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<h3>Job Description</h3>
Lead Quality Excellence in Innovative Biotechnology
 
Ready to mentor a growing microbiology team while driving FDA/EPA product compliance? Our client, an established biotech company in Ohio, specializes in cutting-edge microbial solutions for environmental applications.
 
Your Impact: Lead OTC drug efficacy studies, disinfectant testing, and preservative challenge tests while developing team expertise. You'll manage FDA audits, streamline validation processes, and ensure cGMP/GLP compliance across diverse product portfolios.
 
Key Responsibilities:
 
<ul>
<li>Conduct hands-on efficacy testing for FDA OTC drugs and EPA-registered products</li>
<li>Mentor microbiologists in USP methods, aseptic techniques, and validation protocols</li>
<li>Lead investigations, write SOPs, and manage CAPA processes</li>
<li>Execute environmental monitoring and continuous improvement initiatives</li>
</ul>
 
Requirements:
<ul>
<li>Bachelor's in Microbiology/Biology + 5+ years regulated industry QC experience</li>
<li>FDA OTC and EPA disinfectant testing expertise required</li>
<li>Proven leadership skills with method validation and audit experience</li>
</ul>
 
Package: Market-competitive salary + bonuses, full benefits, career growth in collaborative, innovation-focused environment.
 
Ready to make your mark in biotech leadership?
 
Confidential search by Pave Talent. Apply now - we'll contact qualified candidates within 48 hours. Complete privacy guaranteed.

Microbiologist

<h3>Job Description</h3>
Job Description
Interpret, Analyze and extract roadway data from street-level imagery to provide location and descriptive information about roadway infrastructure to be used in GIS databases. Create, edit and manage GIS data layers. Creation of maps for customers.&nbsp;
Position Requirements&nbsp;
<ul>
<li>
Able to work independently and as part of a team&nbsp;
</li>
</ul>
<ul>
<li>
Excellent communication skills&nbsp;
</li>
<li>
Able to follow set procedures and rules for data extraction&nbsp;
</li>
<li>
Able to understand and carry out oral and written instructions&nbsp;
</li>
<li>
Ability to work a minimum of 40 hours per week during business hours&nbsp;
</li>
<li>
Possession of and ability to maintain a valid driver’s license and automobile insurance coverage consistent with the law&nbsp;
</li>
</ul>
<ul>
<li>
Available for travel (up to 30%)&nbsp;
</li>
<li>
Bachelor’s degree or higher in Geography, GIS or related fields&nbsp;
</li>
<li>
At least one year of hands-on experience and demonstrated proficiency with ESRI GIS Software&nbsp;
</li>
</ul>
Expected Requirements&nbsp;
<ul>
<li>
Excellent driving record&nbsp;
</li>
<li>
Excellent knowledge of ArcGIS Desktop and ArcGIS Online&nbsp;
</li>
<li>
Development and maintenance of databases; data creation/editing/conversion&nbsp;
</li>
<li>
Map production; GIS creation and editing&nbsp;
</li>
<li>
Spatial Analysis, mapping, modeling and reporting&nbsp;
</li>
</ul>
<ul>
<li>
Provide user support for GIS web application&nbsp;
</li>
<li>
Provide end user support for GIS application&nbsp;
</li>
<li>
Provide GIS training, working with staff and customers&nbsp;
</li>
<li>
Ability to interface with potential new and existing clients needs&nbsp;
</li>
</ul>

