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<h3>Job Description</h3>
Job DescriptionCompany Description 
At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits.
Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries—from food and water to pharmaceuticals and advanced materials. We help the world’s top companies ensure their products are safe, authentic, and accurately labeled.
Job Description 
<ul>
<li>
Cell Culture &amp; Bioprocessing
<ul>
<li>Conduct lab-scale cell culture studies (shake flask → fed-batch bioreactor → harvest)</li>
<li>Support characterization of cell banks and manufacturing processes</li>
</ul>
</li>
<li>
Purification &amp; Inactivation
<ul>
<li>Perform affinity chromatography and viral inactivation for cell culture activities</li>
</ul>
</li>
<li>
Cell Banking
<ul>
<li>Execute cGLP cell banking for research use</li>
</ul>
</li>
<li>
Data Analysis &amp; Reporting
<ul>
<li>Analyze large datasets statistically</li>
<li>Draft technical reports for commercial filings</li>
<li>Present technical topics in cross-functional meetings</li>
</ul>
</li>
<li>
Collaboration &amp; Support
<ul>
<li>Coordinate lab schedules with broader scientific teams</li>
<li>Provide technical support to Manufacturing for troubleshooting and process improvements</li>
</ul>
</li>
<li>
Continuous Improvement
<ul>
<li>Develop and drive scientific or business improvement initiatives</li>
</ul>
</li>
<li>
Technical Expertise
<ul>
<li>Understand antibody manufacturing processes</li>
<li>Proficient in Microsoft Suite (Word, Excel, PowerPoint)</li>
</ul>
</li>
</ul>
Qualifications 
<ul>
<li>Education: Bachelor’s degree in Life Sciences (Chemistry or Biochemistry preferred)</li>
<li>Experience: Strong cell culture skills and demonstrated competence</li>
<li>Work Authorization: Authorized to work in the U.S. indefinitely without restrictions or sponsorship</li>
<li>Candidates currently living within a commutable distance of&nbsp;Rensselaer, NY&nbsp;are encouraged to apply</li>
</ul>
 Additional Information 
<ul>
<li>
This position is&nbsp;Wednesday-Saturday, 6:00 AM - 4:30 PM.&nbsp;
<ul>
<li>
Training will take place on a Monday-Friday, 8:00 AM - 4:30 PM schedule.
</li>
</ul>
</li>
<li>
Pay: $21.50 - $22.50 per hour
</li>
<li>
Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.
</li>
<li>
#LI-EB1
</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Biochemist - Process Characterization and Controls (Wed-Sat)

<h3>Job Description</h3>
Job DescriptionPerforming critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you. When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, ddPCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment.&nbsp;&nbsp;Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation.&nbsp;In this role, we will rely on you to:
<ul>
<li>Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and ddPCR) and handling DNA/RNA</li>
<li>Experience with procedures for the extraction and quantification of nucleic acids</li>
<li>Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level</li>
<li>Experience with cell culture is preferred</li>
<li>Plan and carry out assigned experiments. Including method development,&nbsp;method validation, sample analysis, data calculation, interpretation &amp; review, and troubleshooting</li>
<li>Design experiments &amp; evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary</li>
<li>Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects</li>
<li>Perform all aspects of the job in a way that supports the company brand, mission, vision, and values</li>
</ul>
To qualify specifically for this role, you will have:
<ul>
<li>Bachelor’s, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment</li>
<li>Experience with design, method development, validation, and sample analysis</li>
<li>Experience with GLP requirements and Good Documentation Practices (GDP)</li>
<li>Manage material, equipment, and instrumentation</li>
<li>Analyze and interpret data, prepare summary tables, and review raw data</li>
<li>Assist with the preparation and review of SOPs, study plans, and reports</li>
<li>Ability to multi-task and meet deadlines</li>
<li>Excellent verbal and written communication and organizational skills</li>
<li>Self-motivated and driven</li>
<li>Flexible and adaptable – able to work independently and/or in a team environment</li>
<li>Ability to troubleshoot and problem-solve – Critical Thinking</li>
</ul>
(Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.)&nbsp;WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work.&nbsp;WHAT YOU’LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days.&nbsp;You will grow in your career with KCAS University.&nbsp;You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach.&nbsp;You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer.&nbsp;Learn more about the Benefits at KCAS Bio&nbsp;&nbsp;WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields.&nbsp;Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another’s growth. At KCAS Bio, we advance both great science AND great people.&nbsp;Learn more about what it is like to work at KCAS Bio&nbsp;KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to <a href="mailto:kcasrecruiting@kcasbio.com" target="_blank">kcasrecruiting@kcasbio.com</a>&nbsp;or call 913-248-3000 (for TTY assistance call 711) and ask for Human Resources.&nbsp;IND123
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Associate Scientist, BioPharma Molecular

