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<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
<ul>
<li>Perform analytical testing of medium to high complexity on drug substance/drug product using instrumentation including, but not limited to, compendial testing (e.g. description, EP color/clarity, VOI, osmolality), pH, HIAC, MFI, HPLC, UPLC, icIEF, GC, TOC, Karl Fischer, FTIR, UV, LC/MS, and NMR.</li>
<li>Initiate Trackwise events and participate in conducting investigations</li>
<li>Execute method qualifications</li>
<li>Document test results in notebooks and reports</li>
<li>Perform technique training with new analysts</li>
</ul>
Qualifications 
The ideal candidate would possess:&nbsp;&nbsp;&nbsp;
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>&nbsp;Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Proficiency in IT related skills such as Microsoft excel, word, PowerPoint etc&nbsp;&nbsp;&nbsp;&nbsp;</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s or M.S. degree with a science concentration (chemistry, biology, or related fields) with at least 2 years of related industry experience</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&nbsp;</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.

Bioanalytical Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is a global leader in analytical testing, operating over 950 labs in 60 countries with 65,000 employees. EAG Laboratories, part of Eurofins, offers advanced services in analytical chemistry, microscopy, surface analysis, and engineering sciences—including failure analysis, product reliability, and ATE testing. We support clients across the product lifecycle, from R&amp;D to manufacturing. Serving diverse industries, EAG delivers expert insights and tailored solutions. Our engineers and scientists collaborate with clients to solve complex challenges and deliver actionable results. We foster a growth mindset, empowering individuals to drive success while meeting evolving technological and business needs.
Job Description 
EAG Laboratories is seeking a skilled Scientist to support our analytical services including Electron Microscopy and Atom Probe. We work with leading-edge technology companies across a wide range of industries, helping to design and manufacture the electronics of tomorrow. The ideal candidate will thrive in a collaborative, research-driven environment focused on precision and innovation. &nbsp;
This is an exciting opportunity for a talented Scientist to join our Milpitas (Nanolab) team and contribute to high-impact analytical services. You’ll play a key role in customer interaction, specimen preparation, data collection, and analysis to support our clients. &nbsp;
A typical day will consist of multiple activities, including:&nbsp;
<ul>
<li>
Collaborate with team members to deliver high-quality analysis to clients. &nbsp;
</li>
</ul>
<ul>
<li>
Prepare TEM (Transmission Electron Microscopy)&nbsp;and APT (Atom Probe Tomography)&nbsp;specimens using FIB (Focused Ion Beam).
</li>
</ul>
<ul>
<li>
Operate CAMECA LEAP for data acquisition and data analysis using AP Suite6 software.
</li>
</ul>
<ul>
<li>
Perform routine maintenance to ensure optimal equipment performance.
</li>
</ul>
<ul>
<li>
Coordinate with equipment vendors to minimize downtime. &nbsp;
</li>
</ul>
<ul>
<li>
Conduct data processing and reporting.&nbsp;
</li>
</ul>
<ul>
<li>
Document and report analytical findings clearly and accurately.&nbsp;
</li>
</ul>
<ul>
<li>
Work cross-functionally with internal teams on integrated microscopy projects. &nbsp;
</li>
</ul>
This&nbsp;position works with companies that deal with defense-related activities and is subject to&nbsp;ITAR&nbsp;(International Traffic in Arms Regulations).&nbsp;All considered applicants must be U.S. Persons as defined by ITAR:
<ol>
<li>U.S. Citizen</li>
<li>U.S. Permanent Resident (i.e. “Green Card Holder”)</li>
<li>Political Asylee or Refugee</li>
</ol>
Work Schedule:&nbsp;
<ul>
<li>
Monday to Friday, *5:00 PM – 2:00 AM&nbsp; &nbsp;*(+10% shift differential will apply)
</li>
</ul>
Qualifications 
<ul>
<li>
MS or PhD degree&nbsp;in Materials Science and Engineering or a related field.
</li>
<li>
MUST HAVE minimum 2 years of experience on specimen preparation using APT, FIB and&nbsp;TEM.
</li>
<li>
Skilled in handling delicate, chip-sized samples with precision tools. &nbsp;
</li>
<li>
Strong communication skills and ability to work effectively in a team. &nbsp;
</li>
<li>
Comfortable working in a fast-paced, dynamic environment. &nbsp;
</li>
<li>
Excellent problem-solving and interpersonal skills. &nbsp;
</li>
</ul>
Preferred Qualifications:&nbsp;
<ul>
<li>
Skilled with APT data analysis using customized coding programs. 
</li>
<li>
Experience with CAMECA LEAP instrument.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with automated specimen fabrication using FIB/SEM systems. &nbsp;
</li>
</ul>
<ul>
<li>
Experience and knowledge with semiconductor technologies and processes. 
</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours).</li>
<li>The person in this position needs to occasionally move about inside the office or laboratory to access file cabinets, machinery, equipment etc.</li>
<li>Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead.</li>
<li>Must be able to remain in a stationary position 90% of the time.</li>
<li>Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting.</li>
<li>Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota.</li>
</ul>
The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. &nbsp;&nbsp;
We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you.&nbsp;&nbsp;
Employees are expected to comply with ISO 27001 standard and company requirements for Information security. &nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;
 Additional Information 
Compensation is aligned with market standards for the region and tailored to individual qualifications and experience.
What It’s Like to Work Here:
<ul>
<li>Teamwork:&nbsp;Be inspired by your leaders, be encouraged by your teammates and be supported in all parts of your journey working with us.</li>
<li>Learning &amp; Development:&nbsp;take on career development programs and goal setting to create big possibilities for your career and life. Develop within the company; be mentored and grown as a leader.</li>
<li>Diversity &amp; Authenticity:&nbsp;we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day.</li>
</ul>
Benefits &amp; Perks to Foster Work/Life Balance:
✓ 401k Company Matching
✓ Wellness Program
✓ Volunteer Time off
✓ Education Assistance
✓ Fitness Reimbursement
✓ …and more!
If you enjoy being immersed in technology, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today!
Eurofins&nbsp;EAG&nbsp;Laboratories&nbsp;is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the Company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law.&nbsp; The Company’s policy is to recruit, hire, train, promote and administer all employment-related matters&nbsp;based on&nbsp;an individual's qualifications,&nbsp;abilities&nbsp;and efforts without regard to protected status.&nbsp;
#EAGlaboratories
Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

