field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionAnalyst III (Hybrid – Detroit, MI)Pay Rate: $39.00/hour Type: Long-Term Contract (Possible Extension or Direct Hire) Benefits: Available Description: We are seeking an experienced Analyst III to support our Preventative Maintenance Organization Start-Up Group. This role will focus on problem solving, process creation, documentation, and work order reviews to optimize business systems and workflows. The successful candidate will combine technical expertise with business acumen to bridge user needs and system capabilities. Responsibilities:
<ul>
<li>Review, analyze, and evaluate business systems and user requirements.</li>
<li>Document and translate business processes clearly using process mapping and other tools.</li>
<li>Write detailed user requirements, program functions, and steps required to develop or modify computer programs.</li>
<li>Collaborate with business stakeholders to gather and define requirements.</li>
<li>Coordinate tasks with others as needed to ensure timely project completion.</li>
<li>Apply knowledge of accounting or finance concepts to solve business challenges in preventative maintenance and operations.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in a relevant field.</li>
<li>5–7 years of experience gathering business system requirements and documenting processes.</li>
<li>Strong PC skills and knowledge of MS Office tools.</li>
<li>Experience in accounting or finance (minor, coursework, or practical experience).</li>
<li>Strong analytical, problem-solving, and communication skills.</li>
</ul>
Work Location: Hybrid – Detroit, MI Company DescriptionUsing the best business practices obtained from many years of experience in Business, Law, and Recruiting and Staffing, the Founders at CrossFire Group (“CrossFire”) started in downtown Royal Oak, MI more than a decade ago. With backgrounds in Information Technology (IT) and the Legal Industry, CrossFire began placing by IT and Legal Professionals in contract and direct-hire positions throughout the Midwest. Since our founding, CrossFire has grown into a full-service Human Capital Solutions Organization. We are proud of now providing full services beyond recruiting and staffing. Our portfolio of services includes HR supply chain management, human resources consulting, and many customized Human Resource related services. 
<h3>Company Description</h3>
Using the best business practices obtained from many years of experience in Business, Law, and Recruiting and Staffing, the Founders at CrossFire Group (“CrossFire”) started in downtown Royal Oak, MI more than a decade ago. With backgrounds in Information Technology (IT) and the Legal Industry, CrossFire began placing by IT and Legal Professionals in contract and direct-hire positions throughout the Midwest.\r\n\r\nSince our founding, CrossFire has grown into a full-service Human Capital Solutions Organization. We are proud of now providing full services beyond recruiting and staffing. Our portfolio of services includes HR supply chain management, human resources consulting, and many customized Human Resource related services.

Analyst III

<h3>Job Description</h3>
MSR Technology Group DBA Infomatics has been an Inc 500/5000 corporation for the last 7 years in a row. We have an urgent need for Electronics Research Engineer, and this is an Onsite role in Ann Arbor, MI. Please find the job details below.
 
Title: Electronics Research Engineer
Location: Ann Arbor, MI
Duration: Long Term Contract 
Pay Rate: $45 per hour on W2 
 
Job description (Duty &amp; Responsibility):
<ul>
<li>Conduct work to meet project targets and key performance indicators (e.g. reports, and project milestones)</li>
<li>Design and develop custom electronic circuits for proof-of-concept devices and demonstration units, create schematic diagrams, PCB layouts, and component specifications. Perform circuit simulation and analysis using industry-standard tools.</li>
<li>Design compact, robust packaging solutions for electronic assemblies. Ensure electromagnetic compatibility (EMC) and shielding requirements. Collaborate with team mates on enclosure design, thermal control and integration.</li>
<li>Design control circuits for laser systems and optical components. Implement laser safety protocols and interlock systems. Develop precision timing and synchronization circuits for chip-scale laser applications.</li>
<li>Work with vendors to build and test prototype circuits and assemblies. Conduct performance validation and troubleshooting. Document test procedures and results</li>
<li>Ability to work within and contribute to cross-disciplinary research teams with key deliverables including prototypes, intellectual property, and publications (an active interest in publishing is highly desirable)</li>
<li>Willingness to participate in, support, and contribute to work-place safety culture and activities.</li>
</ul>
 
