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<h3>Job Description</h3>
Metrologist Job Category: Service Contract Act Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: Local * * * The Opportunity: CACI is looking for a Metrologist to join the team at the Naval Surface Warfare Center, Carderock Decision's (NSWCCDs) Fabrication Team. In this role, you will utilize high precision measurement equipment (coordinate measurement machines (CMMs), laser tracker equipment, ultrasonic devices, calipers, verniers, electronic protractors, squares, height gauges, depth gauges, indicators, and micrometers) and perform computerized spatial analysis. Calibrate equipment then measure item geometry and spatial relationships. This includes small and large-scale items requiring dimension and tolerance analysis to determine accuracy. Shall restrain items to prevent hog and sag deformation prior to measurement. Provide Tolerance Measurement Study upon completion. Perform preventative and routine maintenance and calibration of measurement equipment as needed and issue calibration Responsibilities: 
<ul>\n
<li>Prepare measurement reports per customer specifications. Determine if first article parts are acceptable.</li>
\n
<li>Implement new innovative practices to promote part accuracy, and proficiency. This may include, but is not limited to, new reporting templates or formats that better facilitate the documentation, reporting, and tracking of precision measurement activities.</li>
\n
<li>Use Polyworks Metrology Software to inspect high tolerance finished components designed with minimal fixturing to preform article inspection.</li>
\n
<li>Use Polyworks to advise shop management, supervisors, and planners, during the planning and costing phase, on the difficulty, complexity and potential issues which may arise during the inspection process.</li>
\n
<li>Analyze and diagnose problems which may arise during the inspection process. Utilize Polyworks or Spatial Analyzer to determine root cause of potential issues and develop methods and processes to ensure that similar issues are reduce or eliminate in future tasks.</li>
\n
<li>Use Polyworks software to perform Laser Tracker measurements according to the Model Fabrication Facility policies and standard practices</li>
\n
<li>Adhere to the Model Fabrication Facility policies and standard practices were applicable.</li>
\n
<li>Design specialized tooling fixtures to be used to support the production of complex machined components</li>
\n
<li>Applies knowledge of engineering disciplines in structural design, weld design materials applications and prototype design • Skilled in the interpretation of complex engineered drawings, sketches and verbal communications</li>
\n</ul>
\n Qualifications: Required: 
<ul>\n
<li>High School diploma or equivalent.</li>
\n
<li>Experience with utilizing high precision measurement equipment (coordinate measurement machines (CMMs), laser tracker equipment, ultrasonic devices, calipers, verniers, electronic protractors, squares, height gauges, depth gauges, indicators, and micrometers) and performing computerized spatial analysis</li>
\n
<li>Knowledge of manufacturing trades including industrial and commercial manufacturing processes to contribute to the engineering design and development function</li>
\n
<li>Ability to collect and analyze data in test samples and fabrication mockups and apply the data collected to the fabrication of future high cost components and models</li>
\n
<li>Experienced in inspecting and dimensionally verifying components and models to ensure compliance with dimension specified in drawings, specifications and control documents.</li>
\n
<li>Experience with generating and delivering measurement reports per customer specifications</li>
\n
<li>Thorough understanding of geometric dimensioning and tolerance practices, including NIST.</li>
\n
<li>Ability to read and work from highly detailed drawings and specifications.</li>
\n
<li>Desire to learn, ask questions, and take initiative within safety and skills limitations.</li>
\n</ul>
\n Physical: 
<ul>
<li>Office, industrial and construction settings; the work requires the employee to spend most of the day standing, kneeling, or sitting in awkward positions. S/he will lift weights up to 80 lbs. S/he will work from ladders and scaffolds, also trenches, and hard to reach places by bending, stretching, and stooping</li>
</ul>
\n Working Conditions: 
<ul>\n
<li>Contractor will frequently work inside and outside of buildings. S/he will work in cold weather. S/he may be working in the hot sun. S/he will work in environments where ventilation or respirators may be necessary. S/he must be safety minded about themselves and others. S/he will check tools and equipment, and see their capacities are not exceeded; and that tools are kept in a safe working condition.</li>
\n
<li>Physical: (1) Lift up to 80 lbs. (2) Work in Industrial and Test Facility Environment including cranes, fork trucks and vehicle operations.</li>
\n
<li>Hazardous Duty: Incumbent performs work in industrial settings where the potential for hazards exists. However, the use of engineering controls, materials substitution and personal protective equipment reduce or eliminate hazard exposure. Incumbent is regularly exposed to the hazard of: noise, electrical shock, wet surfaces, and climbing. The contractor will occasionally use hazardous materials e.g. various oils and solvents. The contractor is occasionally exposed to high work and confined space.</li>
\n</ul>
\n Desired: 
<ul>\n
<li>Possess a working knowledge of machining and sheet metal processes.</li>
\n
<li>Familiarity with NAVSEA, Navy, or other military standards for fabrication</li>
\n
<li>Experience with PolyWorks and Spatial Analyzer</li>
\n</ul>
\n What You Can Expect: A culture of integrity. At CACI, we place character and innovation at the center of everything we do. As a valued team member, you'll be part of a high-performing group dedicated to our customer's missions and driven by a higher purpose - to ensure the safety of our nation. An environment of trust. CACI values the unique contributions that every employee brings to our company and our customers - every day. You'll have the autonomy to take the time you need through a unique flexible time off benefit and have access to robust learning resources to make your ambitions a reality. A focus on continuous growth. Together, we will advance our nation's most critical missions, build on our lengthy track record of business success, and find opportunities to break new ground - in your career and in our legacy. Your potential is limitless. So is ours. Learn more about CACI here. Pay Range: This posting is for a position covered by the Service Contract Labor Standards (SCA). The pay and benefits provided for this position will meet or exceed the minimum required amounts detailed in the wage determination issued by the Department of Labor and made applicable to this position, as incorporated into CACI's government contract for the work location. Minimum Required Hourly Wage: $35.64 There are a host of other factors that can influence final salary including, but not limited to, geographical location, relevant prior work experience, specific skills and competencies, education, and certifications. Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives. We offer competitive compensation, benefits and learning and development opportunities. Our broad and competitive mix of benefits options is designed to support and protect employees and their families. At CACI, you will receive comprehensive benefits such as; healthcare, wellness, financial, retirement, family support, continuing education, and time off benefits. Learn more here. CACI is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, age, national origin, disability, status as a protected veteran, or any other protected characteristic.

