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<h3>Job Description</h3>
Job DescriptionJob Title: Analytical ChemistJob Description
We are seeking a skilled Analytical Chemist who can perform release and in-process testing for materials and finished products. The candidate should be proficient in using various laboratory instruments and adept at interpreting chromatography data. This role requires the ability to perform and review complex calculations, document GMP activities accurately, and adhere to all applicable procedures and specifications.
Responsibilities
<ul>
<li>Conduct release and in-process testing for materials and finished products.</li>
<li>Perform wet and analytical chemistry analysis on raw materials, intermediates, and API products.</li>
<li>Operate and maintain laboratory instruments including HPLC, FTIR, UV-Vis, KF, and ICP-MS.</li>
<li>Prepare and standardize volumetric solutions.</li>
<li>Interpret and review analytical data to ensure material meets specifications for release.</li>
<li>Document all GMP activities accurately and legibly.</li>
<li>Provide information and documentation responses for customer complaints or returns.</li>
<li>Perform and review critical and complex calculations.</li>
<li>Write procedures, test methods, protocols, reports, and material specifications.</li>
<li>Support compliance with internal and regulatory procedures through training and review.</li>
<li>Meet deadlines as provided by management.</li>
<li>Perform routine maintenance and troubleshooting on laboratory instrumentation.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency with laboratory instrumentation including HPLC, FTIR, UV-Vis, KF, and ICP-MS.</li>
<li>Ability to perform and interpret complex calculations.</li>
<li>Clear documentation skills for GMP activities.</li>
<li>Experience with chromatography data management systems such as Chemstation or Chromeleon.</li>
<li>3-5 years of experience as a chemist in the industry.</li>
<li>BS Degree in Sciences such as Chemistry, Biochemistry, or Biology.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with analytical development and method development or validations.</li>
<li>Familiarity with Excel and data management systems.</li>
<li>Experience with GC is a plus.</li>
</ul>
Work Environment
The position is within a quality laboratory of an API/F&amp;F/Specialty Chemical company. The role requires occasional presence on the manufacturing floor. The working hours are from Monday to Friday, 3 PM to 11 PM on the 2nd shift, with initial training on the 1st shift for at least 6 weeks. The candidate will be the only chemist/laboratory personnel during their shift, with plans to eventually move to a 24-7 operation. The company is expanding its facilities, adding a new building to enhance API manufacturing capabilities and laboratory operations. Annual pay raises are based on performance, averaging 4% of salary yearly.
Job Type &amp; Location
This is a Contract to Hire position based out of St Francis, WI.
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 St Francis,WI.
Application Deadline
This position is anticipated to close on Dec 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Chemist