<h3>Job Description</h3>
Job DescriptionDescription:
As a Project Geotechnical Engineer, you will play a key role in managing some of the most exciting and technically challenging projects across the United States and the Pacific region! Our geotechnical team works on a variety of transportation, energy, development, and natural resources projects. Responsibilities include planning field programs, conducting technical briefings with field staff, and project management tasks including budgeting and client communications. You will also be responsible for performing engineering analyses and preparing technical reports, as well as conducting regular site visits, overseeing field explorations and construction observations. As a project manager, you will be responsible for mentoring and overseeing the work of junior staff.
 
Essential Duties and Responsibilities
<ul>
<li>Lead or coordinate the development and implementation of field exploration programs and construction observation projects. Ensure that work performed is consistent with project plans and specifications as well as in accordance with safety guidelines.</li>
<li>Assists with business-development activities such as identifying potential new clients, attending conferences or professional association meetings, etc.</li>
<li>Partners with marketing development team to develop compelling relationships for federal pursuits tied to the Indo-Pacific region.</li>
<li>Partners with marketing development team to develop compelling relationships for federal pursuits tied to the Indo-Pacific region.</li>
<li>Assist with training junior technical and technician staff.</li>
<li>Complete engineering analyses and calculations. Develop moderately complex conceptual models.</li>
<li>Complete moderately complex spatial analyses.</li>
<li>Lead the generation of technical reports including completion of routine reports, figures, tables, etc.; Assist senior staff in completing portions of large, complex reports, figures, tables, etc.</li>
<li>Support project management tasks such as budget planning, general field report reviews, and proposal development. Manage small projects under the supervision of a certified professional engineer or geologist as required.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Civil Engineering required; Master’s degree with a Geotechnical Engineering focus strongly preferred.</li>
<li>Minimum 4 years of relevant experience is required.</li>
<li>At least one year of project management experience.</li>
<li>PE license required.</li>
<li>Professional-level verbal and written communication skills are a must.</li>
<li>Valid driver’s license required.</li>
</ul>
Physical Requirements/Work Environment
<ul>
<li>All candidates are subject to completing a background check, and reference check.</li>
<li>All candidates are required to participate in our medical surveillance program.</li>
<li>Ability to perform a wide range of physical activities and do heavy work including exerting up to 50 pounds of force on occasion.</li>
<li>Ability to perform consistent work on a PC with prolonged sitting and view of a monitor/screen.</li>
<li>Ability to travel for short-term and long-term assignments as needed.</li>
<li>All employees are responsible for conducting their work in a safe manner. This includes identifying potential safety hazards and reporting them to the designated project manager in a timely manner and participating in project safety briefings. This also includes wearing appropriate safety equipment when working in the field and completing all required health &amp; safety training prior to beginning fieldwork.</li>
</ul>
Our best estimate of the salary range for this position, located in Guam, is $84,600 – $119,200 annually. Compensation offered will be based on a variety of individual factors, including education and experience, as well as internal equity. GeoEngineers’ salary ranges are reviewed and updated each year and employees are eligible for pay increases based on individual performance. As part of our competitive total rewards package, employees in this role may also be eligible for our annual year-end bonus offering, subject to program eligibility requirements.
 
At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits here.
 
Our Commitment to Belonging at GeoEngineers
When people feel they can bring their whole selves to work, that they have a voice and are supported and respected, it creates trust and a feeling of belonging— employees then flourish, grow their careers, and do the best work of their lives. A culture of belonging allows our employees to thrive and our company to prosper. This is a journey, and we are committed to doing the work, learning and evolving as we go.
 
GeoEngineers is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances.
 
GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at <a href="mailto:hr@geoengineers.com" target="_blank">hr@geoengineers.com</a> or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis.
 
We welcome and encourage individuals from all backgrounds and experiences to apply for openings on our team. We would love for you to join us!
 
