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<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, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.
Responsibilities Include:&nbsp;
<ul>
<li>Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment</li>
<li>90% Method development,&nbsp;qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
<ul>
<li>May include technology transfer activities, regulatory support, and possible project team participation</li>
</ul>
</li>
<li>10% Analytical testing
<ul>
<li>Liquid Chromatography&nbsp;and Plate-Based&nbsp;</li>
</ul>
</li>
<li>Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.&nbsp;</li>
<li>Experience working in a GMP/GLP environment&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives</li>
<li>Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>BS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>2 years of demonstrated work experience with cell-based assays</li>
</ul>
</li>
<li>Or MS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>6 months of Demonstrated experience with cell-based assays&nbsp;</li>
</ul>
</li>
<li>Experience with&nbsp;experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<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 holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioassay Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
LGC Clinical Diagnostics, part of the LGC Group, has more than 30 years of experience as a leading and trusted global IVD quality manufacturer, with particular expertise in quality measurement tools (QMT) and reagents. Focused on five key areas – clinical biochemistry and immunoassay, serology, molecular diagnostics, clinical genomics, and reagents – it has around 450 employees across its four FDA-registered and ISO 13485-certified facilities in the USA and Ireland, and an ISO 9001-certified facility in England.
 LGC Clinical Diagnostics partners with IVD and biopharmaceutical developers, CROs and academic institutions covering the entire diagnostic pipeline, from concept and early-stage research to accelerated product development and, ultimately, routine clinical use. It develops and manufactures a comprehensive portfolio of premium catalogue and custom-developed diagnostic quality solutions and component materials for the IVD and extended life sciences industry through its four brands, Maine Standards Company, SeraCare, The Native Antigen Company and Technopath Clinical Diagnostics. Together, they serve 7,500+ customers in over 120 countries, providing products for more than 20 clinical application areas, including infectious diseases, NIPT, diabetes, cardiac disease and oncology. lgcclinicaldiagnostics.com
Job Description 
The Scientist I, New Product Development –position will work with and report to the Scientist II Serology or Senior Scientist New Product Development – Serology &amp; Toxicology. This role will support LGC Clinical Diagnostics purpose of advancing the understanding of disease in order to enable precision diagnostics. As a Scientist I, this position will work with cross functional teams to bring innovative, multiplexed toxicology quality control materials to market to serve the diagnostics and blood screening community.&nbsp; This scientist will support timelines and priorities and be a contributor to team’s workflow as needed to meet internal and external customer needs. This scientist will also support serology new product development as needed.&nbsp;
To perform this job successfully, an individual must be able to capably perform each of the following essential functions:&nbsp;
<ul>
<li>Proactively communicates upward and cross-functionally with colleagues to build relationships throughout the organization to clearly articulated goals and priorities.</li>
<li>Provide technical support for product development and manufacture of new products including IVD controls, reference materials, and QC panels.</li>
<li>Provide support for cross-site new product development.</li>
<li>Provide support for investigations and trouble-shooting activities, as needed, for technical manufacturing issues</li>
<li>Development of new product specifications and modification of existing specifications to ensure reliable and repeatable manufacturing.&nbsp; Products must be developed using LGC Clinical Diagnostics design control process to ensure compliance with CE and FDA guidelines.</li>
<li>Critically analyses data and communicates conclusions to the team.</li>
<li>Supports and assists in technical transfers of products into manufacturing.</li>
</ul>
Qualifications 
Minimum Qualifications: 
<ul>
<li>Knowledge of and ability to assess and understand toxicology-based IVD diagnostic tests and immunoassay systems.&nbsp;</li>
<li>Willingness to work in BSL-2 laboratory and DEA regulated areas with personal protective equipment for handling potentially infectious or hazardous material.</li>
<li>Experience with stage gate design control processes.</li>
<li>Demonstrates strong organizational skills to coordinate multiple projects, meet deadlines, solve problems, focus on priorities, and communicate effectively with collaborators.</li>
<li>Ability to work independently and thrive in a fast-paced environment, adaptable to changes in development priorities.</li>
<li>Accurate and strong verbal and written communication skills with outstanding attention to detail.</li>
<li>Proficient in statistical data analysis and articulating conclusions from data, raising issues with insight into implications based on data.</li>
<li>Flexible and able to work effectively in a variety of environments and situations.</li>
<li>Individual who actively seeks continuous learning and development.</li>
<li>Willingness to accommodate less than 5% travel time if necessary.</li>
</ul>
Preferred Qualifications: 
<ul>
<li>Bachelor’s degree in Biology, Chemistry, or a related area, with a preference for Immunology.</li>
<li>5+ years of experience in a laboratory environment, product development, or technical operations.</li>
<li>Experience working in a BSL-2 laboratory and a DEA regulated laboratory.&nbsp;</li>
<li>Proficiency in basic and advanced laboratory techniques (e.g., pipetting, balance use, centrifugation, use of BSC hoods, safety procedures, etc).</li>
<li>Experience with manufacturing in a cGMP environment.</li>
<li>Familiarity with diagnostic and medical device requirements, including ISO 13485.</li>
<li>Experience with toxicology biomarkers is preferred.</li>
<li>Familiarity with toxicological test methods, platforms, and data analysis is preferred.</li>
</ul>
 Additional Information 
Join LGC and become part of a team that values collaboration, integrity, and brilliance in all we do. We are committed to encouraging a workplace where everyone can thrive and contribute to our mission.
Our values:
• PASSION
• CURIOSITY
• INTEGRITY
• BRILLIANCE
• RESPECT
Equal opportunities:
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, parental responsibilities, religion, or belief. Shortlisting, interviewing, and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
For more information about LGC, please visit our website <a href="http://www.lgcgroup.com" target="_blank">www.lgcgroup.com</a>
#scienceforasaferworld

