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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
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: 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 DescriptionJob Title: Chemical OperatorJob Description
As a Chemical Operator, you will be responsible for operating various chemical mixing and compounding equipment, including pumps, valves, and hoses. You will also utilize sit-down forklifts to transport materials across the site, follow specific batch sheets, and document all relevant information. Precise measurement of raw materials and performing quality control checks on finished, in-process, and raw materials are essential tasks.
Responsibilities
<ul>
<li>Operate chemical mixing and compounding equipment, pumps, valves, and hoses.</li>
<li>Use sit-down forklifts to transport materials to shipping and receiving areas.</li>
<li>Follow batch sheets and accurately document all related information.</li>
<li>Utilize measuring equipment to weigh raw materials to correct proportions.</li>
<li>Perform mathematical calculations to ensure correct material quantities and percentages.</li>
<li>Conduct quality control checks on finished, in-process, and raw materials.</li>
</ul>
Essential Skills
<ul>
<li>Experience in blending, mixing, and compounding chemicals.</li>
<li>Ability to follow batch sheets, formulas, and ingredient lists.</li>
<li>Understanding of the operation of pumps and hoses (hydraulic, air, electric, etc.).</li>
<li>Capability to operate complex production equipment.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma, HSED, or GED.</li>
<li>Minimum of 2 years of experience in mixing, blending, or compounding, or 2 years in food, chemical, or pharmaceutical manufacturing operations.</li>
</ul>
Work Environment
This role is based in a manufacturing facility with about 35 production personnel. You will work closely with a team of 2 to 4 people per blend, interacting with production and QA/QC staff. The environment can be dirty and hot due to machines operating at high temperatures and the nature of the products being manufactured, such as oils and lubricants. The position is a 1st shift role, with hours from 5:00 a.m. to 1:30 p.m., requiring flexibility for overtime and occasional Saturday work. Teamwork is highly emphasized, and all safety standards and ISO regulations must be followed.
Job Type &amp; Location
This is a Contract to Hire position based out of NEW BERLIN, WI.
Pay and Benefits
The pay range for this position is $18.00 - $25.00/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 NEW BERLIN,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.

Chemical Operator

<h3>Job Description</h3>
Job Description
What You'll Be Owning: 
As a Senior Geospatial Research Analyst - Production Manager you will be responsible for supporting DoD geospatial and all-source analysis and production, including supervising analysis, research, and production.
What You Must Have:
<ul>
<li>TS/SCI Security Clearance Required</li>
<li>Bachelor's degree in Geography, Geospatial Science, GIS, Remote Sensing, Environmental Science, Computer Science, Business Analytics or a closely related field; or 5+ years minimal experience creating geospatial analytic products in these fields of study or supporting DoD geospatial and all-source analysis and production, including supervising analysis, research, and production.</li>
<li>Expertise, knowledge, and capability to both apply and lead geospatial analytics and all-source intelligence methodologies, theories, and frameworks; and AI/ML, data quality, enrichment, and stewardship processes and techniques to research to:
<ul>
<li>Solve and articulate complex geospatial and all-source intelligence analytic problems.</li>
<li>Develop and oversee data stewardship techniques and best practices.</li>
<li>Collaborate with other data providers and analysts to improve access to key data.</li>
<li>Leverage the knowledge of peers to better understand analytic trends and initiatives.</li>
<li>Working knowledge of Esri ArcGIS Enterprise systems and data steward tools, catalogs, techniques, and processes.</li>
</ul>
</li>
</ul>
What Would Be Nice to Have: 
<ul>
<li>Certifications or training in Esri GIS or related technologies (e.g., ArcGIS Pro, ArcGIS REST API), Python, R, JSON, HTML/XML, SQL, NoSQL, PostgreSQL, Open-Source Intelligence (OSINT), and All-Source Intelligence analytic methodology are advantageous but not required.</li>
</ul>
Why Choose GRVTY
The toughest national security challenges demand vision and ingenuity, not just resources. We deliver mission and technical expertise to outpace our adversaries. We're purpose-built to tackle the most entrenched, systemic national security issues around the world.
We partner with our customers to help them overcome challenges in every corner of technology and defense—including the ones still being explored. Our growing capabilities create complementary advantages, giving on-the-ground operations the edge they need to succeed. We muster everything we have to answer every challenge presented, every day of our lives.
At GRVTY, we believe that when our employees thrive, our company thrives. That's why we offer a comprehensive and competitive benefits package designed to support your well-being, growth, and work-life balance.
• Robust health plan including medical, dental, and vision 
• Health Savings Account with company contribution 
• Annual Paid Time Off and Paid Holidays 
• Paid Parental Leave 
• 401k with generous company match 
• Training and Development Opportunities 
• Award Programs 
• Variety of Company Sponsored Events

