<h3>Job Description</h3>
Job DescriptionDescription:
Company Description: Quantus is a growing Pennsylvania-based Life Sciences Equipment Services provider supporting facilities regulated by the FDA, ISO, and EMA throughout the Mid-Atlantic region. Our customers include many of the most innovative pharmaceutical and biotech organizations in the country, and our reputation is built on responsiveness, compliance, and technical excellence.
 
Our Microbiology Laboratory in Blue Bell, PA plays a key role in supporting customer quality programs through fast turnaround testing, strong documentation practices, and expert technical support.
 
Position Summary
We are hiring a Microbiologist to support daily laboratory operations and microbiology testing services for regulated life sciences customers. This role is ideal for a hands-on microbiology professional who thrives in an organized lab environment, values strong cGMP / GDP compliance, and takes pride in delivering accurate results with reliable turnaround times.
This is an in-person role in Blue Bell, PA, working as part of a high-performing team in a growing laboratory environment.
Requirements:
Laboratory Operations &amp; Sample Handling
Support daily lab operations including sample receipt, labeling, documentation review, and workflow execution
Maintain lab readiness through supply inventory support, stocking, and coordination of laboratory consumables
Follow all internal SOPs and customer requirements to maintain compliance and audit readiness
Support equipment readiness and lab organization, including incubators and controlled lab areas
Microbiology Testing &amp; Analysis
 
Perform microbiological testing services such as:
Biological Indicator (BI) Testing
Microbial Enumeration (including plate-based methods and reporting)
USP Water Testing support (as assigned, based on qualifications)
Organism Identification using Bruker MALDI-TOF
Subculture, Gram Staining, and isolate handling
Growth Promotion Testing (GPT) and quality control testing support
Support other microbial testing services based on customer needs and lab capability
 
Incubation &amp; Result Reporting
Track sample incubation schedules and ensure proper handling throughout incubation lifecycle
Read plates and interpret microbiological results accurately
Complete reports and documentation in alignment with GDP, cGMP, and client expectations
Communicate issues, deviations, and questionable results appropriately and in a timely manner
Quality, Compliance, and Continuous Improvement
 
Maintain strict adherence to Good Documentation Practices (GDP) and applicable quality requirements
Support internal quality procedures including documentation review and corrective actions as needed
Identify inefficiencies and propose practical process improvements to support scaling lab throughput
Foster a culture of consistency, accountability, and continuous improvement
 
Required Qualifications
Bachelor’s degree in Microbiology, Biology, Chemistry, or related Life Sciences discipline
3+ years of microbiology laboratory experience (regulated industry strongly preferred)
Working knowledge of GMP and GDP expectations, with strong documentation habits
Experience performing microbiology testing such as enumeration, organism handling, and incubation workflows
Proficiency with computers and lab documentation tools (Microsoft Office and email required)
Comfortable working in a structured environment with high attention to detail and timelines
Ability to lift up to 50 lbs, and perform physical work including standing, bending, kneeling, and light equipment handling
Valid driver’s license and ability to pass background and drug screening
 
Preferred Qualifications
Experience working in pharmaceutical, biotech, compounding pharmacy, cleanroom, or other regulated environments
Familiarity with environmental monitoring concepts (classified areas, controlled spaces, trending, etc.)
Hands-on experience with Bruker MALDI-TOF or similar microbial identification tools
Experience supporting internal audits, customer audits, or inspection readiness
 
What Success Looks Like in This Role
Accurate, compliant test execution with minimal documentation errors
Consistent turnaround time performance and predictable throughput
Strong ownership of assigned workflows, incubation schedules, and reporting deliverables
Clear communication and teamwork, especially during high-volume periods
Proactive mindset toward lab organization, compliance, and continuous improvement

Microbiologist

<h3>Job Description</h3>
Canyon Labs exists to raise the standard of services in the Medical Device and Pharmaceutical markets by providing streamlined and expert solutions in technical consulting, sterilization, analytical testing and packaging.
 
We are committed to ensuring that quality services are delivered by meeting or exceeding customer expectations, continuously improving the effectiveness of the quality system, and ensuring compliance with regulations, standards and directives.
 
Position Title: Microbiologist I
Location: Onsite at Canyon Labs in Bluffdale, UT
Schedule: Monday – Friday 8:00AM – 5:00PM
Overtime: 1 – 2 Saturdays a month required
Hourly Pay Range: $24.00 - $26.00
 
Microbiologist I Overview:
The Microbiologist I is responsible for performing routine microbiological testing in support of product release, environmental monitoring, and method development or validation activities. This role works under direct supervision and follows established laboratory procedures and good documentation practices in a GMP/GLP-compliant environment.
 
