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<h3>Job Description</h3>
Job DescriptionCompany Description 
Trove Brands is a privately-held house of brands including BlenderBottle®, Owala®, EcoBrite™, and Whiskware®. Our patented and best-selling products are designed to simplify and improve everyday life with leading-edge innovation, incomparable quality, and aspirational style.
A career at Trove Brands is not about punching the clock. It’s about embracing exciting and fast-paced opportunities that sharpen your skills, drive innovation, and play an integral role in growing our global reach. Your work will not only impact the company, it will impact the lives of millions of people around the world. When you step up to a career at Trove, you step up to cutting-edge excellence. You sign up for bold action and invigorating synergy. You agree to face—and break through—new challenges every single day.
Job Description 
We are seeking a highly motivated and detail-oriented R&amp;D Scientist I to join our dynamic Research &amp; Development team, with a focus on sports nutrition product innovation. This role will support the development and optimization of products across a variety of delivery formats including powders, ready-to-drink (RTD) beverages, baked/freeze-dried goods, and extruded items. The ideal candidate will combine a strong scientific foundation with creativity and practical execution to deliver innovative, consumer-accepted products from concept to commercialization.
This is an exciting opportunity for someone who thrives in a collaborative, fast-paced environment and is passionate about performance nutrition, functional ingredients, and food science.
Key Responsibilities:
<ul>
<li>Support the development of innovative sports nutrition products in various delivery formats.</li>
<li>Utilize the latest research and trends in nutritional science and biochemistry to guide development decisions and optimize product efficacy.</li>
<li>Apply a deep understanding of physical and organic chemistry principles to drive product optimization and flavor development.</li>
<li>Participate in and contribute to sensory evaluation studies; collect and interpret data to guide formulation adjustments for consumer acceptability.</li>
<li>Conduct stability testing and troubleshoot formulation challenges with minimal supervision.</li>
<li>Collaborate cross-functionally with Marketing, Project Management, Supply Chain, Quality Assurance, Regulatory, Legal, and external partners to ensure timely and compliant product launches.</li>
<li>Operation of laboratory equipment including mixers, pH meters, Brix refractometers, density testers, and other analytical tools.</li>
<li>Develop formulas considering ingredient claims, interactions in formulation, and implications for certificate of analysis standards.</li>
<li>Manage multiple product development projects simultaneously, ensuring they are completed on time, within budget, and in alignment with strategic goals.</li>
<li>Ensure exemplary record keeping, reporting, and documentation of all project activities in both written and electronic formats.</li>
<li>Maintain a clean, organized, and safe laboratory environment in compliance with internal policies and safety standards.</li>
<li>Awareness of regulatory requirements to ensure product claims and nutrition facts panels meet applicable standards (FDA, DSHEA, etc.).</li>
<li>Coordinate and communicate effectively with contract manufacturing organizations (CMOs); support scale-up trials and commercial production activities.</li>
<li>Refine and standardize raw material specifications.</li>
</ul>
Qualifications 
<ul>
<li>Strong understanding of ingredient functionality, food chemistry, and sensory science.</li>
<li>Proficient in formulating food and beverage products with time and budget constraints.</li>
<li>Demonstrated ability to work independently and manage multiple priorities effectively in a dynamic environment.</li>
<li>Excellent communication and interpersonal skills; ability to explain technical concepts to cross-functional stakeholders.</li>
<li>Detail-oriented with strong analytical, organizational, and project management abilities.</li>
<li>Familiarity with Microsoft Office Suite (Excel, Word, PowerPoint); experience with formulation and nutritional software (e.g., ESHA) is a plus.</li>
<li>Experience with basic statistical analysis tools and research methodologies.</li>
<li>Strong problem-solving mindset with a proactive and flexible approach to R&amp;D challenges.</li>
<li>Minimum: Bachelor of Science (B.S.) in Food Science, Food Chemistry, Nutritional Sciences, or a related scientific discipline.</li>
<li>Preferred: Advanced coursework or background in nutritional biochemistry.</li>
<li>Experience: Minimum of 2+ years of relevant experience in food product development, preferably in sports nutrition, functional foods, or nutraceuticals.</li>
<li>Hands-on experience with contract manufacturing or co-manufacturing environments is highly desirable.</li>
<li>Understanding of regulatory frameworks related to food labeling and nutrition claims.</li>
<li>Willingness to travel up to 25% for production trials, vendor visits, and other project needs.</li>
</ul>
 Additional Information 
Our culture is passionate, entrepreneurial, and energetic. We value innovation through collaboration. And while we work smart and hard, we also connect and celebrate with equal gusto. We host team-building activities, athletic events, and seasonal celebrations to foster community and reward accomplishments. Bottom line? You’ll love it here.
