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<h3>Job Description</h3>
Job Description
Job Title: Preclinical Research Assistant
Job Description
We are seeking a dedicated Preclinical Research Assistant to support the Study Director and Preclinical Sponsor Representatives in the preparation and conduct of preclinical research studies. These studies aim to develop products or procedures utilizing in-vivo, ex-vivo, and in-vitro models.
Responsibilities
<ul>
<li>Setup study binders as per local procedures.</li>
<li>Develop study-specific data sheets.</li>
<li>Support the study director in addressing QAU audit findings.</li>
<li>Quality check all study-related documentation throughout the study lifecycle.</li>
<li>Document study data as required by protocol and SOP.</li>
<li>Archive study files according to SOP.</li>
<li>Interface with principal investigators and contributing scientists for studies conducted on-site and at contract laboratories.</li>
<li>Support the study director with the preparation of draft study protocols and reports.</li>
<li>Coordinate project/study logistics.</li>
<li>Request study-specific equipment and instrumentation.</li>
<li>Collaborate with study coordinator to request and schedule studies to meet project timelines.</li>
<li>Place animal orders in accordance with protocol and study schedule.</li>
<li>Request ordering of appropriate animal-related drugs to meet protocol and SOP requirements.</li>
<li>Coordinate receipt, submission, and transfer of test and/or control articles.</li>
<li>Support the conduct of histopathology work tasks, including management, transfer, and receipt of histology specimens to an external laboratory.</li>
</ul>
Essential Skills
<ul>
<li>Experience with preclinical animal research, including comfort with large animals such as dogs, sheep, and pigs.</li>
<li>Willingness to learn and strong record-keeping experience.</li>
<li>Proficiency in Microsoft Suite.</li>
<li>Experience in a GLP-regulated environment.</li>
<li>Knowledge of both human and animal anatomy/physiology.</li>
<li>Surgical support experience, comfortable assisting during surgical procedures.</li>
<li>Ability to understand and precisely follow Standard Operating Procedures.</li>
<li>Meticulous attention to detail to identify and correct discrepancies/errors.</li>
<li>Strong background in data collection, data management, and data integrity.</li>
<li>Ability to set priorities and manage time effectively to meet deadlines.</li>
<li>Demonstrated ability to work both independently and as part of a team.</li>
<li>Strong organizational and project management skills.</li>
<li>Safety-minded in workspace organization and conduct.</li>
<li>Accountability for one's own actions and work.</li>
<li>Basic computer proficiency in Outlook, Word, Excel, and PowerPoint.</li>
<li>Excellent verbal, written, and interpersonal communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Biology, Zoology, Animal Science, Engineering, Mathematics, or a closely related STEM field preferred. Equivalent education and experience may be substituted.</li>
<li>Leadership and public speaking skills are preferred but not required.</li>
<li>Surgical Research Specialist (SRS) certification is preferred but not required.</li>
<li>Associates may be asked to bring their own device (BYOD) for this role, unless other arrangements have been made to provide a laptop.</li>
</ul>
Work Environment
This Actalent Services LLC position requires working onsite. 
Job Type &amp; Location
This is a Contract position based out of Cincinnati, OH.
Pay and Benefits
The pay range for this position is $28.00 - $32.00/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 Cincinnati,OH.
Application Deadline
This position is anticipated to close on Jan 17, 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.

