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<h3>Job Description</h3>
Job DescriptionCompany Description 
At Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the healthcare industry. As an integral part of our team, you'll have the opportunity to join our quest for better health care, no matter where you work within the Northwestern Medicine system. We pride ourselves on providing competitive benefits: from tuition reimbursement and loan forgiveness to 401(k) matching and lifecycle benefits, our goal is to take care of our employees. Ready to join our quest for better?
Job Description 
The Manager, Laboratory Support Services reflects the mission, vision, and values of NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
Responsibilities:
<ul>
<li>Leads by example; models I-CARE values (Integrity, Compassion, Accountability, Respect and Excellence) in daily work and interactions.</li>
<li>Helps all employees make the connection between CDH values, their daily work and patient and customer satisfaction. Holds staff accountable for modeling service standards and behaviors.</li>
<li>Sets clear expectations for continuous quality and service improvement. Uses internal and external benchmark data and best practices to establish specific targets, timelines and metrics for improvement projects.</li>
<li>Encourages those who identify problems, potential solutions and opportunities for improvement. Supports and empowers staff in piloting new ideas and solutions.</li>
<li>Creates an environment of partnership, collaboration, seamless quality and service enhancement across teams, departments and divisions of the organization.&nbsp;</li>
<li>Stays informed of current and emerging issues and trends for areas of accountability, CDH organization and healthcare industry. Communicates and educates staff on requirements, changes, advances, opportunities, directions and projections for the future.</li>
<li>Thinks and acts in ways that support CDH strategy, vision and plans. Identifies opportunities for new business growth and development, expansion of current services, etc.</li>
<li>Practices fiscal accountability. Encourages staff and team accountability by involving them in budget preparation, identifying ideas for increasing efficiency, cost savings, developing and growing the business and existing services.</li>
<li>Measures and monitors budget and business development plans; provides ongoing updates to staff.</li>
<li>Achieves or exceeds budget and business growth and profitability targets.</li>
<li>Makes effective hiring decisions; completes the 90-day NEWMAN orientation process for new employees.</li>
<li>Identifies staff's individual skills and interests; provides timely, positive, constructive feedback; addresses performance gaps as they occur with clear action plans and timelines for improvement.</li>
<li>Supports ongoing learning and skill development for self and staff; provides coaching and mentoring; assigns stretch goals, cross-training and other opportunities for career development within CDH.</li>
<li>Involves staff in planning and decision-making as appropriate. Holds staff accountable for follow-through and results.</li>
<li>Facilitates change readiness and agility among staff and teams.</li>
<li>Uses timely, effective communication methods to update staff on departmental and organizational priorities and progress.</li>
<li>Creates a culture of respectful communication by listening, demonstrating approachability, practicing meeting, voicemail and e-mail courtesy.</li>
<li>Asks for staff input; encourages diverse perspectives and solutions, drawing from staff, peers, physicians, patients and other stakeholders.</li>
<li>Demonstrates ability to communicate effectively across departments and sectors of organization; within all levels of management; with patients, visitors, other customers, etc.</li>
<li>Acknowledges and celebrates individual and team contributions.</li>
<li>Works in a cooperative and collaborative manner with the sales and service representatives to meet new and existing client need.</li>
<li>Fully supports through management accountability for customer service the growth of the reference laboratory.</li>
</ul>
Qualifications 
Required:
<ul>
<li>Bachelor's of Science in Medical Technology within two years of hire.&nbsp;</li>
<li>One to three years' experience in a&nbsp;CAP accredited laboratory.</li>
</ul>
Preferred:
<ul>
<li>Three or more years' experience in a&nbsp;CAP accredited laboratory.&nbsp;</li>
<li>Medical Technologist Certification.</li>
</ul>
 Additional Information 
Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status.
Background Check
Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check.&nbsp; Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act.
Benefits
We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our&nbsp;Benefits&nbsp;section to learn more.
Sign-on Bonus Eligibility:&nbsp;Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.&nbsp;

