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<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
<ul>
<li>Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.</li>
<li>Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.</li>
<li>Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.</li>
<li>Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure compliance with international regulations such as FDA and EMA.</li>
<li>Work collaboratively with R&amp;D and production teams to support product development and release.</li>
<li>Provide technical support and training to junior team members or other departments.</li>
</ul>
Essential Skills
<ul>
<li>3-7 years of routine testing experience using HPLC and dissolution techniques.</li>
<li>Proficiency in working with solid oral dosage forms, raw materials, and finished products.</li>
<li>Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.</li>
<li>Strong understanding of Pharma GMP practices.</li>
<li>Competence in laboratory applications including wet chemistry, titration, and chromatography.</li>
<li>Basic computer skills in MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>Ability to document and record analytical experiments and results as per cGMP guidelines.</li>
<li>Strong problem-solving skills and attention to detail.</li>
<li>Knowledge of regulatory guidelines such as GMP and GLP.</li>
</ul>
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type &amp; Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Job Description

POSITION SUMMARY The Microbiology Supervisor is responsible for the operation of Microbiology section of the clinical laboratory.&nbsp; The Microbiology Supervisor facilitates the implementation of hospital and laboratory policies and procedures.&nbsp; Responsible for assisting in training new employees, supervising both Clinical Laboratory Scientists and laboratory phlebotomist’s workload organization, and monitoring daily maintenance and quality control. This person will report to the Lab Manager Implements good public relations by representing the laboratory directly to patients, physicians and hospital staff at all times.
ESSENTIAL DUTIES AND RESPONSIBILITIES
<ul>
<li>Responsible for assisting with the selection of methodology and instrumentation to perform laboratory tests appropriate for the patient population served.&nbsp; Responsible for the validation and implementation of new instrumentation.&nbsp; Ensures the standardization of tests methodologies, procedures, instrumentation, and reference ranges.</li>
<li>Verifies test procedures performed and established the laboratory’s test performance characteristics, including, but not limited to the linearity, precision and accuracy of each test and test system.</li>
<li>Ensures participation in and successful completion of a quality control and approved proficiency testing program commensurate with the services offered.&nbsp; Troubleshoots any problems with the proficiency testing program.&nbsp; Establishes parameters for acceptable level of analytic performance.&nbsp; Ensures that quality is maintained throughout entire testing process from order entry through results reporting.</li>
<li>Reviews the work of others to ensure that tests are performed in accordance with prescribed standards.</li>
<li>Assists in maintaining and optimizing work standards to assure a reasonable turnaround time of test results.</li>
<li>Troubleshoots equipment problems.</li>
<li>Maintains inventory control of supplies and reagents in his/her section(s).</li>
<li>Schedules, organizes and delineates duties of personnel.</li>
<li>Assists manager in performance evaluations of the employees in his/her sections.</li>
<li>Responsible for the operation of the Microbiology department.</li>
<li>Works closely with the Laboratory Manager to meet the administrative and financial goals of the department</li>
<li>Responsible for meeting the service and quality goals of the department. Assumes responsibility for daily operations and meets CLIA requirements for microbiology</li>
<li>Provides clinical microbiology consultations to medical and hospital staff</li>
<li>Present micro data reports clearly and concisely to management, including QC performance metrics and trends</li>
<li>Proactively identifies and implements improvements and lean initiatives</li>
<li>Responsible for the technical and scientific oversight of the department including assisting in hiring of personnel, training/competency assessment and input for performance review of the staff in their designated area.</li>
<li>Responsible for making clinical/technical decisions in the resolution of testing/reporting issues, maintenance of the quality and security of department instrumentation, quality control documentation and meeting hospital goals to ensure accurate and timely patient care.</li>
<li>Responsible for maintaining procedure manuals for all testing performed and the documentation required for regulatory and licensing organizations</li>
<li>Oversee and manage team schedule of staff and PTO request.&nbsp;</li>
<li>Work collaboratively with other department leaders to have a more efficient workflow for the Clinical laboratory.&nbsp;</li>
<li>Responsible for ensuring staff compliance with hospital policies and meeting regulatory requirements within their assigned areas (e.g. coordinate meal breaks, corrected reports, attendance, overtime and punctuality)</li>
<li>Setting an example- must always be conscious of how his / her words and actions will be perceived.</li>
<li>Attend minimum of three (3) leadership seminar/workshop annually</li>
<li>Performs additional duties as directed by the by the Laboratory Director or Manager which are necessary for the efficient operation of the laboratory.</li>
</ul>
Job Requirements