Requirements:
<ul>
<li>Required minimum education and experience:</li>
<li>Doctorate in Electrical Engineering or other applicable area, or Masters in Electrical Engineering with equivalent experience.</li>
</ul>
 
Requirements:
<ul>
<li>Circuit Design: Proficiency in analog and digital circuit design, mixed-signal systems, understanding of RF</li>
<li>CAD Tools: Experience with Altium Designer, KiCad, or similar PCB design software</li>
<li>Simulation: Knowledge of SPICE, LTSpice, or equivalent circuit simulation tools</li>
<li>Programming: Familiarity with programming (C/C++, Python) to drive circuits via lab bench</li>
<li>Test Equipment: Proficiency with oscilloscopes, spectrum analyzers, network analyzers, and laser measurement equipment</li>
</ul>
 
Preferred Skills:
<ul>
<li>Experience with integrated photonic interconnect.</li>
<li>Familiarity with 3D modeling software (SolidWorks, AutoCAD).</li>
<li>Experience with rapid prototyping techniques (3D printing, CNC machining).</li>
<li>Background in RF/microwave circuit integration.</li>
<li>Familiarity with work style of research institutes.</li>
</ul>
 
If you have the above skills/experience, please share your resume in confidence to:
 
Recruiter Name: Sravan
Email: <a href="mailto:sravan@msrtechnologies.com" target="_blank">sravan@msrtechnologies.com</a>
 
EOE

Electronics Research Engineer

<h3>Job Description</h3>
Job Title: Formulation Scientist – Skin Health
Duration: 12-Month Contract
Work Hours: Monday – Friday, 8:30 AM – 5:00 PM
Locations: Skillman, NJ 08558 (4 days/week) / Summit, NJ 07901(1 day/week; may fluctuate based on business needs)
 
Position Summary
We are seeking a motivated and detail-oriented Product Development Scientist to join our client’s Skin Health division. The successful candidate will be responsible for hands-on formulation work, batch processing, and laboratory testing to support new product development. This position requires strong organizational skills, technical documentation, and collaboration with cross-functional teams in a dynamic product development environment.
 
Key Responsibilities
<ul>
<li>Prepare and process a high volume of formulation batches in the laboratory.</li>
<li>Perform formulation and product development activities at both Skillman and Summit sites.</li>
<li>Conduct laboratory testing, evaluations, and stability studies to ensure product quality and performance.</li>
<li>Maintain accurate and detailed documentation of experimental data and batch records.</li>
<li>Organize, label, and deliver product samples as required.</li>
<li>Follow established formulation guidelines and equipment setup procedures.</li>
<li>Support product scale-up and process optimization activities.</li>
<li>Ensure compliance with technical standards, regulatory requirements, and project timelines.</li>
</ul>
 
Education:
<ul>
<li>Bachelor’s degree in Chemistry, Chemical Engineering, or a related scientific discipline.</li>
</ul>
 
Experience:
<ul>
<li>Minimum 2 years of formulation experience (inclusive of internship and industry experience).</li>
<li>Experience in product development preferred but not mandatory.</li>
<li>Knowledge of basic raw materials and lab equipment setup.</li>
<li>Prior experience in skin care or consumer goods is a plus but not required.</li>
<li>Strong analytical, problem-solving, and time management skills.</li>
<li>Excellent documentation and communication abilities.</li>
<li>Flexibility to work between multiple lab locations as needed.</li>
</ul>
 
Interview Process
<ul>
<li>Virtual interview conducted via Microsoft Teams.</li>
</ul>

