Css Scientific Jobs in Usa

Kelly Science and Clinical FSP is currently seeking a Clinical Scientist for a long-term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.

Clinical Scientist

(Clinical Research/Clin Ops)

Description of Services

• Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g, adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management
• May support a single study or multiple studies
• May lead a study with limited scope (e.g., Survival Follow-up)
• May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Minimum Years of Experience

• At least 2 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years, required
• TA-specific experience required for postings in Oncology. TA-specific experience in IDV and GSM preferred
• Indication specific experience preferred
• Experience reviewing and resolving study related data issues such as: issued queries, resolved queries, accurate review of medical records, identify any errors in data by performing data review that require further clarification with the study sites, etc., required
• Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience, preferred
• Demonstrated oral and written communication skills
• Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required. One Note experience preferred.

Educational Requirements

• Degree in Life Sciences
• BS/BA/MS/PhD

Biologist/Environmental Scientist – New Mexico

Location: Southwestern New Mexico

Base: Deming, New Mexico

Landhawk Consulting LLC is seeking several Biologists/Environmental Scientists to join our growing environmental and cultural resources team in New Mexico. Established in 2012, Landhawk is a multidisciplinary environmental consulting firm of 25 professionals with expertise spanning natural resources, cultural resources, and water resource management. Our team includes wildlife biologists, archaeologists, environmental scientists, aquatic ecologists, and permitting specialists who support infrastructure and compliance projects across Texas and the greater Southwest.

The successful candidate will assist in biological regulations compliance, construction monitoring, and biological surveys within the New Mexico border region. This position offers hands-on experience working with diverse environmental projects in support of state and federal environmental compliance programs.

Position Details and Expectations

Interested candidates should submit a detailed resume or CV, along with unofficial transcripts, outlining relevant field and project experience such as biological survey work, construction monitoring, and biological resource documentation in New Mexico and the surrounding border region. Candidates should have experience or interest in endangered plant species survey, nesting bird surveys, and biological resource monitoring in support of environmental compliance. Familiarity with the avian communities and flora of southwestern New Mexico.

Responsibilities:

• Perform routine inspections and oversee construction to ensure compliance with environmental regulations

• Monitor the state and condition of stormwater related best management practices (BMPs)

• Conduct biological monitoring

• Assist with vegetation surveys

• Perform weekly migratory nesting bird surveys

• Relocate wildlife including but not limited to protected reptile species, injured birds, and some aquatic organisms when found

• Produce daily, and occasionally weekly reports regarding information collected from field inspections

• Conduct biological surveys

Minimum Qualifications:

o Valid state driver's license

o Bachelor's degree in biology, environmental science, or related fields of study

o Excellent writing skills

o High attention to detail

o Ability and willingness to travel periodically in Texas

o Ability to meet deadlines consistently

o Proficient in MS Office Suite

o Ability to work effectively with remote staff

o Ability to work with minimal supervision

o Must be able to pass a background check

Preferred qualifications include:

 Experience identifying native flora and fauna found in New Mexico.

 2 years of experience conducting a combination of biological monitoring surveys, migratory nesting bird surveys, vegetation surveys, and stormwater BMP inspections.

Compensation and Benefits:

- Landhawk Consulting offers competitive compensation tailored to each candidate's experience, qualifications, and technical expertise.

- Positions may be full-time or part-time, with hybrid and field-based assignments primarily in New Mexico and surrounding regions.

- 15 days paid vacation, up to 40 hours of annual sick leave, and 11 paid holidays are provided to salaried employees.

- Retirement plan with employer match.

- Access to in-person and virtual training programs, mentorship, and career development opportunities.

- Paid travel time, GSA per diem, and mileage reimbursement.

- Bonuses may be available based on performance and project contributions.

Background Check Notice:

All employment offers are contingent upon the successful completion of a background check. This may include verification of employment history, education credentials, driving record, and criminal background review.

About Landhawk Consulting:

Founded in 2012, Landhawk Consulting LLC is a multidisciplinary environmental consulting firm providing services across Texas and the greater Southwest. Our team of 25 professionals includes experts in natural resources, cultural resources, and water resource management. Landhawk's archaeologists, biologists, environmental scientists, and permitting specialists work collaboratively to support infrastructure, compliance, and conservation projects for public and private clients.