Scientist I, New Product Development

<h3>Job Description</h3>
Job Description
We are seeking a skilled GIS/Construction&nbsp;Field Engineer Specialist to join our innovative team. This role combines cutting-edge geospatial technology with precise engineering to ensure construction projects are executed with maximum accuracy and efficiency. The ideal candidate will have expertise in GPS layout systems, drone operation, and advanced survey technologies, including Ground Penetrating Radar (GPR), LIDAR, and photogrammetry. This position offers a unique opportunity to work at the intersection of traditional surveying and emerging digital technologies in the construction industry.
Responsible for performing skilled digital mapping involving the preparation and maintenance of digital maps and providing Geographic Information System (GIS) support. Also responsible for systems analysis, maintenance, and update of the Geographic Information System (GIS) data, as well as implementing precise geospatial data collection and layout services for construction projects. This full-time position requires expertise in both field work and technical data processing. You will report directly to the Survey Manager or Project Superintendent and play a critical role in ensuring construction accuracy from groundbreaking through project completion.
Responsible for the highly technical work that is involved in analyzing, evaluating and enhancing of the existing Geographic Information System (GIS) and will assist in designing solutions and technical procedures to process GIS data. Also utilizes Geographic Information System techniques to provide a better understanding of certain variables in a given geographic location. Extracts data from GIS software and uses varying analysis methods to arrive at results.
Tasks:
<ul>
<li>
Prepares and maintains digital maps and provides Geographic Information System (GIS) support. Converts hand drawn maps into a digital format for use in a Geographic Information System (GIS) database.
</li>
<li>
Serves as a technician on projects involving GIS studies that require data creation, editing and manipulation and provides supportive mapping data and analysis upon request.
</li>
<li>
Maintains a variety of spatial data layers and associated attributes.
</li>
<li>
Produces printed maps, showing a variety of map features.
</li>
<li>
Well verse in the precepts and practices, including, but are not limited to, Geo-reference imagery, reading and interpreting engineering plans, survey drawings, design plans, etc.
</li>
<li>
Imports, edits and converts AutoCAD files to ESRI features.
</li>
<li>
Creates reports using ArcGIS software.
</li>
<li>
Utilizes Geographic Information System techniques to provide a better understanding of certain variables in a given geographic location among varying types of data such as spatial and database analysis.
</li>
<li>
Familiar with standard concepts, practices, and procedures within the fields of Land Surveying, Urban Development, Utilities and Environmental Studies.
</li>
<li>
Maintains current knowledge with respect to relevant state-of-the-art technology, equipment and/or systems. Maintains knowledge and continues to educate on the trends and practices of the field.
</li>
<li>Operate advanced GPS layout systems to perform construction staking with precision of ±2mm, ensuring all elements are positioned according to engineering specifications</li>
<li>Plan and execute drone flight missions for aerial mapping, volumetric calculations, and 3D modeling of construction sites</li>
<li>Process and analyze survey data using specialized software to generate accurate site models and layout coordinates</li>
<li>Conduct subsurface utility detection using Ground Penetrating Radar (GPR) technology</li>
<li>Perform LIDAR scanning for precise topographical mapping and as-built documentation</li>
<li>Apply photogrammetry techniques to create detailed visual records and measurements of construction progress</li>
<li>Interpret construction plans and translate complex design data into field layout instructions</li>
<li>Maintain calibration and proper functioning of all survey equipment</li>
<li>Communicate findings and coordinate with project managers, superintendents, and subcontractors</li>
<li>Prepare comprehensive technical reports documenting survey results and construction layout activities</li>
<li>
Well versed in the precepts and practices, including, but are not limited to, Geo-reference imagery, reading and interpreting engineering plans, survey drawings, design plans, etc.
</li>
<li>
Imports, edits and converts AutoCAD files to ESRI features.
</li>
<li>
Maintains and updates spatial data layers and associated attributes using GIS, creates reports, and quality map products using ArcGIS software.
</li>
<li>
Familiar with standard concepts, practices, and procedures within the fields of Land Surveying, Urban Development, Utilities and Environmental Studies.
</li>
<li>
Maintains current knowledge with respect to&nbsp;relevant state-of-the-art technology, equipment and/or systems. Maintains knowledge and continues to educate on the trends and practices of the field.
</li>
<li>
Provides training and technical assistance to GIS end users.&nbsp;
</li>
</ul>
Minimum Requirements:
Bachelor’s Degree in Geography, Geomatics, Urban Planning, Civil Engineering or related field with Geographic Information System (GIS) coursework is required. Certification as Geographic Information System Professional (GISP) is preferred. A minimum of five (5) years of GIS experience with at least two (2) years of experience working with ArcGIS Databases, AutoCAD and knowledge and understanding of GPS hardware and software packages. Knowledge and understanding of GIS/GPS database and principles, database, cartographic, geographic, statistical and mathematical theory sufficient to perform geographic analyses is required.

