
</li>
<li>
May require repetitive motions, including pipetting and sample handling.
</li>
<li>
For All Levels: May occasionally require extended hours, including weekends, to meet project deadlines.
</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.Austin, TX$69,700—$87,100 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Research Associate/Senior Research Associate

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Formulation Scientist Location: Lexington, MA 02421 Duration: 6 months+ (Possible Extension) Pay Rate: $37.97/hr. on w2 TOP SKILLS PER MGR: 1. Experience in preparing injectable formulations for animal studies 2. Experience creating ELN entries and managing formulation requests / workflows 3. Highly communicative and able to quickly solve problems as they arise JOB DESCRIPTION: About the Department: Our Research &amp; Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Seattle reflect the full R&amp;D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&amp;D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&amp;D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients. The Position: Client is seeking a highly motivated formulation scientist to join its Pharmaceutical Research Sciences department in Lexington, Massachusetts. The candidate will be responsible for the formulation and characterization of peptides, proteins, small molecules, and bioconjugates. Relationships: This position reports to the Head of Pharmaceutical Formulation Sciences. Internal relationships include project teams and research colleagues in Lexington MA. Individual Contributor: does not manage other employees or contingent workers. Essential Functions:
<ul>
<li>Prepare peptide and protein injectable formulations for in vitro and in vivo studies including selection of buffers, excipients, surfactants and conducting the relevant biophysical characterization and stability studies</li>
<li>Collaborate with cross-functional teams to ensure the selected dosage form meets the desired biophysical and biochemical profile and contribute to early screening strategies and execution</li>
<li>Operate, maintain, and troubleshoot lab instruments such as biophysical and analytical characterization equipment</li>
<li>Conduct laboratory work in a safe, efficient manner that ensures a safe working environment for colleagues</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor's Degree required. Degree within subject matter expertise (biological, biochemical, or pharmacological sciences) preferred</li>
<li>2+ years’ relevant technical experience required</li>
<li>Strong knowledge and expertise in biophysical characterization and injectable formulation development</li>
<li>Experience with spectroscopy, calorimetry, light scattering, and other biophysical methods for peptide and protein injectable formulations is a plus</li>
<li>Proficient in data analysis and interpretation for drawing conclusions and making recommendations</li>
<li>Experience in managing projects and working collaboratively with cross-functional teams</li>
<li>Excellent scientific communication skills and ability to engage with stakeholders effectively</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN)</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical industries a plus.</li>
</ul>
 #sczr2

Research Associate Formulation Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
<ul>
<li>Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.</li>
<li>Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.</li>
<li>Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.</li>
<li>Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure compliance with international regulations such as FDA and EMA.</li>
<li>Work collaboratively with R&amp;D and production teams to support product development and release.</li>
<li>Provide technical support and training to junior team members or other departments.</li>
</ul>
Essential Skills
<ul>
<li>3-7 years of routine testing experience using HPLC and dissolution techniques.</li>
<li>Proficiency in working with solid oral dosage forms, raw materials, and finished products.</li>
<li>Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.</li>
<li>Strong understanding of Pharma GMP practices.</li>
<li>Competence in laboratory applications including wet chemistry, titration, and chromatography.</li>
<li>Basic computer skills in MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>Ability to document and record analytical experiments and results as per cGMP guidelines.</li>
<li>Strong problem-solving skills and attention to detail.</li>
<li>Knowledge of regulatory guidelines such as GMP and GLP.</li>
</ul>
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type &amp; Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $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 East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 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 DescriptionCompany Description
We are Olsson. We engineer and design solutions that improve the world around us. As a company, we promise to always be responsive, transparent, and focused on results – for our people, our clients, and our company.
We're a people-centric firm, so it's no surprise our greatest asset is our people. The impact this creates is an environment that encourages our people to grow and be creative with their talents. This approach builds a culture that is uniquely Olsson. It allows us to grow our people as we grow our business. This, in turn, creates a lasting impact on the world around us.
Job Description
As one of our student interns on the Geotechnical team you will perform meaningful, hands-on, real-world work that will transform your classroom experience and help you envision your future career. Your experience will involve assisting our geotechnical engineering staff putting together geotechnical reports and appendices. You'll get an introduction to Olsson's culture that will help you evaluate our firm as a career choice. This position may occasionally assist with working in the lab and in the field performing various types of testing and reporting.
Freshman and sophomores are encouraged to apply. 