Scientist (Materials Analysis, APT) | EAG Laboratories

<h3>Job Description</h3>
Job Description
About Cleerly
We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. 
Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. 
At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. 
While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter, for some roles like sales or external facing roles travel could be up to 90% of the time.
About the Opportunity
We are seeking a highly skilled Staff Scientist to lead the design, development, validation of innovative clinical workflow that can directly impact the diagnosis and treatment for heart disease. In this senior-level role, you are responsible for architecting a cutting-edge product that integrates our existing technologies while pushing the boundary of innovation in cardiac vascular imaging. You will also represent the company in strategic research collaborations with leading academic and clinical institutions, driving innovation at the intersection of AI and cardiovascular health.
Responsibilities
<ul>
<li>Research and develop state-of-the-art AI and non-AI algorithms for coronary CT/fluoroscopy imaging applications.</li>
<li>Implement efficient and robust image processing pipeline to solve challenging problems in low latency environments.</li>
<li>Translate product and clinical requirements into algorithmic specifications in collaboration with Product and Clinical teams.</li>
<li>Partner with Regulatory Affairs to support regulatory submissions (e.g., 510(k), De Novo, PCCP), including generating evidence and documentation.</li>
<li>Collaborate with engineering teams to deploy AI and non-AI based solutions in clinical practice.</li>
<li>Communicate findings and strategy to internal stakeholders and leadership through clear technical documentation, presentations, and demos.</li>
<li>Contribute to intellectual property development through patents and scientific publications.</li>
<li>Mentor junior scientists and foster a culture of technical excellence and scientific rigor.</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Computer Science, Data Science, Biomedical Engineering, Biomedical Imaging, or a related technical field, with 5+ years combined postdoc and/or industry experience; OR an M.S. with 8+ years of relevant experience.</li>
<li>R&amp;D experience in medical image processing, including classical image processing algorithm, optical flow analysis, 2D&amp;3D rigid/deformable image registration</li>
<li>Proven track record of publications in top-tier medical imaging or computer vision conferences and journals (e.g., MICCAI, IEEE TMI, CVPR, Medical Image Analysis).</li>
<li>Strong experience in C++ and Python.</li>
<li>Experience of developing and applying graph processing or GNN(graph neural network) </li>
<li>Prior experience with ITK, OpenCV, VTK, CMake, Slicer is a plus</li>
<li>Prior experience with cardiac motion modelling or tracking is a plus</li>
<li>Excellent interpersonal, cross-functional, and cross-cultural collaboration skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>5+ years of industry experience in AI-based medical device development or clinical deployment.</li>
<li>Experience supporting FDA regulatory submissions for ML-based software, including familiarity with De Novo, 510(k), and PCCP pathways.</li>
<li>Deep domain knowledge in cardiovascular imaging and CT interpretation workflows.</li>
</ul>
TTC*:
NY: $270,000 - $310,000 CO: $265,000 - $305,000
*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.).
Each role at Cleerly has a defined salary range based on market data and company stage. We typically hire at the lower to mid-point of the range, with the top end reserved for internal growth and exceptional performance. Actual pay depends on factors like experience, technical depth, geographic location, and alignment with internal peers.
Working at Cleerly takes HEART. Discover our Core Values:
<ul>
<li>H: Humility- be a servant leader</li>
<li>E: Excellence- deliver world-changing results</li>
<li>A: Accountability- do what you say; expect the same from others</li>
<li>R: Remarkable- inspire &amp; innovate with impact</li>
<li>T: Teamwork- together we win</li>
</ul>
Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.
OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.
By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (<a href="https://cleerlyhealth.com/privacy-policy" target="_blank">https://cleerlyhealth.com/privacy-policy</a>). All official emails will come from @cleerlyhealth.com email accounts. 
#Cleerly

Staff Scientist, Imaging Systems

<h3>Job Description</h3>
Job Description
Are you detail-oriented and passionate about maintaining high-quality standards in a fast-paced environment? We're looking for a fill-time Post Processing Technician I to join our team in the Processing Department. Available shifts include Monday through Friday 7:30AM - 4:00PM or Friday through Monday 7:00AM - 5:30PM. This position plays a vital role in supporting the post-processing process, ensuring compliance, and maintaining product quality from start to finish. If you're excited to work with a dedicated team in a dynamic setting, this could be the perfect opportunity for you!
As a Post Processing Technician I, you will be responsible for performing routine tasks across all processing areas, working under the guidance of the Processing Supervisor and Post Processing Technician III. Your responsibilities will include conducting green waste disposal processes, trimming batches by hand and machine, and assisting with the dry and cure processes. You'll play a role in maintaining quality control measures, ensuring batches meet product standards, and supporting inventory management by keeping accurate records. In addition, you will be expected to keep your workspaces and machinery clean, sanitized, and organized to maintain operational efficiency.
Previous experience is preferred but not required. The ideal candidate will have a keen eye for detail and the ability to focus on sensitive and complex tasks. Strong verbal and written communication skills, flexibility, and adaptability are essential to succeed in this role. You must be able to stand for extended periods, lift up to 50 lbs occasionally, and perform manual tasks requiring fine motor skills. Safety is a priority, and you will be required to maintain balance while using ladders or performing tasks such as stooping, kneeling, or reaching.
If you're ready to be part of a supportive team in an evolving environment and are excited about contributing to our post-processing process, we encourage you to apply today!

