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<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Manufacturing Support TechnicianJob Description
As a Chemical Manufacturing Support Technician, you will collaborate closely with the Chemical Manufacturing Technician to prepare and clean reactors. You will adhere to standard operating procedures (SOPs) and current Good Manufacturing Practices (cGMPs) to ensure batch completions, involving real-time documentation, weight checks, component counting, and material preparation.
Responsibilities
<ul>
<li>Assist in the preparation and cleaning of reactors alongside the Chemical Manufacturing Technician.</li>
<li>Follow SOPs and cGMPs for batch completion, including documentation, weight checks, and component counting.</li>
<li>Handle, consolidate, inspect, and prepare materials for production.</li>
<li>Perform basic math calculations and chemical handling operations.</li>
</ul>
Essential Skills
<ul>
<li>1-2 years of experience in Chemical Operating or Chemical Handling.</li>
<li>Basic math skills for calculations.</li>
<li>Knowledge of chemical handling, blending, titration, and analytical chemistry.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma.</li>
<li>Experience in pharmaceutical, API, GDP, method validation, and method development.</li>
</ul>
Work Environment
The position is within an Active Pharmaceutical Ingredient (API) Manufacturing facility that is highly regulated and requires personal protective equipment (PPE). This includes wearing gloves, a full-face respirator, and occasionally a Tyvek suit to prevent getting wet. Normally, a uniform is worn instead of Tyvek. The primary cleaning agent used is citric acid, with no hazardous chemicals involved. The work schedule is flexible, requiring at least 8.5-hour shifts starting between 6-9 am, Monday to Friday, totaling 40 hours a week, with opportunities for overtime as needed. The position may transition to a permanent role with a night shift schedule of 12-hour shifts on a 2-2-3 rotation from 6 p.m. to 6:30 a.m., offering a shift differential and a yearly bonus.
Job Type &amp; Location
This is a Contract to Hire position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $21.00 - $21.00/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 Germantown,WI.
Application Deadline
This position is anticipated to close on Jan 23, 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.

Chemical Manufacturing Support Technician

<h3>Job Description</h3>
Job Description
Job Title: Microbiology Operations Manager
Job Description
The Microbiology Operations Manager is a pivotal role responsible for leading and managing a department that ensures compliance with SOPs for testing client samples. This position requires overseeing a diverse team and ensuring efficient and safe testing across various product categories.
Responsibilities
<ul>
<li>Oversee daily operations of a team of approximately 20–25 staff within the Micro department, ensuring efficient testing across different product categories.</li>
<li>Develop and maintain systems to ensure proper methodologies are used in conformance with client requirements, and lead PCR and classical micro testing oversight.</li>
<li>Administer HR programs including recruitment, retention, compensation, training and development, EEO, and performance appraisals.</li>
<li>Interpret data and guide correction of discrepancies prior to release to Client Services and clients, ensuring data aligns with accepted methods.</li>
<li>Ensure corrective actions effectively eliminate errors and that documentation and follow-up meet SOP requirements.</li>
<li>Support company initiatives and partner with Operations, QA, and other leaders to implement methods, and train teams for complete understanding.</li>
<li>Communicate emerging client requirements to departmental personnel and align resources accordingly.</li>
<li>Interface with internal and external auditors to demonstrate quality systems and accreditation compliance with regulations.</li>
<li>Maintain expertise in food science and microbiology through resources and peer learning, and maintain a strong working knowledge of LIMS.</li>
<li>Champion corporate quality and continuous improvement, proactively initiating actions to prevent or minimize departures from the quality system or test procedures.</li>
<li>Address resource needs such as turnaround time requirements, overtime limits, turnover, and work stoppage, ensuring appropriate materials are available.</li>
</ul>
Qualification
<ul>
<li>A degree in Microbiology, Food Science, Biology, or a related field.</li>
<li>A minimum of 8 years of experience in microbiology testing environments, with proven success in high-volume operations and team leadership.</li>
<li>Expertise in PCR and culture-based methods, method verification and validation, and LIMS proficiency.</li>
<li>Experience with CAPA, SOP authoring and updating.</li>
<li>Knowledge of quality and regulatory standards and customer audits.</li>
<li>Strong problem-solving skills and accountability.</li>
<li>Comfortable interfacing with customers and conducting third-party testing.</li>
</ul>
Job Type &amp; Location
This is a Permanent position based out of Chicago Heights, IL.
Pay and Benefits
The pay range for this position is $70000.00 - $100000.00/yr.
Benefits include but not limited to Medical, Dental, Vision.
Workplace Type
This is a fully onsite position in Chicago Heights,IL.
Application Deadline
This position is anticipated to close on Jan 23, 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.

