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<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>Personal Time Off</li>
<li>Expense Stipend ($530 bi-weekly)</li>
</ul>
 Summary/Objective The goals of Archbolds Internship Program are to train students to develop independent research skills and to foster professional interactions between Interns and (a) their supervisor, (b) resident staff and visiting scientists, and (c) other Interns. The internship will be located at Buck Island Ranch, an operational cattle ranch and an experimental field station, with a heavy focus on applied ecology. We are thinking both locally and globally. Archbold Biological Station and its partner site University of Florida Range Cattle Research Center (UF RCREC) are part of the Long-term Agroecosystem Research Network (LTAR <a href="https://ltar.ars.usda.gov" target="_blank">https://ltar.ars.usda.gov</a> ), a network of 19 agroecosystems across the United States that seek to address the grand challenge of maintaining multiple ecosystem services in food production systems. To apply: Please write a cover letter including why you are interested in this position, how it would further your career goals, and when you are available to start. Include a resume that has contact information for 3 references. Preferred start date: Sept/October 2025 Interns will: 
<ul>
<li>Get the opportunity to work on a variety of projects, including wetland restoration and management, precipitation manipulation to simulate the effects of drought and flooding, and water retention on ranchlands.</li>
<li>Experience life on a cattle ranch in a collaborative environment</li>
<li>Assist with our different research projects (see our two documentaries <a href="https://www.youtube.com/watch?v=y6_WhY3aZB0" target="_blank">https://www.youtube.com/watch?v=y6_WhY3aZB0</a>, <a href="https://www.youtube.com/watch?v=rGV_G6dnYHg" target="_blank">https://www.youtube.com/watch?v=rGV_G6dnYHg</a>).</li>
<li>Dedicate remaining time to designing and implementing an independent research project that fits within our research program, with a report and a presentation at the end of internship. </li>
</ul>
Essential Duties and Responsibilities 
<ul>
<li>Average 20 hours per week on assigned duties (depending on needs of Research Program) while being mentored by Research Program Director or someone designated by Research Program Director.</li>
<li>The position requires substantial ecological field work. Fieldwork consists of being out in pastures and wetlands, for collection of forage, soil, manure, or other samples.</li>
<li>Assigned duties may include field and/or laboratory work, data collection and entry, statistical analyses, literature reviews, curation of collections, participating in education-related events, and training other lab members</li>
<li>Present a research Seminar at the end of the internship based on independent research project.</li>
<li>Submit a final copy of the research report to the Research Program Director and the Librarian in both electronic and hard copy at the end of the internship.</li>
</ul>
Additional Duties and Responsibilities 
<ul>
<li>Design and implement an independent research project that fits within the research program, with basic research materials provided.</li>
<li>Gather weekend and holiday weather or other Station/Ranch data collection upon request</li>
<li>Assist with unanticipated Station/Ranch issues, such as helping during adverse weather occurrences, reporting power outages and fires, and providing guidance to visitors requesting assistance during off hours</li>
<li>Assist with reasonable requests from maintenance, kitchen, housekeeping, and facilities staff, etc.</li>
</ul>
Work Environment - The incumbent must be able to work in conditions that include inclement weather, heat and humidity. The incumbent will also work in an office environment, and routinely use standard office equipment such as computers, phones, photocopiers, projectors and fax machines. The incumbent may occasionally work in a laboratory setting with possible exposure to potentially hazardous materials and is required to wear appropriate protective clothing and equipment when handling these materials. Physical Demands - The demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand, walk, or sit for long periods of time; and occasionally required to lift, push and pull items up to 50 pounds; climb stairs; reach stoop, bend, kneel, crouch or crawl; talk or hear. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to focus. Position Type/Expected Hours of Work - An incumbent in this position generally works an average of 20 hours per week, typically but not always Monday through Friday on assigned duties. Early morning, evening and weekend hours may be required with little or no notice. Incumbents will also spend an average of 20 hours per week on an independent research project. Travel - Incumbents may occasionally travel to field sites or to Archbold Biological Station for seminars. Required Education and Experience 
<ul>
<li>Recent graduate with Bachelor of Science or Bachelor of Arts degree required</li>
</ul>
Competencies and Additional Eligibility Qualifications 
<ul>
<li>An understanding of and commitment to the Archbold mission</li>
<li>Ability to work extended periods independently and with initiative under minimal supervision</li>
<li>Ability to perform assigned tasks with accuracy and attention to detail</li>
<li>Familiarity with a scientific discipline and procedures</li>
<li>Possess valid drivers license with good driving record as determined by Archbolds insurance carrier.</li>
</ul>