Post Processing Technician 1

<h3>Job Description</h3>
Job Description
Laboratory Data Analyst-Laboratory Express
$25-$32/hr | Full-time | Entry Level | Training Provided
About the Role
Laboratory Express is seeking a Laboratory Data Analyst to analyze testing data, generate reports, and support quality improvement initiatives. Perfect for analytical professionals wanting to apply data skills in the growing healthcare diagnostics field.&nbsp; &nbsp;
Key Responsibilities&nbsp;
1. &nbsp;Analyze laboratory test results and identify trends and &nbsp;patterns
2. &nbsp;Create comprehensive reports and dashboards for management and clients&nbsp;
3. &nbsp;Monitor quality control data and investigate statistical anomalies&nbsp;
4. &nbsp;Maintain and optimize laboratory information systems and databases
5. &nbsp;Generate regulatory compliance reports and documentation&nbsp;
6. &nbsp;Collaborate with laboratory staff to improve testing processes and efficiency
7. &nbsp;Support research projects with statistical analysis and data visualization&nbsp;
Requirements&nbsp;
1. &nbsp;Bachelor degree in data analysis, statistics, life sciences of related fields preferred.
2. &nbsp;Strong analytical and problem-solving skills
3. &nbsp;Proficiency in Excel, database management and statistical software&nbsp;
4. &nbsp;Experience with data visualization tools (Tableau, Power B1) a plus
5. &nbsp;Excellent attention to detail and accuracy in data handling&nbsp;
6. &nbsp;No laboratory experience-comprehensive training in laboratory operations and medical terminology&nbsp;
What We Offer
Company DescriptionLaboratory Express is one of the leading companies equipping healthcare providers. 
<h3>Company Description</h3>
Laboratory Express is one of the leading companies equipping healthcare providers.

Laboratory Data Analyst-Laboratory Express

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today!&nbsp;&nbsp;
Job Description 
Job Summary: Execute bioassays and support method qualification in a GMP environment while leading team operations and collaborating with clients.
Key Responsibilities:
<ul>
<li>
Assay Execution: Perform cell-based and surrogate bioassays (e.g., ligand-binding ELISA) in plate-based format under GMP standards.
</li>
<li>
Method Support: Conduct qualification and transfer of analytical test methods.
</li>
<li>
Documentation &amp; Compliance: Record work in lab notebooks/e-notebooks, verify data integrity, and report results via electronic systems.
</li>
<li>
Team Leadership: Coach and develop team members, coordinate workflow, monitor daily tasks to meet turnaround times (TAT), and manage performance reviews and training records.
</li>
<li>
Strategic Collaboration: Partner with leadership and clients to implement business directives and support growth planning.
</li>
</ul>
Qualifications 
<ul>
<li>
Education &amp; Experience: Bachelor’s degree in biology, chemistry, or related field 4+ years of relevant lab experience, including GMP operations.
</li>
<li>
Work Authorization: Must be authorized to work in the U.S. indefinitely&nbsp;without restriction or need for sponsorship.
</li>
<li>
Technical Skills: Proficiency in reporter-gene assays, cell culturing, cell counting, cell banking. Strong computer, scientific, and organizational skills.
</li>
<li>
Leadership &amp; Collaboration: Demonstrated leadership experience with a focus on employee engagement, morale, and retention. Ability to work independently and collaboratively with internal and external clients.
</li>
<li>
Communication &amp; Work Style: Excellent written and verbal communication skills. Detail-oriented, self-motivated, adaptable, and able to manage multiple tasks in a fast-paced environment. Proactive and solution-oriented with strong prioritization skills.
</li>
<li>
Compliance &amp; Documentation: Ability to maintain accurate records, follow instructions, and adhere to company policies
</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&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.

