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<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Operator
Job Description
The operator will be responsible for monitoring computer software sensors throughout the facility and recording any variances in readings. This role is essential in a company dedicated to producing ethanol from recycled products.
Responsibilities
<ul>
<li>Monitor computer software sensors throughout the facility.</li>
<li>Record readings and note any variances on an hourly basis.</li>
<li>Monitor and adjust liquid and steam levels for efficient operation.</li>
<li>Monitor the pH levels of wastewater discharge and record test results.</li>
<li>Safely start, monitor, and shut down the Evaporation System.</li>
<li>React to abnormal conditions, breakdowns, and emergencies.</li>
<li>Unload and load tanker trucks, railcars, syrup trucks, totes, barrels, and kegs.</li>
<li>Submit work orders for equipment and facilities requiring maintenance.</li>
</ul>
Essential Skills
<ul>
<li>Experience in production and machine operation.</li>
<li>Proficiency in computer operation for monitoring production activities and sensors.</li>
<li>Knowledge of chemical mixing and general labor tasks.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in a production environment is advantageous.</li>
<li>Capability to handle emergency situations effectively.</li>
</ul>
Why Work Here?
Join a small manufacturing company located in the heart of Louisville. Enjoy the opportunity to work in a dynamic environment with a supportive team on a night shift schedule of 7p-7a, following a 2-2-3 rotation.
Work Environment
Work in a non-temperature controlled distilling environment, which is non-unionized. Safety gear such as steel-toed boots, safety glasses, and a hard hat are required when in the production area. Most tasks will be completed in an office setting.
Job Type &amp; Location
This is a Permanent position based out of Louisville, Kentucky.
Pay and Benefits
The pay range for this position is $41600.00 - $45760.00/yr.
Healthcare benefits Dental benefits Vision benefits Retirement benefits 401k Vacation
Workplace Type
This is a fully onsite position in Louisville,KY.
Application Deadline
This position is anticipated to close on Sep 22, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Chemical Operator

<h3>Job Description</h3>
Job Description
Job Title: Microbiology Lab Technician
Job Description
We are seeking a skilled Microbiology Lab Technician to perform Bioburden testing on medical device products and support the Microbiology team. This role involves media preparation and sterilization using aseptic techniques during sample preparation. The technician will recognize malfunctions in laboratory equipment and either notify management or perform simple repairs, along with conducting preventative maintenance and laboratory housekeeping. Adhering to procedures related to data documentation, laboratory safety, and good laboratory practices is crucial. The role also includes LAL testing and training on USP 61 and USP 62.
Responsibilities
<ul>
<li>Conduct Bioburden testing on medical device products.</li>
<li>Support the Microbiology team in daily operations.</li>
<li>Prepare and sterilize media utilizing aseptic techniques.</li>
<li>Recognize and address malfunctions in laboratory equipment.</li>
<li>Perform preventative maintenance and housekeeping in the laboratory.</li>
<li>Follow protocols for data documentation, laboratory safety, and good laboratory practices.</li>
<li>Perform LAL testing and undergo training on USP 61 and USP 62.</li>
</ul>
Work Environment
Join a dynamic Bio department with approximately 20 team members. The labs, while separated, collaborate closely with R&amp;D and Chemistry labs, ensuring a clean and efficient work environment. The position is for the 2nd shift, Monday through Friday, from 3 pm to 12 am. Benefit from working in a brand-new 74,000 square foot lab that fosters teamwork among Micro, R&amp;D, Chemistry, Design and Verification, Calibrations, and Stability Lab teams. Enjoy quarterly team outings and be part of a tight-knit group with ample opportunities for growth and advancement.
Pay and Benefits
The pay range for this position is $22.00 - $26.00/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 Mundelein,IL.
Application Deadline
This position is anticipated to close on Sep 18, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Microbiology Lab Technician

<h3>Job Description</h3>
Job DescriptionJob Title: Associate Scientist
Job Description
The Associate Scientist processes clinical samples and conducts validation/verification studies of Next Generation Sequencing (NGS)-based molecular assays within specific turnaround times.