We are committed to delivering high-quality, defensible work products and fostering a culture of professionalism, mentorship, and scientific excellence across every discipline we serve.

Conducts Research and product development activities for all BQ manufactured products. Brings key skills and knowledge in new product ideas/concepts and troubleshooting. Able to initiate product and /or processing concepts from idea to final production start-up. Spearhead new technology development and its application into all baked good areas. Develop and implement productivity project. Chef-oriented professional with culinary knowledge to support product development through planning, preparation, and execution of customer demonstrations.

Key Job Responsibilities:

• Strong ability to independently develop bakery formulations with hands on bench scale bakery product development and ability to scale up to commercial level.
• Ability to work in fast paced environment and manage multiple projects at a time.
• Introduction of new products and processes to BQ bakeries, Collaborate and influence internal and external project teams (Teams are made up of R&D, Product Developers, Project Managers, Quality, Regulatory, Engineering, Packaging, Factories, Marketing, Purchasing, and Supply Chain, etc.) to develop, industrialize, and launch Innovation and Renovation projects. Do a robust complaint reduction exercise and mitigate key risks and ensure vertical start up.
• Design and execute experimentation using established procedures, interpret results and translate results into possible solutions. Describe/demonstrate research results or experimental protocols to colleagues in a professional manner.
• Contribute to key product improvement, cost reductions, new products, development, knowledge building or other technically based, business driven objectives.
• Strong ability to collaborate with other team member and cross functional partners, proactively benefiting from team members technical abilities and being adaptive to ensure speed and agility.
• Advise and guide, other R&D team members and other departments throughout BQ, on scientific/technical matters as necessary.
• To prepare product and process specifications and process operating guides for new product launches and existing products as required. Ensure effective knowledge transfer to bakeries and operations teams and follow up to ensure product consistency and desired production efficiencies are achieved. Interface with operations personnel in all facilities to implement product development objective effectively and efficiently to completion.
• To write reports/memos from time to time on status of developments
• Deal effectively and professionally with outside ingredient and equipment suppliers to meet R&D objectives (keeping Purchasing & Engineering informed).
• Ensure effective communication with all R&D members of product development team and other internal BQ stakeholders.
• To lead in special projects concerning products, processes, equipment, and facility concepts and design.
• Ability to travel as required for bakery trials, internal and external meetings.
• Strong commitment to and support of Bimbo QSR values, ethics, goals, and objectives.
• Plan, prepare, and execute customer demonstrations, including ingredients preparation, show execution and presentation of culinary applications.

______________________________________________________________

Education and Work History:

Education/Certification:

B.S. degree in Grain/Cereal Science, Bakery Science, or Food/Agricultural/Biological Sciences.

Culinary degree or proven experience in customer-facing culinary presentations and product demonstrations

Experience:

• Minimum of 1 year of experience in Research and Development of foods, preferably in the bakery industry. Formulating and/or troubleshooting experience is desired.
• Completion of the AIB Residence course preferred.
• Knowledge of the baking process and functionality of ingredients.
• Proven excellent work record with demonstrated high levels of initiative and self-direction.
• Regulatory affairs: basic knowledge about national and international food regulations of food and its processes.
• Quality Standards: basic knowledge of safety standards (HACCP, FSSC 22000, BRC) and their implications in food development and processing.
• Knowledge of Statistical Process Control, statistical design of experiments, and data collection and analysis preferred.

____________________________________________________________________________

Qualifications and Skill:

• Demonstrated strong problem-solving and critical-thinking skills.
• Excellent organizational and communication (written and oral) skills.
• Excellent verbal and written communication skills.
• Excellent project management skills with ability to prioritize multiple activities simultaneously.
• Computer skills and proficiency with word processing, spreadsheet, database, and other software/applications.
• Willing to travel as required.