We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies.
Requirements:

Project Geotechnical Engineer - Pacific Region

<h3>Job Description</h3>
Job DescriptionCompany Description 
Vitol is a leader in energy and commodities. Vitol produces, manages and delivers energy and commodities to consumers and industry worldwide.&nbsp;In addition to its primary business of trading, Vitol is invested in infrastructure globally, with $10+billion invested in long-term assets.
Vitol’s customers include national oil companies, multinationals, leading industrial companies and utilities. Founded in Rotterdam in 1966, today Vitol serves its customers from some 40 offices worldwide. Revenues in 2024 were $331bn.
For more information: vitol.com
Job Description 
Vitol is seeking a Quantitative Risk Analyst to join our Market Risk team, with a focus on portfolio-level market risk across commodities. In this role, you will assess, monitor, and report market risks across Vitol’s dynamic trading portfolios, providing quantitative insights that support risk management and commercial decision-making.
Key Responsibilities:
<ul>
<li>Analyze and monitor market risk exposures across portfolios, including VaR, stress testing, and scenario analysis</li>
<li>Develop, implement, and enhance quantitative risk models</li>
<li>Support deal structuring and option modelling for complex transactions</li>
<li>Collaborate with trading, risk, and technology teams to ensure robust risk measurement and reporting</li>
<li>Prepare regular and ad-hoc risk reports for senior management, highlighting key risk drivers and portfolio sensitivities</li>
<li>Identify and communicate emerging risks and market trends specific to commodities</li>
<li>Support the development and maintenance of risk systems, tools, and dashboards, leveraging Vitol’s internal platforms</li>
<li>Contribute to the ongoing improvement of risk management frameworks, policies, and procedures</li>
<li>Ensure compliance with internal risk limits and regulatory requirements</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree or higher in a quantitative field (e.g., Mathematics, Statistics, Finance, Engineering, Physics)</li>
<li>Strong understanding of energy/commodity markets, derivatives, and risk management concepts</li>
<li>Proficiency in quantitative analysis, statistical modeling, and programming (e.g., Python, R, MATLAB)</li>
<li>Experience with risk measurement techniques such as VaR, stress testing, and scenario analysis</li>
<li>Experience in deal structuring and option modelling for energy or commodity markets</li>
<li>Excellent analytical, problem-solving, and communication skills</li>
<li>Ability to work independently and collaboratively in a fast-paced, global environment</li>
<li>Direct experience in energy, commodities, or financial trading, with a focus on power and gas, is highly desirable</li>
</ul>
 Additional Information 
All your information will be kept confidential according to EEO guidelines.

Quantitative Risk Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated&nbsp;soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets.
Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace ®. We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees.
Why join Clean Earth?&nbsp;
In addition to competitive pay, we also offer:&nbsp;
<ul>
<li>Health benefits available Day 1&nbsp;</li>
<li>401k available Day 1&nbsp;</li>
<li>10+ paid holidays/year&nbsp;</li>
<li>Free HAZWOPER training and certification&nbsp;</li>
<li>Overtime opportunities&nbsp;</li>
<li>Ability to be cross-trained into different roles&nbsp;</li>
</ul>
Job Description 
Performs various assigned tasks and physical labor to ensure proper off-site treatment and disposal of customers’ hazardous waste materials in accordance with environmentally responsible and cost-effective practices and Clean Earth policies, practices, and procedures. The ability to oversee a small project/job with supervision of personnel.
Primary Responsibilities (Essential Functions):
• Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations.
• Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract.
• Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed.
• Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle
• Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures.
• Maintain a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations.
• Follows, understands, and promotes by example, all Health &amp; Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &amp;Safety plans/JSA’s as outlined in the procedures and policies.
• Perform unknown field testing for classification and packaging for transportation and disposal.
• Mentor and assist new employees in field work duties.
• Complete site walks to inventory and assess requirements for potential and awarded work.
• Assist sales in creating estimates for lab pack work.
• Performs other duties as assigned.
• Lead/coordinate field service/lab pack jobs requiring multiple personnel/days.
Qualifications 
• Associate College degree in area of General Science or equivalent experience
• Commercial Driver’s License (CDL) with Hazardous Material endorsement and a clear record
• Moderate to extensive travel with 20% overnight travel
• Physical ability to lift and move material of various weights frequently exceeding 55 lbs.
• Basic understanding of chemistry through general chemistry or biology
• Advanced knowledge of EPA and DOT
• Minimum one (1) year lab pack experience  40-hour OSHA HAZWOPER (29 CFR 1910.120)
• 40 hours Depack Experience
• 8 hours DOT Training
• PPE Training which includes Respirators
Preferred Qualifications:
EDUCATION/CREDENTIALS:
• BS/BA in science related field.
MEASURES OF PERFORMANCE:
 Completion of the following curriculum:
• Clean Earth Lab Pack I Training – (24 hours)
• RCRA/DOT refresher course
• Department of Transportation
• Lab Pack definitions and procedures
• Lab pack Field Program
• Introduction to High Hazardous Cylinder Assessment course
• Customer Interactions
• Waste Management Methods
• On-Site Expectations
• Manifest/ LDR Completion • Health &amp; Safety course(s)
• Customer Approach • Forklift Training
• Local Facility Capabilities
• CPR/First Aid/Blood-borne Pathogen training
• State regulations (if applicable)
• All required local training
DEMONSTRATED KNOWLEDGE, SKILLS, AND ABILITIES:
• Strong communication skills to interact with customer to provide information, explanations, and/or instructions
• Team Player • Attention to detail
• Ability to work independently using initiative and effective communication to solve challenges.
• Demonstrate proficiency to operate a computer with Windows based programs (i.e., Microsoft excel and word)
• Demonstrates extensive Lab Pack knowledge (i.e., US EPA, DOT, and chemical properties)
WORKING ENVIRONMENT:
• Customer sites, plant, labs
• Indoor/Outdoor and associated weather conditions
This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position.
This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements.
 Additional Information 
Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching.&nbsp;
We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.&nbsp;
If you have a difficulty applying for any job posted on Harsco Clean Earth’s website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free (833) 209-2659 and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response.&nbsp;