Operations Manager Microbiology

<h3>Job Description</h3>
Job Description
Polymer Chemist – Advanced Composites &amp; Resin Formulation

Polymer Chemist

<h3>Job Description</h3>
Job DescriptionIrvine Clinical Research, a research site specializing in late phase clinical trials in Mild Cognitive Impairment, Alzheimer’s Disease, and Depression, is seeking applicants for a Research Assistant. They will provide administrative support to our team of physicians, psychologists, and research coordinators. This position is designed for an ambitious individual who is willing to start at an entry-level role and work their way up quickly.Job Duties
<ul>
<li>Warmly greet and assist study participants at the front and back office, especially older adults</li>
<li>Coordinate and troubleshoot scheduling for participant visits</li>
<li>Learn complex research protocols quickly and assist with data entry and quality</li>
<li>Assist doctors, clinicians, and research coordinators with study participant visits as needed</li>
<li>Provide clerical and administrative support</li>
</ul>
Job Requirements
<ul>
<li>Excellent communication and social skills in spoken and written English</li>
<li>Attention to detail and the ability to handle multiple tasks with precision</li>
<li>Willingness to commit to at least 2 years of growth and development</li>
</ul>
This is a full-time employment position based in-person at our clinic in the Alzheimer’s Orange County building in Irvine. The starting salary for this position is approximately $23/hr (approximately $47,480 per year). Depending on job performance, there is a possibility for growth. The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.

Research Assistant

<h3>Job Description</h3>
Job Description
Associate degree preferred with 2+ years chemical manufacturing experience, knowledge of 5S, organic chemical syntheses experience on reactors, Forklift Certified, and trained in EPA, ERCRA HAZWOPER.
 Perform chemical syntheses of active pharmaceutical ingredients (APIs) in strict accordance with written procedures and standard chemical safety practices
 Work on multikilogram scale organic chemical syntheses with reactors larger than 100 gallons
 Record accurate reaction notes, making observations throughout the process
 Maintain a meticulous work environment: return all equipment to the appropriate storage location; clean all tools, equipment, and surroundings after use.
 Conform to applicable safety regulations including proper handling of chemicals and use of all designed safety equipment and PPE
 Maintain meticulous inventory logs of raw materials and finished product.
 Collect and discard chemical waste in accordance with applicable internal, safety, and regulatory requirements.
 Accurately maintain waste and disposal logs.

