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<h3>Job Description</h3>
Job Description
We are seeking an experienced and results-driven Sales Representative to join our team in the specialized field of chemical transportation and logistics. The ideal candidate will have 3–5 years of proven success in selling transportation services to clients in the chemical industry, with a strong understanding of hazmat regulations, bulk freight logistics, and customer relationship management.
Key Responsibilities:
<ul>
<li>
Identify and pursue new business opportunities within the chemical manufacturing and distribution sectors.
</li>
<li>
Build and maintain strong, long-term relationships with key decision-makers and logistics managers.
</li>
<li>
Present and sell trucking and freight solutions tailored to hazardous materials and chemical transport.
</li>
<li>
Negotiate contracts and pricing while ensuring compliance with regulatory standards (e.g., DOT, EPA, OSHA).
</li>
<li>
Collaborate with operations and dispatch teams to ensure customer satisfaction and service delivery.
</li>
<li>
Maintain an up-to-date CRM with client interactions, leads, and pipeline progress.
</li>
<li>
Attend trade shows, industry conferences, and client meetings as needed.
</li>
</ul>
Requirements:
<ul>
<li>
3–5 years of experience in sales, specifically within the chemical industry or hazmat transportation sector.
</li>
<li>
Strong knowledge of DOT regulations, hazmat classifications, and bulk liquid or dry freight logistics.
</li>
<li>
Proven ability to meet or exceed sales targets in a competitive B2B environment.
</li>
<li>
Excellent communication, negotiation, and presentation skills.
</li>
<li>
Proficiency with CRM systems and Microsoft Office Suite.
</li>
<li>
Self-motivated with strong organizational and time-management skills.
</li>
<li>
Willingness to travel regionally as required.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Bachelor’s degree in Business, Logistics, Chemistry, or related field.
</li>
<li>
Existing network of chemical industry clients or logistics contacts.
</li>
<li>
Experience with tanker, ISO tank, or intermodal transportation services.
</li>
</ul>

Sales Representative (Chemical Industry)

<h3>Job Description</h3>
Job Description
Ergon's Paragon Technical Services is seeking an experienced Analytical Chemist to lead laboratory-based research and development efforts focused on bituminous materials used in the asphalt paving industry, in our Hattiesburg, MS, location. This role requires expertise in High-Performance Liquid Chromatography (HPLC) and Gel Permeation Chromatography/Size Exclusion Chromatography (GPC/SEC) to analyze the properties of asphalts, polymers, and process oils. The ideal candidate will thrive in a dynamic, research-driven environment and contribute to innovative product development.
Education and Experience Requirements:
<ul>
<li>Bachelor's degree in chemistry required (Graduate degree preferred).</li>
<li>Minimum 3 years of experience in analytical chemistry (5+ years preferred).</li>
<li>Proven expertise in HPLC and/or GPC/SEC instruments; experience with Agilent equipment is a plus.</li>
<li>Strong ability to work independently in a deadline-driven research setting.</li>
<li>Effective time management and organizational skills.</li>
<li>Commitment to data accuracy, integrity, and laboratory excellence</li>
</ul>
Duties and Responsibilities:
<ul>
<li>Conduct and oversee HPLC and GPC/SEC testing for bituminous materials.</li>
<li>Develop a deep understanding of the SAR-AD instrument and its applications.</li>
<li>Ensure laboratory data integrity, verifying accuracy and reevaluating questionable results.</li>
<li>Maintain meticulous lab records and documentation that align with industry standards.</li>
<li>Stay current with relevant testing requirements and methodologies (ASTM, AASHTO, etc.).</li>
<li>Perform routine calibration and maintenance of laboratory equipment.</li>
<li>Organize lab space effectively, ensuring cleanliness and proper inventory management.</li>
<li>Collaborate with the Technical Director and Research Team, providing updates on ongoing projects.</li>
<li>Comply with Environmental, Health &amp; Safety (EHS) regulations and company policies.</li>
<li>Support broader research initiatives through analysis, reporting, and teamwork.</li>
<li>Optional: Contribute to peer-reviewed publications based on research findings.</li>
</ul>
Why Ergon Inc.? 
At Ergon, we are a relationship-driven, family-owned company that values each employee's growth and contributions. Headquartered in Flowood, Mississippi, we take pride in maintaining a close-knit, small-company atmosphere while offering exceptional career opportunities. Our comprehensive benefits package includes:
<ul>
<li>Competitive pay</li>
<li>401(k) matching &amp; profit sharing</li>
<li>Health, Dental, Vision, and Life Insurance</li>
<li>Short- and Long-Term Disability Plans</li>
<li>Additional voluntary benefits</li>
<li>Paid holidays, vacation, and sick leave</li>
<li>Tuition assistance</li>
</ul>
At Ergon Inc., we live by our core values: 
<ul>
<li>Empowered Service: Together, we're committed to delivering unparalleled service. We do what's right, provide solutions, and foster stronger relationships with our teams and customers. Employee safety is our top priority and the first consideration in all aspects of our service. That's empowered service.</li>
<li>Selfless Leadership: We lead with compassion and put those around us before ourselves. We don't say we're experts; we demonstrate it through technical expertise, category innovation, and care for what we do. We call this selfless leadership.</li>
<li>Purposeful Growth: We believe employee and company growth go hand in hand. We build our legacy together to ensure future success through purposeful growth. The company has continually reinvested tremendously back into the business, not just growing for the sake of growing but growing carefully and strategically.</li>
<li>Respectful Relationships: Together, we foster a culture of respect, acceptance, and diversity of ideas and people. Our differences make us stronger. We're united by our shared values, constantly forging respectful relationships.</li>
</ul>
Come and join the Ergon team!
Must be able to pass a pre-employment drug screen and background check. A clean MVR is required.
We are an EEO/AAP employer.
Job Role: Analytical Chemist
Location: Hattiesburg, MS
 Job Posted by ApplicantPro