POSITION REQUIREMENTS
A.&nbsp; &nbsp;Education
<ul>
<li>Bachelor’s degree – Science</li>
</ul>
B.&nbsp; Qualifications/Experience
<ul>
<li>2-5 years Microbiology Clinical Laboratory Experience</li>
<li>CA Clinical Laboratory Scientist License or Clinical Microbiologist Scientist License</li>
<li>2 years leadership experience in an acute care setting required</li>
</ul>
C.&nbsp; &nbsp;Special Skills/Knowledge
<ul>
<li>Strong interpersonal and organizational skills.&nbsp; Proficient with computer.</li>
</ul>
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#LI-AJ1

Microbiology Supervisor - Full Time Days

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical EngineerJob Description
We are seeking a skilled Chemical Engineer to perform all chemical process functions related to chemical batching. This role involves conducting root cause analysis (RCA) to troubleshoot batching issues and implementing corrective and preventive actions (CAPAs) for both internal and external challenges. You will be responsible for scaling up and commercializing new formulas, adjusting existing formulas, and validating all manufacturing and quality processes and specifications. Additionally, you will perform in-process batch adjustments, support production scaling to meet product specifications, and analyze production and laboratory data to optimize processes and reduce costs.
Responsibilities
<ul>
<li>Conduct root cause analysis for customer complaints and internal production issues.</li>
<li>Ensure all batch adjustments are executed accurately when raw materials or formulas change.</li>
<li>Scale up and commercialize new formulas and products, ensuring correct implementation.</li>
<li>Analyze production data and quality data to identify optimization and cost reduction opportunities.</li>
<li>Participate in the disposition of non-conforming materials and support deviation management.</li>
<li>Mentor and coach fellow engineers and quality and production personnel in continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>1-5 years of experience in chemical engineering or chemical process engineering.</li>
<li>Ability to diagnose and resolve customer complaints and internal production issues.</li>
<li>Experience with root cause analysis and implementation of CAPA.</li>
<li>Expertise in chemical manufacturing, quality control, and process engineering.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Degree in Chemical Engineering or a related field.</li>
<li>Experience in scale-up and commercialization processes.</li>
<li>Familiarity with chemical equipment and laboratory practices.</li>
<li>Knowledge of new product development and chemical processing.</li>
</ul>
Work Environment
This position operates in a chemical manufacturing environment, working across offices, laboratories, production areas, and production labs. The role follows a first shift schedule from Monday through Friday, with flexible working hours typically ranging from 40 to 45 hours per week, extending to 50 hours during major projects or issues. You will collaborate with various organizational levels, including R&amp;D, Quality, Production, Maintenance, Customers, Sales, and leadership roles.
Job Type &amp; Location
This is a Permanent position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
This company offers health insurance, dental insurance, vision insurance, 401k match, bonuses, etc. They also provide paid vacation and paid holiday.
Workplace Type
This is a fully onsite position in Germantown,WI.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Chemical Engineer