Metrologist

<h3>Job Description</h3>
Job DescriptionDescription:
Summary
This position provides research, data analysis and operational support to and laboratory members for research projects involving symbiont technology, citrus greening disease, cotton leafroll dwarf virus and other projects as assigned. 
 
Essential Job Functions
<ul>
<li>Conduct research as directed by a supervisor, including:
<ul>
<li>Executing laboratory and/or field research, and interpreting the resulting data</li>
<li>Maintaining knowledge of relevant scientific literature </li>
<li>Maintain biological material such as plants or microorganism collections</li>
<li>Maintain laboratory notebooks and electronic records</li>
<li>Assisting with the preparation of reports, manuscripts and presentations</li>
<li>Operates with complete oversight by the PI, research scientists, and/or specialists in the lab</li>
<li>Training colleagues on techniques/equipment</li>
<li>Give presentations</li>
<li>Has the capacity to operate semi-autonomously with moderate oversight by the PI, research scientists, and/or specialists in the lab</li>
<li>Design experiments to support questions/hypotheses from PI/supervisors</li>
<li>Collaborate with principal investigators (PIs) in formulating research questions and hypotheses</li>
<li>Has the capacity to operate completely autonomously with minimal oversight by the PI, research scientists, and/or specialists in the lab</li>
</ul>
</li>
<li>Participate in professional development activities, which may include:
<ul>
<li>Regular meetings regarding the progress and direction of research with the supervisor or in group meetings</li>
<li>Participating in Institute seminars and events</li>
<li>Participating in activities to develop communication, management and other soft skills</li>
<li>Participating in BTI committees/societies</li>
<li>Attending conferences</li>
<li>May perform some of the duties of a lab manager if there is no such position in the group such as, oversee the maintenance of research databases and the organization of research files for the entire lab</li>
<li>Other duties as assigned</li>
</ul>
</li>
</ul>
Requirements:
Required Experience and Knowledge
Prior experience with symbiont technology and making symbiont technology plasmids is required. Prior experience maintaining hemipteran insect colonies for vector biology research is required. Prior experience working in a research laboratory or group is required, as well as the ability to work independently. 
Prior experience submitting documents to support federal field trial permits to EPA and USDA is required. 
Supervisory Responsibilities
No direct supervisory responsibilities. May provide mentoring to undergraduate student workers.
Communication Skills
Effective written and verbal communication and interpersonal skills required. Ability to maintain accurate lab notebooks and electronic records in English. Ability to draft publications and sections of grant proposals. Ability to speak effectively one-on-one or in small groups, and to present information to groups internal and external to the Institute.
Computer Skills
The position requires the proficiency in basic business applications, and may require use of scientific programs.
Travel
Occasional travel to off-site meetings or conferences. Occasional fieldwork may be required.
Physical Demands and Working Conditions
Some physical exertion may be required such as long periods of standing, recurring bending and occasional lifting. Ability to lift up to 50 pounds. The work is often conducted in a laboratory setting with regular use of chemicals or equipment/materials requiring use of personal protective equipment and routine precautions. May require occasional early morning, evening or weekend work.

