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<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today!
Job Description 
Key Responsibilities:
<ul>
<li>Generate ADCs and related modalities using advanced conjugation techniques (e.g. cysteine, lysine, site-specific and related biorthogonal chemistries).</li>
<li>Purify reagent proteins/antibodies (up to 100 mg scale) using gravity or chromatography-mode with various FPLC methods (affinity, ion exchange, hydrophobic interaction, size-exclusion) and tangential flow filtration under supervision.</li>
<li>Apply protein chemistry/analytical techniques such as mass spectrometry, SDS-PAGE, and analytical SEC to assess protein quality.</li>
<li>Analyze and summarize experimental data and maintain accurate records in client-provided electronic lab notebooks (ELNs).</li>
<li>Collaborate effectively with team members and cross-functional partners, proactively communicating issues and seeking guidance when needed.</li>
<li>Stay flexible and open to learning new techniques and technologies as project needs evolve.</li>
</ul>
Leadership Responsibilities:
<ul>
<li>Supports and monitors the performance of the team of employees</li>
<li>May participate in new hire interviews</li>
<li>Supports the on-boarding process of new employees</li>
<li>Disseminate administrative communications</li>
<li>Demonstrate and promote the company's vision</li>
<li>Ensure adherence to highest quality and efficiency standards in laboratory operations&nbsp;</li>
<li>Ensure coverage and performance for all shifts, and work duties&nbsp;</li>
<li>Performs administrative tasks for team member growth and development</li>
<li>Adeptly balance technical lab work with leadership responsibilities</li>
<li>Foster morale and teamwork&nbsp;</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>M.S. in Biochemistry or related field with at least 2 years of industry experience in protein purification, bioconjugation, or relatable work experience; or a B.S. Biochemistry or related field with at least 3 years of industry experience in protein purification, bioconjugation, or relatable work experience</li>
<li>Experience with protein purification techniques such as FPLC, SDS-Page, SEC, TFF etc.</li>
<li>Experience in mentoring, training, or leading others</li>
<li>Flexible, able to multi-task, open to learn new techniques as needed, good communication skills and able to flag issues when arise and seek help.</li>
<li>Highly detail-oriented and collaborative, able to analyze and summarize data upon training, document data properly in an electronic lab notebook (ELN).</li>
<li>Must be eligible to work indefinitely in the United States without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience in mentoring, training, or leading others in a pharmaceutical industry setting</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday – Friday, 8am-5pm with overtime as needed.&nbsp;Candidates currently living within a commutable distance of&nbsp;Louisville, CO&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<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 holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
<li>Base Compensation: $72,800-$89,440&nbsp;per year</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioconjugation Scientist - Group Leader

<h3>Job Description</h3>
Job Description
An Analytical Chemist role in Greenwood, SC is now available through Adecco Healthcare and Life Science. In this position, you will be responsible for performing chemical and physical testing on raw materials, work-in-process and finished product samples to ensure quality and safety of consumers.
Position type: Minimum 6-month+ temp/contract
Pay rate: $21.00/hr.

Shift:
The work hours are from 1:00pm-1:30am (with a 30-minute lunch)
Week 1: Monday, Tuesday, Friday, Saturday and Sunday
Week 2: Wednesday and Thursday

Responsibilities:

• Under minimal supervision performs / reviews analytical testing of Raw Materials, Work-In-Process,
Finished Products for product approval and releases.
• Performs physical and chemical testing in accordance with standard procedures, utilizing wet-chemistry and basic instrumental techniques.
• Maintains accurate, up-to-date and concise laboratory notebooks and records.
• Works as a member of the Laboratory Team to complete all required tasks in a timely manner.
• Understand and precisely follows Standard Operating Procedures, global methods, local methods and
published standard or compendia methods i.e. USP, AOCS, ASTM.
• Provides training to employees on new and existing Standard Operating Procedures (SOP).
• Provides support to the Operations personnel with analytical equipment and testing procedures.
• Capable of operating and performing basic troubleshooting on analytical instruments (HPLC,
Autotitrator, Karl Fischer, NIR, UV-Vis and FTIR).
• Responsible for daily/monthly instrument calibrations to ensure all instruments are working properly.
• Support laboratory equipment validations by executing or assisting vendors with Installation.
• Assist the manufacturing site with product, equipment, and Cleaning &amp; Sanitizing (C&amp;S) validations by
performing all required tests in a timely manner.
• Participates on Out of Specification (OOS) investigations to collect the necessary samples and
information to complete Laboratory Investigation Reports (LIR).
• Supports, maintains and reviews data to identify trends and draw conclusions.
• Understands and applies basic laboratory safety instructions, reagent handling precautions, and disposal of chemical waste according to local environmental regulations.
 