Responsibilities
<ul>
<li>Serve as a technical contributor for the Molecular/NGS laboratory and perform clinical tasks with precision.</li>
<li>Prepare and isolate nucleic acids from oncology specimens, such as DNA/RNA extraction from FFPE tissues and blood samples.</li>
<li>Operate complex laboratory equipment, including high throughput liquid handlers and Illumina sequencers (NovaSeq6000), and perform instrument maintenance procedures.</li>
<li>Review and troubleshoot NGS sequencing runs.</li>
<li>Evaluate and implement new NGS technologies.</li>
<li>Demonstrate and execute excellent laboratory best practices and troubleshooting principles.</li>
<li>Support the timely processing and reporting of oncology samples to internal and external collaborators.</li>
<li>Pay attention to detail and precisely follow instrument and assay SOPs.</li>
<li>Maintain detailed notes of experimental parameters with proper documentation.</li>
<li>Independently perform lab procedures with minimal supervision.</li>
<li>Prepare reports and presentations to communicate results in group meetings.</li>
<li>Support FDA, NYS DOH, CAP/CLIA, and other regulatory agency inspections.</li>
<li>Provide support and contribute to QC and QA activities as needed.</li>
<li>Participate in training sessions and workshops.</li>
<li>Collaborate with MDs and Molecular Pathologists.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of experience in molecular diagnostics and/or high throughput clinical laboratories.</li>
<li>Experience working with typical oncology specimens, including Formalin-fixed (FFPE) tissue samples and blood in clinical and/or high-volume molecular diagnostics settings.</li>
<li>Demonstrated understanding of molecular biology techniques and best troubleshooting principles.</li>
<li>Experience with clinical oncology NGS assays, including DNA and RNA-seq (TSO500, MSK, etc.), WES protocols, and various target-enrichment approaches.</li>
<li>Experience working in CAP/CLIA regulatory environments, WA state requirements, and HIPAA regulations, with an understanding of the importance of patient data privacy.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with Clarity LIMS/LabVantage software is preferred.</li>
<li>Technologist in Molecular Biology, MB(ASCP) certification is preferred.</li>
</ul>
Work Environment
The work environment involves handling complex laboratory equipment and working with oncology specimens. The role requires adherence to CAP/CLIA regulatory standards and patient data privacy regulations. There is a focus on precision, thorough documentation, and collaboration with medical professionals.
Job Type &amp; Location
This is a Contract position based out of Bothell, Washington.
Pay and Benefits
The pay range for this position is $45.00 - $60.00/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 Bothell,WA.
Application Deadline
This position is anticipated to close on Sep 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Description:&nbsp;
The Biologics CMC Development team at AbbVie in the Bay Area has a long and rich history of biologics development.&nbsp;&nbsp; Located in a new state of the art facility in South San Francisco, the team leverages its comprehensive end-to-end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing complex biologic therapies, such as bi-specifics and novel modalities, to human clinical studies and eventual licensure.&nbsp;
The Cell Line Development Group in South San Francisco, CA is seeking an Associate Scientist II to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position the candidate will perform hands-on CHO cell line development for pipeline assets and support the establishment of automation capabilities in the group to increase throughput. The successful candidate will contribute to the evaluation and implementation of an automated liquid handler for cell culture workflows.