Research Technician III

<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 
We are looking for an experienced Scientist I/Mechanical Engineer to join our Injection Device Development team to help us accelerate AbbVie’s combination of products from proof-of-concept through submission, industrialization and launch.
Our team has end-of-end accountability for commercial development, submission, industrialization and marketed product support for injection devices that enable the delivery of AbbVie’s innovative medicines. During our work we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing, and other cross-functional colleagues to ensure timeliness, robustness and market success.
As a Scientist I/Mechanical Engineer at AbbVie you will be part of a multi-disciplinary team of professionals working at the intersection of engineering and biopharmaceuticals. The problems you would help to solve relate not only to the function of innovative injection systems, but also the way in which they interact with drug products and the human body. You would be responsible for advancing programs that combine proven delivery systems with viable commercial drug assets. If you are a self-motivated person who thrives on solving complex problems and are excited by the idea of putting life-changing therapies in the hands of patients, this might be the opportunity for you.
Responsibilities
<ul>
<li>Design and execute laboratory studies supporting product development and on-market investigations</li>
<li>Support design transfer and industrialization activities</li>
<li>Maintain product design documentation</li>
<li>Support product design changes and continuous improvement effort</li>
<li>Perform statistical data analysis</li>
<li>Perform 3D and 2D CAD development in PDM environment</li>
<li>Develop protocols, and document test results</li>
<li>Position required up to 25% of travel time</li>
</ul>
Preferred Qualifications:
<ul>
<li>BS in Mechanical or Biomedical Engineering (MS preferred)</li>
<li>3-5 years of experience (MS up to 2 years) ideally in the medical device, drug delivery or other regulated industry</li>
<li>Strong communication skills (both written and verbal)</li>
<li>Strong design and analytical skills</li>
<li>Experience with:
<ul>
<li>Laboratory environment, experiment planning, material control and recordkeeping</li>
<li>Physical prototyping (including 3D printing, manual machining, etc) and reverse engineering</li>
<li>3D CAD modeling, detailed engineering drawings, product database management environment and GD&amp;T</li>
<li>Statistical analysis tools</li>
<li>Manufacturing processes</li>
<li>Design controls (in accordance with ISO 13485 / CFR 820.30)</li>
<li>Toolroom environment</li>
</ul>
</li>
<li>Knowledge of material properties, material selection and testing methodologies</li>
<li>The ability to follow assigned schedules and work in team environment</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education with typically 5 years of experience, or Master’s Degree or equivalent education with typically two years of experience.</li>
<li>Theoretical and practical knowledge to carry out the job functions.</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;ofthis 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.&nbsp;​
</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>
</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 anybonus,&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 soleand&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>

Scientist I Medical Device Mechanical Engineer

<h3>Job Description</h3>
Job Description
Position Overview
We are seeking an Engineer, Scientist, or Programmer with strong Python skills to support a wide variety of analytical, computational, and technical tasks. This position is fully on-site in Doylestown Borough, Pennsylvania and requires 25–50% travel based on project needs.
Work Location: Doylestown, PA 18901 (On Site)
Schedule:&nbsp;Monday - Friday 8 hours per day
Travel required 25-50%
Responsibilities
<ul>
<li>Develop, test, and maintain Python-based tools, models, and analytical workflows</li>
<li>Perform technical analysis, modeling, simulation, and data processing</li>
<li>Support mission-driven research across multi-domain topics</li>
<li>Coordinate with the owner to deliver high-quality products</li>
<li>Maintain strict adherence to federal security protocols</li>
<li>Adapt to changing project requirements</li>
</ul>
Required Qualifications
<ul>
<li>Must have a strong proficiency in Python programming</li>
<li>3 years of experience preferred in engineering, computer science, physics, mathematics, or related field</li>
<li>Ability to obtain and maintain a U.S. government security clearance</li>
<li>On-site work required in Doylestown Borough, PA</li>
<li>Willingness to travel 25–50%</li>
<li>Strong problem-solving and analytical skills</li>
<li>Able to work independently in a small business environment</li>
</ul>
Highly Preferred
<ul>
<li>Degree in Aerospace, Electrical or Mechanical Engineering</li>
<li>Active security clearance (Secret or higher)</li>
<li>Experience supporting defense, government, or national-security missions</li>
<li>Familiarity with modeling, simulation, scientific computing, or data analysis</li>
</ul>
Core Values
Intensity — purposeful focus and disciplined execution
Insight — clarity of thought and analytical rigor
Integrity — professionalism, reliability, and ethical conduct
Company DescriptionAbout Good Multi-Domain Solutions, LLC Good Multi-Domain Solutions, LLC is a small, high-performance defense and technology consulting and engineering service firm delivering impactful solutions across multiple mission domains. We maintain a strong commitment to our core values: Intensity, Insight, and Integrity. About the Founder Good Multi-Domain Solutions, LLC is led by Brandon Lowell Good, Ph.D., who served over 16 years with the Department of the Navy. In his final five years of federal service, he was a Program Technical Director in the Maritime Domain at the Office of Naval Research. The company’s current work includes supporting programs that contribute to the advancement of next-generation maritime and multi-domain platforms across several naval communities. Dr. Good focuses on delivering versatile, high-performance solutions through advanced computational analysis, streamlined development processes, and close collaboration with government and industry partners. His current efforts emphasize developing systems that combine information from multiple sources to enable more capable and adaptable platforms. 
<h3>Company Description</h3>
About Good Multi-Domain Solutions, LLC\r\nGood Multi-Domain Solutions, LLC is a small, high-performance defense and technology consulting and engineering service firm delivering impactful solutions across multiple mission domains. We maintain a strong commitment to our core values: Intensity, Insight, and Integrity.\r\n\r\nAbout the Founder\r\nGood Multi-Domain Solutions, LLC is led by Brandon Lowell Good, Ph.D., who served over 16 years with the Department of the Navy. In his final five years of federal service, he was a Program Technical Director in the Maritime Domain at the Office of Naval Research. The company’s current work includes supporting programs that contribute to the advancement of next-generation maritime and multi-domain platforms across several naval communities. Dr. Good focuses on delivering versatile, high-performance solutions through advanced computational analysis, streamlined development processes, and close collaboration with government and industry partners. His current efforts emphasize developing systems that combine information from multiple sources to enable more capable and adaptable platforms.

