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<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
<ul>
<li>Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.</li>
<li>Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.</li>
<li>Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.</li>
<li>Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure compliance with international regulations such as FDA and EMA.</li>
<li>Work collaboratively with R&amp;D and production teams to support product development and release.</li>
<li>Provide technical support and training to junior team members or other departments.</li>
</ul>
Essential Skills
<ul>
<li>3-7 years of routine testing experience using HPLC and dissolution techniques.</li>
<li>Proficiency in working with solid oral dosage forms, raw materials, and finished products.</li>
<li>Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.</li>
<li>Strong understanding of Pharma GMP practices.</li>
<li>Competence in laboratory applications including wet chemistry, titration, and chromatography.</li>
<li>Basic computer skills in MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>Ability to document and record analytical experiments and results as per cGMP guidelines.</li>
<li>Strong problem-solving skills and attention to detail.</li>
<li>Knowledge of regulatory guidelines such as GMP and GLP.</li>
</ul>
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type &amp; Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $35.00/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 East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 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.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Job Description

POSITION SUMMARY The Microbiology Supervisor is responsible for the operation of Microbiology section of the clinical laboratory.&nbsp; The Microbiology Supervisor facilitates the implementation of hospital and laboratory policies and procedures.&nbsp; Responsible for assisting in training new employees, supervising both Clinical Laboratory Scientists and laboratory phlebotomist’s workload organization, and monitoring daily maintenance and quality control. This person will report to the Lab Manager Implements good public relations by representing the laboratory directly to patients, physicians and hospital staff at all times.
ESSENTIAL DUTIES AND RESPONSIBILITIES
<ul>
<li>Responsible for assisting with the selection of methodology and instrumentation to perform laboratory tests appropriate for the patient population served.&nbsp; Responsible for the validation and implementation of new instrumentation.&nbsp; Ensures the standardization of tests methodologies, procedures, instrumentation, and reference ranges.</li>
<li>Verifies test procedures performed and established the laboratory’s test performance characteristics, including, but not limited to the linearity, precision and accuracy of each test and test system.</li>
<li>Ensures participation in and successful completion of a quality control and approved proficiency testing program commensurate with the services offered.&nbsp; Troubleshoots any problems with the proficiency testing program.&nbsp; Establishes parameters for acceptable level of analytic performance.&nbsp; Ensures that quality is maintained throughout entire testing process from order entry through results reporting.</li>
<li>Reviews the work of others to ensure that tests are performed in accordance with prescribed standards.</li>
<li>Assists in maintaining and optimizing work standards to assure a reasonable turnaround time of test results.</li>
<li>Troubleshoots equipment problems.</li>
<li>Maintains inventory control of supplies and reagents in his/her section(s).</li>
<li>Schedules, organizes and delineates duties of personnel.</li>
<li>Assists manager in performance evaluations of the employees in his/her sections.</li>
<li>Responsible for the operation of the Microbiology department.</li>
<li>Works closely with the Laboratory Manager to meet the administrative and financial goals of the department</li>
<li>Responsible for meeting the service and quality goals of the department. Assumes responsibility for daily operations and meets CLIA requirements for microbiology</li>
<li>Provides clinical microbiology consultations to medical and hospital staff</li>
<li>Present micro data reports clearly and concisely to management, including QC performance metrics and trends</li>
<li>Proactively identifies and implements improvements and lean initiatives</li>
<li>Responsible for the technical and scientific oversight of the department including assisting in hiring of personnel, training/competency assessment and input for performance review of the staff in their designated area.</li>
<li>Responsible for making clinical/technical decisions in the resolution of testing/reporting issues, maintenance of the quality and security of department instrumentation, quality control documentation and meeting hospital goals to ensure accurate and timely patient care.</li>
<li>Responsible for maintaining procedure manuals for all testing performed and the documentation required for regulatory and licensing organizations</li>
<li>Oversee and manage team schedule of staff and PTO request.&nbsp;</li>
<li>Work collaboratively with other department leaders to have a more efficient workflow for the Clinical laboratory.&nbsp;</li>
<li>Responsible for ensuring staff compliance with hospital policies and meeting regulatory requirements within their assigned areas (e.g. coordinate meal breaks, corrected reports, attendance, overtime and punctuality)</li>
<li>Setting an example- must always be conscious of how his / her words and actions will be perceived.</li>
<li>Attend minimum of three (3) leadership seminar/workshop annually</li>
<li>Performs additional duties as directed by the by the Laboratory Director or Manager which are necessary for the efficient operation of the laboratory.</li>
</ul>
Job Requirements