Key Responsibilities:
<ul>
<li>Perform CHO cell line development, including transfection, selection, single cell subcloning, growth and productivity screening, cell banking and stability assessment of cell banks.</li>
<li>Support the evaluation and implementation of liquid handlers like Tecan, Biomek or Hamilton for cell culture workflows.</li>
<li>Culture mammalian cells across multiple scales and formats, from 96-well plates up to shake flasks.</li>
<li>Operate instruments like ViCell automated cell counter, Octet, Clone Select Imager, microscope, HPLC, Ambr®15, Beacon, SONY flow cytometer and liquid handlers (Tecan, Biomek and Hamilton). Share responsibility for equipment maintenance.</li>
<li>Co-author cell line development technical reports that meet expectations of regulatory agencies for all stages from IND to BLA.&nbsp;</li>
<li>&nbsp;Collaborate closely with cell culture, purification, analytical and formulation development colleagues to meet project timelines.</li>
<li>Actively support opportunities to execute improvements to the cell line development workflow, including automation, assessment of new technologies and equipment.&nbsp;</li>
<li>May generate data for internal or external conferences or consortia.&nbsp;</li>
<li>Display effective organization, verbal and written communication skills, and adherence to good documentation practices.</li>
</ul>
Qualifications 
Required:
<ul>
<li>Associate Scientist II: BS with a minimum of 3 years or MS with no minimum of experience</li>
<li>Proficient in aseptic mammalian cell culture techniques. Understanding of cell biology and bioprocess engineering concepts.</li>
</ul>
<ul>
<li>Familiarity with lab automation. Prior experience in scripting, operating and troubleshooting liquid handlers like Tecan, Biomek and Hamilton for automated, high throughput cell culture activities.</li>
<li>Previous experience developing automated high throughput solutions in cell line development or cell culture process development to improve process efficiency.</li>
<li>Must enjoy a hands-on laboratory-focused role in a CMC multidisciplinary team with&nbsp;excellent attention to detail and detailed daily record keeping proficiency.</li>
<li>Demonstrated ability to independently generate precise, reliable and reproducible data promptly.</li>
<li>Demonstrated ability to learn, understand and master new experimental techniques.</li>
<li>Demonstrated ability&nbsp;to work collaboratively within and outside of&nbsp;the&nbsp;group.</li>
<li>Demonstrated ability&nbsp;to co-author technical reports&nbsp;and presentations.</li>
<li>Proficient with Microsoft Office software and able to learn new software applications for frequently used instruments like, Beacon, CSI, Sony MA900, Octet analyzer software. Able to multi-task and work within timelines.</li>
<li>Strong communication skills – verbal, written, scientific data presentation.</li>
</ul>
Preferred:
<ul>
<li>Programming/data science languages skills, such as R, Python, and SQL.</li>
<li>Prior experience performing statistical analysis and visualization using JMP, SIMCA, Spotfire and Power BI.</li>
<li>Experience handling ambr15 operation, Beacon and flow sorter</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist II - Cell Line Development

<h3>Job Description</h3>
Job Description
The position of Research Scientist, Filtration Product Development is a team member responsible for aspects of the design and development of new polymeric membranes for Life Science markets. This may include working with a team of membrane scientists to develop new generation of hollow fiber membranes and taking sole responsibility for membrane characterization (water flux, porometry, etc.), as well as performance testing. General Responsibilities include, but are not limited to, the following: Study and understand requirements for CTQs of membranes used in bioprocess, execute membrane testing (morphology and performance), plan and execute scaled-down filtration applications. Effectively lead research projects within R&amp;D, including proper planning, daily benchwork, control and completion. Maintain detailed and accurate records of all experiments and graph all relevant trend data along with the appropriate controls. Maintain all instruments and equipment in excellent condition, keep all work areas neat and clean, and follow all safety procedures without exception. Perform other functions required for the development and/or support of new products, as required.
QUALIFICATIONS: BS or equivalent in Biochemistry/biology/chemistry or related field (MS or PhD preferred) with min. 3 years focus on bioprocess. Previous exposure to characterization of membranes with respect to separation characteristics, pore size, both in direct and/or tangential flow applications is highly desired. Experience with cell culture, small scale bioreactors, filtration, and analytical techniques is required. Ability to analyze data, interpret results, and make informed decisions based on experimental data. Able to rapidly refine tech/marketing info through literature reading and form ideas/protocols to present to team. Excellent working knowledge of current instrumentation, robotics, and automation is desired. Strong ability to think outside the box and apply your skills creatively to solve problems. Outgoing personality with excellent English. Able to work independently with minimum supervision.
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Research Scientist - Filtration & Product Development

<h3>Job Description</h3>
JOB SUMMARY
*Cytology experience needed (Big plus if they have experience keeping up with regulations surrounding Cytology.)