Analytical Chemist

<h3>Job Description</h3>
Job Description
Job Title: Civil/Geotechnical Engineer
***Work Location: Atlanta, GA ***
Salary: Based on experience and will be discussed with manager in interview
Duties/Responsibilities:
<ul>
<li>Civil/site engineering and design for government buildings, test stands, recreational facilities, roadways, parking lots, laboratory facilities, etc.</li>
<li>Perform boring layout for utility clearance, supervising drill rigs, classifying soils, logging borings</li>
<li>Perform and supervise field exploration, including SPT sampling, rock coring, pile testing</li>
<li>Assist in developing a variety of layouts, drawings, and designs</li>
<li>Work under supervision of a project manager or senior-level team member</li>
<li>Working knowledge of AutoCAD and Slope Stability Analysis</li>
</ul>
Education/Experience:
<ul>
<li>Bachelor's Degree in Civil or Geotechnical Engineering</li>
<li>1-3 years’ experience with Geotechnical engineer knowledge</li>
<li>1-3 years’ experience preparing Geotechnical Engineering reports, including site investigations, soil analysis, and foundation recommendations</li>
<li>Experience and skill in application of CAD software, specifically Civil 3D and associated civil software packages are highly desirable.</li>
<li>At least 1 year of experience working on GDOT projects preferred</li>
<li>Ability and willingness to assist designers, drafters, and other staff members where needed.</li>
<li>Ability to effectively communicate with internal and external partners including clients, sub consultants, and utility companies</li>
<li>Must have a valid driver’s license and be insurable</li>
</ul>
Physical Requirements:
<ul>
<li>Physically mobile in and around construction sites and field assignments</li>
<li>Ability to carry required instruments and equipment</li>
<li>Ability to lift 50 pounds</li>
<li>The worker is subject to variable climate and environmental conditions including but not limited to extreme cold and heat.</li>
</ul>
Benefits:
<ul>
<li>Competitive salary based on experience.</li>
<li>Comprehensive health, dental, and vision insurance.</li>
<li>Retirement savings plan with company match.</li>
<li>Paid time off and holidays.</li>
<li>Professional development and career advancement opportunities.</li>
<li>A supportive and collaborative work environment.</li>
</ul>
Equal Opportunity Employer (U.S.) all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, or any other characteristic protected by law. Accura uses E-Verify in its hiring practices to achieve a lawful workplace. <a href="http://www.dhs.gov/everify" target="_blank">www.dhs.gov/everify</a>
Company DescriptionAccura Engineering specializes in providing engineering, construction inspection and management and environmental services to federal, state and local clients. As a federal contractor, Accura Engineering completed projects for the US Department of Defense including the Army Corps of Engineers, Army, Navy and Air Force for more than 10 years. We also work with other federal agencies including NASA, GSA, Bureau of Prisons, Environmental Protection Agency, among a few. As a state and local contractor, Accura has completed projects for Georgia Department of Transportation as well as numerous cities and counties. 
<h3>Company Description</h3>
Accura Engineering specializes in providing engineering, construction inspection and management and environmental services to federal, state and local clients. \r\n\r\nAs a federal contractor, Accura Engineering completed projects for the US Department of Defense including the Army Corps of Engineers, Army, Navy and Air Force for more than 10 years. We also work with other federal agencies including NASA, GSA, Bureau of Prisons, Environmental Protection Agency, among a few. As a state and local contractor, Accura has completed projects for Georgia Department of Transportation as well as numerous cities and counties.

