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<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
As a Quality Control Chemist, you will be responsible for performing routine analysis of raw materials, in-process, and finished products. This includes conducting tests such as titrations, FTIR, GC, HPLC, Color, and using a viscometer. Your role involves performing calculations for batch tests in a lab environment using instrumentation and physical test methods. You will follow setup procedures and work instructions for laboratory equipment while adhering to customer and company quality standards. Safety is paramount, so you must follow all safety rules and regulations, including the use of appropriate PPE at all times.
Responsibilities
<ul>
<li>Conduct routine analysis of raw materials, in-process, and finished products.</li>
<li>Perform tests including titrations, FTIR, GC, HPLC, Color, and viscometer.</li>
<li>Carry out calculations for batch tests using lab instrumentation and physical test methods.</li>
<li>Set up and operate laboratory equipment according to established procedures.</li>
<li>Ensure compliance with customer and company quality standards.</li>
<li>Follow all safety rules and regulations, using appropriate PPE at all times.</li>
</ul>
Essential Skills
<ul>
<li>Minimum 1 year of industry experience in analytical testing, troubleshooting, and quality assurance.</li>
<li>Proficiency in gas chromatography (GC), high-performance liquid chromatography (HPLC), and FTIR.</li>
<li>Strong understanding of quality control processes in chemical manufacturing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Chemistry or other Sciences preferred; AS in Chemistry is acceptable.</li>
<li>Experience in chemical manufacturing is preferred.</li>
<li>Familiarity with basic laboratory equipment (GC/LC/FTIR) and techniques (titration, liquid-liquid partition).</li>
</ul>
Work Environment
You will work independently on the night shifts in the lab, handling chemical products. The lab is equipped with newer equipment to assist with testing. The work schedule is a 12-hour night shift, following a 2/2/3 non-rotating pattern in a 7-day x 24-hour chemical operation, from 7PM to 7AM. The role offers opportunities for cross-training and education in certifications, contributing to employee development and career growth.
Job Type &amp; Location
This is a Contract to Hire position based out of Greensboro, NC.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 Greensboro,NC.
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.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist - Architectural PaintJob Description
Join our dynamic team as a Chemist in the Architectural Paint division, where you will be instrumental in testing and developing new paint materials. Your role will involve mixing chemicals and additives to create innovative architectural paint, ensuring that quality standards are met and environmental impacts are considered.
Responsibilities
<ul>
<li>Test new architectural paint materials within a laboratory setting.</li>
<li>Mix chemicals and additives to create architectural paint, ensuring quality standards and environmental considerations are met.</li>
<li>Select appropriate resins, pigments, additives, and solvents to achieve desired paint properties such as adhesion, durability, color, and gloss.</li>
<li>Conduct laboratory testing including viscosity, draw downs on different substrates, stain resistance, and application testing.</li>
<li>Provide technical support for key innovation projects and customer services.</li>
<li>Ensure lab safety by following general safety procedures.</li>
<li>Perform hands-on work in the lab to deliver reliable results.</li>
<li>Collaborate with scientists and technicians to plan and execute technical lab work.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemistry, particularly in paint and coating.</li>
<li>Knowledge of polymer chemistry.</li>
<li>Experience with viscosity, application testing, draw down, and stain resistance.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Diploma with 5+ years of hands-on paint/coating lab experience.</li>
<li>Associates degree with 2+ years of hands-on paint/coating lab experience.</li>
<li>Bachelor's degree with co-op or industrial internship preferred.</li>
<li>Experience in making paint or coatings, with a preference for architectural paint.</li>
<li>Experience conducting lab testing such as viscosity and application testing.</li>
<li>Knowledge of rheology and viscosity.</li>
</ul>
Work Environment
Work within the Applications Lab, a specialized environment that fosters innovation and technical excellence. You will be part of a team that is committed to developing cutting-edge solutions in architectural paint, with access to expert training and tutoring.
Job Type &amp; Location
This is a Contract to Hire position based out of Wilmington, DE.
Pay and Benefits
The pay range for this position is $26.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Wilmington,DE.
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.

