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<h3>Job Description</h3>
Job Description
Job Location:160 McLean Drive,&nbsp;Romeo, MI 48065
Position Type: Direct Hire&nbsp;
 
 
Education Qualification:
 
• Bachelor’s Degree (chemistry or material science) with 10+ years of product development experience
• Masters with 5+ years of product development experience or
• PhD in the sciences, typically in chemistry or material science.
 
&nbsp;Job Requirements:
 
•&nbsp; &nbsp; At least 5 years of experience leading and mentoring research and development personnel toward the identification and development of new technologies in a business setting. Select skills in technical/scientific disciplines, as required. &nbsp;
• Very adept at maintaining and improving safety requirements in the laboratory and work space.
• Select skills in technical/scientific disciplines, as required. &nbsp;
• Versed in scientific methods, laboratory apparatus, and communication skills.
 
Responsibilities of this position:
 
•&nbsp; &nbsp; Identify and create new technologies in structural and/or environmental sealing polymeric materials and processes through a technically fundamental approach. &nbsp;
•&nbsp; &nbsp; Develop fundamental knowledge on the relationship of materials, processes, structures, and properties. &nbsp;
•&nbsp; &nbsp; Lead a set of R&amp;D personnel to independently plan and execute research and development projects to explore new technologies, products, or modes of problem solution.
•&nbsp; &nbsp; Provide mentorship to less-experienced associates. &nbsp;
•&nbsp; &nbsp; Generate and interpret data in context of problem resolution and effectively communicate findings and direction to other departments in the organization.
•&nbsp; &nbsp; Maintain and expand expertise in a set of scientific areas, including physical, chemical, analytical, or formulation principles and methods. &nbsp;
•&nbsp; &nbsp; Help develop mechanistic understanding of current products and processes. &nbsp;
• Cultivate global collaboration in the internal and external scientific community. &nbsp;
• Support patent activities through filing activities, patent surveillance, and defense of our intellectual property. &nbsp;
• Serve as a champion of safety practices in the laboratory and office environments.
• Provide leadership to technicians and specialists. &nbsp;
• Very competent with self-directed work.
• Construction, maintenance, and safety responsibilities for laboratory workspace and equipment.
Company DescriptionZobility (RGBSI), is dedicated to providing the highest quality of services to our clients and employees. We are proud to be the primary partner to top companies in the automotive, aerospace &amp; defense, IT, media &amp; entertainment, sports, energy, and finance industries. As a result of our clients' continued growth, we are looking for energetic, personable professionals to partner with these leading US companies 
<h3>Company Description</h3>
Zobility (RGBSI), is dedicated to providing the highest quality of services to our clients and employees. We are proud to be the primary partner to top companies in the automotive, aerospace &amp; defense, IT, media &amp; entertainment, sports, energy, and finance industries. As a result of our clients' continued growth, we are looking for energetic, personable professionals to partner with these leading US companies

Senior Scientist (R&D)

<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
This position will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations.
Responsibilities
<ul>
<li>Prepare and follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and logbooks</li>
<li>Able to identify, design, and implement process improvements</li>
<li>Comply with GMP protocols</li>
<li>Operate large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)</li>
<li>Assist other chemists within the Manufacturing group during synthesis and purification of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Mobile phase preparation</li>
<li>Column Packing</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Perform oligonucleotide/intermediate analysis via LCMS</li>
<li>Assist in scale up/process development from small/mid-scale chemistry</li>
<li>Communicate with cross-functional groups such as Process Development, Analytical Development, Quality Control, Quality Assurance, etc.</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
<li>Track and update raw material usage in D365 ERP software</li>
<li>Act as production campaign lead</li>
<li>Assist with new personnel training</li>
<li>Address and resolve production challenges proactively, utilizing analytical and critical thinking skills</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in a scientific field</li>
<li>5-10 years experience in a similar position</li>
<li>Good verbal and written communication skills</li>
<li>Ability to work in a team environment</li>
<li>Ability to pay attention to detail</li>
</ul>
Preferred:
<ul>
<li>Experience working in a GMP setting and controlled documentation</li>
</ul>
Wisconsin pay range $85,000—$95,000 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

Associate Manufacturing Scientist III

<h3>Job Description</h3>
Job Description
Leukemia Research Scientist: Tampa, FL
Children's Cancer Research Group Laboratory is looking for a research scientist to direct, plan, supervise and execute laboratory research projects regarding the etiology of acute leukemias. A Ph.D., an appropriate background and experience is required. Must be able to personally perform the laboratory tests.&nbsp; Competitive salary and benefits provided. Resumes ONLY (do not personally deliver a resume. It will not be considered) Please send resume with the required qualifications only to:
<a href="mailto:ctebbi@childrenscancerresearchgroup.org" target="_blank">ctebbi@childrenscancerresearchgroup.org</a>&nbsp;