Agroecology Research Intern - Research Internship in grazing lands

<h3>Job Description</h3>
Job DescriptionBiomechanics Lab Associate

Department: Performance Science
Reports To: Senior Biomechanist
Job Status: Full-time, Exempt

Description:
Built upon our storied legacy, the New York Yankees look to attract the best possible talent not just on the field but in the front office as well. It is our shared responsibility to maintain the first-class reputation associated with the franchise in all aspects of our business. 
The New York Yankees Performance Science department is accepting applications for a Biomechanics Associate. Reporting to the Senior Biomechanist, this individual will serve as a research technician and manage operations in the Performance Science Laboratory. This position is based in Tampa, FL.

Primary Responsibilities:
This individual will assist the Senior Biomechanist in managing the day-day operations in the Performance Science Laboratory and also oversee the processing and delivery of other biomechanical data feeds.

Data Collection and Processing 
<ul>
<li>Coordinate with stakeholders to schedule data collection in the lab </li>
<li>Oversee the preparation, setup, calibration and take-down of all materials and technologies related to biomechanics </li>
<li>Manage data collection procedures and documentation </li>
<li>Meticulously tag and upload biomechanical data feeds according to standard conventions </li>
<li>Oversee timely and rigorous processing of motion capture data </li>
</ul>

Laboratory Maintenance 
<ul>
<li>Ensure that all equipment is fully operational at all times </li>
<li>Regularly interface with vendors to troubleshoot and ensure that software is up to date and running in the most optimal manner</li>
<li>Maintain inventory of lab materials</li>
</ul>

Administrative 
<ul>
<li>Conduct reviews to summarize scientific literature</li>
<li>Remain abreast of technological advancements in biomechanical measurement </li>
<li>Adhere to ethical protocols when working with human subjects and protect privacy of all data </li>
<li>Oversee lab Intern personnel </li>
<li>Develop and maintain documentation to outline data collection and processing methods across all technologies </li>
</ul>

Qualifications and Experience:
<ul>
<li>This individual must possess a Bachelor’s degree (Master’s degree preferred) in kinesiology, biomechanics, engineering (biomedical or mechanical) or a related field</li>
<li>Demonstrated ability and experience with biomechanical data collection and analysis is essential.</li>
<li>Success in this position requires expertise in optical motion capture hardware and software. </li>
</ul>
This is a contract position through October 31st, 2026.
 

This description is intended to describe the type of work being performed by a person assigned to this position. It is not an exhaustive list of all duties and responsibilities required of the employee. The New York Yankees are an Equal Opportunity Employer. The Company is committed to the principles of equal employment opportunity for all employees and applicants for employment.

Biomechanics Lab Associate

<h3>Job Description</h3>
Job DescriptionJob Title: Industrial Chemist Job Description
A full-time opportunity is available for a skilled Industrial Chemist to conduct chemical analysis and support laboratory operations in a pharmaceutical manufacturing environment. The role involves testing raw materials, intermediates, and finished products to ensure compliance with established standards.
Responsibilities
<ul>
<li>Analyze chemical and physical properties of various substances.</li>
<li>Perform routine testing and documentation of pharmaceutical materials.</li>
<li>Prepare solutions, conduct extractions, filtrations, and other lab techniques.</li>
<li>Audit lab data and maintain accurate records.</li>
<li>Interpret results and compile technical reports.</li>
<li>Investigate out-of-specification (OOS) results per standard procedures.</li>
<li>Operate and maintain lab instruments such as HPLC, ICP/MS, UV, and IR.</li>
<li>Develop and execute protocols and standard operating procedures.</li>
<li>Follow safety guidelines and contribute to method development.</li>
<li>Carry out additional tasks as assigned by supervisors.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, IR, FTIR, ICP/MS, and other analytical lab equipment.</li>
<li>Strong understanding of Chemistry, Wet chemistry, Analytical chemistry, and Quality control.</li>
<li>Experience with GCMS.</li>
<li>1–3 years of experience in an industrial or pharmaceutical lab setting.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Chemistry or a related field.</li>
<li>Fluent in English and Spanish.</li>
<li>Familiarity with GMP and GLP standards.</li>
</ul>
Work Environment
The role is based in a clean room laboratory with desk and bench workstations. The working hours are Monday to Friday, from 4:15 pm to 12:45 am. The environment is dynamic and inclusive, offering opportunities for professional growth, collaboration, and continuous learning in a supportive setting.
Job Type &amp; Location
This is a Permanent position based out of Davie, Florida.
Pay and Benefits
The pay range for this position is $62400.00 - $62400.00/yr.
Paid Time Off 401k Holiday Benefits
Workplace Type
This is a fully onsite position in Davie,FL.
Application Deadline
This position is anticipated to close on Sep 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Chemist

