field_job_employment_type

field_job_occupational_field_parents_all

field_job_experience

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
 NOW HIRING ENTRY LEVEL CANDIDATES FOR A MEDICAL DEVICE MANUFACTURING ROLE! 
Location – Mira Mesa, CA 
Shift – 1st Shift (4:00AM – 2:30PM Monday – Thursday)
Pay Rate - $17.40/HR
Job Description
Join our dynamic team in the packout department where we have fully transitioned to an automated packaging line. As a Clean Room Assembler, you will play a crucial role in ensuring the seamless operation of our advanced machinery by monitoring screens for errors, checking for defects, and replenishing materials.
Responsibilities
<ul>
<li>Monitor the machine screens closely for any errors and reset when necessary.</li>
<li>Check for defects in the cartridges being packed by the robots.</li>
<li>Load materials into the staging area and replenish parts as they get used.</li>
<li>Monitor inventory levels at each station to prevent machine stoppages.</li>
<li>Perform manual packaging tasks occasionally when required.</li>
<li>Strong attention to detail to monitor machines effectively.</li>
<li>Ability to work in a fast-paced environment, ideally with experience from fast food or similar industries.</li>
<li>Trainable with a good work ethic and punctuality.</li>
<li>Ability to work as a team player.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with tool work instruction and assembly in a cleanroom setting.</li>
<li>Familiarity with production, machine operating, and automated lines.</li>
<li>Experience with mechanical assembly, medical devices, and GMP standards.</li>
</ul>
If you are interested and qualified, please apply directly with your updated resume!
Pay and Benefits
The pay range for this position is $17.40 - $17.40/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in San Diego,CA.
Application Deadline
This position is anticipated to close on Nov 3, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Description
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. MUST HAVE: Bilingual in English + Spanish • Creating and maintaining patient charts for all assigned studies. • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts. • Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials. • Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication. • Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection. • Communicating with study participants, caregivers, third party vendors and laboratories as needed. • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks. • Aiding Coordinators in the facilitation of study monitoring visits. • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants. • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
 
Skills
bilingual
 
Top Skills Details
bilingual
 
Additional Skills &amp; Qualifications
soft skills: personable, goal driven, eager to grow into CRC role • Interest in and knowledge of specific study indications. • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.). • Skilled in organization and record maintenance. • Skilled in developing and maintaining effective working relationships with supervisors and co- workers. • Strong personal initiative and attention to detail. • Ability to react calmly and effectively in emergency situations. • Ability to interpret, adapt and apply guidelines and procedures. • Ability to clearly communicate both orally and verbally.
 
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $39520.00 - $45760.00/yr.
Benefits package available. Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, &amp; Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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.

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Research AssociateJob Description
We are currently seeking an experienced Research Associate to join the Cell Therapy Process Development team. This role offers an exciting opportunity to lead or support the development and improvement of cell therapy manufacturing processes, contributing to the advancement of cutting-edge therapies. The ideal candidate will possess a strong experience in cell therapy or biopharmaceutical development, process optimization, and technology transfer, and be passionate about making an impact in the evolving field of cell therapy.
Responsibilities
<ul>
<li>Design and execute experiments to optimize and improve processes for cell therapy manufacturing, including media preparation, cell expansion and harvest, and product formulation. Analyze experimental data and present results in a clear and actionable manner to stakeholders.</li>
<li>Provide technical expertise in the development and implementation of new techniques and technologies. Support troubleshooting and process improvement initiatives.</li>
<li>Collaborate closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure the successful transfer of processes into GMP clinical and commercial manufacturing.</li>
<li>Support the characterization and validation of cell therapy processes, ensuring compliance with regulatory guidelines and internal standards. Conduct process performance qualification (PPQ) studies and support clinical trial material production.</li>
<li>Ensure all process development activities adhere to GMP and applicable regulatory standards. Support regulatory filings and audits as needed.</li>
<li>Prepare and review technical documentation, including process development reports, batch records, SOPs (Standard Operating Procedures), and change controls.</li>
<li>Identify potential risks in process development and manufacturing, and implement strategies for mitigation, ensuring the successful advancement of cell therapy programs.</li>
</ul>
Essential Skills
<ul>
<li>Aseptic technique and operation</li>
<li>Experience in cleanroom and sterile processing</li>
<li>Cell culture and cell therapy expertise</li>
<li>Process development knowledge</li>
<li>Understanding of GMP standards</li>
<li>Proficiency in laboratory work and decontamination procedures</li>
<li>Ability to troubleshoot and analyze batch records</li>
<li>Knowledge in molecular biology and biopharmaceutical processes</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related field.</li>
<li>2+ years of experience in cell therapy and/or biopharmaceutical process development.</li>
<li>Strong problem-solving abilities and critical thinking skills.</li>
<li>Ability to effectively work in cross-functional teams, meet deadlines, and prioritize multiple projects.</li>
<li>Strong verbal and written communication skills, including technical writing.</li>
<li>Understanding of GMP, GLP, and regulatory requirements for cell-based therapies.</li>
<li>Experience with regulatory submissions and support for inspections is a plus.</li>
</ul>
Work Environment
The role is based in a lab and office setting, specifically within a cleanroom environment with level 10k and 100k specifications. Responsibilities include maintaining sterile gowning certification and adhering to sterile gowning procedures.
Pay and Benefits
The pay range for this position is $70000.00 - $75000.00/yr.
See company website for details on what is offered for FTE's.
Workplace Type
This is a fully onsite position in Winston Salem,NC.
Application Deadline
This position is anticipated to close on Oct 31, 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.

