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<h3>Job Description</h3>
Job Description:
• Plan and execute assigned particle characterization tasks as well as other applicable physical analytical chemistry tasks utilizing standard procedure and technical understanding of various techniques to complete assigned tasks
• Independently generate precise, reliable and reproducible data in a timely manner. Document the experimentation per the regulatory requirements.
• Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.
• Collaborate with various functions (i.e. formulation, analytical, process engineering) to integrate particulate analysis into finished dosage forms and complete projects under aggressive timeline
• Ensures safety requirements are met when performing tasks.
• Ensures timely delivery of high-quality precise data.
• Apply basic computer skills including word processing, spreadsheets, and instrument related systems.
• Presents findings of defined experiments to larger audiences.
 
Requirements/Qualifications
• BS/BA in Chemistry, Material Science, Pharmaceutical Sciences or related field with minimum 5 yrs lab experience (pharmaceutical industry preferred) or master’s degree with minimum 2 yrs lab experience (pharmaceutical industry preferred).
• Experienced in particulate matter characterization and investigation within pharmaceutical, biotechnological, or relevant scientific environments
• Experience utilizing analytical instruments relevant to visible and sub-visible particle characterization such as visual inspection, Laser Obscuration (LO), Dynamic Light Scattering (DLS), Flow imaging, Laser Diffraction (LD), optical microscope, spectroscopy (FTIR/Raman), and Scanning Electron Microscope/Energy Dispersive X-Ray Spectroscopy (SEM/EDX)
• Background working with lyophilized and/or spray dried pharmaceutical products, particularly with peptide, lipid and/or mRNA preferred
• Familiarity with regulatory requirement regarding particulate matter in pharmaceuticals preferred
• Experience utilizing additional materials science techniques such as Thermo Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Dynamic Vapor Sorption (DVS), and PXRD would be a plus
• Strong documentation, problem-solving, communication, and teamwork skills. Able to present experimental findings to larger groups

Particle Science Chemist

<h3>Job Description</h3>
Responsibilities may include the following and other duties may be assigned. 
<ul>
<li>Conducts exploratory research to produce new knowledge and potential products; conceives, organizes, promotes, and executes ideas and plans to increase chemistry's role in and contribution to the discovery and chemical approaches to meet exploratory objectives in product discovery.</li>
<li>Develops research proposals to provide a technically and economically sound basis for developing and evaluating new or improved products, synthetic methods, processes, and analytical and physical testing techniques. </li>
<li>Recommends utilization of the results or changes in the scope of work or termination of projects. </li>
</ul>
Preferred Qualifications:
<ul>
<li>Advanced degree in chemistry or chemical engineering or related technical field;</li>
<li>5+ years of experience in R&amp;D within medical device or pharmaceutical industries;</li>
<li>Experience with new product development and sustaining project support;</li>
<li>Expertise in combination device analytical test method development and validation: HPLC, GC, dissolution, bioassay;</li>
<li>Formulation and testing experience with adhesives, cyanoacrylates preferred;</li>
<li>Expertise with analytical instrumentation, including troubleshooting: dissolution USP Apparatuses, HPLC-DAD, GPC, GC-FID/MS, Karl Fischer, FT-IR and UV-Vis; </li>
<li>Strong problem-solving capabilities;</li>
<li>Solid oral and written communication skills;</li>
<li>Ability to manage and prioritize multiple tasks and lead projects;</li>
<li>Experience in moderate and complex data analyses using statistical techniques;</li>
<li>Experience of using chromatography software: Empower and MassHunter;</li>
<li>Experience using common electronic documentation software (e.g. MAP, Agile or equivalent).</li>
</ul>