Paint Chemist

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Mechanistic Pharmacology Intern – RNAi Mechanisms &amp; Functional Genomics will support discovery research at Arrowhead Pharmaceuticals by contributing to fundamental studies aimed at understanding the cellular mechanisms that drive the activity of Arrowhead's proprietary RNAi therapeutic platform (TRiM). This internship provides hands-on exposure to cutting-edge laboratory and computational approaches used to interrogate RNAi biology, pharmacodynamics, and gene knockdown mechanisms. The intern will work closely with experienced scientists on defined research projects that generate insights critical to drug development and discovery strategy.
This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Complete onboarding activities including shadowing team members, skill assessments, learning core laboratory techniques, and reviewing foundational scientific background.</li>
<li>Execute one of two predefined research projects within the Mechanistic Pharmacology group.</li>
<li>Support execution of a CRISPR-based screening project to identify cellular pathways and factors that enable productive RNAi-mediated target gene knockdown, including analysis and validation of screening hits.</li>
<li>Support studies investigating the relationship between cellular uptake, RISC loading, and mRNA degradation activity to better understand RNAi pharmacokinetics and pharmacodynamics.</li>
<li>Learn and apply laboratory methodologies fundamental to Mechanistic Pharmacology research, including:
<ul>
<li>Tissue culture</li>
<li>Quantitative PCR (qPCR)</li>
<li>siRNA and plasmid transfection</li>
<li>Protein biochemistry and analysis</li>
<li>Confocal and live-cell fluorescence microscopy</li>
<li>Flow cytometry</li>
</ul>
</li>
<li>Collect, analyze, and interpret experimental data using tools such as GraphPad Prism, FACSDiva, FlowJo, Design and Analysis (Thermo Fisher), CellProfiler, ZEN Suite, ImageJ/FIJI, Microsoft Excel, and Benchling.</li>
<li>Read and critically evaluate primary scientific literature to contribute to hypothesis generation and data interpretation.</li>
<li>Present project updates in weekly group meetings.</li>
<li>Prepare final deliverables, including a scientific poster and a ~20-minute presentation summarizing project objectives, results, and learnings.</li>
</ul>
Requirements:
<ul>
<li>Currently enrolled in a bachelor's degree program at an accredited university or college and majoring in a scientific discipline such as Biochemistry, Biology, Chemistry, Engineering, Genetics, or a related scientific discipline.</li>
<li>Excellent verbal and written communication skills, including comfort presenting in group settings.</li>
<li>Strong problem-solving and organizational skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Ability to lift up to 40 lbs.</li>
<li>Willingness and ability to spend 75% of the workday walking the facility and 25% at a desk.</li>
</ul>
Preferred:
<ul>
<li>Fundamental understanding of cell biology and biochemical principles.</li>
<li>Previous laboratory experience and familiarity with basic lab techniques.</li>
<li>Curiosity, enthusiasm for discovery science, and willingness to learn new approaches and techniques.</li>
</ul>
Wisconsin pay range $9,240—$9,240 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Mechanistic Pharmacology - RNAi Mechanisms & Functional Genomics