Manager of Laboratory Support Services

<h3>Job Description</h3>
Aramco energizes the world economy.
\n\n
Aramco occupies a special position in the global energy industry. We are one of the world’s largest producers of hydrocarbon energy and chemicals, with among the lowest Upstream carbon intensities of any major producer.
\n\n
With our significant investment in technology and infrastructure, we strive to maximize the value of the energy we produce for the world along with a commitment to enhance Aramco’s value to society.
\n\n
Headquartered in the Kingdom of Saudi Arabia, and with offices around the world, we combine market discipline with a generations’ spanning view of the future, born of our nine decades experience as responsible stewards of the Kingdom’s vast hydrocarbon resources. This responsibility has driven us to deliver significant societal and economic benefits to not just the Kingdom, but also to a vast number of communities, economies, and countries that rely on the vital and reliable energy that we supply.
\n\n
We are one of the most profitable companies in the world, as well as amongst the top five global companies by market capitalization.
\n\n\n\nOverview\n\n\n
We are seeking Risk &amp; Resource Geoscientist to join our Unconventional Resources Exploration and Characterization Department (URECD).
\n
URECD is responsible for identifying and evaluating Unconventional Resources across the Kingdom, leveraging integrated subsurface studies to challenge traditional perspectives and drive portfolio growth. We collaborate with asset teams to advance appraisal and field development plans, ensuring a comprehensive approach to exploring, characterizing, and developing these resources.
\n
As a Risk &amp; Resource Geoscientist, you will lead risk and resource evaluations across all subsurface assets. You will work closely with exploration, appraisal, and development teams; ensuring best approaches are applied for the integration of both geologic and engineering data for risk and resource estimates. and You will provide independent technical evaluations of wells, fields, and technical studies.
\n\n\n\n\nKey Responsibilities\n\n\n
As the successful candidate you will be required to perform the following:&nbsp;
\n
<ul>\n
<li>Assess and evaluate petroleum systems and plays interpretation workflows and products.</li>
\n
<li>Interrogate completed technical evaluations of wells and fields, and associated technical studies.</li>
\n
<li>Evaluate seismic, log, and core data to characterize subsurface structures, facies, and fluid distributions.</li>
\n
<li>Evaluate drilling, completions, production, and diagnostics data to understand reservoir performance.</li>
\n
<li>Provide guidance to geoscientists to accurately define the subsurface using geological maps, cross-sections, and grids; that incorporate seismic, sedimentological, petrophysical, and geomechanically data, etc.</li>
\n
<li>Work collaboratively with professionals across all geoscience and engineering disciplines.</li>
\n
<li>Review pre-drill and post-drill well/field evaluations.</li>
\n
<li>Complete independent risk &amp; resource assessments.</li>
\n
<li>Compile and present technical reports summarizing key technical risks and challenges.</li>
\n
<li>Mentor other geoscience professionals.</li>
\n</ul>
\n\n\n\n\nMinimum Requirements\n\n
<ul>\n
<li>As the successful candidate you will hold Bachelor's degree in Geosciences (Geology, Geophysics, or equivalent) from a recognized and approved program, an advanced degree is preferred.</li>
\n
<li>10-15 years of experience in the Exploration and Production (E&amp;P) industry, including a depth of experience in multiple unconventional plays including both source rock, and tight sand/carbonate plays.</li>
\n
<li>Experience in resource estimation and technical risk assessment, for portfolio evaluation.</li>
\n
<li>Proficiency in two or more of the following subsurface disciplines; seismic interpretation, QI, structural geology, stratigraphy, sedimentology, petrophysics, geomodelling, geochemistry, basin modeling, and geomechanics.</li>
\n
<li>Integrated work experience with reservoir engineering, drilling, completions, and production teams to; monitor drilling/stimulation operations, evaluate production &amp; diagnostics testing, execute field development, and commercial evaluation.</li>
\n
<li>Ability to work independently and make real-time decisions</li>
\n
<li>Excellent communication and interpersonal skills to facilitate collaboration and knowledge sharing.</li>
\n
<li>Proficiency in industry-standard software packages for seismic interpretation, geological modeling, data visualization and analytics, and resource assessment (Petrel, GeoX, etc.)</li>
\n</ul>
\n\n\n\nJob Post Duration \n\n\n
Job posting start date: 10/05/2025
\n
Job posting end date: 10/05/2026
\n\n\n\n\nWork Location and Work Schedule \n\n
Work Location: Within Saudi Arabia – To be specified in Job offer&nbsp; Work Schedule: Full Time - To be specified in Job offer
\n\n\n
Working environment 
\n\n
Our high-performing employees are drawn by the challenging and rewarding professional, technical and industrial opportunities we offer, and are remunerated accordingly. 
\n\n
At Aramco, our people work on truly world-scale projects, supported by investment in capital and technology that is second to none. And because, as a global energy company, we are faced with addressing some of the world’s biggest technical, logistical and environmental challenges, we invest heavily in talent development. 
\n\n
We have a proud history of educating and training our workforce over many decades. Employees at all levels are encouraged to improve their sector-specific knowledge and competencies through our workforce development programs – one of the largest in the world.
\n\n\n