Job Title: Clinical Research Associate (CRA) – Oncology

Location: Boston, MA (Hybrid or Remote, with travel)

Reports to: Director of Clinical Operations

Our client is a Boston-based biotechnology company dedicated to developing innovative oncology therapies that address unmet medical needs. The team is driven by scientific rigor, patient-centricity, and collaboration to advance cutting-edge cancer treatments from early development through late-stage clinical trials.

Position Summary

The Clinical Research Associate (CRA) will support the planning, execution, and monitoring of oncology clinical trials in compliance with ICH-GCP, FDA regulations, and company SOPs. The CRA will serve as a key liaison between investigative sites and the clinical operations team, ensuring data integrity, patient safety, and operational excellence across assigned studies.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials
• Ensure protocol compliance, data accuracy, informed consent integrity, and patient safety
• Monitor AE/SAE reporting, protocol deviations, and essential documentation
• Train and support site staff and maintain strong site relationships
• Review and maintain study documentation and Trial Master File (TMF)
• Track site performance, identify risks, and proactively resolve issues
• Collaborate cross-functionally and provide timely monitoring reports
• Support audit and inspection readiness

Qualifications

• Bachelor's degree/Master's degree in Life Sciences, Nursing, or a related field (required)
• 2+ years of CRA experience in clinical research (oncology preferred)
• Experience monitoring interventional clinical trials (Phase I–III preferred)
• Knowledge of Good Clinical Practices (GCP), clinical monitoring, study site oversight and management.
• Strong knowledge of ICH-GCP and FDA regulations
• Excellent communication, organizational, and problem-solving skills
• Ability to manage multiple sites and travel up to 30%

Offer

• Salary 100-150k (depending on level of experience)
• Career development opportunities in a growing oncology-focused organization
• Collaborative, mission-driven work environment in the Boston biotech hub

Research Technician II — Hall Lab

Are you fascinated by the bizarre world of small, wiggly, often regenerative invertebrates?

The Stowers Institute for Medical Research is seeking a Research Technician II to join the Hall Lab.

Our lab is motivated by the simple premise that we shouldn't be limited to studying biology only in established "model" organisms. We are developing a suite of molecular and imaging tools to enable genetic engineering in diverse emerging model organisms, with the goal of understanding how stem cells support regeneration across the tree of life.

Roles & Responsibilities

The selected candidate will work closely with the PI to support the lab's research efforts by:

• Developing and refining techniques to maintain and expand an array of emerging model invertebrates (with a strong emphasis on flatworms).
• Contributing to molecular cloning that support transgenesis and gene editing strategy development.
• Performing experiments to characterize regeneration, life history traits, and phenotype variation across species.
• Maintaining thorough documentation (protocols, experimental records, colony/line tracking) and contributing to lab organization and best practices.

The ideal candidate is curious, creative, and resilient in the face of experimental setbacks. They work independently when needed, communicate clearly, and consistently incorporate feedback to improve.

What You'll Be Doing

• Animal husbandry to maintain several species of emerging model flatworms and related invertebrates.
• Working with the Invertebrate Culture Facility to develop and implement more automated, standardized husbandry workflows.
• Characterizing life-cycle traits and regenerative capabilities across diverse flatworm species (including phenotyping with immunohistochemistry and in situ hybridization, and performing genetic perturbations with CRISPR and RNAi).
• Performing molecular cloning using techniques such as bacterial transformation, minipreps, PCR, gel electrophoresis, restriction digestion, Golden Gate assembly, and Gibson assembly.

What We Offer

• Close mentorship and support to help you meet your scientific and professional goals.
• The opportunity to work with unusual and exciting emerging model organisms in the field of regenerative biology.
• The opportunity to work closely with our fantastic technology centers while gaining important leadership skills.
• Professional development opportunities (lab meetings, institute seminars, and conference attendance as appropriate).
• Competitive compensation and benefits (medical, dental, vision, 403(b)), and relocation assistance as applicable.
• Campus perks including café access, and fitness facilities.

Minimum Qualifications

• BS or MS in a relevant field (e.g., Molecular Biology, Bioengineering, Synthetic Biology, Biophysics, Chemical Biology, Ecology, Microbiology, or related discipline).
• 3+ years of laboratory experience.