<h3>Job Description</h3>
Job Description Geotechnical Engineer 
Location: Denver, Colorado Experience Level: 5-10 years
 About the Company 
They are a leading engineering consulting firm specializing in geotechnical and geo-structural solutions for underground construction, tunneling, trenchless technology, and complex foundation systems. Their team is known for practical, constructable designs and innovative approaches to challenging infrastructure projects.
 Role Overview 
This position is ideal for an experienced Geotechnical Engineer who wants to take on technical leadership responsibilities while remaining hands-on with design and fieldwork. You will work on high-profile underground and infrastructure projects, collaborating with multidisciplinary teams to deliver safe, efficient, and cost-effective solutions.
 Key Responsibilities 
<ul>
<li>Lead geotechnical evaluations for tunnels, shafts, slopes, and foundation systems.</li>
<li>Develop and review excavation support and foundation designs.</li>
<li>Prepare engineering drawings and details using CAD/BIM tools.</li>
<li>Conduct site visits for construction observation and troubleshooting.</li>
<li>Perform advanced design computations and prepare technical reports.</li>
<li>Mentor junior engineers and contribute to project management tasks.</li>
<li>Collaborate with clients and internal teams to ensure project success.</li>
</ul>
 Minimum Requirements 
<ul>
<li>BS in Civil or Geological Engineering; MS preferred.</li>
<li>5-10 years of geotechnical engineering experience.</li>
<li>Strong technical background in underground or geo-structural projects.</li>
<li>Proficiency with AutoCAD/Civil 3D and geotechnical analysis software.</li>
<li>Excellent communication and organizational skills.</li>
<li>Ability to travel and perform fieldwork as needed.</li>
</ul>
 Preferred Qualifications 
<ul>
<li>PE license in Colorado (or ability to obtain within 6 months).</li>
<li>Experience with tunneling, trenchless, or ground improvement projects.</li>
<li>Familiarity with structural analysis tools and advanced modeling.</li>
</ul>
 Compensation &amp; Benefits 
<ul>
<li>Salary Range: $95,000-$130,000 annually, based on experience.</li>
<li>Benefits: Comprehensive health coverage, 401(k) with match, paid time off, professional development support, and performance-based bonuses.</li>
</ul>
 Company DescriptionLVI Associates exists to enable exceptional careers around the world; we connect exceptional talent, with exceptional opportunities. We believe that every professional should benefit from the advice of a trusted partner throughout their career. We provide that partnership to mid to senior level professionals within the Energy, Environmental &amp; Infrastructure spaces through our network of micro-specialist consultants. Each team within LVI Associates focuses on a specialist area of Energy &amp; Infrastructure. I specialise in sourcing and placing senior level candidates within the bridges and highway construction spaces. Make LVI Associates your career partner; ensure your career journey is exceptional. 
<h3>Company Description</h3>
LVI Associates exists to enable exceptional careers around the world; we connect exceptional talent, with exceptional opportunities.\r\n\r\nWe believe that every professional should benefit from the advice of a trusted partner throughout their career.\r\n\r\nWe provide that partnership to mid to senior level professionals within the Energy, Environmental &amp; Infrastructure spaces through our network of micro-specialist consultants.\r\n\r\nEach team within LVI Associates focuses on a specialist area of Energy &amp; Infrastructure. I specialise in sourcing and placing senior level candidates within the bridges and highway construction spaces. \r\n\r\nMake LVI Associates your career partner; ensure your career journey is exceptional.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Job Title: Application Chemist
Job Description
We are seeking a temporary full-time project lead to execute, coordinate, and document a defined portfolio of collaborative initiatives between the Chemical Analysis Division (CAD) and the Bioprocessing Collaboration Center (BCC). These initiatives focus on reducing adoption barriers, enabling automation readiness, and expanding product positioning across spectroscopy, process analytics, and bioprocess monitoring platforms.
PAY - $40 - $45
Responsibilities
<ul>
<li>Develop and manage project timelines, milestones, and deliverables for nine identified CAD–BCC projects.</li>
<li>Coordinate seed unit placements, tracking, and evaluation for various instruments including SmartRaman DXR, AIO, TruScan, NanoDrop, PrimaPro, MAX-IR, and Process16.</li>
<li>Support competitive benchmarking and comparison analyses versus alternative vendor technologies.</li>
<li>Facilitate cross-functional meetings with CAD product managers, engineers, BCC scientists, and PSG stakeholders.</li>
<li>Compile and analyze evaluation data, particularly for comparative and automation-readiness projects.</li>
<li>Prepare technical summaries, application notes, and white papers highlighting findings and recommendations.</li>
<li>Contribute to OPC-UA standardization documentation and develop automation-readiness frameworks with vendors.</li>
<li>Conduct paper-based assessments for PrimaPro, MAX-IR, summarizing technical fit and market opportunity.</li>
<li>Liaise between CAD Division, BCC, and PSG to ensure alignment of study objectives and resource allocation.</li>
<li>Collaborate with automation vendors and partners for data collection and technical validation.</li>
<li>Prepare summary presentations and internal reports for leadership reviews and roadmap discussions.</li>
<li>Develop a standardized utilization process for PSG seed placements.</li>
<li>Establish frameworks for competitive analysis and product validation consistency across CAD platforms.</li>
</ul>
Essential Skills
<ul>
<li>Strong understanding of analytical instrumentation including Raman, FTIR, NIR, UV-Vis spectroscopy, and process analytics.</li>
<li>Familiarity with automation protocols and industrial communication standards such as OPC-UA and PLC integration.</li>
<li>Experience with bioprocess development workflows and/or pharma/biopharma process analytical technology (PAT).</li>
<li>Ability to conduct data analysis, compile findings, and write technical reports, application notes, or white papers.</li>
<li>Proven ability to manage multiple parallel projects and coordinate cross-functional teams.</li>
<li>Competence in tracking deliverables, scheduling milestones, and ensuring on-time reporting.</li>
<li>Strong organizational and communication skills with ability to interface between technical and commercial teams.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Chemical Engineering, Chemistry, Analytical Chemistry, Biotechnology, or related field.</li>
<li>3+ years of experience in analytical development, process analytics, or instrumentation applications.</li>
<li>Familiarity with CAD product lines or competing analytical technologies is highly advantageous.</li>
</ul>
Work Environment
The position requires full-time commitment, with a schedule from Monday to Friday, 8am to 5pm. This is a 12-month term with potential for renewal or conversion based on results and business needs. The role is based on-site at BCC, with coordination across CAD product teams.
Job Type &amp; Location
This is a Contract position based out of Saint Louis, MO.
Pay and Benefits
The pay range for this position is $40.00 - $45.00/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 Saint Louis,MO.
Application Deadline
This position is anticipated to close on Dec 26, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Application Chemist

