field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Type Full-time Description Job Summary: Validate parts and assemblies against the design intent by collecting points gathered by using a coordinate measure machine. Education and Experience: 
<ul>\n
<li>Associate degree and three (3) years related experience and/or training; or equivalent combination of education and experience.</li>
\n
<li>A minimum one (1) year programming CMM, Faro equipment and Polyworks software experience a plus.</li>
\n
<li>CMM Level III certification preferred.</li>
\n</ul>
\n Required Skills and Abilities: 
<ul>\n
<li>Minimum one (1) year of experience operating Laser Tracker and Articulated Arm PCMM's either Faro,</li>
\n
<li>Leica, or API using Spatial Analyzer or Polyworks.</li>
\n
<li>Experience with ERP systems, preferably IFS.</li>
\n
<li>Demonstrated excellent attention to detail and ability to work independently.</li>
\n
<li>Excellent attendance record including job stability.</li>
\n
<li>Must have the ability to change and adapt to new situations.</li>
\n
<li>Must be able to read and understand blueprints and drawings.</li>
\n
<li>Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers and decimals.</li>
\n</ul>
\n Competencies: 
<ul>\n
<li>Upholds Safety &amp; Quality Standards</li>
\n
<li>Embodies Esprit de Corps</li>
\n
<li>Relentless Customer Focus</li>
\n
<li>Conveys Integrity, Trust &amp; Professionalism</li>
\n
<li>Executes with Excellence &amp; Velocity</li>
\n</ul>
\n Requirements Responsibilities and Duties: 
<ul>\n
<li>Operate Portable Coordinate Metrology Machine(s) to verify various products are in dimensional accordance with drawings and specifications.</li>
\n
<li>Operate PCMM's to assist trades in fit-up i.e. live fit.</li>
\n
<li>Conduct regular maintenance on PCMM and inspection equipment.</li>
\n
<li>Collect and analyze data using Spatial Analyzer.</li>
\n
<li>Understand geometric dimensioning and tolerancing (GD&amp;T).</li>
\n
<li>Uses calipers, micrometers, and other hand inspection tools as required </li>
\n
<li>Performs other related duties as assigned.</li>
\n
<li>Responsible for housekeeping in the department.</li>
\n
<li>Performs other related duties as assigned. </li>
\n</ul>
\n Travel Requirements: As needed to facilities within the Southeast region. Physical Requirements: 
<ul>\n
<li>May be required to stand, walk, sit, reach with hands and arms, climb or balance, stoop or kneel regularly.</li>
\n
<li>Lift up to 50 pounds.</li>
\n</ul>
\n Work Environment: 
<ul>\n
<li>Exposure is frequent to moving mechanical parts, airborne particles - eye protection is required, and fumes, machine vibration, and noisy conditions, high temperatures, and occasional to a restricted space work area.</li>
\n
<li>All Keel locations are tobacco free where appropriate.</li>
\n</ul>
\n Relevance and Importance to Quality Objectives: Keel is committed to continually improve effectiveness and awareness; this is communicated to all team members to ensure everyone is aware of: 
<ul>\n
<li>the quality policy</li>
\n
<li>relevant quality objectives</li>
\n
<li>their contribution to the effectiveness of the quality management system, including the benefits of improved importance</li>
\n
<li>the implications of not conforming with the quality management system requirements</li>
\n
<li>relevant quality management system documented information and changes thereto</li>
\n
<li>their contribution to product or service conformity</li>
\n
<li>their contribution to product safety</li>
\n
<li>the importance of ethical behavior</li>
\n</ul>
\n Equal Employment Opportunity Statement Keel provides equal employment opportunities (EEO) to all team members and applicants for employment without regard to race, (including traits historically associated with race such as hair texture and protective hairstyles), color, religion, sex, sexual orientation, gender identity or expression, national origin, age, genetic information, service in the uniformed services, status as a protected veteran or spouse thereof, height, weight, marital or familial status, disability, or any other characteristic protected by law. In addition to federal law requirements, Keel complies with applicable state and local laws governing nondiscrimination in employment in every location in which Keel has facilities. To provide equal employment and advancement opportunities to all individuals, employment decisions at Keel will be based on merit, qualifications, and abilities. This policy applies to all terms and conditions of employment, including recruitment, recruitment advertising, hiring, job assignment, promotion, demotion, discipline, termination, layoff, recall, transfer, leaves of absence, compensation, or rates of pay, benefits, and selection for training. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by Keel where appropriate. Management retains the right to add to, or change, the responsibilities and/or duties of this position at any time including the elimination of this position. The team member understands that his/her job description is for operational purposes and is not intended to be an employment contract. The employment relationship remains "at-will."

