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<h3>Job Description</h3>
Job Title: Biologist (3-5 years)
Location: Boston, MA 02210
Duration: 6-month term to begin with, and then extend for another 12-month
 
Qualifications:
Required:
1. MSc with 3+ years, or PhD with 0+ years of relevant experience in a scientific discipline such as molecular/cell biology, genetics, virology, or related field (same as "Education" section below)
2. Proficiency in cell culture and molecular biology techniques (transfection, molecular cloning)
Preferred: Knowledge or preferably experience in AAV and/or baculovirus
 
Responsibilities:
Drive the viral vector process to deliver internal productions of recombinant AAVs and baculoviruses
Design and execute molecular/cellular experiments, including PCR techniques and cell culture, to support bioprocess sample testing to guide the process optimization
Manage experimental workflows and vector inventory through electronic lab notebook documentation of experimental data, protocols, and reports
Assist in the group efforts on vector expression system upgrade, cell line development and characterization, and AAV capsids
 
Comments/Special Instructions
The Start and End dates are flexible. I would like a 6-month term to begin with, and then extend for another 12-month if the contractor worker is capable for the work and fits in the team.

Biologist

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Production TechnicianJob Description
As a Chemical Production Technician, your role will involve processing raw materials and chemicals following a batch record to mix the correct chemicals to create the final product. You will utilize various machines to measure the amount of raw material, take samples for lab quality testing, and operate a crane to lift large chemical bags. This is a physical role requiring you to climb stairs to reach the top of tanks and use computer skills to monitor and control tank levels. You will be suited in a full uniform and respirator mask due to chemical exposure and must be open to performing other work-related duties as assigned.
Responsibilities
<ul>
<li>Read batch records and recipes; check balances to ensure the correct amount of raw material is added.</li>
<li>Measure chemicals of raw material to be added and use math skills for accuracy.</li>
<li>Operate machines for mixing raw materials and ensure proper chemical mixing and formulation.</li>
<li>Report with attention to detail and follow instructions while working independently.</li>
<li>Exhibit physical strength for lifting or moving up to 50 pounds.</li>
</ul>
Essential Skills
<ul>
<li>Experience in machine operation, utility technician, and production technician roles.</li>
<li>Proficiency in quality control, scale operation, and measurement equipment.</li>
<li>Ability to work with formulation and chemical mixing processes.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma or GED.</li>
<li>2-4 years of manufacturing experience preferred.</li>
<li>Ability to take initiative, learn, and collaborate with a team.</li>
</ul>
Why Work Here?
Our family-like atmosphere creates a positive work environment where employees feel comfort and compassion from their leader and team. Our culture is centered on core values: Responsive, Attitude, Proactive, Integrity, Dependability, and Safety. We are committed to creating a diverse and inclusive work environment where all employees feel valued and have the opportunity to succeed. The Des Moines site has grown immensely in the last 5 years, adding multiple buildings to the plant while maintaining a family-like culture.
Work Environment
This is a fully on-site position within a manufacturing facility in Des Moines, Iowa. You will be working in a shift of 2nd shift from Monday to Friday, starting between 2pm to 4pm for 8hr/10hr shifts. The environment includes a chemical plant, with exposure to moving equipment, mechanical parts, fumes, airborne particles, chemicals, and biological hazards. Dress code includes uniforms, steel-toed boots, hair nets, and showering after the shift.
Job Type &amp; Location
This is a Contract to Hire position based out of Des Moines, IA.
Pay and Benefits
The pay range for this position is $21.00 - $22.00/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 Des Moines,IA.
Application Deadline
This position is anticipated to close on Feb 2, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Formulator