Senior Chemist

<h3>Job Description</h3>
Job Description
Apply Here: <a href="https://secure.onehcm.com/ta/ECI.jobs?ShowJob=721612865&amp;TrackId=ZipRecruiter" target="_blank">https://secure.onehcm.com/ta/ECI.jobs?ShowJob=721612865&amp;TrackId=ZipRecr…</a>
Measurement Technician - New Construction Homes &amp; Apartments
Técnico de Medición - Casas y Apartamentos de Nueva Construcción
ENGLISH -&nbsp;Español Abajo
As a measurement technician, you will travel by company car throughout Southern California to new home and apartment construction locations to take on-site wall measurements, verify the measurements to the cabinet drawings, then confirm plumbing locations and soffit heights --- all to prepare for a successful cabinetry installation.&nbsp;&nbsp;
Requirements, Skills, and Responsibilities (not all-inclusive):
<ul>
<li>Valid CA driver's license.</li>
<li>Clean driving record.</li>
<li>Good driving habits.</li>
<li>Safely and confidently drive the streets and freeways of Southern California.</li>
<li>Follow California traffic laws (vehicles are equipped with GPS and driving behavior monitoring).&nbsp;</li>
<li>Regular &amp; Punctual attendance - work is appointment and production based.</li>
<li>Skillfully use and read a tape measure.</li>
<li>Ability to visualize a finished and installed product from production drawings.</li>
<li>Identify and respond to a hazardous job site situation.</li>
<li>Ability to identify a problem, then consider and plan a solution.&nbsp;</li>
<li>Great customer service attitude:&nbsp;professional and&nbsp;courteous with&nbsp;customers, other trades, and&nbsp;coworkers.</li>
<li>Communicate in English as it relates to the job to walk job site&nbsp;with superintendent, builder personnel, or other trades.&nbsp;</li>
<li>Spanish is a plus.</li>
<li>Conscientious and accurate when recording measurements and verifying drawings.&nbsp;</li>
<li>Good numerical ability.&nbsp;</li>
<li>Good listening and communication skills.</li>
<li>Read&nbsp;and interpret common business correspondence.</li>
<li>Basic computer, tablet, and cell skills.</li>
<li>Sit, bend, stoop, crouch, kneel, climb&nbsp;stairs, reach, walk, stand, talk, hear, speak, read, navigate&nbsp;construction site uneven terrain; use fingers, hands, arms.</li>
<li>Moderate noise level.&nbsp;</li>
<li>Work environment temperature is&nbsp;dependent upon current weather conditions.</li>
</ul>
Pay: The wage range is $18 to $21 per hour depending on experience.
Work Schedule:&nbsp;Monday through Friday. Start time varies but may be as early as 5am.&nbsp; Typically scheduled 8 hours per day but may vary up to 12 hours per day depending on work location. Daily and weekend overtime may be a frequent requirement.
Benefits - Health, dental, vision, life, disability insurances; paid time off; paid sick leave; 401k; EAP (employer assistance plan).
Excel Cabinets, Inc. is an Equal Opportunity Employer.&nbsp;Qualified applicants are considered for employment without regard to age, race, color, religion, sex, national origin, sexual orientation, disability, veteran, or other protected status. If you need assistance or an accommodation during the application process because of a disability, it is available upon request by contacting us.
Employment with Excel Cabinets, Inc. is at-will. This means that the terms of employment may be changed with or without notice, with or without cause, including, but not limited to termination, demotion, promotion, transfer, compensation, benefits, work schedule, and duties.
Excel Cabinets, Inc. will consider qualified applicants with a criminal history pursuant to the California Fair Chance Act. You do not need to disclose your criminal history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if Excel Cabinets, Inc. is concerned about a conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report.
ESPAÑOL&nbsp;- English above
Técnico de Medición - Casas y Apartamentos de Nueva Construcción