Metrology Technician

<h3>Job Description</h3>
Job Description
Chemical Operator – Fort Mill, SC
Schedule:
<ul>
<li>Full-Time (40 hours/week)</li>
<li>3rd Shift: 12-hour schedule (2-2-3 rotation)</li>
<li>Hours: 7:00 PM – 7:00 AM</li>
<li>Must be available every other weekend</li>
</ul>
Pay:
<ul>
<li>Starting at&nbsp;$20.00/hour and up, based on experience</li>
</ul>
Benefits:
<ul>
<li>401(k)</li>
<li>Holiday Pay</li>
<li>Medical Insurance</li>
</ul>
About the Company
Join one of America’s leading custom and toll manufacturers of specialty organic chemicals. We produce organic intermediates, polymers, and colorants for customers around the world. We’re growing and looking for a reliable&nbsp;Chemical Operator&nbsp;to join our team!
Job Summary
As a Chemical Operator, you’ll be responsible for:
<ul>
<li>Mixing and blending chemicals</li>
<li>Following batch sheets for daily tasks</li>
<li>Performing general labor duties as needed</li>
</ul>
What We’re Looking For
<ul>
<li>Team-oriented and self-motivated</li>
<li>Willing to learn and accept training</li>
<li>Detail-focused with mechanical/electrical aptitude</li>
<li>Experience as a Chemical Operator is a plus, but not required</li>
</ul>
Requirements
<ul>
<li>Good problem-solving and time management skills</li>
<li>Familiarity with PPE (including respirators)</li>
<li>Ability to read batch sheets and MSDS</li>
<li>Previous experience in chemical manufacturing is a plus</li>
</ul>

Chemical Operations Specialist

<h3>Job Description</h3>
Job DescriptionDescription:
As a Project Geotechnical Engineer or Geologist, you will play a key role in managing some of the most exciting and technically challenging projects! Our geotechnical team works on a variety of transportation, energy, development, and natural resources projects. Responsibilities include planning field exploration programs, conducting technical briefings with field staff, and project management tasks including budgeting and client communications. You will also be responsible for performing engineering analyses and preparing technical reports and proposals, as well as conducting regular site visits, attending client meetings, and overseeing field explorations and construction observations. As a project manager, you will also be responsible for mentoring and overseeing the work of junior staff. 
 