Biochemist Group Leader - Bioassay

<h3>Job Description</h3>
Job DescriptionActively hiring for production associates for a large Printing company located in Stratford, CT. This is a 4-6 month contracted job with the opportunity to join the company permanently as they ramp up these upcoming months. We are looking for dedicated workers who are open to working overtime. Please submit an application with your resume attached to be considered for the position.
Location: Stratford, CT
Pay: 1st - $17.00/hr, 2nd - $17.50/hr
Shift: 1st - 6:00am-6:00pm, 2nd - 6:00pm-6:00am - Monday - Friday
Job Description:
This role involves sorting and preparing outbound packages in accordance with USPS standards. The Cleanroom Technician ensures all outputs are produced and verified based on specifications, assisting in the processing of daily scheduled jobs and maintaining quality control standards.
Responsibilities:
<ul>
<li>Sort and prepare outbound packages according to USPS standards.</li>
<li>Confirm that all outputs are produced based on specifications and verify them before leaving the facility.</li>
<li>Assist the Mailing Distribution Manager in processing scheduled jobs.</li>
<li>Ensure all outputs are sorted in appropriate USPS containers.</li>
<li>Use a scanner and computer to verify job counts into proprietary software.</li>
<li>Scan EOBs and booklets to ensure 100% piece count before mailing.</li>
<li>Perform QC inspections on each job according to departmental guidelines.</li>
<li>Verify successful submission of reprints by other departments.</li>
<li>Collaborate with other departments to achieve manufacturing goals.</li>
<li>Perform general housekeeping, including trash removal and facility upkeep.</li>
</ul>
Essential Skills:
<ul>
<li>Experience navigating web browsers.</li>
<li>Basic math and reading skills.</li>
<li>Excellent critical thinking and problem-solving abilities.</li>
<li>Ability to work well individually and in a team setting.</li>
<li>Safety-conscious mindset.</li>
<li>Excellent interpersonal skills.</li>
<li>Organizational skills and attention to detail.</li>
<li>Quality-oriented focus.</li>
<li>Ability to safely lift up to 50lbs.</li>
<li>Ability to stand for long periods and perform physical activities such as walking, stooping, kneeling, twisting, and bending.</li>
</ul>
Additional Skills &amp; Qualifications:
<ul>
<li>Familiarity with cleanroom environments.</li>
<li>Experience in general production or packaging.</li>
<li>Machine operation experience.</li>
</ul>
Why Work Here?:
This is a great opportunity to enter the manufacturing industry with no prior skills required, just a willingness to work hard. The position offers full benefits and the flexibility to work longer hours if desired.
Work Environment:
The job is set in a very clean, temperature-controlled environment, similar to a cleanroom. Teamwork is essential in this role.
Apply today and we will reach out after reviewing your resume.
Job Type &amp; Location
This is a Contract to Hire position based out of Stratford, CT.
Pay and Benefits
The pay range for this position is $17.00 - $17.50/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 Stratford,CT.
Application Deadline
This position is anticipated to close on Nov 14, 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 DescriptionDescription:
Equipment &amp; Controls, Inc. is a successful and innovative Emerson Impact Partner. ECI provides an entrepreneurial opportunity for each employee to achieve our common mission of Delivering Successful Customer Outcomes 100% of the Time.?Our customer base includes?oil and gas, chemical, power, food and beverage, mining and metals, life sciences, pulp and paper, refining, petrochemical, OEM and nuclear industries. With offices in Pennsylvania, West Virginia, and Ohio, ECI is the region’s leader in process control and industrial automation products and solutions. We seek individuals that share our passion for excellence.
 