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist Job Location: Bellefonte, PA Duration: 6 Months+ (Possible Extension) EXPERIENCE: BS or AS degree and 1-2 yrs experience, or HS Diploma/equivalent and 5+ yrs experience Description: Roles that are responsible for the analysis, development, and operation of quality and risk management systems. Activities include developing standards for quality, documentation and processes as well as continuous improvement and preventive activities. Monitors and documents that procedures, processes, equipment, and systems meet specifications and quality standards. Drives improvement of processes and procedures. A Quality Control Chemist completes a variety of laboratory processes and procedures in the scheduling, evaluation, and review of stock and specialty chromatography products. Responsibilities include, but are not limited to:
<ul>
<li>Reviewing test results for conformance to specifications.</li>
<li>Performing advanced gas and/or liquid chromatography operations according to documented methods to evaluate stock and/or custom chromatography products</li>
<li>Testing all product groups</li>
<li>Selecting and preparing appropriate standards and solutions as required for product evaluation.</li>
<li>Working with manufacturing and/or R&amp;D departments to resolve nonconformances.</li>
<li>Executing experiments, analyzing, and reporting on results.</li>
<li>Recommending process or system improvements when possible and taking a leadership role in addressing improvements.</li>
<li>Reviewing test results for conformance to specifications.</li>
<li>Generating and maintaining records of systems, procedures, and test results.</li>
<li>Entering and evaluating QC data using PC and lab automation systems.</li>
<li>Performing routine maintenance and troubleshooting of chromatographic instrumentation and related equipment.</li>
<li>Assisting analyst with product scheduling and review of test results</li>
<li>Writing/modifying standard operating procedures and related quality documentation</li>
<li>Assisting in training other QC chemists.</li>
</ul>
 #sczr2

Quality Control Chemist

<h3>Job Description</h3>
Job Description
About the Role
 
The Site Assessment and Remediation practice at AKRF delivers value on projects of all scopes and sizes, from individual lots and single-use buildings to large-scale mixed-use developments, corporate and institutional campuses, renewable energy facilities, and infrastructure improvements. We seek an entry level environmental scientist/geologist/engineer to support our growing Site Assessment and Remediation practice in delivering healthier, safer, and more sustainable sites to our clients. This position is based out of our New York City Office. The position entails field-related assignments in the NYC-metro area, which requires local travel. Non-field assignments will be conducted in hybrid.

Job Responsibilities:
<ul>
<li>Phase I Environmental Site Assessments.</li>
<li>Phase II/Subsurface/Remedial Investigations including logging borings and soil, groundwater, soil vapor, and indoor air sampling.</li>
<li>Remediation oversight and community air monitoring related to brownfield redevelopment.</li>
<li>Oversight of subcontractors such as drillers, excavation companies, and remedial contractors. </li>
<li>Data interpretation, report preparation and writing (Work Plans, Phase II and Remedial Investigation Reports, Remedial Plans, etc.).</li>
</ul>
Essential Requirements:
<ul>
<li>Bachelor’s and/or Master’s degree in Environmental, Chemical, or Civil Engineering, Geology, or Environmental Science.</li>
<li>Up to 3 years of experience in the environmental assessment and remediation field. New York City experience is preferred.</li>
<li>OSHA 40-hour HAZWOPER Certification preferred.</li>
<li>A valid driver’s license and willingness to drive in the NYC-metro area.</li>
<li>Excellent communication skills, both written and verbal.</li>
<li>Strong attention to detail with the ability to manage multiple priorities at once.</li>
<li>Familiarity with EQuIS a plus.</li>
</ul>
Compensation
 
Compensation will range from $65k to $72k, and commensurate with experience. 
 
Why Work at AKRF
 
Founded in 1981, AKRF is an award-winning consulting firm with 400 planners, engineers, designers, economists, ecologists, geologists, historians, archaeologists, acousticians, and many other types of professionals guided by the belief that to be original is to be transformative. 
 
Professionals join and remain at AKRF for our corporate-casual environment that values flexible work schedules and locations, and balances award-winning projects with social impact initiatives, charitable giving, and plenty of fun and games. We foster a diverse, equitable, and inclusive environment where employees are respected and valued in honor of their identities; we strive to deliver on this promise every day. Our cookie exchanges and ice cream socials are quite the treat.
 