Lab Pack Chemist II

<h3>Job Description</h3>
Job Description
Divergent is a technology company that has architected, invented, built, and commercialized an end-to-end factory system called the Divergent Adaptive Production System (DAPS) that comprehensively uses machine learning to optimally engineer, additively manufacture, and flexibly assemble complex integrated vehicle structures and subsystems. Products created using DAPS are superior in performance, lower in cost, rapidly customizable to meet mission and customer-specific requirements, faster to market, and scalable on demand to high volume production. Divergent is a qualified Tier 1 supplier to global automotive OEMs, and Divergent is now expanding to support mission critical needs in the Aerospace and Defense sector. Join us to be a part of this transformative journey, where your impact will shape the future of technology and production.
Purpose
The Metrology Programmer creates, maintains, and optimizes inspection programs and templates across PC-DMIS, ZEISS Inspect, and PolyWorks for CMMs, portable arms, and GOM/ATOS optical systems. This role not only builds robust, efficient programs but also performs hands-on inspections, operates advanced metrology equipment, and supports technicians with reporting and data validation as needed. 
 Acting as both a technical anchor and a collaborative guide, the Metrology Programmer ensures inspection accuracy, drives standardization, manages programming priorities, and elevates team capability. Through deep expertise, disciplined execution, and a steady presence on the floor, this role enables precise, compliant measurement results that uphold engineering requirements and strengthen production quality. 
The Role
<ul>
<li>Develop, edit, and maintain metrology programs/templates across CMMs, portable arms, and optical systems to drive consistency and efficiency. </li>
<li>Perform dimensional inspections using CMMs, portable arms, GOM/ATOS, and conventional tools to verify parts against CAD and engineering requirements. </li>
<li>Interpret and apply engineering documentation, including 2D drawings, 3D models, GD&amp;T, and related specifications. </li>
<li>Support and prepare First Article Inspection Reports (FAIRs) in accordance with internal and industry standards. </li>
<li>Review and validate supplier and subcontractor FAIRs and production inspection records when required. </li>
<li>Collaborate with cross-functional teams to meet quality, throughput, and delivery targets. </li>
<li>Guide and mentor technicians on program execution, workflow standards, and proper equipment use/maintenance. </li>
<li>Clearly communicate non-conformances and inspection results to Manufacturing, Engineering, and leadership. </li>
<li>Maintain and improve standard program libraries, templates, and best practices to elevate metrology capability. </li>
<li>Perform additional duties assigned to support overall quality objectives and cross-functional alignment. </li>
</ul>
Basic Qualifications
<ul>
<li>Ability to lawfully access information and technology that is subject to US export controls </li>
<li>Well demonstrated experience with 2D and 3D inspections using a CMM, preferably utilizing PCDMS, Hexagon and GOM-ATOS inspection software applications </li>
<li>Working knowledge of inspection and documentation procedures </li>
<li>Ability to interpret GD&amp;T and engineering drawing </li>
<li>Strong attention to detail and ability to work independently in a fast-paced environment. </li>
<li>Aerospace manufacturing experience </li>
<li>Ability to work effectively with diverse team members </li>
<li>Excellent communication and interpersonal skills. </li>
<li>Ability to multi-task and streamline day-to-day operations. </li>
</ul>
Preferred Qualifications
<ul>
<li>Machining Shop experience </li>
<li>Bachelor's degree in mechanical engineering, Manufacturing Engineering, or related technical field. </li>
</ul>
Work Environment
<ul>
<li>This role is based in a dynamic manufacturing setting and may require standing and handling precision equipment for extended periods of time. </li>
<li>Must be able to lift at least 25 lbs. </li>
<li>Company Uniform must be worn while working. </li>
<li>PPE must be worn while working. </li>
</ul>
Compensation
At Divergent, our pay range is based on the level of the job. For this role, we will consider candidates at levels S04 - S05 as evaluated through our interview process. 
<ul>
<li>Specialist / S04: $46.00 - $63.00</li>
<li>Senior Specialist / S05: $110,160.00 - $151,470.00</li>
</ul>
Pay Range$46—$72.82 USD
What We Offer:
<ul>
<li>Holistic Compensation Package: Enjoy a world-class compensation package that includes a competitive salary, equity plan, and discretionary results-based incentive bonus opportunities, ensuring you're truly valued for your contributions.</li>
<li>Wellness and Time Off: Embrace a healthy lifestyle with paid vacation, sick time, and company holidays, including a year-end shutdown to recharge. We support growing families with paid parental leave, recognizing the importance of bonding time.</li>
<li>Comprehensive Health and Wellness: Prioritize your well-being with our comprehensive health and wellness benefits, offering both HMO and Premium PPO options. Additionally, benefit from company-sponsored life insurance and short and long-term disability coverage for peace of mind.</li>
<li>Investment in Growth: We're committed to your professional development. Take advantage of reimbursement opportunities for learning and development initiatives, empowering you to continuously expand your skill set and reach peak performance.</li>
<li>Collaborative and High-Performing Environment: Join our collaborative, dynamic, and high-performing team within a fast-paced, mission-driven company. Together, we're disrupting the traditional manufacturing industry, fostering innovation, and integrating people and technology to reduce our footprint. </li>
</ul>
 Equal Employment Opportunity Divergent is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected characteristic. Divergent provides affirmative action in employment for qualified Individuals with Disabilities and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. EEO Poster 
In order to adjust to changes in our business, it may become necessary to add, remove or modify certain duties and responsibilities, or to reassign you to another job position. From time to time you may be asked to work on special projects or to assist with other work. Your cooperation and assistance in performing such additional work is expected. E-Verify: Right to Work Our company participates in E-Verify. E-Verify is a program that electronically confirms a candidate's eligibility to work in the United States after completing the Employment Eligibility Verification (Form I-9). The information provided on the Form I-9 is compared to the records contained in the Social Security Administration and Department of Homeland Security (DHS) databases. This helps employers verify the identity and employment eligibility of newly hired employees. Eligibility to Work Poster (English) | Eligibility to Work Poster (Spanish) Los Angeles Fair Chance Initiative for Hiring Ordinance (FCIHO) Pursuant to the Los Angeles Fair Chance Initiative for Hiring Ordinance (FCIHO), we will consider for employment qualified applicants with arrest and conviction records.
No agencies, no solicitations, and no calls please.