Essential Duties and Responsibilities
<ul>
<li>Lead or coordinate the development and implementation of field exploration programs and construction observation projects. Ensure that work performed is consistent with project plans and specifications as well as in accordance with safety guidelines.</li>
<li>Assist with training junior technical and technician staff.</li>
<li>Complete engineering analyses and calculations including: pavement design, slope stability, bearing capacity, settlement, shallow and deep foundations, retaining walls, and seismic design.</li>
<li>Lead the generation of technical reports including completion of routine reports, figures, tables, etc. Assist senior staff in completing portions of large, complex reports, figures, tables, etc.</li>
<li>Lead the generation of construction plans and specifications for slope stabilization, soil nail walls, soldier pile and tieback walls, and ground improvement projects.</li>
<li>Lead project management tasks such as attending project meetings, budget and schedule planning, staffing and task assignments, deliverable preparation, and proposal development.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Civil Engineering or Geology required; Master's degree with a Geotechnical Engineering focus strongly preferred.</li>
<li>Minimum 4 years of relevant experience is required. Highway, bridge, heavy civil project related geotechnical experience preferred.</li>
<li>At least one year of project management experience.</li>
<li>PE and/or LG license required.</li>
<li>Professional-level verbal and written communication skills are a must.</li>
<li>Valid driver’s license is required.</li>
</ul>
Physical Requirements/Work Environment
<ul>
<li>All candidates are subject to completing a background check, and reference check.</li>
<li>All candidates are required to participate in our medical surveillance program.</li>
<li>All candidates are subject to complete drug/alcohol testing.</li>
<li>Ability to perform a wide range of physical activities and do heavy work including exerting up to 50 pounds of force on occasion.</li>
<li>Ability to perform consistent work on a PC with prolonged sitting and view of a monitor/screen.</li>
<li>Ability to travel for short-term and long-term assignments as needed.</li>
<li>All employees are responsible for conducting their work in a safe manner. This includes identifying potential safety hazards and reporting them to the designated project manager in a timely manner and participating in project safety briefings. This also includes wearing appropriate safety equipment when working in the field and completing all required health &amp; safety training prior to beginning fieldwork.</li>
</ul>
Our best estimate for the salary range for a Project Geotechnical Engineer role in Missouri is $87,200 - $122,900 annually. Our best estimate for the salary range for a Project Geologist role in Missouri is $76,200 - $107,400 annually. Compensation offered will be based on a variety of individual factors, including education and experience, as well as internal equity. GeoEngineers’ salary ranges are reviewed and updated each year and employees are eligible for pay increases based on individual performance. As part of our competitive total rewards package, employees in this role may also be eligible for our annual year-end bonus offering, subject to program eligibility requirements.
 
At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits here.
 
Our Commitment to Belonging at GeoEngineers
 
When people feel they can bring their whole selves to work, that they have a voice and are supported and respected, it creates trust and a feeling of belonging— employees then flourish, grow their careers, and do the best work of their lives. A culture of belonging allows our employees to thrive and our company to prosper. This is a journey, and we are committed to doing the work, learning and evolving as we go.
 
GeoEngineers is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances. 
 
GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at <a href="mailto:hr@geoengineers.com" target="_blank">hr@geoengineers.com</a> or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis. 
 
We welcome and encourage individuals from all backgrounds and experiences to apply for openings on our team. We would love for you to join us!
 
We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies.
Requirements:

Project Geotechnical Engineer or Geologist

<h3>Job Description</h3>
Job Description
Interested in this role? Email or call/text Grace Williams directly to be considered at grawilliams@actalentservices. com | 317 - 567 - 6610
Responsibilities
<ul>
<li>Perform analytical studies including GLP certifications of various materials to support the registration and production of active ingredients and formulated crop protection products.</li>
<li>Ensure all data is generated and documented in compliance with GLP regulations, SOPs, best practices, and study protocols.</li>
<li>Process and interpret the quality of analytical data, troubleshoot, and implement solutions for experimental challenges to meet study requirements.</li>
<li>Support the daily operations of analytical laboratories by maintaining instrumentation and lab areas.</li>
<li>Collaborate closely with the GLP Certifications Team and Product Chemistry Subject Matter Experts to efficiently conduct experiments and communicate results to stakeholders.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Biology, Chemistry, Biochemistry, or related disciplines; Chemistry preferred.</li>
<li>0-3 years of experience in a professional laboratory setting (6+ months preferred).</li>
<li>Proficiency in working in a fast-paced, multi-tasking, and customer-focused environment.</li>
<li>Ability to demonstrate flexibility to accommodate urgent projects.</li>
<li>Commitment to environmental health and safety values.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in analytical, chemistry, laboratory environments.</li>
<li>Familiarity with HPLC, NIR, GLP, GMP, Quality Control, and QC testing.</li>
</ul>
Work Environment
Work a 1st shift from 8am to 5pm, Monday through Friday. 
INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:
﻿**INTERVIEWS AVAILABLE THIS WEEK**
<ul>
<li>I am scheduling interviews for this position and conducting phone interviews as early astoday. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams.</li>
<li>HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com and/or CALL/TEXT ME: 317 567 6610</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Indianapolis, IN.
Pay and Benefits
The pay range for this position is $20.00 - $22.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Indianapolis,IN.
Application Deadline
This position is anticipated to close on Nov 11, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Entry Level Analytical Chemist - HIRING NOW