Leukemia Research Scientist

<h3>Job Description</h3>
Job Description
Position Purpose: 
We are seeking an analytical chemist with general laboratory experience including creation of standards/spiking mixes, sample preparation, and sample analysis as well as familiarity with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms. The focus of this role will be on providing technical support to Signature Science’s quality assurance (QA) contracts for defense and homeland security programs as well as commercial proficiency testing (PT) programs, including HazMat PT, hemp/cannabis PT, and custom PT programs. The successful candidate will also support internal Signature Science quality programs through maintenance of the quality management system and QA laboratory support. 

Essential Duties and Responsibilities:
<ul>
<li>Assist with planning and implementation of chemical analysis proficiency tests for methods such as gas chromatograph mass spectrometry (GC/MS), Fourier transform infrared spectroscopy (FTIR), percent moisture determination, liquid chromatography with tandem mass spectrometry (LC-MS/MS), high performance liquid chromatography - ultraviolet (HPLC-UV), and Raman. Activities include developing proficiency test plans, performing laboratory pilot testing, preparing and verifying proficiency test samples, and packaging samples for shipment.</li>
<li>Perform laboratory activities related to the preparation and verification of proficiency test samples, as detailed below: o Creation of standards/spiking mixes, o Sample creation, o Sample extraction/dilution, and sample analysis, using techniques such as GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and Raman.</li>
<li>Maintain laboratory equipment and laboratory records.</li>
<li>Perform laboratory inventories, purchase laboratory supplies, and maintain appropriate purchasing records.</li>
<li>Evaluate special study and proficiency test data, identify data trends and other issues, and help prepare reports.</li>
<li>Lead or assist with the validation and/or verification of new methods</li>
<li>Contribute to the development and revision of internal and external quality documents based on ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and Clinical Laboratory Improvement Program (CLIP) standards, as applicable.</li>
<li>Perform internal audits of Signature Science systems and procedures against relevant internal or external standards such as ISO/IEC 17025, ISO/IEC 17043, and ISO 17034.</li>
<li>Regularly communicate with internal laboratory staff to help resolve laboratory or other quality-related issues.</li>
<li>Other activities may include: o Assisting client laboratories in preparing for external ISO/IEC 17025 accreditation audits and attend assessments as an advocate for the client laboratory o Communicating with external laboratory staff to help resolve QA, PT, or other quality-related issues o Providing feedback and help prepare auditee corrective actions packets for submission to the accreditation body or certification body o Providing ISO/IEC 17025 training or training on other quality topics to clients o May serve as a task leader on one or more projects </li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li> General chemistry laboratory experience (e.g., creation of standards/spiking mixes, sample extraction/dilution, and sample analysis).</li>
<li>Knowledge of and/or experience with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms.</li>
<li>General quality management experience, preferably in an analytical laboratory setting.</li>
<li>Proficiency in MS Word, MS Excel, and MS PowerPoint.</li>
<li>Strong written and verbal communication skills.</li>
<li>Proactive, self-starter Preferred knowledge, skills, and abilities include:</li>
<li>Laboratory experience with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms.</li>
<li>Experience assessing data for trends.</li>
<li>Analytical laboratory auditing experience.</li>
<li>Knowledge and experience with relevant quality standards, including ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and/or CLIP.</li>
<li>Ability to lead small teams and ensure accurate and timely submission of project deliverables.</li>
</ul>

Education/Experience:
<ul>
<li>Bachelor degree (or higher) in chemistry, biochemistry, or related field.</li>
<li>At least 3 years experience performing analytical chemistry laboratory work</li>
</ul>
 
Certificates and Licenses:
None upon hire
 
Clearance:
Candidate must be able to obtain a Secret level security clearance.