What We Offer
 
We provide employees with a benefit package that reflects our respect for your workplace contributions, professional goals, and personal priorities. The benefits program at AKRF includes:
<ul>
<li>Medical, Dental, Vision insurance</li>
<li>Vacation and Sick time</li>
<li>Flexible work schedules and locations</li>
<li>401(k) retirement plan with employer matching</li>
<li>Additional Voluntary Life Insurance</li>
<li>Short- and Long-Term Disability</li>
<li>Stock Ownership</li>
<li>Tuition Reimbursement</li>
<li>Training and professional development courses</li>
<li>Opportunities for community outreach through internal networks</li>
<li>Charitable donation match</li>
<li>Transit/parking program</li>
</ul>
Equal Opportunity Company
 
AKRF enforces a policy of equal employment opportunity in our daily operations. The firm has a demonstrated history of hiring, training, developing, promoting and retaining minority group members and women. All employment-related decisions are based solely on relevant criteria and without regard to race, color, religion, age, sex, pregnancy, national origin, age, physical or mental disability, marital status, sexual orientation, sexual identity, caregiver status, military/veteran status or citizenship status, or any other characteristic protected by federal, state, or local law.

Environmental Scientist/Geologist/Engineer

<h3>Job Description</h3>
Job Description
When you join Groundwater &amp; Environmental Services, Inc. (GES), you are not a number – you become the reason for our success. You’ll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world’s leading organizations solve their most complex environmental challenges.
We work hard, and we have a lot of fun while we’re at it. Our core values are centered on doing what’s right – for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. 

Groundwater &amp; Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks an experienced Geologist or Environmental Scientist to support environmental remediation project activities in Southern California. 

<ul>
<li>Under general supervision, provides project management support including client involvement, work plan and proposal preparation, project scheduling and deadline tracking, budget evaluation and analysis, and technical editing and report finalization. </li>
<li>Must be a detail-oriented team player able to multi-task, and possess strong communication, analytical, organizational, problem-solving, planning, technical writing, delegation, mentoring, and time management skills. </li>
<li>Executes, supervises, and documents field aspects of environmental site assessment and remediation activities using standard operating procedures (SOPs). Conducts compliance assessment (e.g., facility response plan compliance), remedial testing, operation, maintenance, and monitoring (OM&amp;M), short-term remedial events (e.g., chemical injection, groundwater and vapor extraction), and other project-support field activities.</li>
<li>Self-performs or directs junior staff in the installation of soil borings, monitoring wells, remediation activities, waste management and disposal, and other field requirements using standard operating procedures (SOPs). Self-performs and may direct junior staff in the performance of engineering design, permitting, OM&amp;M, remedy process optimization, and environmental compliance.</li>
<li>Acts as the primary author for site work plans and proposals for routine scopes of work on low/medium priority projects, and co-author for complex scopes of work including comprehensive site characterizations and remedial actions. Co-authors comprehensive site characterizations and remedial action plans. These reports contain multiple level and interrelated interpretations and conclusions as well as provide recommendations based upon conclusions with focus on conceptual site model development.</li>
<li>May manage various level priority projects by providing technical, regulatory, and financial project support. Technical responsibilities may include monitoring contaminant concentrations, fate and transport analysis, QA/QC of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Provides technical, regulatory, and financial project support for O&amp;M sites. Technical responsibilities may include monitoring contaminant concentrations, site remediation activities, quality of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Knowledgeable of pertinent regulations and their application to the compliance and progression of the projects. </li>
<li>Performs hydrogeological assessments regarding groundwater flows to identify contamination impact and related concerns. </li>
<li>Researches information relating to identifying geological formations and soil delineation studies and prepares reports and geological maps based on the findings.</li>
<li>Participates in the identification of viable remedial solutions consistent with all federal, state, and local regulations </li>
<li>Procures and manages subcontractors and vendors for completion of project tasks (e.g., trenching and excavation, system construction, and electrical work), including supplier bid package development.</li>
</ul>

Skills &amp; Requirements:
<ul>
<li>A Bachelor's degree or higher in geology, environmental science, engineering or related scientific discipline.</li>
<li>4+ years of related experience.</li>
<li>GIT or EIT a plus</li>
<li>Must be detail-oriented, and a team player with good communication, analytical, organization, and time management skills.</li>
</ul>


Our comprehensive benefits include: medical, dental, vision, prescription, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Continuing Education/Training Course Assistance, Bonus Plan, and more.