Chemical Operator

<h3>Job Description</h3>
Job Description
Description
• Prepare samples for analytical and microbiological testing of nutraceutical products, supplement ingredients, utilities, and environmental samples. • Perform Quality Control microbiological testing for food and nutraceutical manufactured products. • Conduct environmental monitoring of cleanrooms, including air, surface, and personnel monitoring. • Collect water samples per approved schedules and ensure timely testing and documentation. • Perform and review microbiological assays, including: o Gram stain o Sterility testing o Microbial identification o Growth promotion testing o Plate reading and interpretation • Perform and review visual inspection of finished products. • Perform microbiological utility testing, including water system monitoring. • Perform and oversee microbiological testing of probiotic raw materials and finished products, including: o Enumeration of probiotic strains o Strain verification o Stability and viability assessment • Enter data accurately into laboratory systems, trend microbiological data, and prepare reports and presentations for management review. • Assist with investigations related to out-of-specification (OOS) results and deviations associated with microbiological testing. • Perform routine maintenance and cleaning of laboratory equipment and laboratory spaces. • Review and approve final product microbiological test results to support product release. • Support audits and inspections (internal, customer, NSF, regulatory) as needed. • Perform other duties as assigned to support Quality and Manufacturing operations.
Skills
Environmental monitoring, gram staining, sterility testing, Microbiology, Aseptic technique, Quality control, Bioburden, Plating, Media, Sop, swabbing, strain verification, enumeration of probiotic strains, plate reading, probiotic raw materials, trending reports, deviation, out of spec, water testing, air monitoring, surface testing, NSF, GMP, microbiological testing
Top Skills Details
Environmental monitoring,gram staining,sterility testing,Microbiology
Additional Skills &amp; Qualifications
• Bachelor’s degree in microbiology, Biology, or a related scientific discipline. • Hands-on experience with microbiological techniques, including: o Environmental air monitoring o Water testing o Surface monitoring • Experience with aseptic techniques and cleanroom operations. • Ability to grow and work within aseptic core and support cleanroom areas. • Knowledge of GMP regulations, SOPs, and Quality Control processes in a commercial manufacturing environment. • Ability to lift- up to approximately 25 lbs. • Ability to pass a vision exam for visual inspection activities. • Proficiency in Microsoft Word, Excel, PowerPoint, and related applications. • Strong interpersonal, verbal, and written communication skills. • Ability to work effectively in a fast-paced, small company environment with minimal supervision. • Flexibility to adjust workload based on changing priorities and to work overtime as needed. Preferred Qualifications • Experience with probiotic microbiological testing, including enumeration, identification, and stability studies of probiotic strains (strongly preferred). • Experience in dietary supplement, nutraceutical, food, or pharmaceutical manufacturing environments. • Familiarity with NSF certification requirements and regulatory expectations for
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Contract to Hire position based out of Chatsworth, CA.
Pay and Benefits
The pay range for this position is $20.00 - $40.00/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 Chatsworth,CA.
Application Deadline
This position is anticipated to close on Jan 23, 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.

Microbiologist

<h3>Job Description</h3>
Job DescriptionDIHO Consulting USA is seeking a Geotechnical Engineer on behalf of our client for their Southeast Louisiana Area offices.
The successful candidate will provide engineering and consulting services for a wide variety of projects and clients, primarily in the Energy Market Sector. Our client offers training and support necessary for career advancement, with the objective of developing the candidate into a departmental management role. Their Southeast Louisiana operations are well established in the local market and have an experienced engineering support staff in place.
We are looking for a candidate with excellent communication skills, a strong desire for career advancement, and sound leadership qualities.
Responsibilities
<ul>
<li>Prepare technical proposals.</li>
<li>Execute geotechnical engineering project assignments.</li>
<li>Work with and provide mentorship to engineering support staff.</li>
<li>Manage and coordinate geotechnical field and laboratory assignments.</li>
<li>Perform engineering analyses and prepare reports.</li>
<li>Maintain client expectations for project quality and schedule.</li>
</ul>
Requirements
<ul>
<li>Bachelors Degree in Civil Engineering.</li>
<li>PE License or active EIT Certification.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Benefits
This position includes a comprehensive benefits package provided by our client, which includes:
<ul>
<li>Flexible work schedule.</li>
<li>Health, Vision, Dental, Disability, and Life Insurance.</li>
<li>401(k) Retirement Program with up to 4% employer match after eligibility period.</li>
<li>120 hours of Paid Time Off (PTO) annually.</li>
<li>9 company-paid holidays.</li>
</ul>