Supervisory Responsibilities:
May serve as a task leader on one or more projects
 
Working Conditions/ Equipment:
<ul>
<li>Ability to work in varying conditions to include: traditional office environments with sedentary extended periods required for voluminous data analysis via office automation;</li>
<li>Climate controlled laboratory environments requiring extended periods of standing when performing laboratory analyses, or during audits and SOP observation;</li>
<li>Mobile laboratories, subject to wide ranges of temperature and humidity requiring extended periods of standing, stooping or kneeling in confined spaces; conference, classrooms or theaters that involve extended periods of standing for training delivery or command briefings; and outdoors in various weather and lighting conditions including heat, humidity, cold, snow, bright sun, and dark night.</li>
<li>Exposure to various chemical and biological materials associated with an analytical lab or facility.</li>
<li>Ability to wear required personal protective equipment (PPE) including gloves, coats or gowns, shoe cover, tyvek coveralls, safety glasses, respirators, and/or PAPRs.</li>
<li>Subject to medical monitoring based on lab functions.</li>
</ul>

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.

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Associate QA Chemist

<h3>Job Description</h3>
Job DescriptionThis is an Associate Scientist/Scientist role in the Bioanalytical Group to help developing, qualifying/validating bioanalytical methods, and analyzing small and large molecule in different biological matrix. Experienced in analytical techniques such as ELISA, MSD, PCR is preferred. Job title and compensation will be based on candidates credentials

Associate Scientist/Scientist

<h3>Job Description</h3>
Job Description
Our client, leading leader in biotechnology and diagnostics, is looking for Chemist/Scientist based out of Indianapolis, IN. If you are interested in discussing further, please review the details below. 
 
Duration: Long term contract (Possibility of further extension) 
Pay Rate: $45/hr on W2 DOE 
 
Job Summary: 
Executes all pre-clinical scientific research and/or development strategies in research and development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. The Opportunity:
As a Scientist, you will provide testing support for product and process research and development (including design, development, analysis, troubleshooting, etc). You will apply sound experimental design, perform complex scientific research to support research and development of product formulations and/or analytical methods. Possess an in-depth knowledge and experience in the field of analytical chemistry, electrochemistry, biosensors, in-vitro diagnostics, and/or biomedical engineering. Your duties will be dynamic and complex often involving research, analysis, and solution development. 
Qualifications: 
· Applies deep and intensive knowledge of scientific principles. 
· Performs laboratory based studies and experimentation to generate data relevant to various product development projects specifically, the Diabetes Care portfolio. 
· Test and assess innovative technologies as part of our Research and Early Development Scouting efforts.
· Bachelor’s degree in Chemistry, Biochemistry, or a related Life Sciences field with 5 years of relevant experience or Master of Science/PhD with 2 years of relevant experience
· 2+ years of experience in, biomedical or analytical chemistry 
· 2+ years of experience in the field of biosensors 
 
Preferred: 
· More than 5 years of progressive work experience in an appropriate scientific field. 
· Previous Lab based role / safety focused role 
 
If interested, please send your updated resume at <a href="mailto:hr@dawarconsulting.com" target="_blank">hr@dawarconsulting.com</a>/<a href="mailto:akansha@dawarconsulting.com" target="_blank">akansha@dawarconsulting.com</a>

Chemist/Scientist

<h3>Job Description</h3>
Job DescriptionPosition overview The Metrology Specialist – Metrology Systems Sales is responsible for driving sales growth of advanced metrology systems across New England and New York, with a primary focus on managing and supporting distributor partners and key end‑user accounts. The role is mid‑level, owning a defined territory and full sales cycle for capital metrology solutions including vision systems, optical comparators, and force/material testing systems. Key responsibilities
<ul>
<li>Achieve territory order and revenue targets for all metrology systems by executing a structured territory plan covering New England and New York.</li>
<li>Develop, manage, and support authorized distributor partners through joint sales calls, training, opportunity reviews, and structured growth plans.</li>
<li>Identify, qualify, and close new business at end‑user accounts in medical device, aerospace, automotive, job shops, and general manufacturing.</li>
<li>Plan and conduct onsite and virtual product demonstrations, presentations, and technical discussions to align metrology solutions with customer quality and production requirements.</li>
<li>Coordinate applications studies, sample measurements, and pre‑sale evaluations with internal applications and product specialists to validate solutions and support proposals.</li>
<li>Maintain an accurate pipeline, forecast, and account plans in the company CRM, providing regular territory updates and competitive feedback to sales leadership.</li>
<li>Represent the company at regional trade shows, distributor open houses, and industry events to generate leads and strengthen brand presence in precision metrology.</li>
</ul>
Required qualifications and experience
<ul>
<li>3–7 years of successful B2B technical or capital equipment sales experience, preferably in metrology, precision measurement, or related industrial automation.</li>
<li>Working knowledge of dimensional inspection practices, including experience with vision systems, optical comparators, CMMs, force/material testing, or similar measurement technologies.</li>
<li>Ability to read engineering drawings and interpret GD&amp;T, and to communicate credibly with quality, manufacturing, and engineering stakeholders.</li>
<li>Proven experience working through and with distributors or manufacturer’s reps, including joint account planning and opportunity management.</li>
</ul>
Skills and attributes
<ul>
<li>Strong territory planning, organization, and time‑management skills, with high personal accountability for results.</li>
<li>Consultative selling style with solid questioning, discovery, and value‑based closing skills in multi‑stakeholder environments.</li>
<li>Excellent verbal and written communication skills, including delivering technical presentations and training to distributor sales teams and customers.</li>
<li>Comfortable working remotely in the field with frequent regional travel (up to ~60–70%) across New England and New York.</li>
</ul>
Reporting and location
<ul>
<li>Reports directly to the Director of Sales – Metrology Systems, who leads North American sales for vision systems, optical measuring projectors, and force measurement systems.</li>
<li>Candidate should reside within the territory (New England or New York) with convenient access to major customer hubs and distributor locations.</li>
</ul>
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tlGHTqUI9M