Risk & Resource Geoscientist

<h3>Job Description</h3>
Responsibilities:
<ul>
<li>Excellent employment opportunity for a Clinical Laboratory Associate in the Ames, IA area.</li>
<li>Additional Information: Shift 8-4, Hours 40hrs/week</li>
<li>Prepare labels and label clinical study samples.</li>
<li>Assist in collection of clinical study samples or necropsy.</li>
<li>Aliquot clinical study samples. (serum, swab effluents, fecal samples, animal tissue samples).</li>
<li>Maintain electronic inventory of clinical study samples.</li>
<li>Accurately record all laboratory activities and techniques on data capture forms, research notebooks, and raw data notebooks as appropriate.</li>
<li>Review and contribute to protocols, planning, and execution.</li>
<li>Create and prepare submissions to diagnostic laboratories and to AVRC laboratories.</li>
<li>Compile testing information from outside labs and AVRC labs for statistical and reporting within clinical teams</li>
<li>Support clinical teams with document scanning, manual data entry and quality control of data entry.</li>
<li>Receives samples, plans, and executes processing and delivery to the appropriate lab for testing.</li>
<li>Ability to Plan and create a weekly schedule from multiple lists</li>
<li>Maintain number lists with minimal transposition</li>
<li>Initiates, executes, completes, and communicates duties and related issues</li>
</ul>
 
Experience:
<ul>
<li>A.A.S. or B.S.</li>
<li>Effective organization and time management skills.</li>
<li>Effective oral and written communication skills.</li>
<li>Handling of veterinary laboratory specimens</li>
<li>Experience with the safe and appropriate use of BSL2 organisms preferred.</li>
<li>Hand eye coordination</li>
<li>Aseptic technique</li>
<li>Proactive and resourceful.</li>
<li>Ability to work across groups and take direction from multiple scientists.</li>
<li>Competent with Microsoft Office software.</li>
<li>Exceptional interpersonal skills; High level of comfort/ease interacting with all levels of the organization.</li>
<li>Maintains a constructive and positive attitude for working on projects and for working at Company.</li>
<li>Follow Research &amp; Development policies and procedures to maintain high quality standards and follow best practices.</li>
</ul>