<h3>Job Description</h3>
Job Description
Quality Assurance Chemist
Onsite - Gurnee IL 
Who We Are: 
PurposeBuilt Brands, rooted in a legacy dating back to Weiman, stands as a pioneer in crafting top-tier products for specialty surfaces. Our beloved brands, including Weiman, Goo Gone, Green Gobbler, Biokleen, Gonzo, Magic, Wright’s, Stone Care International, Urnex, Five Star, and Micro-Scientific, are preferred choices among consumers and seasoned professionals alike.
At PBB, we seek to hire employees who bring a level of engagement, drive, and performance that pushes business forward. We work together and are motivated by positive results, while continuously thriving in a scrappy environment. We believe our greatest assets are the talented and passionate employees who are motivated by our purposeful work. Our company may be 60 years old, but the real growth is just getting started.
The Role:
The Quality Assurance Chemist is responsible for ensuring finished products are made to quality specifications. This position will oversee the quality of a product from raw materials to finished product. The position will also be responsible for ensuring that the quality lab is maintained and sufficient to perform lab testing. The Quality Assurance Chemist will work directly with production, research and development, and supply chain departments.
What You Will Do:
<ul>
<li>Perform chemical and microbial testing of batches and make adjustments as needed </li>
<li>Inspect raw materials including chemicals, packaging components, and labels </li>
<li>Assist Quality Technicians and production with finished product inspections </li>
<li>Calibrate and maintain lab equipment </li>
<li>Troubleshoot lab equipment </li>
<li>Inspect and approve FDA product for release </li>
<li>Assist in validation of lab equipment (IQ, OQ, PQ) </li>
<li>Assist with product validations </li>
<li>Maintain quality assurance lab </li>
<li>Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. </li>
</ul>
What You Will Bring:
<ul>
<li>Bachelor’s Degree in a science discipline or equivalent experience </li>
<li>2-5 years previous lab experience</li>
<li>Basic understanding of chemistry and laboratory equipment (e.g., pH meter, viscometer, UV-Vis, gas chromatograph, FTIR, auto titrator, etc.). </li>
<li>Strong computer skills (proficient in MS Word, Excel, PowerPoint, and use of Access databases). </li>
<li>Excellent verbal and written communication skills. </li>
<li>Ability to problem solve and good math skills. </li>
<li>Strong attention to detail and organizational skills. </li>
<li>Understanding of manufacturing processes </li>
</ul>
Hours: Monday – Friday, 5:00 p.m. – 2:00 a.m.
Benefits:
PBB offers a wide range of benefits because we understand no two employees are the same. We want our employees to feel empowered to set their day up for success, whether that's in the office or remote.
What We Offer:
Flexible work options (fully remote, hybrid, onsite)
Generous paid time off
Competitive salaries and bonus incentives
401K company match
Competitive medical, dental, &amp; vision insurance
Pet insurance
Annual fitness stipend
Unmatched employee discount on all products
Summer Hours
LinkedIn learning membership
Job Title: 
Quality Assurance Chemist
PBB Job Code:
QAC
Mercer Job Code:
QLT.03.006.P10
FLSA Status:
Exempt
Reports To: 
QA Manager
Job Function:
Quality
Work Location:
Gurnee IL 
Travel Required:
None

Quality Assurance Chemist

<h3>Job Description</h3>
Job Description
Description
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
 
Skills
Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry
 
Top Skills Details
Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control
 
Additional Skills &amp; Qualifications
Frist Shift- General Shift: 8:30AM – 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They’re hiring across levels (QC Chemist II &amp; III). QC Chemist II should be between 2-3 years’ experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I’d prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. • Bachelor's degree (BS or BA), physical sciences required • Master's degree preferred • Minimum of 3-5+ years' experience. • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets.
 