Metrology Specialist

<h3>Job Description</h3>
Job Description
Reports to: Shift Supervisor
These jobs require some moderate/heavy lifting. Optima is a 24-hour operation; thus, candidates must be able and willing to workdays, nights, weekends, and holidays. A High School diploma/GED and math skills are required. Work as directed by the Shift Supervisor, including primarily:
• Setting up pumps, hoses, etc. for use
• Setting up reactors, tanks, etc. for use
• Climbing into reactors and tanks to clean and inspect them
• Lifting bags of raw materials (20 to 50 lbs. each)
• Recording data on batch sheets, etc.…
• Working 12-hour shifts, sometimes at nights and weekends
• Working outside in the elements year round
• Pumping and general handling of chemicals (some toxic, flammable, corrosive)
• Wearing protective equipment (suits, respirators, gloves, etc.…)
• Moving material containers using lift devices as well as limited physical adjustments by hand with appropriate support.
• Filling of containers of various sizes
• Pressurizing, pulling vacuum, heating, and cooling of equipment as needed
• Loading and unloading of tanker truck by pressure or pump.
• Other general plant maintenance and cleanup as directed.
• Maintain a neat and clean working environment.
• Stay Clean Shaved for full face respirator usage.
• Follow all procedures and standards.
• Report to work on time as scheduled.
• Progress through the operator Area qualifying examines within designated timeline.
• Training other employees.
• Follow instruction via supervisors/ assistant Supervisors.
Company Description<a href="http://www.optimachem.com" target="_blank">www.optimachem.com</a> 
<h3>Company Description</h3>
<a href="http://www.optimachem.com" target="_blank">www.optimachem.com</a>

Chemical Operator

<h3>Job Description</h3>
Job Description
Adesis Inc. - a subsidiary of Universal Display Corporation (Nasdaq: OLED), a global leader in organic light emitting diodes - is a premier contract development and manufacturing organization (CDMO) accelerating our clients’ success in the biotech, pharmaceutical and specialty chemistry industries through our innovative chemistry and solutions. Adesis Inc. encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/ pharmaceutical hub. Our business model provides clients with organic chemistry services in three areas: early-stage research, scale-up and development, and specialty manufacturing. We specialize in organic and organometallic synthesis, from milligrams to multi-kilogram quantities, and our exceptional technical team prides ourselves in our ability to solve challenging chemistry problems for our growing client base. Adesis is an extraordinary company looking for extraordinary talent! Our mission is to accelerate our clients’ success through innovative chemistry and solutions, and we offer promising careers in an inclusive work environment aligned with our values of innovation, ownership and integrity. Job Summary The Analytical Chemist I will support the Quality Control laboratory by performing analytical testing of raw materials, in-process samples, intermediates, and finished products. The technician will ensure compliance with ISO-9001 Standards, internal procedures, and client-specific requirements while maintaining accurate documentation and supporting laboratory operations. Essential Duties and Responsibilities Include the following. Other duties may be assigned.
<ul>
<li>
Perform routine analytical testing using techniques such as HPLC, GC, LC-MS, UV-Vis, FTIR, and wet chemistry methods.
</li>
<li>
Execute raw material, in-process, release, and stability testing in accordance with SOPs and regulatory guidelines.
</li>
<li>
Prepare, standardize, and document test solutions and reagent.
</li>
<li>
Calibrate and maintain analytical instruments; promptly report malfunctions.
</li>
<li>
Maintain accurate laboratory records in compliance with Good Documentation Practices (GDP).
</li>
<li>
Identify and correct problems with instruments in QC lab. Identify and communicate problems and solutions related to process, procedure, and materials to Analytical team lead and QC Chemists.
</li>
<li>
Maintain cleanliness and organization of lab by following safety, regulatory, and chemical hygiene plan
</li>
<li>
Perform daily record keeping in electronic lab notebook,
</li>
<li>
Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste
</li>
<li>
Assist in OOS/OOT investigations and support root cause analysis.
</li>
<li>
Attend and participate in QC Team meetings. Develop team skills.
</li>
<li>
Participate in continuous improvement initiatives to optimize laboratory efficiency and data integrity.
</li>
</ul>