Preferred Qualifications

• Hands-on experience with molecular biology and/or genetics (cloning, PCR, gel electrophoresis, etc.).
• Comfort with careful organization and recordkeeping (tracking cloning projects, animal lines, and experimental details).
• Familiarity with sequence/plasmid design tools (e.g., Geneious, Benchling, SnapGene).
• Imaging experience (widefield fluorescence, confocal, or similar).
• Strong attention to detail and observational skill (e.g., recognizing "happy worms," regeneration phenotypes, and subtle health changes).
• A love and excitement for the organisms we work with.

How to Apply

Please compile the following materials into a single PDF and name the file using the format:

LastName_2026_HallLab_RTechII.pdf

Submit applications to:

Application materials:

• Cover letter
• Statement of career goals and research interests (1 page max)
• Summary of prior research experience
• CV
• Unofficial college transcripts
• Contact information for up to three professional references

We look forward to reviewing your application!

• Design and synthesize small-molecule analogs to support SAR campaigns.
• Develop and execute efficient synthetic routes, including multi-step syntheses and late-stage diversification strategies.
• Utilize parallel or high-throughput approaches to generate focused compound libraries.
• Troubleshoot and optimize challenging reactions with scientific rigor and independence.
• Scale synthesis of intermediates and final compounds from milligram to decagram quantities.
• Collaborate closely with Medicinal Chemistry and cross-functional project teams to advance program goals.
• Coordinate with external CRO partners to plan and troubleshoot synthetic activities.
• Purify and characterize compounds using NMR, LC-MS, and related analytical techniques.
• Maintain high-quality electronic lab documentation suitable for IP and regulatory standards.
• Clearly communicate experimental rationale, progress, and results to internal and external stakeholders.

• M.S. or Ph.D. in Organic Chemistry or related discipline with 4+ years of pharmaceutical or biotechnology industry experience.
• Strong foundation in modern synthetic organic chemistry with demonstrated application of enabling technologies (e.g., photocatalysis, electrochemistry, transition metal–mediated transformations).
• Experience with parallel synthesis, high-throughput experimentation, or automated reaction platforms preferred.
• Proven ability to design and execute robust, scalable multi-step syntheses.
• Experience delivering high-quality compounds across varying scales.
• Prior experience working effectively with CRO partners.
• Excellent documentation practices and strong analytical interpretation skills.
• Strong communication skills and collaborative mindset.

• Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
• Health Savings Account (HSA) (for employees working 20+ hours per week)
• Life & Disability Insurance (for employees working 20+ hours per week)
• MetLife Voluntary Benefits
• Employee Assistance Program (EAP)
• 401K Retirement Savings Plan
• Direct Deposit & weekly epayroll
• Referral Bonus Programs
• Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice:

As a Senior Environmental Scientist at Intrepid you will assist the Environmental Manager with execution of our mine site environmental compliance and permitting responsibilities.

You will be responsible and should excel at the following:

Leading air, water and waste management compliance inspections.

Managing and arranging for disposal of universal, and hazardous wastes.

Assisting operations with implementation of best practice operational controls for environmental compliance

Developing and maintaining positive professional relationships with regulatory personnel

Overseeing the compilation of all relevant environmental data, statistics and information required by management, government bodies and agencies

Maintaining and submitting various records related to permit requirements

Overseeing the preparation and review of permit documents

Leading environmental special projects (groundwater sampling, compliance stack testing, etc)

Project management and contractor oversite

Be the environmental lead on continuous improvement projects

Perform other duties as assigned

REQUIRED QUALIFICATIONS

5+ years of experience in environmental roles

Bachelor's Degree in Environmental Science, Engineering, Geology, Civil or Mining Engineering, or related technical field

Valid Driver's License

Proficiency with Google Earth and Microsoft Suite, including: Microsoft Outlook, Microsoft Word and Microsoft Excel required.