Metrology Engineer

<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 
Pay Range: $67k/Yr.- $92k/Yr.
Shift: 8:45am- 5pm
The Associate Food Scientist focuses on prototype formulation, understanding ingredient functionality, and working with suppliers to source ingredients for new products. The Associate Food Scientist also support pilot plant production runs, shelf life studies, and learn the basic requirements to produce GMP products for testing.
Essential Duties and Responsibilities:
•&nbsp;&nbsp; &nbsp;Demonstrates and promotes the company vision •&nbsp;&nbsp; &nbsp;Regular attendance and punctuality •&nbsp;&nbsp; &nbsp;Applies GMP/GLP in all areas of responsibility, as appropriate •&nbsp;&nbsp; &nbsp;Under direction, independently executes: o&nbsp;&nbsp; &nbsp;bench-top experiments and formulation work o&nbsp;&nbsp; &nbsp;nutritional and component analysis o&nbsp;&nbsp; &nbsp;pilot plant trials, shelf life studies, and sensory studies o&nbsp;&nbsp; &nbsp;experimental design •&nbsp;&nbsp; &nbsp;Plans activities such as calculating ingredient quantities, production timing, and planning own weekly schedule&nbsp; •&nbsp;&nbsp; &nbsp;Supports pilot plant trials; prepares samples for processing, operates processing and/or packaging equipment, and collects data. Produces samples of good quality. •&nbsp;&nbsp; &nbsp;Interfaces with ingredient suppliers; orders ingredients and requests documentation. Seeks out information/facilities to get the job completed. &nbsp;&nbsp; •&nbsp;&nbsp; &nbsp;Makes suggestions for modifications in experimental approach and proactive feedback on next steps based on results. •&nbsp;&nbsp; &nbsp;Occasionally (up to 10% of time) has to travel overnight, weekends, interstate and/or international travel. &nbsp; •&nbsp;&nbsp; &nbsp;Must demonstrate excellent communication and interpersonal skills; must be a team player who is professional and presentable. •&nbsp;&nbsp; &nbsp;Assists in writing reports, methods, protocols and SOPs. •&nbsp;&nbsp; &nbsp;Keeps updated and educated on relevant news, literature and findings in the industry. &nbsp; •&nbsp;&nbsp; &nbsp;Networks with individuals outside of Covance •&nbsp;&nbsp; &nbsp;Trains and assists less experienced staff •&nbsp;&nbsp; &nbsp;Completes all required training courses. •&nbsp;&nbsp; &nbsp;Learns and demonstrates departmental procedures and policies •&nbsp;&nbsp; &nbsp;Viewed as a resource across multiple teams •&nbsp;&nbsp; &nbsp;Performs other related duties as assigned •&nbsp;&nbsp; &nbsp;Conducts all activities in a safe and efficient manner •&nbsp;&nbsp; &nbsp;Performs other duties as assigned &nbsp;
Qualifications 
Education Minimum Required: •&nbsp; &nbsp; Masters of Sciences degree in Food Science or an allied science is required&nbsp; •&nbsp;&nbsp; &nbsp;Bachelor of Science in Food Science or allied science with a minimum of one year practical experience&nbsp;
Experience Minimum Required: •&nbsp;&nbsp; &nbsp;Demonstrates understanding of food GMP’s and FDA requirements for process adequacy. •&nbsp;&nbsp; &nbsp;Basic knowledge of computers and software programs •&nbsp;&nbsp; &nbsp;Must be able to work with both lab and pilot scale food processing machinery.
 Additional Information 
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.
Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Food Scientist

<h3>Job Description</h3>
Job Description
At Relativity Space, we're building rockets to serve today's needs and tomorrow's breakthroughs. Our Terran R vehicle will deliver customer payloads to orbit, meeting the growing demand for launch capacity. But that's just the start. Achieving commercial success with Terran R will unlock new opportunities to advance science, exploration, and innovation, pioneering progress that reaches beyond the known.