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 13, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist II, III

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
<ul>
<li>Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post packaging support</li>
<li>Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods</li>
<li>Set up and analysis of drug substance and drug product stability samples</li>
<li>Method development and validation of analytical methods for drug substance and drug product</li>
</ul>
Qualifications 
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Experience with eLN, LIMS and data trending are a plus</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor’s degree in chemistry or other science related degree concentration, or equivalent directly related experience</li>
<li>Laboratory experience and some experience in GMP analytical chemistry, preferred</li>
</ul>
 Additional Information 
<ul>
<li>Position is Monday-Friday 8:00am – 5:00pm overtime as needed.</li>
<li>Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.</li>
<li>Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: NMR Scientist Location: San Diego CA -92121 ( Onsite ) Duration -6 months Pay Range: $86.25/hr. on w2 Job Description:
<ul>
<li>Troubleshoot and resolve technical issues with NMR spectrometers</li>
<li>Solve complex regio- and stereoisomer structures by NMR</li>
<li>Lead and coordinate NMR lab relocation activities</li>
<li>Drive automation and workflow improvements</li>
<li>Advanced degree in Chemistry or related field, with demonstrated NMR structure elucidation experience</li>
<li>Proficiency in Bruker NMR platforms</li>
<li>Experience with NMR hardware and troubleshooting</li>
<li>Excellent interpersonal and communication skills</li>
<li>Commitment to safety and collaboration</li>
<li>Be part of a collaborative team making a real difference in drug discovery</li>
<li>Work onsite in a state-of-the-art lab environment</li>
</ul>
 Hard Skills:
<ul>
<li>Experience with NMR hardware and troubleshooting</li>
<li>Solve complex regio- and stereoisomer structures by NMR</li>
<li>Lead and coordinate NMR lab relocation activities</li>
</ul>
 Interview Process:
<ul>
<li>Team Call (Camera On)</li>
<li>Onsite Interview</li>
<li>Initial Duration: 6-m with potential to extend</li>
</ul>
 What You Will Achieve
<ul>
<li>As a Senior Scientist in the Oncology Analytical and Synthesis Technologies Open Access group, you will be at the center of a pivotal operation within Medicinal Chemistry. </li>
<li>You will be part of a group in Client that comprises experts in the major scientific disciplines involved in the discovery and preclinical development of small molecule drugs. Specifically, you will be involved in the structural analysis of a broad range of achiral/chiral small molecule compounds primarily through NMR spectroscopy as well as responsible for implementing novel technologies/workflows to expedite such processes.</li>
<li>You will play a vital role as a key contributor in large, multi-disciplinary matrix teams from project inception through to delivery of clinical drug candidates. You will provide key contributions to the implementation of analytical chemistry strategies through development and execution of innovative techniques that help to revolutionize expedite our approach to the discovery and development of small molecule and synthetically derived drugs.</li>
<li>Your significant experience of applying knowledge of principles, concepts, and practices of the analytical chemistry discipline and specifically NMR will make you a critical member of the team. Your skill and knowledge will help in making decisions that require choosing among limited options. You are proactive in contributing to all team discussions and creating an environment of collaboration.</li>
<li>It is your innovative scientific temperament that will help in making Client ready to achieve new milestones and help patients across the globe.</li>
</ul>
 Why Patients Need You
<ul>
<li>Purpose is to deliver breakthroughs that change patients’ lives. </li>
<li>Research and Development is at the heart of fulfilling Client purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most.</li>
<li>Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.</li>
</ul>
 How You Will Achieve It
<ul>
<li>Contribute to achievement of immediate work group goals and collaborate with other team members.</li>
<li>Build effective partnerships with other research lines, in particular synthetic medicinal chemistry, technology, pharmaceutical sciences and process chemistry groups.</li>
<li>Develop efficient approaches to the structural elucidation of primarily small molecule compounds through developing an expertise in NMR-based methodologies.</li>
<li>Drive the utilization of the most contemporary and effective analytical/purification instrumentation combined with automated technologies.</li>
<li>Communicate work clearly and concisely to internal stakeholders through written and verbal communications.</li>
</ul>
 Qualifications Must-Have
<ul>
<li>Bachelor's Degree</li>
<li>2+ years of experience</li>
<li>Experience in compound structural analysis by NMR-based and Mass Spectrometry methods.</li>
<li>Working knowledge of NMR-instrumentation and hardware.</li>
<li>Familiarity with standard laboratory techniques and working knowledge of HPLC and purification techniques.</li>
<li>Interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment</li>
<li>Effective communication skills</li>
</ul>
 Nice-to-Have
<ul>
<li>Broad knowledge of various analytical software packages (e.g. Agilent, ACD Labs, Bruker, etc).</li>
<li>Proficiency with basic NMR instrument upkeep and troubleshooting issues.</li>
<li>Experience with logistics around lab set-up after a site move.</li>
<li>Familiarity with development/execution of workflows for the parallel purification and analysis of compound libraries.</li>
</ul>
 Education :
<ul>
<li>What is the minimum education experience required?:BA or Masters Open to PhD</li>
</ul>
 #sczr2