<h3>Job Description</h3>
Job DescriptionAerotek is Hiring Cleanroom Technicians
📍 Allentown, PA
&amp;#x1F4B0; Pay: $22–$28/hr (based on experience) + 15% Night Shift Differential
⏱ Shifts:
<ul>
<li>Day Shift: 6:00 AM – 6:00 PM</li>
<li>Night Shift: 6:00 PM – 6:00 AM</li>
</ul>
Why You’ll Love This Opportunity
<ul>
<li>Great Pay + Built‑In Overtime with 12‑hour shifts</li>
<li>Choose the Shift That Fits Your Schedule – day or night</li>
<li>Clean, Modern Facility – full cleanroom gear provided</li>
<li>Convenient On‑Site Amenities including cafeteria and breakroom</li>
<li>Real Career Growth in a fast‑expanding semiconductor industry</li>
</ul>
What You’ll Do
<ul>
<li>Operate advanced equipment used in semiconductor processing</li>
<li>Perform photolithography, etching, substrate cleaning, and related tasks</li>
<li>Set up and maintain manual and computer‑controlled machinery</li>
<li>Work as part of a team to process wafers and optical components</li>
<li>Monitor quality and make adjustments as needed</li>
<li>Maintain a clean, safe, and organized workspace</li>
</ul>
What We’re Looking For
<ul>
<li>High school diploma or GED</li>
<li>Basic Microsoft Excel &amp; Word skills</li>
<li>Ability to stand for long periods and lift up to 20 lbs</li>
<li>Strong manual dexterity; comfortable using microscopes</li>
<li>Reliable, motivated, and eager to learn new technical skills</li>
</ul>
Ready to Step Into a High‑Tech Career?
<ul>
<li>If you’re looking for stable work, long‑term growth, and a clean, modern environment—this is the place to start.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Breinigsville, PA.
Pay and Benefits
The pay range for this position is $22.50 - $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 Breinigsville,PA.
Application Deadline
This position is anticipated to close on Jan 23, 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.

Cleanroom Technician

<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:
Leads cross-functional collaborations on identifying and developing consumer eyecare products (artificial tears, gels and ointments). Leads the direction, planning, and interpretation of clinical trials or research activities within consumer eye care innovation of one or more programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality data supporting consumer eye care product scientific and business strategy.
Responsibilities:
•Serves as an in-house expert in identification and development of consumer eye care products. As required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May participate in or lead clinical development contributions to due diligence or other business development activity.
• Serves as a champion for innovation in consumer eye care. Actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
•Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff.
•May have responsibility for leading clinical study teams, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for ensuring agreed-upon study enrollment and overall timelines for key deliverables.
•Primary responsibility for and ownership of design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents.
•May oversee the work of Medical and/or Scientific Directors and of Clinical Scientists working on the same or related programs.
•May serve on or co-chair Integrated Evidence Strategy Team(s), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In the role of Co- Chair, responsibilities may include supervision of matrix team members; serving as Clinical Research representative to lend clinical development or medical expertise to Asset Development Teams (ADTs).
•Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. May represent AbbVie at key external meetings.
•Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
•Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Qualifications 
•Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, OD, MD, PharmD) preferred.
•At least 8 years of product development experience with 5 years of experience in consumer eye care in the pharmaceutical industry, academia, or equivalent.
•Direct experience in leading cross-functional and translational development preferred.
•Ability to run a complex clinical research program independently.
•Proven leadership skills and ability to bring out the best in others on a cross-functional global team. Must be able to lead through influence.
•Ability to interact externally and internally to support a global scientific and business strategy.
•Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
•Must possess excellent oral and written English communication skills.
•Ability to exercise judgment and address complex problems and create solutions for one or more projects.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientific Director, Clinical Development - Consumer Eye Care Product Development