Qualifications
 
Required:
• Bachelor of Science Degree in Chemistry with at least 2 years’ experience in an Analytical laboratory.
• Working knowledge and practical experience with cGMP and FDA regulations in a chemistry laboratory
• Familiar with quality systems (i.e. Laboratory Investigation Reports (LIR), Corrective and Preventive
Actions (CAPA), calibration, validation, change control, etc.).
• Good team player with strong relationship building skills.
• Communicate Effectively - Clearly and simply expresses ideas and concepts.
• Ability to gather relevant information efficiently and apply logic in solving problems and making
decisions; using data to support recommendations; weighing risks and predicting benefits and costs.
• Ability to plan, prioritize and adapt to circumstances as needed.
• Set a positive example for conducting business in an ethical manner, managing stress, and creating a
pleasant and balanced work environment.
• Proficient knowledge of computer and computer software: Excel, Word, Power Point, etc.
 
Preferred:
• Bachelor’s degree in Chemistry or related sciences major
• 2+ years of experience in an Analytical laboratory
• 1+ years of experience in the pharmaceutical, medical device, cosmetic or consumer products
industries.
• Experience with common Analytical Laboratory instrumentation (i.e. HPLC, NIR, Autotitrators, Karl
Fischer, UV-Vis and FTIR)

Why work for Adecco?
<ul>
<li>
Weekly Pay
</li>
<li>
401(k) Plan
</li>
<li>
Skills Training
</li>
<li>
Excellent medical, dental, and vision benefits
</li>
</ul>

Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or other paid leave required by Federal, State, or local law, as well as Holiday pay upon meeting eligibility criteria. IMPORTANT: This job is being recruited for by Adecco’s Medical and Science division, not your local Adecco Branch Office.

Equal Opportunity Employer/Veterans/Disabled

 Pay Details: $21.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.adecco.com/en-us/candidate-privacy" target="_blank">https://www.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: 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.

Chemist - 2nd shift

<h3>Job Description</h3>
Job DescriptionDescription:
The Research Assistant Intern will work with multi-disciplinary teams within Vivex Biologics, Inc. and assist a Research Scientist with early-stage development activities and product development.
 Requirements:
 
Duties and responsibilities
<ul>
<li>Assist with early stage and product development projects.</li>
<li>Assist and conduct research on existing and developed products.</li>
<li>Develop design of experiments and execute accordingly under supervision as assigned.</li>
<li>Deliver protocols, reports, and presentation as required.</li>
<li>Other duties as assigned.</li>
</ul>
 
Qualifications
<ul>
<li> Bachelor’s or master’s (or currently enrolled) in Biochemistry, Chemical Biology, or a related life sciences or health-science discipline; minimum GPA of 3.0.</li>
<li>Strong foundational knowledge of biochemistry and biology, with a solid understanding of human anatomy and chemistry relevant to laboratory research.</li>
<li>Demonstrated strong hands-on laboratory skills, with extensive practical experience in biochemistry-focused laboratory environments.</li>
<li>Proven proficiency in core wet-lab techniques, including precise pipetting, sample preparation, reagent handling, and execution of biochemical assays (e.g., protein quantification, enzymatic assays, ELISA or similar analytical assays).</li>
<li>Ability to accurately collect, analyze, and interpret experimental data, with strong attention to detail and adherence to laboratory protocols.</li>
<li>Excellent verbal and written communication skills, including technical writing, data reporting, and documentation of experimental results.</li>
<li>Strong analytical, problem-solving, troubleshooting, and organizational skills, with the ability to support experimental planning and execution.</li>
<li>Proficiency in Microsoft Office applications (Excel, Word, PowerPoint); familiarity with GraphPad Prism, Microsoft Visio, and Microsoft Project is preferred.</li>
</ul>

Applicants must be legally authorized to work in the United States. Vivex will not provide sponsorship or employment for candidates who require the 24-month STEM Optional Practical Training (OPT) extension. Please note this is not an offer of immigration sponsorship. 
 