<h3>Job Description</h3>
Job Description
About the Team:
The Sensors Division specializes in the development of advanced sensor systems, with a particular focus on airborne and surface-based radar, space-based sensing, electronic warfare, and underwater acoustics. This position is within the Space Missions and Sensing (SMS) Sector of the Sensors Division. In this sector, we develop and deliver technology to advance space-based sensing, space control, and counter-sensing missions.
The Role:
The SMS Sector is seeking a Senior RF signal processing scientist to support algorithm development in a Research &amp; Development environment. In this role, you will be an integral part of a team developing a cutting-edge space-based radar system. Your responsibilities will include utilizing and advancing existing signal processing algorithms and analytics tools. This position offers significant opportunities for career growth within a fast-paced and rapidly expanding company.
What you will do:
<ul>
<li>Design signal processing and data exploitation algorithms that support day to day satellite operations</li>
<li>Conduct performance analysis through simulations and real-world testing to validate system performance</li>
<li>Communicate effectively with internal teams and stakeholders to convey technical concepts and project updates</li>
</ul>
Who you are:
<ul>
<li>Active Security Clearance at the Secret (S) level</li>
<li>BS or MS in Physics, Applied Mathematics, Electrical Engineering</li>
<li>3-5+ years of experience depending on degree</li>
<li>Radar signal processing, statistical signal processing background (detection, estimation)</li>
<li>Proficiency in MATLAB and/or Python programming languages</li>
</ul>
Even Better:
<ul>
<li>Past experience in space-based remote sensing (e.g. SAR, signal exploitation)</li>
<li>Expertise in linear algebra, mathematical optimization a plus</li>
<li>PhD in Applied Mathematics, Electrical Engineering with research background related to radar, radar signal processing in lieu of experience</li>
</ul>
Pay Information Full-Time Salary Range: $134,000 - $184,000
The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate's experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions.
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Senior RF Signal Processing Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist OperatorJob Description
The Chemist Operator will be responsible for producing Active Pharmaceutical Ingredients using chemical reactors. This role requires following specific Batch Records to ensure the production of a consistent product.
Responsibilities
<ul>
<li>Handle various unit operations, such as reactions, filtration, distillation, drying, and milling, on raw materials and various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document instructions per batch sheet to produce products in accordance with all cGMP guidelines.</li>
<li>Set up equipment, including vessels, tanks, centrifuges, and dryers, for proper processing. Clean and verify equipment and vessels.</li>
<li>Record observations of operating conditions.</li>
<li>Drive and operate a fork truck.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in Chemical Operation or Batching, 1-5 years preferred.</li>
<li>Knowledge of GMP guidelines from food, chemical, or pharmaceutical industries.</li>
<li>Understanding of Analytical Chemistry and Chemical Operating.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma with experience, or an Associate's or Bachelor's degree in Sciences, preferably in Chemical Technology or Chemistry.</li>
<li>Experience in GC and Batching processes.</li>
</ul>
Work Environment
The work environment is a clean laboratory and production setting. Initial training will be on the first shift for 3-6 months, after which the role will transition to a permanent shift from 6 p.m. to 6:30 a.m., following a 2-2-3 schedule, including working every other weekend. The company is expanding its innovation hub, offering growth opportunities into leadership positions for those who excel.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $24.00 - $26.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Grafton,WI.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Chemist Operator

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology AnalystJob Description
The Microbiology Laboratory Analyst II/III or Senior Analyst will be a vital part of the team, contributing to both general and complex laboratory testing, sample management, and laboratory maintenance. The role involves collaborating with the team to achieve the goals of the Microbiology Services Department, as well as performing both routine and non-routine laboratory duties.
Responsibilities
<ul>
<li>Perform microbiological tests in strict accordance with SOPs, cGMP, cGLP, USP, EP, ISO/IEC, and other applicable regulatory requirements.</li>
<li>Conduct cleaning and disinfection validations, both manual and automated.</li>
<li>Execute Container Closure Integrity Tests (CCIT) and Package Integrity Evaluations.</li>
<li>Perform custom studies and additional testing as per client requests.</li>
<li>Engage in method development, modification, verification, and assist with method validation testing.</li>
<li>Participate in method transfer activities and suitability studies under leadership guidance.</li>
<li>Support Quality Management System investigations for non-conformance or out-of-specification results.</li>
<li>Complete assigned CAPA tasks and change controls.</li>
<li>Maintain laboratory cleanliness, safety, and compliance with cGMP standards.</li>
<li>Conduct regular inventory of reagents, consumables, and materials.</li>
<li>Prepare in-house reagents, stock solutions, media, and microbial suspensions.</li>
<li>Perform biowaste autoclave sterilization cycles and other laboratory housekeeping tasks.</li>
<li>Maintain accurate and complete test records.</li>
<li>Ensure audit readiness at all times.</li>
<li>Deliver results within predetermined turnaround times (TAT) with accuracy.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in aseptic technique.</li>
<li>Experience with cleaning and disinfection validation.</li>
<li>Strong knowledge of GMP and GLP standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS/BA in Biology, Pharmaceutical Sciences, Biotechnology or equivalent, with a preference for a Microbiology degree and 2+ years of relevant experience in microbiology.</li>
<li>Associate degree in a related scientific discipline with 5+ years of experience in a microbiology or related laboratory.</li>
<li>High school diploma with 7+ years of experience in a microbiology or related scientific laboratory.</li>
<li>2+ years of GMP/GLP laboratory or FDA experience is required.</li>
<li>Additional training certifications and self-learning are advantageous.</li>
</ul>
Work Environment
The role requires the ability to lift up to 30 pounds and stand for extensive periods (up to 6 hours). Ergonomics will be utilized to perform repetitive motion tasks with hands and arms. The position involves working in a BSC/LAF and at the lab bench for most of the day (up to 8 hours). Candidates must be able to tolerate the smell of Gram-negative organisms and laboratory disinfectants, and work safely with Biosafety Level II (BSL II) microorganisms and bloodborne pathogens. Proficiency in navigating computer systems is required. Flexibility to work off shift hours and weekends when needed is essential.
Job Type &amp; Location
This is a Contract to Hire position based out of Hercules, CA.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hercules,CA.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Microbiology Analyst