EEO Statement
GRVTY, is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran and will not be discriminated against on the basis of disability. 
Anyone requiring reasonable accommodations should email <a href="mailto:recruiting@grvty.com" target="_blank">recruiting@grvty.com</a> or call 703-544-7930 with requested details.  A member of the HR team will respond to your request within 2 business days. 
Know Your Rights: Workplace Discrimination is Illegal (eeoc.gov)  
Please review our current job openings and apply for the positions you believe may be a fit. If you are not an immediate fit, we will also keep your resume in our database for future opportunities.

Senior Geospatial Research Analyst - Production Manager

<h3>Job Description</h3>
Job DescriptionFounded in 1964, TTL is an engineering design firm focused on delivering integrated infrastructure solutions for public and private clients. From site and corridor selection to due diligence, design, and construction services, TTL is a trusted partner providing single-sourced custom solutions for complex infrastructure development. With more than 500 team members across the Southern United States, TTL provides a wide range of services including civil and geotechnical engineering; transportation design and CEI; environmental consulting and remediation; construction materials engineering and testing; and surveying, GIS and mapping services.

At TTL, we are driven to serve our clients, our communities, and each other. TTL not only provides a great work/life balance, but we provide excellent employee benefits such as a robust health &amp; dental plan, vision, 401(k), flexible spending accounts, and generous paid time off (PTO) accrual.

For more information, please go to <a href="http://www.ttlusa.com" target="_blank">www.ttlusa.com</a>.

Build your legacy at TTL
Geotechnical Field Logger - San Antonio, TX
TTL, Inc. has a need for a full-time, geotechnical field logger. This full-time position provides technical field support for geotechnical engineering projects for both private and public sectors. This person must have a good safety record and be able to communicate effectively with other team members and clients. Primary responsibilities include:
<ul>
<li>Collecting soil samples</li>
<li>Preparing field boring logs</li>
<li>Conduct field testing on collected soil samples and record pertinent drilling information</li>
<li>Locate and stake boring locations</li>
<li>Notify utility locators of proposed drilling locations</li>
<li>Conduct field electrical earth resistivity testing</li>
<li>Ensure general safety of drilling crew</li>
<li>Participate in safety meetings</li>
</ul>
Requirements
<ul>
<li>Must have a valid driver’s license and a safe driving record</li>
<li>H.S. Diploma or GED equivalent</li>
<li>Must be able to work independently as well as in a team environment</li>
<li>Must be able to work in all types of weather and field conditions</li>
<li>Must be able to work outside typical daily 8 am to 5 pm hours</li>
<li>Must be able to travel for extended periods of time</li>
<li>Must have basic computer skills for time and expense entry</li>
<li>Must be able to communicate effectively with fellow employees and drillers</li>
<li>Must be able to read plans and maps</li>
<li>Must be able to lift 50 pounds</li>
<li>Must be able to travel between Texas, Oklahoma, Arkansas and Louisiana.</li>
<li>Schedule is 12 days on 4 days off cycle</li>
</ul>
Job Type: Full-time
This position is subject to a pre-employment drug and motor vehicle record check. 
TTL is an EEO/AAP employer.