Shift Mon-Fri 8a-5p
The Manager of Lab supervises technical and support personnel while overseeing the daily the operations of the Laboratory. This includes ensuring that regulatory requirements are met, monitoring test systems to ensure they are in control, and supervising staff, including all activities relative to work assignments, hiring/termination, performance reviews, orientation, and professional development.
ESSENTIAL FUNCTIONS OF THE ROLE
<ul>
<li>Manages the daily functions of the laboratory to ensure it runs efficiently. Performs all delegated functions as defined by facility CLIA Director.</li>
<li>Prepares schedules, coordinates job assignments, and monitors personnel including the selection, orientation, training, assignments, evaluations, discipline, and discharge of employees.</li>
<li>Ensures staff has the necessary training, experience, and competencies required to perform their duties by coordinating continuing education and providing in-services and orientations.</li>
<li>Maintains appropriate personnel and patient records in accordance with established policies and procedures.</li>
<li>Assist with budgeting, provides information about supplies, personnel, and equipment, seeks avenues of cost containment, and plans long-term purchases or capital equipment.</li>
<li>Establishes and implements quality assurance programs and maintains standards and records that document compliance with regulatory agencies.</li>
<li>Ensures the review of all quality control, proficiency testing, instrument maintenance, and quality assurance records, and any associated corrective action.</li>
<li>Provides input/support in the selection/purchase of capital equipment and the development of yearly budgets.</li>
</ul>
KEY SUCCESS FACTORS
<ul>
<li>Knowledge of laboratory regulations, protocols and procedures.</li>
<li>Statistical and critical thinking abilities.</li>
<li>Ability to comprehend and communicate instructions.</li>
<li>Ability to perform laboratory protocols and procedures.</li>
<li>Knowledge of safety and infection control standards.</li>
<li>Ability to work in a team environment.</li>
<li>Provides training and opportunities for continuing education.</li>
<li>Ability to make operational choices around how work gets done quality and productivity standards, measurable goals for employees and project teams, etc.</li>
<li>Ability to use broader targets to regulate how best to use resources to meet schedules and goals.</li>
<li>Ability to make or approve effective hiring and termination judgments.</li>
<li>Ability to evaluate and recommend changes to policies, and establish procedures that affect the managed organization.</li>
<li>Basic business knowledge, including but not limited to: annual planning and goal setting, adherence to budgets, employee compensation, compliance and risk management.</li>
<li>General computer skills, including but not limited to: Microsoft Office, information security, scheduling and payroll systems, electronic medical documentation, and email.</li>
</ul>
BENEFITS
Our competitive benefits package includes the following
<ul>
<li>Immediate eligibility for health and welfare benefits</li>
<li>401(k) savings plan with dollar-for-dollar match up to 5%</li>
<li>Tuition Reimbursement</li>
<li>PTO accrual beginning Day 1</li>
</ul>
Note: Benefits may vary based upon position type and/or level
QUALIFICATIONS
\n\n
<ul>\n\t
<li>EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification</li>
\n\t
<li>EXPERIENCE - 4 Years of Experience</li>
\n\t
<li>CERTIFICATION/LICENSE/REGISTRATION -</li>
\n</ul>
\n\n
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;ASCP-BloodBanking Technologist (ASCP-BB), ASCP-Chemistry Technologist (ASCP-C), ASCP-Cytogenetics Technologist (ASCP-CG), ASCP-Cytologist (ASCP-CT), ASCP-Hematology Technologist (ASCP-H), ASCP-Microbiology Technologist (ASCP-M), Molecular Biology Technologist (ASCP-MB), ASCP-Pathologist Asst (ASCP-PA), ASCP-Blood Banking Specialist (ASCP-SBB), ASCP-Chemistry Specialist (ASCP-SC), ASCP-Hematology Specialist (ASCP-SH), ASCP-Microbiology Specialist (ASCP-SM): Must have ONE of the following:
\n\n
<ul>\n\t
<li>ASCP-BB</li>
\n\t
<li>ASCP-C</li>
\n\t
<li>ASCP-CG</li>
\n\t
<li>ASCP-CT</li>
\n\t