Microbiologist I Primary Responsibilities:
<ul>
<li>Perform a wide range of microbiological tests and assays according to established protocols and procedures.</li>
<li>Conduct environmental monitoring (EM) and water testing (bioburden).</li>
<li>Prepare media, reagents, and cultures according to SOPs.</li>
<li>Maintain laboratory cleanliness and aseptic conditions.</li>
<li>Record data accurately and in compliance with Good Documentation Practices (GDP).</li>
<li>Participate in equipment use, maintenance, and calibration activities.</li>
<li>Assist with microbiological investigations and deviations, as needed.</li>
<li>Follow all safety procedures and report incidents immediately.</li>
<li>Support ongoing method verification or validation under supervision.</li>
</ul>
 
Microbiologist I Qualifications
<ul>
<li>Understanding of a quality system and its development, documentation and implementation to domestic and internal standards or requirements.</li>
<li>General microbiology understanding and problem-solving skills in the pharmaceutical and medical device testing industries.</li>
<li>Working synergistically with other team members.</li>
<li>Advanced computer skills in MS Office and Adobe.</li>
<li>Excellent multitasking, project management and time management skills.</li>
<li>Admirable work ethic with proven abilities to work independently and proactively to drive positive change.</li>
<li>Ability to quickly adapt to change.</li>
<li>Bachelor's degree (preferred) from an accredited university in a life science discipline (Microbiology, Molecular Biology, Biology, Medical Laboratory Sciences)</li>
</ul>
 
Canyon Labs offers several benefits as part of your total compensation, including but not limited to:
<ul>
<li>Paid Time Off, Sick Time, and Paid Holidays</li>
<li>Medical, Dental and Vision Insurance</li>
<li>Long term disability insurance, life insurance</li>
<li>401(k) with company match up to 4%</li>
</ul>
 
At Canyon Labs, we are committed to creating a diverse and inclusive workplace. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, veteran status, or any other protected characteristic under applicable laws.