<h3>Job Description</h3>
Job Description
MOVING YOUR WORLD by focusing on your success:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow.&nbsp; We stand behind our core values: trust, creating value, respect, reliability, and integrity. Ours is a culture that fosters creativity and empowerment, values work/life balance, and gives you the freedom to excel. At FUCHS we aim to nurture your capabilities, ideas and career.
&nbsp;
Salary:
FUCHS offers a competitive salary commensurate with experience in a similar position. The salary range for this position is $22.00 - $27.00 per hour, but actual salary will vary depending upon a new hire’s experience and qualifications as well as internal equity.
&nbsp;
Your responsibilities:
The Compounder works in the production department and is responsible for manufacturing of specialty lubricants. The Compounder must follow product folders to ensure all specification levels are met.&nbsp; The Compounder must adhere to all regulations, policies, and procedures for health, safety, and environmental compliance.
<ul>
<li>Wear mandatory PPE at all times.</li>
</ul>
<ul>
<li>Set up and operate production equipment in accordance with current good manufacturing practices and standard operating procedures</li>
<li>Review folder, calculate requirements, and verify weight of material</li>
<li>Documents production by completing forms, reports, logs, and records of equipment and batches</li>
<li>Locate material and supplies, and verify lots and weights according to the manufacturing order</li>
<li>Prepare and load raw materials into equipment</li>
<li>Must complete daily assigned tasks to meet production volume and schedule</li>
<li>Ensure that end products conform to FUCHS quality standards in accordance with 6S standards</li>
<li>Prepare finished goods for shipment by packing, labeling and loading on dock</li>
<li>Ensure that work environment is maintained clean, safe and organized</li>
<li>Keep equipment operating by following operating instructions; troubleshooting breakdowns;</li>
<li>Updates job knowledge by participating in training opportunities</li>
<li>Utilization of lean manufacturing techniques throughout production</li>
</ul>
<ul>
<li>Maintains material-handling equipment by completing pre-use inspections</li>
<li>Maintains inventory by identifying, labeling, and placing materials and supplies in stock; recording location of inventory</li>
</ul>
<ul>
<li>Responsible for responding to assigned corrective actions per the CAR system</li>
<li>Some heavy lifting (up to 75-lbs.) may be required</li>
<li>Ability to stand for long periods of time</li>
</ul>
&nbsp;
Qualifications we are looking for:
<ul>
<li>High school diploma or equivalent</li>
<li>2+ years working in chemical manufacturing experience</li>
<li>Computer literate required</li>
</ul>
<ul>
<li>Experience in a manufacturing environment</li>
<li>Mechanical ability preferred</li>
<li>Knowledge of material handling equipment</li>
</ul>
&nbsp;
&nbsp;
These are your benefits:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow as professionals.&nbsp; In this role, you will have the opportunity to work on projects that will expand your experience and challenge your abilities in the global marketplace.&nbsp; The position also offers an excellent compensation package and a comprehensive suite of benefits.&nbsp;Detailed benefit information can be found at this link: <a href="https://fuchs.com/us/en/benefits" target="_blank">https://fuchs.com/us/en/benefits</a>.
&nbsp;
FUCHS Lubricants Co. is an equal employment opportunity (EEO)/AA employer and strongly supports diversity in the workplace (m/f/d/v).
&nbsp;
Do you have any questions?&nbsp;Rosalinda Almanza (<a href="mailto:rosalinda.almanza@fuchs.com" target="_blank">rosalinda.almanza@fuchs.com</a>) will be more than happy to answer them!