GIS / Construction Field Engineer Specialist

<h3>Job Description</h3>
UniTech seeks reliable, self-motivated, team players for positions at our facilities across the United States. There are several potential job openings. Visit our website for a list of locations <a href="http://www.UniTechUS.com/locations" target="_blank">www.UniTechUS.com/locations</a>. UniTech is the world’s leader in the supply of radiological protective clothing. Our customers include Nuclear Power Plants and the Department of Energy (DOE). Our facilities offer nuclear laundry and material decontamination services.
 Health Physics Technician The Health Physics Technician position involves a wide range of responsibilities to support all facets of operation.
 • Perform radiological surveys involving various instrumentation to monitor fixed and non-fixed contamination and radiation levels. • Survey plant work areas, support areas, perimeter boundaries and the environment. • Calibrate and perform daily quality control of handheld and laboratory instruments including automated gas flow proportional counting systems. Liquid scintillation counters and gamma spectroscopy at select locations. • Collect and analyze air samples at fixed and portable air sample locations. • Collect and analyze water samples and assist in the operation and maintenance of wastewater treatment systems. • Perform surveys to support the receipt and shipment of radioactive materials regulated as Hazardous Materials by the Department of Transportation (DOT) • Utilize various software packages to input data, evaluate results of analysis, print and maintain reports. • Calibrate and maintain specialized instrumentation including Automated Laundry Monitors (ALMs), personnel monitors, pipe monitors, respirator monitors, and a variety of specialized instrumentation manufactured for our specific needs. • Package, sample, inventory, and maintain records of radioactive waste. • Issue personnel, area, and environmental Thermoluminescent Dosimeter (TLDs) and Self Reading Personnel Dosimeters (SRPDs) and assist in the management of the dosimetry program. • Perform personnel in-vivo bioassays (chest counts). • Perform assays to release materials and equipment from radiological controls. • Support plant operations and special projects.
Health Physics Technicians are candidates for internal promotion
 Qualifications 
Education: Associate’s degree in health physics or nuclear engineering or a bachelor’s degree in engineering, mathematics, or science curriculum. • Practical experience in radiological safety. • Able to perform the position responsibilities with reasonable accommodations. • Computer proficiency: Microsoft Word®, Microsoft Excel®, etc. • Able to learn custom software. • Shift work may be required. • Able to read, analyze, and interpret technical procedures and information. • Proficient in communication, verbally and in written reports. • Language: English required. Spanish and other languages are helpful. • Strong problem-solving skills. • Able to stand throughout an 8-hour shift. • Able to lift and carry up to 50 lbs. • Professional credential (or ability to achieve) desired: National Registry of Radiation Protection Technologists (NRRPT).
About UniTech and UniFirst
UniTech Services Group, Inc. is a wholly owned subsidiary of UniFirst Corporation. UniTech became the first licensed provider of radiological laundry services in the United States in 1957. UniTech&amp;#x2BC;s management team boasts over 250 years of experience in nuclear protective clothing, respiratory protection, nuclear laundry and materials decontamination. UniFirst is recognized on the Forbes “Platinum 400 - Best Big Companies” List. With over 14,000 employee Team Partners and more than 250 facilities throughout the United States, Canada, Mexico and Europe. UniFirst is an equal opportunity employer. We do not discriminate in hiring or employment against any individual based on race, color, gender, national origin, ancestry, religion, disability, age, or any other factor protected by antidiscrimination laws.
Compensation: &nbsp;$30.00 - $35.00/hr
Benefits include: • 401K with Company MatchProfit Sharing • Health Insurance, Dental, Vision • Employee Assistance Program • Life Insurance • Supplemental Life Insurance • Long Term Disability • Paid Vacation • Sick Time • Paid Holidays • Direct Payroll Deposit • Tuition Reimbursement • 30% Employee Discount • Employee Referral Program • And Much More