<h3>Job Description</h3>
Job Description
 
LABORATORY SUPERVISOR 
1.0 Corporate Job Title
Laboratory Supervisor
2.0 Reporting Relationships
Laboratory Manager
3.0 Position Summary
Assists Management in the responsibility for all day-to-day laboratory operations. Represents the policies, ethics, and culture of the company in a leadership role. Assists and understudies Lab Manager through closely monitoring lab-related customer service, troubleshooting, and problem solving. Supervises and coordinates activities of personnel engaged in performing chemical and physical tests required for quality control of processes and products
4.0 Minimum Requirements
• Bachelor’s degree from four-year college or university or Associates degree or equivalent from two-year college or technical school; or a minimum of three years related experience and/or training; or equivalent combination of education and experience. 
• Ability to define problems, collect data, establish facts, and draw valid conclusions. 
• Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
5.0 Responsibilities
• Ensures all lab staff has adequate resources to perform all aspects of work required.
• Ensures all lab staff are adequately trained to safely perform all required job functions and that competency records are maintained.
• Ensures compliance with all corporate policy procedures in the laboratory.
• Assists Lab Manager regarding sales, profits, costs and expenses to meet/ exceed budgeted financial expectations for the laboratory.
• Provides employee motivation and champions the Quality system, including SQC, Calibrations, Quality Assurance, Training, and Round Robins.
• Communicates with lab staff and management to promote empowerment and accountability.
• Obtains and maintains an in-depth knowledge of local market requirements.
• Understands customer requirements and organizes lab procedures, schedules and staffing to provide for meeting/exceeding same.
• Fosters customer confidence in CCC laboratory work.
• Supports the ISO certificate(s) and manages corrective/preventive actions.
• Reviews local laboratory operations for all aspects of the continuous improvement process.
• Recommends measures to improve testing procedures, use of equipment, and needs for new equipment. Conducts research to develop custom procedures as needed, working in conjunction with senior lab management.
• Maintains open communication with the Lab Manager.
• Represents CCC by appearance and conduct. Behaves ethically at all times; Ensures compliance in all areas
• Ensures laboratory practices meet or exceed company policy and industry standards.
• Establishes or adjusts work schedules to meet testing requirements and control costs.
• Assists with maintaining time, training, calibration, QC and testing records.
• Other duties as may be assigned by Lab Management, and/or senior management.
6.0 Fitness for Duty – Physical Demands
Workday may consist of 8-12 hours however this can vary day to day and shift to shift. Some of the retain work is performed outdoors, wearing full Personal Protective Equipment (PPE), and could include possible exposure to high and low temperatures for a prolonged duration of time. Laboratory work is normally performed indoors under climate-controlled conditions. 
All times listed in the table below are approximate. 
• Maximum Lift-Floor to knee; Knuckle to waist; Waist to shoulder
Weight Up to 45 lbs.- Duration/Day Up to 1 hours.
• Walking
Weight Up to 45 lbs. -Duration/Day Up to 10 hours
• Pushing-Pulling
Weight Variable-Duration/Day Up to 1 hour
• Carrying
Weight Up to 45 lbs.- Duration/Day Up to 2 hours
• Ascend/Descend Ladder/Stair
Weight Up to 45 lbs.- Duration/Day Up to 1 hour
• Extended Reach
Weight Up to 45 lbs.- Duration/Day Up to 1 hour
• Standing
Weight Up to 45 lbs.- Duration/Day Up to 12 hours
• Crouch/Squat/Knee
Weight Up to 45 lbs.- Duration/Day Up to 1 hour
• Tool use
Weight 5-8 lbs.- Duration/Day Up to 1 hour
• Sitting
Weight 5-8 lbs. -Duration/Day Up to 6 hours
• Driving
Weight N/A- Duration/Day Up to 6 hours
All are required to perform this position
This document contains Confidential and Proprietary information which is the property of Camin Cargo Control. None of the information contained herein may be disclosed, reproduced, distributed or used without prior written consent from Camin. All rights reserved.
 
 
 Shift Schedule: Mon - Fri 8:00am to 5:00pm / nights and alternating weekends on-call

Laboratory Supervisor

<h3>Job Description</h3>
Job Description
Duties include but are not limited to:
<ul>
<li>Monitoring the entire Revtech wheat pasteurization system to ensure that the process is running at optimum performance and the finished product produced meets all targeted specifications</li>
<li>Measuring and recording the required parameters of the pasteurization process</li>
<li>Monitoring and recording magnet findings and other food safety documents</li>
<li>Organize, lead, and perform maintenance and sanitation programs for the pasteurization system</li>
<li>Maintain maintenance and sanitation records</li>
<li>Assist in the packing/warehouse operation when necessary</li>
<li>Responsibility to proactively offer facility and system improvements</li>
<li>Actively participate in workplace safety and food safety training</li>
<li>Actively participate in facility’s food safety team</li>
<li>Responsibility to comply with all food safety and work place safety policies</li>
<li>Responsibility to report any issues involving food safety and sanitation</li>
<li>Responsibility to observe and report any unusual activity regarding site security</li>
<li>Perform other duties as required</li>
</ul>
 