<h3>Job Description</h3>
Job DescriptionJob Title: In vivo Research Associate Location - Foster City, CA 94404 Duration:18 Months+ (Possible Extension) Pay Range: $45 - $50/hr. on w2 Description:
<ul>
<li>We are seeking a highly motivated In Vivo Research Associate to join our Oncology in vivo pharmacology team. </li>
<li>The selected candidate will provide in vivo study support for evaluating Client oncology therapeutics in pre-clinical models and will be responsible for daily in vivo study execution, data analysis and organization, as well as project team responsibilities. </li>
<li>A minor amount of scheduling flexibility, including off-shift and weekend, may be required.</li>
<li>The successful candidate will be proficient in murine handling techniques including various dosing routes (IV, IP, PO, RO, subcutaneous), in-life and terminal blood collection, and handling of tissues during necropsy and processing for ex vivo analysis. </li>
<li>The day-to-day responsibilities will include daily dosing, daily tumor measurements, tissue collections, and assisting with various aspects of study and facility maintenance.</li>
<li>In addition to daily hands-on lab responsibilities, the position will have project team responsibilities including attending meetings to determine appropriate study design, organization of data, and presentation of results.</li>
</ul>
 Qualifications &amp; Prior Experience:
<ul>
<li>MS or BS with a minimum of 2-3 years of post-graduate hands on experience or demonstrate equivalent work experience with murine models of cancer, inflammation and/or immunology</li>
<li>Strong biology background with understanding of basic pharmacology</li>
<li>Demonstrated ability to design, execute, and analyze experiments</li>
<li>Excellent organizational and communication skills, along with the ability to work effectively in a multidisciplinary team environment</li>
<li>Proficiency with MS suite including powerPoint, Excel, and word. Demonstrated ability to analyze and graph data using GraphPad prism or equivalent</li>
</ul>
 Additional Experience:
<ul>
<li>Experience with more advanced in vivo techniques: surgery, anesthesia</li>
<li>Experience with StudyLog data collection software is desired</li>
<li>Experience with tissue culture is desired</li>
<li>Experience with in vivo imaging is desired</li>
</ul>
 #sczr2

In vivo Research Associate

<h3>Job Description</h3>
Job DescriptionJob Title: R&amp;D Formulation Scientist - Soft GelJob Description
We are looking for an experienced R&amp;D Formulation Scientist specializing in soft gels to join our innovative team. You will partner closely with sales and customers to support product requirements and technical needs, develop formulations for various products, and collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency.
Responsibilities
<ul>
<li>Develop formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations.</li>
<li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li>
<li>Assist with analytical testing and quality assessments.</li>
<li>Perform hands-on work in the Product Development laboratory.</li>
<li>Utilize analytical instrumentation including GC, HPLC, and ICP-MS.</li>
<li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li>
<li>Work effectively with a predominantly Spanish-speaking laboratory team.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of R&amp;D formulation experience.</li>
<li>Bachelor's Degree in Food Science, Chemistry, or related field.</li>
<li>Expertise in soft gels.</li>
<li>Experience in the nutraceutical industry.</li>
<li>Skilled in HPLC, GC, and ICP.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bilingual skills are a plus.</li>
<li>Experience with raw materials and quality control.</li>
<li>Knowledge of analytical chemistry and fish oils.</li>
</ul>
Work Environment
The position will report to the Quality Director until a future R&amp;D Director is hired. Initially, there will be only two R&amp;D formulators on the team until the acquisition expands the team. The work schedule is Monday to Friday, 8 AM to 5 PM, 100% on-site. The dress code is business casual.
Job Type &amp; Location
This is a Permanent position based out of Clifton, NJ.
Pay and Benefits
The pay range for this position is $75000.00 - $90000.00/yr.
401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&amp;D department!
Workplace Type
This is a fully onsite position in Clifton,NJ.
Application Deadline
This position is anticipated to close on Jan 30, 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.

R&d Formulation Scientist - Soft Gel

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Location: Oceanside, CA 92056 Duration: 5 months+ (Possible Extension) Pay Rate: $42.00 - $48.50/Hour. on W2 Hours: Monday – Friday, 8 am – 5 pm Essential Duties and Job Functions:
<ul>
<li>Under general supervision, develops and validates bioassays to support biological drug development.</li>
<li>Plans and executes assigned experiments that support Process Development activities and project goals.</li>
<li>Proactively seeks out senior personnel to discuss potential solutions to problems.</li>
<li>Participates in group meetings to share test results.</li>
<li>Demonstrates ability to recognize anomalous and inconsistent results and interpret experimental outcomes.</li>
<li>Develops skills in data analysis and ability to evaluate quality of data.</li>
<li>Operates scientific equipment (Plate reader and Softmax software for ELISA, cell culture techniques), selects appropriate methods and techniques to perform experiments, and prepare related reports</li>
<li>Plans and organizes details of experiments with guidance.</li>
<li>Demonstrates good verbal communication skills and interpersonal skills to provide insight into the processes used to achieve results of assigned tasks.</li>
<li>Be able to work in a fast-paced and highly collaborative working environment.</li>
<li>Must have basic understanding of ELISA and cell based assays.</li>
<li>Responsible for data analysis using SoftMax Pro software and graphic display of data using Excel and Power Point presentation formats.</li>
</ul>
 Academic Level: BSc or MSc Knowledge, Experience and Skills:
<ul>
<li>2+ years of experience with BS degree in a relevant scientific discipline.</li>
<li>1+ years of experience with MS degree in a relevant scientific discipline.</li>
</ul>
 #sczr2