Must be proficient in reading, analyzing and interpreting scientific data and information

Demonstrated experience in mining or other heavy industry environments

Able to communicate effectively to management and hourly work force

Experience working with federal, state and local environmental permitting preferred

Experience with Clean Water Act, Clean Air Act, Resource Conversation and Recovery Act

Knowledge of NEPA, MSHA, OSHA, DOT and other regulatory requirements preferred

OPPORTUNITIES

Medical plans with prescription drug coverage, dental insurance and vision insurance

401(K) with immediate vesting and generous employer match

Work-life balance with family-friendly work schedules

Opportunity to grow within position through Intrepid's career path program

SCHEDULE AND WORK ENVIRONMENT

9/80 schedule: Monday – Thursday, 9-hour workdays, Fridays worked, 8-hour workday, with every other Friday off. Schedule subject to change.

Work environment will vary from a climate controlled office to loud processing and loadout facilities, construction sites and remote field locations

Noise levels will vary from low to high

Employees are required to wear safety attire and personal protective equipment (PPE).when applicable.

PHYSICAL REQUIREMENTS

Job conditions require sitting up to 2/3 of work time, and hearing over 2/3 of work time. Standing, walking, using hands, reaching with hands, climbing and stooping up to 2/3 of the time depending on job responsibilities. Must be able to lift up to 50 lbs. Up to 1/3 of the work time, the environment may consist of moving mechanical parts and high/precarious places. Typical noise levels vary from low to high (ex: business office, industrial and construction sites)

A pre-placement physical and hair follicle drug test will be required for anyone selected for this opportunity. Placement into the position will not be made until the results are received and cleared by Intrepid.

ABOUT US

Intrepid is an entrepreneurial organization committed to developing unique and environmentally sound ways of extracting minerals of global importance to multiple industries. While our legacy potassium products hold a strong reputation in the agriculture and feed industries, the expansion of our water, brine and other solutions contributes to the oil and gas industries to support energy resources. This diversification of products and customers expands our growth

and impact beyond yesterday's needs. Working at Intrepid, you will experience the commitment, teamwork, and growth in every role and experience.

About the Role

Genesee Polymers Corporation has management's commitment to be a world-class organization and a culture of excellence with the company's focus on best practices and has created an environment for continuous improvement. Our quality system utilizes ISO 9001:2015 as its quality platform. As the Research and Development Chemist, you will have the autonomy to recommend and establish quality control processes and test methods to ensure that our products meets the quality specifications required by our Customers and by the nature of the product itself.

As a member of our Research and Development team, you will stay abreast of the latest technology in sustainability and R&D management in order reach our Quality goals and objectives. Highly visible to senior leadership, you will strive year over year for continuous improvement in the quality control department. You will chart a course of continued success by educating and training our other quality control technicians on new policies and procedures, while collaborating with staff for understanding, agreement, and compliance to Standard Operating Procedures, Work instructions, and other documented processes pertaining to the R&D department.

Responsibilities

• Record research and development data and post in the ERP system
• Work on R&D projects based on demand from Customers
• Analyze and evaluate reaction process to create a successful R&D batch
• Consult with technical director of sample creation results and communicate proper course of action.
• Maintain good electronic record keeping of steps in development for future reference
• Create and maintain SDS submission and TDS on existing and new products
• Maintain all governmental regulatory compliance including but not limited to Chemical Waste disposal profile and manifest, SARA Title II reporting, REACH, SVHC, Conflict mineral reporting, Prop 65, etc.

Qualifications

• Chemistry degree and three years related experience or training; or equivalent combination of education and experience

Required Skills

• Primary knowledge of Silicone Polymers
• Experience in a laboratory for chemical industry is required
• Ability to work independently and remain self-motivated
• Passionate about taking the company's best practices to a higher level of performance
• Strong analytical and scientific skills
• Computer literate in Windows-based database programs and MS Office products
• Ability to write technical papers and document research and development project
• ERP experience a plus
• Chemical Batch manufacturing experience a plus
• Possess excellent organization skills and the ability to prioritize, meet deadlines and multitask independently
• Ability to think independently, communicate thoroughly, and influence the implementation of the appropriate corrective and preventative actions
• Ability to make independent judgments to manage and facilitate company programs/policies as they relate to the R&D department
• Positively interact and influence front-line supervisors and field personnel to create a standardized work environment
• Leadership skills and a proactive mindset and not reactive
• Project management experience a plus

Driven by People. Powered by Opportunity.