Geotechnical Field Logger

<h3>Job Description</h3>
Job Description

Position: Research Associate II - Myers Lab
Job Type: Full-Time
INSTITUTE OVERVIEW
The HudsonAlpha Institute for Biotechnology (<a href="http://www.hudsonalpha.org" target="_blank">www.hudsonalpha.org</a>) is a non-profit organization with the mission to use biotechnology and basic biological research to make important discoveries, improve human health, stimulate economic development, inspire young people to seek careers in science and teach members of the public the importance of science in their everyday lives. Located in Cummings Research Park in Huntsville, Alabama, one of the world's leading science and technology parks, HudsonAlpha's campus contains state-of-the-art laboratories for biological research and development, as well as education, in the areas of genomics, genetics and personalized medicine.
DEPARTMENT OVERVIEW
Dr. Richard M. Myers is a Faculty Investigator and Chief Scientific Officer of the HudsonAlpha Institute for Biotechnology. His laboratory uses genomic, genetic, molecular biology, and cell biology approaches to study problems in human neurobiology and gene regulation on a genome-wide level. We especially seek to understand how germline and somatic DNA sequence variation, epigenetics, and the environment affect the levels of transcription of genes in cell-type specific manners in the human nervous system. We focus on normal, healthy brain function as well as diseases, including Huntington disease, Alzheimer disease, Parkinson disease, psychiatric disorders, and amyotrophic lateral sclerosis, often in the context of differential responses to therapeutic agents. In addition, we work on neuropsychiatric disorders, and with Dr. Greg Cooper's lab at HudsonAlpha, on understanding the causes and mechanisms of unexplained diseases in children. Our experimental and computational work include genome-scale analysis of cis-acting regulatory sequences, DNA binding proteins and epigenetic action involved in human gene regulation and disease, as well as the development of molecular biomarkers for early detection and monitoring of diseases relevant to neuroscience.
While not required, subject area familiarity and/or interest in genetics, genomics, neuroscience, neuropsychiatric diseases, and/or neurodegenerative diseases is desirable. Project areas include study of gene regulation for genes implicated in normal human biology as well as disease, novel analysis approaches for associating genetic variation with gene expression, and genome-wide approaches relevant to disease as well as genome function in the brain more broadly.
POSITION SUMMARY
This Research Associate (RA) position is in the Myers Lab supporting genomics research projects in a variety of basic and applied areas, including global genomic assays and functional characterization. The activities of the RA include: molecular techniques including restriction digests, ligations, annealing, gel electrophoresis, quantification of nucleic acids, bacterial cloning, nucleic acid extractions; mammalian cell culture using fully consented cell lines; preparation of samples for next-generation sequencing; and other cellular and molecular biology protocols. This position requires exacting attention to detail, strong organizational skills, and the ability to work as part of a team as well as independently.
The Research Associate carries out research protocols as determined by the Principal Investigator. The Associate follows procedures exactly as outlined, ensuring the consistency of research practices and, ultimately, helping ensure the consistency and integrity of project outcomes. The Associate also provides feedback in the case that procedures are not producing expected results.
The Research Associate must understand laboratory procedure and safety. In addition to a general knowledge of the overall objectives of the research project, the Associate must have an understanding of the tactical methodology in particular. The Associate works under the direction of a graduate student, postdoctoral fellow, research assistant with supervisory responsibilities, senior scientist, or the lab Principal Investigator, communicating progress and advising of any issues that arise. The Associate must be able to adapt to modifications in protocol, changes in equipment or upgrades in software, as well as adjustments to the scope of research projects.
JOB SPECIFIC TASKS
<ul>
<li>Hands-on laboratory work, executing research assignments according to existing protocols </li>
<li>Communicates with lab colleagues regarding shared equipment and reagent usage, experimental results, and any potential troubleshooting</li>
<li>This position will periodically require limited weekend hours for performance of mammalian cell culture and/or molecular cloning procedures but will not exceed 40 total hours per week</li>