Research Associate

<h3>Job Description</h3>
Job Description
Job Title: Department Supervisor – TEM&nbsp;&nbsp; Department: Asbestos/TEM&nbsp; Reports To: Program Manager &nbsp;
FLSA: Exempt&nbsp; Location: Pittsburgh, PA&nbsp; Employment Type: Full-Time&nbsp; Position Summary&nbsp;
We are seeking a highly skilled and experienced Transmission Electron Microscopy (TEM) Supervisor to manage and support the daily operations of the asbestos TEM laboratory. The ideal candidate will possess strong expertise in electron microscopy, sample preparation, and instrument maintenance. This role involves supervising users, managing equipment, maintaining lab protocols, and contributing to high-level imaging and analysis projects.&nbsp;
Key Responsibilities:&nbsp;
TEM Operations &amp; Supervision&nbsp;
<ul>
<li>
Oversee the operation, calibration, and maintenance of TEM instruments and related equipment.&nbsp;
</li>
</ul>
<ul>
<li>
Ensure optimal performance and uptime of TEM systems (e.g., JEOL, FEI, Hitachi, etc.).&nbsp;
</li>
</ul>
<ul>
<li>
Supervise day-to-day activities in the microscopy lab, ensuring safe and effective operations.&nbsp;
</li>
</ul>
<ul>
<li>
Train and support users in sample preparation, instrument use, and image/data analysis.&nbsp;
</li>
</ul>
User Support &amp; Training&nbsp;
<ul>
<li>
Assist staff across departments in planning and conducting TEM analysis.&nbsp;
</li>
</ul>
<ul>
<li>
Provide hands-on training and develop instructional materials for new users.&nbsp;
</li>
</ul>
<ul>
<li>
Monitor and manage user scheduling, usage logs, and adherence to protocols.&nbsp;
</li>
</ul>
Technical Expertise &amp; Imaging&nbsp;
<ul>
<li>
Prepare and analyze samples using standard and advanced techniques for asbestos analysis.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Perform high-resolution imaging and elemental analysis (e.g., EDX, SAED).&nbsp;
</li>
</ul>
<ul>
<li>
Interpret and troubleshoot complex imaging data in collaboration with principal investigators.&nbsp;
</li>
</ul>
Lab &amp; Equipment Management&nbsp;
<ul>
<li>
Maintain lab supplies, consumables, and inventory related to electron microscopy.&nbsp;
</li>
</ul>
<ul>
<li>
Schedule and coordinate preventive maintenance and service with equipment vendors.&nbsp;
</li>
</ul>
<ul>
<li>
Ensure compliance with safety regulations and waste disposal protocols.&nbsp;
</li>
</ul>
Administrative &amp; Reporting&nbsp;
<ul>
<li>
Maintain documentation including SOPs, maintenance logs, and user training records.&nbsp;
</li>
</ul>
<ul>
<li>
Stay current with advances in TEM and asbestos analysis to recommend upgrades as needed.&nbsp;
</li>
</ul>
<ul>
<li>
Prepare client reports.&nbsp;&nbsp;
</li>
</ul>
Required Qualifications:&nbsp;
<ul>
<li>
Bachelor’s or Master’s degree in Materials Science, Geology, Chemistry, Biology, or related field.&nbsp;
</li>
</ul>
<ul>
<li>
3+ years of hands-on experience with transmission electron microscopy.&nbsp;
</li>
</ul>
<ul>
<li>
3+ years of hand-on experience with asbestos analysis&nbsp;
</li>
</ul>
<ul>
<li>
Prior experience in a supervisory, training, or core facility support role.&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in sample preparation, instrument operation, and digital image analysis.&nbsp;
</li>
</ul>
<ul>
<li>
Strong communication and organizational skills.&nbsp;
</li>
</ul>
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Transmission Electron Microscopy Supervisor

