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<h3>Job Description</h3>
Job Description
Overview
Serves as Medical Radiation Physicist in the Cancer Centers of Northern Arizona Healthcare's two cancer centers. Involved in both clinical and machine physics, serving as directed in the leadership, development, implementation and technical aspects of the Radiation Oncology programs. The Medical Radiation Physicist works under the direction of and is supervised by the Chief Medical Radiation Physicist, the Radiation Oncologist(s) and the Department Director performing physics service in accordance with the American College of Radiology Standards of practices as required by regulatory agencies and may work collaboratively with other department's medical physicists to address common programmatic needs. 
Responsibilities
Clinical* In conjunction with the Chief Medical Radiation Physicist and the Radiation Oncologist, assists with the physics needs for the Brachytherapy program; including High Dose Rate (HDR) and Low Dose Rate (seed implant). * Assists with oversight of the treatment planning program. * May direct Intensity Modulated Radiation Therapy IMRT) treatment planning and program operations, as directed or delegated. * In collaboration with the Radiation Oncologist(s), assists with the Stereotactic RadioSurgery program (SRS) and directs the Stereotactic Brain Radiotherapy Program (SBRT). * Participates in the Cancer Center's quality assurance program. * May directs proficiency testing of radiation oncology equipment for acceptance and on a periodic basis. * Performs chart reviews and therapy calculations, dosimetry assistance and facilitates treatment plan development and reviews, as delegated.Administrative* Assists with the Radiation Safety Program in the cancer centers. * May supervise or work collaboratively with the Lead Dosimetrist, Staff Dosimetrists, Lead Radiation Therapist and Staff Therapists. * May coordinate or provide direction to the BioMedical Technologist assigned to Radiation Oncology. * Provides interface with the Arizona Department of Radiation Protection, maintains licensure for the facilities, and serves as primary liaison with other state and federal regulatory agencies for Radiation Oncology, as delegated or directed. * Coordinates, as directed, with the designated Radiation Safety Officer for Flagstaff Medical Center and Verde Valley Medical Center on radiation licensure, radiation exposure monitoring and reporting.Technical* Assists with Radiation Safety Compliance and reporting. * Competent in three dimensional treatment planning. * Competent in brachytherapy treatment planning, including HDR and seed implants. * Knowledge of calibration of Linear Accelerators and other radiation sources. * Expert in clinical dosimetry and treatment planning for external beams and implant sources, patient set-up and computerized treatment planning.Compliance/Safety* Responsible for reporting any safety-related incident in a timely fashion through the Midas/RDE tool; attends all safety-related training programs; performs work in a safe manner; monitors work environment for possible safety issues and ensures others are also performing work in a safe manner. * Stays current and complies with state and federal regulations/statutes and company policies that impact the employee's area of responsibility. * If required for the position, ensures all certifications and/or licenses are up-to-date and valid prior to expiration dates. * Completes all company mandatory modules and required job-specific training in the specified time frame. 
Qualifications
EducationMaster's Degree in Medical Physics or a closely related discipline- Required PhD in Medical Physics - PreferredCertification &amp; Licensures Completion of Part 1 of Certification by the American Board of Radiation Therapy Physics or Radiological Physics- Required BLS Certification completion- Required within 90 days of hireExperienceMinimum 2 years Clinical experience in a Radiation Therapy department- Required Experience in the following areas- Preferred • HDR and LDR treatment planning using Eclipse BrachyVision and VariSeed. • Familiarity with ARIA Record and Verify System Version 11 and higher. • Varian Linac Commissioning, Calibration and QA. • CT Simulation. • Image Guidance to Generate Treatment Plans as well as for Patient Setup. Healthcare is a rapidly changing environment and technology is integrated into almost all aspects of patient care. Computers and other electronic devices are utilized across the organization and throughout each department. Colleagues must have an understanding of computers, and competence in using computers and basic software programs.CALL REQUIRED: Must be able to physically show upNo