Como técnico de medición, viajará en automóvil de la empresa por todo el sur de California a nuevas ubicaciones de construcción de casas y apartamentos para tomar medidas de paredes en el sitio, verificar las mediciones según los planos del gabinete, luego confirmar las ubicaciones de plomería y las alturas del sofito --- todo para prepararse para una instalación exitosa de gabinetes.
Requisitos, habilidades y responsabilidades (no todo incluido):
<ul>
<li>Licencia de conducir válida de CA.</li>
<li>Historial de manejo limpio.</li>
<li>Buenos hábitos de conducción.</li>
<li>Conduzca con seguridad y confianza por las calles y autopistas del sur de California.</li>
<li>Siga las leyes de tránsito de California (los vehículos están equipados con GPS y monitoreo del comportamiento de conducción).</li>
<li>Asistencia regular y puntual: el trabajo se basa en citas y producción.</li>
<li>Usa y lee hábilmente una cinta métrica.</li>
<li>Capacidad para visualizar un producto terminado e instalado a partir de planos de producción.</li>
<li>Identificar y responder a una situación peligrosa en el lugar de trabajo.</li>
<li>Capacidad para identificar el problema, luego considerar y planificar la solución.</li>
<li>Gran actitud de servicio al cliente: profesional y cortés con los clientes, otros oficios y compañeros de trabajo.</li>
<li>Comunicarse en inglés; Camine por el lugar de trabajo con el superintendente, el personal de construcción u otros oficios.</li>
<li>El español es un plus.</li>
<li>Concienzudo y preciso al registrar las medidas y verificar los dibujos.</li>
<li>Buena capacidad numérica.</li>
<li>Buenas habilidades de escucha y comunicación.</li>
<li>Leer e interpretar la correspondencia comercial común.</li>
<li>Conocimientos básicos de informática, tableta y celular.</li>
<li>Siéntate, agacharte, agacharse, arrodillarse, subir escaleras, alcanzar, caminar, pararse, hablar, escuchar, hablar, leer, navegar por terrenos irregulares del sitio de construcción; Usa los dedos, las manos, los brazos.</li>
<li>Nivel de ruido moderado.</li>
<li>La temperatura del ambiente de trabajo depende de las condiciones climáticas actuales.</li>
</ul>
Horario de trabajo: de&nbsp;lunes a viernes. La hora de inicio varía, pero puede ser tan pronto como a las 5 a.m.&nbsp; Por lo general, se programa 8 horas por día, pero puede variar hasta 12 horas por día según el lugar de trabajo. Las horas extras diarias y de fin de semana pueden ser un requisito frecuente.
Beneficios: Aseguranzas de salud, dentales, visión, de vida; días pagados libre;&nbsp;licencia por enfermedad con goce de sueldo;&nbsp;401k; EAP (Plan de Asistencia al Empleado)
Excel Cabinets, Inc. es un empleador que ofrece igualdad de oportunidades. Los solicitantes calificados son considerados para el empleo sin distinción de edad, raza, color, religión, sexo, origen nacional, orientación sexual, discapacidad, veterano u otro estado protegido. Si necesita asistencia o una adaptación durante el proceso de solicitud debido a una discapacidad, está disponible a pedido, poniéndose en contacto con nosotros.
Excel Cabinets, Inc. considerará a los solicitantes calificados con antecedentes penales de conformidad con la Ley de Oportunidad Justa de California.&nbsp;No necesita revelar sus antecedentes penales ni participar en una verificación de antecedentes hasta que se le haga una oferta de trabajo condicional. Después de hacer una oferta condicional y realizar una verificación de antecedentes, si Excel Cabinets, Inc. está preocupado por la convicción que está directamente relacionada con el trabajo, se le dará la oportunidad de explicar las circunstancias que rodearon la condena, proporcionar evidencia atenuante o impugnar la exactitud del informe de antecedentes.
El empleo con Excel Cabinets, Inc. es a&nbsp;la&nbsp;voluntad, lo que significa que usted o la Compañía tienen derecho a terminar la relación laboral con o sin previo aviso o causa. El empleador tiene derecho a cambiar los términos y condiciones de empleo, incluidos, entre otros, el despido, la degradación, la promoción, la transferencia, la compensación, los beneficios, el horario de trabajo y los deberes.