Working conditions
Job may require work inside the controlled cleanroom manufacturing area where the intern would be exposed to tissue processing.
 
Physical requirements
The job may entail occasional requirement to stand for extended periods of time and lifting heavy objects of up to 30 lbs.
 
Direct reports
No direct reports.
 
Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job any time. 
VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, transfers, leaves of absence, compensation, and training.
VIVEX Biologics complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.

Research Assistant - Intern

<h3>Job Description</h3>
Job Description
Join the V3 Team and take your career to the next level! We are seeking an experienced and passionate Field Ecologist to join our Ecological Restoration team in our West Chicago office. As a Field Ecologist, you will play a crucial role in studying and understanding natural ecosystems, wildlife habitats, and environmental processes. Your work will contribute to conservation efforts, ecological research, and sustainable land management. The ideal candidate will have a minimum of 5 years of field experience and, ideally, hold a Commercial Driver’s License (CDL).
 
About Us

V3 is more than just a place to work. It is a place where you can make an impact, build your skills, create your path and dive into meaningful, rewarding work that is challenging, inspiring and fun!

As a civil engineering consulting firm, we transform communities. Our diverse array of specialties includes civil engineering, contracting, environmental, planning, landscape architecture and surveying services. We believe in excellence in all we do and have an unwavering commitment to success. We have over 425 employees, with offices in six states and one in Canada. We are a growing firm and that creates exciting opportunities for our staff!

Key Responsibilities
<ul>
<li>Carry-out tasks related to ecosystem restoration and management.</li>
<li>Application of herbicide (hand wicking, backpack spraying, etc.).</li>
<li>Perform general field labor and manual weed removal by hand, mowing, weed whipping.</li>
<li>Installation of native plant plugs and erosion control.</li>
<li>Conduct brush clearing, tree cutting and general chainsaw work.</li>
<li>Participate in prescribed burning.</li>
<li>Coordinate with construction foreman, project managers and ecologists.</li>
<li>Assist with other duties as assigned or requested.</li>
<li>Facilitate site assessments, field monitoring, and reporting.</li>
<li>Project administration (define and input work orders, daily logs, and contract administration).</li>
</ul>

Qualifications
<ul>
<li>Associate/Bachelor degree in an environmental discipline with 5 years of relevant experience.</li>
<li>A passion for ecosystems, natural resource conservation, and the outdoors.</li>
<li>Demonstrate proficient knowledge of native and non-native plant species of the Chicago region.</li>
<li>Background in natural area installation and management and/or agricultural knowledge related to planting and seeding in natural areas.</li>
<li>Licensed herbicide applicator or ability to obtain the license through the state of Illinois state herbicide exam.</li>
<li>Ability to perform physical labor throughout the year (lift/carry minimum 50 lbs).</li>
<li>Competent in the use hand tools and equipment.</li>
<li>Strong work ethic and willingness to perform multiple tasks.</li>
<li>Valid driver’s license.</li>
<li>Excellent communication skills and work ethic.</li>
</ul>

Benefits

<ul>
<li>Competitive salary and performance-based bonuses</li>
<li>Comprehensive health, dental and vision insurance </li>
<li>Health Savings Account with V3 funding contribution</li>
<li>Retirement plan with up to 6% company match</li>
<li>Paid time off, holidays and volunteer paid time off</li>
<li>Professional development opportunities</li>
<li>Collaborative and supportive work environment </li>
<li>Explore our website at <a href="http://www.v3co.com" target="_blank">www.v3co.com</a> to learn more about us! </li>
</ul>
 
Join Our Team! If you are ready to join a growing firm with a vibrant culture, where you can learn from our experienced staff who are experts in their field, submit your resume today! 