Engineer - Scientist - Programmer

<h3>Job Description</h3>
Job Description
EnSafe is seeking a Senior Hydrogeologist to join our team of environmental professionals working on complex and rewarding projects across the countrybased out of any of EnSafe’ soffices listed.
EnSafe is an employee-owned global environmental consulting and engineering firm. We strive to provide cutting-edge, creative solutions for our clients. EnSafe specializes in custom solutions in Environmental Management and Planning, Civil Design Engineering, Environmental Restoration, Natural &amp; Water Resources, Health &amp; Safety, and Technology, with offices operating within the U.S. 
What We Are Looking For
As Senior Hydrogeologist, you will lead and contribute to multidisciplinary projects involving environmental site investigation, remediation, groundwater modeling, and regulatory compliance. We offer a workplace culture that promotes autonomy, continuous learning, and professional growth. 
What You Will Be Doing: 
<ul>
<li>Designing, directing, and executing complex site investigations, including the planning and implementation of drilling, geophysical logging, aquifer testing, sampling of various media, and installation of monitoring and recovery wells.</li>
<li>Leading project teams in developing conceptual site models and conducting contaminant fate and transport evaluations.</li>
<li>Managing and overseeing field activities, ensuring health and safety compliance, subcontractor coordination, and efficient scheduling.</li>
<li>Interpreting hydrogeologic data and synthesizing field and analytical results to support reporting, risk assessments, remedial design, and regulatory decision-making.</li>
<li>Practical use of advanced groundwater models to support site characterization and remediation/optimization strategies.</li>
<li>Writing and reviewing technical reports, work plans, sampling plans, and standard operating procedures (SOPs).</li>
<li>Serving as a technical advisor, mentoring junior staff, performing quality control reviews, and helping the next generation of hydrogeologists grow.</li>
<li>Interfacing with clients and regulatory agencies as a subject matter expert, providing strategic guidance, presenting findings, and supporting negotiations.</li>
<li>Performing optimization of passive and active remedial alternatives, including LTM.</li>
<li>Building, calibrating, and validating analytical and numerical soil, groundwater, surface water, sediment, and indoor air (attenuation) modeling.</li>
<li>Providing litigation support for discovery, affidavits, deposition, and trial.</li>
<li>Performing sequence stratigraphy evaluations and reporting.</li>
<li>Performing statistical evaluations, background studies, and associated reporting.</li>
<li>Travel up to approximately 30% may be required, including occasional overnight trips.</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's or Master’s degree in Hydrology, Hydrogeology, Geology, Engineering, or a closely related field.</li>
<li>15–20 years of professional experience, preferably in environmental consulting. </li>
<li>Professional Geologist or Engineer licensure (by exam).</li>
<li>Strong background in hydrogeologic site characterization, groundwater flow and transport modeling and analysis, and environmental remediation/remedy optimization.</li>
<li>Proficiency with regulatory programs including CERCLA, RCRA, and state-specific programs.</li>
<li>Demonstrated ability to lead projects and teams, manage multiple priorities, mentor/supervise employees, and communicate effectively with diverse audiences.</li>
<li>Advanced skills in data analysis, report writing, and preparation of maps, tables, charts, and figures.</li>
<li>Experience using hydrogeologic modeling tools, including but not limited to MODFLOW, MT3D codes, VISTAS, EVS, etc. </li>
<li>Familiarity with GIS applications.</li>
<li>Excellent verbal and written communication skills. </li>
<li>Current 40-hour HAZWOPER certification.</li>
</ul>
About EnSafe
EnSafe began as a two-person firm in 1980, navigating complex regulatory compliance issues on behalf of our clients. We nurture our people with growth and development opportunities. We build enduring, trustful relationships with each of our clients, with a focus on high ethical and safety standards. We build this reputation by attracting high-quality people and retaining them for the long term.
At EnSafe, we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this or other roles at our company.
EnSafe is committed to being an EEO employer and all qualified candidates will receive consideration without regard to race, color, religion, national origin, citizenship, age (except for bona fide occupational qualifications), sex, disability, sexual orientation, gender identity, marital status, military or veteran status, any other status protected by federal, state, or local law, or association with a person on the basis of one or more of the foregoing.
Check us out on the web at <a href="http://www.ensafe.com" target="_blank">www.ensafe.com</a>