Among the many benefits our team members enjoy are:
<ul>
<li>Comprehensive medical, dental, and vision care</li>
<li>401k package with employer matching</li>
<li>Paid Time Off</li>
<li>Maternity/Paternity leave</li>
<li>Full indoor basketball/volleyball&nbsp;court</li>
<li>Fully equipped fitness center (cardio, weights, functional fitness area, lockers and showers, etc.)</li>
<li>Yoga studio</li>
<li>Meditation/Nap room</li>
<li>And much more!</li>
</ul>
Trove Brands is an equal opportunity employer.
This is a fully in-office position in Lehi, Utah.&nbsp;
Phone calls regarding this position are not accepted.

R&D Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins 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 
The hand-held Raman testing laboratory analysts in the Analytical Quality Control Operations (AQCO) organization will serve as a technical resource to execute material identification test method validations and transfers, to support installation of hand-held Raman applications in Quality Control testing labs and materials receipt areas.&nbsp; The hand-held Raman testing analyst has primary responsibility for executing approved protocols for method validation and transfer, generating the data necessary to complete studies, training analysts in receiving laboratories, and participating in investigations of protocol deviations or protocol execution issues.&nbsp; The analyst may also participate in generating documentation, including methods, protocols, reports and change controls in support of these activities. The hand-held Raman testing analyst should have familiarity with basic laboratory operations and must be capable of operating in a cGMP laboratory environment.
<ul>
<li>Execute approved protocols for method validation and transfer, with accurate documentation of execution steps and data in an electronic notebook or other electronic execution system.</li>
<li>Provide hands-on training and oversight to receiving laboratories before and during method transfers, including troubleshooting for execution difficulties.</li>
<li>Assist with investigations into protocol or method execution errors or difficulties in successful testing.</li>
<li>Author methods, protocols, and reports to support new materials or transfer existing methods to new laboratories.</li>
<li>Technically review validation or transfer data generated by other analysts.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry or related physical sciences field, or at least 1-3 years of laboratory experience in a cGMP pharmaceutical Quality Control laboratory.</li>
<li>Fundamental knowledge of requirements in a cGMP environment.</li>
<li>Effective communication and self-management</li>
<li>Effective interpersonal skills with the ability to work within a cross-functional, interdisciplinary team environment</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Additional Skills/ Preferences:
<ul>
<li>Experience using Electronic Laboratory Notebooks and electronic document repositories.</li>
<li>Prior experience with Raman spectroscopic testing</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, Monday-Friday, 8:00 am - 5:00 pm, with potential for weekends or holiday work if needed</li>
<li>Candidates currently living within a commutable distance of Indianapolis, IN, 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.

Raman (Hand-Held) Testing Laboratory Analyst

<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.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
The Laboratory Analyst has some knowledge of commonly used microbiological concepts, practices and procedures. This person has working knowledge of formulations for various media used in the laboratories’ techniques. The person in this position should be able to work independently when necessary.
***** This lab will relocate to our North Kingstown location within 2-4 months or so*****.&nbsp; &nbsp;
Must live a commutable distance to North Kingstown, RI
Compensation- $22/24/hour (DOE) plus Benefits&nbsp; Schedule is Mon-Fri&nbsp; 1st shift
Responsibilities:
• Responsible for receipt of and proper logging in of all samples received into the laboratory.
• Responsible for ensuring the correct analysis is performed on all samples received into the laboratory.
• Ensures that proper Quality Control/Quality Assurance tests are performed on all analyses for the day.
• Correctly utilizes all QC/QA documentation/logbooks.
• Assists MLT III to ensure that the QA/QC task schedule is completed as necessary.
• Input and review data entry from the bench sheets to the Laboratory Information Management System (currently Element).
• Interface with clients
• Conducts all laboratory tasks as needed.
• SOP revision as needed
• Work with MLT III and LD to order supplies necessary for the day to day running of the laboratory.
• Responsible for running routine and non-routine, specialized microbiological analyses.
• Perform field work as necessary.
• Prepare media necessary for various analyses in the laboratory.