<li>ASCP-H</li>
\n\t
<li>ASCP-M</li>
\n\t
<li>ASCP-MB</li>
\n\t
<li>ASCP-PA</li>
\n\t
<li>ASCP-SBB</li>
\n\t
<li>ASCP-SC</li>
\n\t
<li>ASCP-SH</li>
\n\t
<li>ASCP-SM</li>
\n\t
<li>CHS-ABHI</li>
\n\t
<li>CHT-ABHI</li>
\n\t
<li>CLS</li>
\n\t
<li>MLS</li>
\n\t
<li>MT</li>
\n\t
<li>SCT</li>
\n\t
<li>SCYM</li>
\n\t
<li>SMB.</li>
\n</ul>
\n\n
 \n&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Cert Histocompatibility Spec (CHS-ABHI), Cert Histocompatibility Techno (CHT-ABHI), Clinical Laboratory Scientist (CLS), Medical Laboratory Scientist (MLS), Medical Technologist (MT), Specialist in Cytology-ASCP (SCT), Specialist in Cytometry-ASCP (SCYM), Molecular Biology Spec-ASCP (SMB): . \n&nbsp;

Cytopathology/Lab Manager

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist
Job Description
As a Quality Control Chemist, you will play a crucial role in analyzing raw materials, intermediates, and finished products through routine and non-routine analysis using advanced techniques such as GC and HPLC. You will prepare samples, standards, and reagents, ensuring accuracy and compliance with established procedures and regulatory requirements.
Responsibilities
<ul>
<li>Conduct routine and non-routine analysis of raw materials, intermediates, and finished products using GC and HPLC.</li>
<li>Prepare samples, standards, and reagents according to established procedures.</li>
<li>Interpret and document analytical results accurately and timely.</li>
<li>Maintain and calibrate laboratory instruments and equipment.</li>
<li>Ensure compliance with internal SOPs, GMP, and regulatory requirements.</li>
<li>Assist in method development and validation as needed.</li>
<li>Collaborate with cross-functional teams to support production and R&amp;D.</li>
<li>Maintain a clean and organized laboratory environment.</li>
<li>Participate in investigations of out-of-specification results and deviations.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in laboratory techniques and material handling.</li>
<li>Experience with quality assurance, inventory control, and sampling.</li>
<li>Basic QC testing and quality control skills.</li>
<li>Knowledge of chemistry, UV/Vis, gas chromatography, refractive index, specific gravity, total alcohol, total aldehyde, acid values.</li>
<li>Hands-on experience with GC and HPLC instrumentation and software (e.g., Agilent, Waters).</li>
<li>Strong understanding of analytical chemistry principles and GMP practices.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>AA degree in a science field or BS degree in Chemistry (Preferred).</li>
<li>Strong attention to detail and ability to learn unique processes.</li>
<li>Previous experience in a GMP food and beverage environment is a plus.</li>
<li>2 years of experience in a QC laboratory setting, preferably in the flavor, food, or pharmaceutical industry.</li>
</ul>
Work Environment
You will work alongside other chemists and flavorists in a lab setting, occasionally visiting the production floor as needed. The environment encourages collaboration and requires a strong understanding of GMP processes. This family-owned company offers a supportive work culture with benefits like raises upon permanent employment, company events such as softball games and holiday parties, and fun activities like Chic-Fil-A Days.
Job Type &amp; Location
This is a Contract to Hire position based out of Abingdon, Maryland.
Pay and Benefits
The pay range for this position is $23.00 - $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 Abingdon,MD.
Application Deadline
This position is anticipated to close on Sep 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
🚗 Why us? Your car and your home are the two most expensive things you’ll ever own — and the hardest to manage. At Jerry.ai, we’re building the first super app to help everyday Americans take control of both. From insurance and financing to repairs and real estate, we’re reimagining what it means to own and maintain your car and home. This is a $5 trillion+ problem — and we’re the only company tackling it end to end.
2024 was a milestone year for Jerry.ai. We delivered nearly 50% year-over-year revenue growth while reaching profitability for the first time in our history.