Measurement Technician

<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>We are looking for a Cryptanalytic Computer Scientist who can apply their expertise in computer science, mathematics, and engineering to design, develop, and evaluate algorithms and techniques for solving complex cryptographic and security-related problems. The ideal candidate will create and utilize mathematical models and methods to study cryptographic systems, analyze vulnerabilities, and develop solutions to secure sensitive information. Additionally, you will work on high-performance computing projects to optimize cryptographic processes and address security challenges across diverse computing environments.</li>
</ul>
The Level 2 Cryptanalytic Computer Scientist shall possess the following capabilities:
<ul>
<li>Design, develop, and evaluate algorithms and techniques for solving complex cryptographic and security-related problems.</li>
<li>Create and utilize mathematical models and methods to study cryptographic systems, analyze vulnerabilities, and develop solutions to secure sensitive information.</li>
<li>Work on high-performance computing projects to optimize cryptographic processes and address security challenges across diverse computing environments.</li>
<li>Requires someone with a strong networking background to support EDO analytics. An ideal candidate would have python, pyspark, and GM experience.</li>
</ul>
Qualifications:
<ul>
<li>Master's Degree with 3 years of relevant experience</li>
<li>Bachelor's Degree with 5 years of relevant experience</li>
<li>Associates degree with 7 years of relevant experience</li>
<li>Degree must be in Computer Science, Computer Engineering, Electrical Engineering, Mathematics, or a related field with at least one programming and at least 4 upper-level math classes (Calculus and above).</li>
<li>Relevant experience must be in a computer science area (i.e. theoretical or applied), designing/developing/using/evaluating mathematic models, methods, and/or techniques (e.g. algorithm or development) to study issues and solve problems, engineering (electrical or computer), and/or high-performance computing.</li>
</ul>
Must Have an ACTIVE TS/SCI With Full-Scope Poly or be CCA Eligible. 
 Job Posted by ApplicantPro

Cryptanalytic Computer Scientist 2

<h3>Job Description</h3>
Job DescriptionTitle: Quality Control Microbiologist Location: Durham, North CarolinaHire Type: Long-term Contract, OnsitePay Rate: $24.00/hour (W2, with full employee benefits) Overview:Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive aFull Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental &amp; vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan. Job Summary: The QC Microbiology Analyst is responsible for performing microbiological testing to ensure product quality and compliance with FDA and GMP regulations. This role involves testing product and stability samples, maintaining accurate documentation, supporting investigations, and contributing to continuous improvement initiatives in a fast-paced medical device/diagnostics environment. Job Duties:
<ul>
<li>Perform microbiological testing on finished products, stability samples, and special test requests per SOPs.</li>
<li>Prepare and manipulate microbial cultures and stocks using aseptic technique.</li>
<li>Document and review test results for accuracy and compliance with GDP, GLP, GMP, and HSE requirements.</li>
<li>Support audits by maintaining logbooks, calibration records, and laboratory cleanliness.</li>
<li>Enter and manage data in the Laboratory Information Management System (LIMS).</li>
<li>Assist with laboratory investigations and document invalid test results.</li>
<li>Maintain training compliance with departmental processes and procedures.</li>
<li>Follow PPE and safety protocols in all laboratory activities.</li>
<li>Participate in continuous improvement initiatives and maintain 6S standards in lab areas.</li>
<li>Perform additional duties as assigned.</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor’s Degree in Microbiology, Biology, Biochemistry, or related life science preferred.</li>
<li>In lieu of a Bachelor’s Degree, will consider Associate’s Degree with 2+ years of relevant regulated industry experience (GMP preferred).</li>
<li>Prior microbiology lab and sterile/aseptic technique experience preferred.</li>
<li>Strong organizational, multitasking, and communication skills.</li>
<li>Knowledge of microbiological testing, quality principles, and data entry/analysis software.</li>
<li>Ability to problem solve and troubleshoot independently.</li>
<li>Team-oriented with initiative to drive improvements.</li>
<li>Ability to read and follow SOPs while maintaining safety and HSE compliance.</li>
</ul>
 Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.