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The Microbiology &amp; Sterilization Specialist will be instrumental in supporting integration, remediation, and sustainment activities related to sterilization, microbiology, and environmental control processes. This role involves assessing current practices, updating procedures, and ensuring compliance with applicable standards and regulatory requirements. The specialist will work closely with cross-functional teams to maintain robust sterilization and microbiological control programs that ensure product quality and patient safety.
Responsibilities
<ul>
<li>Conduct updated gap assessments of existing microbiology and sterilization processes, procedures, and controls.</li>
<li>Identify deficiencies and develop remediation plans to align with regulatory expectations and industry standards.</li>
<li>Update, revise, and improve procedures related to sterilization, microbiological testing, and environmental monitoring.</li>
<li>Serve as a steward for the enforcement and implementation of relevant standards and regulations within the Quality and Sterilization domains.</li>
<li>Ensure alignment with ISO (EO sterilization), FDA regulations, GMP requirements, and internal quality system procedures.</li>
<li>Support routine GQO activities related to sterilization oversight and environmental control programs.</li>
<li>Provide technical guidance on bioburden, endotoxin testing, and environmental monitoring practices.</li>
<li>Support cleanroom operations, sterilization validation activities (IQ/OQ/PQ), and ongoing compliance initiatives.</li>
<li>Collaborate with cross-functional partners to ensure consistent application of microbiological and sterilization best practices.</li>
</ul>
Essential Skills
<ul>
<li>Minimum 3 years of experience in EO sterilization or microbiology within the medical device or pharmaceutical industry.</li>
<li>Hands-on experience with sterilization validation (IQ/OQ/PQ), cleanroom operations, and regulatory compliance.</li>
<li>Demonstrated ability to assess and remediate sterilization or microbiological processes.</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Irvine, CA.
Pay and Benefits
The pay range for this position is $40.00 - $48.00/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 Irvine,CA.
Application Deadline
This position is anticipated to close on Jan 24, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
Are you looking to progress in your career with a fast-growing food safety company? Are you a hardworking, collaborative team member ready to hit the ground running and get the job done? Then we are looking for you!
What we do:
Matrix Sciences provides a uniquely comprehensive scope of laboratory, advisory, research, agsciences, and data management services that support our customers’ confidence in bringing safe, quality food to market. 
The Matrix Sciences Microbiology lab performs testing for pathogens, bacteria, yeast, molds and other organisms in a variety of food, products and packaging, as well as in support of our clients’ environmental monitoring programs. 
Why it matters:
This work allows clients to identify potential contamination before it impacts their products and helps them feel confident that their products meet their quality standards and are safe for consumption in the market.
Role Summary:
Within the Microbiology department, this role is responsible to performs all aspects of routine and non-routine microbiological testing of food and environmental samples. This role includes weekend and evening hours.
What you’ll do:
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ul>
<li>Perform microbiological analysis of food and environmental samples using conventional plating techniques as well as PCR and ELISA instrumentation. </li>
<li>Identify microorganisms by microscopic examination of physiological and cultural characteristics.</li>
<li>Perform cultural confirmations for pathogens. </li>
<li>Ensure accurate and complete traceability and documentation of testing activities performed, including LIMS result entry.</li>
<li>Review result for accuracy and suitability prior to approval, initiating additional testing per client requests if required. </li>
<li>Identify, communicate and document non-conformities with samples, instrumentation and methodologies, assisting with troubleshooting as assigned. </li>
<li>When required, assist with method verification activities as directed by assigned staff. </li>
<li>Perform routine and non-routine instrument maintenance and routine troubleshooting. </li>
<li>Referring to LIMS, ensure client expectations for turnaround time are met, communicating with Lead Microbiologists and Supervisor on status or potential delays. </li>
<li>Review of controlled documents and procedures.</li>
<li>For methods within area of responsibility, provide training for other laboratory staff. </li>
<li>Participate in quality system activities, including maintenance of test and training records. </li>
<li>Identify and assist with implementation of process improvements.</li>
<li>Adhere to lab safety procedures and reporting standards.</li>
<li>Follow written Standard Operating Procedures and Work Instructions.</li>
<li>Other duties may be assigned to assist with the operations of the lab.</li>
</ul>
What you have:
<ul>
<li>Bachelor’s Degree in Sciences, preferably Microbiology, plus 2 years in laboratory experience (or equivalent combination).</li>
<li>Ability to distinguish colors as required for Microbiological testing. </li>
<li>Demonstrated ability to work with a team.</li>
<li>Positive outlook with the ability to adapt to a changing environment.</li>
</ul>
What we offer:
<ul>
<li>Medical </li>
<li>Dental </li>
<li>Vision </li>
<li>401(k) </li>
<li>Commuter Benefits</li>
<li>Short-Term &amp; Long-Term Disability</li>
<li>Accident &amp; Critical Illness</li>
<li>Life Insurance </li>
<li>LifeLock Protection</li>
<li>Tuition Reimbursement </li>
</ul>
Location:
<ul>
<li>Mount Prospect, IL</li>
</ul>
EEO Statement
Matrix Sciences International Inc. is an Equal Opportunity Employer. Matrix Sciences is committed to a policy of Equal Employment Opportunity for all applicants and employees. We treat all employees and applicants in conformance with both the spirit and letter of federal, state, and local employment discrimination laws, regulations, and Executive Orders. The Company makes all employment decisions without regard to a person's race, color, religion, gender (including gender identity or expression), national origin, ancestry, sex, sexual orientation, medical condition, marital status, age, physical or mental disability, genetic information, veteran status, uniform services membership status or any other characteristic protected by law. Discrimination, retaliation or harassment based upon any of these factors is wholly inconsistent with how we do business and will not be tolerated.
 Wednesday - Sunday 12 PM - 8:30 PM

<h3>Job Description</h3>
Job Description:
 
Ensure that lab cleanliness and biosafety standards are maintained, including proper handling and disposal of biological materials.
Develop and qualify new microbiological or biological testing methods (e.g., microbial limits, endotoxin testing, cell-based assays).
Train other analysts to perform biological assays and microbiological procedures.
Perform visual inspections of biological samples and finished products for contamination or abnormalities.
Participate in internal assessments and audits related to biological testing and biosafety compliance.
Identify and troubleshoot issues with biological testing equipment (e.g., incubators, autoclaves, biosafety cabinets).
Evaluate new biological technologies and methods (e.g., PCR, ELISA, flow cytometry) and recommend their implementation.
Serve as a technical liaison between microbiology/biology labs and other departments, vendors, or contractors.
Coordinate biological and microbiological testing with contract laboratories and vendors.
Write technical reports or documentation such as deviation reports, biological testing protocols, and microbial trend analyses.
Write or revise standard operating procedures for biological and microbiological quality control.
Supply biological quality control data necessary for regulatory submissions.
Receive and inspect biological raw materials (e.g., cell lines, reagents, growth media).
Review data from contract microbiology labs to ensure accuracy and regulatory compliance.
Prepare or review method transfer documentation for biological assays, including technical transfer protocols or reports.
Perform validations or transfers of biological and microbiological methods in accordance with applicable guidelines.
Participate in out-of-specification and contamination investigations and recommend corrective actions.
Monitor biological testing procedures to ensure compliance with established specifications and protocols.
Investigate or report questionable biological test results.
Interpret biological test results, compare them to specifications, and make recommendations on data suitability for release.
Identify biological quality problems and recommend solutions.
Evaluate biological testing methods and procedures for potential improvements.
Complete documentation needed to support biological testing procedures, including data capture forms and equipment logbooks.
Calibrate, validate, or maintain biological lab equipment.
Compile biological test data and perform appropriate statistical or trend analyses.
Conduct routine and non-routine biological and microbiological analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Libertyville, IL.
Pay and Benefits
The pay range for this position is $22.00 - $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 Libertyville,IL.
Application Deadline
This position is anticipated to close on Jan 28, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job DescriptionSalary: 
At Argenta, were more than a company were a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. 
 