GIS Technician

<h3>Job Description</h3>
Job Description
POSITION TITLE: Chemical Mixer
DEPARTMENT: Paste – Plant 2 
SALARY: $23.00/hour
SHIFT: 1st Shift Only - 6:30am to 2:30pm
POSITION SUMMARY:
Mix and prepare batches of paste, manufactured with both brazing and soldering alloys. Perform all necessary tests to assure the finished product will meet all quality specifications.
ESSENTIAL FUNCTIONS &amp; RESPONSIBILITIES: 
· Verify cleanliness of required equipment before starting
· Gather pots, beaters, carts, utensils, bases, powders and other ingredients as prescribed
· Do all mathematical conversions necessary to properly record tare and material weights on various types of scales
· Verify all weights with 2nd party weight check procedure
· Perform viscosity tests at appropriate temperatures and record all results
· Prepare batches of paste for the paste adjuster
· Exercise care during process to avoid contamination, cover pots with plastic between processes
· Interact with our computer operating system to attain information and accurately issue materials to each shop order
· Calculate quantity conversions based on material and proportion variances of customer order if required
· Package finished product into drums and/or other packaging containers when required
· Clean/maintain production equipment and work area to an excellent level
· Commit to following the Quality Policy established procedures and guidelines as required by the current ISO 9001 standards. Seek opportunities for continuous process improvement as a commitment to the Quality Policy
· Adhere to prescribed safety rules and regulations
· Maintain organization and cleanliness in work areas
· Perform other duties as assigned or directed
ESSENTIAL REQUIREMENTS:
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong math and conversion skills</li>
<li>Ability to lift and move heavy objects both manually and with basic material handling equipment</li>
<li>Able to read and understand written instruction</li>
<li>Maintain accurate, legible paperwork</li>
<li>Basic computer skills involving Windows operating systems and Microsoft office programs</li>
<li>Must be able to wear air purifying respirator as required</li>
</ul>
Fusion Incorporated offers a competitive compensation plan plus comprehensive benefits that include:
• Medical, Dental, Prescription and Vision Coverage
• 401(K) program with Company Match and discretionary Profit-Sharing
• Company paid Life and Accidental Death and Dismemberment Insurance
• Company paid Short-Term Disability and Long Term Disability
• Paid Vacation and Sick Days, Holidays, Bereavement Leave, Jury Duty
• Discretionary Company Bonus programs
Fusion Inc. is committed to adhering to the requirements of the Americans with Disabilities Act (ADA) and will make every effort to reasonably accommodate qualified individuals with disabilities.
Company DescriptionWe are a well-established manufacturing company located in Lake County, Ohio, with a proud history of over 80 years in business. Known for our commitment to quality, innovation, and long-term customer relationships. We take pride in our skilled workforce and are dedicated to providing a safe and rewarding workplace for all employees. 
<h3>Company Description</h3>
We are a well-established manufacturing company located in Lake County, Ohio, with a proud history of over 80 years in business. Known for our commitment to quality, innovation, and long-term customer relationships. We take pride in our skilled workforce and are dedicated to providing a safe and rewarding workplace for all employees.

Chemical Mixer

<h3>Job Description</h3>
Job DescriptionGeotechnical Engineer
Job Title: Geotechnical Engineer Job Location: Duquesne, PA Salary: $75K-125K Requirements: 5+ years of civil engineering/geotechnical engineering required. Experienced with Retaining wall and slope stability design also required. Position Overview: We are seeking a skilled Geotechnical Engineer to join our team. The ideal candidate will be responsible for conducting geotechnical investigations, analyzing data, and designing foundations, retaining walls, and other structures. This position plays a crucial role in ensuring the stability and safety of construction projects. Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations and soil testing to assess site conditions</li>
<li>Analyze data and prepare geotechnical reports for projects</li>
<li>Design foundations, retaining walls, and other earth structures</li>
<li>Evaluate slope stability and provide recommendations for land development</li>
<li>Collaborate with civil engineering teams to integrate geotechnical solutions into overall project design</li>
<li>Ensure compliance with relevant codes and regulations</li>
<li>Provide technical support during construction and monitor site conditions</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree in Geotechnical Engineering or Civil Engineering</li>
<li>E.I.T. (Engineer in Training) certification or P.E. (Professional Engineer) certification preferred</li>
<li>5+ years of experience in geotechnical engineering/civil engineering</li>
<li>Strong knowledge of soil mechanics and foundation design</li>
<li>Experience with retaining wall and slope stability design</li>
<li>Proficiency in geotechnical software and data analysis tools</li>
</ul>
Benefits
<ul>
<li>Medical</li>
<li>Vision</li>
<li>Dental</li>
<li>401(K) Match</li>
<li>Bonus</li>
<li>Generous PTO</li>
<li>And More!&nbsp;</li>
</ul>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. This job was first posted by CyberCoders on 06/05/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please contact a member of our Human Resources team to make arrangements.