Required Qualifications
<ul>
<li>
Bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field.
</li>
<li>
QC analytical laboratory experience in a pharmaceutical, biotech, or CDMO environment, preferred.
</li>
</ul>

Technical Skills:
<ul>
<li>
Hands-on experience with HPLC, GC, and spectroscopic techniques.
</li>
<li>
Familiarity with cGMP, ICH, and USP/EP guidelines preferred.
</li>
<li>
Strong analytical and problem-solving skills with attention to detail.
</li>
</ul>

Other Skills:
<ul>
<li>
Proficiency in Microsoft Office and laboratory data systems (e.g., Empower, Open Lab CDS, Mass hunter and LIMS) is a plus.
</li>
<li>
Excellent written and verbal communication skills.
</li>
<li>
Strong organizational skills and ability to work both independently and in a team setting.
</li>
</ul>

Current Benefits at UDC:
<ul>
<li>
Competitive base salary and annual bonus program
</li>
<li>
Medical/Prescription Drug coverage, Dental, and Vision for employees and family
</li>
<li>
Option between Flexible Spending account (FSAs) or Health Savings Account (HSA)
</li>
<li>
Group Term Life insurance, short term disability, and long-term disability benefits for employees
</li>
<li>
Employee Stock Purchase Plan (ESPP)
</li>
<li>
401(k) company contribution
</li>
<li>
Annual charitable matching gift
</li>
<li>
Generous Paid Time Off
</li>
</ul>
Annual compensation range: $65k-$75k

Analytical Chemist

<h3>Job Description</h3>
Job Description
Our Story
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow.
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program (ESOP) and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage — with medical premiums either paid by Superior or highly subsidized — so you and your family can access great benefits with minimal cost.
You’ll also join a supportive team, where paid training and experienced coworkers help you learn, grow, and succeed from day one.
At SUPERIOR, you get more than a job — you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to success.
What We’re Looking For
We are currently seeking a Chemical Handler to work at our Arnold, MO location.
This role is responsible for:
<ul>
<li>Daily production</li>
<li>Unloading raw materials</li>
<li>Completing paperwork</li>
<li>Maintaining a safe operation</li>
</ul>
Schedule:
<ul>
<li>Full-time, 1st shift</li>
<li>Monday–Friday, 7:30 a.m. – 5:00 p.m.</li>
<li>Additional hours may be required</li>
</ul>
What You’ll Do
You will:
<ul>
<li>Transfer products into and out of pails, drums, and totes using transfer pumps and hoses</li>
<li>Read paperwork with chemical amounts and blending instructions</li>
<li>Pull product samples and submit them to the Lab for quality control</li>
<li>Label containers and secure closures</li>
<li>Inspect, label, store, and prepare products for shipment</li>
<li>Stage, load, and unload pails, drums, and totes</li>
<li>Operate a forklift</li>
<li>Wear required PPE for safety</li>
<li>Keep your work area safe, clean, and orderly</li>
<li>Lift and/or move 55 lbs</li>
<li>Cross-train in areas such as shipping/receiving, bulk handling, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventive maintenance, and yard truck spotting</li>
</ul>
Candidates Should Possess
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Effective verbal and written communication skills to work with co-workers, chemists, administrative staff, delivery personnel, and management</li>
</ul>
What We Offer
At Superior, we take care of our people. Our comprehensive benefits package includes:
<ul>
<li>Medical Insurance – 100% company-paid HDHP or a low-cost PPO option</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>401(k) Retirement Plan</li>
<li>Flexible Spending Accounts (FSA)</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Dental, Vision &amp; Life Insurance</li>
<li>Short-Term &amp; Long-Term Disability (STD &amp; LTD)</li>
<li>Paid Training from day one</li>
</ul>
Join a company that invests in you — personally, professionally, and financially.
EOE including disability/veteran/drug free

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