Minimum Requirements
<ul>
<li>High school diploma or equivalent</li>
<li>Knowledge of Microsoft Office preferred</li>
<li>Willingness to work all shifts and weekends when required</li>
<li>Physically able to perform all milling requirements including but not limited to:
<ul>
<li>Ability to walk stairs and climb up and down bulk trailers during the course of a nine hour shift</li>
<li>General cleaning</li>
<li>General mill maintenance and repair</li>
</ul>
</li>
</ul>

Qualifications Desired
<ul>
<li>Electrical knowledge and experience including (electric motors, variable frequency drives, prox sensors)</li>
<li>Mechanical knowledge and aptitude</li>
<li>Automation knowledge and experience is a plus</li>
<li>Problem solving skills</li>
<li>Positive attitude – hands-on leadership skills</li>
<li>Self-motivated</li>
</ul>

Thermal Processing Technician

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Computational Discovery Chemistry Intern will join Arrowhead Pharmaceuticals' Discovery Research organization and play an active role in contributing to the expansion of data infrastructure and computational tools within the Computational Chemistry Core. This this role will focus on database development, data analysis, and coding of new tools that support in-silico drug design and AI/ML-driven discovery efforts. The intern will work under the guidance of senior scientists and computational leaders, gaining exposure to applied data science, bioinformatics, and machine learning within a pharmaceutical research environment.
This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Expand and maintain databases supporting computational chemistry and discovery research initiatives.</li>
<li>Program new tools for automated data extraction to support both new and existing databases.</li>
<li>Develop tools for quality control (QC) analysis of biological efficacy data and apply them to collected datasets.</li>
<li>Create tools for streamlined processing of in-silico–generated data.</li>
<li>Contribute to ongoing discovery efforts, including:
<ul>
<li>Development of generative AI / machine learning models for physicochemical and structural prediction of drug molecules.</li>
<li>Development of models integrating biological, bioinformatic, and in-silico calculated data.</li>
</ul>
</li>
<li>Assist with data analysis, visualization, and interpretation to support applied drug discovery efforts.</li>
<li>Collaborate with computational chemists, data scientists, and discovery stakeholders.</li>
<li>Present project updates in weekly group meetings.</li>
<li>Prepare final deliverables, including a scientific poster and a ~20-minute presentation summarizing project objectives, results, and learning.</li>
</ul>
Requirements:
<ul>
<li>Currently enrolled in a bachelor's degree program at an accredited university or college and majoring in computer science or a related field.</li>
<li>Basic command-line experience (Bash/Shell) in Unix and/or Linux environments.</li>
<li>Experience coding in Python (preferred), or demonstrated proficiency in Julia, JavaScript/TypeScript, or R.</li>
<li>Experience with relational databases and query languages such as SQL.</li>
<li>Excellent verbal and written communication skills, including comfort presenting in group settings.</li>
<li>Strong problem-solving and organizational skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Ability to lift up to 40 lbs.</li>
<li>Willingness and ability to spend 25% of the workday walking the facility and 75% at a desk.</li>
</ul>
Preferred:
<ul>
<li>Exposure to applied bioinformatics, including HTC/HPC environments and/or HT-seq analysis.</li>
<li>Interest in AI/ML applications within drug discovery and computational chemistry.</li>
<li>Strong curiosity, initiative, and eagerness to build scalable tools in a scientific research setting.</li>
</ul>

Wisconsin pay range $9,240—$9,240 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Computational Discovery Chemistry

<h3>Job Description</h3>
Job Description
Title: QC Analyst
Location: LaPorte, TX
 
Who we are:
Voted one of the Nation's Best and Brightest Companies to Work for, Kuraray America, Inc. (KAI) is a global leader in specialty chemical, fiber, and resin production. With top-of-the-line research and production facilities and a vast network of supplies from around the world, Kuraray leads the industry in specialty dental, fiber, resin, and elastomer products. Kuraray America is a wholly owned subsidiary of Kuraray Company, Ltd. Based in Tokyo, Japan. Kuraray has operations in 32 countries and employs more than 11,000 employees, including over 800 in the United States.
Why Kuraray:
Kuraray is building a better tomorrow, today. Our team members are dedicated to expanding our business with committed professionals who share essential values such as integrity, excellence, teamwork, and accountability.
As a part of Kuraray America, Inc., our team shares the advantages of working for the leader in specialty chemicals, resins, and fibers. Our international presence and resources allow us to be a world-leading innovator in the industries we service. Yet, despite our size, our people are more than just a number. As a new team member, you can expect to earn responsibility quickly. Our commitment to our people is visible in our comprehensive benefits package. As a Kuraray team member, you will have the opportunity to enjoy competitive salaries and benefits, incentive opportunities, and an excellent work environment.
 