• Laboratory maintenance.
• Work evenings, weekends, holidays as needed on a rotating basis.
Qualifications 
Minimum Qualifications:
<ul>
<li>An Bachelor’s degree in Microbiology or a related field.</li>
<li>A high school diploma or equivalent.</li>
<li>2 years’ experience in a microbiology laboratory performing various environmental analyses.</li>
<li>Strong interpersonal skills</li>
<li>Proficiency in Microsoft Office.</li>
<li>Good customer service skills.</li>
<li>Must be able to perform light lifting and light housekeeping duties</li>
<li>Must be able to tolerate unpleasant odors</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li>
<li>Perform other duties as assigned</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
We support your development!&nbsp;Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity!&nbsp;Eurofins network of companies believe in strength and innovation through diversity, being an&nbsp;Equal Opportunity Employer.&nbsp;We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us!&nbsp;We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company description:&nbsp;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 discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
We do not offer Visa Sponsorship for this role.
Eurofins is a&nbsp;M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Analyst I, Environment Testing

<h3>Job Description</h3>
Job DescriptionCompany Description 
Leap Consulting Group supports clinical diagnostics and clinical research organizations through a full range of services supporting the end-to-end digital and technology needs of the lab, from the digital front door to the pre-analytical lab bench process (LIMS, instrumentation, automation, etc.), and all of the complex processes for report writing, revenue cycle, and patient engagement before and after testing.
Leap provides turnkey services starting with strategic planning through full implementation and everything in between for CLIA, CAP, NYS CLEP, and FDA-compliant laboratories. Leap’s lab practice is led and staffed by veteran laboratory leaders from high-volume, high-complexity laboratories across the United States. In addition to lab-centric capabilities, Leap offers full capabilities across digital, cloud, and the rest of the IT ecosystems.
Job Description 
We’re looking for experienced laboratory professionals — former bench technologists, R&amp;D scientists, or lab operations specialists — who are excited to apply their laboratory expertise to be client-facing and working directly on client lab projects building the latest and greatest in clinical laboratory workflows and laboratory software system implementations.
This is a hands-on, problem-solving role — you’ll work alongside scientists, engineers, and clinicians to make lab systems work better, not sell software or convince people why they need to do better - everyone is working together to make it better.
This role is not a generic IT business analyst position — it’s designed for individuals with deep understanding of how labs actually function, from sample accessioning to reporting. If you have great IT analyst skills we need those too, but we are currently not hiring for those. Please do not apply here if you are not deeply experienced in clinical laboratory and/or LIMS.
This is a role reporting into our Healthcare Practice Lead focused on supporting several laboratory initiatives including digital-front-doors, preanalytical systems, LIMS, lab automation, bioinformatics, revenue cycle, and other related needs. The role requires Laboratory Operations and/or Laboratory IT awareness, a background in digital transformation or information systems, and ideally exposure to clinical laboratory revenue cycle. The person in this role would be a smart, inquisitive, experienced clinical laboratory or health system technology business analyst or functional technical analyst.&nbsp;
From Buy vs. Build Analysis, to System Sourcing projects, to big picture planning, and down to the real roll-up-your-sleeves implementation requirements gathering, technical design, and partnering with your software engineering peers to deliver solutions. In this position, you will work closely with Leap client’s business, clinical, and technology leaders to understand their needs, design and develop innovative solutions, and tackle complex challenges. The people in this role will help clients articulate their requirements, prioritize their needs, develop detailed specifications, and at times will lead implementations in Agile methodologies often supporting a mixed team of both Leap provided and client employee engineering resources. The ideal candidate will be well spoken, extremely organized, and able to succinctly capture every detail. You should also be able to ask questions to clients to ensure there are no gaps in the analysis conducted and be an effective communicator when there have been changes in the requirements.
As is the nature of digital transformation consulting, the right people for this role find themselves adaptable and flexible in an environment where change is the only constant. The ideal candidate finds clarity in ambiguity and shifts priorities quickly as new client considerations, challenges, and opportunities arise.&nbsp;
You should excel in managing projects, driving product development, and analyzing business needs, all while thriving in a fast-paced and collaborative environment.
This role is a hybrid position based in our Bergen County NJ offices. Hybrid expectations include 4 days a week in office, 1 day remote, exclusive of client-related-travel which would be as required.
