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<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the Head of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
0–2 years post-PhD or 2–5 years of industry/academic R&amp;D experience (not QC/manufacturing).
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: flexible schedule, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Research Associate I / II

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to perform testing and evaluations of raw materials, bulk, and finished products following written procedures. The role involves ensuring compliance with GMP requirements and maintaining accurate documentation records. You will develop an understanding of various testing methodologies and maintain neat and organized work areas.
Responsibilities
<ul>
<li>Perform testing and evaluations of raw materials, bulk, and finished products in accordance with written procedures.</li>
<li>Ensure test results meet current specifications prior to completion and approval.</li>
<li>Troubleshoot out-of-specification situations and perform batch adjustments as needed.</li>
<li>Maintain compliance with current regulatory expectations and practices, such as USP.</li>
<li>Document monthly Key Quality Incidents and out-of-specification situations, determining root causes and suggesting solutions.</li>
<li>Utilize data to focus improvement efforts, ensuring customer requirements and regulatory regulations are met.</li>
<li>Understand and maintain a culture of 'lean action' within the department.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in Chemistry.</li>
<li>0-2 years of quality control industry experience in pharma, cosmetics, or food.</li>
<li>Proficiency in laboratory techniques such as wet chemistry, FTIR, and quality control.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus.</li>
</ul>
 Pay and Benefits
The pay range for this position is $25.00 - $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 Minneapolis,MN.
Application Deadline
This position is anticipated to close on Sep 1, 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
Job Type: Full-Time
Reports To: President and Vice President of Operations
Job Summary:
We are seeking an experienced Chemical Plant Manager to oversee daily operations at our chemical manufacturing facility. The ideal candidate will have a strong background in chemical engineering, process management, and hands-on experience in formulating, scaling, and producing polymers. This position requires comprehensive knowledge of chemical handling, process safety, and production optimization.
Key Responsibilities:
· Lead, supervise, and coordinate all aspects of plant operations related to polymer synthesis and chemical processing.
· Manage day-to-day plant activities including production scheduling, equipment maintenance, quality control, and personnel oversight.
· Monitor and optimize production processes for efficiency, yield, and quality, particularly in the manufacture of water-based, solvent-based, or specialty polymers.
· Ensure compliance with OSHA, EPA, and other regulatory requirements, including proper chemical handling, storage, and disposal.
· Oversee raw material procurement and inventory control of monomers, catalysts, surfactants, solvents, and other chemicals.
· Work closely with R&amp;D and QA teams to scale up lab-developed polymers to full-scale production.
· Develop and maintain standard operating procedures (SOPs), batch sheets, and safety protocols.
· Train and mentor plant staff in chemical safety, operational procedures, and emergency response.
· Analyze data and implement continuous improvement strategies for process reliability, safety, and cost-effectiveness.
· Manage capital improvement projects, plant expansions, and equipment upgrades.
Qualifications:
· Bachelor’s degree (or higher) in Chemical Engineering, Chemistry, or Polymer Science.
· Minimum 5 years of experience in a chemical or polymer manufacturing plant, with at least 2 years in a supervisory or management role.
· Strong working knowledge of polymerization techniques (e.g., emulsion, suspension, solution, bulk).
· Familiarity with chemical process equipment (reactors, mixers, filtration units, etc.).
· Proficient in chemical handling protocols, hazard communication (GHS), and personal protective equipment (PPE) use.
· Experience with batch processing, process control systems (PLC/SCADA), and ISO/GMP standards is preferred.
· Excellent leadership, communication, and problem-solving skills.
Preferred Skills:
· Experience with waterborne acrylics, polyurethanes, styrene-butadiene, or specialty resin systems.
Work Environment:
· Manufacturing plant environment with regular exposure to chemicals, high temperatures, and production machinery.
· Must be able to wear required PPE and respond to emergencies when necessary.
Compensation &amp; Benefits:
· Competitive salary commensurate with experience
· Health insurance
· SIMPLE IRA (SIRA) retirement plan
· Paid time off and holidays
· Relocation assistance (if applicable)
Job Type: Full-time
Pay: $90,257.70+
Benefits:
<ul>
<li>401(k)</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Monday to Friday</li>
</ul>
Application Question(s):
<ul>
<li>Do you have a chemical background?</li>
</ul>
Education:
<ul>
<li>Bachelor's (Required)</li>
</ul>