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Position Summary
We are looking for an Intern to join VTC’s Research division during the summer of 2026 for a 10-week period. This energetic, self-starting individual is seeking analytical experience in economics, tourism, or in state government and will assist with producing reports and generating insights from VTC’s data sources. The selected intern will gain valuable experience working alongside a dedicated team and will become familiar with the mission and goals of a state destination marketing organization (DMO). We aim to offer the intern with direct mentorship to cultivate their skills and help them develop into being a proficient professional in the tourism industry. The responsibilities of the intern may vary based on the applicant’s interest and experience, as well as the particular research areas the team is pursuing at the time. 
Interns will complete a project and develop a presentation to be shared with staff at the end of the internship. They will be part of an organization-wide cohort, providing networking and professional development opportunities throughout the summer.
Duties:
<ul>
<li>Produces monthly &amp; weekly reporting for VTC’s key data sources and subscriptions</li>
<li>Responds and fulfills requests from travel industry members for travel or visitor insights across Virginia</li>
<li>Interprets visitor and travel industry data and provides insights to stakeholders in other VTC divisions </li>
<li>Analyzes quantitative data and presents data analysis in a visually compelling format</li>
<li>Assists in designing and developing industry reports for internal VTC consumption</li>
<li>Attend local tourism summits or related events alongside VTC Research staff, as needed </li>
<li>Assist in other project-related tasks, as needed</li>
</ul>
Knowledge and Skills Required:
<ul>
<li>Interest in economics, hospitality, business, or state government</li>
<li>Excellent planning, organizational, and communication skills </li>
<li>Proficient with Microsoft Office – especially working with data in Excel and developing insight-oriented presentations in PowerPoint</li>
<li>Basic experience working with large data sets using Python (a plus, but not required)</li>
</ul>
Qualifications Preferred:
The ideal intern excels in their academic studies and is comfortable translating data into insights for non-technical audiences. This individual has a high degree of intellectual curiosity and is a self-starter with the ability to learn new topics and concepts quickly. Pursuit of a bachelor’s or graduate degree in social science (economics, public policy), business, data analytics, tourism management, or a related field is preferred.
VTC is flexible on a full or part-time arrangement. Full-time candidates should be prepared to work approximately 3 days a week in our Richmond office and up to 2 days from home. Part-time candidates work 3 days a week in our Richmond office.
All candidates must submit a resume and cover letter through our website <a href="https://www.vatc.org/about/employment/" target="_blank">https://www.vatc.org/about/employment/</a> Internship Period: June 1, 2026 – August 6, 2026 (10 weeks) Salary: Undergrad Students - $15 per hour, Graduate Students - $17 per hour Application deadline: February 06, 2026 
VTC is an Equal Opportunity Employer. All applicants are considered for employment without regard to race, sex, color, national origin, religion, sexual orientation, gender identity or expression, age, veteran status, political affiliation, genetics, or against otherwise qualified individuals with disabilities. It is VTC’s intent that its employment and personnel policies and practices conform to all applicable federal, state, and local laws and regulations regarding non-discrimination and affirmative action. Applicants requiring more information or requiring assistance may contact VTC Human Resources at 1-804-545-5634 or <a href="mailto:vtchr@VEDP.org" target="_blank">vtchr@VEDP.org</a>. TDD 1-800-828-1120.