Research Associate

<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 
Purpose:
We are seeking a highly skilled Senior Scientist to join our Global Material and Parenteral Packaging Science team, a core component of Product Development Science &amp; Technology (PDS&amp;T). The successful candidate will help lead the development of Container Closure Systems (CCS) for novel parenteral and biotechnological products (NBEs), supporting the advancement of some of AbbVie’s most strategic pipeline assets, including monoclonal antibodies, antibody-drug conjugates, and therapeutic toxins.
In this role, you will be considered a subject matter expert (SME) in characterizing CCS—including vials, prefilled syringes, and prefilled cartridges—with an emphasis on Container Closure Integrity (CCI). You will lead the design and execution of novel scientific methods to critically evaluate container closure performance and integrity using force analyzers, developing and validating analytical methods, providing technical expertise for CCS qualification in pharmaceutical manufacturing, and evaluating and implementing cutting-edge CCI and characterization technologies.
<ul>
<li>Leverage deep technical expertise and available characterization data (force/torque, dimensional, material properties) to proactively identify, analyze and resolve key project hurdles and critical assumptions related to CCS design and integrity of new parenteral drug products, namely liquid drug preparations of biotechnological drugs in vials, pre-filled syringes and cartridges as well as lyophilizates.</li>
<li>Identify and seize opportunities to investigate and incorporate novel CCS materials, components, or integrity technologies that align with the long-term strategy and enhance product stability and manufacturability.&nbsp; This includes actively contributing to the technical evaluation and implementation of CCIT methods and continuous improvement based on a holistic CCI strategy aligned to current regulatory requirements.</li>
<li>Responsibility for development and validation of robust CCI methods according to GxP requirements, ensuring they are scientifically sound and fit-for-purpose across all phases of drug development.</li>
<li>Technical support of the continuous landscaping programs for innovative CCS, including hands-on implementation and comprehensive characterization based on various CCI techniques.</li>
<li>Initiate and drive strategic technical collaborations with AbbVie partner labs, external contract labs, and manufacturing sites to facilitate method transfer, technology adoption, and successful project delivery.</li>
<li>Coordination of external suppliers for materials, equipment, and contract services needed to perform work.</li>
<li>Authoring comprehensive, scientifically sound reports (e.g. lab reports, development reports or risk assessments) that could serve as critical source documents for authority submissions.&nbsp; Ensure all work is documented according to applicable GxP and internal procedural requirements.</li>
<li>Take responsibility for transferring ownership and maintaining lab equipment. Ensure required maintenance schedule, proper documentation, and training new users.</li>
<li>Mentoring and support for new colleagues and interns/contractors to build group expertise.</li>
<li>Presentation of project data as well as SME topics in internal global teams and effectively communicate technical conclusions and strategic recommendations.</li>
<li>Compliance with all relevant work safety requirements.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Degree from an accredited University in pharmacy/biology/biotechnology/chemistry/process engineering/material sciences/physics or related areas.</li>
<li>Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and typically 4 years of experience.</li>
<li>Possesses thorough technical and scientific understanding of parenteral drug product development and CCI test methods.</li>
<li>Understanding of relevant scientific literature and ability to apply theoretical framework to solving problems within their scientific discipline in a timely manner.</li>
<li>Scientific expertise in statistical data analysis</li>
<li>Knowledge of CAD/3D printing and/or µCT analysis is an advantage.</li>
<li>Ability to work concurrently on multiple projects, work in teams, and manage priority conflicts.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to establish comprehensive scientific and project related documentation.</li>
<li>Ability to communicate CCI strategies and content to broad audiences internally and externally.</li>
<li>Strong motivation and proactive approach to lab responsibilities</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education and typically 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Possess thorough theoretical and practical understanding of own scientific discipline.</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>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, I Global Material and Parenteral Packaging Sciences