Key Responsibilities:
<ul>
<li>
Portfolio and Program Management:
<ul>
<li>
Partner with clients to define a product or program vision, strategy, and roadmap in alignment with business goals and stakeholder needs
</li>
</ul>
</li>
<li>
Business Analysis:
<ul>
<li>
Able to understand complex lab workflows and communicating future state changes to developers
</li>
<li>
Perform gap analysis to identify discrepancies between current processes and desired outcomes
</li>
<li>
Translate bench-side workflows into system requirements
</li>
<li>
Document process maps that mirror the flow of specimens through the lab
</li>
<li>
Collaborate with engineers to digitize and automate R&amp;D and QC processes
</li>
<li>
Be able to handle changes in workflow and how to address them when those blockers occur
</li>
<li>
Facilitate meetings to gather requirements, develop solution plans, and drive alignment with business stakeholders
</li>
<li>
Participate in detailed design sessions with the technical teams to define the implementation approach based on requirements gathered
</li>
</ul>
</li>
<li>
Project Management:
<ul>
<li>
Handle project ambiguity, complexity, and interdependencies with an organized and structured approach
</li>
<li>
Assess and prioritize new information and requirements, integrating them seamlessly into project deliverables
</li>
<li>
Identify and manage project risks and issues
</li>
<li>
Maintain project documentation, ensuring all project deliverables are documented, updated, and communicated effectively
</li>
</ul>
</li>
<li>
Facilitation &amp; Communication:
<ul>
<li>
Maintain situational awareness and resolve conflicts efficiently to keep projects on track
</li>
<li>
Ensure clear and effective communication across all levels of the organization
</li>
</ul>
</li>
<li>
Adaptability &amp; Creative Problem Solving:
<ul>
<li>
Demonstrate a proactive approach to identifying and addressing challenges
</li>
<li>
Embrace and manage chaos with a continuous learning mindset, adapting to evolving requirements and challenges
</li>
</ul>
</li>
<li>
Detail Orientation &amp; Strategic Vision:
<ul>
<li>
Dive into the details to ensure precision and accuracy while maintaining a strategic, high-level perspective
</li>
<li>
Communicate complex technical concepts in a way that is accessible to non-technical stakeholders, effectively bridging the gap between technical and business perspectives
</li>
<li>
Stay strategic without losing the detail - it is an art more than a science
</li>
</ul>
</li>
<li>
Execution &amp; Results:
<ul>
<li>
Demonstrate dependability and reliability with a focus on clear thinking and meticulous attention to detail
</li>
<li>
Produce detailed stories to drive development and be reliable for QA testing
</li>
</ul>
</li>
</ul>
If you are an energetic and multifaceted professional who can embrace uncertainty, think on their feet, and effectively manage shifting priorities to drive projects forward, with the ability to navigate both technical details and strategic business goals, we encourage you to apply and help us drive impactful solutions for our clients!
Keywords:&nbsp;LIMS, LIS, ELN, middleware, automation, genomics, pathology, molecular diagnostics, assay development, quality control, sample tracking, data integrity, CLIA, CAP, HL7, FHIR, lab workflow optimization
Qualifications 
Minimum Qualifications:
<ul>
<li>
Education: BA/BS Required
</li>
<li>
Experience: Minimum of 3-5 years working at the bench and/or as a Business Analyst or Functional Technical Analyst, preferably in a clinical laboratory&nbsp;
</li>
<li>
Be comfortable communicating in-person, by phone, over video, as well as collaboration chat tools such as Slack and Teams
</li>
<li>
Be a self-starting independent team player who is both professional and kind to colleagues and customers
</li>
<li>
Be tech savvy and ideally consider yourself 'fairly technical'
</li>
<li>
Proven experience in project management, product management, and business analysis
</li>
<li>
Strong facilitation, communication, and conflict resolution skills
</li>
<li>
Ability to manage multiple projects simultaneously and prioritize tasks effectively
</li>
<li>
Ability to manage complexity and ambiguity in a structured and organized manner
</li>
<li>
Demonstrated ability to drive results and deliver innovative solutions
</li>
<li>
Proficiency in discussing technical details and translating them into business value
</li>
<li>
Experience in performing gap analysis and creating business process flows
</li>
</ul>
Preferred Qualifications:
Knowledge, experience, or proficiency in most or all of the following:&nbsp; &nbsp; &nbsp;
<ul>
<li>
Acting as a liaison between technical operations and solutions providers
</li>
<li>
Documenting, analyzing, and recommending solutions to complex problems
</li>
<li>
Information Technology and Software Development business cycles
</li>
<li>
Healthcare Digital Physician and/or Patient Portals
</li>
<li>
Revenue Cycle Management
</li>
<li>
Laboratory Operations
</li>
<li>
Bioinformatics
</li>
</ul>
 Additional Information 
<ul>
<li>Be comfortable communicating in-person, by phone, over video, as well as collaboration chat tools such as Slack</li>
<li>Be a self-starting independent team player who is both professional and kind to colleagues and customers</li>
<li>Be tech savvy and ideally consider yourself 'fairly technical'</li>
</ul>
All your information will be kept confidential according to EEO guidelines.