<h3>Job Description</h3>
Job DescriptionJob title: Chemist Job Location: Sunnyvale, CA, 94085 Job Duration: 12 months Shift Timing: M-F, 1st Shift Pay rate: $35-39/hr on W2. Position Summary The Polymer / Process Development Chemist will provide technical expertise, hands-on experimentation, and process development support for the Resin Synthesis team, focusing on polymerization, grafting, functionalization, and scale-up of specialty chromatographic resins. This role bridges R&amp;D and Operations, enabling robust, efficient, and scalable manufacturing processes that meet quality, yield, and performance requirements. The ideal candidate is a self-driven chemist with strong polymer chemistry fundamentals, experience in translating bench-scale methods into production-scale processes, and a passion for continuous improvement in a fast-paced manufacturing environment. Key Responsibilities:
<ul>
<li>Process Development &amp; Scale-Up</li>
<li>Develop, optimize, and document polymerization, grafting, and functionalization processes for new and existing resin products.</li>
<li>Conduct small-scale and pilot-scale experiments to evaluate reaction conditions, kinetics, reagent ratios, mixing profiles, and heat transfer characteristics</li>
<li>Support production scale-up activities including DOE studies, process mapping, and parameter window definition.</li>
<li>Partner with R&amp;D to transfer new resin technologies into manufacturing using structured tech-transfer methodologies.</li>
</ul>
 Manufacturing Support
<ul>
<li>Serve as the on-floor technical resource for Resin Synthesis, troubleshooting deviations, out-of-trend results, or process bottlenecks.</li>
<li>Analyze batch data to identify trends in yields, particle size distributions, reaction profiles, and other critical QC metrics</li>
<li>Collaborate with engineers, manufacturing chemists, and QC analysts to resolve in-process issues and implement corrective/preventive actions.</li>
<li>Support validation, verification, and characterization of equipment, reactors, filters, and analytical tools.</li>
</ul>
 Data Analysis &amp; Documentation
<ul>
<li>Maintain accurate laboratory notebooks, development reports, and process summaries.</li>
<li>Generate and update batch records, SOPs, work instructions, and training materials for resin processes.</li>
<li>Support creation of risk assessments (pFMEA), control plans, and critical parameter monitoring systems.</li>
<li>Summarize experimental findings and present recommendations to cross-functional teams.</li>
</ul>
 Quality &amp; Compliance
<ul>
<li>Ensure all development and manufacturing activities comply with internal Quality Management Systems (QMS), SOPs, and safety requirements.</li>
<li>Evaluate raw materials, supplier changes, and material qualifications that impact resin performance.</li>
<li>Participate in nonconformance investigations, CAPA activities, and root cause analysis.</li>
</ul>
 Continuous Improvement
<ul>
<li>Identify opportunities for yield improvement, cycle time reduction, and waste minimization.</li>
<li>Lead or support PPI/Lean projects targeting process robustness, reagent utilization, and scale-up efficiency.</li>
<li>Contribute to long-term process roadmaps, resin portfolio improvements, and modernization initiatives (e.g., digital instructions, Dozuki integration).</li>
</ul>
 Required Qualifications
<ul>
<li>Bachelor’s, Master’s, or PhD in Chemistry, Polymer Chemistry, Chemical Engineering or related field.</li>
<li>2+ years (BS), 1+ years (MS), or 0–2 years (PhD) of industry experience in polymer synthesis, organic synthesis, or process development.</li>
<li>Demonstrated experience with polymerization techniques (e.g., suspension, emulsion, grafting, cross-linking).</li>
<li>Hands-on familiarity with lab-scale and pilot-scale equipment: jacketed reactors, overhead stirring, reflux systems, filtration units, ovens, vacuum systems, particle sizing instruments.</li>
<li>Strong data analysis skills; ability to interpret batch data, reaction profiles, and analytical characterization results .</li>
<li>Excellent written communication and documentation skills.</li>
</ul>
 Preferred Qualifications
<ul>
<li>Experience working in regulated manufacturing environments (ISO 9001 or similar).</li>
<li>Knowledge of chromatographic resin chemistry (anion exchange, cation exchange, polymer grafting, silica bonding).</li>
<li>Experience with Design of Experiments (DOE) and process characterization.</li>
<li>Familiarity with scale-up methodologies, heat/mass transfer considerations, and mixing studies.</li>
<li>Understanding of QMS concepts including change control, validation, risk assessments, and CAPA.</li>
<li>Working knowledge of Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) preferred.</li>
</ul>
#sczr2