Qualifications
You are passionate about:
<ul>
<li>Working collaboratively with others</li>
<li>Having ownership in the work you do</li>
<li>Using your talents to positively affect communities</li>
</ul>
You bring to the team:
<ul>
<li>Strong communication skills.</li>
<li>Ability to contribute and work well on a team.</li>
<li>Proficiency in Microsoft Excel, Word, and Outlook.</li>
<li>Problem-solving and decision-making skills.</li>
<li>The ability to work in a constant state of alertness and safe manner.</li>
<li>The ability to work during the school year in addition to the summer.</li>
</ul>

#LI-DNI



Additional Information
Olsson specializes in engineering and design, client advisory services, planning, field services, and environmental. Improving the world has been our mindset from the very beginning, back when Olsson first opened for business in 1956. And it will be our mindset for years to come.
As an Olsson employee, you will:
<ul>
<li>Receive a competitive 401(k) match</li>
<li>Be empowered to build your career with tailored development paths</li>
<li>Have the possibility for flexible work arrangements</li>
<li>Engage in work that has a positive impact on communities</li>
<li>Participate in a wellness program promoting balanced lifestyles</li>
</ul>
In addition, full-time employees will receive our traditional benefits package (health care, vision, dental, paid time off, etc.) and the opportunity to participate in a bonus system that rewards performance.

Olsson is an Equal Opportunity Employer. We encourage qualified minority, female, veteran, and disabled candidates to apply and be considered for open positions. We do not discriminate against any applicant for employment or any employee because of race, color, religion, national origin, sex, sexual orientation, gender identity, gender, disability, age, military status, or other protected status.
Olsson understands the importance of privacy and is committed to protecting job applicants' personal information. Pursuant to the California Consumer Privacy Act, as amended by the California Privacy Rights Act (collectively, the "CCPA"), this notice explains Olsson's practices regarding the collection, use, and disclosure of personal information for job applicants residing in California. Please read this Notice carefully to understand our privacy practices.
For more information about the types of information we collect and how we use it in connection with your general access and use of our website, please review our general California Privacy Notice here.

Student Internship - Geotechnical

<h3>Job Description</h3>
Job DescriptionJob Title - R&amp;D scientist Location - Temecula CA Duration -12 months+ (Possible Extension) Pay Range - $48 - $54/hr. on w2 Shift: 8 am – 5 pm Mon - Fri Description: Must have a PhD in Pharmacology, formulation science or biology Skills: formulation science, cell culture/assay, self-starter New focus area for client: PepProduct drug delivery 
<ul>
<li>As an integral part of our innovation team, the R&amp;D scientist provides much needed new product development and scale-up capacity for the realization of R&amp;D mission. </li>
<li>Under the supervision of a Sr. Scientist or R&amp;D leaders, the scientist will contribute to the new formulation and assay development and scale-up for a reproducible and sustainable production methods and procedures. </li>
<li>The scientist is expected to set a high-quality standard for accuracy, in following good laboratory practices, and in complying with all safety regulations.</li>
<li>Develop hands-on skills expertise in nano/microparticle formulations (e.g., lipid nanoparticle and polymer nanoparticles) and conjugation chemistry</li>
<li>Maintain knowledge &amp; expertise in technical areas of formulation characterization and assay development</li>
<li>Expand experiences in immunology and chemical biology</li>
<li>Engage with internal innovation team in formulating project concepts</li>
<li>Validate technical prototypes</li>
<li>Perform result analysis</li>
<li>Document all the innovation work</li>
<li>Support product launch and post-launch follow ups</li>
<li>Collaborate with group members and stakeholders</li>
<li>Lend insights into drug discovery and virtual demo tailed description of the services you require.</li>
</ul>
 #sczr2

R&D scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist OperatorJob Description
The Chemist Operator will be responsible for producing Active Pharmaceutical Ingredients using chemical reactors. This role requires following specific Batch Records to ensure the production of a consistent product.
Responsibilities
<ul>
<li>Handle various unit operations, such as reactions, filtration, distillation, drying, and milling, on raw materials and various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document instructions per batch sheet to produce products in accordance with all cGMP guidelines.</li>
<li>Set up equipment, including vessels, tanks, centrifuges, and dryers, for proper processing. Clean and verify equipment and vessels.</li>
<li>Record observations of operating conditions.</li>
<li>Drive and operate a fork truck.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in Chemical Operation or Batching, 1-5 years preferred.</li>
<li>Knowledge of GMP guidelines from food, chemical, or pharmaceutical industries.</li>
<li>Understanding of Analytical Chemistry and Chemical Operating.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma with experience, or an Associate's or Bachelor's degree in Sciences, preferably in Chemical Technology or Chemistry.</li>
<li>Experience in GC and Batching processes.</li>
</ul>
Work Environment
The work environment is a clean laboratory and production setting. Initial training will be on the first shift for 3-6 months, after which the role will transition to a permanent shift from 6 p.m. to 6:30 a.m., following a 2-2-3 schedule, including working every other weekend. The company is expanding its innovation hub, offering growth opportunities into leadership positions for those who excel.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $24.00 - $26.50/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 Grafton,WI.
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 Operator