<h3>Job Description</h3>
Job DescriptionActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong background in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Associate Scientist

<h3>Job Description</h3>
Job Description
DCS Corp has an immediate opening for a Tech ELINT Analyst supporting the USRL and 513th Electronic Warfare Squadron.
Essential Job Functions:
The Tech ELINT Analyst will work with other members of the Operational Mission Data Analysis Team providing Tech ELINT support for Mission Data analysis and file generation for advanced 5th generation fighter aircraft. The ideal candidate’s responsibilities will include:
Process and evaluate Tech ELINT/Electronic Warfare data to support MD analysis, development, and Lab testing.
Conduct ELINT signals analyst of operational systems derived from radar emissions data.
Develop MD products by utilizing signals analysis tools, techniques, and procedures.
Provide detailed feedback and support by performing ELINT validation and verification of Intelligence products used in mission data file generation, mission data group management, and lab testing.
Required Skills:
Due to the sensitivity of customer related requirements, U.S. Citizenship is required.
Must have a high school diploma plus 16+ years of experience. Will also consider a candidate with an associate degree and at least 10 years' of relevant experience or a candidate with a bachelor’s degree and at least 8 years’ experience. 
Must have current Top Secret/SCI security clearance.
Minimum 5 years’ experience as Technical ELINT and/or Electronic Warfare analyst.
Experience with developing Tech ELINT and/or Electronic Warfare data reports.
Desired Skills:
Course work in engineering, computer/data science, or other related technical/scientific fields.
Experience with instructing and/or providing training.
Experience with Tech ELINT/Electronic Warfare analysis products and software such as Aspen, or Martes as well as software such as MATLAB and Python.
Military ELINT Signal Analyst Program (MESAP) Graduate.
SIGE 3810/4810 Intermediate/Advanced Tech ELINT Analysis course.
Experience working for an Intelligence Production Center.
Familiarity or experience with Artificial Intelligence/Mission Learning.