Chemist

<h3>Job Description</h3>
Job Description
QC Chemist Job Description
Position Overview:
The Quality Control Chemist reports directly to Quality Laboratory Management and plays a key role in supporting laboratory operations through accurate and timely testing. This position requires strong time management skills to meet testing deadlines and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting techniques.
Schedule:
This position will be on a 2nd shift: Monday - Thursday 3:30pm - 11:30 and Friday 1:30pm - 9:30pm.
Key Responsibilities
Testing:
Perform Release, Stability, and Special Request testing on finished products and raw materials in compliance with Standard Operating Procedures (SOPs), in-house methods, and compendial standards.
Execute in-house methods independently and accurately with minimal supervision.
Team Collaboration:
Adapt to changes in testing schedules and support continuous improvement initiatives within the lab.
Assist in training new laboratory personnel and document training per established SOPs and Nutramax guidelines.
Safety:
Maintain a safety-first approach and remain vigilant of surroundings while performing laboratory tasks.
Ensure all equipment used in testing is properly calibrated and maintained.
General Duties:
Train on and operate various laboratory instruments, including but not limited to: Laboratory Balances, HPLC, GC, Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration instruments.
Complete assigned projects within established timelines while balancing testing responsibilities.
Stay informed on updates from USP, FDA, and other regulatory bodies to ensure compliance with analytical standards and documentation practices.
Assist in investigating Out-of-Specification (OOS) results as needed.
Perform additional duties as required to support company objectives.
Communicate effectively across departments and work collaboratively within a team environment.
Maintain regular and reliable attendance.
Additional Skills &amp; Qualifications
Experience: 2–5 years in a laboratory setting, preferably in a cGMP environment. Familiarity with GC and/or LC instrumentation.
Skills: Strong interpersonal skills, self-motivation, and ability to work with individuals at all organizational levels.
Education: Bachelor’s degree in Chemistry required; concentrations in Biochemistry, Inorganic, Physical, or Polymer Chemistry are preferred.
Job Type &amp; Location
This is a Permanent position based out of Lancaster, SC.
Pay and Benefits
The pay range for this position is $70000.00 - $80000.00/yr.
Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families. Educational Assistance: Opportunities for training and professional development to support career growth. Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration. Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally. Employee Recognition &amp; Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures. Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere.
Workplace Type
This is a fully onsite position in Lancaster,SC.
Application Deadline
This position is anticipated to close on Dec 26, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology Lab TechnicianJob Description
Perform microbiological testing on cosmetic products in accordance with USP , USP , USP Suitability, and USP standards. Conduct method suitability testing to validate sterility procedures and eliminate antimicrobial interference. Prepare and analyze samples for microbial enumeration and identification of objectionable organisms. Maintain, calibrate, and clean laboratory equipment to ensure sterility and accuracy. Document all procedures, results, and deviations in compliance with ISO standards. Develop and revise Standard Operating Procedures (SOPs) for microbiological testing workflows. Ensure strict adherence to safety protocols and laboratory best practices. Communicate findings and updates to the Lab Manager and relevant stakeholders.
Responsibilities
<ul>
<li>Perform microbiological testing on cosmetic products according to regulatory standards.</li>
<li>Conduct method suitability testing to validate sterility procedures.</li>
<li>Prepare and analyze samples for microbial enumeration and identification.</li>
<li>Maintain, calibrate, and clean laboratory equipment to ensure sterility.</li>
<li>Document procedures, results, and deviations in compliance with ISO standards.</li>
<li>Develop and revise Standard Operating Procedures (SOPs) for workflows.</li>
<li>Ensure strict adherence to safety protocols and laboratory best practices.</li>
<li>Communicate findings and updates to relevant stakeholders.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in microbiological techniques and regulatory protocols.</li>
<li>Bachelor’s degree in Microbiology, Biology, or a related field.</li>
<li>Minimum 2 years of experience in a microbiology lab, preferably in cosmetics or pharmaceutical testing.</li>
<li>Knowledge of GMP/GLP/GCP standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Hands-on experience with USP , , Suitability, and testing protocols.</li>
<li>Familiarity with ISO quality management systems.</li>
<li>Proven ability to create and maintain SOPs.</li>
<li>Experience with Preservative Efficacy Testing.</li>
</ul>
Work Environment
The role involves working in a small bench lab for 3rd party cosmetics testing. The technician will be the sole lab operator reporting to the laboratory manager.
Job Type &amp; Location
This is a Contract to Hire position based out of Phoenix, AZ.
Pay and Benefits
The pay range for this position is $21.00 - $24.00/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 Phoenix,AZ.
Application Deadline
This position is anticipated to close on Dec 26, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Microbiology Lab Technician