<h3>Job Description</h3>
Job Description
Responsibility/Requirements:
· Perform analysis of plating solutions
· Treat batch tanks
· Assist in trouble shooting issues, as they arise
· Perform ICP, titration and dilutions for chemical analysis, will train
· Perform tank maintenance
· Responsible for accurate data entry into True Chem software, will train
· Operate forklifts
· Focus on 6S practices
· High responsibility to safety issues
· Observes all company policies and procedures
· Maintain high level of performance
· Actively participate in continuous improvement initiatives by identifying and providing suggestions on areas of improvement.
· High school diploma or equivalent
· 1-2 years of lab or chemical experience preferred
· Must be proficient in the use of computers and programs
· Able to lift 55 pounds as a part of daily routine
· Licensed Waste Water Treatment Operator preferred
· Ability to work with and move drums up to 850 lbs using a drum dolly and totes using forklift in tight areas
3rd shift hours: Sunday - Wednesday – 8:00 pm – 6:30 am (4 day, 10 hour shifts)
Training:
The employee will train on 1st shift for approximately 2-3 weeks.
Benefits:
60 days - Insurance Benefits available (Medical, Dental, Vision, &amp; Life)
90 days – 401K/Roth
Vacation and Flex Time
Holiday Pay
Payday every Friday!
Company DescriptionElectro-Spec is a diversified automated electroplating company that utilizes PLC automation for many of its processes. (i.e. Gold, Silver, Nickel, Tri-M3, Electroless Nickel, and Passivation) We are a dynamic company, well known in the plating industry for the high quality work we have produced in Indiana since 1959. We have a casual, team-oriented work environment; we also provide opportunities for career growth and advancement to employees at all levels at both locations. 
<h3>Company Description</h3>
Electro-Spec is a diversified automated electroplating company that utilizes PLC automation for many of its processes. (i.e. Gold, Silver, Nickel, Tri-M3, Electroless Nickel, and Passivation) We are a dynamic company, well known in the plating industry for the high quality work we have produced in Indiana since 1959. We have a casual, team-oriented work environment; we also provide opportunities for career growth and advancement to employees at all levels at both locations.

Chemical / Waste Treatment Operator - 3rd shift

<h3>Job Description</h3>
Job DescriptionPOURLINE OPERATOR Email your resume over to <a href="mailto:desoto@wisestaffinggroup.comJob" target="_blank">desoto@wisestaffinggroup.comJob</a> Summary:* Pay Rate: $20 hr. * 1st shift: 6am -2:30pm * Full time: M-F 40hrs weekly * Location: Terrel1 75160 Requirements: * Must be able to pass Respirator Test (PLHCP) and wear a Respirator.* Visually inspect buns during production and storage. * Assist pouring line operator during foam shut down procedure.* Maintain and clean the curfew saw or ski before and after each foam pour.* Operate the rack and gantry or skis during production runs. * Maintain a clean and safe work area. * Possess some computer knowledge.* Inspect and maintain gantry and rack area. * Mark and identify each bun and complete production paperwork for the saw area. * Forklift experience required. * Must be dependable and maintain a good attendance record, understand and perform all instructions. * Must be able to lift up to 50 lbs. Why Wise:* Medical, Dental, Vison &amp; Life insurance available! * Direct deposit - Weekly pay!* Apply here or @wisestaffinggroup.com today! #WeeklyPay #TempToPerm #Terrell#ImmidiateHire #Warehouse