Senior Hydrogeologist

<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 Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.
Responsibilities:
<ul>
<li>Leads the statistical programming activities for projects with lower complexity.</li>
<li>Leads the statistical programming activities for studies.</li>
<li>Develop SAS programs for the creation of ADaM data sets following CDISC standards.</li>
<li>Develop SAS programs for the creation of Tables, Listings and Figures.</li>
<li>Validation of ADaM data sets, Tables, Listings and Figures.</li>
<li>Create specifications for the structure of ADaM data sets for individual studies and integrated data.</li>
<li>Create documentation for regulatory filings including reviewers guides and data definition documents</li>
<li>Leads the development of standard SAS Macros and participates in the development of standard operating procedures.</li>
<li>Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.</li>
</ul>
*This is a US remote based position
Qualifications 
<ul>
<li>MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience.</li>
<li>Indepth understanding of SAS programming concepts and techniques related to drug development.</li>
<li>Fundamental understanding of CDISC Standards.</li>
<li>Fundamental understanding of the drug development process, including experience with regulatory filings.</li>
<li>Ability to communicate clearly both oral and written.</li>
<li>Ability to accurately estimate effort required for study related programming activities.</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;ofthis 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.&nbsp;​
</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 anybonus,&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 soleand&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>

Senior Statistical Analyst (Remote)

<h3>Job Description</h3>
Job Description
FORT VALLEY STATE UNIVERSITY (FVSU), a state and land-grant institution of the University System of Georgia, invites applications for the position of Research Professional.
Fort Valley State University, the only 1890 land-grant university in Georgia, is a comprehensive institution that provides an education to over 2,800 students including graduate students. The university is located in the town of Fort Valley in Peach County, the original site of the state's peach industry. Its 1,365-acre (5.52 km2) campus is Georgia's second-largest public university in area.
Fort Valley State University is an affirmative action, equal opportunity institution and does not discriminate against applicants, students, or employees on the basis of race, gender, ethnicity, national origin, sexual orientation, religion, age, disability, or marital or veteran status.
 
JOB SUMMARY:
We are looking for a highly qualified Research professional with advanced knowledge in animal parasitology, stress physiology, nutrition, microbiology, and meat quality. The role involves designing and conducting research studies, overseeing laboratory operations, publishing in peer [1] reviewed journals, and utilizing advanced laboratory and molecular techniques. This position supports our mission to enhance animal health, productivity, and product quality through innovative and applied research.
 
ESSENTIAL DUTIES/RESPONSIBILITIES:
<ul>
<li>Conduct advanced research on animal stress physiology, nutrition, growth, reproduction, parasitology, and meat quality, integrating laboratory and field-based approaches. </li>
<li>Design, implement, and evaluate experiments involving small ruminants (e.g., goats), including blood, meat, and rumen sampling, and analyze physiological and biochemical responses.</li>
<li>Utilize advanced molecular and laboratory techniques, including ELISA, mRNA extraction, PCR, RT-PCR, western blotting, calorimetry, hematology, and blood chemistry analysis. Maintain and calibrate a wide range of laboratory instruments (spectrophotometers, plate readers, hematology analyzers, biochemistry analyzers, calorimeters, etc.). </li>
<li>Manage animal herds during research, including monitoring behavior, welfare, stress responses, and productivity. </li>
<li>Supervise and train students and research staff in laboratory techniques, experimental design, data collection, and analysis.</li>
<li>Use of machine learning based image classification to identify different Lespedeza species, classify FAMACHA scores for anemia detection, and detect mastitis in animals. </li>
<li>Analyze data using statistical and bioinformatics tools (Microsoft Office 365 tools, SAS), prepare detailed reports, and contribute to scientific publications.</li>
<li>Collaborate with multidisciplinary teams, present research findings at professional conferences.</li>
</ul>
 