Geotechnical Engineer

<h3>Job Description</h3>
Job DescriptionAdvanced Chemical Mixer, $17/hr – Pontiac, MIAre you experienced in chemical mixing and looking for a role where you can fast-track into more advanced liquid mixing operations? Are you ready to grow within a company that specializes in surface chemistry solutions with over 40 years in the industry? If you're eager to take on more responsibility and be part of a growing team, this opportunity is for you!Qualifications:
<ul>
<li>At least 1–2 years of experience mixing chemicals in a manufacturing or industrial setting </li>
<li>Must be able to stand, walk, and crouch throughout the shift </li>
<li>Ability to lift up to 50 lbs </li>
<li>Comfortable with PPE and safety procedures around chemicals </li>
</ul>
Skills:
<ul>
<li>Strong attention to detail and understanding of batch formulations </li>
<li>Ability to follow written and verbal instructions and record accurate data </li>
<li>Basic math and measurement skills required </li>
<li>Familiarity with industrial mixers and the ability to troubleshoot minor equipment issues </li>
<li>Team player with a positive attitude and willingness to learn new processes </li>
</ul>
As an Advanced Chemical Mixer, you'll be responsible for mixing chemical powders and liquids used in surface treatments for metal forming and industrial applications. You’ll begin with dry mix processes and will be fast-tracked to handle liquid mixing responsibilities. Attention to detail, safety, and process accuracy are crucial in this role. This is a great opportunity for someone who is ready to grow into a lead mixing position. Let’s go to work! Apply online today. Workbox Staffing Benefits:
<ul>
<li>Weekly Pay </li>
<li>Hire-in Opportunities </li>
<li>Benefits including Health, Life, and Dental </li>
<li>Veteran Friendly and Equal Opportunity Employer </li>
</ul>