Geotechnical Engineer

<h3>Job Description</h3>
MAJOR DUTIES AND RESPONSIBILITIES
Responsibilities include, but are not limited to:
<ul>
<li>Provide critical analytical support for regulatory submissions, including Investigational Device Exemptions (IDEs), Premarket Approvals (PMAs), or combination product filings across various global regions.</li>
<li>Lead method development, validation, and transfer for drug substances and drug products using HPLC, GPC, GC, UV-Vis, FTIR, thermal analysis and USP Apparatus 7 dissolution testing.</li>
<li>Design and perform analytical testing for assay, purity, residual solvents, degradation products, and drug release profiles, in accordance with ICH, EMA, USP and FDA requirements.</li>
<li>Author and review technical reports, stability protocols/reports, specifications, and analytical CMC documentation to support regulatory submissions.</li>
<li>Investigate and resolve complex analytical challenges and laboratory investigations (e.g., OOS, OOT) with thorough root-cause analysis and data interpretation with report.</li>
<li>Develop and revise Standard Operating Procedures (SOPs), Installation-Operation-Qualification of existing and/or new equipment and analytical software.</li>
<li>Develop and revise analytical specifications for drug substances and drug products in collaboration with cross- functional team members. Serve as subject matter expert (SME) during internal and external audits and inspections; ensure compliance with cGMP, GLP, ISO, and FDA regulations.</li>
<li>Collaborate cross-functionally with R&amp;D, Quality, Regulatory Affairs, and Manufacturing teams to align analytical strategies with project goals and timelines during various stages of development.</li>
<li>Mentor junior scientists and analysts, providing scientific and technical guidance to support high-quality data generation, critical review, and reporting.</li>
<li>As part of the analytical team member, maintain, trouble-shoot and calibrate (if needed) analytical equipment performances with documentation, mentoring junior members (as needed).</li>
<li>Maintain up-to-date knowledge of evolving analytical technologies, regulatory expectations, and industry trends for drug substance and drug products.</li>
</ul>
 
QUALIFICATIONS
Experience &amp; Education: 
<ul>
<li>Bachelor’s degree (Master’s preferred) in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or a related field required</li>
<li>Minimum 10 years (BSc) or 8 years (MSc) of hands-on analytical experience in pharmaceuticals, medical devices, or combination products</li>
<li>Strong expertise in analytical method development, validation, and CMC analytical sections for regulatory submissions such as IDE or IND, PMA or NDA</li>
<li>Demonstrated hands-on proficiency (but not limited to) with HPLC, GC, LC-MS, UV-Vis, thermal analysis and dissolution testing per USP &lt;711&gt; </li>
<li>Proven experience authoring SOPs and establishing analytical specifications for both drug substances and drug products</li>
<li>Solid understanding of ICH, EMA, USP, FDA, and ISO guidelines for analytical testing and regulatory compliance</li>
<li>Skilled in technical writing with the ability to generate clear, concise, and defensible scientific documentation</li>
<li>Strong individual contributor with a proven track record of delivering results and experience mentoring junior team members</li>
<li>Experience in leading laboratory investigations, driving root cause analysis and implementation of corrective actions to support quality and process improvements</li>
<li>Proficiency in chromatography software (e.g., Empower, ChemStation) and familiarity with LIMS or electronic data systems is a plus</li>
<li>Critical reviewing and releasing analytical data packages, and assisting in day-to-day team scheduling and workflow coordination</li>
<li>Experience in working with CROs establishing expectations and resolutions (if needed), critical reviewing and releasing their data packages</li>
</ul>

Principal Analytical Chemist

<h3>Job Description</h3>
Job Description
<ul>
<li>Position: Clinical Laboratory Supervisor</li>
<li>Location: Las Vegas, Nevada </li>
<li>Employment Type: Full-Time</li>
</ul>
 
We are seeking a qualified Laboratory Supervisor with a strong background in clinical laboratory science and a passion for hands-on benchwork. This is an excellent opportunity for an experienced professional who is ready to take on a leadership role while staying actively involved in day-to-day testing operations. We are looking for a person with experience in the Chemistry, Hematology, and Immunology departments for general diagnostic testing. Additionally, Coagulation, TB testing is a plus.
 