Clinical Laboratory Associate

<h3>Job Description</h3>
Imagery Intelligence Analysis SME The Opportunity: With cloud-based tools, faster GPUs, and the explosion of connected devices, geospatial data has more potential than ever. A skilled geospatial and remote sensing analyst can turn that data into mission critical information. If that sounds like you, we have an opportunity for you! As a geospatial and remote sensing analyst at Booz Allen, you'll work with a team of analysts to extract meaning and context from a variety of data sources. Using resources like SOCET GXP and iSpy, you'll develop new ways to find patterns and connections to answer our Army's needs. On our team, you'll also use your skills to leverage satellite and airborne remote sensing solutions, and you'll analyze data to assess meaning and potential intent. You'll analyze and provide geospatial solutions for priorities like infrastructure, topography, human geography, and intelligence. Your geospatial skills will come in handy as you produce formal reports to make sure decisionmakers have the timely information they need. Work with us as we turn data into knowledge to support our warfighters and protect our national security. Join us. The world can't wait. You Have: 
<ul>\n
<li>Experience in the application of space-based GEOINT</li>
\n
<li>Experience with photogram met ric principles and techniques</li>
\n
<li>Experience c ond ucting Foundational Military Intelligence analysis and baseline reporting</li>
\n
<li>Experience with object-based production ( OBP ) , structured observation management ( SOM ) , and activity-based intelligence ( ABI ) </li>
\n
<li>Experience with analytic modeling</li>
\n
<li>Knowledge of the full spectrum of U.S. Government and commer cia l satellite capabilities, including tasking and collection processes and protocols</li>
\n
<li>Knowledge of GEOINT Army, National System for GEOINT ( NSG ) , or Intelligence Community ( IC ) policies </li>
\n
<li>Knowledge of GEOINT sof tware, including Remote View, SOCET GXP, or ArcGIS</li>
\n
<li> Active TS/SCI clearance; willingness to take a polygraph exam </li>
\n
<li>Bachelor's degree in a Remote Sensing, Cartography, or Geography field and 15+ years of experience in Intelligence Analysis, Master's degree in a Remote Sensing, Cartography, or Geography field and 10+ years of experience in Intelligence Analysis, or Doctorate degree in a Remote Sensing, Cartography, or Geography field and 5+ years of experience in Intelligence Analysis</li>
\n</ul>
\n Nice If You Have: 
<ul>\n
<li>Experience with commer cia l visualization sof tware</li>
\n
<li>Experience with non-traditional GEOINT data sources</li>
\n
<li>Experience using the Microsoft Office suite of tools</li>
\n
<li>Experience with data analytics and COTS statistical sof tware such as SPSS, SAS, or MATLAB</li>
\n
<li>Ability to collaborate with partners across the IC and DoD on technical or substantive topics</li>
\n
<li>Ability to present intelligence information via multimedia presentations and written reports</li>
\n
<li> TS/SCI clearance with a polygraph </li>
\n
<li>GPC-II Imagery Certification</li>
\n</ul>
\n Clearance: Applicants selected will be subject to a security investigation and may need to meet eligibility requirements for access to classified information ; TS/SCI clearance is required. Compensation At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen's benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page. Salary at Booz Allen is determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The projected compensation range for this position is $77,500.00 to $176,000.00 (annualized USD). The estimate displayed represents the typical salary range for this position and is just one component of Booz Allen's total compensation package for employees. This posting will close within 90 days from the Posting Date. Identity Statement As part of the application process, you are expected to be on camera during interviews and assessments. We reserve the right to take your picture to verify your identity and prevent fraud. Work Model Our people-first culture prioritizes the benefits of flexibility and collaboration, whether that happens in person or remotely. 
<ul>\n
<li>If this position is listed as remote or hybrid, you'll periodically work from a Booz Allen or client site facility.</li>
\n
<li>If this position is listed as onsite, you'll work with colleagues and clients in person, as needed for the specific role.</li>
\n</ul>
\n Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, local, or international law.

Imagery Intelligence Analysis SME

<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.
Job Description 
Job Summary:&nbsp;Eurofins BPT-Columbia&nbsp;is looking for a&nbsp;Senior Scientistto join our Biologics Raw Materials team located in Columbia, Missouri. This individual will be a subject matter expert in testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.
Responsibilities include (but are not limited to):
<ul>
<li>Designing, carrying&nbsp;out, and performing&nbsp;simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).</li>
<li>Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.</li>
<li>Analyze data with software including Empower and effectively communicate results.</li>
<li>Train and mentor junior staff.</li>
<li>Utilize laboratory information management system (LIMS) with proficiency.</li>
<li>Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.</li>
<li>Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s degree and 3 years of experience working in a cGMP laboratory OR PhD and minimum 1 year(s) of experience working in a cGMP laboratory</li>
<li>Industrial experience with method establishment and cGMP validations are highly desirable</li>
<li>Authorization to work in the U.S. without restriction or sponsorship</li>
</ul>
The Ideal Candidate Would Possess:
<ul>
<li>Previous experience working in a CRO/CDMO adhering to cGMP regulations</li>
<li>Ability to conduct work efficiently, analyze data to ensure accuracy and report quality data.</li>
<li>Good problem solving, time management, communication, and interpersonal skills.</li>
</ul>
 Additional Information 
Position is full-time, Monday-Friday 8am-4:30pm, plus additional hours, as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.
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.