Formulation Scientist

<h3>Job Description</h3>
Subsurface Geologist
 
Location: Remote – Houston, TX
&amp;#x1F539; Highlights
<ul>
<li>Interpret seismic and well data to define reservoir structure and quality</li>
<li>Collaborate with drilling and reservoir teams for field development planning</li>
<li>Drive geologic modeling to support exploration and production</li>
</ul>
 
&amp;#x1F6E0;️ Job Overview
The Subsurface Geologist integrates geophysical, geological, and petrophysical data to characterize reservoirs and identify development opportunities. You’ll generate 3D geologic models, interpret logs, and advise drilling on target selection and risk assessment. This role requires strong technical skills, an analytical mindset, and experience translating data into actionable field development insights.
 
&amp;#x1F393; Requirements
<ul>
<li>Bachelor’s or Master’s in Geology, Geophysics, or Earth Sciences</li>
<li>7+ years of experience in subsurface mapping and stratigraphic interpretation</li>
<li>Proficiency in Petrel, Kingdom, or GeoFrame</li>
<li>Strong understanding of basin analysis and structural geology</li>
<li>Experience working in unconventional or tight-rock plays</li>
</ul>
 
&amp;#x1F305; About Us + Why Join Us
We are redefining the way geoscience and engineering intersect — using data and innovation to create smarter, more sustainable energy solutions. Join a collaborative team that values curiosity and technical excellence.

Subsurface Geologist

<h3>Job Description</h3>
Company Description
Veolia is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia designs and implements innovative solutions for decarbonization, depollution, and resource regeneration, supporting communities and industries in their ecological transformation.
 
Within this framework, Water Tech brings together a dedicated team of experienced professionals committed to tackling the world’s most complex challenges related to water scarcity, quality, productivity, and energy.
Together, we pursue a shared mission to create a more sustainable future.
 
Job Description
As a Junior Process Chemist, you will work closely together with the Manufacturing plants, Technology, Global Engineering and Regional Quality and EHS functions to support variable process chemistry activities related to high risk operations and chemical manufacturing operations. You will coordinate the NAM tolling activities for products for which Veolia does not have the in-house capabilities.
 
In this critical role, you’ll provide technical guidance, direction and training to plant staff and operators on process chemistry and process safety, ensuring awareness and adhesion to operational parameters and safety limits. You’ll lead and provide onsite support for new and/or improved processes, provide on-time coverage for troubleshooting, participate in root cause analysis and implement corrective and preventive actions.
 
Additionally, you will be responsible for supporting different new business opportunities, manufacturing process optimization, and cost-out initiatives in the business. If you like the idea of doing meaningful work with a company that’s doing big things to create a cleaner, more sustainable world for us all, here’s more!
 