Health Physics Technician - UniTech

<h3>Job Description</h3>
Job DescriptionDescription:
Knight Federal Solutions is a trusted provider to industry leading prime contractors, the Department of Defense and the Intelligence Community. We have established a company culture that supports our employees, their families and the communities in which they live and work. When you join our team you belong to a group of people that work hard, strive for greatness and care about people.
 
Our hard work is evident in everything we do. Whether it be supporting large government programs in the areas of Simulation and Training, Information Technology, Intelligence or Engineering we always strive to be the best. It is for this reason that we have been recognized as a World Class Team Supplier by Northrop Grumman and were also named one of Florida’s fastest growing companies by Inc. Magazine.
 
As Knight Federal Solutions continues to grow, we look forward to hiring the best and the brightest to join us in our success!
 
Job Duties 
<ul>
<li>Conducts analysis using intelligence and information from multiple sources to assess, interpret, forecast, and explain a range of national security issues and developments that are regional or functional</li>
<li>Provides all-source analytic support to collections, operations, investigations, and other defense intelligence analytic requirements</li>
</ul>
Requirements:
<ul>
<li>At least 3 years of experience conducting analysis relevant to the specific labor category with at least a portion of the experience within the last 2 years</li>
<li>Bachelor’s degree in an area related to the labor category from a college or university accredited by an agency recognized by the U.S. Department of Education </li>
<li>The candidate will need to have Mandarin language proficiency at the DLPT 3 level with the ability to read and analyze technical documents, grey literature, and academic journals. </li>
<li>Demonstrates comprehensive mission knowledge and skills that affirm completion of all developmental training and experiences for the labor category</li>
<li>Demonstrates ability to communicate understanding from information that may be incomplete, indirect, highly complex, seemingly unrelated, and technically advanced</li>
<li>Demonstrates ability to structure analysis based on trends in reporting and a range of analytic perspectives from other analysts, organizations, and intelligence disciplines</li>
<li>Demonstrates ability to work independently with minimal oversight and direction</li>
<li>Demonstrates ability to collaborate and work with other IC members on information sharing, driving collection, and addressing analytic disputes and conflict resolution</li>
<li>Demonstrates ability to develop concise, insightful, and comprehensive products for defense intelligence</li>
<li>Demonstrates ability to recognize nuances and resolve contradictions and inconsistencies in information</li>
<li>Demonstrates working knowledge using complex analytic methodologies, such as structured analytic techniques or alternative approaches, to examine biases, assumptions, and theories to eliminate uncertainty, strengthen analytic arguments, and mitigate surprise</li>
<li>Structured analytic techniques include, but are not limited to, Analysis of Competing Hypotheses, Devil’s Advocacy, High-Impact / Low-Impact Analysis, Red Team Analysis, and Alternative Futures Analysis</li>
<li>Demonstrates understanding of intelligence collection capabilities and limitations, including but not limited to technical sensors/platforms and human intelligence sources related to the labor category</li>
<li>Demonstrates understanding of evaluating collected intelligence reporting, engaging with collection managers, and developing collection requirements</li>
<li>Demonstrates ability to lead teams in researching multifaceted or critical problems. Guides in selecting, designing, and applying analytic methodologies</li>
<li>Uses argument evaluation and validated analytic methodologies to challenge differing perspectives</li>
</ul>
Knight Federal Solutions provides equal employment opportunities to all qualified individuals without regard to race, color, religion, sex, gender identity, sexual orientation, pregnancy, age, national origin, physical or mental disability, military or veteran status, genetic information or any other protected classification.