Senior Scientist: Biologics Raw Materials

<h3>Job Description</h3>
Job DescriptionJob Title: R&amp;D Chemical TechnicianJob Description
We are seeking a dedicated R&amp;D Chemical Technician to support chemical operations throughout our facility. This role involves assisting the team with tasks related to handling chemicals, chemical transfer, and packaging, as well as other essential duties in the laboratory and facility.
Responsibilities
<ul>
<li>Assist with chemical operations and handling throughout the facility.</li>
<li>Support chemical transfer and packaging processes.</li>
<li>Participate in various tasks required in the laboratory and across the facility.</li>
</ul>
Essential Skills
<ul>
<li>Experience in chemical handling and manufacturing processes.</li>
<li>Knowledge of Safety Data Sheets (SDS) and Good Manufacturing Practices (GMP).</li>
<li>Strong attention to detail.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>1 year of experience in chemical manufacturing or handling is preferred.</li>
</ul>
Work Environment
The position operates within a chemical manufacturing facility. The work is conducted during the day shift, and the environment supports the development and manufacturing of fire suppression chemicals. The facility is currently expanding, offering growth and cross-training opportunities for the right candidate.
Job Type &amp; Location
This is a Contract to Hire position based out of Green Bay, WI.
Pay and Benefits
The pay range for this position is $20.00 - $24.00/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 Green Bay,WI.
Application Deadline
This position is anticipated to close on Dec 19, 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.

R&d Technician

<h3>Job Description</h3>
Join a global community of talented professionals to shape the future of AI. Earn up to $15 USD/hr and additional rewards based on quality of submission.
\n
Outlier is committed to improving the intelligence &amp; safety of AI models. Owned and operated by Scale AI, we’ve recently been featured in Forbes for partnering experts with top AI labs to provide the high quality data for LLMs. We believe AI can only perform as well as the data it’s trained on. That’s why we work with contributors from all over the world, who help improve AI models by providing expert human feedback. This data has led to AI advancements for the world's leading AI labs and large language model builders. We’ve built a best-in-class remote work platform for our freelance contributors to provide valuable, specialized skills, and we in turn strive to provide them with a positive experience based on our core pillars of reliability, transparency, and flexibility.
\n
What you will be doing
\n
We are looking for someone who speaks fluent English to contribute their expertise toward training and refining cutting-edge AI systems.
\n
<ul>\n
<li>Adopt a “user mindset” to produce natural data to meet the realistic needs you have or would use AI for.</li>
\n
<li>Use the tool of rubrics to address user needs in a structured way.</li>
\n
<li>Evaluate AI outputs by reviewing and ranking reasoning and problem-solving responses from large language models.</li>
\n
<li>Contribute across projects depending on your specific skillset and experience.</li>
\n</ul>
\n
What we’re looking for
\n
<ul>\n
<li>Education: Bachelor’s degree or higher (or currently enrolled).</li>
\n
<li>Analytical and Problem-Solving Skills: Ability to develop complex, professional-level prompts and evaluate nuanced AI reasoning.</li>
\n
<li>Strong Writing: Clear, concise, and engaging writing to explain decisions or critique responses.</li>
\n
<li>Attention to Detail: Commitment to accuracy and ability to assess technical aspects of model outputs. Nice to Haves:</li>
\n
<li>Experience in fields like literature, creative writing, history, philosophy, theology, etc.</li>
\n
<li>Prior writing or editorial experience (content strategist, technical writer, editor, etc.).</li>
\n
<li>Interest or background in AI, machine learning, or creative tech tools.</li>
\n</ul>
\n
Compensation and benefits
\n
Earn up to $15 USD/hr, paid out weekly
\n
Rates vary based on quality, accuracy, and time spent. Paid via PayPal &amp; AirTM
\n
Free access to Model Playground
\n
Interact, experiment and engage with leading large language models free of cost
\n
Flexible schedule and time commitment
\n
No contracts, no 9-to-5. You control your schedule. (Most experts spend 5-10 hours/week, up to 40 hours working from home
\n
Join a global community of Coding experts
\n
Join a global network of experts contributing to advanced AI tools
\n
Disclaimer: For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.
\n
Equal Opportunity Employer: Outlier is committed to fostering a diverse and inclusive work environment. We welcome applicants from all backgrounds and celebrate diversity in our workforce.