Key Characteristics:
<ul>
<li>Serves as regional process chemistry expert, representing global standards in meetings and projects while ensuring safety requirements and operational consistency across manufacturing sites.</li>
<li>Leads tolling strategy and execution, including supplier qualification, SOP development, audits, and scale-up support to optimize cost and quality outcomes.</li>
<li>Champions process safety initiatives and continuous improvement through implementation of hazardous material standards, safety programs, and lean/digital optimization methods.</li>
</ul>
Duties &amp; Responsibilities 
<ul>
<li>Represent Global Process Chemistry in team meetings and projects to ensure process chemistry and process safety requirements are covered from a regional point of view while ensuring consistency with global standards.</li>
<li>Support Cost-out initiatives by investigating the best operational strategy, in-house production vs tolling.</li>
<li>Coordinate the regional tolling activities by assembling and providing toll manufacture SOPs, conducting onsite EHS and Quality audits, and following up on completion of corrective actions. Being a critical part of the qualification team through the entire qualification process, providing guidance and support during scale-up trials, ensuring safe operation, and delivering products meeting quality expectations.</li>
<li>Implement the company’s internal standards for hazardous processes (e.g. flammable materials, combustible dust handling and neutralization reactions) in cooperation with the Process Safety Chemist and support the manufacturing sites during plant upgrades.</li>
<li>Implement, maintain, and improve all aspects of the company's process safety program.</li>
<li>Drive and support continuous system and process improvements based on Digitization and Lean Six Sigma methodology.</li>
</ul>
Qualifications
Knowledge, Skills &amp; Abilities:
<ul>
<li>Knowledge:</li>
<li>Expert understanding of process chemistry principles and global safety standards</li>
<li>Comprehensive knowledge of chemical manufacturing processes and hazardous material handling</li>
<li>In-depth understanding of quality management systems and audit procedures</li>
<li>Advanced knowledge of Lean Six Sigma methodology and digital optimization tools</li>
<li>Thorough understanding of tolling operations and supplier qualification processes</li>
<li>Skills:</li>
<li>Ability to develop and implement process safety programs and protocols</li>
<li>Proficiency in conducting EHS and quality audits</li>
<li>Strong analytical skills for cost-benefit analysis and operational strategy development</li>
<li>Excellence in SOP development and documentation</li>
<li>Advanced project management capabilities</li>
<li>Skilled in digital tools and process improvement methodologies</li>
<li>Abilities:</li>
<li>Capacity to lead cross-functional teams and influence stakeholders</li>
<li>Ability to balance multiple projects while maintaining attention to detail</li>
<li>Capability to translate technical requirements into practical applications</li>
<li>Strong problem-solving abilities in complex manufacturing environments</li>
<li>Excellent communication skills for presenting technical information to various audiences</li>
</ul>
Education &amp; Experience Required:
<ul>
<li>Master's Degree in Science, Chemistry, or Chemical Engineering (or equivalent experience)</li>
<li>Proven experience with chemical plant processes and process safety protocols</li>
<li>Demonstrated ability to develop and conduct Process Safety training programs</li>
<li>Track record of promoting and maintaining safety compliance culture in chemical industry settings</li>
<li>Experience in conducting quality and compliance audits</li>
<li>Strong verbal and written communication skills</li>
<li>Willingness and ability to travel up to 10% of time</li>
</ul>
Preferred:
<ul>
<li>Two (2) years of professional experience with chemical manufacturing operations</li>
<li>Knowledge of industry safety standards and regulations</li>
<li>Familiar with NFPA 30 standard, OSHA regulations, Process Safety Management</li>
<li>Familiar with Brilliant fulfilment / Lean Manufacturing / Six Sigma</li>
<li>Expertise with chemical process instrumentation</li>
<li>Knowledge of SAP is helpful</li>
</ul>
Additional Information
At Veolia, we realize diverse teams make smarter decisions, deliver better results, and build stronger
communities. We’re an organization that champions diversity and inclusion at every rung of the ladder
and are proud to be an equal opportunity workplace. 
● Medical, Dental, &amp; Vision Insurance Starting Day 1!
● Life Insurance
● Paid Time Off
● Paid Holidays
● Parental Leave
● 401(k) Plan - 3% default contribution plus matching!
● Flexible Spending &amp; Health Saving Accounts
● AD&amp;D Insurance
● Disability Insurance
● Tuition Reimbursement
 
Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this
posting. The Company reserves the right to modify this information at any time, subject to applicable
law.
****Applicants are required to be eligible to lawfully work in the U.S. immediately; employer will not
sponsor applicants for U.S. work authorization (e.g. H-1B visa) for this opportunity****
VWTS does not accept unsolicited resumes from external recruiting firms. All vendors must have a
current and fully executed MSA on file before submitting candidates. Any unsolicited resumes and
candidate profiles will be deemed the property of VWTS, and no fee will be due.