All Source Analyst

<h3>Job Description</h3>
Job Description Description:
Job Title: Lab Supervisor Department: Quality Control / Laboratory Reports To: Lab Manager Type: Full-Time 
 
Note: This position requires applicants to successfully pass a pre-employment, as well as an annual pulmonary function test (PFT). This position may expose the employee to isocyanates which are chemicals known to be respiratory irritants and sensitizers. While TSE provides personal protective equipment (PPE) to its employees working around such chemicals, the most current and best available medical data indicate that individuals with pre-existing respiratory conditions including but not limited to asthma, chronic bronchitis, emphysema, and the like are at high risk of experiencing serious, and possibly fatal reactions to isocyanates, even at concentrations below the legally permissible exposure level (PEL). Therefore, due to this direct threat to their safety, TSE does not hire individuals with pre-existing respiratory conditions to work in this position. 
 
Position Summary: The Lab Supervisor supports the Lab Manager in the day-to-day operations of the laboratory within a chemical manufacturing environment. This role ensures effective execution of laboratory processes, supervises lab personnel in the absence of the Lab Manager, and contributes to maintaining ISO 9001 compliance. The Lab Supervisor plays a key role in quality control for raw materials, in-process products, and final finished goods, and also assists with training new team members and scheduling lab activities. 
 
Key Responsibilities:
<ul>
<li>Supervise laboratory staff and daily lab activities in coordination with or in the absence of the Lab Manager. </li>
<li>Assist in scheduling lab shifts and tasks to ensure timely completion of testing and quality activities. </li>
<li>Perform quality control testing on incoming raw materials, in-process batches, and final products, ensuring conformance to company specifications and regulatory standards. </li>
<li>Approve or reject finished products based on lab results and quality standards. </li>
<li>Participate in ISO 9001 quality management system activities, including audits, documentation, and continuous improvement efforts. </li>
<li>Help oversee adherence to safety and compliance protocols within the lab environment. </li>
<li>Provide guidance and training to new lab employees to ensure accurate and consistent testing practices. </li>
<li>Support investigation of non-conformances and contribute to root cause analysis and corrective actions. </li>
<li>Maintain and calibrate lab instruments and ensure accurate recordkeeping of test results and logs. </li>
<li>Assist the Lab Manager in data review, reporting, and development of lab-related procedures and policies. </li>
</ul>
Teamwork is essential for TSE's continued success, so Teamwork is an essential function of every employee's job. Teamwork drives positive results every day. Teamwork promotes positive customer relations and results in exceeding the expectations of our customers. Teamwork benefits every employee since it grows our business and increases our sales. With Teamwork, we all succeed. Without it, we all suffer. Teamwork with co-workers in the same department is just the beginning. Teamwork with every other employee, department and division is the Teamwork that is required to succeed. WE ARE TSE.
Requirements:
Qualifications:
<ul>
<li>Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific field. </li>
<li>3+ years of experience in a chemical laboratory setting; prior supervisory or team lead experience preferred. </li>
<li>Familiarity with ISO 9001 quality systems and documentation practices. </li>
<li>Strong understanding of laboratory safety protocols, chemical testing, and quality control procedures. </li>
<li>Excellent organizational and communication skills. </li>
<li>Proficiency with lab data systems and Microsoft Office Suite. </li>
<li>Ability to lead by example and maintain a team-oriented, high-performance work environment. </li>
</ul>
Working Conditions: This position is primarily based in a laboratory environment and requires the use of appropriate personal protective equipment. Some exposure to chemicals, noise, and equipment is expected.
 