V3 IS AN EQUAL OPPORTUNITY EMPLOYER: Veteran/ Disability

Field Ecologist

<h3>Job Description</h3>
Job DescriptionCompany Description 
In a world of vibrant color, INX stands out by blending art, science, and sustainability into every drop of ink we make.&nbsp; We’re globally recognized for our innovation, and we’re A Great Place to Work-Certified™ company!
INX International is the third largest producer of inks in North America with full-service subsidiaries in Europe and South America. We offer a complete line of ink and coating solutions technology for commercial, packaging and digital applications. We expertly blend pioneering technology with a deep commitment to the environment. Dedicated to coloring a safe and sustainable future one print at a time, you can see our color chemistry on beverage cans, food and household packaging, clothing, banners, billboards and more.&nbsp;
Investing in and protecting our employees is the key to our success.&nbsp; Our average employee has been with us 12 years, and we recognize the significant experience and the continuous dedication of our team members.&nbsp;
We’re acti vely seeking new talent with new ideas as we continue to provide sustainable products, service and innovation to the printing and packaging markets.
Join us in coloring a safe and sustainable future!
Job Description 
This role offers a range of $87,000 to $95,000 annually. Actual compensation will be based on qualifications such as experience, education, certifications, and skills, as well as geographic considerations.
The Analytical Chemist will perform analytical tests with some direction from the Lab Manager and/or project leader.&nbsp; Understands method development and can apply the principles to non-routine testing.&nbsp; Have potential to become a project leader and be responsible for shepherding a project form inception through preparation/submission of report.&nbsp; Will maintain, organize and lead multiple projects at a time.&nbsp; Highly organized, have knowledge of industry standards, such that he/she can move analytical methods towards work instructions, regulated methods, SOPs, and/or ASTMs.
Proficiency will be required in the following: GC/MS, GC/FID, GCqTof, HRMS or LC/MS/MS as well as&nbsp;in the use of GC-FID, GC-Mass Spectrometry, FTIR, DSC, UV-Vis and particle size analysis.&nbsp;
As Analytical R&amp;D Chemist you will be responsible to:
<ul>
<li>Prepare internal and external reports.</li>
<li>Prepare and maintain&nbsp;data for formal submission outside of INX</li>
<li>Assist with raw material and finished good analysis and evaluation.</li>
<li>Support day to day laboratory activities by performing routine analytical tests with strict adherence to SOP and GLP when necessary</li>
<li>Perform non-routine analytical tests.</li>
<li>Utilize literature and patent searches to support non-routine tests, troubleshooting, and root cause analysis.</li>
<li>Develop new methods for the analytical lab.</li>
<li>Maintain, organize, and lead multiple projects at a time.</li>
<li>Evaluate instrument system suitability.</li>
<li>Work&nbsp;independently with some supervision of lab manager and/or project leader.</li>
<li>Facilitate&nbsp;cross lab discussion for project progression, completion and/or analysis.</li>
<li>Maintain a clean and orderly work environment according to 5S guideline and 5S Best Practices at the respective facility</li>
</ul>
Qualifications 
To perform your job as expected, you will be required to have:
<ul>
<li>BA or BS in chemistry or science with 5+ years of experience; or&nbsp;MS in chemistry with 3+ years of experience; PhD in Chemistry with 1+ years of experience.</li>
<li>Proficiency&nbsp;using MS Office.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency&nbsp;in separation and extraction techniques for analytical analysis and characterization.</li>
<li>Proficiency at equipment and experimental troubleshooting.</li>
<li>Proficiency&nbsp;in quantitative and qualitative laboratory tests.&nbsp;</li>
<li>Proficiency&nbsp;in quantitative analysis.</li>
<li>Proficiency&nbsp;in Analytical methods, laboratory equipment, and HPLC/MS and/or GC/MS.</li>
<li>Proficiency&nbsp;at analytical instrumentation analysis software.</li>
<li>Have basic understanding of ink formulation and components as it pertains to analytical analysis and daily analytical activities.</li>
</ul>
 Additional Information 
We offer a competitive salary with excellent benefits including medical, dental, vision, life insurance, disability, pet insurance, HSA and FSA, long-term care, 401(k), and more. Through our programs, which now include Paid Volunteer Time Off and Paid Parental Leave, we support the needs of our employees, their dependents, and their communities by providing a benefit package that is easy to understand, easy to access, and affordable for all our employees.
Don’t just choose a job; choose a career that emphasizes employee growth in a safe, environmentally conscious culture. &nbsp; Embark on your Colorful Career with us!
We require post-offer, pre-employment drug screens, physicals, and background checks.
Equal Opportunity Employer: disability/veteran.