NMR Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
Scientist&nbsp;responsibilities include, but are not limited to the following:
<ul>
<li>Perform a wide range of analyses (routine and non-routine) primarily but not limited to the biochemistry&nbsp;test areas of Biopharmaceutical Services</li>
<li>Review and evaluate raw data for acceptability</li>
<li>Set up and validate new analytical or related processes used by the department</li>
</ul>
Qualifications 
The ideal candidate would possess:
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Bachelor's degree in biology, biochemistry, molecular, cell biology, or other related degree concentration, or&nbsp;equivalent directly-related experience&nbsp;</li>
<li>Prior laboratory experience</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is full-time, Monday-Friday, 8am - 4&nbsp;pm., with overtime as needed.&nbsp;Candidates currently living within a commutable distance of Lancaster, Pennsylvania are encouraged to apply.&nbsp;
Excellent full-time benefits including:
<ul>
<li>Comprehensive medical coverage, dental, and vision options.</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientist I - Biochemistry

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom TechnicianJob Description
We are seeking a dedicated Cleanroom Technician to join our team in Hebron, KY. This role involves working from 7:30 am to 4:00 pm, Monday through Friday. The ideal candidate will play a key role in utilizing technology for efficient inventory management.
Responsibilities
<ul>
<li>Utilize RF Scanner device for inventory management.</li>
<li>Perform inventory transfers efficiently and accurately.</li>
<li>Engage in assembly, inspection, and packaging duties in a cleanroom environment.</li>
</ul>
Essential Skills
<ul>
<li>Experience with RF scanner devices.</li>
<li>Proficient in assembly, cleanroom operations, inspection, and packaging.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Prior cleanroom experience is advantageous.</li>
<li>Strong attention to detail and ability to follow procedures.</li>
</ul>
Why Work Here?
Join a global company that offers a supportive work environment with laid-back management. 
Work Environment
The facility is very clean and climate-controlled, providing a comfortable working environment. The company values a laid-back management style and promotes a positive work culture.
Job Type &amp; Location
This is a Contract to Hire position based out of Hebron, Kentucky.
Job Type &amp; Location
This is a Contract to Hire position based out of Hebron, KY.
Pay and Benefits
The pay range for this position is $17.00 - $18.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hebron,KY.
Application Deadline
This position is anticipated to close on Nov 20, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

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