Chemical Compounder

<h3>Job Description</h3>
Job Description
About AIRCO AIRCO is a world leader in carbon conversion technology, paving the way to global energy security by transforming CO₂ into a valuable resource. Its proprietary AIRMADE™ Technology is an adaptable platform that allows any industry to efficiently produce high-demand, fully-formulated synthetic fuels from waste CO₂ and hydrogen.
The company has commercial partnerships with airlines including JetBlue and Virgin Atlantic, amongst others, and has been awarded multiple government contracts, including with NASA and the United States Department of Defense's Defense Innovation Unit. The company has received industry recognition through awards such as Time Best Inventions, Inc. Best in Business, Fast Company World Changing Ideas, and the XPrize for Carbon Removal.
AIRCO's many accolades include winning the prestigious Green Chemistry Challenge Award from the Environmental Protection Agency in October 2023, an award given to organizations that reinvent processes to reduce the generation of hazardous substances and byproducts. AIRCO was also declared a winner for the World Economic Forum UpLink Sustainable Aviation Challenge, which accelerates the development of promising technology pathways that enable widespread uptake of SAF.
The Position
AIRCO is seeking a Senior Scientist to join our team. This role will report to the Director, Research, and will contribute to the development of heterogeneous catalysts for the production of Sustainable Aviation Fuel (SAF) from CO2, supporting AIRCO's business Growth. This role is based in New Britain, PA with travel as needed to Brooklyn, NY.
What you get to do
<ul>
<li>Design and execute experiments independently with minimal supervision to meet the project goals</li>
<li>Synthesis, characterization, and testing of heterogeneous catalysts</li>
<li>Catalyst stability testing and scale-up support </li>
<li>Record, analyze, interpret, and present data to stakeholders</li>
<li>Supervise and mentor chemists and technicians involved in catalyst synthesis and testing</li>
<li>Collaborate cross functionally with Development and Engineering teams</li>
</ul>
What you bring to AIRCO
<ul>
<li>PhD in Chemistry or Chemical Engineering</li>
<li>0-5 years of post-doctoral, academic, or industrial experience in heterogeneous catalyst development in academic or industrial setting </li>
<li>Ability to work in a hands-on laboratory setting with minimal supervision</li>
<li>Ability to learn new techniques related to catalyst synthesis and testing</li>
<li>Maintain a safe and compliant working environment, adhering to all relevant regulations, standards, and guidelines</li>
<li>Good communication and presentation skills, with the ability to effectively communicate technical information to both technical and non-technical audiences</li>
<li>Ability to work independently and collaboratively in a fast-paced, multidisciplinary team environment</li>
</ul>
Bonus Points
<ul>
<li>Prior experience in fixed-bed reactor set-up and maintenance</li>
<li>Experience in characterization techniques such as BET, TPR, TGA, SEM, Mercury Porosimetry </li>
</ul>
 Working at AIRCO - In addition to standard medical and dental benefits, that kick in Day 1, we provide:
Comprehensive Health Benefits
<ul>
<li>Full coverage for employee base premiums on health, dental, and vision insurance.</li>
<li>70% coverage for spouse and dependent base premiums.</li>
<li>Choose between base plans or enhanced options to fit your needs.</li>
</ul>
Health Savings &amp; Flexibility
<ul>
<li>Access company-sponsored HSA and FSA accounts to save on healthcare and dependent care expenses.</li>
</ul>
Income Protection &amp; Insurance
<ul>
<li>Company-paid Short-Term Disability insurance.</li>
<li>Optional Long-Term Disability and Life Insurance plans.</li>
</ul>
Time Off &amp; Leave
<ul>
<li>Flexible and generous paid time off, including national holidays and sick leave.</li>
<li>Paid family leave to support you during important life moments.</li>
</ul>
Retirement Savings
<ul>
<li>Tax-deferred 401(k) plan with a 3% company match to help you invest in your future.</li>
</ul>
Commuter Benefits
<ul>
<li>Pre-tax savings on transit and parking, plus monthly company contributions.</li>
</ul>
Additional Perks
<ul>
<li>Ancillary benefits through Sequoia, including pet insurance and financial wellness programs.</li>
<li>Employee wellness program to support your well-being.Inclusive of Wellhub &amp; One Medical. </li>
<li>Company-sponsored events and programs that promote an inclusive and values-driven workplace.</li>
<li>In person weekly catered lunch every Wednesday.</li>
</ul>
At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
Don't meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIRCO we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles
This position requires access to technology, software and other information that is subject to governmental access control restrictions, due to export controls, security classification and/or designation as Controlled Unclassified Information. Employment in this position is conditioned on the candidate's ability to obtain and maintain appropriate government authorization to access technology or information, to the extent required, including without limitation a security clearance, export license, or other documentation required to establish authorization to receive access to such items technology or information.
We may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to Company facilities and information systems, as we deem appropriate, in order to ensure compliance with applicable government access control restrictions.
I consent to transfer my data to Air Company in the U.S. and to its use in accordance with the Air Company Privacy Policy, and I opt in to receiving information from Air Company. Air Company does not sell or share personal information to third parties within the meanings given under applicable laws.