<h3>Job Description</h3>
Job Description
Job Title: Preclinical Research Assistant
Job Description
We are seeking a dedicated Preclinical Research Assistant to support the Study Director and Preclinical Sponsor Representatives in the preparation and conduct of preclinical research studies. These studies aim to develop products or procedures utilizing in-vivo, ex-vivo, and in-vitro models.
Responsibilities
<ul>
<li>Setup study binders as per local procedures.</li>
<li>Develop study-specific data sheets.</li>
<li>Support the study director in addressing QAU audit findings.</li>
<li>Quality check all study-related documentation throughout the study lifecycle.</li>
<li>Document study data as required by protocol and SOP.</li>
<li>Archive study files according to SOP.</li>
<li>Interface with principal investigators and contributing scientists for studies conducted on-site and at contract laboratories.</li>
<li>Support the study director with the preparation of draft study protocols and reports.</li>
<li>Coordinate project/study logistics.</li>
<li>Request study-specific equipment and instrumentation.</li>
<li>Collaborate with study coordinator to request and schedule studies to meet project timelines.</li>
<li>Place animal orders in accordance with protocol and study schedule.</li>
<li>Request ordering of appropriate animal-related drugs to meet protocol and SOP requirements.</li>
<li>Coordinate receipt, submission, and transfer of test and/or control articles.</li>
<li>Support the conduct of histopathology work tasks, including management, transfer, and receipt of histology specimens to an external laboratory.</li>
</ul>
Essential Skills
<ul>
<li>Experience with preclinical animal research, including comfort with large animals such as dogs, sheep, and pigs.</li>
<li>Willingness to learn and strong record-keeping experience.</li>
<li>Proficiency in Microsoft Suite.</li>
<li>Experience in a GLP-regulated environment.</li>
<li>Knowledge of both human and animal anatomy/physiology.</li>
<li>Surgical support experience, comfortable assisting during surgical procedures.</li>
<li>Ability to understand and precisely follow Standard Operating Procedures.</li>
<li>Meticulous attention to detail to identify and correct discrepancies/errors.</li>
<li>Strong background in data collection, data management, and data integrity.</li>
<li>Ability to set priorities and manage time effectively to meet deadlines.</li>
<li>Demonstrated ability to work both independently and as part of a team.</li>
<li>Strong organizational and project management skills.</li>
<li>Safety-minded in workspace organization and conduct.</li>
<li>Accountability for one's own actions and work.</li>
<li>Basic computer proficiency in Outlook, Word, Excel, and PowerPoint.</li>
<li>Excellent verbal, written, and interpersonal communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Biology, Zoology, Animal Science, Engineering, Mathematics, or a closely related STEM field preferred. Equivalent education and experience may be substituted.</li>
<li>Leadership and public speaking skills are preferred but not required.</li>
<li>Surgical Research Specialist (SRS) certification is preferred but not required.</li>
<li>Associates may be asked to bring their own device (BYOD) for this role, unless other arrangements have been made to provide a laptop.</li>
</ul>
Work Environment
This Actalent Services LLC position requires working onsite. 
Job Type &amp; Location
This is a Contract position based out of Cincinnati, OH.
Pay and Benefits
The pay range for this position is $28.00 - $32.00/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 Cincinnati,OH.
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.

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Production ChemistJob Description
We are seeking a dedicated and detail-oriented Production Chemist to join our team. The ideal candidate will be responsible for managing and handling all raw materials for chemical operations and ensuring the creation of new chemical compounds by operating chemical manufacturing equipment.
Responsibilities
<ul>
<li>Manage and handle all raw materials for chemical operations.</li>
<li>Operate chemical manufacturing equipment following specific chemical formulas.</li>
<li>Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met.</li>
<li>Work with chemical engineers and R&amp;D personnel to scale up processes.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry or a related science field.</li>
<li>Experience in precise chemical manufacturing processes.</li>
<li>Proficiency in chemistry, chemical processing, and chemical synthesis.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience working in a laboratory setting.</li>
<li>Ability to work collaboratively with R&amp;D personnel, scale-up, and process teams.</li>
</ul>
Work Environment
The role involves working in a chemical manufacturing environment. Initial training will be conducted from Monday through Friday during first shift hours (6 am to 2:30/3:30 pm). After three to four weeks, the position will transition to a weekend day shift, working from 6:00 pm to 6:00 am on Friday, Saturday, and Sunday.
Job Type &amp; Location
This is a Contract to Hire position based out of Milwaukee, WI.
Pay and Benefits
The pay range for this position is $29.50 - $29.50/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 Milwaukee,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.

Production Chemist

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Vernon Hills, IL.
Pay and Benefits
The pay range for this position is $22.00 - $24.00/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 Vernon Hills,IL.
Application Deadline
This position is anticipated to close on Jan 25, 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.

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