Compensation details: 55000-55000 Yearly Salary
 
PI8a40a48ac15b-25405-37612465

Lab Supervisor

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom TechnicianJob Description
Join our team as a Cleanroom Technician, where you will play a crucial role in ensuring the quality and safety of production processes in a highly controlled environment. This position offers a rotating shift schedule that requires dedication and flexibility, with opportunities for skill enhancement and career growth.
Responsibilities
<ul>
<li>Visually inspect IV bags for weight, functional and cosmetic defects, and seal integrity.</li>
<li>Load units into pasteurization carts in a specified order.</li>
<li>Support local manufacturing operations and supply components to cell culture and purification areas.</li>
<li>Operate general production equipment such as parts washers and autoclaves.</li>
<li>Complete relevant paperwork following GDP/GMP guidelines.</li>
<li>Manually clean portable equipment and small parts.</li>
<li>Participate in Continuous Improvement Teams.</li>
<li>Receive and distribute supplies into the production area as necessary.</li>
<li>Perform daily cleaning of the production area to maintain GMP standards.</li>
<li>Fulfill other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>High school diploma or GED required.</li>
<li>At least 1 year of production or warehouse experience.</li>
<li>Ability to pass a vision test with perfect 20/20 vision and a color vision test.</li>
<li>Strong communication skills for effective interviewing.</li>
<li>Good written and verbal communication skills.</li>
<li>Understanding of cGMP regulations.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Comfortable working in a GMP environment with strict attire requirements (no makeup, no jewelry, scrub attire).</li>
<li>Ability to work on a rotating schedule, including weekends.</li>
<li>Must be able to train on the first shift for two days in Libertyville before reporting to the Round Lake site.</li>
<li>Commitment to not miss work within the first five weeks.</li>
<li>Must be okay with THC drug testing.</li>
<li>Ability to provide a copy of high school diploma or GED.</li>
</ul>
Why Work Here?
Enjoy working in an extremely clean and quiet environment that prioritizes precision and quality. Our company fosters a culture of continuous improvement and professional development, offering opportunities for advancement and skill enhancement.
Work Environment
Work in a cleanroom environment where contractors must wear cleanroom gowns, hair nets, beard guards (if applicable), gloves, and closed-toe shoes. The environment is extremely clean and quiet, with strict dress code requirements to maintain GMP standards.
Pay and Benefits
The pay range for this position is $21.00 - $22.68/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 Round Lake,IL.
Application Deadline
This position is anticipated to close on May 23, 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 Description
The Meteorologist II, under general supervision, performs scientific environmental tests, analyzes test data, develops or prepares graphs and figures, and summarizes results in test reports. Personnel will be required to work in a team environment on the Upper Air (UA) Operations and Maintenance (O&amp;M) Team located at the Sterling Field Support Center in Sterling, VA. 
One of the main functions of the position, is to assist the NWS field operations in performing synoptic soundings. This is accomplished by performing helpdesk duties during the synoptic windows. Specific duties include but are not limited to:
<ul>
<li>Obtain an upper air observing certification within 30 days of employment (long-term employment contingent on meeting this requirement)
<ul>
<li>Will also be required to demonstrate proficiency on multiple systems</li>
</ul>
</li>
<li>Test and analyze upper air observation software, hardware, and equipment</li>
<li>Record and analyze meteorological and engineering data from primarily upper air based meteorological systems and sensors both at the SFSC and at remote test sites</li>
<li>Evaluate sensors and system performance with respect to NWS specifications and requirements. </li>
<li>Perform real-time on-site and remote clinical weather observations in support of meteorological sensor testing during non-business hours/weekends/holidays</li>
<li>Become a subject matter expert for Help Desk-style support of the radiosonde systems
<ul>
<li>Work schedule will include shift work on a scheduled basis
<ul>
<li>Morning Shift - 6am-2pm EDT (5am - 1pm EST)</li>
<li>Evening Shift - 2pm - 10pm EDT (1pm-9pm EST) or,</li>
<li>Normal Shift ~ 8am - 4:30pm.</li>
</ul>
</li>
<li>Work schedule will include some weekends and holidays</li>
</ul>
</li>
<li>Conducting scientific environmental tests using radiosondes and laboratory equipment</li>
<li>Develop, maintain, and modify meteorological algorithms</li>
<li>Prepare test plans, test reports, various support documentation, and training materials</li>
<li>Provide status briefings to government clients on the progress of testing</li>
<li>Participate in on-site tours of the facility to outside entities</li>
<li>Assist with training new UA employees on UA equipment, practices, and safety</li>
<li>Implementation of new UA assets: development and research for implementation, installation, and testing</li>
<li>Perform installations and training of new systems at NWS locations (Travel Possibly Required)</li>
<li>Personnel may be required to assist with Upper Air Chamber and Laboratory testing- Individuals would be trained and certified on the equipment to complete this if tasking is assigned</li>
<li>Other Duties as Assigned</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor degree in Meteorology, Earth Science, or similar engineering or science discipline</li>
<li>0-2 years of experience setting up scientific tests </li>
<li>0-2 years utilizing data analysis tools such as MS Excel, MATLAB, or Python to perform statistical analysis of data</li>
</ul>
 