We are looking for a proactive and dependable leader who takes initiative, maintains high standards, and values teamwork. We are a family-owned operation with multiple locations.
 
We are open to relocating the right candidates based on their experience and qualifications.
Compensation:
$100,000+ yearly
Responsibilities:
<ul>
<li>Oversee daily laboratory operations, including testing and workflow coordination</li>
<li>Perform complex testing procedures and ensure accuracy and compliance</li>
<li>Experience with LabDAQ is a plus</li>
<li>Must be able to do daily benchwork</li>
<li>Support and supervise laboratory staff, including training and performance evaluation</li>
<li>Monitor and maintain quality assurance and regulatory standards</li>
<li>Collaborate with management to identify process improvements and support laboratory growth</li>
</ul>
Qualifications:
Minimum Requirements:
<ul>
<li>Active Nevada Laboratory Supervisor License (required)</li>
<li>ASCP Certification Required</li>
<li>Minimum of 5 years' experience in a clinical laboratory environment</li>
<li>Strong working knowledge of chemistry, hematology, coagulation, and general diagnostic testing</li>
<li>Demonstrated experience in supervising or mentoring staff</li>
<li>Excellent critical thinking, organizational, and communication skills</li>
<li>Ability to work independently while contributing to a team-focused environment</li>
<li>Familiarity with CLIA regulations, quality control practices, and laboratory safety protocols</li>
<li>Understanding and application of quality control and assurance procedures are critical for reliable lab results</li>
<li>The ability to analyze data, solve problems, and make informed decisions is important for a supervisor</li>
</ul>
About Company 
Reference Laboratory located in Las Vegas, NV

Clinical Laboratory Supervisor (Nevada Based Laboratory)

<h3>Job Description</h3>
Job Description
Who we are: Our product is progress.
At JDS Consulting, progress is the way we do business. Progress represents the rapid and streamlined manner in which we move clients from initial requests to final delivery. And progress represents the infrastructure improvements we make by delivering innovative yet practical solutions for every step of the life cycle. We measure progress by the value we bring to your investments, the reputation we build for excellence, and the lives we improve by creating safe, sustainable and fulfilling spaces where people live, work, travel, and play.
JDS Consulting, Raleigh, NC growing engineering firm is seeking to add a position within the department and expand in the Charlotte market. We are seeking individuals to work in our Construction Field Inspection Department on local projects. What we are looking for in 2025: Employee experience &amp; quality of life Risk management Communication &amp; customer service Lastly Financial profitability
Requirements/Responsibilities:
Our preferred candidates will have 1+ years of field engineering experience or 1+ years of construction management experience. Job focus will be on soils inspections and reporting. Company phone, vehicle, and gas card will be provided. All full-time employees at JDS are salaried. Pay is commensurate with experience
<ul>
<li>Must have excellent written and oral communication skills, solid math skills, and reliability.</li>
<li>Provide detailed daily reports of observations.</li>
<li>Observe work and verify compliance with plans and specifications.</li>
<li>Interact and communicate effectively with client representatives.</li>
<li>Must be authorized to work in the US.</li>
<li>Candidate(s) will be subject to both inside and outside environmental conditions, in addition to hazards at construction sites, including heights, heavy equipment, and possible highway traffic.</li>
<li>Must be able to stand and walk on uneven surfaces.</li>
<li>A valid driver's license and acceptable driving record are required.</li>
</ul>
Benefits (After 60 Days of Employment):
<ul>
<li>15 Paid days off per year, plus sick days</li>
<li>Full Medical &amp; Dental Coverage for Employees</li>
<li>Short &amp; Long Term Disability</li>
<li>Life Insurance</li>
<li>Bonus Program</li>
<li>Retirement Plan</li>
<li>Job Type: Full-time</li>
</ul>
Qualifications:
Required education: High school or equivalent Required experience: 1+ years of field engineering experience or 1+ years of construction management experience Soil and Material Testing: 1 year Required license or certification: N/A Edit job description
Job Types: Full-time
Expected hours: 40 per week
Benefits:
 