1st shift - Advanced Chemical Mixer

<h3>Job Description</h3>
Job Description
Everytown for Gun Safety, the nation’s largest gun violence prevention advocacy group, is seeking a Research Intern for the Fall 2025 semester. Everytown’s Research Department studies how gun violence occurs in America and identifies the best policies and interventions to prevent and address it. In this role, the Intern will support and contribute to Everytown’s research of various types of gun violence, who it impacts, and how it impacts different communities in diverse ways. Interns are expected to work 15 hours (combination of in-person and remote) per week.
Primary Responsibilities:
<ul>
<li>
Conduct and write literature reviews, and critically analyze new research to support both day-to-day and longer-term research on gun violence prevention in the US;
</li>
<li>
Contribute to drafts of analytically rigorous and credible research materials, including memos, factsheets, and blog posts for a wide range of audiences;
</li>
<li>
Collect, clean, and conduct basic data analysis of gun violence-related datasets;
</li>
<li>
Collaborate on the development and execution of online content;
</li>
<li>
Assist the team in routine research administrative tasks, as and when required;
</li>
<li>
Support data accuracy for EveryShot by reviewing entries, flagging errors, and helping ensure incidents are categorized and displayed correctly;
</li>
<li>
Interact regularly with Everytown staff across all departments to ensure effective coordination and delivery of research program activities.
</li>
</ul>
Note: This position can be hybrid, with some days in the New York City office, or fully remote.
The minimum pay rate for this position is $17.00 per hour.
Dates: Anticipated start date September 22, 2025 through January, 2026
The candidate must meet the following requirements:
<ul>
<li>
Be currently enrolled in an undergraduate program;
</li>
<li>
Demonstrated ability to write well &amp; produce written materials for non-technical audiences;
</li>
<li>
Have exceptional attention to detail;
</li>
<li>
Some previous experience conducting basic data analysis on social science datasets is preferred;
</li>
<li>
Willingness to take initiative on projects;
</li>
<li>
Ability to quickly learn and adapt to a fast-paced environment;
</li>
<li>
Excellent collaboration and communication skills. 
</li>
</ul>
 
Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
About Everytown for Gun Safety Support Fund
Everytown for Gun Safety Support Fund (the “Everytown Support Fund”) is the education, research, and litigation arm of Everytown for Gun Safety, the largest gun violence prevention organization in the country with nearly ten million supporters. The Everytown Support Fund seeks to improve our understanding of the causes of gun violence and help to reduce it by conducting groundbreaking original research, developing evidence-based policies, communicating this knowledge to the American public, and advancing gun safety and gun violence prevention in communities and the courts. Learn more at <a href="http://www.everytownsupportfund.org" target="_blank">www.everytownsupportfund.org</a>.
Everytown for Gun Safety provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws.
Candidates who identify as members of historically underrepresented groups are highly encouraged to apply. 
You can learn about the framework that guides our work by viewing Everytown's Organizations Values

Research Intern - Fall 2025

<h3>Job Description</h3>
Job Description
About the Role
The Acoustics Department at AKRF is seeking a Senior Acoustical Consultant to be based out of New York City, NY or Mt. Laurel, NJ office. This individual will work with the department to provide noise and vibration analysis and review on a broad range of public and private development projects. The potential candidate will have the opportunity to work in an environment of encouragement and collaboration to help AKRF shape the future of the region.
Job Responsibilities:
<ul>
<li>Supervise, manage, and contribute to noise and vibration impact analyses for environmental review of land development, transportation, energy production/distribution, infrastructure, and other project typologies</li>
<li>Supervise and conduct noise and/or vibration modeling (CadnaA, TNM, FTA, HUD, etc.)</li>
<li>Direct and conduct noise and vibration field measurements and acoustical testing</li>
<li>Develop mitigation and noise/vibration control recommendations</li>
<li>Contribute to and review noise and vibration chapters for CEQR, SEQRA, NEPA and other environmental review documents (e.g., EAS, EIS)</li>
<li>Interact with clients, teaming partners, and review agencies</li>
<li>Review site plans/architectural drawings</li>
<li>Assist with HVAC and mechanical noise calculations, vibration isolation recommendations, engineering calculations</li>
<li>Day-to-day project communication and coordination with clients and other design consultants.</li>
</ul>
Essential Requirements:
<ul>
<li>7-10 years’ experience</li>
<li>Bachelor’s degree in acoustics, physics, mechanical, electrical or architectural engineering</li>
<li>Familiarity with NEPA and state-level environmental review</li>
<li>Project management and client interaction experience</li>
<li>Preferred experience with CEQR Technical Manual/Noise (E) designations</li>
<li>Preferred experience with environmental noise and vibration and architectural acoustics</li>
<li>Ability to manage and meet multiple deadlines</li>
<li>Strong written and verbal communication skills</li>
<li>Ability to work both independently and collaboratively</li>
<li>Superior attention to detail and organizational ability</li>
</ul>
Compensation
Compensation will range from $100k to $120k, 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.