Groundwater &amp; Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

Mid-Level Environmental Scientist, Geologist, or Engineer

<h3>Job Description</h3>
Job DescriptionHIRING FOR CLEANROOM ASSEMBLERS WITH SOLDERING EXPERIENCE IN FRIDLEY! $22-27/HOUR.Job Description
We are seeking a meticulous and skilled Clean Room Assembler to join our team. In this role, you will be responsible for assembling IPG or pacemakers, catheters, sub-assemblies, and complete catheter builds within a clean room environment. This position involves working under a microscope, handling small components, and ensuring the highest quality in new product development.

Responsibilities
<ul>
<li>Read and interpret work instructions and production drawings.</li>
<li>Assemble IPG or pacemakers, catheters, and sub-assemblies in a clean room environment.</li>
<li>Perform tasks under a microscope and use small hand tools for precision work.</li>
<li>Conduct visual inspections and document work accurately.</li>
<li>Trim parts, solder pacemaker enclosures and wires, and package final products.</li>
<li>Work on various projects, adapting to different assembly needs.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of assembly and/or manufacturing experience in the medical device industry.</li>
<li>1+ year of experience with soldering or welding.</li>
<li>Strong written and verbal communication skills for reading work orders and following instructions.</li>
<li>Ability to document work in travelers, QMS systems, or ERP systems.</li>
<li>High school diploma or GED equivalent.</li>
<li>Hand dexterity and patience for working with small components, both under a microscope and without.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with catheter and guidewire assembly.</li>
<li>Familiarity with clean room protocols and documentation.</li>
</ul>
Why Work Here?
Join a company that offers comprehensive benefits including group health, dental, and vision insurance, as well as a Health Savings Account and Flexible Spending Accounts. Enjoy company-paid benefits such as Employee Life Insurance and Long Term Disability. Take advantage of voluntary benefits and a robust 401(k) plan with a Safe Harbor Contribution. Benefit from accrued Paid Time Off, Floating Holidays, and Paid Parental Leave. Work in a supportive environment with a focus on employee well-being and work-life balance.

Work Environment
You will work in a state-of-the-art, clean facility with a great break room. The company fosters a collaborative atmosphere through various events, lunches, and gatherings. The position is based in a clean room, primarily involving work under a microscope. The work schedule is Monday through Thursday from 5 am to 3:30 pm on the first shift.
Job Type &amp; Location
This is a Permanent position based out of Minneapolis, MN.
Pay and Benefits
The pay range for this position is $22.00 - $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 Minneapolis,MN.
Application Deadline
This position is anticipated to close on Jan 16, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler - IMMEDIATE HIRING

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
As a Quality Control Chemist, you will be responsible for performing routine analysis of raw materials, in-process, and finished products. This includes conducting tests such as titrations, FTIR, GC, HPLC, Color, and using a viscometer. Your role involves performing calculations for batch tests in a lab environment using instrumentation and physical test methods. You will follow setup procedures and work instructions for laboratory equipment while adhering to customer and company quality standards. Safety is paramount, so you must follow all safety rules and regulations, including the use of appropriate PPE at all times.
Responsibilities
<ul>
<li>Conduct routine analysis of raw materials, in-process, and finished products.</li>
<li>Perform tests including titrations, FTIR, GC, HPLC, Color, and viscometer.</li>
<li>Carry out calculations for batch tests using lab instrumentation and physical test methods.</li>
<li>Set up and operate laboratory equipment according to established procedures.</li>
<li>Ensure compliance with customer and company quality standards.</li>
<li>Follow all safety rules and regulations, using appropriate PPE at all times.</li>
</ul>
Essential Skills
<ul>
<li>Minimum 1 year of industry experience in analytical testing, troubleshooting, and quality assurance.</li>
<li>Proficiency in gas chromatography (GC), high-performance liquid chromatography (HPLC), and FTIR.</li>
<li>Strong understanding of quality control processes in chemical manufacturing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Chemistry or other Sciences preferred; AS in Chemistry is acceptable.</li>
<li>Experience in chemical manufacturing is preferred.</li>
<li>Familiarity with basic laboratory equipment (GC/LC/FTIR) and techniques (titration, liquid-liquid partition).</li>
</ul>
Work Environment
You will work independently on the night shifts in the lab, handling chemical products. The lab is equipped with newer equipment to assist with testing. The work schedule is a 12-hour night shift, following a 2/2/3 non-rotating pattern in a 7-day x 24-hour chemical operation, from 7PM to 7AM. The role offers opportunities for cross-training and education in certifications, contributing to employee development and career growth.
Job Type &amp; Location
This is a Contract to Hire position based out of Greensboro, NC.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 Greensboro,NC.
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.