Sr. Scientist

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

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

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

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

Research Associate/Senior Research Associate

<h3>Job Description</h3>
Job DescriptionResponsibilities
<ul>
<li>Lead the Machine Learning and Applied Science team through strategic roadmaps to support business initiatives with high impact.</li>
<li>Guide the teams technically, engaging in architecture definition, implementation of best practices, and troubleshooting when needed.</li>
<li>Mange the team through all phases of machine learning development, from concept and design to deployment and monitoring.</li>
<li>Stay ahead of state-of-the-art research and industry trends in machine learning, computer vision, pricing algorithms, and related fields.</li>
<li>Collaborate with other Engineering and Product teams to evaluate requirements and use cases for new systems.</li>
<li>Invest in the career development of the team members, develop future leaders, and create a culture of cohesion and teamwork.</li>
<li>Participate in talent acquisition processes to ensure that we have world class engineers across all skill and experience levels.</li>
<li>Establish metrics to measure the productivity of the team, hold people accountable and identify people issues early.</li>
</ul>
Requirements and Qualifications
<ul>
<li>PhD or MS in Computer Science, Statistics, Operations Research or a relevant quantitative discipline. PhD is strongly preferred.</li>
<li>5+ years of industry experience, with at least 1+ years of experience leading machine learning teams preferably in computer vision or pricing domain.</li>
<li>2+ years of experience as a hands-on senior, staff, or principal engineer with demonstrated end-to-end ownership of a machine learning project before transitioning into managing teams.</li>
<li>Expert level knowledge in Python and SQL for model development and statistical analysis.</li>
<li>Proficiency in ML frameworks such as TensorFlow, PyTorch, or scikit-learn.</li>
<li>Proficiency in edge computing, distributed systems, and cloud platforms (e.g., AWS, GCP, Azure).</li>
<li>Strong foundation in data structures, algorithms, and optimization techniques.</li>
<li>Experience with common program management (MS Project, Visio, etc.) and productivity (Confluence, Jira, etc.) tools.</li>
<li>Excellent written and verbal communication skills with a proven ability to present complex technical information in a clear and concise manner to a variety of audiences.</li>
<li>Previous experience working inside innovative, high-growth environments is a plus.</li>
<li>Publications or patents in relevant fields such as machine learning, computer vision, or optimization is a plus.</li>
</ul>
Company DescriptionStaffSource is committed to creating long-term partnerships where we can truly affect both clients’ and candidates’ lives for the better. Our success is rooted in matching talented professionals with environments that suit their goals, personalities, lifestyles, and skills. A perfect placement allows candidates to thrive in their new role and hiring managers to fill their openings with top talent that aligns with both the needs of their team and the company’s culture. Founded in 2003, StaffSource now has a 20+ year company history with business units operating within Information Technology, Accounting and Finance, Sales, Executive Search and more. Still headquartered in Knoxville, TN and lead by our founder John Sharpe, we are now serving clients and candidates all across the United States. We conduct national, regional, and localized talent searches based on the specific needs of each client and the unique goals of top talent everywhere. 
<h3>Company Description</h3>
StaffSource is committed to creating long-term partnerships where we can truly affect both clients’ and candidates’ lives for the better. Our success is rooted in matching talented professionals with environments that suit their goals, personalities, lifestyles, and skills. A perfect placement allows candidates to thrive in their new role and hiring managers to fill their openings with top talent that aligns with both the needs of their team and the company’s culture.\r\n\r\n Founded in 2003, StaffSource now has a 20+ year company history with business units operating within Information Technology, Accounting and Finance, Sales, Executive Search and more. Still headquartered in Knoxville, TN and lead by our founder John Sharpe, we are now serving clients and candidates all across the United States. We conduct national, regional, and localized talent searches based on the specific needs of each client and the unique goals of top talent everywhere.

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