Senior Acoustical Consultant

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom Assembler
Job Description
A career in this role is purposeful, committed, and driven by the mission to alleviate pain, restore health, and extend life for millions globally. As a Cleanroom Assembler, you will play a crucial role in the production and packaging of components for medical devices in a clean room manufacturing environment.
Responsibilities
<ul>
<li>Perform a variety of tasks ranging from repetitive to non-repetitive production assembly operations following Good Manufacturing Practices and Standard Operating Procedures.</li>
<li>Work from visual aids, method layouts, diagrams, schematics, process flow sheets, and written or verbal assembly instructions.</li>
<li>Set initial layouts and use a variety of tools to prepare products.</li>
<li>Make continuity checks on work in process and completed.</li>
<li>Conduct quality inspections on the processing line in accordance with quality specifications.</li>
<li>Operate packaging machines.</li>
<li>Box and apply labeling materials.</li>
</ul>
Essential Skills
<ul>
<li>No experience required for the assembler role.</li>
<li>General labor skills.</li>
<li>Ability to work in cleanroom conditions.</li>
<li>Basic assembly and production skills.</li>
<li>Medical assembly knowledge.</li>
<li>Must be able to work 2nd or 3rd shift- no 1st shift available. </li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in a clean room manufacturing environment is a plus.</li>
<li>Experience using measuring devices and hand tools is beneficial.</li>
</ul>
Why Work Here?
Join a nationwide company that offers an air-conditioned and sit-down job environment. Be part of a high-performing team committed to improving healthcare worldwide through meaningful innovations.
Work Environment
Work in a clean room environment requiring personal protective equipment such as eyewear, ear plugs, hair net, and protective gowning. The role offers a 2nd shift schedule, Monday through Friday, from 2:30 PM to 10:30 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Grand Rapids, Michigan.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/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 Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Sep 24, 2025.
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.