POSITION REQUIREMENTS
A.&nbsp; &nbsp;Education
<ul>
<li>Bachelor’s degree – Science</li>
</ul>
B.&nbsp; Qualifications/Experience
<ul>
<li>2-5 years Microbiology Clinical Laboratory Experience</li>
<li>CA Clinical Laboratory Scientist License or Clinical Microbiologist Scientist License</li>
<li>2 years leadership experience in an acute care setting required</li>
</ul>
C.&nbsp; &nbsp;Special Skills/Knowledge
<ul>
<li>Strong interpersonal and organizational skills.&nbsp; Proficient with computer.</li>
</ul>
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#LI-AJ1

Microbiology Supervisor - Full Time Days

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical EngineerJob Description
We are seeking a skilled Chemical Engineer to perform all chemical process functions related to chemical batching. This role involves conducting root cause analysis (RCA) to troubleshoot batching issues and implementing corrective and preventive actions (CAPAs) for both internal and external challenges. You will be responsible for scaling up and commercializing new formulas, adjusting existing formulas, and validating all manufacturing and quality processes and specifications. Additionally, you will perform in-process batch adjustments, support production scaling to meet product specifications, and analyze production and laboratory data to optimize processes and reduce costs.
Responsibilities
<ul>
<li>Conduct root cause analysis for customer complaints and internal production issues.</li>
<li>Ensure all batch adjustments are executed accurately when raw materials or formulas change.</li>
<li>Scale up and commercialize new formulas and products, ensuring correct implementation.</li>
<li>Analyze production data and quality data to identify optimization and cost reduction opportunities.</li>
<li>Participate in the disposition of non-conforming materials and support deviation management.</li>
<li>Mentor and coach fellow engineers and quality and production personnel in continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>1-5 years of experience in chemical engineering or chemical process engineering.</li>
<li>Ability to diagnose and resolve customer complaints and internal production issues.</li>
<li>Experience with root cause analysis and implementation of CAPA.</li>
<li>Expertise in chemical manufacturing, quality control, and process engineering.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Degree in Chemical Engineering or a related field.</li>
<li>Experience in scale-up and commercialization processes.</li>
<li>Familiarity with chemical equipment and laboratory practices.</li>
<li>Knowledge of new product development and chemical processing.</li>
</ul>
Work Environment
This position operates in a chemical manufacturing environment, working across offices, laboratories, production areas, and production labs. The role follows a first shift schedule from Monday through Friday, with flexible working hours typically ranging from 40 to 45 hours per week, extending to 50 hours during major projects or issues. You will collaborate with various organizational levels, including R&amp;D, Quality, Production, Maintenance, Customers, Sales, and leadership roles.
Job Type &amp; Location
This is a Permanent position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
This company offers health insurance, dental insurance, vision insurance, 401k match, bonuses, etc. They also provide paid vacation and paid holiday.
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 Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist OperatorJob Description
The Chemist Operator will be responsible for producing Active Pharmaceutical Ingredients using chemical reactors. This role requires following specific Batch Records to ensure the production of a consistent product.
Responsibilities
<ul>
<li>Handle various unit operations, such as reactions, filtration, distillation, drying, and milling, on raw materials and various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document instructions per batch sheet to produce products in accordance with all cGMP guidelines.</li>
<li>Set up equipment, including vessels, tanks, centrifuges, and dryers, for proper processing. Clean and verify equipment and vessels.</li>
<li>Record observations of operating conditions.</li>
<li>Drive and operate a fork truck.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in Chemical Operation or Batching, 1-5 years preferred.</li>
<li>Knowledge of GMP guidelines from food, chemical, or pharmaceutical industries.</li>
<li>Understanding of Analytical Chemistry and Chemical Operating.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma with experience, or an Associate's or Bachelor's degree in Sciences, preferably in Chemical Technology or Chemistry.</li>
<li>Experience in GC and Batching processes.</li>
</ul>
Work Environment
The work environment is a clean laboratory and production setting. Initial training will be on the first shift for 3-6 months, after which the role will transition to a permanent shift from 6 p.m. to 6:30 a.m., following a 2-2-3 schedule, including working every other weekend. The company is expanding its innovation hub, offering growth opportunities into leadership positions for those who excel.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $24.00 - $26.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Grafton,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.