NAM JR Process Chemist

<h3>Job Description</h3>
Job Description
We are looking to hire a Medical Physicist who will be primarily located at the Oncology Paris Cancer Center, which is a community-based cancer center treating an average of 40 patients per day.
Additionally, the center has very active PSI and HDR programs, treating more than 300 HDR treatments per year
The Paris radiation therapy team consists of one Radiation Oncologist, one Chief Medical Physicist, two site Medical Physicists (shared across the region), two Dosimetrists, three Radiation Therapists, and one CT Technologist.
While operationally independent, the center is part of a network POD that consists of two nearby, fully staffed, centers located in Mt Pleasant and Greenville in the North East Texas region.
Periodic travel to the other two sites is required based on the POD dynamic and staff coverage.
Responsibilities
The essential responsibilities beyond daily clinical tasks include:
<ul>
<li>Periodic evaluation of all equipment for continued utility, appropriateness, reliable performance, age, and condition to make recommendations on practical life span, obsolescence, and replacement</li>
<li>Contribute to the design and implementation of all aspects of the quality management program that includes the use of external beam radiotherapy equipment as well as the review and proposal of changes to procedures followed by radiation therapy staff</li>
<li>Assist in the management of radiation oncology information systems, including development of usage protocols, maintenance, and data storage</li>
<li>Radiation safety duties for the practice, including assisting with employee monitoring, reports, and regulatory issues</li>
<li>Lead or participate in clinical projects to improve department processes or patient treatments</li>
</ul>
Preferred Experience:
<ul>
<li>Eclipse, and Oncentra treatment planning systems</li>
<li>HDR planning and treatment.</li>
<li>ARIA ROIS and Mosiaq ROIS</li>
<li>SBRT and SRS procedures</li>
</ul>
Qualifications
The ideal candidate will have
<ul>
<li>CAMPEP Accredited Residency Program in Medical Physics</li>
<li>Valid Texas Medical Board license</li>
<li>American Board of Radiology certification or board eligible</li>
<li>Preferred two years of experience as a certified medical physicist</li>
<li>Working knowledge of SRS, SBRT, and HDR</li>
<li>Experience with Varian linear accelerators</li>
<li>Experience with Eclipse Planning system</li>
<li>Experience with Oncentra Planning system</li>
<li>Strong organization and oral / written communication skills</li>
</ul>
Required Citizenship / Work Permit / Visa Status US Citizen / Green Card holder
Must-Haves CAMPEP Accredited Residency Program in Medical Physics Valid Texas Medical Board license American Board of Radiology certification or board eligible Preferred two years of experience as a certified medical physicist

Medical Physicist

<h3>Job Description</h3>
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Lead Scientist I, Manufacturing Sciences for Cytiva is responsible cross functional work with manufacturing, product engineering, R&amp;D, QC, RRP and the customer to develop new processes within manufacturing to successfully produce new custom products, support manufacturing through improvements to our processes, and support quality investigations
This position is part of the Manufacturing Sciences located in Logan, UT and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
<ul>
<li>
Utilize knowledge of chemistry, biology and manufacturing to manage custom cell culture media qualification for pharma customers
</li>
</ul>
<ul>
<li>
Identify, develop and qualify current process improvements to ensure first time success with new custom cell culture media products
</li>
</ul>
<ul>
<li>
Use Broad expertise in biotechnology and manufacturing to resolve urgent issues with current and new custom products and drive to root cause and effective corrective actions
</li>
</ul>
<ul>
<li>
Prepare and present written and oral presentations for new product processes and applications both internally and externally
</li>
</ul>
<ul>
<li>
Drive projects with manufacturing, QC, QA, QE to implement process changes and improvements to ensure first time success for each new custom product
</li>
</ul>
Who you are:
<ul>
<li>
MS in Biology, Biochemistry or related field with 3+ years experience
</li>
<li>
Experience with cell culture techniques, filtration processes and biochemical analytical techniques.
</li>
<li>
Excellent oral and written communication skills
</li>
</ul>
It would be a plus if you also possess previous experience in:
<ul>
<li>
Cell culture media manufacturing experience
</li>
</ul>
LI#KP1
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