MINIMUM QUALIFICATIONS:
<ul>
<li>Master's degree in animal science, veterinary science, or related field. </li>
<li>At least 3 years of research experience in animal science, stress physiology, nutrition, parasitology, or related areas.</li>
</ul>
 
PREFERRED QUALIFICATIONS:
<ul>
<li>DVM or Equivalent degree.</li>
<li>Research experience of at least five years in Animal Sciences or related degree. </li>
<li>Hands-on experience with large-scale animal research projects and conference presentations.</li>
<li>Had prior experience working with small ruminants. </li>
<li>Knowledge of bioinformatics and statistical analysis for large datasets (e.g., metabolomics, RNA-seq).</li>
</ul>
 
REQUIRED SKILLS AND KNOWLEDGE:
<ul>
<li>Expertise in animal physiology, nutrition, parasitology, microbiology, and meat science.</li>
<li>Proficiency with molecular biology and analytical techniques (PCR, ELISA, RNA-seq, western blotting, calorimetry, metabolomics). </li>
<li>Strong publication record in peer-reviewed journals. Experience managing and researching small ruminants, including blood and tissue sampling. </li>
<li>Ability to supervise and mentor students and contribute to collaborative research teams. </li>
<li>Strong written and verbal communication skills; proven ability to present findings at scientific meetings.</li>
</ul>
 
WORKING CONDITIONS:
<ul>
<li>Research laboratories, animal research facilities, and field environments. </li>
<li>Everyday activities include responding to emails, phone calls, and team discussions in addition to the research duties. </li>
<li>Requires handling animals, biological samples, and specialized lab equipment.</li>
<li>May involve extended hours during data collection, animal management, and field experiments</li>
</ul>
 
USG Core Values Statement 
The University System of Georgia is comprised of our 26 institutions of higher education and learning, as well as the System Office. Our USG Statement of Core Values are Integrity, Excellence, Accountability, and Respect. These values serve as the foundation for all that we do as an organization, and each USG community member is responsible for demonstrating and upholding these standards. More details on the USG Statement of Core Values and Code of Conduct are available in USG Board Policy 8.2.18.1.2 and can be found on-line at <a href="https://www.usg.edu/policymanual/section8/C224/#p8.2.18_personnel_conduct" target="_blank">https://www.usg.edu/policymanual/section8/C224/#p8.2.18_personnel_condu…</a>
 
Additionally, USG supports Freedom of Expression as stated in Board Policy 6.5 Freedom of Expression and Academic Freedom found on-line at <a href="https://www.usg.edu/policymanual/section6/C2653" target="_blank">https://www.usg.edu/policymanual/section6/C2653</a>. 
 Job Posted by ApplicantPro

