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city

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<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>
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.

Sr Associate - Molecular Biology

<h3>Job Description</h3>
Job DescriptionDescription:
ENTRY LEVEL ROLE
On the job training
 
SALARY:
17-18/hr
 
Signing Bonus
$1000 paid after 90 days
 
SHIFT:
Nights: 7p.m.-7:30a.m. (Urgently Hiring)
Days: 7a.m.-7:30p.m.
 
SUMMARY
Tends reactors by performing the following duties.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
<ul>
<li>Weigh and/or measure specific quantities of varying types of ingredients. Mix ingredients in proper sequence and proportions.</li>
<li>Tend mixing equipment and maintain desired control over time, heat, pressure, color or other variables.</li>
<li>May perform blending, filtration and drying operations.</li>
<li>May test according to prescribed procedures and specifications.</li>
<li>Maintain batch, time, weight, color, pressure, heat, production and/or other records as required.</li>
<li>Fill drums and buckets as needed.</li>
<li>Cross training throughout CASE production</li>
<li>Maintain a clean and safe work environment.</li>
<li>Troubleshooting with supervisor to devise solutions to any foreseen difficulties.</li>
<li>Must perform standard duties using the Vantage computer software.</li>
</ul>
 
Teamwork is essential for TSE’s continued success, so Teamwork is an essential function of every employee’s job. Teamwork drives positive results every day. Teamwork promotes positive customer relations and results in exceeding the expectations of our customers. Teamwork benefits every employee since it grows our business and increases our sales. With Teamwork, we all succeed. Without it, we all suffer. Teamwork with co-workers in the same department is just the beginning. Teamwork with every other employee, department and division is the Teamwork that is required to succeed. WE ARE TSE.
Requirements:
SAFETY TRAINING To perform this job successfully, an individual must complete and maintain the following Safety Training requirements.
General Safety Orientation Forklift Safety Training Respiratory Protection Training Confined Space Entry Training Hazard Communications Training HAZWOPER Awareness Training Lock-Out/Tag-Out Training
Personal Protective Equipment Training Hearing Protection Training
Heat Stress Training Machine Guarding Training Fall Protection Training
 
QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION AND/OR EXPERIENCE
High school diploma or general education degree (GED); or one to three months related experience and/or training; or equivalent combination of education and experience. Forklift experience a plus. The employee must complete all applicable departmental training requirements within 90 days to retain this position; this includes all safety programs designed for the Chemical Operator position.
CERTIFICATES, LICENSES, REGISTRATIONS
Must have a valid driver’s license. Forklift experience preferred.
LANGUAGE SKILLS
Ability to read and comprehend simple instructions, short correspondence, memos, and Quality System Documentation. Ability to write simple correspondence. Ability to effectively present information in one-on-one or small group situations.
MATHEMATICAL SKILLS
Ability to add and subtract two-digit numbers and to multiply and divide with 10’s and 100’s. Ability to perform these operations using weight measurement, volume, and distance.
REASONING ABILITY
Ability to apply common sense understanding to carry out detailed tasks or operations, given written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations.
PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; and talk or hear. The employee is occasionally required to reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move more than 100 pounds. Specific vision abilities required by this job include close vision.
Employees in this position are required to wear a full face respirator and comply with TSE Respiratory Protection Program and Title 29 CFR 1910.134. Employees with facial hair or other conditions that would compromise the facepiece-to-face seal cannot work in this position. Examples of these conditions include beards or sideburns that interfere with the facepiece seal or valve function, certain dentures or dental conditions, facial deformities (e.g., scars, deep skin creases, prominent cheekbones), or the use of jewelry or headgear that projects under and interferes with the facepiece seal.
WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is frequently exposed to wet and/or humid conditions, fumes or airborne particles, and toxic or caustic chemicals. The employee is occasionally exposed to high, precarious places and outside weather conditions. The noise level in the work environment is usually moderate.
 