<li>Immediately reviews initial outcomes for quality and consistency, and participates in team discussions regarding short-term and long-term goals</li>
<li>Maintains an accurate and up-to-date laboratory notebook and tracks work as required by the project or supervisor</li>
<li>Participates in general lab maintenance such as cleaning freezers, shared lab space and equipment, and stocking and/or ordering shared reagents and consumables</li>
<li>Other duties as assigned</li>
</ul>
EDUCATION AND REQUIRED SKILLS EXPERIENCE
<ul>
<li>Master's degree in a life or physical science field requiring hands-on laboratory work with 5 years experience, or a bachelor's degree in a life or physical science field requiring hands-on laboratory work and 7 years experience</li>
<li>Meticulous attention to detail, both in actual laboratory practice and in documentation</li>
<li>Excellent laboratory skills, including proficiency in pipetting, documentation, and procedure (clinical, sterile, or molecular, depending on the needs of the laboratory)</li>
<li>Ability to accurately convert measurements as required</li>
<li>Ability to understand protocols, clarify as needed, and perform protocols with consistency, as demonstrated through previous laboratory experience</li>
<li>Ability to operate basic equipment (thermal cycler, gel electrophoresis, tabletop centrifuge, etc.) and troubleshoot basic problems</li>
<li>While not required, experience with mammalian cell culture is preferred</li>
</ul>
Physical Demands/Environmental Factors/Mental Functions
ADA Requirements – The physical demands, work environment factors, and mental functions described below are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Disclaimer - All job requirements are subject to possible revision to reflect changes in the position requirements or to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a threat or risk to the health and safety of themselves or other employees. This job description in no way states or implies that these are the only duties which will be required in this position. Employees will be required to follow other job-related duties as requested by their supervisor/manager (within guidelines and compliance with Federal and State Laws). Continued employment remains on an "at-will" basis.
Physical Demands
<ul>
<li>Must be able to remain in a stationary position (sit or stand) for prolonged periods (50% of the time).</li>
<li>Frequently moving between work areas.</li>
<li>Frequently moving, transporting, and positioning materials up to 30 pounds.</li>
<li>Vision abilities required by this job include close vision, distance vision, and depth perception.</li>
<li>Frequent operation of common office equipment (e.g. computers, mobile devices, calculators, copiers, scanners) and laboratory equipment.</li>
<li>Frequently position self (e.g. stoop, crouch, crawl, bend) and pull/push, grasp/squeeze, wrist flexion/extension, reach to operate and maintain laboratory equipment.</li>
</ul>
Environmental Factors
<ul>
<li>Exposure to chemical, mechanical and electrical hazards, and hazardous physical substances and fumes, and airborne particles.</li>
<li>Noise level in the work environment is usually moderate.</li>
</ul>
Mental Functions
<ul>
<li>Continuous mental and visual attention, requiring sustained attention and observation.</li>
<li>Excellent fine motor skills and hand control in order to pipette accurately. </li>
<li>Ability to sustain focus during research procedures (to maintain protocol such as order of operations). </li>
<li>Ability to visually observe results and record outcomes on lab logs and/or PC.</li>
<li>Extensive documentation skills, good attention to detail, and exceptional organizational skills are required.</li>
<li>Communicate effectively, both orally and in writing, in the English language.</li>
<li>Requires the ability to adapt to change efficiently.</li>
<li>Ability to independently lead and conduct research, and to evaluate, interpret and present complex scientific data.</li>
<li>Capacity to work productively within functionally diverse teams as well as collaborate with external investigators and partners in academic and industrial settings.</li>
<li>Ability to prioritize issues and use sound judgment to recognize when additional consultation and/or help is needed.</li>
<li>Comfortable working on multiple projects at one time.</li>
<li>Strong logical thinking and deduction skills.</li>
<li>Ability to effectively present ideas and information in a variety of formats to a wide range of audiences.</li>
<li>Positive, flexible, and professional attitude.</li>
</ul>
It is the policy of HudsonAlpha Institute for Biotechnology, in accordance with all applicable laws, to recruit, hire, train, and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, disability, genetic information, sexual orientation, veteran status, or any other basis prohibited by applicable law.
 Job Posted by ApplicantPro