Research Professional

<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.
Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie’s R&amp;D, is a global organization that is responsible for discovering and optimizing drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA etc.) for all therapeutic areas across discovery.
Job Description 
The Principal Data Architect is a visionary leader in the development and success of our cloud-native data platform, which supports the development and integration of predictive and generative machine learning solutions in drug discovery scientist workflows. This role requires a strong ability to see both the big picture and the details, and to work cross-functionally with both wet lab scientists, ML engineers, software engineers, data engineers, and data infrastructure engineers, among others.
This position reports to the Head of AI/ML in Biotherapeutics and Genetic Medicine (BGM) and will serve as a trusted advisor to senior leadership. This role is pivotal in driving our organization towards becoming a leader in the application of artificial intelligence, ensuring that AI and ML initiatives are built on a robust, resilient, and scalable data foundation that grows with the organization.
Key responsibilities:
<ul>
<li>Drive the vision, execution, implementation, adoption, and continuous improvement of a robust, scalable data platform as the foundation for the execution of AbbVie’s AI/ML strategy, particularly within BGM.&nbsp;</li>
<li>Define data models and architectures that collect, store, structure, access, and connect datasets generated across a dozen different lab groups, enabling downstream uses (ML model development, operational reports, lab documentation, etc.).&nbsp;</li>
<li>Collaborate closely with wet lab scientists, especially the Head of Lab Data Products, and automation engineers to maximize the utility of data captured by lab automation workflows.&nbsp;</li>
<li>Collaborate closely with data scientists, and deployment engineers, to ensure data pipelines support both machine learning model development and deployment into production. &nbsp;</li>
<li>Co-develop and execute a strategy that maximizes FAIR-fication of BGM data and in concert with wider BGM strategic goals.&nbsp;&nbsp;</li>
<li>Communicate the impact of a robust data platform to AbbVie’s drug pipeline, using both user stories and KPIs that allow measurement of the value added.&nbsp;</li>
<li>Multiply impact of the data platform by championing and communicating the principles behind connected data, data stewardship, data-as-a-product, and cloud-first and cloud-native architectures.&nbsp;</li>
<li>Collaborate with data infrastructure and data governance experts across AbbVie to ensure that data governance principles and policy are optimally implemented.&nbsp;&nbsp;</li>
<li>Ensure alignment and coordination of data infrastructure initiatives with existing AbbVie initiatives such as Convergence, and ARCH.</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in&nbsp;computer science, data science, computational biology, computational chemistry, computational biophysics, or related field with typically 16+ (BS) years, 14+ (MS) years, or 8+ (PhD) years of &nbsp;experience in data architecture&nbsp;with a track record of designing enterprise data platforms.&nbsp;&nbsp;</li>
<li>Deep technical skills in data modeling, data integration, implementation of data storage solutions, data pipelines, and integration with AI/ML.&nbsp;&nbsp;</li>
<li>Production programming expertise in SQL, python, or Java.&nbsp;</li>
<li>Experience building cloud data infrastructure solutions using AWS, Azure, or GCP.&nbsp;</li>
<li>Familiar with both wet and dry lab scientific principles and processes, able to foresee and prevent data platform-originating failure modes.&nbsp;</li>
<li>Experience with cross-functional team leadership, and track record of collaboration excellence.&nbsp;</li>
<li>Previous experience in the pharmaceutical or biotechnology sectors.&nbsp;&nbsp;</li>
<li>Experience managing both team member delivery and career development.&nbsp;</li>
<li>Exceptional interpersonal and communication skills, and strong evidence of ability to build stakeholder alignment.&nbsp;&nbsp;</li>
<li>Ability to integrate data governance principles into everyday decision making.&nbsp;</li>
</ul>
The position is located at Worcester, MA site as a full time in office or hybrid (3 days per week) role.&nbsp;
 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 thetime&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.&nbsp;​
</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 anybonus,&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 soleand&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 II- Data Architecture, Biotherapeutics and Genetic Medicine

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Essential Duties and Responsibilities: 
<ul>
<li>Demonstrates strong client service skills, teamwork, and collaboration</li>
<li>Applies GMP/GLP/ISO 17025 compliance standards in all areas of responsibility, as appropriate</li>
<li>Recognizes errors, identifies root causes, and applies process improvements</li>
<li>Assists in Method Development and execute method validation protocols</li>
<li>Oversees sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, ICP, pH, moisture, Karl Fischer, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.)</li>
<li>Assists in Method Development and executes method validation protocols</li>
<li>Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision</li>
<li>Makes recommendations for technical improvements, as needed</li>
<li>Provides analysis support for method validation as needed</li>
<li>Ensures that the quality policy program is understood, implemented, and maintained at all levels of the organization; identifies, prevents, or corrects any departures from the quality system</li>
<li>Performs work for both routine and non-routine work as specified by a separate and applicable technical job description for the individual</li>
<li>Develops and implements operational improvements</li>
<li>Coaches, trains, and develops others within the group with respect to their personal development and effective implementation of operational improvements</li>
<li>Coordinates workflow and performs daily monitoring to meet TAT</li>
<li>Conducts semiannual performance reviews, interviews applicants, keeps training records up to date for assigned employees, and performs succession planning in preparation for growth</li>
<li>Confronts and addresses problems, concerns, and performance issues</li>
<li>Coaches and develops individuals and teams to maximize performance</li>
<li>Fosters motivation and positive morale</li>
<li>Monitors and approves employees’ time worked through the time-entry system</li>
<li>Expands self-awareness and develops leadership skills as defined; attends applicable leadership training based on identified needs</li>
<li>Performs and/or assigns other duties as requested to ensure the smooth operation of the department</li>
<li>Provides analysis support for method validation as needed</li>
<li>Evaluates, reviews, and approves data by other analysts</li>
<li>Trains new analysts in laboratory techniques and procedures</li>
<li>Writes, edits, and updates SOPs, WI and other documentation</li>
<li>Documents results appropriately in notebooks, LIMS, or on testing forms</li>
<li>Possesses strong computer, scientific, quality orientation, and organizational skills</li>
<li>Provides clear feedback</li>
<li>Communicates (oral and written) effectively and shows attention to detail</li>
</ul>
<ul>
<li>Keeps accurate records, follows instructions, and complies with company policies</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in Chemistry, Biology, or other related degree concentration, or&nbsp;equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>7+ years of related experience</li>
<li>1 – 3 years supervisory experience</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, Monday - Friday&nbsp;8am to 5 pm</li>
<li>Ability to work overtime as required.</li>
<li>Tasks require repetitive motion and standing for long periods of time.</li>
<li>May be required to respond to off-shift operational issues.</li>
<li>Candidates currently living within a commutable distance of Winston-Salem, NC&nbsp;are encouraged to apply.</li>
<li>Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Chemist Group Leader- Inorganics Lab