Research Analyst AI Content (Remote)

<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.
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>
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 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.
Job Description 
Members of the Metrology team support processes for laboratories at Viracor with a focus on maintaining CLIA, CAP and NYDOH, GxP accreditation by using and maintaining procedures and software or other methods to perform, train, document, assist others to ensure complete and appropriate documentation of required tasks and records. The Laboratory Metrology Technician (Tech) is responsible for conducting and documenting cleaning, calibration, preventive maintenance functions, and documenting excursions from expected performance as outlined by management in the laboratory areas.
Laboratory Metrology Technician&nbsp;responsibilities include, but are not limited to, the following:
Level I –
<ul>
<li>Perform and/or assist with instrument maintenance such as plate readers and washers, liquid handling equipment, front end lab automation equipment, centrifuges, balances, etc.</li>
<li>Responsible for performing and documenting cleaning of the laboratory areas and equipment</li>
<li>Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.</li>
<li>Maintain cleaning and maintenance records as required</li>
<li>Instrument calibration activities and documentation including environmental monitoring system and laboratory equipment as directed (Pipettes/Temperature probes)</li>
<li>Respond to and document environmental alerts, ensuring documentation of actions taken/escalate as needed</li>
<li>Instrument power cycles/UPS maintenance as required</li>
<li>Inventory management and upkeep of pipettes including supplying backups and replacements as requested</li>
<li>Maintain proper records in equipment tracking software by documenting actions and maintaining schedule of required activities</li>
<li>Administration duties within the department and investigation activities which includes providing documentation as requested by internal or external auditors</li>
<li>Obtain and maintain proficiency in software programs or tools used in department</li>
<li>Support development of system and process improvements that would enhance compliance to requirements</li>
<li>Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies</li>
<li>Adhere to policies and protocols in the laboratory</li>
<li>Work closely and communicate with other laboratory associates to complete daily activities efficiently</li>
<li>Represent department and the organization favorably and in accordance with established company standards and associate attributes at all times</li>
<li>Other duties as assigned by management</li>
</ul>
Level II –
Fully meets the responsibilities of Level I plus the following:
<ul>
<li>Highly proficient in multiple processes managed by the department</li>
<li>Able to train, assist users or clients with questions and/or issues, participate in validation of updates</li>
<li>Provide training and orientation of testing personnel as directed (pipettes and environmental monitoring)</li>
<li>Maintenance of Laboratory equipment schedules, including management of calibration/maintenance tracking program/software, temperature monitoring system, and pipette calibration program, ensuring that calibrations are correct and current.</li>
<li>Understand and demonstrate proficiency with quality monitoring activities such as quality indicators and quality reporting related to equipment and monitoring such as KPIs for Quality Meeting</li>
<li>Communicates Metrology area needs to Facilities, Testing and Manufacturing personnel</li>
<li>Contacts suppliers/vendors as required</li>
<li>Participate in data reporting, internal or external client reports as requested, using Excel or other software utilized for reporting, trending, and tracking</li>
<li>Participate in continual quality improvement projects company-wide</li>
<li>Participate in creation/revision of SOPs and training materials for the department as required and ensure policies and procedures are monitored and updated to include regulatory changes</li>
<li>Other duties as assigned by managemen</li>
</ul>
Qualifications 
Basic Minimum Education Qualifications:
<ul>
<li>Level I: GED or High school Diploma</li>
<li>Level II: BA/BS in biological, physical, chemical or clinical laboratory science preferred.</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Level II: minimum of 2 years’ experience in a regulated laboratory (CAP/CLIA and/or GxP), as Laboratory Quality Tech I, or similar experience in Laboratory process ownership, e.g. laboratory technical roles.</li>
<li>Knowledge of the clinical laboratory environment preferred, including basic terminology, protocols and practices</li>
<li>Ability to initiate tasks and work efficiently with minimal supervision</li>
<li>Comfortable working in a laboratory setting</li>
<li>Knowledge of basic computer programs such as Microsoft Excel and Word including common applications in laboratory use</li>
<li>Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices</li>
<li>Position may require working hours outside of the normal work schedule when necessary</li>
<li>Ability to keep sensitive information confidential</li>
<li>Working knowledge of good laboratory practices and laboratory test methodologies.</li>
<li>Ability to identify aberrant data and potential quality/compliance concerns escalating to management.</li>
<li>Familiarity with six sigma scoring as applied to metrics/KPIs for quality</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
The Ideal Candidates Possesses the Following:
<ul>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work proactively in a self-directed manner, taking initiative as required</li>
<li>Ability to make sound decisions with little or no supervision, including generating test data, performing analysis, and escalating when appropriate</li>
</ul>
Physical Requirements:
<ul>
<li>Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead</li>
<li>Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting</li>
<li>Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours)</li>
<li>Ability to lift and move items weighing up to 50 pounds</li>
<li>Using assistance as available, must have physical ability to push/pull heavy loads (may be in excess of 100 pounds</li>
<li>Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation</li>
<li>Ability to continuously operate a personal computer for extended periods of time (4 or more hours)</li>
<li>Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions</li>
</ul>
 Additional Information 
Position is part-time, working Thursday-Saturday: 7:00 pm - 11:00 pm and Sunday 3:00 pm -11:30 pm,&nbsp;with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS 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 Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Metrology Technician (Part-Time)