Clinical Lab Business Analyst - Hybrid On-site

<h3>Job Description</h3>
Job DescriptionCompany Description 
Are you ready to take the next step in your career and join a company that truly values your contributions? At Eurofins PSS, we offer more than just a job—we provide a rewarding, enriching, and fulfilling career path with opportunities for growth and advancement.
As part of our team, you’ll work in state-of-the-art laboratories alongside passionate professionals dedicated to the testing, development, and advancement of life-saving drug products. Together, we’re making the world a healthier and happier place to live.
Eurofins PSS is a global leader in life sciences, delivering a unique range of analytical testing services that help ensure the safety, authenticity, and accuracy of products and their ingredients. We partner with some of the world’s largest companies to make life and our environment safer, healthier, and more sustainable.
Our people are our chemistry—and we’re looking for talented individuals like you to join us in making a difference.
Job Description 
Advance your scientific career in Indianapolis, a thriving center for pharmaceutical and biotech innovation. We’re seeking a Metrologist Group Leader to oversee equipment maintenance, qualification, and team development in a GMP-regulated lab environment. This is a full-time leadership role with relocation assistance provided to support your move.
Why Relocate to Indianapolis?
<ul>
<li>Affordable cost of living with vibrant urban and suburban options</li>
<li>Expanding life sciences and pharmaceutical ecosystem</li>
<li>Relocation support and onboarding assistance to help you settle in smoothly</li>
</ul>
What You’ll Do
<ul>
<li>Lead equipment maintenance and qualification activities across lab operations</li>
<li>Troubleshoot technical issues and serve as a subject matter expert on lab instrumentation</li>
<li>Collaborate cross-functionally with internal teams, vendors, and global quality groups</li>
<li>Recommend and implement process improvements to enhance lab efficiency</li>
<li>Supervise and mentor team members, manage workflow, and conduct performance reviews</li>
<li>Ensure compliance with GMP standards and maintain accurate documentation</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in physical sciences (e.g., chemistry, physics)</li>
<li>4+ years of lab experience, including leadership responsibilities</li>
<li>Strong troubleshooting skills and familiarity with CMMS systems</li>
<li>Excellent communication, organizational, and team leadership abilities</li>
<li>Authorization to work in the U.S. indefinitely without sponsorship</li>
<li>Willingness to relocate to Indianapolis – relocation support is available</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&nbsp;</li>
<li>Position is located in downtown Indianapolis, IN.&nbsp;</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>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Metrologist Group Leader - Relocation Opportunity to Indianapolis

<h3>Job Description</h3>
Job Description
We are looking for a Senior Chemical Engineer to join a state-of-the-art EV/Hybrid battery recycler. This position will be responsible for the development and implementation of new processes and products as multiple lithium-ion battery recycling facilities are established across the US, as well as the oversight of existing projects. The ideal candidate will have experience with process design, chemical synthesis, and process control. This role will be responsible for developing and implementing a wide range of projects that are critical to the company’s growth.