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Production TechnicianJob Description
As a Chemical Production Technician, you will be responsible for processing raw materials and chemicals by following a batch record to mix the correct chemicals together to create the final product. This role requires the operation of various machines to measure the amount of raw material to be added into the tank, taking samples for lab quality checks, and lifting large plastic bags using a crane. This is a physical role involving activities like pushing material out of bags using a mixing device, climbing stairs to access tank tops, and operating machines to monitor and control tank levels.
Responsibilities
<ul>
<li>Read and interpret batch records and recipes.</li>
<li>Check balances to ensure the correct amount of raw material is added.</li>
<li>Measure chemicals accurately for addition.</li>
<li>Operate machinery for mixing raw materials.</li>
<li>Sign off on documents verifying the correct type and amount of materials.</li>
<li>Perform other work-related duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Experience in machine operation, utility or production technician roles.</li>
<li>Ability to read and follow batch records.</li>
<li>Strong mathematical skills for measuring chemicals.</li>
<li>Attention to detail in reporting and documentation.</li>
<li>Ability to follow instructions and work independently.</li>
<li>Physical strength to lift or move up to 50 pounds.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>2-4 years of manufacturing experience preferred.</li>
<li>High School Diploma or GED required.</li>
<li>Capability to learn and collaborate effectively with a team.</li>
<li>Dependability and initiative without being overbearing.</li>
</ul>
Why Work Here?
Our work environment fosters a family-like atmosphere that encourages high performance through comfort and compassion from leaders and peers. We are committed to a diverse and inclusive workplace where employees feel safe, valued, and empowered to succeed. Our Des Moines site has experienced significant growth and maintains a close-knit culture despite being part of a national company.
Work Environment
This is a fully on-site position located in a manufacturing facility in Des Moines, Iowa. You will work a 2nd shift from Monday to Friday, with shifts starting between 2 pm to 4 pm, lasting 8 to 10 hours. The role is within a chemical plant, where you'll be exposed to moving equipment, mechanical parts, fumes, airborne particles, chemicals, and biological hazards. The dress code includes uniforms, steel-toed boots, and hair nets, with a requirement to shower after each shift.
Job Type &amp; Location
This is a Contract to Hire position based out of Des Moines, IA.
Pay and Benefits
The pay range for this position is $20.00 - $21.75/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Des Moines,IA.
Application Deadline
This position is anticipated to close on Dec 26, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Formulator