Compensation details: 17-18 Hourly Wage
 
PId3626e1ec893-25405-35851856

CHEMICAL OPERATOR I

<h3>Job Description</h3>
Chemical Production Engineer: Nutriceuticals
Houston, TX
 
Our client, a growing global nutraceutical company, has an opportunity for a Chemical Production Engineer. In this role, you will be responsible for evaluating current processes and optimizing the production capability and reliability to meet business needs as well as leading ongoing efforts to identify and implement process improvement opportunities.
 
Responsibilities:
<ul>
<li>Monitor production processes and identify and resolve deficiencies.</li>
<li>Monitor and trend direct production materials consumption and optimize usage and cost.</li>
<li>Monitor and trend utilities consumption and lead initiatives to optimize usage.</li>
<li>Provide day-to-day troubleshooting support to operations.</li>
<li>Provide process documentation and operating instructions. Issue lessons-learned reporting to operations.</li>
<li>Define and provide technical specifications for process, equipment, and new technology applications.</li>
<li>Assist with the installation, start-up and validation of conformance to design specification for new technology, equipment and processes.</li>
<li>Develop best practices, routines, and innovative solutions to improve production rates and quality of output.</li>
<li>Establish business case, performs risk analysis, and develop detailed opportunities to meet business needs.</li>
<li>Update and maintain relevant documentation for process trending, initiatives, and opportunities.</li>
<li>Report on a regular basis all key information to the management team.</li>
</ul>
 
Requirements:
<ul>
<li>Bachelor's degree in chemical engineering.</li>
<li>Minimum of 5 years of equivalent experience.</li>
<li>Proven manufacturing plant experience, preferably in nutraceutical, pharmaceutical, biotech, or food manufacturing.</li>
<li>Experience with equipment reliability analysis and methods for improvement.</li>
<li>Must understand industry regulatory compliance standards and their application to the manufacturing process.</li>
<li>Knowledgeable of FDA requirements for the industry: HACCP and cGMP (Change control, CAPA, deviation, audit, validation)</li>
<li>Process control &amp; continuous improvement experience.</li>
<li>Experience with Batch and continuous processing.</li>
<li>Experience in applied process design engineering.</li>
<li>Knowledge of interpreting laboratory analytical data related to process.</li>
<li>Knowledge of AutoCAD, simulation software, programing software (ALLEN BRADLEY).</li>
<li>Read, analyze, and interpret common scientific and technical journals, P&amp;ID’s, drawing/designs, and legal documents.</li>
<li>Strong analytical and problem-solving skills (leading root cause analysis).</li>
<li>Proficient with Microsoft Office Suite or related Software.</li>
<li>Experience with project management.</li>
<li>Excellent verbal and written communication skills.</li>
</ul>

Chemical Production Engineer: Nutraceuticals-Houston, TX

<h3>Job Description</h3>
Operations Research Analyst, Senior The Opportunity: As an operations analyst, you're passionate about exploring the root cause of an issue and then analyzing, reporting, and developing recommendations for a creative solution. We need an experienced research analyst like you to help us solve complex problems for our clients. On our military operations and research analysis team, you'll lead the evaluation of data assessment strategies, such as statistical analysis, evaluation, and mission analysis, to deliver solutions. You won't go at it alone, you'll work alongside a team to conduct research, prepare graphs and charts, and analyze and interpret programmatic or cost data such as life cycle cost models and estimates, cost and benefit analyses, M&amp;S outputs, operational data and models, and what-if analysis. Once documented, you'll develop assessments and recommendations to impact future force planning decisions for the Department of Defense. In this role, you'll use your passion for analytics and statistics to devise modeling and measuring techniques utilizing mathematics, statistical methods, engineering methods, operational mathematics techniques, and other principles and laws of scientific and economic disciplines. Use your operations research knowledge combined with your understanding of the Department of Defense to advance the Department's future force planning decisions. Join us. The world can't wait. You Have: 
<ul>\n
<li>5+ years of experience conducting operations research analysis</li>
\n
<li>Experience with the defense management of forces, units, equipment, or infrastructure data</li>
\n
<li>Experience contributing to analytic teams consisting of operations research, data science, and data visualization analysts</li>
\n
<li>Knowledge of the DoD's Planning, Programming, Budgeting, &amp; Execution (PPBE) process and associated data</li>
\n
<li>Ability to communicate effectively and draft clear and concise analysis findings</li>
\n
<li>Top Secret clearance</li>
\n
<li>Bachelor's degree</li>
\n</ul>
\n Nice If You Have: 
<ul>\n
<li>10+ years of experience conducting operations research analysis</li>
\n
<li>Experience supporting the DoD's PPBE process</li>
\n
<li>Experience with software tools such as Tableau, Qlik, or similar</li>
\n
<li>Experience with programming languages or analytical software suites, including Python, SAS, R, MATLAB, or other languages</li>
\n
<li>Knowledge of advanced data science techniques, including the application of Artificial Intelligence and Machine Learning</li>
\n
<li>Master's degree in Mathematics, Statistics, Operations Research, or Data Analytics</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; Top Secret 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 $69,400.00 to $158,000.00 (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.