R&D Analytical Chemist

<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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
<ul></ul>
Job Description 
The Senior Scientist ensures study design; execution and reporting align with regulatory and client project specifications. The Senior Scientist provides critical client consultation throughout study life cycle and ensures lab compliance to study design. This role will support Electrophysiology projects including cardiac safety screening in a GLP-compliant electrophysiology lab and serve as a Principal Investigator for regulated studies. This role requires technical expertise, portfolio leadership, leadership competencies, and proficiency in client communication within a contract research organization.
Senior Scientist — Regulatory Cardiac Safety/Electrophysiology (Scientist II) responsibilities include, but are not limited to, the following:
The Senior Scientist is a scientific leadership position, responsible for providing guidance and alignment between our customer base, the industry at large, commercial teams and service operations. This role is a hands-on laboratory-based role and will be collaborative and influential in a broad network of business functions in support of delivering high quality services to our valued customers, and driving business growth, brand recognition, and alignment with Eurofins core competencies. This position will train and mentor junior staff, responsible to take informed decision to move projects ahead, set direction, champion change and directly contribute to achieving departments goals and strategies.
<ul>
<li>Develops client and stakeholder relationships through technical leadership and collaboration</li>
<li>Manages client projects in all phases of study life cycle from study design to reporting</li>
<li>Provides guidance and oversight for compliance and scientific integrity of the studies to ensure that studies are performed in a compliant manner</li>
<li>Understands and follows all procedures and processes required for work performed under Regulatory Compliance (i.e. GxP, FDA/GLP and GCP, OECD, CLIA, etc.) and completes annual GLP training</li>
<li>Directs investigations of service operations, such as deviation reports, non-conforming reports, corrective action reports, etc. Produces documentation according to established standards</li>
<li>Drafts and approves operations documents to assure consistency with regulatory standards and requirements. (I.e. SOPs, batch records, training records, etc.)</li>
<li>Responsible for data generation, review, analysis review and ensuring accuracy and integrity of reporting</li>
<li>Provides scientific guidance that supports technical writing and final review of Validation Plans and Reports as required</li>
<li>Supports client services team in generating proposals, RFPs, study plans and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis</li>
<li>Completes required training and supports 100% of Employee Health and Safety requirements</li>
<li>Manages responsible use of confidential IT and business systems, as required</li>
<li>Ensures accurate data management and reporting, with the highest integrity, and manages quality control on project data and reports</li>
<li>Accountable for delivering to unit and site key performance metrics (quality, delivery on time)</li>
<li>Supports site goals and demonstrates Eurofins' competencies, as defined in the job plan</li>
<li>Provides training to colleagues and external end users, when required</li>
<li>Performs other duties, as assigned</li>
</ul>
<ul></ul>
Qualifications 
Basic Minimum Education Qualifications:
<ul>
<li>
M.A. or M.S. with minimum 5 years relevant experience
</li>
</ul>
OR
<ul>
<li>
Ph.D. with minimum 3 years relevant experience
</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Demonstrated experience in manual patch clamp electrophysiology in a GLP-compliant laboratory is a plus.</li>
<li>Scientific expertise in Ion Channel electrophysiology and applications to execute safety pre-clinical studies.</li>
<li>Technical experience and knowledge in supporting compound cardiac safety profiling within drug discovery programs, from early drug discovery to IND submission life cycle.</li>
<li>Experience developing client relationships, supporting technical correspondence, drafting and presenting scientific proposals to clients.</li>
<li>Experience in drafting and executing equipment and method validation according to 21CFR11 compliance.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.&nbsp;</li>
</ul>
The Ideal Candidate Possesses the Following:
<ul>
<li>Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health.</li>
<li>Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations.</li>
<li>Demonstrates a working understanding of international regulatory requirements and aptitude to stay relevant on topical scientific publications.</li>
<li>Ability to support project management, plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources.</li>
<li>Demonstrated experience in working effectively with lab operations, business development, marketing, and outsourcing stakeholders.</li>
<li>Experience with leading and influencing cross-functional teams effectively</li>
</ul>
 Additional Information 
Position is full-time,&nbsp;with overtime as needed. Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply.
<ul>
<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>
</ul>
Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Scientist -- Regulatory Cardiac Safety/Electrophysiology (Scientist II)

