<h3>Job Description</h3>
Job Title: Microbiologist
Job Location: Indianapolis, IN (Onsite- Locals only)
 
 
About the Job:
 
As the Microbiologist, you are responsible for coordinating and performing tests for SARS-CoV-2 and other targets of public health concern in wastewater 
and water samples. Duties include sample examination and analyses, recording, interpreting, and result reporting of test results. You are responsible for completing all required Quality Control, compliance with all certification requirements, and maintaining all required safety standards. 
 
 
What You'll Need for Success:
• Four (4) year degree (B.S. or B.A.) in a biological science.
• Experience performing RNA/DNA extraction and PCR testing is required.
• Extensive knowledge of the principles, theories, and practices of molecular testing.
• Specialized knowledge of current molecular scientific methods and testing procedures.
• Specialized knowledge of and ability to use a full range of molecular and standard technical equipment
• Ability to compile, analyze, evaluate, and prepare laboratory reports.
• Extensive knowledge of laboratory safety practices and principles.
• Aware of state and federal laws, rules, regulations, and policies concerning the program area.
• Ability to effectively communicate technical information both verbally and in writing and maintain
productive working relationships.
• Ability to satisfactorily participate in proficiency testing programs.

Microbiologist

<h3>Job Description</h3>
• Four (4) year degree (B.S. or B.A.) in a biological science.
• Experience performing RNA/DNA extraction and PCR testing is required.
• Extensive knowledge of the principles, theories, and practices of molecular testing.
• Specialized knowledge of current molecular scientific methods and testing procedures.
• Specialized knowledge of and ability to use a full range of molecular and standard technical equipment
• Ability to compile, analyze, evaluate, and prepare laboratory reports.
• Extensive knowledge of laboratory safety practices and principles.
• Aware of state and federal laws, rules, regulations, and policies concerning the program area.
• Ability to effectively communicate technical information both verbally and in writing and maintain
productive working relationships.
• Ability to satisfactorily participate in proficiency testing programs.

<h3>Job Description</h3>
Job Description
Part Time Shift: Every other Saturday and Sunday 7:00am-3:30pm Hourly Pay Range: $25.00-$30.00 (Based on experience)
POSITION SUMMARY 
Performs lab testing and associated activities within the Microbiology section, including Serology, Virology and Parasitology.
Essential Position Duties 
<ul>
<li>Reviews the daily specimen management report.</li>
<li>Troubleshoots and maintains the LIS and instruments interface and software.</li>
<li>Performs Clostidium difficile assays.</li>
<li>Resolves client problems as needed.</li>
<li>Performs and records all quality assurances systems required to maintain precision and accuracy, including proficiency testing.</li>
<li>Performs other tasks and procedures in Microbiology as required which are commensurate with education, training and experience.</li>
<li>Assists in maintaining adequate inventory of supplies.</li>
<li>Record lot numbers and ensures compliance with State requirements for documentation of lot numbers with quality control and specimen records.</li>
<li>Performs all clerical functions associated with the department.</li>
<li>Reads bacterial and viral cultures. Performs biochemical identification procedures as necessary and record MIC results. </li>
<li>Follows all safety protocols as outlines in safety manual.</li>
<li>Identifies and pursues self improvement needs.</li>
<li>Seeks coaching/mentoring when appropriate.</li>
<li>Performs other duties as assigned</li>
</ul>
Compliance Responsibilities 
<ul>
<li>Participates in required orientation, Compliance and HIPAA training programs.</li>
<li>Cooperates with monitoring and audit functions and investigations.</li>
<li>Participates, as requested, in process improvement responsibilities.</li>
</ul>
POSITION QUALIFICATIONS 
Core Competencies/Skill Sets 
<ul>
<li>Excellent verbal and written communication skills.</li>
<li>Detail oriented and organizational skills.</li>
<li>Exercises accuracy and precision in completion of prescribed tasks and treatments.</li>
</ul>
Professional Experience/Educational Requirements 
<ul>
<li>Bachelor’s degree or MT (ASCP or equivalent preferred); Associates degree with MLT</li>
<li>Minimum of one (1) year experience in the area of Microbiology.</li>
<li>Some computer experience required.</li>
</ul>
Certification/Licensure
<ul>
<li>Must qualify as a clinical laboratory technologist under CLIA regulations.</li>
</ul>
Benefits:
TridentCare offers a competitive wage and robust benefit package to full time employees. Part time employees are eligible for many of the same below, pro-rated. Benefits include:
<ul>
<li>Two weeks of vacation time</li>
<li>Health Insurance after 30 days!</li>
<li>Sick time</li>
<li>8 paid holidays</li>
<li>Same day pay available</li>
<li>Medical insurance allowance, giving you the freedom to customize your plan to fit your needs</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Disability insurance</li>
<li>Company paid life insurance</li>
<li>401(k)</li>
</ul>
#MBX