Chemist Operator

<h3>Job Description</h3>
Job Description
Description
Work closely with the Senior Chemist and/or Technical Director to improve the functionality, performance, and application of chemical products. Adjust, refine, or optimize existing product formulations based on feedback from sales engineers, field service personnel, and customers. Replicate specific water qualities and system conditions to conduct testing of new and existing products, ensuring accuracy and relevance to real-world applications. Review, perform, and verify quality control parameters to support consistent production standards. Prepare documentation, technical reports, and presentations as required by the Senior Chemist and/or Technical Director. Maintain accurate laboratory records, test data, and research files in accordance with internal documentation standards. Collaborate with the R&amp;D and QC teams to support product troubleshooting, root-cause analysis, and continuous improvement initiatives. Follow all laboratory safety protocols and maintain clean, organized, and compliant laboratory workspaces. Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
The Research &amp; Development Chemist supports the development of new products, enhancement of existing formulations, and testing efforts required for innovation and continuous product improvement. This role also supports Proton Software by providing accurate data, application insights, and testing results that inform internal and external stakeholders.
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of Plant City, FL.
Pay and Benefits
The pay range for this position is $24.00 - $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 Plant City,FL.
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.

R&D Chemist

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
The Laboratory Associate is primarily responsible for the support and upkeep of R&amp;D laboratories based in Austin, TX. The scope of support includes inventory management, supply ordering and tracking, Clinical Sample ordering and tracking, vendor communication, laboratory safety checks and audits, corrective actions, and communication with various R&amp;D teams as needed. The Laboratory Associate is also responsible for assisting equipment support personnel with critical tasks such as equipment installation, calibration, maintenance, repair, and daily laboratory checks as needed.
PRIMARY RESPONSIBILITIES: 
<ul>
<li>Track Laboratory Support Requests using established systems, regularly update requestors and ensure timely request resolutions</li>
<li>Clear and effective communication with R&amp;D teams to ensure requests are adequately resolved</li>
<li>Communicate with vendors to obtain price quotes, equipment demonstrations, equipment deliveries, order updates, tracking information etc</li>
<li>Submit purchase requests using established systems and track purchases through delivery to the requestor</li>
<li>Conduct regular inventory checks of laboratory spaces to ensure adequate supplies are available</li>
<li>Perform regular safety checks of the laboratory spaces and monitor chemical and biohazardous waste streams in accordance with environmental health and safety requirements</li>
<li>Contribute to laboratory safety newsletters</li>
<li>Assist with regular safety audits and perform corrective actions as needed</li>
<li>Handle shipping and receiving of materials, chemicals and equipment in compliance with safety and regulatory standards</li>
<li>Provide feedback on lab processes, suggesting improvements for efficiency, safety, and cost-effectiveness</li>
<li>Assist with instrument installations and qualifications per equipment protocols as needed</li>
<li>Perform routine equipment maintenance procedures as needed</li>
<li>Perform routine laboratory equipment checks as needed</li>
</ul>
QUALIFICATIONS:
<ul>
<li>BS/BA in biomedical engineering, biological sciences or related fields</li>
<li>Industry-related experience, especially in supporting laboratories, preferred</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES: 
<ul>
<li>Excellent communication (verbal and written) and interpersonal skills</li>
<li>Excellent attention to detail, organization, and accuracy</li>
<li>Excellent adaptability in a fast-changing environment</li>
<li>Self-motivated</li>
<li>Ability to work independently and as part of a team</li>
<li>Maintain a high level of professionalism and responsibility</li>
<li>Comply with company policies</li>
</ul>
PREFERRED SKILLS: 
<ul>
<li>Inventory management skills</li>
<li>Customer Service skills</li>
<li>Experience working in BSLI and BSLII laboratories as well as familiarity with Biosafety requirements and guidelines as established by applicable regulatory bodies such as OSHA and CDC</li>
<li>Familiar with DNA Isolation and Purification, PCR, Cell Culture, Next Generation Sequencing, etc</li>
<li>Familiar with LIMS</li>
</ul>
PHYSICAL DEMANDS &amp; WORK ENVIRONMENT: 
<ul>
<li>Duties are typically performed in an office and/or laboratory setting</li>
<li>This position requires the ability to use a computer keyboard, communicate over the telephone and read printed material</li>
<li>Ability to lift 40lbs</li>
<li>This position requires the ability to squat, bend, and reach</li>
<li>Duties may occasionally require working outside normal working hours (evenings and weekends)</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.Austin, TX$19.52—$25 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Lab Associate