Desired Skills
<ul>
<li>Scientific writing experience </li>
<li>Scientific testing experience </li>
<li>Procedural drafting &amp; editing</li>
<li>Understanding of Upper Air meteorological sensors and NWS Observing Programs</li>
<li>Understanding of NWS field operations and deployment strategies and methods</li>
<li>Ability to work with an inter-disciplinary and diverse team of scientists and technicians</li>
<li>Ability to multi-task and have outstanding verbal and written communication (MS Office) </li>
<li>Ability to lift and carry up to 50 lbs.</li>
<li>Completing field and outdoor work in all weather conditions</li>
<li>Customer Service- willing to work with sites in all situations </li>
</ul>
Axiom offers competitive compensation packages including comprehensive medical/dental/life insurance and matching 401(k) contribution.
 
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
 Job Posted by ApplicantPro

Meteorologist II

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are looking for a highly motivated scientist to join our Rheumatology team at our Cambridge, MA office. The ideal candidate should be driven, experienced, collaborative, adaptable, and productive. They will support in vitro research efforts for our existing early-stage through late-stage discovery portfolio programs. Responsibilities include conducting, analyzing, and reporting on in vitro assays to explore key biological questions related to rheumatic diseases, such as RA, Systemic Sclerosis and Psoriatic Arthritis. The candidate should apply fundamental scientific principles to research and be skilled in laboratory techniques such as pipetting, cell culture, molecular biology and ELISA. In addition, a candidate with experience in fibroblast cultures and functional assays (proliferation, migration and invasion) and model development is preferred.
Responsibilities
<ul>
<li>Scientific Research: Design and execute precise in vitro experiments to advance understanding of rheumatic disease biology.</li>
<li>Lab Techniques: Skillfully use methods like pipetting, cell culture, molecular biology, ELISA, fibroblasts functional assays (proliferation, migration, invasion), fibroblasts-based model development and flow cytometry to collect quality data.</li>
<li>Data Analysis: Analyze and interpret results accurately, creating reports and presentations to share with teams.</li>
<li>Protocol Development: Follow and adapt experimental protocols while implementing new methods as needed.</li>
<li>Lab Management: Maintain equipment and manage supplies to ensure efficient lab operations.</li>
<li>Literature Review: Review literature for insights that aid experimental design and contribute ideas.</li>
<li>Collaboration: Work with cross-disciplinary teams, offering scientific expertise to drive project progress.</li>
<li>Documentation: Accurately maintain and update lab notebook and lab inventories of cell stocks, reagents etc.</li>
</ul>
Qualifications 
<ul>
<li>Education/ Years of Experience: Bachelor’s or Master’s degree in Biology or a closely related discipline with typically 0-2 (MS) or 3-5+ (BS) years’ experience.</li>
<li>Professional Experience: Demonstrated proficiency in cell culture techniques with a strong grasp of molecular biology, including practical expertise in fibroblasts culture.&nbsp; Fibroblasts related functional assays (proliferation, migration and invasion assays with incucyte), flow cytometry and ELISA are strongly preferred. Experience with data analysis and use of PowerPoint, Excel and GraphPad Prism and maintenance of data records on electronic lab notebooks.</li>
<li>Communication Abilities: Excellent verbal and written communication skills, with the capability to explain complex scientific ideas clearly and encourage collaborative dialogue.</li>
<li>Interpersonal Capabilities: Proven ability to thrive in a team-oriented setting, displaying strong interpersonal and teamwork skills.</li>
<li>Organizational Skills: Outstanding time management and organizational abilities, adept at handling multiple priorities and tasks effectively.</li>
<li>Learning Aptitude: A proactive and adaptable learner with the ability to independently generate and assess data, while quickly acquiring and applying new skills.</li>
</ul>
Position will be hired based on level of experience - Associate Scientist II or Scientist I&nbsp;
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist II or Scientist I, Rheumatology