Cleanroom Assembler

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Local Delivery Translational Sciences (LDTS) organization at AbbVie, leads the strategy, generation, analyses, interpretations, and reporting of non-clinical data and communications/agreements with global regulatory agencies in the areas of Translational Pharmacology, Non-clinical Pharmacokinetics, Exposure-Response, Immunogenicity, and Biopharmaceutics. &nbsp;The organization supports all phases of non-clinical development, supporting all new molecular entities across multiple therapeutic areas.
The organization is responsible for defining the relationship between drug exposure (e.g., concentrations in blood/ local tissue) and efficacy and safety measures in non-clinical models to select the optimal dose, dosing intervals, and biomarkers for FIH studies.
The organization provides critical support for conducting technical due diligence of new business opportunities (both in-licensing and out-licensing) by assessing probability of success for achieving the Target Product Profile (TPP). It also contributes to responses to defend our intellectual properties and extension of patent protection, provides critical support for life-cycle management of marketed products, responds to questions from post-marketing safety, legal, pharmaceutical manufacturing and regulatory for marketed products world-wide, and publication of scientific information in patents and manuscripts.
The LDTS group at AbbVie, is seeking a Principal Research Scientist – Modeling and Simulation.&nbsp; As a member of multidisciplinary teams, this individual will contribute both Pharmacokinetic and Modeling and Simulation (M&amp;S) expertise to lead efforts to build in silico drug models that describe the relationship(s) between exposure (drug, antibody, biomarker) and response (pharmacodynamic, toxicodynamic) for both desired and undesired effects.&nbsp; These models will support formulation development as well as early-stage clinical development activities utilizing various sources of data from both nonclinical models and humans.&nbsp; This individual should be comfortable with exploratory analyses and non-conventional modeling beyond systemic drug development including ophthalmology, neurotoxin, and aesthetics/dermatology.&nbsp; This scientist should be proactive, inquisitive, a self-starter who is eager to learn and thrives in a fast pace and independent environment, with a desire to interact as a modeling and simulation expert with matrix project teams.
Specific responsibilities include:
<ul>
<li>Apply PK and PK/PD modeling/simulation to guide the design and execution of in vivo preclinical animal experiments and/or early-stage clinical trials.</li>
<li>Identify opportunities to apply and develop modeling and simulation strategies across the R&amp;D portfolio, with a focus on ophthalmology, neurotoxin, and aesthetics/dermatology.</li>
<li>Integrate M&amp;S knowledge to contribute to optimizing translational sciences strategies.</li>
<li>Analysis of PK/PD data, both clinical and nonclinical, through the use of sophisticated mathematical and statistical modeling and simulation tools to support dose selection, study design and proof-of-concept.</li>
<li>Identify and monitor vendors and consultants or engage internal resources as appropriate to meet project deliverables.</li>
<li>In collaboration with other stakeholders, conduct and integrate data analyses and summarize modeling outcomes to support IND, CTA, IMPD, NDA, and BLA filing and regulatory correspondences.&nbsp;</li>
<li>Exploratory analyses and non-conventional modeling beyond systemic drug development with a focus on locally-administered/acting products.</li>
<li>Maintain awareness of current technologies in PK/PD and PBPK modeling.</li>
<li>Develop close and effective partnerships with other nonclinical and clinical pharmacology/PKPD and biomarker scientists, safety scientists, research scientists, clinicians and project teams.</li>
<li>Design and provide scientific oversight of preclinical PK/TK studies</li>
<li>At project level, establish and maintain effective collaborations with key stakeholders to facilitate data integration for biomarker selection, candidate nomination/selection, and human dose prediction</li>
</ul>
Qualifications 
<ul>
<li>BS with typically&nbsp;14+ years of experience OR MS with typically 12+ years of experience OR&nbsp;PhD with typically 6+ years of experience in Pharmaceutical Sciences, Quantitative Pharmacology, Biomedical/Chemical Engineering, Pharmacometrics or related field,</li>
<li>&nbsp;2+ years of experience in PK/PD modeling &amp; simulation, quantitative pharmacology, and/or applied population PK in the pharmaceutical industry.&nbsp;&nbsp;</li>
<li>Academic and/or industry experience in either physiologically-based pharmacokinetic (PBPK) modeling or population PK/PKPD modeling.</li>
<li>Strong knowledge of biology (mechanism of action)/pharmacology, toxicology, clinical immunology, protein sciences, statistics, and pharmaceutical development</li>
<li>Ability to learn new areas of biological sciences and build on solid foundation of quantitative skills to develop models.</li>
<li>Data manipulation and programming skills and ideally with the use of programs such as SAS, R, S+ or similar programs.</li>
<li>Experience using Phoenix WNL,GastroPlus, and SimCyp</li>
<li>Scientific publications in area of specialization.</li>
</ul>
<ul>
<li>Effective written and verbal communication skills.</li>
<li>Strong ability to collaborate with others.</li>
<li>Ability to keep up-to-date with and propose the implementation of scientific and technological developments in the area of modeling.</li>
<li>The successful candidate is required to have ability to work within a diverse workforce.</li>
</ul>
Preferred Experience
<ul>
<li>Experience with biologics including gene therapy</li>
<li>Experience with general programming and data analysis tools/languages such as R, Matlab, Berkeley Madonna, ADAPT, etc.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
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This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
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<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
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</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Principal Research Scientist - Modeling and Simulation