Joining Relativity means becoming part of something where autonomy, ownership, and impact exist at every level. Here, you're not just executing tasks; you're solving problems that haven't been solved before, helping develop a rocket, a factory, and a business from the ground up. Whether you're in propulsion, manufacturing, software, avionics, or a corporate function, you'll collaborate across teams, shape decisions, and see your work come to life in record time. Relativity is a place where creativity and technical rigor go hand in hand, and your voice will help define the stories we're writing together. Now is a unique moment in time where it's early enough to leave your mark on the product, the process, and the culture, but far enough along that Terran R is tangible and picking up momentum. The most meaningful work of your career is waiting. Join us.
About the Team: 
The Stage Manufacturing team turns design into reality, owning the build of Terran R's primary structures. This isn't about turning the same bolt every day; it's about building the systems to build the rocket. Engineers and technicians work side by side, with deep collaboration and real-time feedback, to shape how we build better and faster. With a manifest and a launch date, it's up to the team to deliver on Terran R: solving challenges in real time, optimizing for scale, and constantly improving processes. As the vehicle evolves, so will the factory, with opportunities to apply automation, machine learning, and advanced technologies. What we build here sets the blueprint for the future of scaled launch.
This is a 2nd shift position with a standard schedule of 3:00 PM – 1:30 AM PT, Monday through Friday. The role includes a 10% shift differential added to the base pay. Please note that this position is structured around a baseline expectation of a 50-hour workweek, which may include occasional overtime as needed to meet operational goals.
About the Role:
<ul>
<li>Set up and operate orbital tube welding machine and necessary purge equipment. </li>
<li>Prep, assemble, fit up, and tack complex fluids assemblies at on assemblies at elevated heights. </li>
<li>Verify weld quality visually and using a borescope system. </li>
<li>Collaborate with leadership and team members</li>
</ul>
About You:
<ul>
<li>4+ years of OTW experience </li>
<li>Experience with welding and tacking </li>
<li>Experience with aerospace mechanical assembly </li>
<li>Comfortable working in a confined space. </li>
<li>Ability to read engineering drawings </li>
</ul>
Nice to haves but not required: 
<ul>
<li>Familiarity with COPV's </li>
<li>Experience with rigging and crane operations </li>
<li>Familiar with AWS D17.1. </li>
<li>Experience with cutting tools</li>
</ul>
Benefits: 
<ul>
<li>100% health care coverage on your first day</li>
<li>Quarterly wellness stipend to use on health and wellness</li>
<li>Partnership with Modern Health with access to 8 therapy &amp; coaching sessions and mental health resources</li>
<li>Discounts on gym memberships, travel and entertainment through PerkSpot</li>
<li>Unlimited onsite snacks</li>
<li>Free lunch on Mondays and Fridays</li>
<li>Annual learning and development stipend</li>
<li>PPE Stipend</li>
<li>Pet Insurance through Fetch</li>
<li>Company Paid Life Insurance, Short Term Disability, and Long Term Disability</li>
<li>Up to 12 weeks salary continuation for paid pregnancy disability leave</li>
<li>8 Weeks company paid parental leave</li>
<li>Access to One Medical </li>
</ul>
At Relativity Space, we are committed to transparency and fairness in our compensation practices. Actual compensation will be determined based on experience, qualifications, and other job-related factors. Compensation is only one part of our total rewards package. Relativity Space offers competitive salary and equity, a generous PTO and sick leave policy, parental leave, an annual learning and development stipend, and more! To see some of the benefits &amp; perks we offer, please visit here.
Hiring Range:$35.25—$45.65 USD
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
If you need a reasonable accommodation, please contact us at <a href="mailto:accommodations@relativityspace.com" target="_blank">accommodations@relativityspace.com</a>.