<ul>
<li>401(k)</li>
<li>Dental Insurance</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Vision insurance</li>
</ul>
 
Schedule:
 
<ul>
<li>8-hour shift</li>
</ul>
 
Ability to Relocate:
 
<ul>
<li>Greenville, SC: Relocate before starting work (Required)</li>
</ul>
 
Work Location: On the road

GEOTECHNICAL ENGINEERING TECHNICIAN I

<h3>Job Description</h3>
Job Description
Drug Hunter™ (drughunter.com) is an essential knowledge platform for industry R&amp;D innovators turning molecules into medicines. The Drug Hunter research team distills the science behind emerging drugs and technologies into concise but scientifically rich, searchable reports. Drug Hunter subscribers include many of the world’s leading innovative biotechnology and pharmaceutical companies and top-tier investors.
The Industry Research Scientist will play a crucial role in building relationships with our members through product and feature demonstrations and trainings, facilitating events and workshops highlighting the power of the Drug Hunter platform, and creating and curating high-quality educational content for Drug Hunter’s audience of industry professionals. This role requires scientific expertise, a strong understanding of industry trends, and exceptional communication skills to distill complex information into engaging resources.
Key Responsibilities:
<ul>
<li>Conduct engaging demonstrations to technical audiences including PhD medicinal chemists, showcasing the capabilities of the Drug Hunter platform</li>
<li>Develop and deliver presentations tailored to Drug Hunter members and prospects working in small molecule drug discovery</li>
<li>Present highlights in small molecule drug discovery featuring content curated from Drug Hunter to inform and inspire audiences</li>
<li>Stay informed and report on the latest trends, breakthroughs, and developments in small molecule drug discovery within the pharmaceutical and biotechnology industries.</li>
<li>Synthesize information from multiple sources into concise, insightful educational content (e.g., reviews on scientific concepts, drug targets, modalities, and technologies).</li>
<li>Prepare educational articles and summaries based on webinars, interviews, and recordings on a regular basis.</li>
<li>Develop and review a variety of educational resources for Drug Hunter members, including cheat sheets, calculators, posters, and directories.</li>
<li>Create and review engaging social media posts to promote Drug Hunter articles, events, and webinars.</li>
<li>Prepare and review content for newsletters, ensuring relevance and value for different audience segments.</li>
<li>Collaborate cross-functionally with editorial, marketing, business development, sales, and product teams to develop presentations, webinars, demos, and articles.</li>
<li>Contribute to the production of video and audio content for educational and marketing purposes.</li>
<li>Attend and organize mixers, dinners, and other networking events</li>
<li>Other duties as required</li>
</ul>
Requirements
<ul>
<li>Ph.D. in chemistry, pharmacology, biochemistry, or a related scientific field.</li>
<li>3+ years of experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery.</li>
<li>Strong scientific writing, editing, and data synthesis skills.</li>
<li>Ability to independently research and distill complex scientific topics for a professional audience.</li>
<li>Digitally native, comfortable with social media, software, databases, literature search tools, and new technologies and platforms, and eager to apply new best practices to a growing organization</li>
<li>Proven ability to collaborate effectively across teams in a remote work environment.</li>
<li>Ability to work independently and collaboratively in an extremely fast-paced, dynamic environment and meet strict deadlines </li>
</ul>
Preferred Qualifications:
<ul>
<li>Familiarity with Drug Hunter's platform and tools</li>
<li>Established network within the pharmaceutical and biotechnology industries</li>
<li>Experience with scientific content creation and data analysis</li>
</ul>
Instructions To Apply:
Your application should include:
<ol>
<li>A resume or CV</li>
<li>A cover letter stating why you are excited about this opportunity</li>
<li>A draft for a social media post about a recent ground-breaking development in small molecule drug discovery illustrated with an image written independently by you </li>
</ol>
Applications are considered on a rolling basis.
Benefits
Why join Drug Hunter?
<ul>
<li>Be part of a dynamic and innovative team that is at the forefront of the pharmaceutical industry and scientific innovation</li>
<li>Contribute to a platform that influences drug discovery and development worldwide</li>
<li>Engage with leading experts and industry partners, expanding your professional network</li>
<li>Enjoy a flexible work environment with opportunities for growth and professional development</li>
</ul>
Drug Hunter provides industry-leading benefits, including the following:
<ul>
<li>Competitive salary, variable compensation, and equity</li>
<li>Broad range of medical, dental, vision, and life insurance plans for employees and their dependents, including generous coverage for a platinum PPO healthcare plan</li>
<li>Short-term disability and long-term disability insurance</li>
<li>Cancer and critical illness coverage</li>
<li>Up to 12 weeks paid parental leave (after 1 yr tenure) and childcare FSA plan</li>
<li>401(k) + employer match (3-5%)</li>
<li>Home office set up stipend for fully remote employees</li>
<li>Learning and development support</li>
<li>Generous and flexible vacation and leave policies</li>
</ul>