<h3>Job Description</h3>
Job DescriptionJob Title: Director of Research and DevelopmentJob Description
Seeking a highly skilled and visionary R&amp;D Director to lead formulation development and production scale-up efforts. This role involves creating innovative, high-quality cosmetic, hand, and body care formulations, ensuring regulatory compliance, and taking products from lab prototypes to mass production.
Responsibilities
<ul>
<li>Lead formulation development and innovation for cosmetics, hand, and body care products.</li>
<li>Oversee scale-up from lab prototypes to mass production while maintaining quality and consistency.</li>
<li>Ensure compliance with regulatory and safety standards (FDA, EU, GMP).</li>
<li>Manage and mentor a team of chemists and technicians.</li>
<li>Collaborate with marketing, production, QA, supply chain, and external partners.</li>
<li>Stay current with market trends, emerging ingredients, and technologies.</li>
<li>Manage R&amp;D projects, budgets, and timelines from concept to commercialization.</li>
</ul>
 Essential Skills
<ul>
<li>Proficiency in Chemistry and Formulation.</li>
<li>Experience in R&amp;D and people management.</li>
<li>Proven track record in scaling products from lab to mass production.</li>
<li>Strong understanding of cosmetic chemistry and regulatory compliance.</li>
<li>8–10 years of R&amp;D experience, with at least 5 years in a leadership role within cosmetics or personal care.</li>
</ul>
 Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Chemistry, Chemical Engineering, Cosmetic Science, or related field (Master’s/Ph.D. preferred).</li>
<li>Proven experience in developing unique formulations.</li>
<li>Exceptional leadership, project management, and collaboration skills.</li>
</ul>
 Work Environment
Onsite manufacturing environment, full-time, Monday-Friday. Enjoy comprehensive benefits including health, dental, and vision insurance, life insurance, a 401(k) plan, and paid time off.
Job Type &amp; Location
This is a Permanent position based out of Clearwater, Florida.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
Health, dental, and vision insurance
Life insurance
401(k)
Paid time off
Workplace Type
This is a fully onsite position in Clearwater,FL.
Application Deadline
This position is anticipated to close on Sep 24, 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.

Director Of R&D

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist
Job Description
As a Quality Control Chemist, you will play a crucial role in analyzing raw materials, intermediates, and finished products through routine and non-routine analysis using advanced techniques such as GC and HPLC. You will prepare samples, standards, and reagents, ensuring accuracy and compliance with established procedures and regulatory requirements.
Responsibilities
<ul>
<li>Conduct routine and non-routine analysis of raw materials, intermediates, and finished products using GC and HPLC.</li>
<li>Prepare samples, standards, and reagents according to established procedures.</li>
<li>Interpret and document analytical results accurately and timely.</li>
<li>Maintain and calibrate laboratory instruments and equipment.</li>
<li>Ensure compliance with internal SOPs, GMP, and regulatory requirements.</li>
<li>Assist in method development and validation as needed.</li>
<li>Collaborate with cross-functional teams to support production and R&amp;D.</li>
<li>Maintain a clean and organized laboratory environment.</li>
<li>Participate in investigations of out-of-specification results and deviations.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in laboratory techniques and material handling.</li>
<li>Experience with quality assurance, inventory control, and sampling.</li>
<li>Basic QC testing and quality control skills.</li>
<li>Knowledge of chemistry, UV/Vis, gas chromatography, refractive index, specific gravity, total alcohol, total aldehyde, acid values.</li>
<li>Hands-on experience with GC and HPLC instrumentation and software (e.g., Agilent, Waters).</li>
<li>Strong understanding of analytical chemistry principles and GMP practices.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>AA degree in a science field or BS degree in Chemistry (Preferred).</li>
<li>Strong attention to detail and ability to learn unique processes.</li>
<li>Previous experience in a GMP food and beverage environment is a plus.</li>
<li>2 years of experience in a QC laboratory setting, preferably in the flavor, food, or pharmaceutical industry.</li>
</ul>
Work Environment
You will work alongside other chemists and flavorists in a lab setting, occasionally visiting the production floor as needed. The environment encourages collaboration and requires a strong understanding of GMP processes. This family-owned company offers a supportive work culture with benefits like raises upon permanent employment, company events such as softball games and holiday parties, and fun activities like Chic-Fil-A Days.
Job Type &amp; Location
This is a Contract to Hire position based out of Abingdon, Maryland.
Pay and Benefits
The pay range for this position is $23.00 - $25.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Abingdon,MD.
Application Deadline
This position is anticipated to close on Sep 23, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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