Operations Research Analyst, Senior

<h3>Job Description</h3>
Summary: 
Responsible for the collection and protection of intellectual property, technical customer support, review and approval of numerous key documents and processes involved in the development of new personal care products. This position requires a science background and an analytical mind with an eye for detail-oriented work.
 
Essential Duties and Responsibilities:
<ul>
<li>Behavior: Exhibit team player qualities of cooperation and coordination; professional interaction in all business contacts, all day, every day</li>
<li>Attendance: Present for work when scheduled is a mandatory function. Work hours may extend pass normal business hours based on the workload of the department.</li>
<li>Safety: Your compliance and enforcement of all company safety rules, procedures and guidelines is essential. Reporting of safety issues is mandatory.</li>
<li>Provide internal and external customer technical support via information and document creating, gathering, dissemination. Manage the collection and dissemination of information for customer specific systems.</li>
<li>Management and maintenance of formulations software including, but not limited to collecting, entering, and updating product formulations, raw materials, components, and vendors.</li>
<li>Review &amp; Approval of key developmental documents which have high impact within the organization and must be accurate: Ingredient Statements, Specification Setups, SAP Group BOM entries, Raw Material Setups, Quantitative Ingredient Statements</li>
<li>Out of Specification investigations including customer 3rd party testing deviations.</li>
<li>Alternate Raw Material review/approval.</li>
<li>Conversion project form generation.</li>
<li>National Brand evaluations and Competitor analysis – physical property testing and organoleptics evaluations.</li>
<li>Provide technical support to lab personnel including but not limited to: Triangle evaluations, SAP assistance, internal software system assistance, and equipment function training (i.e. viscometers and pH meters).</li>
<li>Submission of products for 3rd party review</li>
<li>Reviewing and repurposing 3rd party test reports</li>
<li>Archival of raw material and product documentation in multiple systems</li>
<li>Equipment calibration and maintenance as needed: Viscometers, pH Meters, Thermometers, Incubators</li>
<li>Store checks: Shopping for product samples as needed for product evaluations, 3rd party testing, special projects, etc.</li>
</ul>
 
Supervisory Responsibilities:
None
 
Education Requirements:
A Bachelors Degree in Chemistry or related science; three years of related experience and/or training.
 
Experience Requirements:
<ul>
<li>At least three (3) years of laboratory work or Quality Systems Auditing experience is required in addition to the education requirement. </li>
<li>Proficient in Excel; basic understanding of Word. </li>
<li>Ability to work with mathematical concepts such as probability and statistical inference and apply concepts such as fractions, percentages, and ratios to practical situations </li>
</ul>
 