513 EWS USRL Intel/Tech ELINT Analyst

<h3>Job Description</h3>
Job DescriptionOverview Ansible Government Solutions, LLC (Ansible) is currently recruiting a Therapeutic Medical Physicist to provide onsite services to eligible beneficiaries of the West Palm Beach VA Medical Center located at 7305 N Military Trl, West Palm Beach, FL 33410. &nbsp;If you accept employment with Ansible, you must also acknowledge that any assigned schedule is subject to change at the direction of either Ansible or its customers. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities&nbsp;
<ul>
<li>Shall be available, when necessary, for consultation with the Radiation Oncologist and to provide advice or direction to technical staff when radiation treatments are being planned or when patients are being treated. Where possible, should be present to observe and/or help supervise complicated simulations and/or treatment set-ups. Contractor’s Medical Physicist must be present at the machine during patient setup for SBRT/SRS and IGRT.</li>
<li>Shall specify and monitor method(s) to calculate MUs or treatment times and ensure independent review(s) of such calculations. Any individual having appropriate training and experience as defined in this PWS may perform the initial calculation(s). Independent review of said calculation(s) shall be performed within a specified time period.</li>
<li>Shall develop and maintain a method for the weekly and systematic review of the charts of all patients under radiation treatment. All methods shall be approved by the VA Chief of Staff or designee. Contractor’s Medical Physicist shall perform a final chart review at the end of the course of radiation treatment in order to confirm that the prescribed dose has been delivered, and to document the total doses delivered to critical structures. All charts are subject to quality reviews by the facility’s Chief of staff or designee.</li>
<li>Responsible for data input into the planning system, which should be based upon measured beam data for the radiation beams in question, and for output from the planning system(s).</li>
<li>Responsible for understanding the calculation algorithm and should document those conditions for which the algorithm and measured data are in disagreement by more than 5%. The output of the planning system should be periodically tested by comparisons to direct measurements of the radiation beams. Contractor’s Medical Physicists shall ensure that all users of the treatment planning system receive appropriate training.</li>
<li>Shall provide advice and consultation, to VA and third-party clinical engineers, for the operation, maintenance, and troubleshooting of the VA RADIATION ONCOLOGY’s linear accelerators and CT simulation equipment, all of their relevant accessories and the computerized network interconnectivity; record and verification systems.</li>
</ul>
Qualifications
<ul>
<li>Master's degree in Medical Physics or related field&nbsp;</li>
<li>Board Certification in Medical Physics or Therapeutic Medical Physics by the American Board of Radiology (ABR)&nbsp;</li>
<li>Minimum 2 years of continuous working experience within the last 3 years in therapeutic medical physics&nbsp;</li>
<li>Experience with:&nbsp;
<ul>
<li>Varian Linear Accelerators (TrueBeam with Brain Lab Accessories)&nbsp;</li>
<li>Image Guided Radiation Therapy (IGRT) including Cone Beam CT&nbsp;</li>
<li>Eclipse treatment planning system and ARIA record &amp; verify system&nbsp;</li>
<li>Treatment modalities including 2D/3D Conformal, SRS, SRT, SBRT, and IMRT/VMAT&nbsp;</li>
<li>IMRT QA systems (e.g.,&nbsp;MapCheck)&nbsp;</li>
<li>CT Simulators&nbsp;</li>
<li>Superficial X-ray machines&nbsp;</li>
</ul>
</li>
<li>Experience in a healthcare system with ACR or&nbsp;APEx&nbsp;certification preferred&nbsp;</li>
<li>Strong analytical and problem-solving skills&nbsp;</li>
<li>Excellent communication and teamwork abilities&nbsp;</li>
<li>Proficiency&nbsp;in computer systems and networking related to radiation oncology&nbsp;</li>
<li>Ability to pass a government background check and complete required VA training&nbsp;</li>
</ul>
All candidates must be able to:
<ul>
<li>Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift</li>
<li>Lift up to 50 lbs from floor to waist</li>
<li>Lift up to 20 lbs</li>
<li>Carry up to 40 lbs a reasonable distance</li>
<li>Push/pull with 30 lbs of force</li>
</ul>
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. 
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A0c4FdbU62

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job Description
Chemist
Description
<ul>
<li>Perform routine and non-routine analysis of raw materials, in-process samples, and finished products using HPLC and GC.</li>
<li>Develop, validate, and optimize analytical methods and SOPs for nutraceutical formulations.</li>
<li>Maintain and calibrate laboratory instruments including HPLC, GC, and other analytical equipment.</li>
<li>Ensure compliance with cGMP, FDA, and internal quality standards.</li>
<li>Document and report analytical results accurately and timely using LIMS or equivalent systems.</li>
<li>Support R&amp;D initiatives by providing analytical data for new product development.</li>
<li>Participate in internal audits and assist in regulatory inspections.</li>
<li>Collaborate with cross-functional teams including Quality Assurance, Production, and R&amp;D.</li>
</ul>
Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Chemistry, Biochemistry, or related field.</li>
<li>2+ years of experience in analytical testing using HPLC and GC, preferably in the nutraceutical, pharmaceutical, or food industry.</li>
<li>Strong understanding of cGMP, FDA regulations, and laboratory safety practices.</li>
<li>Proficiency in method development and troubleshooting analytical instrumentation.</li>
<li>Excellent organizational, communication, and documentation skills.</li>
</ul>
Pay and Benefits
The pay range for this position is $25.00 - $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 Orlando,FL.
Application Deadline
This position is anticipated to close on Sep 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job DescriptionpcActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong experience in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $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 Fort Lauderdale,FL.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