Business Unit/Department: Reliability Solutions Group
 
Location: Solon, Lima, or Columbus, Ohio
 
Essential Duties and Responsibilities:
<ul>
<li>Support customers in process control instrumentation and equipment startup with focus on flow measurement equipment</li>
<li>Verify, troubleshoot and resolve instrumentation and equipment communications</li>
<li>Inspect instrument wiring, power and grounding of installation</li>
<li>Set up instruments with Hart 475 field communicator</li>
<li>Work with onsite installation crew</li>
<li>Replace/install instrumentation and equipment</li>
<li>Troubleshoot failed instruments and equipment</li>
<li>Develop solutions to resolve instrumentation and equipment problems</li>
<li>Calibration of measurement and flow transmitters</li>
<li>Providing clear and effective documentation of services provided to customers</li>
</ul>
Requirements:
<ul>
<li>Technical Degree or equivalent field experience. 5+ years experience with Rosemount products is preferred</li>
<li>Familiarity with Rosemont and Micro Motion</li>
<li>Familiarity with Foxboro, Endress&amp;Hauser, Yokogawa, and other instrumentation</li>
<li>Ability to use hand and power tools, including drills, saws, shovels, picks, wrenches, tube benders and tube cutters.</li>
<li>Understand instrumentation and be able to read blueprints.</li>
<li>Understand and be able to perform electrical work. 480V experience is preferred</li>
<li>Ability to work with electrical conduit and fittings is a plus.</li>
<li>Be proficient in MS Word, Excel and Outlook.</li>
<li>Familiarity with TCP/IP, networking fundamentals, Modbus, RS232/485, and Hart communications</li>
<li>Experience managing customer projects and working independently</li>
<li>Current driver’s license</li>
<li>Proficient with MS Office suite</li>
<li>Ability to work any overtime that is required to complete a particular assignment (occasional weekend work)</li>
<li>Ability to travel out of town and work in the field when required.</li>
</ul>
Core Competencies:
<ul>
<li>WORK COLLABORATIVELY - Promote an inclusive and positive work environment that encourages collaboration and team building across all levels of the organization.? Work with others to resolve obstacles that may prevent the organization from achieving its mission.</li>
<li>CUSTOMER FOCUS - Demonstrate the desire and knowledge to understand customer needs.? Provide personalized, professional, and courteous service, accurate information, continuous communication, and the ability to handle customer concerns in an appropriate manner.</li>
<li>INTEGRITY - Behave ethically, act fairly, and take responsibility for accomplishing work goals.</li>
</ul>
Additional Details:
We provide our team with everything needed for success, including world-class products, company vehicle for work/personal use, excellent continuous training, and all necessary work equipment. We reward hard work and success with a competitive base salary and benefits package, as well as a retirement savings program, which includes 401(k) with company match and profit sharing. Salary is based on experience. EEO/AA/M/F/Veteran/Disability