Competencies:
<ul>
<li>Excellent organizational skills, with the ability to prioritize and execute tasks in a fast paced high volume environment required</li>
<li>Understanding of what it takes to get a basic project to market</li>
<li>Ability to manage basic projects through the organization</li>
<li>Able to report on project progress</li>
<li>Solid understanding of the commercialization process</li>
<li>Preference towards collaborating on group projects rather than working individually</li>
<li>High standards for quality of work</li>
<li>Enthusiastic, with a positive attitude and passion for innovation</li>
<li>Strong information management and communication skills</li>
<li>Efficient management of time and use of resources</li>
<li>Inspires confidence and trust by being dependable and honest</li>
<li>Intrinsic drive to support team goals by learning and applying new skills and concepts</li>
<li>Good listening skills and willingness to accept constructive criticism and learn from mistakes</li>
<li>Logical approach to judgement and decision making based on original thinking, direct experience, and high quality, independently verifiable evidence</li>
<li>Eager to learn </li>
<li>Excellent written and verbal communication skills are critical</li>
<li>Ability to deal with ambiguity</li>
<li>Exhibit a team based approach</li>
<li>Interpersonal savvy</li>
<li>Priority setting</li>
<li>Process management</li>
<li>Drive for results</li>
</ul>
 
Certificates, Licenses, Registrations:
DOT Hazmat certification and GHS SDS certification may be provided.
 
Travel: 
Limited
 
Work Environment: 
This job operates in a professional laboratory and office environment. This role routinely uses standard office equipment and standard laboratory equipment such as hot plates, pH meter, viscometer, Ross miles foam height apparatus, mixers, balances, computers, phones, photocopiers, filing cabinets and fax machines. 
 
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to fingers, handle or feel; and reach with hands and arms. Frequently lifts 5-50lbs packages from floor to shelf, table, or cart.

R & D - Formulation Chemist

<h3>Job Description</h3>
EMM Research is seeking a dynamic and self-motivated Research Associate to join our team in New York City. As a Research Associate, you will play a crucial role in supporting our investment banking operations by providing comprehensive research and analytical support to assist our clients and decision-makers.
 
Responsibilities:
<ul>
<li>Conduct comprehensive market research and analysis, delivering valuable insights into diverse industry sectors, market trends, and investment opportunities.</li>
<li>Gather and synthesize financial data, market reports, and relevant information from various sources to facilitate informed decision-making</li>
<li>Prepare concise and informative research reports, presentations, and investment memoranda for clients and internal stakeholders</li>
<li>Stay updated on industry news, regulatory changes, and economic developments, and provide timely updates to the team</li>
<li>Collaborate with team members to ensure the delivery of high-quality research and analysis</li>
<li>Proactively track project progress and updates in the internal ticketing system, ensuring accurate documentation of events such as calls, meetings, and activity uploads</li>
<li>Utilize timers on all work to accurately capture time spent on tasks and projects, contributing to efficient project management and resource allocation</li>
</ul>
 
Requirements:
<ul>
<li>Bachelor's degree in history, library studies, communications, or a related field</li>
<li>At least one year of corporate experience</li>
<li>Strong analytical and quantitative skills</li>
<li>Excellent communication, both written and verbal</li>
<li>Self-motivated and able to work independently as well as in a team</li>
<li>Demonstrated ability to meet deadlines and manage multiple tasks simultaneously</li>
<li>4x on site, 1 day remote | Central NYC location</li>
</ul>
 
If you are a dedicated and enthusiastic professional looking to advance your career EMM Research offers an exciting opportunity to work with a dynamic team in the heart of New York City.

Research Associate

<h3>Job Description</h3>
Job Summary:
Our client is seeking Lab Technician – Biology/Microbiology to join their team! This position is located in St. Louis, Missouri.
 
Duties:
<ul>
<li>Document microorganisms in online databases</li>
<li>Develop and implement in planta and in vitro assays</li>
<li>Implement sterile techniques throughout the entire pipeline</li>
<li>Prepare different substrates and growth mediums</li>
<li>Keep good data records and ensure proper labeling</li>
</ul>
 
Desired Skills/Experience:
<ul>
<li>Bachelor's degree in Biology, Microbiology, Microorganism, etc.</li>
<li>Able to work in a fast-paced environment and with a dynamic team</li>
<li>Comfortable working independently and within a team</li>
</ul>
 
Benefits:
<ul>
<li>Medical, Dental, &amp; Vision Insurance Plans</li>
<li>Employee-Owned Profit Sharing (ESOP)</li>
<li>401K offered</li>
</ul>
 
The approximate pay range for this position starting at $43,000. Please note that the pay range provided is a good faith estimate. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and location. We comply with local wage minimums.

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