Medical Radiation Physicist

<h3>Job Description</h3>
Job Description
Job Title: Geotechnical Engineer Company: MTA Engineers NWA Location: Northwest Arkansas (On-site with field work required) Employment Type: Full-time
About Us
MTA Engineers in NWA is a growing engineering firm committed to delivering high-quality, data-driven solutions across a wide range of civil and geotechnical projects. We're seeking a motivated and detail-oriented Geotechnical Engineer to join our team in Northwest Arkansas. This is an exciting opportunity for a skilled professional who thrives on technical challenges, client interaction, and field-based work.
Key Responsibilities
<ul>
<li>Lead and support geotechnical engineering projects from inception through completion</li>
<li>Conduct geotechnical field explorations, including drilling, soil sampling, and groundwater measurements</li>
<li>Perform analyses including slope stability, karst investigations, and expansive soil evaluations</li>
<li>Complete foundation evaluations and construction site inspections</li>
<li>Prepare comprehensive geotechnical reports and deliver technical recommendations</li>
<li>Manage projects, including proposal development, client communication, execution, and reporting</li>
<li>Perform Construction Materials Testing and special inspections (foundation inspections, proof rolling, etc.)</li>
<li>Build and maintain strong client relationships in the Northwest Arkansas region</li>
<li>Analyze and interpret laboratory and field data using “standard” engineering software</li>
<li>Conduct field work to ensure data quality and accuracy</li>
</ul>
&nbsp;Qualifications
Required:
<ul>
<li>Licensed Professional Engineer (P.E.) in the State of Arkansas</li>
<li>Bachelor’s degree in civil engineering</li>
<li>Minimum 5 years of geotechnical engineering experience</li>
<li>Valid driver’s license and reliable transportation</li>
<li>Strong knowledge of geotechnical drilling techniques and field procedures</li>
<li>Excellent written and verbal communication skills</li>
</ul>
Preferred:
<ul>
<li>Experience with client development in Northwest Arkansas</li>
<li>Proficiency in geotechnical software and report writing</li>
<li>Strong organizational and project management abilities</li>
</ul>
What We Offer
<ul>
<li>Competitive salary based on experience</li>
<li>Paid time off</li>
<li>Medical, dental, and vision benefits</li>
<li>Opportunities for professional growth and advancement</li>
<li>Collaborative team environment</li>
<li>A chance to work on diverse and impactful geotechnical projects across the region</li>
</ul>

Geotechnical Engineer

<h3>Job Description</h3>
Description 
Summary:
A professional who assists in the organizational development, management, and administration of Oncology Research activities. Is responsible for the coordination and administration of clinical trials under the direction of the Principal Oncology Investigator in accordance with the standards of good clinical practice.&nbsp;&nbsp;
Responsibilities:
<ul>
<li>Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders.</li>
<li>Consistent with the ANA Scope and Standards of Practice, provides nursing care utilizing the nursing process, including assessment, diagnosis, planning, intervention and evaluation for assigned patients.</li>
<li>Addresses increasingly complex psychological, emotional, cultural, and social needs of patient and families in accordance with their level of practice.</li>
<li>Using the appropriate protocol, administers medications and treatments; monitors for side-effects and effectiveness of the treatment prescribed.</li>
<li>Documents patient history, symptoms, medication, and care given.</li>
<li>Assess learning needs and provides education to patients, family members and/or care givers; identify issues and resources.&nbsp;</li>
</ul>
Requirements:
<ul>
<li>Associate’s Degree in Nursing</li>
<li> Previous Oncology or Research experience&nbsp;</li>
<li>RN License in state of employment or compact&nbsp;</li>
<li>BLS </li>
</ul>
Work Schedule: 
8AM - 5PM Monday-Friday
Work Type: 
Full Time

Registered Nurse Clinical Research Senior-Research Industry-Full Time

<h3>Job Description</h3>
Job DescriptionDescription:
Job Title: Chemical Operator Department: Manufacturing Reports To: Shift Supervisor
Build Your Future with Toll Solutions – Where Chemistry Meets Innovation!
Are you looking for a hands-on career where you can make a real impact in the chemical industry? At Toll Solutions, we specialize in high-quality, custom chemical manufacturing for industrial markets. We are growing, and we need motivated individuals who thrive in a dynamic environment. If you’re ready to be part of an innovative team, this opportunity is for you!
Why Toll Solutions?
<ul>
<li>Industry Leader – We partner with top companies to create specialty chemical solutions that power industries worldwide.</li>
<li>Career Growth – We invest in our employees through training, certifications, and advancement opportunities.</li>
<li>Commitment to Safety &amp; Quality – We set the standard in chemical manufacturing with a culture of excellence and safety.</li>
</ul>
What You’ll Do as a Chemical Operator:
<ul>
<li>Operate and monitor chemical processing equipment such as reactors, mixers, and filtration systems.</li>
<li>Measure, blend, and transfer raw materials with precision to ensure product quality.</li>
<li>Maintain accurate batch records and perform in-process quality checks.</li>
<li>Package products in drums, totes, and other containers according to specifications.</li>
<li>Troubleshoot and maintain equipment to support continuous operations.</li>
<li>Follow all safety protocols, wear required protective equipment, and contribute to our strong safety culture.</li>
</ul>
What You’ll Gain:
<ul>
<li>Competitive Pay &amp; Benefits – Including health, dental, and retirement plans.</li>
<li>On-the-Job Training – No experience? No problem! We provide hands-on training to set you up for success.</li>
<li>Stability &amp; Growth – Join a company that values its employees and promotes from within.</li>
<li>Engaging Work Environment – Be part of a collaborative team that values safety, quality, and innovation.</li>
</ul>
Join Us at Toll Solutions!
If you’re ready to start a rewarding career with a company that values its people, apply today! Take the next step toward a future in chemical manufacturing with Toll Solutions.
 