<h3>Job Description</h3>
Job DescriptionRelocation + Sign on Bonus Offered + ESOP Profit Sharing + You Voice Matters + Employee Owned (share in the success!) + Opportunity to Build in an Established and Well Known Brand This Jobot Job is hosted by: Chelsea Piekarski Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $130,000 - $200,000 per year 
A bit about us:
 We are a 100% employee-owned engineering and consulting firm with a 60+ year history of delivering geotechnical, environmental, and materials testing expertise across the U.S. Our teams partner with clients in municipal, K-12, commercial, and institutional markets to design practical, reliable solutions that strengthen infrastructure and communities. What makes us unique is our ownership model: every employee is also an owner, sharing directly in the company’s success. That mindset drives collaboration, accountability, and long-term commitment. We’re in active growth mode, expanding our footprint and building key markets with an entrepreneurial approach backed by decades of technical excellence. Joining us means stepping into a culture where your expertise is valued, your career path is supported, and you have a true voice in shaping the company’s future. 
Why join us?
 
<ul>
<li>Last year ESOP paid 11% (of base + bonus) TRULY UNMATCHED COMPENSATION POTENTIAL</li>
<li>Opportunity to build and shape a growing market — not just maintain work</li>
<li>Direct impact on strategy and growth trajectory ($2M market scaling to $5M+)</li>
<li>Leadership pathway with mentoring and succession built into role design</li>
<li>Highly supportive VP leadership — straightforward, invested in people</li>
<li>Employee-owned company with strong benefits, PTO, 401(k), and ESOP</li>
</ul>
 
Job Details
 We are seeking a Geotechnical Manager to lead and grow our San Antonio practice. This is a mission-critical leadership role with the opportunity to build a team, deepen client relationships, and expand the business from a $2M market toward $5M+. Responsibilities 
<ul>
<li>Provide strategic leadership for geotechnical and construction materials testing projects, ensuring technical excellence and client satisfaction</li>
<li>Build and maintain relationships across municipal, K-12, commercial, and institutional markets; actively pursue new business opportunities</li>
<li>Lead, mentor, and develop junior engineers, cultivating the next generation of technical leaders</li>
<li>Oversee project scoping, budgeting, proposals, and delivery; ensure projects are delivered on time and within budget</li>
<li>Represent the San Antonio office in the market — serve as the “face” of the practice and a trusted advisor to clients</li>
<li>Partner with senior leadership on long-term growth strategy, team expansion, and succession planning</li>
</ul>
 Requirements 
<ul>
<li>BS in Civil, Geotechnical, or related engineering field; Master’s preferred</li>
<li>PE in Texas required</li>
<li>7+ years of geotechnical engineering experience, including leadership of projects and teams</li>
<li>Minimum of 3 years’ experience in the San Antonio market with established client relationships</li>
<li>Strong technical expertise across investigations, lab testing, analysis, recommendations, and reporting</li>
<li>Track record of business development, client management, and market growth</li>
<li>Entrepreneurial drive with ability to build and shape a practice</li>
</ul>
 Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policyCompany DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Geotechnical Manager (relocation offered)

<h3>Job Description</h3>
Job Description
Responsibilities
Artificial Intelligence; Advanced Technology; The very best in patient care. With decades of expertise, we are Radiology Forward. With dynamic cross-training and advancement opportunities in a team-focused environment, the core of our success is its people with the commitment to a better healthcare experience. When you join us as a Research Assistant you will be joining a dedicated team of professionals who deliver quality, value, and access in the 21st century and align all stakeholders- patients, providers, payors, and regulators to achieve the best clinical outcomes.