HPLC Associate Scientist

<h3>Job Description</h3>
Job DescriptionActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong experience in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Sep 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
We Create Products and Brands That People Trust to Clean, Sanitize, and Protect Their Homes and Pools
When you join KIK Consumer Products, you’re joining a team that cares about the work we do and also about each other. We bring exceptional brands and products to consumers that help them protect the health and wellness of their families and the cleanliness of their homes and pools. We are committed to building a culture of performance driven by accountability, collaboration, and agility that enables timely fact-based decision-making and exceptional execution with unwavering ethics. As one of North America’s largest independent manufacturers of consumer products, KIK helps a large portfolio of brands and retailers bring their products to life.
Your Role at KIK
At KIK, we are seeking a detail-oriented Chemical Processor to join our 1st Shift team (Monday - Friday, 5:00 am - 1:30 pm, with occasional overtime as needed). In this role, you will conduct quality checks, perform changeover processes, operate continuous blending/batching equipment for bleach and ammonia products, and follow strict guidelines for wastewater treatment and waste disposal. Candidates must be able to wear a full-face respirator and Level A suit when necessary, adhere to OSHA Hazard Materials Procedures, complete required paperwork, and comply with safety, GMP, and company policies. Attention to detail, strong mathematical skills, and safe chemical handling are essential. You will work around flammable, combustible, and corrosive chemicals. This position offers an hourly rate of $23.00 and is eligible for a 3% quarterly bonus. Apply Today!
What You’ll Be Doing
<ul>
<li>Perform quality checks, titrate bleach and water hardness testing</li>
<li>Operate continuous blending and batching processes for bleach, household cleaners, and ammonia products</li>
<li>Follow guidelines for wastewater treatment and proper disposal of waste materials</li>
<li>Comply with OSHA Hazard Materials Procedures and safety/GMP guidelines</li>
<li>Complete accurate and timely paperwork (batch tickets)</li>
<li>Follow detailed procedures carefully to complete batching processes</li>
<li>Utilize basic mathematical skills for process monitoring</li>
</ul>
What You’ll Bring
<ul>
<li>High school diploma or GED equivalent</li>
<li>3 or more years of experience in processing or batching manufacturing</li>
<li>Strong verbal and written communication skills</li>
<li>Excellent mathematical aptitude and attention to detail</li>
<li>Participation in the site emergency response team</li>
<li>Basic computer skills</li>
<li>Comfortable working around flammable, combustible, and corrosive chemicals, as well as high noise levels, odors, and fumes</li>
<li>Able to wear a full-face respirator and Level A suit as needed</li>
</ul>
Physical Requirements:
<ul>
<li>Able to lift a minimum of 50 lbs</li>
<li>Ability to climb stairs and ladders</li>
<li>Using hands and arms for moving items</li>
<li>Able to stand for prolonged periods, up to 12 hours</li>
</ul>
What You Will Get
We understand compensation is an important factor as you consider the next step in your career. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.
About KIK
We create the products and brands that people trust to clean, sanitize, and protect their homes, pools, and cars. We are one of North America’s largest independent consumer product manufacturers with 16 North American manufacturing facilities. We also operate globally in Canada, Europe, and Australia. We are known for our portfolio of notable brands including Spic and Span® and Comet® cleaning products, Clorox® Pool&amp;Spa™ (under license), BioGuard®, and Natural Chemistry® pool chemicals. We are also the #1 producer in North America of store-brand (“private label”) bleach and a leading private-label provider of laundry detergent and additives, dishwashing products, general-purpose cleaning, and other home care products.
Our global team of over 2,300 employees drives our capabilities in product development, product formulation, strategic sourcing, manufacturing, packaging design, brand marketing, project management, quality assurance, compliance, distribution, and logistics.
Our organization is constantly evolving and is driven by a set of “One KIK” values – a dedication to following through on commitments in a customer-focused, profit-motivated way; while never compromising on safety, ethics, or integrity.
KIK is an Equal Employment Opportunity / Affirmative Action employer. KIK does not discriminate against qualified applicants or employees based on race, color, age, religion, sex, pregnancy, national origin, ancestry, age, physical or mental disability, veteran status, status in uniformed services, sexual orientation, gender identity, gender expression, marital status, genetic information or any other status protected by law.
KIK is also committed to providing reasonable accommodations for applicants and employees with protected disabilities to the extent required by applicable laws. If you require a reasonable accommodation to participate in the job application, or interview process, or to perform the essential functions of the job, please contact Human Resources immediately.
Privacy Policy: <a href="https://www.kikcorp.com/privacy-policy-applicant" target="_blank">https://www.kikcorp.com/privacy-policy-applicant</a>

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