Research Intern

<h3>Job Description</h3>
Job Description
We are looking for a skilled and safety-conscious Chemical Processor to join our metal finishing team. As a Chemical Processor, you will be responsible for operating and maintaining chemical baths and related equipment to process metal components according to specifications. This role is vital in ensuring the highest quality finishes on our products.
Schedule:
M-F 10:00am-6:30PM shift
Key Responsibilities:
<ul>
<li>Prepare and maintain chemical baths used in metal finishing processes, such as plating, anodizing, and coating.</li>
<li>Monitor and adjust chemical concentrations, temperatures, and pH levels to ensure optimal processing conditions.</li>
<li>Load and unload metal parts into chemical baths, ensuring proper handling to prevent damage.</li>
<li>Inspect processed parts to ensure they meet quality standards and specifications.</li>
<li>Perform routine maintenance and cleaning of chemical processing equipment.</li>
<li>Adhere to all safety protocols and environmental regulations while handling chemicals.</li>
<li>Document processing data, including chemical usage, bath conditions, and production output.</li>
<li>Collaborate with the quality control team to address any issues related to the chemical finishing process.</li>
<li>Assist in the disposal of hazardous waste in accordance with company and regulatory guidelines.</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent; technical training in chemistry or a related field is a plus.</li>
<li>Previous experience in chemical processing or metal finishing is preferred.</li>
<li>Strong understanding of chemical safety practices and environmental regulations.</li>
<li>Ability to handle and work with hazardous chemicals safely and responsibly.</li>
<li>Attention to detail and a commitment to maintaining high-quality standards.</li>
<li>Strong problem-solving skills and the ability to troubleshoot processing issues.</li>
<li>Good communication and teamwork skills.</li>
<li>Ability to lift and move materials and equipment as needed.</li>
</ul>
Company DescriptionChanging people lives is what we do, putting them back to work is how we do it! 
<h3>Company Description</h3>
Changing people lives is what we do, putting them back to work is how we do it!

Chemical Processor - Metal Finishing

<h3>Job Description</h3>
Job Description
Job Summary
This role supports complex clinical research and development activities focused on evaluating new procedures, devices, and technologies, particularly within blood quality and transfusion-related research. The position involves conducting laboratory experiments with a high degree of independence, performing advanced biological assays, maintaining accurate documentation, and collaborating closely with scientific and project teams. The role also contributes to assay development, validation, process improvement, and scientific reporting.
Key Responsibilities
<ul>
<li>
Participate in complex clinical research and development studies independently and as part of multidisciplinary research teams
</li>
<li>
Perform blood quality analyses using laboratory instruments such as flow cytometers, hematology analyzers, aggregometers, plate readers, and gamma counters
</li>
<li>
Conduct laboratory experiments and biological assays with minimal supervision
</li>
<li>
Perform radiolabeled in vivo recovery and survival experiments
</li>
<li>
Maintain accurate, detailed records of experimental data, observations, and analyses
</li>
<li>
Summarize and document results, conduct basic analyses, and prepare technical reports
</li>
<li>
Contribute to manuscript preparation for publication in professional journals
</li>
<li>
Support development, validation, and maintenance of laboratory SOPs and assay methods
</li>
<li>
Maintain laboratory equipment and contribute to continuous process improvements
</li>
<li>
Collaborate with scientists and project leaders regarding project progress, observations, and safety procedures
</li>
<li>
Participate in ongoing technical and scientific training to develop expertise within the discipline
</li>
</ul>
Qualifications
Education
<ul>
<li>
Bachelors degree in Biology, Chemistry, Medical Technology, Medical Laboratory Sciences, Biomedical Engineering, or a related field, or an equivalent combination of education and experience
</li>
<li>
Masters degree preferred
</li>
</ul>
Experience
<ul>
<li>
Minimum of one year of experience in a research laboratory
</li>
<li>
Experience in blood banking, hematology, or transfusion medicine preferred
</li>
<li>
Flow cytometry experience highly desirable
</li>
<li>
Background in laboratory, pre-clinical, clinical, or computational studies and scientific writing preferred
</li>
</ul>
Skills &amp; Abilities
<ul>
<li>
Strong proficiency in laboratory techniques with high attention to detail
</li>
<li>
Ability to recognize discrepancies in experimental results
</li>
<li>
Excellent documentation and organizational skills
</li>
<li>
Effective verbal and written communication skills
</li>
<li>
Ability to work collaboratively as part of a research team
</li>
<li>
Broad understanding of scientific principles, theories, and related disciplines
</li>
</ul>
Additional Information
<ul>
<li>
Some travel may be required
</li>
</ul>
This position is well suited for a detail-oriented research professional seeking to contribute to advanced clinical and laboratory research in a collaborative scientific environment.

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