You Will:
<ul>
<li>Greet, register, collect copays, and verify all patient information. Assist team members by notifying patient arrival. Communicate delays in appointments in a timely fashion and offers rescheduling for timely and effective care of patients;</li>
<li>Obtain proper insurance/authorizations and patient information, collects signatures and ensures accuracy and completion of necessary documentation.</li>
<li>Schedules, reschedules or cancels new or current patients, confirms appointments and notifies staff of changes when necessary.</li>
</ul>

If You Are:
<ul>
<li>Passionate about patient care and exercise sound judgement and an ability to remain professional in all situations.</li>
<li>You demonstrate effective and professional communication, interpersonal skills and respect with patients, guests &amp; colleagues.</li>
<li>You have a structured work-approach, understand complex problems are and you are able to prioritize work in a fast-paced environment.</li>
</ul>

To Ensure Success in This Role, You Must Have:
<ul>
<li>High School Diploma</li>
<li>1 year of previous medical office experience and intermediate computer skills</li>
<li>Medical terminology knowledge and recent medical/radiology office work experience is preferred.</li>
</ul>

We Offer: 
<ul>
<li>Comprehensive Medical, Dental and Vision coverages.</li>
<li>Health Savings Accounts with employer funding.</li>
<li>Wellness dollars</li>
<li>401(k) Employer Match</li>
<li>Free services at any of our imaging centers for you and your immediate family.</li>
</ul>
#corpwest

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology AnalystJob Description
The Microbiology Laboratory Analyst II/III or Senior Analyst will be a vital part of the team, contributing to both general and complex laboratory testing, sample management, and laboratory maintenance. The role involves collaborating with the team to achieve the goals of the Microbiology Services Department, as well as performing both routine and non-routine laboratory duties.
Responsibilities
<ul>
<li>Perform microbiological tests in strict accordance with SOPs, cGMP, cGLP, USP, EP, ISO/IEC, and other applicable regulatory requirements.</li>
<li>Conduct cleaning and disinfection validations, both manual and automated.</li>
<li>Execute Container Closure Integrity Tests (CCIT) and Package Integrity Evaluations.</li>
<li>Perform custom studies and additional testing as per client requests.</li>
<li>Engage in method development, modification, verification, and assist with method validation testing.</li>
<li>Participate in method transfer activities and suitability studies under leadership guidance.</li>
<li>Support Quality Management System investigations for non-conformance or out-of-specification results.</li>
<li>Complete assigned CAPA tasks and change controls.</li>
<li>Maintain laboratory cleanliness, safety, and compliance with cGMP standards.</li>
<li>Conduct regular inventory of reagents, consumables, and materials.</li>
<li>Prepare in-house reagents, stock solutions, media, and microbial suspensions.</li>
<li>Perform biowaste autoclave sterilization cycles and other laboratory housekeeping tasks.</li>
<li>Maintain accurate and complete test records.</li>
<li>Ensure audit readiness at all times.</li>
<li>Deliver results within predetermined turnaround times (TAT) with accuracy.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in aseptic technique.</li>
<li>Experience with cleaning and disinfection validation.</li>
<li>Strong knowledge of GMP and GLP standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS/BA in Biology, Pharmaceutical Sciences, Biotechnology or equivalent, with a preference for a Microbiology degree and 2+ years of relevant experience in microbiology.</li>
<li>Associate degree in a related scientific discipline with 5+ years of experience in a microbiology or related laboratory.</li>
<li>High school diploma with 7+ years of experience in a microbiology or related scientific laboratory.</li>
<li>2+ years of GMP/GLP laboratory or FDA experience is required.</li>
<li>Additional training certifications and self-learning are advantageous.</li>
</ul>
Work Environment
The role requires the ability to lift up to 30 pounds and stand for extensive periods (up to 6 hours). Ergonomics will be utilized to perform repetitive motion tasks with hands and arms. The position involves working in a BSC/LAF and at the lab bench for most of the day (up to 8 hours). Candidates must be able to tolerate the smell of Gram-negative organisms and laboratory disinfectants, and work safely with Biosafety Level II (BSL II) microorganisms and bloodborne pathogens. Proficiency in navigating computer systems is required. Flexibility to work off shift hours and weekends when needed is essential.
Job Type &amp; Location
This is a Contract to Hire position based out of Hercules, CA.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/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 Hercules,CA.
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.