<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 
The Toxins group within the Product Development, Science &amp; Technology (PDS&amp;T) - Biologics organization supports manufacturing, process validation, regulatory submission, and continuous improvement for late-stage and commercial manufacturing of biological toxin products at AbbVie. We have an exciting opportunity for a senior scientist I position based in Irvine, CA. This role involves leveraging scientific and bioengineering principles to develop bioassays for analytical testing at drug substance and drug product release and stability time points. The candidate must possess in-depth knowledge and hands-on experience in a range of techniques, including but not limited to molecular cloning, mammalian cell culture, PCR, Western blot, cell sorting, bioassay, microscopy, transfection, HPLC, and mass spectrometry. Moreover, excellent communication skills and the ability to thrive in a multi-disciplinary and cross-functional team environment are essential for success in this role.
Key responsibilities include:
<ul>
<li>Lead scientific initiatives by generating innovative technical ideas and strategic approaches to advance research objectives and overcome experimental challenges.</li>
<li>Demonstrate a strong understanding of project goals, aligning research activities with broader objectives and adapting experimental plans as needed based on new data, project developments, or shifting priorities.</li>
<li>Independently design, execute, and interpret complex experiments with rigorous methodology to ensure reproducibility and accurate data interpretation. Develop, optimize, and implement novel experimental protocols by leveraging emerging technologies to drive scientific progress and solve technical issues.</li>
<li>Maintain advanced, up-to-date expertise in relevant scientific and technical disciplines, applying this knowledge to experimental design, troubleshooting, method development, and integration of best practices from current literature.</li>
<li>Establish and manage clear experimental timelines, closely tracking progress and ensuring timely completion of project deliverables through strong organizational and time-management skills.</li>
<li>Deliver high-quality scientific communication by drafting and editing SOPs, technical reports, publications, presentations, and patent applications according to industry and regulatory standards. Effectively organize, analyze, and present scientific ideas and experimental data to cross-functional teams and stakeholders through impactful written and oral communications.</li>
</ul>
Qualifications 
<ul>
<li>Advanced degree in a relevant field: Ph.D. (with 6+ months biopharmaceutical industry experience preferred), Master’s degree (6+ years industry experience) and Bachler’s degree (8+ years industry experience) in Cell and Molecular Biology, Biochemistry, Biochemical or Biomedical Engineering, Biotechnology, , or closely related disciplines.</li>
<li>Robust research background in neuroscience, with direct expertise in neural cancer cell and primary cell culture, 3D cell models, and complex co-culture systems preferred. Demonstrated hands-on experience in developing and optimizing these models for scientific study or drug discovery applications.</li>
<li>Proficient in RNA microinjection for protein expression and functional evaluations, with a solid understanding of related molecular techniques. Also experienced in the generation of stable cell lines and the design and execution of novel cell-based assays.</li>
<li>Highly skilled in high-resolution imaging and live-cell imaging techniques, including advanced confocal microscopy, fluorescence-based assays, and related methodologies for monitoring cellular processes in real time.</li>
<li>Extensive laboratory experience with molecular cloning, mammalian cell culture, PCR, Western blotting, cell sorting, bioassays, advanced microscopy, transfection procedures, HPLC, and mass spectrometry.</li>
<li>Knowledgeable in genome editing approaches—including CRISPR/Cas9—with a thorough understanding of design, execution, and validation of gene editing experiments.</li>
<li>Previous GxP experience and attention to detail in documentation preferred.</li>
<li>Demonstrated proficiency in computer skills essential for scientific research, including word processing, spreadsheets, presentation software, and advanced data analysis. Capable of analyzing, interpreting, and presenting complex data sets using specialized scientific software (e.g., Python, R, JMP). Experience with laboratory automation platforms (such as Hamilton) is highly desirable.</li>
<li>Proven scientific leadership, demonstrated by being the main author on published research papers and holding patents. Skilled at designing experiments, solving problems creatively, developing thorough experimental plans, and independently troubleshooting and validating results.</li>
<li>Demonstrated ability to stay current with scientific advances, critically assess relevant literature, and quickly integrate emerging concepts and techniques into research projects.</li>
<li>Detail-oriented work style, with a proven record of delivering high-quality and reproducible data within tight timelines.</li>
<li>Strong interpersonal and collaborative skills, enabling effective teamwork within multidisciplinary, cross-functional teams. Able to communicate complex scientific information clearly through both spoken presentations and technical documentation.</li>
<li>Self-motivated and adaptable, with a passion for scientific discovery and a commitment to continuous learning and process improvement.</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;ofthis 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.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of anybonus,&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 soleand&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist I, Cell/Molecular Biology