Primary Responsibilities:
<ul>
<li>Lead the design, installation, and commissioning of chemical processes and equipment.</li>
<li>Provide ongoing process support for plant operation and maintenance.</li>
<li>Support materials and analytical lab development and operation</li>
<li>Own process deliverables for Front End Engineering Design through EPC project phase such as flowsheets, P&amp;IDs, process modeling, control narratives, HAZOPs, etc.</li>
<li>Evaluate and recommend new process technologies to improve recycling and refining, including both technical and economics/financial considerations.</li>
<li>Work with internal and external resources to scale processes from lab to commercial</li>
<li>Support the development of new technology, processes and equipment.</li>
</ul>
Desired Qualifications:
<ul>
<li>5+ years’ experience working in an industrial chemical processing environment</li>
<li>Bachelor’s Degree in Chemical Engineering or related technical discipline</li>
<li>Experience with capital projects</li>
<li>Experience working with EPC’s to execute projects</li>
<li>Experience scaling processes from R&amp;D to Pilot to Commercial scale</li>
<li>Ability to work with and manage external resources to facilitate projects</li>
<li>Experience in hydrometallurgy, mineral extraction and separation</li>
<li>Experience in waste water treatment and pollution control systems a plus</li>
<li>Background in mining &amp; minerals and/or battery recycling processes a plus</li>
<li>Ability to travel domestically and internationally as required</li>
</ul>
Work Environment/Conditions:
Office Location: Work from Home (WFH)
Travel: 20% - 50% to plant site
Plant: Necessary to follow safety protocols and procedures in our and our customer plants. Important to interact with all levels of specialists, team leaders and department managers.

Senior Chemical Process Engineer (FILLED)

<h3>Job Description</h3>
Job Description
Senior Transportation Technician – Inertial Profiler
Requisition Number: 2025-1800-26
S&amp;ME is looking for a motivated and passionate Senior Transportation Technician – Inertial Profiler to join our Construction Services team in Atlanta, Georgia. Are you ready to contribute your education, experience, and knowledge to meaningful projects? Join us at S&amp;ME!
The project locations for this role are Gainesville, Jesup, and Augusta.
As a Senior Transportation Technician specializing as an Inertial Profiler, you will operate advanced profiling equipment to assess pavement smoothness and ride quality across transportation infrastructure projects. Your work supports engineers and project managers by ensuring accurate data collection, analysis, and reporting that directly influences construction quality and compliance. In addition to technical expertise, you will lead and coordinate field activities, mentor junior technicians, and uphold rigorous standards in data integrity and safety. This role bridges high-tech field operations with transportation engineering, contributing to the long-term performance and safety of roadways.
Your Day-to-Day: 
<ul>
<li>Operate and Maintain Inertial Profiling Equipment: Perform frequent calibrations, system checks, and routine maintenance on the inertial profiler vehicle and its components to ensure optimal performance and data accuracy.</li>
<li>Collect and Analyze Pavement Data: Drive the specialized vehicle at controlled speeds to collect surface data, then process it using software to calculate pavement quality indicators such as the International Roughness Index (IRI).</li>
<li>Document Field Activities and Generate Reports: Compose detailed daily diaries and technical reports that include observations, test results, and quantities of work completed. These reports support construction quality control and pavement management programs.</li>
<li>Monitor Contractor Compliance and Construction Quality: Inspect construction work and monitor contractor operations to ensure adherence to project specifications, including erosion and sedimentation control measures.</li>
<li>Lead and Coordinate Technician Teams: Manage and mentor a team of technicians, assigning tasks, reviewing work, and ensuring cohesive execution of field operations and data collection efforts.</li>
</ul>
In this role, you may experience shifting work hours based on project needs and weather conditions, including early mornings, some Saturdays and/or Holidays.
What You Bring:
<ul>
<li>One of the following education/experience combinations:
<ul>
<li>High school diploma/GED with 10+ years of highway-related construction or inspection experience, or</li>
<li>2-year technical degree or higher in Civil Engineering Technology or Surveying Technology with 5+ years of highway-related construction experience</li>
</ul>
</li>
<li>A valid Driver's License</li>
<li>Proficiency in operating and maintaining inertial profiler systems, including GDT-126 and distance-measuring instruments (DMI)</li>
<li>Annual AASHTO test track certification for inertial profiler operation is required and may be obtained within 30 days of hire; additional active certifications, such as ACI, ICC, and DOT in relevant testing areas, a plus</li>
<li>Strong written and verbal communication skills (speaking, reading, and writing) using the English language to effectively interact with contractors, project staff, and team members</li>
<li>A solid understanding of weight, volume, pressure, and measurement units, with the ability to analyze pavement data using specialized software</li>
<li>Skilled in troubleshooting equipment and software issues to ensure consistent and accurate data collection</li>
<li>A high level of precision in observation, documentation, and reporting to support construction quality and pavement evaluation</li>
</ul>
Working Conditions and Physical Demands:
You are willing and able to perform the physical demands of this position with the use of Company-provided Personal Protective Equipment, such as:
<ul>
<li>Outdoor, hands-on work in all weather conditions</li>
<li>Lifting and carrying 40-50 lbs. of materials and equipment</li>
<li>Safely handling field tools and maneuvering equipment on active construction sites</li>
<li>Working outside normal business hours and traveling out-of-town and possibly overnight for assignments as needed</li>
</ul>
We Are S&amp;ME:
At S&amp;ME, we're committed to your growth, professionally and personally. With over 50 years of experience delivering innovative solutions in geotechnical, civil, environmental, and construction materials engineering, we've built a strong foundation for long-term careers. Our team of 1,000+ employee-owners across 10+ states works together to create meaningful impact on our clients and communities. When you join S&amp;ME, you become part of a collaborative, honest, and people-focused culture that invests in your success. 