<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 
What you will learn and work with:
<ul>
<li>Performing routine cell-based assays, including ELISA and cell culture-based methods, to support product testing.</li>
<li>Executing work in a GMP or GMP-like environment, following established protocols and documentation standards.</li>
<li>Supporting GMP testing for drug products, with attention to accuracy and compliance.</li>
<li>Practicing and maintaining environmental containment procedures.</li>
<li>Ensuring proper documentation and reporting aligned with good documentation practices.</li>
<li>Collaborating with cross-functional teams to support quality control and product development timelines.</li>
</ul>
&nbsp;
Qualifications 
Minimum Skills:
<ul>
<li>Bachelor’s or Master’s degree in a relevant life science discipline (e.g., Biotechnology,&nbsp;Biology, Biochemistry, Molecular Biology, or related field).</li>
<li>1-3 years of relevant industrial experience</li>
<li>Hands-on experience with cell culture and ELISA.</li>
<li>Familiarity with working in a regulated/GMP-like lab environment.</li>
<li>Strong attention to detail and adherence to standard operating procedures.</li>
<li>Candidates within a commutable distance of Chesterfield, MO&nbsp;are encouraged to apply</li>
<li>
Authorization to work in the United States indefinitely without restriction or sponsorship
</li>
</ul>
&nbsp;
Desired Skills:
<ul>
<li>Familiarity with OEB-5 compound handling and environmental containment practices.</li>
<li>Familiarity with method qualification or validation under GMP.</li>
<li>Previous work experience in a QC or regulated lab setting.</li>
</ul>
 Additional Information 
<ul>
<li>
Position is full-time, Monday to Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of&nbsp;Chesterfield, MO&nbsp;are encouraged to apply.
What we offer:
· Comprehensive medical coverage, with dental and vision options
· Life and disability insurance
· Paid holidays and vacation.
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.
</li>
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Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Cell-Based Assay Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Visa is a world leader in payments and technology, with over 259 billion payments transactions flowing safely between consumers, merchants, financial institutions, and government entities in more than 200 countries and territories each year. Our mission is to connect the world through the most innovative, convenient, reliable, and secure payments network, enabling individuals, businesses, and economies to thrive while driven by a common purpose – to uplift everyone, everywhere by being the best way to pay and be paid.
Make an impact with a purpose-driven industry leader. Join us today and experience Life at Visa.
Job Description 
Visa Research conducts both applied and fundamental research, aiming to push the boundaries of payment-related technologies on a global scale. We partner with Visa’s technology and product teams, global business units, academic institutions, and government agencies to explore and develop transformative technologies that will shape the future of payments and impact billions of people worldwide.
As a Principal Research Scientist in Quantum Information and Computation, you will play a pivotal role in defining and advancing Visa’s long-term research agenda in this field. You will lead high-impact research initiatives, mentor and develop both junior and senior scientists, and serve as a thought leader influencing Visa’s strategic direction. Your work will focus on pioneering quantum algorithms and computational models applicable to finance and payments — including areas such as portfolio optimization, risk analysis, and derivative pricing.
This role offers the opportunity to guide cutting-edge research from conception to implementation, foster collaborations across internal and external stakeholders, and represent Visa as a leader in the global quantum research community. The ideal candidate will be an established authority in the field, with a distinguished record of research contributions, demonstrated leadership in complex projects, and a passion for developing talent.
Responsibilities:
<ul>
<li>
Lead the formulation and execution of an ambitious, forward-looking research agenda in quantum information and computation, with emphasis on applications to finance and payments.
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<li>
Design, analyze, and prototype novel quantum algorithms and computational models to advance the state-of-the-art.
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<li>
Mentor and coach both junior and senior scientists, fostering technical excellence, innovation, and professional growth.
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<li>
Drive multi-institution collaborations with academia, industry, and government research bodies.
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Publish influential research in top-tier conferences and journals, and present work at leading scientific forums.
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<li>
Engage with business and product leaders to translate research outcomes into strategic opportunities, influencing product and technology roadmaps.
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Stay at the forefront of breakthroughs in quantum computing and related disciplines, assessing their potential impact on Visa’s business.
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Cultivate strong relationships with the global quantum research community to foster collaboration and knowledge exchange.
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<li>
Oversee project lifecycles, ensuring rigor, impact, and alignment with Visa’s long-term vision.
</li>
</ul>
This is a hybrid position. Expectation of days in office will be confirmed by your hiring manager.
Qualifications 
Basic Qualifications: •12 or more years of work experience with a Bachelor’s Degree or at least 10 years of work experience with an Advanced degree (e.g. Masters/MBA /JD/MD), or a minimum of 5 years of work experience with a PhD. Preferred Qualifications: •15 or more years of experience with a Bachelor’s Degree or 12 years of experience with an Advanced Degree (e.g. Masters, MBA, JD, or MD), PhD with 9+ years of experience •PhD in Computer Science, Computer Engineering, Mathematics, Engineering, Physics, or a related field. •7+ years of postdoctoral research experience in quantum computing or related domains. •Internationally recognized research track record, evidenced by high-impact publications, patents, and contributions to the research community. •Proven leadership in guiding large-scale, multi-institution research programs. •Deep expertise in designing quantum computing solutions for financial or related applications. •Proficiency in quantum programming environments such as Qiskit, Cirq, or equivalent platforms. •Hands-on experience deploying and validating algorithms on quantum hardware. •Demonstrated excellence in mentoring scientists at varying career stages.
 Additional Information 
Work Hours: Varies upon the needs of the department.
Travel Requirements: This position requires travel&nbsp;5-10% of the time.
Mental/Physical Requirements: This position will be performed in an office setting.&nbsp; The position will require the incumbent to sit and stand at a desk, communicate in person and by telephone, frequently operate standard office equipment, such as telephones and computers.
Visa is an EEO Employer.&nbsp; Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.&nbsp; Visa will also consider for employment qualified applicants with criminal histories in a manner consistent with EEOC guidelines and applicable local law.
Visa will consider for employment qualified applicants with criminal histories in a manner consistent with applicable local law, including the requirements of Article 49 of the San Francisco Police Code.
U.S. APPLICANTS ONLY: &nbsp;The estimated salary range for this position&nbsp;is $242,100 to $387,800 USD per year, which may include potential sales incentive payments (if applicable).&nbsp; Salary may vary depending on job-related factors which may include knowledge, skills, experience, and location. In addition, this position may be eligible for bonus and equity. Visa has a comprehensive benefits package for which this position may be eligible that includes Medical, Dental, Vision, 401 (k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness Program.