<h3>Job Description</h3>
Job Description
At Redo Cabinets, we are looking to add Measure Technicians to our talented team. The Measure Technician is an essential role that is a trusted pro who ensures accuracy and turns designs into flawless kitchen remodeling projects.&nbsp;The primary function of the measure technician position is the technical evaluation of the job site to determine the manner in which the contracted work will be installed.&nbsp;You will be a W-2 employee. We provide a company vehicle, company tools, health insurance, paid time off, 401(k), and steady inside work. Must have experience measuring kitchen cabinets.
Measure Technician
Measure Technician needed to join our professional team; full-time position with great benefits such as health, dental, vision, 401k with company matching, direct deposit, company vehicle, company supplied tools, paid holidays, and paid time off.
About us
Redo Cabinets is a leader in the home improvement industry and is family owned and operated since 1953. We specialize in cabinet refacing. We pride ourselves on excellent customer service and communication to provide the customer with premium quality work.
Essential Functions:
<ul>
<li>Perform accurate measurements of cabinet components to determine the proper ordering of materials</li>
<li>Complete paperwork for ordering of all materials</li>
<li>Examine and record existing conditions in area(s) in which work is to be performed</li>
<li>Produce necessary drawing(s) for the installer to install the job per the contract specifications</li>
<li>Identify job site problems or irregularities to be addressed by the installer and or need to alter contract specifications</li>
<li>Identify job specifications requiring plumbing and/or electrical contractor</li>
<li>Review the contract and checklist with the customer to confirm expected work to be performed, the materials to be installed and any conditions that may affect scheduling and final outcome of the work performed</li>
<li>Collect measure payment from the customer as indicated on the contract if necessary</li>
<li>Adhere to the scheduled measures appointments as closely as possible without deviation</li>
<li>Project manage during the installation coordinating with the installer and customer questions.</li>
<li>Function as an ambassador for the company by presenting a professional appearance, answering customer questions and concerns in a business like manner, and treating the customer with respect at all times</li>
</ul>
Who You Are:
<ul>
<li>Have knowledge of a kitchen’s composition and an understanding of cabinet layout designs and terminology</li>
<li>Excellent attention to detail</li>
<li>Proficient in measuring and recording cabinet and countertop dimensions</li>
<li>Ability to follow directions and to provide feedback to project manager and sales department</li>
<li>Capable of identifying and addressing installation issues</li>
<li>Prior experience in cabinet refacing and cabinet installation a plus</li>
<li>Must have a valid driver's license with a verifiable safe driving record and no physical limitations to perform the tasks required</li>
<li>Experience with plumbing, electrical, and carpentry a plus</li>
<li>Must have a clear criminal background and will be subjected to a zero-tolerance drug policy</li>
</ul>
What We Offer:
<ul>
<li>Competitive compensation based on experience</li>
<li>Excellent benefits package that includes medical, dental, vision, short-term disability, life insurance, 401(k) with company match, paid vacation, and paid holidays</li>
<li>Company-supplied vehicle and tools</li>
<li>Opportunity for growth and advancement</li>
<li>Family-like work environment</li>
<li>Locally owned business that invests in and appreciates its employees</li>
</ul>
Immediate start is available after successful drug and background screening. We are an Equal Opportunity Employer and value diversity. All employment is decided on the basis of qualifications, merit, and business need.
Company DescriptionAt Redo Cabinets, we’re passionate about transforming kitchens and empowering people. Our team thrives on craftsmanship, collaboration, and doing the right thing every day. We’re a tight-knit crew that supports each other, values growth and reliability, and takes pride in turning houses into homes with beautiful cabinetry. If you want to be part of a motivated, adaptable team where your work matters and your voice is heard, Redo Cabinets is the place to build something meaningful—and grow with us. 
<h3>Company Description</h3>
At Redo Cabinets, we’re passionate about transforming kitchens and empowering people. Our team thrives on craftsmanship, collaboration, and doing the right thing every day. We’re a tight-knit crew that supports each other, values growth and reliability, and takes pride in turning houses into homes with beautiful cabinetry. If you want to be part of a motivated, adaptable team where your work matters and your voice is heard, Redo Cabinets is the place to build something meaningful—and grow with us.