HudsonAlpha - Research Associate II - Myers Lab

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology AnalystJob Description
The Microbiology Laboratory Analyst II/III or Senior Analyst will be a vital part of the team, contributing to both general and complex laboratory testing, sample management, and laboratory maintenance. The role involves collaborating with the team to achieve the goals of the Microbiology Services Department, as well as performing both routine and non-routine laboratory duties.
Responsibilities
<ul>
<li>Perform microbiological tests in strict accordance with SOPs, cGMP, cGLP, USP, EP, ISO/IEC, and other applicable regulatory requirements.</li>
<li>Conduct cleaning and disinfection validations, both manual and automated.</li>
<li>Execute Container Closure Integrity Tests (CCIT) and Package Integrity Evaluations.</li>
<li>Perform custom studies and additional testing as per client requests.</li>
<li>Engage in method development, modification, verification, and assist with method validation testing.</li>
<li>Participate in method transfer activities and suitability studies under leadership guidance.</li>
<li>Support Quality Management System investigations for non-conformance or out-of-specification results.</li>
<li>Complete assigned CAPA tasks and change controls.</li>
<li>Maintain laboratory cleanliness, safety, and compliance with cGMP standards.</li>
<li>Conduct regular inventory of reagents, consumables, and materials.</li>
<li>Prepare in-house reagents, stock solutions, media, and microbial suspensions.</li>
<li>Perform biowaste autoclave sterilization cycles and other laboratory housekeeping tasks.</li>
<li>Maintain accurate and complete test records.</li>
<li>Ensure audit readiness at all times.</li>
<li>Deliver results within predetermined turnaround times (TAT) with accuracy.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in aseptic technique.</li>
<li>Experience with cleaning and disinfection validation.</li>
<li>Strong knowledge of GMP and GLP standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS/BA in Biology, Pharmaceutical Sciences, Biotechnology or equivalent, with a preference for a Microbiology degree and 2+ years of relevant experience in microbiology.</li>
<li>Associate degree in a related scientific discipline with 5+ years of experience in a microbiology or related laboratory.</li>
<li>High school diploma with 7+ years of experience in a microbiology or related scientific laboratory.</li>
<li>2+ years of GMP/GLP laboratory or FDA experience is required.</li>
<li>Additional training certifications and self-learning are advantageous.</li>
</ul>
Work Environment
The role requires the ability to lift up to 30 pounds and stand for extensive periods (up to 6 hours). Ergonomics will be utilized to perform repetitive motion tasks with hands and arms. The position involves working in a BSC/LAF and at the lab bench for most of the day (up to 8 hours). Candidates must be able to tolerate the smell of Gram-negative organisms and laboratory disinfectants, and work safely with Biosafety Level II (BSL II) microorganisms and bloodborne pathogens. Proficiency in navigating computer systems is required. Flexibility to work off shift hours and weekends when needed is essential.
Job Type &amp; Location
This is a Contract to Hire position based out of Hercules, CA.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/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 Hercules,CA.
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.

Microbiology Analyst

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
The Laboratory Associate is primarily responsible for the support and upkeep of R&amp;D laboratories based in Austin, TX. The scope of support includes inventory management, supply ordering and tracking, Clinical Sample ordering and tracking, vendor communication, laboratory safety checks and audits, corrective actions, and communication with various R&amp;D teams as needed. The Laboratory Associate is also responsible for assisting equipment support personnel with critical tasks such as equipment installation, calibration, maintenance, repair, and daily laboratory checks as needed.
PRIMARY RESPONSIBILITIES: 
<ul>
<li>Track Laboratory Support Requests using established systems, regularly update requestors and ensure timely request resolutions</li>
<li>Clear and effective communication with R&amp;D teams to ensure requests are adequately resolved</li>
<li>Communicate with vendors to obtain price quotes, equipment demonstrations, equipment deliveries, order updates, tracking information etc</li>
<li>Submit purchase requests using established systems and track purchases through delivery to the requestor</li>
<li>Conduct regular inventory checks of laboratory spaces to ensure adequate supplies are available</li>
<li>Perform regular safety checks of the laboratory spaces and monitor chemical and biohazardous waste streams in accordance with environmental health and safety requirements</li>
<li>Contribute to laboratory safety newsletters</li>
<li>Assist with regular safety audits and perform corrective actions as needed</li>
<li>Handle shipping and receiving of materials, chemicals and equipment in compliance with safety and regulatory standards</li>
<li>Provide feedback on lab processes, suggesting improvements for efficiency, safety, and cost-effectiveness</li>
<li>Assist with instrument installations and qualifications per equipment protocols as needed</li>
<li>Perform routine equipment maintenance procedures as needed</li>
<li>Perform routine laboratory equipment checks as needed</li>
</ul>
QUALIFICATIONS:
<ul>
<li>BS/BA in biomedical engineering, biological sciences or related fields</li>
<li>Industry-related experience, especially in supporting laboratories, preferred</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES: 
<ul>
<li>Excellent communication (verbal and written) and interpersonal skills</li>
<li>Excellent attention to detail, organization, and accuracy</li>
<li>Excellent adaptability in a fast-changing environment</li>
<li>Self-motivated</li>
<li>Ability to work independently and as part of a team</li>
<li>Maintain a high level of professionalism and responsibility</li>
<li>Comply with company policies</li>
</ul>
PREFERRED SKILLS: 
<ul>
<li>Inventory management skills</li>
<li>Customer Service skills</li>
<li>Experience working in BSLI and BSLII laboratories as well as familiarity with Biosafety requirements and guidelines as established by applicable regulatory bodies such as OSHA and CDC</li>
<li>Familiar with DNA Isolation and Purification, PCR, Cell Culture, Next Generation Sequencing, etc</li>
<li>Familiar with LIMS</li>
</ul>
PHYSICAL DEMANDS &amp; WORK ENVIRONMENT: 
<ul>
<li>Duties are typically performed in an office and/or laboratory setting</li>
<li>This position requires the ability to use a computer keyboard, communicate over the telephone and read printed material</li>
<li>Ability to lift 40lbs</li>
<li>This position requires the ability to squat, bend, and reach</li>
<li>Duties may occasionally require working outside normal working hours (evenings and weekends)</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$19.52—$25 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