Microbiologist/ MLT, Microbiologist

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiologist
Job Description
The Microbiologist will process and analyze patient samples, monitor quality control, ensure all instruments are maintained properly, and enter patient results in their department. This role requires experience and training in the relevant department. The Microbiologist may also conduct training for new employees and work closely with departmental personnel to maintain effective workflow. Compliance with regulatory standards is essential.
Responsibilities
<ul>
<li>Read and follow Departmental Standard Operating Procedures (SOPs).</li>
<li>Demonstrate proficiency in the performance, interpretation, and troubleshooting of assays.</li>
<li>Judge acceptability of quality control results and participate in proficiency testing.</li>
<li>Review performed work for accuracy before releasing it to clients.</li>
<li>Communicate sample issues within and outside the department to ensure proper client communication.</li>
<li>Assist in the evaluation and development of new procedures.</li>
<li>Achieve training goals as established by Human Resources.</li>
<li>Assist supervisors in the daily operation of the department.</li>
<li>Perform maintenance on departmental equipment.</li>
<li>Collaborate with other departmental personnel and the Product Development Department.</li>
<li>Maintain adequate supplies in the department.</li>
<li>Participate in the training of new employees.</li>
<li>Assist in maintaining year-round inspection readiness.</li>
<li>Understand and follow all safety rules and regulations.</li>
<li>Apply value statements and quality principles to work.</li>
<li>Assist in research projects as needed.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in clinical microbiology testing/assays, including blood, wound, and urine cultures.</li>
<li>Experience with microbial identification techniques such as bench biochemicals, Vitek, and MALDI-ToF.</li>
<li>Parasitology microscopic analysis and identification with trichrome and concentrate preparations.</li>
<li>Experience in molecular biology, PCR, and DNA extraction.</li>
<li>Ability to troubleshoot routine issues and train others on sample quantification.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s or Master’s Degree in Biological or Chemical Science, or a degree in Medical Technology.</li>
<li>For an MS degree, 4 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For an MT degree, 6 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For a BS degree, 7 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>Passage of a colorblind test for the Microbiology position.</li>
<li>Strong supervisory skills including mentoring, training, and leadership potential.</li>
</ul>
Work Environment
The work environment is a CLIA-compliant clinical diagnostics laboratory. The role requires meeting educational requirements and maintaining compliance with regulatory standards. Employees benefit from a collaborative culture that values innovation, diversity, and inclusion. Opportunities for professional growth are supported through ongoing training, mentorship programs, and career advancement. The role involves meaningful work that contributes to advancing personalized healthcare.
Job Type &amp; Location
This is a direct placement position based out of Asheville, North Carolina.
Pay and Benefits
The pay range for this position is $52000.00 - $79040.00/yr.
Benefits would be available to them after they complete their time through protouch and would have a waiting/probationary period of 60 days once they are a Genova employee. Once they meet their 60-day waiting period with Genova they are eligible for health, dental, and vision benefits. We offer PPO and HDP plans through Aetna.
After 90 days of employment through Genova you are eligible for 401k. There is an employer contribution. For each dollar you contribute, Genova will match dollar for dollar up to a maximum of 3% and $0.50 on the dollar for the next 2% of compensation. That is 100% vested.
Vacation- When employees are hired, they begin accruing vacation at a rate of 3.08 hours per pay period and up to 80 hours per year.
Personal Leave- Employees will receive personal leave after 6 months of employment. Full time employees will receive 40 hours.
Holidays-After 60 days employees are eligible for paid holidays. The company’s seven paid holidays are: New Year’s Day, Easter, Memorial Day, July 4th, Labor Day, Thanksgiving, Christmas.
Workplace Type
This is a fully onsite position in Asheville,NC.
Application Deadline
This position is anticipated to close on Oct 10, 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.