Measure Tech

<h3>Job Description</h3>
Job Description
Apply Today! Great Company to work for! 
Job Duties:
<ul>
<li>Responsible for maintaining a sterile environment by garbing, cleaning, and acting according to the CGMP guidelines for clean room procedures.</li>
<li>Measure, cut, position, and align tubing and small components for assembly.</li>
<li>Operate cable guns, tubing spreader, bag sealers, tubing cutter and manual cutting devices.</li>
<li>Read instructions and drawing assemblies to identify product specifications.</li>
</ul>
Qualifications:
<ul>
<li>High School diploma or equivalent desired, with a minimum of six months related experience; or equivalent combination of education and experience.</li>
<li>Possess industry-specific training on how to assemble intricate parts or products in a controlled room or facility.</li>
<li>Prepares and assembles necessary parts/products based on Work Order</li>
</ul>
Monday-Friday
Company DescriptionDiscover a workplace that empowers you to thrive, innovate, and build the career you’ve been dreaming of. 
<h3>Company Description</h3>
Discover a workplace that empowers you to thrive, innovate, and build the career you’ve been dreaming of.

Cleanroom Assemblers - 1st shift & 2nd shift

<h3>Job Description</h3>
Job Description
Geotechnical Consultants Inc. (GCI) is a 46-year-old civil engineering company specializing in geotechnical engineering, environmental consulting, field and construction services, special inspections, building envelope services, and steel testing.
We are seeking a full-time Geotechnical Field Representative in the Youngstown, OH area. This position will be responsible for assisting engineers on construction site locations to perform routine testing for project documentation. GCI is looking for individuals who enjoy working outside, ability to work independently, excellent client communication skills, “can do” attitude, willingness to learn new concepts, and ability to achieve needed testing certifications.
General Roles and Responsibilities:
· Provide technical support to the Project Manager through on-site inspections and testing of soils, concrete, asphalt, and other construction materials.
· Perform computations and communicate results through field reports.
· Consistent communication with Project Mangers, client representatives, general contractors, and others to obtain project-appropriate objectives.
· Responsible for maintaining strict quality control and safety standards including cleaning and maintenance of equipment.
· Authority to reject and resolve conflict within scope of authority.
· Willingness to grow and achieve certifications as needed.
Desired Certifications (or ability to achieve):
· Concrete – ACI Field Testing Technician Grade 1-2, NICET Level 1-3, ICC Reinforced Concrete Special Inspector.
· Soils – NICET Level 1-3, ICC Soils Special Inspector.
· Asphalt – NICET Level 1-3, ODOT Level 1-2.
· Masonry – ICC Structural Masonry Special Inspector.
· Structural Steel – ICC Bolt &amp; Weld Special Inspector, AWS Certification.
· ICC Fireproofing Special Inspector
Qualifications:
<ul>
<li>3-5 years' experience in a construction related job, or education related experience, preferred.</li>
<li>Ability to pass drug test and general background check.</li>
<li>Effective speaking and written communication skills.</li>
<li>Valid driver’s license and insurance</li>
<li>Ability to travel up to 4 hours a day and walk/stand up to 8 hours a day.</li>
<li>Desire to work outside in all weather conditions.</li>
<li>Ability to safely lift varying weights from 10-50 pounds, and safely traverse construction sites and project sites</li>
</ul>
&nbsp;
Company DescriptionGCI is an Equal Opportunity Employer committed to compliance with all applicable federal, state, and local equal employment opportunity laws. Since opening our doors in 1979, we’ve upheld the principles of quality work, honest fees, exceptional service, and delivering solid value to our clients. We welcome motivated, self-sufficient individuals who thrive in a team environment and are seeking long-term career growth. GCI offers competitive pay, benefits, paid training, and profit sharing to all full-time employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information, marital status, protected veteran status, political affiliation, military service, parental status, or any other status protected by law. GCI also provides reasonable accommodation for qualified individuals with disabilities, pregnancy-related conditions, and sincerely held religious beliefs, observances, and practices, unless doing so would impose an undue hardship. 
<h3>Company Description</h3>
GCI is an Equal Opportunity Employer committed to compliance with all applicable federal, state, and local equal employment opportunity laws. Since opening our doors in 1979, we’ve upheld the principles of quality work, honest fees, exceptional service, and delivering solid value to our clients.\r\nWe welcome motivated, self-sufficient individuals who thrive in a team environment and are seeking long-term career growth. GCI offers competitive pay, benefits, paid training, and profit sharing to all full-time employees.\r\nAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information, marital status, protected veteran status, political affiliation, military service, parental status, or any other status protected by law. GCI also provides reasonable accommodation for qualified individuals with disabilities, pregnancy-related conditions, and sincerely held religious beliefs, observances, and practices, unless doing so would impose an undue hardship.

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