<h3>Job Description</h3>
Job DescriptionJob Title: Scientist II - Research &amp; Development Location: West Sacramento, CA Duration: 12 Months+ Pay Rate: $30.00-$35.00/Hour on W2 Job Description: This is an on-site position located in West Sacramento, California Client Impactful Work: Life Lab is a CAP accredited CLIA laboratory dedicated to the testing of patients enrolled in partner programs clinical trials. As a part of this team you will have an impact on the development of new cancer tests and assist in the application of new drugs for cancer patients. A day in the Life:
<ul>
<li>Training on new assays</li>
<li>Perform experiments related to clinical trials</li>
<li>Share your results with other team members</li>
</ul>
 Keys to Success: Education
<ul>
<li>A BS degree in Biological Sciences from an accredited college or university.</li>
<li>MS degree in a molecular field preferred</li>
<li>Minimum of 5 years of direct experience in laboratory testing for the specialties performed by the Life Technologies Clinical services Lab is required</li>
</ul>
 Experience:
<ul>
<li>Laboratory based experimental experience in a broad array of molecular biology techniques is required</li>
<li>Demonstrated ability to perform complex data analysis is required.</li>
<li>Hands-on next-generation sequencing is required, with preference given to those individuals familiar with Ion Torrent technology.</li>
</ul>
 Knowledge, Skills, Abilities:
<ul>
<li>Use of computer systems for data entry, retrieval, and analyses involving word processing programs, spreadsheets containing data analyses, and complex computer driven instrumentation</li>
<li>Excellent verbal and written communication skills</li>
<li>Ability to problem solve highly complex analyses</li>
<li>Strong analytical skills</li>
<li>Strong understanding of good laboratory practices and regulatory compliance</li>
</ul>
 Physical Requirements / Work Environment:
<ul>
<li>May handle highly infectious agents and hazardous chemicals.</li>
<li>Sit or stand for long periods of time while using equipment and specimen handling and/or for computer work.</li>
<li>Stretch, Bend or twist to reach into lower or upper cabinets and drawers and squat or kneel to remove or store supplies stored on lower shelves.</li>
<li>Ability to lift up to 40 lbs.</li>
<li>Visual requirements to distinguish colors for analysis; and auditory requirements to hear timers on equipment.</li>
<li>Fine hand manipulation is required to operate equipment, manipulate and pipette specimens.</li>
<li>Work is mainly laboratory-based with some time spent in the office writing up experiments, validation documents, and standard operating procedures.</li>
</ul>
#sczr2

Scientist II - Research & Development

<h3>Job Description</h3>
Job Description
Job Title: Scientist - I
Location: Bothell, WA 98021
Duration: 06 months of Contract (with possible extension)
 
Payrate: $40.00/hr.
Shift timing: Monday–Friday, 8am-4:30pm EST

Job Description
The In Situ Biology team is seeking a motivated associate scientist contractor to assist a team of scientists performing spatial biology experiments aimed at understanding targets for antibody-based therapeutics. The successful candidate will have experience in core histology methodologies, including processing, embedding, and sectioning. The ideal candidate will be energetic and enthusiastic about lab work and flexible in working with different investigators on various projects.
Responsibilities
• Process samples for downstream histological analysis.
• Perform routine histology lab maintenance.
• Perform immunohistochemistry experiments using autostainers.
• Maintain and catalog a biospecimen repository.
• Utilize a LIMS system for documenting experiments.

Qualifications
• 1-2+ years’ experience working in a laboratory.
• BS or BA in in a biological science.
• Experience with histopathology techniques.
• Experience with sectioning a plus, preference given to Histology Technicians (HTs).
• Ability to work collaboratively in a cross-functional research environment.
• Highly organized with the ability to multitask.
• Quick learner with willingness to learn new skills and technologies.
• Excellent teamworking and communication skills and a proactive attitude.
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Biological Scientist

<h3>Job Description</h3>
Job DescriptionOur 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 Louisville, KY 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, 8:00 a.m. – 4:30 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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