Lead Scientist I, Manufacturing Sciences

<h3>Job Description</h3>
All-Source Intelligence Analyst The Opportunity: Our clients need skilled analysts to turn reams of data into actionable intelligence for our government and military every day. If you have strong analytical skills and a problem-solving mindset, are familiar with IC analytic standards, and are ready to help our nation's leaders understand the critical threats and opportunities facing our country, we have an opportunity for you. Join our team as an All-Source Intelligence Analyst. In this role, you'll review reporting from classified and unclassified intelligence streams every day as you build assessments that reflect the priorities of your portfolio. You'll develop specific products by request and propose your own, coordinate with analysts on our team and across the intelligence community (IC), and brief warfighters, senior policymakers, and IC members on our analytic lines. Thanks to our mentoring and training resources, you'll also be able to hone your skills and mature into a stronger analyst. Our world is shifting quickly, and our clients need analysts who can help them stay several steps ahead. Join us. The world can't wait. You Have: 
<ul>\n
<li>Experience in strategic all-source intelligence analysis</li>
\n
<li>Experience with all-source intelligence analysis or U.S. government all-source analytic production</li>
\n
<li>Experience with the Modernized Integrated Database (MIDB) or the Machine-Assisted Rapid-repository System (MARS)</li>
\n
<li>Knowledge of the DoD and wider IC</li>
\n
<li>Ability to develop high-quality deliverables, such as complex written products and formal or informal briefings tailored to clients who range from tactical to strategic levels, including actionable leads</li>
\n
<li>Active TS/SCI clearance; willingness to take a polygraph exam</li>
\n
<li>HS diploma or GED and 6+ years of experience with all-source analysis, Associate's degree and 4+ years of experience with all-source analysis, or Bachelor's degree and 3+ years of experience with all-source analysis</li>
\n</ul>
\n Nice If You Have: 
<ul>\n
<li>Experience as a C4I all-source intelligence analyst</li>
\n
<li>Experience as a telecommunications infrastructure intelligence analyst</li>
\n
<li>Experience providing support for identifying, locating, and tracking deployment of foreign mobile signal, electronic warfare, and SIGINT units that support joint or national C4I functions</li>
\n
<li>Experience with OSINT or GEOINT</li>
\n
<li>Knowledge of the INDOPACOM AOR</li>
\n
<li>TS/SCI clearance with a polygraph</li>
\n
<li>Bachelor's degree in International Affairs, Political Science, Foreign Area Studies, or National Security Studies preferred; Master's degree in International Affairs, Political Science, Foreign Area Studies, National Security Studies, or a related research field a plus</li>
\n</ul>
\n Clearance: Applicants selected will be subject to a security investigation and may need to meet eligibility requirements for access to classified information; TS/SCI clearance is required. Compensation At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen's benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page. Salary at Booz Allen is determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The projected compensation range for this position is $62,000.00 to $141,000.00 (annualized USD). The estimate displayed represents the typical salary range for this position and is just one component of Booz Allen's total compensation package for employees. This posting will close within 90 days from the Posting Date. Identity Statement As part of the application process, you are expected to be on camera during interviews and assessments. We reserve the right to take your picture to verify your identity and prevent fraud. Work Model Our people-first culture prioritizes the benefits of flexibility and collaboration, whether that happens in person or remotely. 
<ul>\n
<li>If this position is listed as remote or hybrid, you'll periodically work from a Booz Allen or client site facility.</li>
\n
<li>If this position is listed as onsite, you'll work with colleagues and clients in person, as needed for the specific role.</li>
\n</ul>
\n Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, local, or international law.

All-Source Intelligence Analyst

<h3>Job Description</h3>
Immediate need for a talented Research Associate Scientific I. This is a 12+ months contract opportunity with long-term potential and is located in Round Lake, IL(Onsite). Please review the job description below and contact me ASAP if you are interested.
 