Pourline Operator

<h3>Job Description</h3>
Job DescriptionPay range: $24.00 to $26.00 per hour, based on experience, plus shift differential pay
 
First several weeks of training on first shift 
Available positions: 3rd shift (M-Th 4x10 hour schedule)

GFS Chemicals is a family owned and operated business in Columbus, Ohio serving customers worldwide since 1928. You will be joining an established, close knit family organization that has been proudly dedicated to quality, service, and innovation in the specialty chemicals market. GFS offers a comprehensive compensation package that includes a generous 401k, profit sharing plan, paid time off, 2:1 HSA match, company paid life insurance, medical, vision, dental, and much more. 
 
Apply now to learn more about GFS Chemicals. Let’s see if we have “Chemistry”!

Qualifications:
<ul>
<li>High school diploma or equivalent; technical or vocational training in chemistry or related field is a plus.</li>
<li>Proven experience as a chemical operator or in a similar manufacturing environment.</li>
<li>Solid understanding of chemical processes, equipment, and safety procedures.</li>
<li>Ability to read and interpret technical documents, including SOPs and manuals.</li>
<li>Strong attention to detail and a proactive approach to problem-solving.</li>
<li>Ability to work effectively in a team and communicate clearly.</li>
<li>Physical ability to lift heavy objects, stand for extended periods, and work in various weather conditions.</li>
<li>Familiarity with operating and troubleshooting process control systems a plus.</li>
</ul>

Essential Responsibilities:
You will be trained in performing fascinating processes to manufacture chemicals used in automotive, pharmaceuticals, electronics, agrochemical, and energy commercial applications. You will learn multiple work centers over time allowing a changing work environment each day.
Daily activities:
<ul>
<li>Utilize pumps to load raw materials into vessels.</li>
<li>Monitor reaction conditions using our electronic PLC systems.</li>
<li>Work closely with Quality Control to test and adjust batches in process.</li>
<li>Package finished goods into containers ranging from 1 liter to 55 gallon drums. </li>
<li>Use a fork-lift to stage pallets of raw materials for upcoming batches.</li>
<li>We empower operators to participate in problem solving and continuous improvement.</li>
<li>Focus on industrial housekeeping and personal protective equipment usage.</li>
<li>Follow written operating procedures including the record keeping of information.</li>
<li>Most importantly.. help to create a positive, productive, and safe work environment.</li>
</ul>
 
 Additional Qualifications
The company will only employ those who are legally authorized to work in the United States for this position. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future are not eligible for hire.
EEO/AA/M/F/Vets/Disabled
No agency calls or emails please!

Chemical Operator - 3rd Shift

<h3>Job Description</h3>
Job DescriptionChemical Operator $23.79 - $25.6212 Hour Swing Shift/ 1st&amp; 3rdShift / Temp - HireWhat Matters Most
<ul>
<li>Competitive Pay of $23.79 - $25.62 per hour plus additional compensation</li>
<li>Schedule: 12-hour shift / Swing 1st &amp; 3rd</li>
<li>Location: Blacksburg, SC</li>
<li>Temporary-to-hire opportunity with career growth and stability</li>
<li>Weekly Pay with direct deposit or pay card</li>
<li>When you work through The Reserves Network, you are eligible to enroll in dental, vision and medical insurance as well as 401K, direct deposit and our referral bonus program</li>
</ul>
Job DescriptionJoin a global manufacturing company and create products that enhance people’s lives and deliver solutions to its customers and communities. As a chemical operator you will play a key role in the chemical manufacturing processes. We are looking to hire experienced and entry-level chemical operators.Responsibilities:
<ul>
<li>Operate a forklift</li>
<li>Operate a computer to manufacture batches</li>
<li>Lifting various raw materials up to 50 lbs.</li>
<li>Perform physical/chemical testing during chemical processing</li>
</ul>
Qualifications and Requirements:
<ul>
<li>High School Diploma </li>
<li>Ability to work in a fast-paced environment</li>
<li>Must be able to climb multiple steps, and lift 50 pounds</li>
<li>Computer experience, window-based software</li>
</ul>
Benefits and Perks:
<ul>
<li>$23.79 - $25.62</li>
<li>Medical Benefits </li>
<li>Temp to Hire</li>
<li>Training &amp; Growth</li>
</ul>
Your New Organization:Join a global manufacturing company and become part of a team that produces products that enhance people’s lives. You will have the opportunity to learn and grow in this position while gaining multiple job certifications to progress to top pay. Your Career Partner:The Reserves Network, a veteran-founded and family-owned company, specializes in connecting exceptional talent with rewarding opportunities. With extensive industry experience, we are dedicated to helping you achieve your professional goals and shine in your field. The Reserves Network values diversity and encourages applicants from all backgrounds to apply. As an equal-opportunity employer, we foster an environment of respect, integrity, and trust in every aspect of employment. The base pay range for this position is $23.79–$25.62, excluding benefits, bonuses, or other compensation. Your final compensation will depend on your skills, qualifications, experience, location, and internal pay equity. Please note, hiring at the top of the range is uncommon to allow room for future growth.