Requirements:
What We’re Looking For:
<ul>
<li>Experience in a chemical or manufacturing setting (preferred but not required).</li>
<li>Basic understanding of chemistry (pH, viscosity, exotherm, etc.).</li>
<li>Strong attention to detail and ability to follow written and verbal instructions.</li>
<li>Ability to perform physical tasks, including lifting 50 lbs and handling large containers.</li>
<li>Forklift experience is a plus.</li>
<li>Team-oriented mindset with a proactive approach to problem-solving.</li>
</ul>

Chemical Operator - 3rd Shift (11pm - 7:30am)

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
Chemist in the Process Development Chemistry Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates.
Responsibilities
<ul>
<li>Work closely with senior chemists on development of new synthetic approaches to desired compounds with an eye toward large-scale synthesis</li>
<li>Cooperate with other chemists in the group in preparation of complex organic constructs</li>
<li>Perform solid-phase synthesis and purification of oligonucleotide drug candidates</li>
<li>Analyze small-molecule and macromolecular targets using standard methods</li>
<li>Maintain a well-documented laboratory notebook</li>
<li>Prepare documentation for transfer of new technologies to the Manufacturing group</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and issues to management, including presentation of findings at team meetings</li>
<li>Coordinate delivery of materials both internally and externally</li>
</ul>
Requirements:
<ul>
<li>BS or MS in chemistry or biochemistry with an excellent understanding of organic and analytical chemistry</li>
<li>Excellent verbal and written communication skills</li>
<li>Strong problem-solving skills</li>
<li>Eagerness to learn new techniques</li>
<li>Experience with synthetic organic chemistry in a laboratory setting</li>
<li>Experience with small-molecule and macromolecule analytical techniques (e.g., HPLC, UV-Vis spectrophotometry, mass spectrometry, NMR, etc.)</li>
</ul>
Preferred: 
<ul>
<li>Experience working with both small molecule or large molecule synthetic targets either in an academic or industrial setting</li>
<li>Experience with solid phase synthesis of oligonucleotides or peptides</li>
<li>Basic familiarity with GLP/GMP regulations</li>
</ul>
Wisconsin pay range $57,000—$70,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Associate Scientist I, CMC Process Development

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
Arrowhead Pharmaceuticals is seeking a Scientist to join the GLP Bioanalytical group within the Clinical Pharmacology and DMPK Department. The successful candidate will focus on internal bioanalytical method transfer, qualification/validation, and sample analysis for pharmacokinetic studies for early and late development phase programs. S/He will have expertise with various analytical platforms including LC/MS/MS, LC-FL, or immunoassays and is well versed in GxP bioanalysis. S/He will interface with different teams to coordinate sample analysis according to the study needs and timelines. S/He will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead development programs. 
Responsibilities
<ul>
<li>Conduct method development/transfer, qualification/validation, and sample analysis of bioanalytical assays via LC-FL, LC/MS/MS or other platforms for non-clinical and clinical studies.</li>
<li>Perform scientific data review and interpretation. Troubleshoot abnormal data and complex method issues as needed</li>
<li>Setup and maintain lab instrumentation and organization</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and issues to management and cross-functional teams</li>
<li>Engage in implementation of new analytical platforms</li>
<li>Engage in development of workflows and procedures</li>
<li>Effectively manage workload with minimal supervision. Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Follow SOPs and stay up to date on regulations. Adhere to Arrowhead values and Good Documentation Practices</li>
<li>Adhere to safe laboratory practices</li>
</ul>
Requirements:
<ul>
<li>B.S. in Chemistry (or related field)</li>
<li>5+ years of relevant GxP experience, M.S. in Chemistry (or related field) with 3+ years of relevant GxP experience.</li>
<li>Familiarity with GxP regulations and approaches to method validations, sample analysis, and data processing</li>
<li>Good documentation practices with excellent organization and attention to detail</li>
<li>Demonstrated innovation, creativity and resilience in problem solving</li>
<li>Excellent oral and written communication skills</li>
<li>Self-motivated team player with a can-do mindset and the ability to thrive in a fast paced, dynamic, multi-disciplinary, matrixed environment</li>
</ul>
Preferred:
<ul>
<li>Method development or troubleshooting experience with various analytical platforms</li>
<li>Project management experience, e.g. principal investigator for bioanalytical studies</li>
<li>Experience with training other scientists and leading lab organization and processes</li>
<li>Experience with sample management under GxP environment</li>
</ul>
Wisconsin pay range $95,000—$115,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Scientist, Bioanalytical