Lab Associate

<h3>Job Description</h3>
Job Description
Summary of Position: 
Under limited supervision, this role leads the formula design, validation and implementation of new products, line extensions, product improvements and cost savings initiatives. This role will also serve as technical assistance to the manufacturing sites and supervisor. 

Essentials for the Role: 
<ul>
<li>Self-directed, independent contributor applying technical skills in problem resolution and execution of development from bench to production scale for new products and product improvements</li>
<li>Lead higher-level technically complex projects and contribute through cross-functional team to execute (Operations, QA, Procurement, Sales, etc.)</li>
<li>Ability to understand manufacturing processes and their implications on formula development </li>
<li>Strong written and verbal communication skills that allow for flexible interactions with R&amp;D, Operations, Food Safety and Business team members </li>
<li>Highly engaged in the organization’s commercialization processes</li>
<li>Independently seek out, apply and share knowledge of competitive activities, industry trends and emerging technology</li>
<li>Utilize technical knowledge to mentor others and drive increased technical depth across the R&amp;D organization</li>
<li>Subject Matter Expert who contributes significantly, directly, and continually to attain results through the generation and application of advanced, specialized knowledge in functional ingredients that drive performance and claims</li>
<li>Identify problems and drive cross-functional exploration to determine root cause with a focus on developing corrective action; apply corrective action to future projects to reduce repeat problem resurrection</li>
<li>Understand and apply product requirements, plant equipment capabilities and processes to drive technology across businesses in problem resolution</li>
<li>Identify and develop research programs to drive cost optimization through formulation and processing efficiencies</li>
</ul>
Important Details: The duties and responsibilities described are not a comprehensive list of all tasks. Additional tasks and duties may be assigned from time to time as necessitated by business needs. 
You’ll fit right in if you have: 
<ul>
<li>Bachelor’s Degree Required: Food Science, Engineering, Chemistry or related field</li>
<li>7 - 10 years of technical experience in industry</li>
<li>Technical knowledge and leadership in baking, dough and/or griddle products formulations and associated technologies </li>
<li>Ability and desire to lead and educate others in technical activities such as formulation and experimental design</li>
<li>Ability to communicate effectively and openly while working with a cross-functional team</li>
<li>Must be a self-starter, independent, organized, energetic, and resourceful</li>
<li>Excellent written and verbal communications skills</li>
<li>Aptitude for technical leadership and project management</li>
<li>Invests time and effort in professional development and supporting customer-centric culture.</li>
</ul>

Work Environment: 
This job operates in a professional manufacturing and R&amp;D lab environment. Must be able to conduct themselves accordingly. Lab hygiene and Good Manufacturing Practices (GMPs) must be followed. 

Physical Demands: 
Role is a hybrid of computer-based work and lab/product development-based work. May require lifting boxes of up to 40 lbs. The physical demands described here are representative of those that must be met by the employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. 

Expected Work Hours: 
This is a full-time position. The employee must be available during “core” business hours between 8:00-5:00 pm, Monday through Friday. 

Travel: 
25 – 35% Headquarters in TN and 3 Manufacturing Facilities in PA 

Equal Employment Opportunity: 
MBC Companies is committed to providing equal opportunity for all employees and applicants without regard to race, color, religion, national origin, sex, age, marital status, sexual orientation, disability, political affiliation, personal appearance, family responsibilities, matriculation, or any other characteristic protected under federal, state, or local law. Each person is evaluated on the basis of personal skill and merit. MBC Companies’ policy regarding equal employment opportunity applies to all aspects of employment including recruitment, hiring, job assignments and promotions, working conditions, scheduling, educational and recreational programs.

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