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.
 
Were in a unique position. We are the worlds only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.
Our uniqueness means:
 
We are ambitious, growing and building a one team culture, guided by our values.
<ul>
<li>
<ul>
<li>We are team players;</li>
<li>We are doers;</li>
<li>We are customer-centric;</li>
<li>We are innovators.</li>
</ul>
</li>
</ul>
We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best paw forward we will make the lives of the animals we care for, better.
 
With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Lets Make It Happen, Together.
 
TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.
 
Argenta is currently looking to fill the role of Microbiologist Iat our Shawnee, KS location. Incumbents in this position are responsible for testing of raw materials, intermediates and finished products according to cGMP's in order to ensure satisfactory levels of microbial quality are met. Fundamental microbiological principles are applied in order to interpret test results. Responsibilities also include monitoring of controlled environments to ensure that manufacturing and testing processes occur under appropriate conditions. The incumbent maintains, compiles and reviews laboratory worksheets to assure accuracy of test data.

On a daily basis, the incumbent must plan for and respond to the analytical needs of a laboratory involved in fast turnaround of pharmaceutical analyses to meet manufacturing deadlines. This planning requires good communication, attention to detail, organization skills and the use of the various analytical instrumentation systems and procedures. All incumbents are responsible for following applicable Division &amp; Company policies and procedures.
 
Key Accountabilities
<ul>
<li>Performs testing of raw material, in-process and finished product samples according to approved procedures.</li>
<li>Perform Environmental monitoring of the manufacturing and laboratory facilities including cleanroom environments, personnel, water systems, compressed gases, and laminar flow hoods.</li>
<li>Identify microbial isolates using manual or automated techniques per written procedures in a timeframe that supports customer requirements.</li>
<li>Prepares media, solutions, materials and equipment to support sampling and testing.</li>
<li>Performs growth promotion and quality testing on media used for microbiological testing, and environmental monitoring in the Microbiology QC Department as needed.</li>
<li>Maintain the record storage systems in a manner that ensures quick and reliable retrieval of the data as needed.</li>
<li>Provide support to laboratory projects and assist other team members as needed.</li>
<li>Adhere to the pertinent aspects of compliance and plant safety programs.</li>
<li>Critical understanding of proper and thorough laboratory investigations</li>
<li>Support QA Operations as required for laboratory investigations</li>
<li>Continuous improvement and assessment of laboratory practices to eliminate over-processing of data</li>
<li>Adhere to GMP and/or GLP standards as required for daily operations</li>
<li>Safety first in the laboratories</li>
</ul>
 
Qualifications
<ul>
<li>BA / BS in a related scientific field such as biology, chemistry, microbiology, or biochemistry.</li>
<li>1+ year laboratory experience, which can include academic experience or microbiology laboratory.</li>
<li>The incumbent should have basic background for the understanding, planning, and execution of laboratory Standard Operating Procedures relating to instrument use, sample analysis, document generation and control, personal safety, and environmental safety.</li>
<li>Knowledge of FDA regulations (or similar regulated environment) to include Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)</li>
<li>Basic computer skills are required.</li>
<li>The incumbent must be able to pass a DEA background check.</li>
<li>Proven, effective written and verbal communication skills.</li>
<li>Demonstrated skills in the use of a wide range of microbiology test methods and instrumentation, including the following:
<ul>
<li>Bioburden testing</li>
<li>Endotoxin testing</li>
<li>Aseptic technique</li>
</ul>
</li>
<li>Water quality sampling and testing</li>
<li>Standing and/or moving &gt;50% of the time</li>
</ul>
 
Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth. Argenta is an equal opportunity employer

Microbiologist I

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Vernon Hills, IL.
Pay and Benefits
The pay range for this position is $22.00 - $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 Vernon Hills,IL.
Application Deadline
This position is anticipated to close on Jan 25, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Mundelein, IL.
Pay and Benefits
The pay range for this position is $22.00 - $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 Mundelein,IL.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Vernon Hills, IL.
Pay and Benefits
The pay range for this position is $22.00 - $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 Vernon Hills,IL.
Application Deadline
This position is anticipated to close on Jan 14, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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