Measurement and Flow Technician (1498)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Members of the Metrology team support processes for laboratories at Viracor with a focus on maintaining CLIA, CAP and NYDOH, GxP accreditation by using and maintaining procedures and software or other methods to perform, train, document, assist others to ensure complete and appropriate documentation of required tasks and records. The Laboratory Metrology Technician (Tech) is responsible for conducting and documenting cleaning, calibration, preventive maintenance functions, and documenting excursions from expected performance as outlined by management in the laboratory areas.
Laboratory Metrology Technician&nbsp;responsibilities include, but are not limited to, the following:
Level I –
<ul>
<li>Perform and/or assist with instrument maintenance such as plate readers and washers, liquid handling equipment, front end lab automation equipment, centrifuges, balances, etc.</li>
<li>Responsible for performing and documenting cleaning of the laboratory areas and equipment</li>
<li>Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.</li>
<li>Maintain cleaning and maintenance records as required</li>
<li>Instrument calibration activities and documentation including environmental monitoring system and laboratory equipment as directed (Pipettes/Temperature probes)</li>
<li>Respond to and document environmental alerts, ensuring documentation of actions taken/escalate as needed</li>
<li>Instrument power cycles/UPS maintenance as required</li>
<li>Inventory management and upkeep of pipettes including supplying backups and replacements as requested</li>
<li>Maintain proper records in equipment tracking software by documenting actions and maintaining schedule of required activities</li>
<li>Administration duties within the department and investigation activities which includes providing documentation as requested by internal or external auditors</li>
<li>Obtain and maintain proficiency in software programs or tools used in department</li>
<li>Support development of system and process improvements that would enhance compliance to requirements</li>
<li>Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies</li>
<li>Adhere to policies and protocols in the laboratory</li>
<li>Work closely and communicate with other laboratory associates to complete daily activities efficiently</li>
<li>Represent department and the organization favorably and in accordance with established company standards and associate attributes at all times</li>
<li>Other duties as assigned by management</li>
</ul>
Level II –
Fully meets the responsibilities of Level I plus the following:
<ul>
<li>Highly proficient in multiple processes managed by the department</li>
<li>Able to train, assist users or clients with questions and/or issues, participate in validation of updates</li>
<li>Provide training and orientation of testing personnel as directed (pipettes and environmental monitoring)</li>
<li>Maintenance of Laboratory equipment schedules, including management of calibration/maintenance tracking program/software, temperature monitoring system, and pipette calibration program, ensuring that calibrations are correct and current.</li>
<li>Understand and demonstrate proficiency with quality monitoring activities such as quality indicators and quality reporting related to equipment and monitoring such as KPIs for Quality Meeting</li>
<li>Communicates Metrology area needs to Facilities, Testing and Manufacturing personnel</li>
<li>Contacts suppliers/vendors as required</li>
<li>Participate in data reporting, internal or external client reports as requested, using Excel or other software utilized for reporting, trending, and tracking</li>
<li>Participate in continual quality improvement projects company-wide</li>
<li>Participate in creation/revision of SOPs and training materials for the department as required and ensure policies and procedures are monitored and updated to include regulatory changes</li>
<li>Other duties as assigned by managemen</li>
</ul>
Qualifications 
Basic Minimum Education Qualifications:
<ul>
<li>Level I: GED or High school Diploma</li>