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiologist Job Description
As a Microbiologist, you will conduct general food microbiological testing, including pathogenic microorganism analysis, under the guidance of the Quality Assurance Supervisor or as outlined in the protocol. You will obtain samples from production, process sample preparations for micro testing, including media preparation as directed, and count and record micro plate counts. Additionally, you will assist in processing samples from receipt through testing, ensuring thorough documentation and recordkeeping, including data entry in the internal electronic system, and communicate promptly with the Quality Assurance Supervisor.
Responsibilities
<ul>
<li>Conduct general food micro testing, including generic pathogenic micro testing.</li>
<li>Obtain and process samples for micro testing, including media preparation.</li>
<li>Count and record micro plate counts.</li>
<li>Conduct specific micro testing under the guidance of the microbiologist.</li>
<li>Assist in processing samples from receipt through testing, including documentation and recordkeeping.</li>
<li>Ensure all steps are completed in a thorough and timely manner as outlined in protocol.</li>
<li>Communicate promptly with the Quality Assurance Supervisor.</li>
<li>Maintain thorough, complete, and timely documentation and recordkeeping according to established SOP.</li>
<li>Adhere to good manufacturing practices (GMP) and good laboratory practices (GLP) at all times.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in microbiology and environmental monitoring.</li>
<li>Expertise in aseptic techniques and microbiology testing.</li>
<li>Experience with sample preparation and media preparation.</li>
<li>Knowledge in bioburden testing and food science.</li>
<li>Experience in food analysis testing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>1-2 years of micro test or food analysis lab experience and basic knowledge of microbiology.</li>
<li>Prior QA/QC experience in food manufacturing is a plus.</li>
<li>B.S. degree in food, chemistry, microbiology, biology, or related field is required.</li>
</ul>
Work Environment
The role requires leading a team of 10 individuals and reporting to the QA Supervisor. It is a fully onsite position with one opening available. The work schedule is on the first shift from 4:00 pm to 12:30 am, and some weekend work may be required to assist the team. The work environment is team collaborative and business casual. The employer covers 80-90% of benefits, including health, medical, vision, and life insurance. Employees receive 7 paid holidays, 5 sick days, floating holidays, and vacation accrual. The organization also hosts team events and is recognized as one of the leading food manufacturers in the world.
Job Type &amp; Location
This is a Contract to Hire position based out of Ayer, Massachusetts.
Pay and Benefits
The pay range for this position is $26.00 - $26.00/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 Ayer,MA.
Application Deadline
This position is anticipated to close on Oct 16, 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.

<h3>Job Description</h3>
Job DescriptionQuality Control - Microbiologist
Job Description
As a Microbiologist, you will be part of a dedicated Quality Control team responsible for ensuring that all finished product testing meets the highest standards of compliance. You will work closely with the Quality Assurance department and other teams to ensure product quality and compliance with customer requirements and regulatory guidelines.
Responsibilities
<ul>
<li>Oversee all quality control aspects of finished product testing.</li>
<li>Ensure product performance compliance with testing standards, IFU, SOPs, and regulatory guidelines.</li>
<li>Manage documentation control duties as per Quality Assurance compliance requirements.</li>
<li>Review, maintain, and interpret microbiology testing results, including growth promotion, biochemical, and AST.</li>
<li>Gain proficiency in all performance benches.</li>
<li>Document testing results and determine product disposition.</li>
<li>Maintain consistency in training within Master Control.</li>
<li>Establish and maintain SOP criteria for inspection and testing.</li>
<li>Maintain department equipment and request consumables as necessary.</li>
<li>Exercise and monitor GMP compliance within the work environment.</li>
<li>Collaborate with the Quality Assurance department as part of a quality team.</li>
<li>Execute Stability Study testing in accordance with QA requirements.</li>
<li>Work alongside Customer Service Representatives to ensure timely product releases.</li>
<li>Participate in continuous improvement programs within the department.</li>
<li>Work in a fast-paced laboratory setting.</li>
<li>Understand and adhere to all safety requirements and procedures.</li>
<li>Assist in maintaining standards according to GMPs, SOPs, and ISO regulations.</li>
<li>Support all company policies and participate in achieving department goals.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in biological sciences with coursework in microbiology</li>
<li>1-2 years of experience in related QC/QA, microbiology laboratory work, or equivalent combination of education and experience.</li>
<li>Familiarity with FDA regulations for medical devices.</li>
<li>Intermediate computer skills, particularly in Microsoft Word, Excel, and PowerPoint.</li>
<li>Experience with SAP is a plus.</li>
<li>Ability to manage tasks efficiently and in an organized manner.</li>
<li>Effective communication skills with various departments regarding quality testing.</li>
<li>Ability to learn new procedures and maintain a scientific and objective approach.</li>
<li>Availability to work weekend shifts when needed.</li>
<li>Self-motivated, highly responsible, and a good team player.</li>
<li>Excellent verbal and written skills in English.</li>
</ul>
Work Environment
This position is based in a laboratory environment, with standard working hours from Monday to Friday, 8 AM to 5 PM. The role may require weekend shifts and overtime as needed. It is a long-term contract opportunity within a pharmaceutical/medical device facility.
Pay and Benefits
The pay range for this position is $23.00 - $25.00/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 Lenexa,KS.
Application Deadline
This position is anticipated to close on Oct 16, 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.