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist Operator LeadJob Description
The Chemist Operator Lead will be responsible for producing Active Pharmaceutical Ingredients (APIs) using chemical reactors. This role involves following specific batch records to ensure consistent product quality.
Responsibilities
<ul>
<li>Handle various unit operations, including reactions, filtration, distillation, drying, and milling, on raw materials and during various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document per batch sheet instructions to produce products in compliance with all cGMP guidelines.</li>
<li>Set up equipment such as vessels, tanks, centrifuges, and dryers for proper processing.</li>
<li>Clean and verify equipment and vessels to maintain operational integrity.</li>
<li>Record observations of operating conditions to ensure optimal performance.</li>
<li>Drive and operate a forklift truck safely and efficiently.</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>Proficiency in operating chemical reactors and handling various unit operations.</li>
<li>Strong understanding of cGMP guidelines and ability to follow batch records.</li>
<li>Experience in setting up and cleaning chemical processing equipment.</li>
<li>Ability to record and analyze operating conditions effectively.</li>
<li>Forklift operation skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>AS Degree in Sciences, with a preference for Chemical Technology or Chemistry.</li>
<li>5-7 years of experience in pharmaceutical chemical operating.</li>
<li>Knowledge of analytical chemistry and experience with GC (Gas Chromatography).</li>
</ul>
Work Environment
The role is based in a clean laboratory and production environment. The work schedule follows a 2-2-3 shift pattern from 6:00 a.m. to 6:30 p.m., including work on alternate weekends. The position offers opportunities for growth into leadership roles as the innovation hub expands.
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 $32.00 - $37.00/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 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 Lead

<h3>Job Description</h3>
Job DescriptionJob Title: R&amp;D Formulation Scientist - Soft GelJob Description
We are looking for an experienced R&amp;D Formulation Scientist specializing in soft gels to join our innovative team. You will partner closely with sales and customers to support product requirements and technical needs, develop formulations for various products, and collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency.
Responsibilities
<ul>
<li>Develop formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations.</li>
<li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li>
<li>Assist with analytical testing and quality assessments.</li>
<li>Perform hands-on work in the Product Development laboratory.</li>
<li>Utilize analytical instrumentation including GC, HPLC, and ICP-MS.</li>
<li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li>
<li>Work effectively with a predominantly Spanish-speaking laboratory team.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of R&amp;D formulation experience.</li>
<li>Bachelor's Degree in Food Science, Chemistry, or related field.</li>
<li>Expertise in soft gels.</li>
<li>Experience in the nutraceutical industry.</li>
<li>Skilled in HPLC, GC, and ICP.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bilingual skills are a plus.</li>
<li>Experience with raw materials and quality control.</li>
<li>Knowledge of analytical chemistry and fish oils.</li>
</ul>
Work Environment
The position will report to the Quality Director until a future R&amp;D Director is hired. Initially, there will be only two R&amp;D formulators on the team until the acquisition expands the team. The work schedule is Monday to Friday, 8 AM to 5 PM, 100% on-site. The dress code is business casual.
Job Type &amp; Location
This is a Permanent position based out of Clifton, NJ.
Pay and Benefits
The pay range for this position is $75000.00 - $90000.00/yr.
401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&amp;D department!
Workplace Type
This is a fully onsite position in Clifton,NJ.
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.