Job ID: 25-89627
 
Pay Range: $28 - $30/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
 
Key Responsibilities:
 
<ul>
<li>Conduct critical chemical and physical analyses on finished product R&amp;D stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&amp;D initiatives. Work under minimum supervision.</li>
<li>Perform chemical assays requiring precise analytical skills and understanding of chemistry principles.</li>
<li>Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules.</li>
<li>Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.</li>
<li>Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.</li>
<li>Use sophisticated laboratory instrumentation (HPLC, pH, UV, titrations, Particle, TOC, Flame photometry, etc) and computer systems to collect and record data.</li>
<li>Follow, understand and comply with *** SOP’s and policies on cGMP’s and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.</li>
<li>Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.</li>
</ul>
 
Key Requirements and Technology Experience: 
 
<ul>
<li>Key skills; Laboratory , Regulatory , Research</li>
<li>Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences, biology) 6 months or more of experience</li>
<li>Analytical chemistry instrumentation experience with pH, UV, titrations, Particle, TOC is preferred but not required.</li>
<li>Must have experience in a regulated environment and strong technical problem-solving skills.</li>
<li>Must have good oral and written communication skills, strong analytical skills and be detail oriented.</li>
<li>Electronic Lab Notebook experience is preferred but not required.</li>
<li>Pharmaceutical GMP laboratory experience is desired.</li>
<li>Empower experience is preferred</li>
<li>Must be able to handle multiple tasks concurrently and in a timely fashion.</li>
<li>Possess relevant laboratory/technical, writing, and computer skills.</li>
<li>Ability to organize and communicate complex information effectively with managers and peers</li>
<li>This is an on-site position.</li>
<li>Physical Activities and Requirements:</li>
<li>Must be able to hand write and use computers for the majority of the work day</li>
<li>Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing</li>
<li>May require standing for extended periods</li>
<li>Must be able to lift up to 10 pounds routinely</li>
<li>Must not be color blind</li>
</ul>
 
Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
 
By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

Research Associate Scientific

<h3>Job Description</h3>
Sr. Associate - Molecular Biology
Thousand Oaks, CA - onsite
3 month contract - possible extension
Pay Rate: $26/hr
 
Job Description:
Key responsibilities include:
1. Follow and execute molecular biology workflows (microbial cell culture, DNA purification, PCR) and operate automated laboratory robotic systems for high-throughput sample preparation and screening.
2. Organize and document laboratory data and experiments in electronic laboratory notebooks
3. Laboratory management (ordering and inventory of consumables)
 
Day to Day Responsibilities:
Execute molecular biology workflows: microbial cell culture, DNA/RNA purification, PCR/qPCR, and sample QC.
Operate, program, and maintain automated laboratory robotic systems for high-throughput sample prep and screening; perform routine calibrations and first-line troubleshooting.
Organize, analyze, and document experiments and results in electronic laboratory notebooks (ELNs) with strong data integrity practices.
Manage laboratory operations: track inventory, order consumables/reagents, receive and label materials, and maintain a clean, safe work environment.
Collaborate cross-functionally to schedule runs, align on assay requirements, and communicate results and issues promptly.
Adhere to safety, biosafety, and quality standards; contribute to SOP writing and continuous process improvement.
 
Basic Qualifications
Master’s degree
OR
Bachelor’s degree and 2 years of experience
OR
Associate’s degree and 4 years of experience
OR
High school diploma / GED and 6 years of experience
 
 
Top 3 Must Have Skill Sets:
Must-Have Skills
1. Molecular biology techniques – PCR, microbial culture, DNA purification.
2. Wet-lab work within last 24 months (no classroom-only experience).
3. Automation experience using platforms such as Hamilton, Tecan, Bravo, or similar.
 
Core molecular biology proficiency: microbial culture, nucleic-acid purification, PCR/qPCR, and basic assay troubleshooting.
 
Laboratory automation experience: operating and maintaining automated liquid handlers/robotic systems for high-throughput workflows (e.g., setup, method execution, error recovery).
 
Data rigor &amp; documentation: accurate, timely ELN record-keeping; organizing datasets, following SOPs, and communicating results clearly.

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