<h3>Job Description</h3>
Job DescriptionQuality Control - Microbiologist
Job Description
As a Microbiologist, you will be part of a dedicated Quality Control team responsible for ensuring that all finished product testing meets the highest standards of compliance. You will work closely with the Quality Assurance department and other teams to ensure product quality and compliance with customer requirements and regulatory guidelines.
Responsibilities
<ul>
<li>Oversee all quality control aspects of finished product testing.</li>
<li>Ensure product performance compliance with testing standards, IFU, SOPs, and regulatory guidelines.</li>
<li>Manage documentation control duties as per Quality Assurance compliance requirements.</li>
<li>Review, maintain, and interpret microbiology testing results, including growth promotion, biochemical, and AST.</li>
<li>Gain proficiency in all performance benches.</li>
<li>Document testing results and determine product disposition.</li>
<li>Maintain consistency in training within Master Control.</li>
<li>Establish and maintain SOP criteria for inspection and testing.</li>
<li>Maintain department equipment and request consumables as necessary.</li>
<li>Exercise and monitor GMP compliance within the work environment.</li>
<li>Collaborate with the Quality Assurance department as part of a quality team.</li>
<li>Execute Stability Study testing in accordance with QA requirements.</li>
<li>Work alongside Customer Service Representatives to ensure timely product releases.</li>
<li>Participate in continuous improvement programs within the department.</li>
<li>Work in a fast-paced laboratory setting.</li>
<li>Understand and adhere to all safety requirements and procedures.</li>
<li>Assist in maintaining standards according to GMPs, SOPs, and ISO regulations.</li>
<li>Support all company policies and participate in achieving department goals.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in biological sciences with coursework in microbiology</li>
<li>1-2 years of experience in related QC/QA, microbiology laboratory work, or equivalent combination of education and experience.</li>
<li>Familiarity with FDA regulations for medical devices.</li>
<li>Intermediate computer skills, particularly in Microsoft Word, Excel, and PowerPoint.</li>
<li>Experience with SAP is a plus.</li>
<li>Ability to manage tasks efficiently and in an organized manner.</li>
<li>Effective communication skills with various departments regarding quality testing.</li>
<li>Ability to learn new procedures and maintain a scientific and objective approach.</li>
<li>Availability to work weekend shifts when needed.</li>
<li>Self-motivated, highly responsible, and a good team player.</li>
<li>Excellent verbal and written skills in English.</li>
</ul>
Work Environment
This position is based in a laboratory environment, with standard working hours from Monday to Friday, 8 AM to 5 PM. The role may require weekend shifts and overtime as needed. It is a long-term contract opportunity within a pharmaceutical/medical device facility.
Pay and Benefits
The pay range for this position is $23.00 - $25.00/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 Lenexa,KS.
Application Deadline
This position is anticipated to close on Oct 15, 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.