R&d Formulation Scientist - Soft Gel

<h3>Job Description</h3>
Job DescriptionProject Scientist/Geologist - PG Project Scientist / Geologist
Location: Walnut Creek, CA&nbsp;
We are an employee-owned Environmental Health, Safety, and Sustainability consulting firm with offices throughout California. Following a recent acquisition, our geographic reach and technical capabilities have expanded significantly, allowing us to serve a diverse portfolio of high-profile institutional clients, including some of the largest companies in the world. Our services include environmental engineering and remediation, vapor intrusion mitigation, compliance and emissions management, industrial hygiene, safety training, and litigation support.
&nbsp;Position Overview
We are seeking a full-time Project Scientist or Geologist to support and manage high-profile environmental projects from initial investigation through site closure. This includes subsurface soil, soil gas, groundwater, and vapor intrusion assessments, as well as remediation planning and execution.
The ideal candidate is entrepreneurial, thrives in a fast-paced consulting environment, and is passionate about mentoring a diverse team. Strong communication skills and a proven track record in business development are essential.
&nbsp;Required Qualifications
<ul>
<li>BS in Geology, Hydrogeology, Environmental Science, Toxicology, or related discipline</li>
<li>Minimum 7 years of environmental consulting experience</li>
<li>California Professional Geologist (PG) license preferred or ability to obtain</li>
<li>40-Hour HAZWOPER Certification</li>
<li>Experience with DTSC, RWQCB, and Bay Area regulatory programs</li>
<li>Demonstrated success in project management and staff mentorship</li>
<li>Exposure to business development activities</li>
</ul>
&nbsp;Desired Skills
<ul>
<li>Expertise in environmental characterization, vapor intrusion, remedial action plans, and remediation oversight</li>
<li>Familiarity with construction management and blueprint interpretation</li>
<li>Proficiency in MS Office (Word, Excel, Outlook)</li>
<li>Experience with CADD, Rockworks, gINT, Revit, or similar software</li>
<li>Strong organizational and time management skills</li>
<li>Self-starter with responsive communication style</li>
<li>Willingness to travel within California (limited)</li>
</ul>
&nbsp;Why Join Us?
<ul>
<li>Be part of a rapidly growing team with high-impact projects</li>
<li>Collaborate with industry leaders in environmental science</li>
<li>Enjoy a supportive, employee-owned culture</li>
<li>Competitive compensation and performance-based incentives</li>
</ul>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. CyberCoders will consider for Employment in the City of Los Angeles qualified Applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring (Ban the Box) Ordinance.This job was first posted by CyberCoders on 11/06/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at <a href="mailto:Benefits@CyberCoders.com" target="_blank">Benefits@CyberCoders.com</a> to make arrangements.

Project Scientist/Geologist - PG

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
The microbiologist will document experiments in accordance with company policies, procedures, and protocols, demonstrating a working knowledge of microbiology tasks and the application of scientific principles and technologies. The role requires collaboration with a team to develop and implement microbiological test procedures that support drug substances, drug products, excipients, compounded sterile preparations, and microbiological sample testing.
Responsibilities
<ul>
<li>Prepare solutions, samples, and standards for use in procedures and manage materials to prevent waste or loss.</li>
<li>Meet requirements for annual gowning and aseptic handling certifications.</li>
<li>Conduct sterility and endotoxin testing in the cleanroom.</li>
<li>Perform environmental monitoring as needed.</li>
<li>Maintain proper waste disposal handling and record keeping.</li>
<li>Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.</li>
<li>Analyze and interpret the outcome of experiments correctly.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Science/Biology.</li>
<li>1+ year of cGMP laboratory or cleanroom experience.</li>
<li>Proficiency in aseptic technique and microbiology.</li>
<li>Experience in cleanroom procedures and environmental monitoring.</li>
<li>Knowledge of sterility and endotoxin testing.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Vernon Hills, IL.
Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Vernon Hills,IL.
Application Deadline
This position is anticipated to close on Jan 14, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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