What We Offer:
We offer exciting project opportunities, ongoing training, and a comprehensive benefits package to support you and your family. This is more than a job; it's a place to grow, thrive, and build a future.
<ul>
<li>Medical, Dental &amp; Vision Plans with HSA and FSA options</li>
<li>100% Employee Stock Ownership Plan (ESOP)</li>
<li>401K with Company Matching</li>
<li>Paid Time Off with Rollover</li>
<li>Maternity/Paternity Leave</li>
<li>Employee Recognition Program</li>
<li>Credential Incentive Program</li>
<li>Mentorship Program</li>
<li>Tuition Reimbursement</li>
<li>Company Vehicle with Fuel Card for Project-Based Work</li>
<li>$2,000 Referral Bonuses &amp; More!</li>
</ul>
If you are seeking a challenging and rewarding career with a firm committed to our employees and providing quality service to our clients, join our team!
This full-time role offers competitive pay based on experience. Candidates must comply with our Fleet Management, Substance Policy, and Reference Check requirements. Only candidates with valid employment eligibility (I-9) will be considered. Visa assistance is not available. S&amp;ME reserves the right to hire internally or externally at any time. No candidate/recruiter calls, personal calls, or walk-ins are accepted.
 Job Posted by ApplicantPro

Senior Transportation Technician - Inertial Profiler

<h3>Job Description</h3>
Job Description
Job Title: General Production Worker 
Shifts Available:
<ul>
<li>3rd Shift: 7:00 PM - 7:00 AM</li>
<li>Rotating schedule (2 days on, 2 days off, 3 days on and every other weekend)</li>
</ul>
Pay Rate:
<ul>
<li>3rd Shift: $19.50 per hour</li>
</ul>
Key Responsibilities:
<ul>
<li>Operate machinery and equipment as trained.</li>
<li>Loading and unloading machines with product or boxes. </li>
<li>Inspect products for defects and ensure quality standards are met.</li>
<li>Maintain a clean and organized work area.</li>
<li>Assist with other production tasks as needed.</li>
<li>Lock out / tag out processes</li>
<li>Minor maintenance on machines</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent.</li>
</ul>
Benefits:
<ul>
<li>Competitive pay rates: $19.50 per hour for 3rd shift.</li>
<li>Health, dental, and vision insurance.</li>
<li>Paid time off and holidays.</li>
<li>Opportunities for overtime.</li>
<li>Career growth and development opportunities.</li>
</ul>
If you are interested, please apply now!
Pay and Benefits
The pay range for this position is $18.00 - $19.50/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 Mc Elhattan,PA.
Application Deadline
This position is anticipated to close on Nov 4, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Technician

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Pharmaceutical Technician Job Description
We are seeking a dedicated Clean Room Pharmaceutical Technician for our 2nd Shift (1pm - 11:30pm), working Sunday through Wednesday with a schedule of four 10-hour shifts. This position plays a crucial role in operating production equipment, including non-sterile filling machines, packaging, and labeling machines. The role involves supplying materials to assigned positions, cleaning equipment and production areas, and inspecting parts and items according to standard operating procedures. Additionally, this position requires basic troubleshooting and training assistance.