Senior Orbital Tube Welder, Second Shift

<h3>Job Description</h3>
Job DescriptionDescription:
Come Live, Work, and Thrive in Anchorage, Alaska
Medical Physicist – Aurora Integrated Oncology Foundation
 
Imagine living where others dream of vacationing, surrounded by majestic mountains, ocean vistas, vibrant wildlife, and endless opportunities for outdoor adventure. In Anchorage, you can enjoy world-class recreation year-round while building a meaningful, rewarding career with a team that truly values you.
Aurora Integrated Oncology Foundation (AIOF) is seeking a compassionate, dedicated, and collaborative Medical Physicist to join our close-knit, mission-driven team. Here, you won’t just be another staff member, you’ll be a respected partner in a workplace built on trust, connection, and exceptional patient-centered care.
 
Why You’ll Love Working with Us
Working in our small-team environment means you’ll enjoy greater autonomy, stronger relationships, and daily opportunities to see the direct impact of your expertise. You’ll have the time to form meaningful bonds with patients and colleagues, and the freedom to shape a warm, respectful, and uplifting clinical environment.
Our Anchorage location offers an unmatched lifestyle—summer hikes, fishing, kayaking, and wildlife viewing; winter skiing, snowboarding, and northern lights; and year-round natural beauty that makes balance and well-being not just possible, but easy. Combined with our center’s commitment to healthy work-life harmony, you’ll have both the time and energy to enjoy everything Alaska has to offer.
 