Position Summary:
The Laboratory Analyst provides analytical support to the Production Department via the testing of both process and final product samples and ensures that all sample analyses adhere to strict standard operating and calibration procedures used in the laboratory. This is a DuPont Shift position.
Responsibilities:
<ul>
<li>Analysis of process samples</li>
<li>Analysis of final product samples</li>
<li>Evaluates reported results for consistency with plant process conditions</li>
<li>Performs routine calibration of laboratory equipment</li>
<li>Conducts non-routine testing of samples using approved detailed procedures &amp; methodology</li>
<li>Provides assistance to Lab Manager, Supervisor and Chemist</li>
</ul>
 
Minimum Qualifications:
<ul>
<li>2 years of laboratory experience in a manufacturing/production environment preferred</li>
<li>HS Degree or equivalent required</li>
<li>Strong computer and hardware skills</li>
<li>Hands-on experience with GC, AA, Titration, viscosity measurement, polymer testing equipment</li>
<li>Hands-on experience with procedures used to calibrate and standardize laboratory test equipment as well as the preparation of reagents</li>
<li>Ability to multi-tasks in a fast-paced, high-energy environment</li>
<li>Strong analytical and problem solving skills</li>
<li>Strong commitment to safety</li>
<li>Excellent oral and written communication skills</li>
</ul>
 
Competencies:
<ul>
<li>Customer Focus
<ul>
<li>Building strong customer relationships and delivering customer-centric solutions.</li>
</ul>
</li>
<li>Business Insight
<ul>
<li>Applying knowledge of business and the marketplace to advance the organization's goals.</li>
</ul>
</li>
<li>Cultivates Innovation
<ul>
<li>Creating new and better ways for the organization to be successful.</li>
</ul>
</li>
</ul>
<ul>
<li>Action Oriented
<ul>
<li>Taking on new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.</li>
</ul>
</li>
<li>Ensures Accountability
<ul>
<li>Holding self and others accountable to meet commitments.</li>
</ul>
</li>
<li>Drives Results
<ul>
<li>Consistently achieving results, even under tough circumstance</li>
</ul>
</li>
<li>Collaborates
<ul>
<li>Building partnerships and working collaboratively with others to meet shared objectives.</li>
</ul>
</li>
<li>Values Difference
<ul>
<li>Recognizing the value that different perspectives and cultures bring to an organization</li>
</ul>
</li>
<li>Communicates Effectively
<ul>
<li>Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences.</li>
</ul>
</li>
<li>Courage
<ul>
<li>Stepping up to address difficult issues, saying what needs to be said.</li>
</ul>
</li>
<li>Instills Trust
<ul>
<li>Gaining the confidence and trust of others through honesty, integrity, and authenticity.</li>
</ul>
</li>
<li>Situational Adaptability
<ul>
<li>Adapting approach and demeanor in real time to match the shifting demands of different situations.</li>
</ul>
</li>
</ul>
 
We offer a competitive compensation package that includes base pay and an annual incentive. This program is designed to reward individual performance and align overall rewards with corporate and team performance.
Our employees benefit from a robust healthcare package that includes wellness reimbursements, along with generous perks such as three weeks of paid time off, ten company holidays, paid parental leave, education reimbursement, and a matching 401k plan, among other offerings. 
 