<h3>Job Description</h3>
Job Description
3V Sigma is a world leading producer of advanced specialty chemicals that range from synthetic polymers to organic chemistry molecules. Through a deep knowledge of chemistry, chemical processes and final market applications we develop and produce chemicals that deliver the high performances customers need. Continuous Innovation, sustained Quality and outstanding Customer Support have been the key ingredients of our success for the last 60 years.
JOB SUMMARY: Process Operator
The Process Engineer will follow all work instructions, equipment operating procedures, quality standards, and safety rules/guidelines while participating in a collaborative, team environment to achieve company goals.
Schedule: Must be available for all shifts to include day, evening, and overnight. Some shifts include weekends and weekend overnight. Shifts are a rotating swing shift.
*Pay Range is $18-$27/hour based on skills, experience, and interview*
Requirements
ESSENTIAL FUNCTIONS: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requests for reasonable accommodations should be directed to the Human Resources Department. 
<ul>
<li>Operation and Control of Process Equipment such as: Reactors, Dryers, Hoppers, Packaging Technology, Valves, Vents, etc</li>
<li>Loading/staging raw materials to production equipment and production areas</li>
<li>Weighing operations to include Gross vs Net weight</li>
<li>Packaging of intermediates and final product through the operation of automated and manual production equipment</li>
<li>Follow Batch Sheet SOP's in accordance with variables: Cycle Time, Temperature, Flow Rate, Weight and Raw Materials</li>
<li>Computer and Control Room Operation to direct processes and/or people</li>
<li>Housekeeping - maintaining a clean, organized, and safe work environment per our Quality Standards and OSHA</li>
<li>Quality Control Sampling of in process material</li>
</ul>
EMPLOYMENT ELIGIBILITY: To be considered for employment you must be legally authorized to work in the United States for any employer and you will not require employment visa sponsorship now or in the future.
Required Education &amp; Experience
<ul>
<li>High School Diploma or Equivalent</li>
<li>1 Year Manufacturing Experience (Preferred)</li>
<li>Follow OSHA standards for wearing a respirator</li>
<li>Basic Computer Skills – i.e. Word, Excel (Preferred)</li>
</ul>
Other Requirements
<ul>
<li>This position is a rotating shift schedule to include day, evenings, and graveyard shifts.</li>
<li>Ability to cover and work Overtime</li>
<li>Previous Forklift Experience (Preferred)</li>
<li>Read, Speak, understand, and follow written instructions in English</li>
<li>Basic Computer Skills – i.e. Word, Excel (Preferred)</li>
<li>Follow OSHA standards for wearing a respirator (Clean Shaven except for mustache), Confined Space, LOTO</li>
</ul>
Working Conditions
<ul>
<li>Occasional exposure to the environment/elements</li>
<li>Normal exposure to environmental temperatures</li>
<li>Regular exposure to moving mechanical parts</li>
<li>Working on and around chemicals</li>
</ul>
Benefits
Available Benefits include: 
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>RX Coverage</li>
<li>Life Insurance</li>
<li>Vacation/PTO</li>
<li>401k Retirement Plan</li>
</ul>
ABOUT 3V SIGMA USA: 
3V Sigma is a leading global producer of specialty chemicals with approximately 500 employees and 4 manufacturing facilities located in United States (Georgetown, SC) and in northern Italy (Mozzo, Grassobbio, Porto Marghera).
Our modern and fully equipped R&amp;D department includes Synthesis and Technology facilities, Application testing centers and Analytical and Quality Control laboratories.
Team work is our way of approaching tasks: our chemists, process engineers, mechanical engineers, operation personnel and managers are continuously in collaboration. In this way, we have been able to create a solid and multidisciplinary technical culture which enables us to provide our customers with innovative technical solutions and with high quality, and price competitive products.
Our proprietary technologies and chemistries, customer support, consistent quality and continuous focus on innovation are what differentiates us from our competitors.
Our Mission is to serve industries supplying high quality and highly innovative products and to serve our customers providing unique solutions and outstanding technical support.
---
3V is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disabilities, or protected veteran status. 
 
Available Benefits include: 
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>RX Coverage</li>
<li>Life Insurance</li>
<li>Vacation/PTO</li>
<li>401k Retirement Plan</li>
</ul>
ABOUT 3V SIGMA USA: 
3V Sigma is a leading global producer of specialty chemicals with approximately 500 employees and 4 manufacturing facilities located in United States (Georgetown, SC) and in northern Italy (Mozzo, Grassobbio, Porto Marghera).
Our modern and fully equipped R&amp;D department includes Synthesis and Technology facilities, Application testing centers and Analytical and Quality Control laboratories.
Team work is our way of approaching tasks: our chemists, process engineers, mechanical engineers, operation personnel and managers are continuously in collaboration. In this way, we have been able to create a solid and multidisciplinary technical culture which enables us to provide our customers with innovative technical solutions and with high quality, and price competitive products.
Our proprietary technologies and chemistries, customer support, consistent quality and continuous focus on innovation are what differentiates us from our competitors.
Our Mission is to serve industries supplying high quality and highly innovative products and to serve our customers providing unique solutions and outstanding technical support.
---
3V is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disabilities, or protected veteran status.

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