Industry Research Scientist

<h3>Job Description</h3>
Job DescriptionAssociate ScientistJob Description
The Associate Scientist will work within a Quality Control (QC) environment, performing product testing in a fast-paced laboratory setting. This role requires proficiency in HPLC, GC, and FTIR techniques to ensure the highest quality standards are met.
Responsibilities
<ul>
<li>Conduct bench-top chemistry tests, including viscosity and pH testing, to generate accurate data.</li>
<li>Test various formulations such as creams, gels, solutions, topicals, foams, and ointments.</li>
<li>Review, interpret, and execute analytical methods to ensure compliance with quality standards.</li>
<li>Collaborate with lab counterparts across multiple shifts to verify analyses and maintain consistency.</li>
<li>Escalate discrepancies to QC management if results do not align with expected outcomes.</li>
<li>Manage a fast-paced and high-pressure workload, typically running two tests per day.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree in a science field, preferably chemistry, organic chemistry, or biochemistry.</li>
<li>6 months to 1 year of undergraduate research/lab or post-academic experience in a chemistry</li>
<li>Proficiency in HPLC and GC techniques.</li>
</ul>
Work Environment
The position operates on a 1st shift schedule, Monday through Friday, from 8am to 5pm. The work environment includes a well-equipped laboratory setting and requires adherence to a professional dress code.
Pay and Benefits
The pay range for this position is $22.00 - $22.00/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 San Antonio,TX.
Application Deadline
This position is anticipated to close on Aug 29, 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.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: General Production WorkerLocation:McElhattan, PA
Shifts Available:
<ul>
<li>3rd Shift: 7:00 PM - 7:00 AM</li>
<li>Rotating schedule (2 days on, 2 days off, 3 days on and every other weekend)</li>
</ul>
Pay Rate:
<ul>
<li>3rd Shift: $19.50 per hour</li>
</ul>
Key Responsibilities:
<ul>
<li>Operate machinery and equipment as trained.</li>
<li>Assemble products according to specifications.</li>
<li>Inspect products for defects and ensure quality standards are met.</li>
<li>Maintain a clean and organized work area.</li>
<li>Assist with other production tasks as needed.</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent.</li>
</ul>
Benefits:
<ul>
<li>Competitive pay rates: $19.50 per hour for 3rd shift.</li>
<li>Health, dental, and vision insurance.</li>
<li>Paid time off and holidays.</li>
<li>Opportunities for overtime.</li>
<li>Career growth and development opportunities.</li>
</ul>
If you are interested please apply now!Pay and Benefits
The pay range for this position is $18.00 - $19.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Mc Elhattan,PA.
Application Deadline
This position is anticipated to close on Sep 6, 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.

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