<h3>Job Description</h3>
Job Description
Cranial Technologies is the only company in the world completely dedicated to researching, diagnosing, and treating plagiocephaly (commonly called flat head syndrome). With over 300,000 babies successfully treated, we are the plagiocephaly experts and the leader in pediatric cranial shaping orthoses. 
Cranial Technologies also provides treatment with EarWell® to correct infant ear shapes without surgery. With over 600,000+ successful outcomes, EarWell® is a proven, non-invasive treatment option for families. 
For over 35 years, Cranial Technologies has provided a superior product, service, and the best possible outcome for every child with cranial asymmetry. We are the leading provider of Head Band Therapy used to treat plagiocephaly in infants.
We are currently looking for a National Traveling Certified Orthotist based out of Washington, DC! This is a full-time position for someone that is looking for an opportunity to practice in a variety of Cranial Technologies locations across the United States. 
This is an exciting opportunity to work outside of traditional orthotics in a niche, pediatric clinical outpatient setting exclusively with infants and their families.
Do love to fly and travel around the United States?
<ul>
<li>In this role you will travel to any state where we have a Cranial Technologies clinic. We're currently in 32 states and are continuing to grow!</li>
<li>Travel is typically on a Sunday afternoon/evening. You work in the clinic Monday – Thursday and fly home Thursday afternoon/evening. You are home every Friday and Saturday! </li>
<li>You will be traveling every week, either to a local clinic or to another state. We are looking for candidates close to a major airport for ease of travel booking! </li>
<li>Cranial Technologies will pay for your travel expenses, and you also get a per diem for your time there. All you need to worry about is treating our babies! </li>
</ul>
Do you thrive in fast paced and new settings?
<ul>
<li>You may be in a different clinic every week working with new teammates and building relationships across the company!</li>
<li>You will be taking over a caseload for another clinician, so you are always meeting new families!</li>
</ul>
What does a clinician do at Cranial Technologies? 
As a Clinician, you will treat infants to reshape head shapes with the DOC Band® and correct ear shapes with EarWell®. Pediatricians and parents alike look to our Clinicians as the experts in evaluation and in treatment of plagiocephaly as well as conditions involving misshapen ears. Our treating Clinicians develop great relationships with our families at every stage of their treatment process. 
We hire from various backgrounds because each background is a great fit in its own way. 
<ul>
<li>PTs and OTs are an excellent fit with their background knowledge of symmetry and asymmetry, cervical anatomy, torticollis, and infant/toddler development. </li>
<li>Certified Prosthetist-Orthotists &amp; Certified Orthotists are also a strong fit because of their hands-on experience with orthotics and direct patient care. </li>
</ul>
A background in pediatrics is preferred, but not necessary as we have a formal training program that includes mentoring.
What we have to offer:
<ul>
<li>You will see visible, measurable changes in two to three weeks</li>
<li>We value our employees and invest in their training and mentorship</li>
<li>Direct patient care with minimal paperwork</li>
<li>No productivity/patient quotas</li>
<li>Cranial Technologies is a national company with future opportunities available in training and mentoring</li>
<li>Travel accommodations and expenses are covered by the company!</li>
</ul>
Qualifications:
<ul>
<li>Certified Orthotist</li>
</ul>
Benefits Package for Cranial Technologies:
<ul>
<li>Medical, Dental, and Vision Insurance</li>
<li>401k Retirement Plan with matching</li>
<li>3.5 Weeks Paid Time Off plus 7 company-paid Holidays</li>
<li>Life Insurance</li>
<li>Short/Long Term Disability Insurance</li>
<li>Clinician Continuing Education Benefit &amp; Licensure Renewal Fees Reimbursed</li>
<li>The pay range for this position is $90,000 - $100,000 plus additional travel bonus. Pay is dependent on the applicant's tenure in their field and relevant experience.</li>
<li>This position is also eligible for quarterly performance bonuses and annual raises.</li>
<li>Many internal growth and promotional track opportunities available.</li>
</ul>
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
You will receive a confirmation email stating your application has been submitted. Once your application has been reviewed, you should receive an update on your status via email. **Please keep an eye on your spam and junk mail**
Please no phone calls to the clinic or offices regarding the position.
If you are unable to submit your application, please email the recruiting department at <a href="mailto:careers@cranialtech.com" target="_blank">careers@cranialtech.com</a> for assistance.

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