Responsibilities
<ul>
<li>Operate assigned equipment per established methods and procedures, including setup, operation, and cleaning.</li>
<li>Ensure configurations are correct, check for leaks or abnormalities, and communicate any issues immediately.</li>
<li>Complete operational documentation as per SOP and manage returned and rejected items.</li>
<li>Review and verify area production documentation for accuracy and real-time recording.</li>
<li>Maintain open communication with management regarding production updates, deviations, and corrective measures.</li>
<li>Exchange work status information with the department, management, and co-workers.</li>
<li>Maintain a clean work environment using appropriate cleaning solutions and methods.</li>
<li>Clean and sanitize designated equipment and tools per established methods and schedules.</li>
<li>Handle and procure raw materials and components as per prescribed methods and procedures.</li>
<li>Maintain Aseptic Process Area sterile gowning qualifications.</li>
<li>Respond immediately to equipment alarms or malfunctions and communicate conditions to experts.</li>
<li>Assist co-workers in the production of finished products according to SOPs and manufacturing instructions.</li>
<li>Receive and ship plant uniforms and scrub uniforms for cleaning.</li>
<li>Stock garments and supplies for clean rooms and sterile core, prepare garments for shipping and sterilization.</li>
<li>Assist with special projects as required or requested.</li>
<li>Promote a safe and harmonious work environment.</li>
<li>Maintain compliance with SOPs, GMPs, and all company policies.</li>
</ul>
Essential Skills
<ul>
<li>Associate or Bachelor's Degree from a regionally accredited institution.</li>
<li>One or more years of previous work experience in a hospital or manufacturing environment or clean room filling preferred.</li>
<li>Experience in a production environment, ideally in a clean room setting.</li>
<li>Basic mechanical skills related to equipment operation.</li>
<li>Knowledge and skill in operating specialized equipment such as filling, wash, and sanitizing equipment.</li>
<li>Knowledge of clean room procedures, preferred but not required.</li>
<li>Knowledge of and compliance with GMP regulations, preferred but not required.</li>
<li>Proficiency in general computer functions like Microsoft Office programs and spreadsheets.</li>
<li>Ability to handle multiple projects or tasks simultaneously.</li>
<li>Advanced problem safety sensitivity to recognize potential safety issues.</li>
<li>Strong time management techniques.</li>
<li>Attention to detail and focus on quality, accuracy, sterility, and aseptic technique.</li>
<li>Effective communication skills with coworkers and management.</li>
<li>Proficiency in math with understanding of measurements and conversions.</li>
<li>Ability to recognize deviations from procedures and communicate immediately.</li>
<li>Critical thinking ability.</li>
<li>Ability to maintain confidentiality of information and processes.</li>
<li>Ability to follow hygiene standards and wear protective attire as required.</li>
<li>Ability to solve practical problems and handle variables where limited standardization exists.</li>
<li>Flexibility in work hours.</li>
<li>Ability to provide motivational support.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in clean room procedures and compliance with GMP regulations is preferred but not mandatory.</li>
</ul>
Work Environment
This role is situated in a clean room, lab, and production environment. Employees must adhere to strict hygiene standards and safety procedures, wearing protective attire as necessary. The position operates during the 2nd shift hours, providing a structured yet flexible work schedule.
Job Type &amp; Location
This is a Contract to Hire position based out of Syracuse, New York.
Pay and Benefits
The pay range for this position is $24.00 - $26.60/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 Syracuse,NY.
Application Deadline
This position is anticipated to close on Nov 12, 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.

Clean Room Pharmaceutical Technician

<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.
Job Description 
Job Summary:&nbsp;Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in&nbsp;method development and/or method validation.
<ul>
<li>Applies GMP in all areas of responsibility, as appropriate.</li>
<li>Performing a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution.</li>
<li>Reading, understanding, and interpreting diverse analytical procedures.</li>
<li>Conducting analytical investigations.</li>
<li>Troubleshoot instrumentation and communicate with vendors when required.</li>
<li>Train and mentor junior staff in laboratory procedures.</li>
<li>Manage and discuss projects with clients.</li>
</ul>
Qualifications 
The Ideal Candidate would possess:
<ul>
<li>Excellent communication (oral and written) and attention to detail.</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Minimum Qualifications:
<ul>
<li>BS or MS degree in analytical chemistry or other related degree concentration.</li>
<li>BS and 4+ years of industry experience, MS and 2+ years of industry experience, or PhD and 1+ years of industry experience.</li>
<li>Experience with forced degradation studies</li>
<li>3-5 years of experience with LC chromatographic validation in a GMP environment.</li>
<li>Authorization to work in the U.S. without immediate or future sponsorship.</li>
</ul>
 Additional Information 
Position is full-time position, Monday - Friday 8:00am - 4pm. Candidates currently living within a commutable distance of Lancaster, PA 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>
To learn more about Eurofins, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
#LI-EB1
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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