<h3>Job Description</h3>
Job Description
Position Type: Contract Onsite Required:
<ul>
<li>Must have a BA or BS degree in Chemistry or closely related science.&nbsp;</li>
<li>Minimum of 1-year relevant experience preferred.&nbsp;</li>
<li>Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE).</li>
<li>Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.</li>
<li>Physical and Environmental:
<ul>
<li>Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching.</li>
<li>While sitting for an extended period of time on a routine basis, incumbent may use the following equipment.&nbsp;</li>
<li>Personal computer, telephone/ other voice communication devices, copier, fax, scanners,&nbsp; or other specialized equipment used in an office setting.&nbsp;</li>
<li>Lift and maneuver equipment and materials weighing up to 20 pounds.</li>
<li>Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums.</li>
<li>Use small hand and power tools to perform incidental maintenance.</li>
<li>Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels.</li>
<li>Equipment and parts could weigh up to 20 pounds.&nbsp;</li>
<li>Requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.</li>
<li>Work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required.&nbsp;</li>
</ul>
</li>
</ul>
&nbsp;Responsibilities:
<ul>
<li>Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures.&nbsp;</li>
<li>Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.</li>
<li>Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.</li>
<li>Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.</li>
<li>Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.</li>
<li>Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency.</li>
<li>Aid other group members as required.</li>
<li>Ensure that equipment and working areas are maintained with good safety and housekeeping practices.</li>
<li>Re-stock chemicals and consumables used in analysis.</li>
<li>Performs other related assignments and duties as required and assigned.</li>
</ul>
Company DescriptionHired by Matrix believes in the human touch and starts every partnership with an in-depth conversation. By talking with our clients about their hiring needs and listening to job seekers describe their career goals, we build an understanding of what they are looking for and work hard to make it happen. 
<h3>Company Description</h3>
Hired by Matrix believes in the human touch and starts every partnership with an in-depth conversation. By talking with our clients about their hiring needs and listening to job seekers describe their career goals, we build an understanding of what they are looking for and work hard to make it happen.

Chemist

<h3>Job Description</h3>
Job Description
We are seeking a Research Associate to become an integral part of our team! You will assist social scientists in educational research and data analysis. Looking to start ASAP Monday -Friday!!
Responsibilities:
<ul>
<li>Gather qualitative and quantitative social science data</li>
<li>Conduct statistical analysis on research data collected</li>
<li>Collaborate with others to identify research needs</li>
<li>Translate complex data into simple textual and visual representations</li>
<li>Summarize findings into presentations and reports</li>
<li>Molecular biology assays</li>
<li>Cell Culture</li>
<li>Manage sample inventory</li>
</ul>
Qualifications:
<ul>
<li>Previous experience in social sciences, educational research, or other related fields</li>
<li>Familiar with fundamental research practices</li>
<li>Deadline and detail-oriented</li>
<li>Excellent written and verbal communication skills</li>
<li>Bachelors' degree in Biology</li>
<li>Strong organizational skill with the ability to track multiple studies, manage inventory, and ensure smooth day-to-day laboratory operations.</li>
</ul>
Company DescriptionInfinity Staffing is a family owned organization whose mission is to provide "Service with a Smile". Our vision is to maintain a strong foundation in an ever changing and evolving marketplace through solid relationships with our clients and candidates. Our number one priority and commitment is to provide a service which enables our clients to attract and retain the very best people available, and our candidates to fulfill their career potential. We are committed to stand out among our competitors and be the one and only choice for staffing solutions. We approach all client projects to the highest ethical and professional level 
<h3>Company Description</h3>
Infinity Staffing is a family owned organization whose mission is to provide "Service with a Smile". \r\nOur vision is to maintain a strong foundation in an ever changing and evolving marketplace through solid relationships with our clients and candidates. Our number one priority and commitment is to provide a service which enables our clients to attract and retain the very best people available, and our candidates to fulfill their career potential. \r\nWe are committed to stand out among our competitors and be the one and only choice for staffing solutions. We approach all client projects to the highest ethical and professional level