And we're just getting started! Our growth is driven by forward-thinking technology; Harvard Business Review covered the success of our chatbot less than a year after its launch and Jerry.ai is getting mentioned in many conversations about our use of GenAI, such as this Forbes article.
&amp;#x1F4BB; About the opportunity
We are looking for a Staff Applied Data Scientist (PhD) who is energized by working with a high caliber team and making a material difference in the lives of millions to join us! Reporting directly to our cofounder/CTO, you will architect and deploy advanced ML models with massive real-world applications (e.g. model &amp; predict user behavior, leverage LLMs and custom-built components to optimize our chatbot &amp; voicebot, etc). Come play a key role in helping us grow from 5M to 50M customers and become a $10B company in the next 4 years!
We have a fast-paced startup culture that empowers you to move quickly, test, iterate, and own projects end-to-end in an environment where your ideas matter and your impact is felt from day one. You’ll work with extremely talented and passionate engineers, data scientists, and analysts from companies like NVIDIA, Meta, Amazon, ByteDance, Square, Robinhood and more.
🫵 How you will make an impact
<ul>
<li>
Develop and architect complex machine learning models to address critical business challenges and drive company-wide strategic initiatives
</li>
<li>
Take ownership of the end-to-end modeling process, from initial ideation to model deployment and maintenance
</li>
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Conduct thorough data preparation and analysis to ensure the quality and relevance of input data for modeling tasks
</li>
<li>
Collaborate closely with cross-functional teams, including Product and Data Engineering to productize and deploy models into production systems
</li>
<li>
Contribute to large-scale company initiatives aimed at solving problems that haven’t yet been touched by anyone at Jerry.ai
</li>
</ul>
🚀 Requirements
<ul>
<li>
PhD in Physics or related field
</li>
<li>
5+ years of experience building and deploying models from scratch.
</li>
<li>
Deep understanding of machine learning algorithms and techniques, with experience in building and deploying models from scratch.
</li>
<li>
Strong analytical and problem-solving skills, with the ability to translate complex business requirements into practical modeling solutions.
</li>
<li>
Passion for real-world application of machine learning, with a desire to make a significant impact on large-scale business initiatives.
</li>
</ul>
While we appreciate your interest and application, only applicants under consideration will be contacted.
Jerry.ai is proud to be an Equal Employment Opportunity employer. We prohibit discrimination based on race, religion, color, national origin, sex, pregnancy, reproductive health decisions or related medical conditions, sexual orientation, gender identity, gender expression, age, veteran status, disability, genetic information, or other characteristics protected by applicable local, state or federal laws. 
Jerry.ai is committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation due to a disability, please contact us at <a href="mailto:recruiting@jerry.ai" target="_blank">recruiting@jerry.ai</a>
The successful candidate’s starting pay will fall within the pay range listed on this job posting, determined based on job-related factors including, but not limited to, skills, experience, qualifications, work location, and market conditions. Ranges are market-dependent and may be modified in the future. In addition to base salary, the compensation may include opportunities for equity grants. 
We offer a comprehensive benefits package to regular employees, including health, dental, and vision coverage, paid time off, paid parental leave, 401(K) plan with employer matching, and wellness benefits, among others. Equity opportunities may also be part of your total rewards package. Part-time, contract, or freelance roles may not be eligible for certain benefits.
About Jerry.ai:
Jerry.ai is America’s first and only super app to radically simplify car ownership. We are redefining how people manage owning a car, one of their most expensive and time-consuming assets.&nbsp;
Backed by artificial intelligence and machine learning, Jerry.ai simplifies and automates owning and maintaining a car while providing personalized services for all car owners' needs. We spend every day innovating and improving our AI-powered app to provide the best possible experience for our customers. From car insurance and financing to maintenance and safety, Jerry.ai does it all.
We are the #1 rated and most downloaded app in our category with a 4.7 star rating in the App Store. We have more than 5 million customers — and we’re just getting started.&nbsp;
Jerry.ai was founded in 2017 by serial entrepreneurs and has raised more than $240 million in financing.
Join our team and work with passionate, curious and egoless people who love solving real-world problems. Help us build a revolutionary product that’s disrupting a massive market.

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