<li>Level II: BA/BS in biological, physical, chemical or clinical laboratory science preferred.</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Level II: minimum of 2 years’ experience in a regulated laboratory (CAP/CLIA and/or GxP), as Laboratory Quality Tech I, or similar experience in Laboratory process ownership, e.g. laboratory technical roles.</li>
<li>Knowledge of the clinical laboratory environment preferred, including basic terminology, protocols and practices</li>
<li>Ability to initiate tasks and work efficiently with minimal supervision</li>
<li>Comfortable working in a laboratory setting</li>
<li>Knowledge of basic computer programs such as Microsoft Excel and Word including common applications in laboratory use</li>
<li>Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices</li>
<li>Position may require working hours outside of the normal work schedule when necessary</li>
<li>Ability to keep sensitive information confidential</li>
<li>Working knowledge of good laboratory practices and laboratory test methodologies.</li>
<li>Ability to identify aberrant data and potential quality/compliance concerns escalating to management.</li>
<li>Familiarity with six sigma scoring as applied to metrics/KPIs for quality</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
The Ideal Candidates Possesses the Following:
<ul>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work proactively in a self-directed manner, taking initiative as required</li>
<li>Ability to make sound decisions with little or no supervision, including generating test data, performing analysis, and escalating when appropriate</li>
</ul>
Physical Requirements:
<ul>
<li>Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead</li>
<li>Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting</li>
<li>Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours)</li>
<li>Ability to lift and move items weighing up to 50 pounds</li>
<li>Using assistance as available, must have physical ability to push/pull heavy loads (may be in excess of 100 pounds</li>
<li>Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation</li>
<li>Ability to continuously operate a personal computer for extended periods of time (4 or more hours)</li>
<li>Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions</li>
</ul>
 Additional Information 
Position is part-time, working Thursday-Saturday: 7:00 pm - 11:00 pm and Sunday 3:00 pm -11:30 pm,&nbsp;with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Metrology Technician (Part-Time)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Crystallization Scientist responsibilities include, but are not limited to, the following&nbsp;:
<ul>
<li>Support crystallization process development activities of the group through laboratory experiments, including solubility screening experiments, kinetic solubility and metastable zone width measurements, and laboratory-scale crystallization experiments.</li>
<li>Hands-on generation of solid-state characterization data using powder X-ray diffraction.</li>
<li>Analysis of product samples for key physical properties, including particle size distribution and particle shape, using optical microscopy and laser diffraction particle size analysis.</li>
<li>Support of technical initiatives that may involve the design, installation, repair, and maintenance of specialized laboratory equipment.&nbsp; Comfortable with multitasking</li>
<li>Independent and systematic</li>
<li>Excellent problem-solving skills</li>
<li>Good written communications, including use of electronic laboratory notebooks</li>
<li>Hands-on experience with relational databases and complex spreadsheets</li>
</ul>
Qualifications 
The ideal candidate would possess&nbsp;:
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Basic Minimum Qualifications&nbsp;:
<ul>
<li>Bachelor's degree in chemistry or chemical engineering or other related degree concentration, or&nbsp;equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>Position is Monday- Friday 8:00 AM- 5:00PM.&nbsp;Overtime as needed.&nbsp; Candidates currently living within a commutable distance of&nbsp;Groton, CT&nbsp;are encouraged to apply.&nbsp;</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.

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