As the Medical Physicist for AIOF, you will be the technical leader in radiation oncology, working in close collaboration with radiation oncologists and a skilled support team. Your work ensures the highest levels of accuracy, safety, and quality in radiation treatment.
You will work with:
<ul>
<li>Varian TrueBeam (VMAT, SBRT, SRS/SRT, 3DCRT, electrons)</li>
<li>Eclipse and ARIA for TPS and EMR</li>
<li>Physics efficiency tools including MIM, Radformation, and ImageOwl</li>
<li>SNC equipment: DQA3, ArcCheck, SRS MapCheck, 1DTank, IC Profiler</li>
<li>IBA Blue Phantom 2 with a comprehensive suite of chambers and electrometers</li>
</ul>
You’ll support two experienced radiation oncologists at Anchorage Radiation Oncology Center, Midtown Anchorage. Your team will consist of three radiation therapists, one dosimetrist, and have the support of other physicists within our organization. Typical patient volume is 25–30 patients —dynamic yet manageable, with a focus on personalized, high-quality care.
Essential Responsibilities
Conduct weekly, monthly, quarterly, and annual QA on linacs, TPS, and CT simulators following manufacturer, AAPM, and IEMA guidelines.
<ul>
<li>Oversee a comprehensive QA program ensuring full regulatory compliance.</li>
<li>Partner with dosimetry to oversee treatment plan quality and accuracy.</li>
<li>Perform routine chart checks and patient-specific QA.</li>
<li>Lead the radiation safety program and ensure compliance with all federal and state regulations.</li>
<li>Drive quality improvement initiatives and RO-ILS safety review processes.</li>
<li>Provide ongoing training for clinical staff regarding medical physics, equipment use, and radiation safety.</li>
<li>Lead annual in-services and support continuing education efforts.</li>
<li>Oversee maintenance, upgrades, and commissioning for radiation oncology equipment.</li>
<li>Troubleshoot clinical systems to support seamless patient care.</li>
<li>Collaborate with radiation oncologists to optimize treatments.</li>
<li>Participate in patient conferences and support development of new procedures and techniques.</li>
<li>Stay current with emerging technologies and treatment advancements.</li>
<li>Contribute to chart rounds, meetings, and initiatives focused on practice improvement.</li>
</ul>
 
Requirements:
<ul>
<li>Board Eligible required; Board Certified strongly preferred (ABR or ABMP)</li>
<li>Master’s, Ph.D., or DMP in Medical Physics</li>
<li>Minimum one year of post-residency clinical experience preferred</li>
</ul>
What We Offer
We believe in supporting your professional success and your personal well-being.
Our comprehensive benefits include:
<ul>
<li>Generous relocation assistance</li>
<li>Competitive salary based on experience and credentials</li>
<li>Robust medical, dental, and vision coverage</li>
<li>Paid time off and holiday pay</li>
<li>Ongoing professional development and continuing education</li>
<li>A team culture built on empathy, integrity, collaboration, and respect</li>
</ul>
Physical Demands &amp; Work Environment
<ul>
<li>Ability to lift/carry up to 25 lbs</li>
<li>Ability to stand or sit for extended periods</li>
<li>Manual dexterity for routine physics tasks</li>
<li>Advanced communication, problem-solving, and analytical skills required</li>
<li>Clinical environment with moderate noise levels</li>
</ul>
 
Join Us in Making a Meaningful Impact
At Anchorage Radiation Oncology Center, every team member contributes to compassionate, high-quality care—and we take pride in supporting each other every step of the way. If you’re seeking a role where your expertise is valued, your work truly matters, and your life outside of work is enriched by breathtaking surroundings and adventure, we’d love to meet you.

Physicist

<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>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Applies the highest quality standard in all areas of responsibility</li>
<li>Demonstrates and promotes the company vision</li>
<li>Demonstrates strong client service skills, teamwork, and collaboration</li>
<li>Proactively plans and multitasks to maximize productivity</li>
<li>Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration</li>
<li>Regular attendance and punctuality</li>
<li>Applies 17025 compliance standards in all areas of responsibility, as appropriate</li>
<li>Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.)</li>
<li>Operates and maintains job-related equipment as required</li>
<li>Performs advanced troubleshooting of laboratory equipment</li>
<li>Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications)</li>
<li>Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation</li>
<li>Assists other staff in the edits and updates of SOPs, WI, and other documentation</li>
<li>Follows all Good Documentation Practices appropriately, including digital platforms</li>
<li>Maintains working areas appropriately (cleaning, disinfecting, etc.)</li>
<li>Possesses strong organizational skills</li>
<li>Provides clear feedback</li>
<li>Keeps accurate records, follows instructions, and complies with company policies</li>
<li>Proactively checks and stays current with all training across multiple learning platforms</li>
<li>Provides instruction/training to new staff</li>
<li>Recognizes errors, identifies root causes, and applies process improvements</li>
<li>Provides analysis support for method validation as needed</li>
<li>Evaluates, reviews, and approves data by other analysts</li>
<li>Independently drafts, edits, and updates SOPs, WI, and other documentation</li>
<li>Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision</li>
<li>Makes recommendations for technical improvements, as needed</li>
<li>Assists in Method Development and executes method validation protocols</li>
<li>Assist in method transfer from the MDV group</li>
<li>Write validation protocols and reports</li>
<li>Communicates effectively with client staff members</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in Chemistry, Biology, or other related degree concentration, or 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>7+ years of related experience</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 Winston-Salem, NC&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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