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiologist Job Description
As a Microbiologist, you will perform tests on finished products and raw materials in accordance with regulatory requirements, following cGMP and cGLP guidelines. This role involves conducting various microbiological analyses, including Gram Staining and using the Plate Method to identify pathogens up to Bio-safety level II. You will also write and update standard operating procedures (SOPs), validate instrument qualifications and methods, and generate technical reports. Additionally, you will provide technical support for the environmental monitoring program and ensure regulatory compliance, while supporting audit activities.
Responsibilities
<ul>
<li>Perform microbiological tests on finished products and raw materials.</li>
<li>Conduct Gram Staining and utilize the Plate Method for pathogen analysis up to Bio-safety level II.</li>
<li>Write and update standard operating procedures (SOPs) and technical reports.</li>
<li>Perform chemistry analysis.</li>
<li>Provide technical support for the environmental monitoring program.</li>
<li>Operate, calibrate, and maintain microbiological instrumentation.</li>
<li>Ensure compliance with regulatory standards.</li>
<li>Support audits.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in microbiology and quality control techniques.</li>
<li>Experience with Gram Staining and Plate Method procedures.</li>
<li>Knowledge of cGMP and cGLP guidelines.</li>
<li>Familiarity with FDA and HACCP regulations.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's Degree in Microbiology, Biology, Biochemistry, or Bacteriology.</li>
<li>Completion of at least 2 microbiology courses or 2 years of laboratory experience.</li>
<li>Experience in an FDA-regulated environment is advantageous.</li>
</ul>
Work Environment
The work environment is a pharmaceutical wet wipe manufacturing setting. Initially, you will train from 8:30 a.m. to 5:00 p.m., Monday to Friday, for approximately 1-2 weeks or until comfortable. After training, the permanent schedule will be 6:00 a.m. to 6:00 p.m. on a 2-2-3 rotation. The position involves 70% laboratory work and 30% administrative tasks, such as writing reports and managing lab inventory. You'll work within a small, collaborative, and fun team in the QC Chemistry &amp; Microbiology Lab.
Job Type &amp; Location
This is a Permanent position based out of Sheboygan, Wisconsin.
Pay and Benefits
The pay range for this position is $54080.00 - $54080.00/yr.
Rockline Industries offers a competitive benefits package that includes comprehensive health insurance, retirement savings plans, and paid time off. Employees have access to wellness programs and resources that support physical and mental health. The company promotes professional development through training opportunities and tuition reimbursement. Rockline also fosters a strong culture of safety, inclusion, and work-life balance across its facilities.
Workplace Type
This is a fully onsite position in Sheboygan,WI.
Application Deadline
This position is anticipated to close on Oct 13, 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.

<h3>Job Description</h3>
Job DescriptionMicrobiologist I
Job Description
We are seeking a dedicated Microbiologist I to join our Quality Control team, supporting our laboratory in a manufacturing setting. The role involves conducting routine microbiological lab testing, ensuring accurate and timely recording of test results into the business integrated module, and leveraging lab reference materials for testing information.
Responsibilities
<ul>
<li>Follow, update, and review quality control lab documentation.</li>
<li>Perform necessary sampling of the facilities and lab areas following established QC protocols.</li>
<li>Conduct microbiology testing of raw materials, intermediate and final products for release to production in a timely and accurate manner.</li>
<li>Interpret results of microbiological testing and document results accurately and promptly.</li>
<li>Troubleshoot QC testing for non-conforming products.</li>
<li>Participate in contamination troubleshooting teams.</li>
<li>Adhere to Good Manufacturing Practices for the care, handling, and storage of food products and report any known or observed violations to management.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in microbiology, laboratory, biology, chemistry, aseptic techniques, and Good Manufacturing Practices (GMP).</li>
<li>Experience with microbiological test methods and the ability to determine specific tests for each raw material or product.</li>
<li>Capability to prepare, culture, and examine samples for microbiological testing.</li>
<li>Competence in performing probiotics enumeration and stability testing.</li>
<li>Skill in preparing product-related microbiology reports for the release of manufactured products.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Minimum of an associate degree in biology, biotechnology, microbiology, or equivalent.</li>
<li>1-2 years of related work experience is preferred.</li>
</ul>
Work Environment
The role requires working in a clean room environment for short periods and handling hazardous materials, including dry ice and gel staining solutions.
Job Type &amp; Location
This is a Contract to Hire position based out of Rochester, New York.
Pay and Benefits
The pay range for this position is $24.00 - $27.00/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 Rochester,NY.
Application Deadline
This position is anticipated to close on Oct 7, 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.

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