Chemical Plant Manager

<h3>Job Description</h3>
Job Description
Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world.
Position: Chemical/Environmental Senior Applications Engineer Location: Remote - Western US
Excellent Benefits:&nbsp;Medical, dental, prescription &amp; vision, HSA &amp; retirement savings (401k) –&nbsp;Generous Company Match! Perks:&nbsp;Incentives/bonus plans, competitive pay, dress for your day, hybrid schedules, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning &amp; development opportunities.&nbsp;&nbsp;
Hours of work:&nbsp;Full-time position with hours Monday-Friday 9:00-5:00 PM
 The Senior Applications Engineer provides the lead technical support for the sale of carbon, equipment, and service in domestic or international markets. This role interfaces with Equipment Engineering, Research and Development, Equipment and Assembly, Product Management, and Sales to provide the technical justification for the use of activated carbon technology in customer applications. The Senior Applications Engineer will assist in the technical development of emerging markets/applications as it pertains to their area of focus, as well as providing lead technical and business support for key global business development groups. This role can also include supervision of entry or intermediate applications engineers &nbsp; &nbsp;Duties and Responsibilities (not limited to) &nbsp;
<ul>
<li>Uses gained technical expertise, know-how and supplied computer models to select appropriate carbon and equipment for liquid and vapor phase applications, and predict performance based upon customer conditions</li>
<li>Set-up and monitor pilot trials in the field and provide design information for future full-scale systems</li>
<li>Interpret data from the lab and the field trials for pilot and full-scale systems to provide technical design and operational recommendations</li>
<li>Trouble shoot customer problems such as short filter run-times or unexpected breakthrough</li>
<li>Provide application engineering support for a geographic region(s) or set of Technical Sales Reps</li>
<li>Called to work with R&amp;D on the development / testing of new carbon products / applications</li>
<li>May also provide technical guidance to engineers with less experience and to overseas colleagues when called upon</li>
<li>Prepares and provides technical training for TSR when new topics, applications, etc. are encountered</li>
<li>Responsible for other general training and assuring consistency of technical messages from TSRs to customers</li>
<li>In coordination with the Technical Director, Market Development Director, and Sales Director, develop strategies and market-specific approaches to expand existing base business and develop new business opportunities through CCC technology adoption</li>
<li>Regularly review and evaluate actual results, report/troubleshoot variances, adjust strategy as appropriate</li>
<li>Provide technical lead for the Business Unit on CCC global initiatives / cross-business segment groups</li>
<li>Working closely with other CCC global regions on projects covering multiple geographic territories</li>
<li>Acts as technical support and back-up contact related to specific projects for Sales team</li>
<li>Serves as liaison between Sales team and internal support teams including Product and Project Management</li>
<li>Review bid specifications for clarity, accuracy and acceptance</li>
<li>Provide recommendations to improve technical quality of bid specifications and prevent undue risk to Calgon Carbon</li>
<li>Serve as main Calgon Carbon contact to customer when Technical Sales Rep is unable to respond to customer</li>
<li>Participate in Industry forums related to emerging markets and existing applications</li>
<li>Attend technical conferences and trade shows to gain technical knowledge and represent Calgon Carbon as a leader in the activated carbon market</li>
<li>Prepare and present papers/posters at conferences, trade shows and virtual opportunities, e.g. webinars</li>
<li>Develop and present technical presentation / training to engineering consultants, clients, regulators, legislators and others to influence selection of treatment solutions</li>
<li>Attendance at conference would be as lead technical personnel &nbsp;</li>
</ul>
Qualifications
<ul>
<li>A bachelor’s degree (B.A. or B.S.), or equivalent from four-year college or university is required (Chemical Engineering or related engineering/chemistry field)</li>
<li>10+ years&nbsp;of experience in the application of carbon adsorption technology to address customer requirements in liquid and gas purification, including carbon modeling, equipment design and development, and equipment functionality is required</li>
<li>5-7 years&nbsp;of experience in the use and troubleshooting of adsorption equipment at customer sites is required</li>
<li>Experience with business/marketing is preferred.</li>
</ul>
 About Calgon Carbon
At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs.
Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron.
In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe.
Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran
 