<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>Perform analytical test methods including HPLC in the GMP environment</li>
<li>Document laboratory work in notebooks/e-notebooks/logbooks/electronic systems. perform data integrity checks, data verification reviews, and communicate results through electronic systems</li>
<li>Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements</li>
<li>Coordinate workflow and perform daily monitoring to meet TAT</li>
<li>Prepare and review job plans, conduct semiannual performance reviews, keep training records up to date for assigned employees, perform succession planning in preparation for growth</li>
<li>Collaborate closely with leaders and clients in implementing overall business directives</li>
</ul>
Qualifications 
<ul>
<li>Experience with HPLC a minimum of 1 year of industry lab.</li>
<li>GMP quality system and lab operations experience</li>
<li>&nbsp;Excellent communication (oral and written) and attention to detail</li>
<li>&nbsp;Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
<li>Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies</li>
<li>Bachelor's degree in biology, chemistry, or other related degree concentration, or&nbsp;equivalent directly related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to work independently and as part of a team, and possess self-motivation, adaptability, and a positive attitude</li>
<li>Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment</li>
<li>Strong focus on quality, teamwork, and productivity</li>
<li>Proactive, positive, solution-oriented leadership style with ability to prioritize and coordinate simultaneous projects with varying deadlines</li>
<li>Strength in employee engagement, morale, and retention&nbsp;</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, Monday - Friday&nbsp;8am to 5 pm</li>
<li>Ability to work overtime as required.</li>
<li>Tasks require repetitive motion and standing for long periods of time.</li>
<li>May be required to respond to off-shift operational issues.</li>
<li>Candidates currently living within a commutable distance of Indianapolis, IN&nbsp;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.

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