Research Associate

<h3>Job Description</h3>
Job Description
<ul>
<li>
The incumbent will work inside/outside the greenhouse and headhouse to support the trait Introgression and initiatives
</li>
<li>
Sampling genetically engineered plant tissue for DNA and Protein testing in search of desired traits.
</li>
<li>
Planting engineered cotton seeds and maintaining suitable conditions for proper growth.
</li>
<li>
Preparing buffer solution to extract protein from cotton leaf.
</li>
<li>
Assisting in plant selection, transplanting, plant placement, and plant care.
</li>
<li>
Candidates must work very well with others, pay attention to detail, and be able to stand for long periods of time.
</li>
<li>
Greenhouse work will include, but not be limited to: water monitoring, cleaning, hanging harvest bags and harvesting, fertilizing, pruning, crossing, re-clipping and stringing plants, cleaning and trashing.
</li>
<li>
The environment can be very hot. Candidates must pay attention to detail and be able to stand for long periods of time.
</li>
<li>
You will be working in a team setting but also independently.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Greenhouse Research Technician

<h3>Job Description</h3>
Job DescriptionJob Description 
Strategic ACI is seeking a Senior GIS Application Developer to provide on-site support in designated Government workspaces primarily in the Washington, DC metropolitan and surrounding areas. Staff in this category work independently to develop GIS tools and applications, perform complex analyses, and develop multi- layered maps accomplished by using an appropriate combination of tools found in the GIS application suite and other programming environments.
Responsibilities:
<ul>
<li>Leads application development team.</li>
<li>Works with other members of a program team (i.e. infrastructure, security, etc.) to ensure applications meet Client IT requirements.</li>
<li>Design and implement data conversion procedures and perform software and database quality control.</li>
<li>Work closely with the GIS user community to determine specific application requirements and specifications.</li>
<li>Perform project planning, requirements analysis, database design and development, and quality assurance and quality control.</li>
</ul>
Qualifications:
Required:&nbsp;
<ul>
<li>US Citizen.</li>
<li>Active Secret Clearance.</li>
<li>Bachelor's Degree with at least 6 years of experience in GIS and related development.</li>
<li>Experience in GIS concepts, computer graphics fundamentals, and relational database fundamentals and concepts is essential.</li>
<li>Experience in the development of complex analysis and mapping projects.</li>
<li>Proficient in the coding of software and manipulating digital databases as well as using GIS programming languages, Internet markup languages, and other, pertinent technologies.</li>
<li>The ability to communicate technical information to non-technical computer users, both orally and in writing.</li>
</ul>
, About Strategic Alliance Consulting, Inc 
Strategic Alliance Consulting Inc. is an Equal Opportunity Employer.
It has been and will continue to be a fundamental policy of Strategic ACI not to discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This policy applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination. Applicants can learn more about the company’s status as an equal opportunity employer by viewing the federal EEO is the Law poster.
Why choose a career with Strategic ACI?
Strategic Alliance Consulting, Inc. believes that our greatest asset is our employees. Our goal is not to meet our staff’s expectations, but to exceed them. Competitive salaries, work-life balance, industry leading benefits packages, and family first values are at the core of Strategic ACI’s culture.
Where benefits meet your needs:
<ul>
<li>Competitive salary</li>
<li>100% benefits paid (Includes: Health, Dental, and Vision premiums) for all full-time employees, and their families</li>
<li>401(k) with 5% match vested at day one</li>
<li>PTO – 3 weeks and 3 days per year, increasing at 5 years service&nbsp;</li>
<li>11 Company Paid Holidays (aligned with Federal Government)</li>
<li>Long term/Short term disability</li>
<li>1.5x salary Life Insurance</li>
<li>$100 per month Cellular Device and IT Resource Benefit&nbsp;</li>
<li>$6,000 Cash in Lieu of Benefits per year, if employee is insured elsewhere</li>
<li>Tuition reimbursement of up to $5,250 per year for college or professional certifications</li>
<li>Retirement Savings 401(k) Contribution - Annually calculated as percentage of salary</li>
</ul>

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