PIe022383bd442-25405-37796249

Chemical/Environmental Senior Applications Engineer

<h3>Job Description</h3>
Job Description
We have immediate opportunity for all levels of Wildlife Biological Monitors for the Central Valley Area. MUST have Wildlife Biological Monitoring Experience in California.
VARIOUS DUTIES AND RESPONSIBILITIES (other duties may be assigned)
<ul>
<li>Experience and knowledge of wildlife species in the Central Valley including small mammals, birds, and reptiles.</li>
<li>Familiarity with state and federal regulations, knowledge of environmental regulatory process is a must.</li>
<li>Experience with monitoring all ground distributing activity including mass grading, grubbing, weed abatement, trenching and any excavation on previously disturbed and undisturbed ground.</li>
<li>Does or oversees field inspections of proposed project areas.</li>
<li>Perform biological monitoring at construction sites to implement mitigation measures.</li>
<li>Conduct field surveys.</li>
<li>Record data for scientific and compliance purposes using company forms and established field methodology.</li>
<li>Ability to read maps.</li>
<li>Prepare daily progress/monitoring reports as needed by the project.</li>
<li>Use GPS equipment (Garmin/Trimble) for field data collection.</li>
<li>Ability to travel to be in the field for extended periods and able to work in rough terrain and challenging weather inclement.</li>
<li>Work independently or as part of a team.</li>
</ul>
VARIOUS DEGREES &amp; SKILLS
<ul>
<li>Master’s or Bachelor’s Degree in Biology or closely related field.</li>
<li>Previous construction monitoring experience in similar California environments.</li>
<li>Knowledge of local, state, and federal environmental regulations.</li>
<li>Team player with the ability to work in a fast-paced environment.</li>
<li>Sound business ethics, including the protection of proprietary and confidential information.</li>
<li>Proficiency in MS Office Applications (Word, PowerPoint, Outlook, Excel) and project tracking software and databases.</li>
<li>Experience with any of the following species: Tipton Kangaroo Rat, San Joaquin Antelope Squirrel, California Tiger Salamander, San Joaquin Kit Fox, Giant Garter Snake</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Biologists, Biology, GPS, endangered species, field surveys, mammal, amphibian)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Wildlife Biologist

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking an experienced Chemical process engineer to oversee daily operations at our chemical manufacturing facility. The ideal candidate will have a strong background in chemical engineering, process management, and hands-on experience in formulating, scaling, and producing polymers. This position requires comprehensive knowledge of chemical handling, process safety, and production optimization.
Key Responsibilities:
· Lead, supervise, and coordinate all aspects of plant operations related to polymer synthesis and chemical processing.
· Manage day-to-day plant activities including production scheduling, equipment maintenance, quality control, and personnel oversight.
· Monitor and optimize production processes for efficiency, yield, and quality, particularly in the manufacture of water-based, solvent-based, or specialty polymers.
· Ensure compliance with OSHA, EPA, and other regulatory requirements, including proper chemical handling, storage, and disposal.
· Oversee raw material procurement and inventory control of monomers, catalysts, surfactants, solvents, and other chemicals.
· Work closely with R&amp;D and QA teams to scale up lab-developed polymers to full-scale production.
· Develop and maintain standard operating procedures (SOPs), batch sheets, and safety protocols.
· Train and mentor plant staff in chemical safety, operational procedures, and emergency response.
· Analyze data and implement continuous improvement strategies for process reliability, safety, and cost-effectiveness.
· Manage capital improvement projects, plant expansions, and equipment upgrades.
Qualifications:
· Bachelor’s degree (or higher) in Chemical Engineering, Chemistry, or Polymer Science.
· Minimum 5 years of experience in a chemical or polymer manufacturing plant, with at least 2 years in a supervisory or management role.
· Strong working knowledge of polymerization techniques (e.g., emulsion, suspension, solution, bulk).
· Familiarity with chemical process equipment (reactors, mixers, filtration units, etc.).
· Proficient in chemical handling protocols, hazard communication (GHS), and personal protective equipment (PPE) use.
· Experience with batch processing, process control systems (PLC/SCADA), and ISO/GMP standards is preferred.
· Excellent leadership, communication, and problem-solving skills.
Preferred Skills:
· Experience with waterborne acrylics, polyurethanes, styrene-butadiene, or specialty resin systems.
Work Environment:
· Manufacturing plant environment with regular exposure to chemicals, high temperatures, and production machinery.
· Must be able to wear required PPE and respond to emergencies when necessary.
Compensation &amp; Benefits:
· Competitive salary commensurate with experience
· Health insurance
· SIMPLE IRA (SIRA) retirement plan
· Paid time off and holidays
· Relocation assistance (if applicable)
Job Type: Full-time
Pay: $90,257.70+
Benefits:
<ul>
<li>401(k)</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Monday to Friday</li>
</ul>
Education:
<ul>
<li>Bachelor's (Required)</li>
</ul>