Principal Research Scientist- Quantum Computing

<h3>Job Description</h3>
Job DescriptionSalary: DOE 
Position: Staff Geologist Location: Austin, TX
 
Mission/ Position Description Summary The mission of a Staff Geologist for HVJ, a leading specialty engineering firm in Texas, is to support the project manager or other staff as directed to assure client satisfaction following the applicable standards, specifications and company guidelines.
 
Responsibilities Include: Performing field work including marking borings, lab testing as needed, logging behind drill rigs (ability to lift 50 lbs. and some travel and alternating shiftwork should be expected) Coordinate field and/or lab assignments Engineering analyses for shallow and deep foundations, retaining walls, slope stability, and settlement. Drafting geotechnical reports for Project Mangers review Assisting Project Managers in Business Development
 
Key Criteria/Requirements: MSCE or BSCE with three to five years of directly related experience. Registered GIT or in the process of becoming one. Excellent written and communication skills and strong math and science skills Valid Texas Driver License Ability to tolerate year round outdoor work Ability to trouble shoot and fix testing equipment a plus Ability to work nights and weekends sometimes traveling within Texas (as needed) Additional Key Expectations: Obtain PG license within 2 years
 
Key Accountabilities: Utilization The amount of time spent working on billable projects. Timeliness/Punctuality Meeting expected deadlines &amp; expected working time. Participation in Professional Organizations One meeting a month towards PE certification/maintenance. Career Development Relevant In-house Training
 
Benefits: 401(k) 401(k) matching Dental, Health &amp; Vision insurance Employer Paid Life, AD&amp;D, &amp; Disability insurance Paid Time Off 8 Paid Holidays Employee Assistance Program Referral Program Professional development &amp; growth opportunities Tuition Reimbursement Casual environment Bonus Eligibility Flexible work environment/arrangements 
 
Physical Requirements: 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 frequently required to sit and talk or hear, and to utilize a computer and software applications such as Microsoft Office. The employee is occasionally required to stand; walk; drive; use hands or fingers; handle or feel objects, tools, or controls; reach with hands and arms; and stoop, kneel, crouch, or crawl. Must be capable of distance driving and have the ability to work weekends and/or shiftwork when required. The employee must occasionally lift and/or move up to 10 pounds and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus.