Applicants must be authorized to work for ANY employer in the U.S.
Learn more at kuraray.us.com/careers/
 Kuraray America, Inc. is an Equal Employment Opportunity/disability/protected veteran status
No third-party candidates accepted.
 Job Posted by ApplicantPro

QC Laboratory Analyst (Laporte)

<h3>Job Description</h3>
Job Description
Overview
Join the Best in Pests℠ – Build Your Future with Orkin!
Are you looking for a hands-on career, not just a job? Do you have experience in construction, roofing, or home improvement, and want to use your skills to build a stable career in a recession-resistant industry? 
At Orkin, we protect what people value most, their homes and businesses. We’ve been the industry leader for more than 120 years, and we’re looking for motivated individuals who are eager to grow, learn, and make a difference. 
No prior pest control experience? No problem. Our award-winning paid training program will equip you with everything you need to know to succeed. 
Why You’ll Love Being an Orkin Pro:
<ul>
<li>Make an Impact: Help customers protect their homes and improve energy efficiency with solutions like attic remediation, crawlspace encapsulation, and radiant barrier installation. </li>
</ul>
<ul>
<li>Earn While You Learn: Get paid while completing industry-leading training—no experience required. </li>
</ul>
<ul>
<li>Career Growth: Advance into leadership, sales, or management with a company that promotes from within. </li>
</ul>
<ul>
<li>Job Stability: Pests don’t stop and neither do we. Enjoy consistent work in a recession-proof industry. </li>
</ul>
<ul>
<li>Tools &amp; Support: Receive a company vehicle, fuel card, mobile device, and all the technology you need to succeed. </li>
</ul>

We are driven by a shared mission and grounded in values that define everything we do: 
<ul>
<li>Safety </li>
</ul>
<ul>
<li>Professionalism </li>
</ul>
<ul>
<li>Empathy </li>
</ul>
<ul>
<li>Integrity </li>
</ul>
<ul>
<li>Innovation </li>
</ul>

 
Responsibilities
What You’ll Do:
<ul>
<li>Inspect and install pest and home protection systems. </li>
</ul>
<ul>
<li>Working collaboratively on a crew of technicians to complete a </li>
</ul>
<ul>
<li>Complete attic and crawlspace services, including encapsulation and insulation </li>
</ul>
<ul>
<li>Light carpentry work </li>
</ul>
<ul>
<li>Communicate clearly with customers. </li>
</ul>
<ul>
<li>Maintain company equipment and complete reports via handheld device. </li>
</ul>

What’s In It for You:
<ul>
<li>Competitive pay starting at $20+ per hour (based on experience) </li>
</ul>
<ul>
<li>Comprehensive benefits: Medical, dental, vision, life, and 401(k) with company match </li>
</ul>
<ul>
<li>Paid time off: Vacation, holidays, and sick leave </li>
</ul>
<ul>
<li>Employee perks: Tuition reimbursement, scholarship programs, and discounts </li>
</ul>
<ul>
<li>Paid training and all tools provided </li>
</ul>
 
Qualifications
What We’re Looking For:

<ul>
<li>Candidates with construction, roofing, HVAC, or maintenance experience (preferred) </li>
</ul>
<ul>
<li>Strong work ethic and commitment to customer service </li>
</ul>
<ul>
<li>Team player with a positive, professional attitude </li>
</ul>
<ul>
<li>Ability to work independently and manage your daily schedule </li>
</ul>
<ul>
<li>Comfortable working in varying weather conditions, confined spaces, and on roofs. </li>
</ul>

Minimum Requirements:

<ul>
<li>High School Diploma or equivalent </li>
</ul>
<ul>
<li>Demonstrated experience using a metal brake to bend or shape metal components </li>
</ul>
<ul>
<li>Valid driver’s license and good driving record </li>
</ul>
<ul>
<li>Ability to obtain a state pesticide license within 90 days (company-paid training) </li>
</ul>
<ul>
<li>Ability to lift 50 lbs., climb ladders, and work safely in attics or crawlspaces </li>
</ul>
<ul>
<li>You must wear PPE, including an OSHA-compliant respirator, as required </li>
</ul>

Orkin is proud to be an Equal Opportunity Employer committed to building a diverse, inclusive team. Veterans and individuals with disabilities are encouraged to apply. 

#ORKAPP

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