Quality Control Microbiologist

<h3>Job Description</h3>
Job Description
Pest Control Technician - Wildlife
Stark Exterminators is looking to hire a full-time Wildlife Technician to provide uncompromised service to Arrow's residential and commercial wildlife control customers through exclusion, trapping, and removal of wildlife. Exclusion includes sealing, caulking, or installation of sheet metal to soffits, gutter lines, roof ridges, vents, voids etc. This work is often done from rooftops or ladders and may require basic carpentry
Our technicians enjoy a company vehicle and other benefits including:
<ul>
<li>generous time off, </li>
<li>11 paid holidays, </li>
<li>401(k) with company match, Roth IRA, </li>
<li>medical, dental and vision insurance, </li>
<li>high deductible HSA, </li>
<li>telemedicine, </li>
<li>disability, cancer, and accident insurance. </li>
<li>health &amp; wellness suite </li>
<li>company-paid + additional, optional, life insurance. </li>
</ul>
 
ABOUT OUR FAMILY OF BRANDS 
Stark Exterminators is part of the Arrow Exterminators family of brands. We have been a family-owned and operated business since our start in 1964. Over the years, we have grown rapidly, and we now have the privilege of servicing 12 states. To ensure the quality and satisfaction of our customers, we have several offices in each state we are in to offer a more personalized approach to our communities. Ranked by revenue, Atlanta-based Arrow Exterminators is the sixth-largest pest and termite control company in the United States! We instill family values in the company culture to create a welcoming work environment and a successful company. We attribute our success to passionate, highly trained team members who are committed to protecting everyone's quality of life.
As Arrow grows and exceeds industry expectations, we are always looking for new talent to bring on board. We know our team has a lot of options and we are humbled that they choose to work with us. That's why we offer competitive compensation, a robust benefits package, and a family-oriented company culture.
A DAY IN THE LIFE OF A WILDLIFE TECHNICIAN
Your primary focus will be to identify, remove, prevent, or repair anything damaged by wildlife. Your first course of action will be to ask questions on the issue your customer is experiencing. Problem-solving will help you form an in-depth inspection of the customer's home to find the source of the issue. Your wealth of knowledge about wildlife will help you determine the best solution and explain to the customer your next steps. Upon the completion of your service, whether it be exclusion, trapping, or removal, you will be responsible for collecting payment due and proposing additional services that would benefit them. Your independence and accountability will help you as you run and schedule your own services. 
Minimum Qualifications:
<ul>
<li>Ability to pass and maintain any state regulatory agency-required licensing/certification exams</li>
<li>Able to pass internal technical exams</li>
<li>Possess a current Driver License's in the state where you work, the ability to operate a motor vehicle, and maintain a driving record consistent with company standards</li>
<li>High school diploma or equivalent</li>
<li>Able to work a 40-hour (minimum) workweek</li>
<li>Willing to work evenings and weekends as needed</li>
</ul>
 
ARE YOU READY TO JOIN OUR TEAM?
If you feel that you would be right for this position, please fill out our initial 3-minute, mobile-friendly application so that we can review your information. We look forward to meeting you! #ArrowExterminators
We are an Equal Opportunity Employer
(The job description is not an exhaustive statement of all the duties, responsibilities, or qualifications of the job, nor is it intended to limit opportunities for necessary modifications).
Stark Exterminators as a PestVets Company is committed to hiring and participating in acts of service for Veterans and active-duty members of the U.S. Military.
 
Stark Exterminators is a Drug-Free Workplace and performs Pre-employment Drug Screens and Background Checks on all employees
 Job Posted by ApplicantPro

Pest Control Technician - Wildlife

<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. ​
</li>
<li>
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>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</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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