Staff Geologist

<h3>Job Description</h3>
Job Description
position summary
Merjent, Inc. (Merjent) is seeking highly motivated and experienced Wetland Field Ecologists to lead, manage, train, and mentor multiple crews in conducting wetland and other ecological surveys in support of utility, transportation, and development projects primarily in the Midwest, with the potential to work throughout the U.S. Primary duties include wetland and stream delineations with additional opportunities to perform threatened and endangered species surveys, functional assessments, habitat assessments, vegetation surveys, and wildlife surveys, in addition to completing associated survey reporting work.
The work environment will consist of both urban and remote field settings, which may include work in adverse weather conditions, and, in some instances, irregular and/or steep terrain. Approximately 80-90% travel is anticipated during the field season, as well as extended (10+ hour) days and/or more than 5-day work weeks. Overtime pay will apply for hours worked in excess of 40 hours per week. 
These are full-time benefits eligible opportunities with an anticipated base wage between $27 to $40 per hour depending on qualifications and experience. Ideal candidates for this position will reside in the Midwest and be familiar with federal and state regulatory agencies and their required protocols. Work schedule is flexible and focused on meeting project and project team needs.

why Merjent?
Merjent is a medium-sized consulting and engineering company dedicated to creating an environment where both people and projects succeed. Merjent has staff located across the United States who may choose a remote, in-office, or hybrid work arrangement. All full-time employees begin their tenure at Merjent with 4 weeks of paid vacation regardless of seniority. In addition, employees receive 10 paid holidays and generous benefits and compensation packages. Merjent supports annual career-related training for employees to become or continue as leaders in their field of expertise. Merjent facilitates organic growth within the company and encourages employees to bring their ideas forward to grow existing and create new service lines within and beyond the currently served sectors of energy, mining, transportation, manufacturing and construction, land development industries, and government. Merjent also invests in its company culture by supporting travel for remote employees to attend in-person team meetings and all-staff events.
The Merjent difference is real – it's based on a commitment to our values, which guides us in how we work with clients and each other. Our commitment to quality and professional integrity encompasses everything we do. We are proud of our reputation for delivering quality work and building long-term, trusting relationships with our clients and with regulatory agencies.

responsibilities
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<li>Conduct wetland delineations according to the 1987 U.S. Army Corps of Engineers Wetland Delineations Manual and applicable regional supplements.</li>
<li>Collect, record, manage, and analyze geospatial data using Trimble and ESRI products.</li>
<li>Prepare technical reports and memos, and other documents for project planning and permitting purposes.</li>
<li>Coordinate with project teams and permitting leads to determine and verify field expectations and data collection requirements.</li>
<li>Perform habitat assessments, functional assessments, vegetation surveys, wildlife surveys, and species-specific surveys (if qualified).</li>
<li>Apply situational awareness to mitigate in-field risks and ensure compliance with industry standards and client-specific safety requirements.</li>
</ul>

qualifications and experience
<ul>
<li>Bachelor's degree or higher in Biology, Ecology, Soil Science, Hydrology, Environmental Science, Natural Resources, or related degree.</li>
<li>Minimum 3 years of experience conducting wetland delineations with at least 1 year experience leading wetland delineation teams.</li>
<li>Knowledge of federal and state wetland regulations. </li>
<li>Experience with USACE Atypical and Problem Wetland Areas methodology is preferred. </li>
<li>Familiarity using Trimble and ESRI products.</li>
<li>Midwest field work experience.</li>
<li>Excellent oral and written technical communication and organizational skills, and ability to strategize on multiple concurrent projects of varying size and complexity.</li>
<li>Competency in general MS Office applications (Word, Excel) required.</li>
<li>Ability to conduct field work for 10+ hours per day, sometimes in adverse conditions carrying equipment up to 25 pounds.</li>
<li>Ability to work weekends, multiple week shifts away from home and regularly work more than 40 hours per week.</li>
<li>Valid driver's license and acceptable driving record and able to pass a pre-employment drug screen.</li>
</ul>

E-Verify
Merjent, Inc. participates with the United States Customs and Immigration Services (USCIS) E-Verify program. We will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Candidates interested in applying should submit a completed Application for Employment (cover letter and resume) to merjent.applicantpro.com.
Merjent, Inc. is an Equal Employment Opportunity/Affirmative Action Employer committed to diversity and inclusion. We are pleased to consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other legally protected factors. Disability-related accommodations during the application process are available upon request.
Merjent is not accepting unsolicited assistance from search firms for this employment opportunity.

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