Chemical Operator

<h3>Job Description</h3>
Job Description
About Us
We are only accepting applications through verified recruitment websites listing our job postings (i.e. LinkedIn, Workable, Indeed, etc). Dymax will only contact potential candidates from email addresses in @dymax.com.
Bomar, part of the Bachmann Chemical &amp; Engineering family of brands is based out of Torrington, Connecticut. With a global presence, Bomar has been a leading innovator of advanced-performance materials for UV/EB energy, light, and other free-radical cure applications. Focused on oligomer synthesis and new product development, we’re able to satisfy unique performance requirements from our global customer base of formulators which use our oligomers, resins, and additives in a variety of applications such as 3D printing, nail coatings, adhesives, industrial coatings and more. 
About You
We’re seeking a results-focused, innovative, self-driven, and well-qualified individual to join our talented team as a Reactor Operator for our Torrington, CT, facility. Here, you will safely produce batch adhesives and oligomer formulations that meet quality, ISO, safety, and internal control standards—while also fulfilling customer expectations and ensuring lines are shipped on time (LSOT). 
You will:
<ul>
<li>Safely operate industrial mixing and powerlifting equipment by setting and controlling mixing parameters according to work instructions, and by using lift trucks, power jacks, and drum dollies to retrieve and replace raw materials and WIP</li>
<li>Promote warehousing and material handling best practices by safely and efficiently transferring raw materials from delivery vehicles to warehouse storage, then to reactor workstations, and finally to racking and staging areas</li>
<li>Maintain a safe, healthy, clean, ergonomic, and productive workplace by practicing safe handling procedures, using PPE as appropriate, following SDS, EH&amp;S, and HazMat requirements, and ensuring proper storage of materials and equipment. </li>
<li>Employ best practices in inventory management by using first-in-first-out controls for raw materials, carefully and consistently recording inventory transactions, and maintaining cycle and stock counts with lot and material traceability. </li>
<li>Create robust work batches by utilizing Work Orders and SOPs, accurately measuring and processing chemical ingredients in the production of finished formulations, recording process information precisely, and taking timely actions to resolve quality concerns. </li>
<li>Reduce quality errors by investigating and identifying sources of errors, predicting future errors, and continuously improving practices and 6-sigma protocols to prevent such errors. </li>
<li>Maintain dependable Enterprise Resource Planning (ERP) records by ensuring transactional accuracy through precise input entries and executing key electronic transfers and search functions.</li>
</ul>
Work Schedule
<ul>
<li>Monday: 6:00 AM – 6:00 PM </li>
<li>Tuesday: 6:00 AM – 6:00 PM </li>
<li>Wednesday: 6:00 AM – 6:00 PM </li>
<li>Thursday: 6:00 AM – 12 PM </li>
<li>Friday (occasional): Overtime into Friday morning as needed </li>
<li>Friday–Sunday: Typically off</li>
</ul>
Requirements
You should have:
<ul>
<li>High school diploma or equivalent; advanced credential preferred. More </li>
<li>3 years of experience in material processing, batch formulations, or chemical manufacturing.</li>
<li>Proficiency with computer programs, including Inventory Management software and Microsoft Office.</li>
<li>Strong math and organizational skills.</li>
<li>Ability to lift and carry weights up to 50 lbs.</li>
<li>Hazwoper training preferred.</li>
<li>After initial training, they are capable of working independently with minimal supervision.</li>
</ul>
Benefits
Our company offers its employees:
<ul>
<li>Attractive salaries</li>
<li>Personal growth opportunities</li>
<li>Excellent benefits packages that include:</li>
</ul>
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401K)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Generous Paid Time Off and Public Holidays</li>
<li>Short-Term and Long-Term Disability</li>
<li>Free uniforms and footwear</li>
<li>Training &amp; Development</li>
<li>Tuition Reimbursement</li>
<li>Wellness Resources</li>
</ul>
Salary: $23 an hour
Sign-on Bonus: $500
Our company takes the compensation of its employees very seriously and considers several factors when determining the total compensation package including but not limited to location, market range, skills, knowledge, experience, and abilities. The base salary range represents the low and high end of our company's salary range for this position. Actual salaries will vary and may be above or below the range. The range listed is just one component of our company's total compensation packages for employees.
Our company provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, domestic violence status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Reactor Operator - Day Shift