Microbiology Analyst

<h3>Job Description</h3>
Job Description
MOVING YOUR WORLD by focusing on your success:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow.&nbsp; We stand behind our core values: trust, creating value, respect, reliability, and integrity. Ours is a culture that fosters creativity and empowerment, values work/life balance, and gives you the freedom to excel. At FUCHS we aim to nurture your capabilities, ideas and career.
&nbsp;
Salary:
FUCHS offers a competitive salary commensurate with experience in a similar position. The salary range for this position is $22.00 - $27.00 per hour, but actual salary will vary depending upon a new hire’s experience and qualifications as well as internal equity.
&nbsp;
Your responsibilities:
The Compounder works in the production department and is responsible for manufacturing of specialty lubricants. The Compounder must follow product folders to ensure all specification levels are met.&nbsp; The Compounder must adhere to all regulations, policies, and procedures for health, safety, and environmental compliance.
<ul>
<li>Wear mandatory PPE at all times.</li>
</ul>
<ul>
<li>Set up and operate production equipment in accordance with current good manufacturing practices and standard operating procedures</li>
<li>Review folder, calculate requirements, and verify weight of material</li>
<li>Documents production by completing forms, reports, logs, and records of equipment and batches</li>
<li>Locate material and supplies, and verify lots and weights according to the manufacturing order</li>
<li>Prepare and load raw materials into equipment</li>
<li>Must complete daily assigned tasks to meet production volume and schedule</li>
<li>Ensure that end products conform to FUCHS quality standards in accordance with 6S standards</li>
<li>Prepare finished goods for shipment by packing, labeling and loading on dock</li>
<li>Ensure that work environment is maintained clean, safe and organized</li>
<li>Keep equipment operating by following operating instructions; troubleshooting breakdowns;</li>
<li>Updates job knowledge by participating in training opportunities</li>
<li>Utilization of lean manufacturing techniques throughout production</li>
</ul>
<ul>
<li>Maintains material-handling equipment by completing pre-use inspections</li>
<li>Maintains inventory by identifying, labeling, and placing materials and supplies in stock; recording location of inventory</li>
</ul>
<ul>
<li>Responsible for responding to assigned corrective actions per the CAR system</li>
<li>Some heavy lifting (up to 75-lbs.) may be required</li>
<li>Ability to stand for long periods of time</li>
</ul>
&nbsp;
Qualifications we are looking for:
<ul>
<li>High school diploma or equivalent</li>
<li>2+ years working in chemical manufacturing experience</li>
<li>Computer literate required</li>
</ul>
<ul>
<li>Experience in a manufacturing environment</li>
<li>Mechanical ability preferred</li>
<li>Knowledge of material handling equipment</li>
</ul>
&nbsp;
&nbsp;
These are your benefits:
FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow as professionals.&nbsp; In this role, you will have the opportunity to work on projects that will expand your experience and challenge your abilities in the global marketplace.&nbsp; The position also offers an excellent compensation package and a comprehensive suite of benefits.&nbsp;Detailed benefit information can be found at this link: <a href="https://fuchs.com/us/en/benefits" target="_blank">https://fuchs.com/us/en/benefits</a>.
&nbsp;
FUCHS Lubricants Co. is an equal employment opportunity (EEO)/AA employer and strongly supports diversity in the workplace (m/f/d/v).
&nbsp;
Do you have any questions?&nbsp;Rosalinda Almanza (<a href="mailto:rosalinda.almanza@fuchs.com" target="_blank">rosalinda.almanza@fuchs.com</a>) will be more than happy to answer them!

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