Chemical Engineer

<h3>Job Description</h3>
Job DescriptionClean Room Assembler: All Shifts Open! - $20/hr!
Shift:
<ul>
<li>1st 6am to 2pm - $17.00</li>
<li>2nd 2pm to 10pm - $19.55</li>
<li>3rd 10pm to 6am - $20.40</li>
<li>Weekend Shift PM or AM - $20.40</li>
</ul>
Responsibilities
• Assemble small parts with precision using tweezers.
• Operate machinery by placing parts in a jig and aligning them on a computer.
• Conduct quality checks using microscopes and magnifying glasses.
• Work in a clean room environment when needed.
• Operate a laser etching machine occasionally.
Essential Skills
• 1+ year of experience in roles requiring attention to detail and quality control using microscopes, micrometers, or calipers.
Additional Skills &amp; Qualifications
• Experience working in a medical-related position is a plus.
• 1+ year of ERP experience is beneficial.
Why Work Here?
Enjoy a generous benefits package that includes 3 weeks of PTO, 11 paid holidays, and a 401k plan with a 6% match. Health, dental, and vision insurance are available from the first day of employment. Additionally, there is an opportunity for tuition reimbursement, supporting your continuous learning and development.
Work Environment
The work environment allows for casual attire, such as jeans and a polo or nice t-shirt. Safety goggles are provided due to the use of lasers, while steel toe boots are not required. If working in the clean room, employees will need to suit up each day.
Job Type &amp; Location
This is a Contract to Hire position based out of Kettering, Ohio.
 Pay and Benefits
The pay range for this position is $19.55 - $20.40/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 Kettering,OH.
Application Deadline
This position is anticipated to close on Aug 31, 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.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
SUMMARY
The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.
• Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance. • Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes. • Uses and maintains HPLC, GC, FTIR, and other instruments. • Assists in performing method validations. • Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc. • Writes and revises SOPs and tests methods as needed. • Follows documented procedures: SOPs, test methods, transfer protocols. • Prepares reports and reviews data. • Follows lab safety procedures. • Performs other tasks, as assigned.
SUPERVISORY RESPONSIBILITIES 
None
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE 
Bachelors of Science in Chemistry.
LANGUAGE SKILLS
 Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
MATHEMATICAL SKILLS 
Able to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Able to apply concepts of basic algebra and geometry.
REASONING ABILITY 
Able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Able to deal with problems involving several concrete variables in standardized situations.
PHYSICAL DEMANDS 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Specific vision abilities required by this job include close vision and depth perception.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

<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 
<ul>
<li>Lead and mentor a team of 10-12 scientists specializing in establishing separation-based assays including HPLC (e.g. SEC, IEX, RPLC), capillary electrophoresis (CE, icIEF), etc. for QC lab implementation to support GMP release and stability testing and for sample testing in PDS&amp;T - Analytical Development to support biologics DS process development, characterization, validation as well as GMP manufacturing investigation activities. &nbsp;Develop high-throughput analytical methods and drive timely delivery of high-quality testing results.</li>
<li>Serve as a primary contact for Analytical Development in AbbVie's CMC teams, supporting both early and late-stage biologics pipeline assets. &nbsp;Balance stakeholder expectations between PDST and other AbbVie analytical functions to ensure effective collaboration.</li>
<li>Develop, communicate, and implement analytical strategies with broader PDS&amp;T analytical functions and CMC business partners. &nbsp;Oversee experimental execution, development, qualification, validation, and transfer of robust analytical methods for QC lab as well as analytical control strategy development.</li>
<li>Guide team to evaluate and select effective analytical technologies and methods for meeting program needs.&nbsp; Evaluate and interpret data trends in release and stability assays. &nbsp;Demonstrate scientific excellence in the analytical characterization of biologics and ensure robust documentation of study findings.</li>
<li>Author and review analytical sections of IND/BLA filings for early and late-stage programs, provide response support to agency information request. &nbsp;Ensure all submissions comply with regulatory requirements and industry standard.</li>
<li>Collaborate with other analytical teams in R&amp;D and PDS&amp;T on program transition, workflow and program strategic alignment.&nbsp; Provide guidance to peers in project management, analytical strategy development, and technical skills related to separation techniques.</li>
<li>Communicate project strategies, issues, and risks to relevant teams. &nbsp;Promote proactive risk resolution within and across functional areas to advance project objectives.</li>
<li>Build a high-performing team to proactively seek method and product understanding, build robust product knowledge and new capability, and advance science and innovation.&nbsp; Lead team to actively publish novel study findings at internal and external conferences and journals.</li>
</ul>
Qualifications 
<ul>
<li>MS or PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline. &nbsp;Minimum of 12+ years (MS) or 8+ years (PhD) of professional experience working in biotech/pharmaceutical setting.</li>
<li>Proven experience managing and leading analytical development activities for biologic development, including mAbs, bispecifics, antibody-drug conjugates, and fusion proteins.</li>
<li>Expertise in protein and impurity analysis techniques such as HPLC, capillary electrophoresis, and other relevant methods. &nbsp;Experience with mass spectrometry and ELISA is a Plus.</li>
<li>Familiarity with USP/ICH guidelines for method development, qualification, and validation. Extensive experience in authoring, reviewing regulatory submissions and responding to agency information requests.</li>
<li>Strong technical and people leadership skills, and demonstrated ability to foster an engaging, inclusive and collaborative team environment.</li>
<li>Ability to quickly comprehend and adapt to new situations, with an open mindset and can-do attitude, demonstrating agility where necessary to address evolving project needs.</li>
<li>Excellent communication, organization and inter-personal skills, effectively managing relationships to enhance team decision-making.</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;
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