<h3>Job Description</h3>
Job Description
Staff Geotechnical Engineer I
 
RESPONSIBILITIES:
The primary responsibilities include, but are not limited to:
<ul>
<li>Performing geotechnical evaluations related to new or expanding landfill facilities, including settlement, slope stability, seepage, evaluation of liner systems, leachate collection and closure cap materials, drainage layer and filtration calculations.</li>
<li>Managing and directing subsurface explorations by soil test borings, CPT, Geoprobe and geophysical methods of site conditions for use in geotechnical evaluation and analysis. </li>
<li>Select, locate and quantify low permeability soils, soils suitable for structural fill, and geotechnical drilling to identify rock and groundwater. </li>
<li>Construction Quality Assurance (CQA), responsibilities from pre-construction to monitoring, sampling, and testing completion and reports to state regulatory agencies during landfill construction projects.</li>
<li>Implements technical requirements to complete client projects by directing field staff to sample, test, and collect data and/or document on-site activities at various client sites.</li>
<li>Evaluates routine laboratory and field data for inclusion in reports.</li>
<li>Performs calculations using engineering formulas and skills.</li>
<li>Prepares reports and correspondence regarding the direction of assigned projects. </li>
<li>A variety of field and office assignments should be expected. </li>
</ul>
POSITION REQUIREMENTS AND BASIC QUALIFICATIONS:
<ul>
<li>Bachelor's degree in Geotechnical Engineering and/or Civil Engineering</li>
<li>0-4 years of working experience in a geotechnical engineering consulting, project management, GeoStructure design, or solid waste landfill CQA position. Salary will be commensurate with experience.</li>
<li>EIT certification or ability to obtain within 1 year. </li>
<li>Able to work out in the field up to 50% of the time, traveling throughout the southeastern United States (Virginia, North Carolina, Tennessee, South Carolina, Georgia, North Floriday and parts of Alabama).</li>
<li>Strong analytical skills and experience with variety of geotechnical analysis, evaluations, and calculations. </li>
<li>Working proficiency in AutoCAD and Civil3D</li>
<li>Working experience with Coal Combustion Residual (CCR) containment is preferred. </li>
<li>Experience providing verbal and written recommendations, producing reports, calculations, technical figures, charts, drawings, and specifications. </li>
<li>Field experience and familiarity with construction sites. </li>
<li>Self-Motivated and ability to manage time and priorities. </li>
<li>Ability to complete projects and tasks on an individual basis, as well as work collaboratively as part of a project team. </li>
<li>History and interest in continued involvement in professional / industry associations.</li>
</ul>
ABOUT BUNNELL-LAMMONS ENGINEERING, INC.:
Bunnell-Lammons Engineering is an environmental consulting firm providing efficient and cost-effective solutions four our clients, resulting in long-term relationships. We service commercial, financial, industrial, municipal, construction, and architectural design engineering clients across the southeast. Our highly qualified staff eagerly turns tough challenges into finished projects. Drawing on the power of combined expertise, we're big believers in teamwork, being proactive and responsive to our client's needs. We recognize that achieving our goals and building our legacy requires both hard work and creativity from all team members. When you join our team, we encourage you to see just what you can achieve as part of our great family-oriented team. 
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