If you're looking for a company that believes in building leaders, you've come to the right place. At Ensolum, you'll sharpen your technical knowledge, manage and oversee projects, develop your leadership skills, and be encouraged to innovate. And you'll do this while working alongside some of the best scientific and engineering experts in the industry.

We're hiring a Project Geologist/Scientist/Engineer to work with our Durango, CO, team. In this role, you'll work on a variety of technical projects from simple to complex. You'll spend time tabulating and analyzing environmental data, making recommendations based on applicable regulations, writing technical reports, and collaborating with others regarding project planning and execution, technical strategies, and financials. Interested? Keep reading.

Responsibilities

As a Project Geologist/Scientist/Engineer at Ensolum, your day-to-day responsibilities will vary, and they will typically include:

• Tabulating and analyzing environmental field and laboratory data
• Applying regulatory policies to clean up the environment
• Recommending technical approaches
• Implementing and ensuring health and safety best practices
• Researching federal and state rules and regulations regarding environmental permitting, compliance, and remediation
• Interfacing with clients and subcontractors
• Preparing proposals, cost estimates, and technical reports
• Managing projects within designated timeframes and budgets

Qualifications

We're always looking for people who are self-motivated, learning-oriented, and client-centric. And to be considered for this role at Ensolum, you'll also need a few more qualification requirements:

• BS in Geology, Environmental Science, Engineering, or related field
• At least 7 years of experience with environmental field sampling, data collection, and report writing
• At least 2 years of experience managing environmental remediation projects and budgets, supervising project staff, and working with Colorado ECMC and New Mexico NMOCD regulations
• Strong technical writing and communication skills
• Safety awareness and understanding of safe work practices
• Valid driver's license, safe driving record, and personal vehicle
• Proficiency with Microsoft Office suite
• Able to pass drug & alcohol screening and background check

It would be great if you also have:

• PE or PG certification in Colorado, New Mexico, Texas, and/or Wyoming
• Current 40-hour HAZWOPER certification

We will provide some assistance with relocation to Durango, CO, for a well-qualified candidate.

Who we are:

Ensolum [en-ˈsō-ləm]

Derived from Latin roots: \"en-\" (within, inside) and \"solum\" (ground, soil).

Noun: A company dedicated to providing innovative and sustainable solutions for environmental challenges through technical expertise in geology, environmental science, and engineering.

Why our clients love us:

Ensolum is a customer focused company that delivers environmental, health, safety, and industrial hygiene services. Ensolum offers comprehensive professional and field services to assess, prevent, and remediate environmental issues related to water, ground, air quality, and facilities. Blending superb technical skills with creativity and business savvy, we focus on reducing or eliminating environmental risks and liabilities economically and expediently.

Ensolum's mission is to combine sustainable environmental solutions with forward thinking, cost effective, innovative and value-added technologies that balance our clients' economic resources and environmental challenges while providing our clients with a competitive advantage.

How to apply:

Submit your application along with your resume and pay requirements. If we'd like to find out more about your qualifications, we'll contact you for a virtual or in-person interview. If not this time, we'll hold onto your resume for consideration of future openings. Please note that you must be legally authorized to work in the US without sponsorship.

Ensolum is an equal opportunity employer.

Chemist

Location: Chicago, IL

We are in search of a Chemist to support laboratory testing, product preparation, troubleshooting, application work, and customer‐focused technical activities in a manufacturing environment.

Responsibilities

• Perform formulation work and apply knowledge of raw materials and coating chemistry.
• Identify technical issues, analyze data, and determine next steps with supervisor guidance.
• Apply key variables and adjust products or parameters under supervision.
• Document all work accurately, maintain lab notebooks, and prepare technical reports.
• Participate in customer trials, adjust priorities to meet deadlines, and represent the organization professionally.
• Execute processes supporting product transition from lab to production and customer use.

Qualifications

• Bilingual Spanish (Required)
• Bachelor's degree in Chemistry or related scientific field.
• Minimum of two years of relevant industry experience; manufacturing experience preferred.
• Strong communication, organizational, and documentation skills.