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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. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
Eurofins Environment testing in Albuquerque, New Mexico offers our customers a wide range of environmental laboratory services. We are experienced in the analysis of organic and inorganic contaminants in drinking water, wastewater, sludge, oil, soil, wastes, solids and air. We are seeking an entry level analyst to join our team!&nbsp;
The Analyst I prepares and analyzes environmental samples using standard&nbsp;analytical techniques according to scientific and EPA methodology in compliance with Eurofins Environment Testing America Quality Assurance programs and standard operating procedures (SOPs).
Essential Duties and Responsibilities:
<ul>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:</li>
</ul>
o Preparation of samples using standard techniques
o Performing chemical analysis using standard techniques
o Calculating data
o Recording and reporting data and any unusual test occurrences to the supervisor
o Performing routine instrument maintenance
<ul>
<li>Responsible for performing job functions in compliance with Eurofins Environment Testing</li>
<li>America’s environmental, health and safety and quality assurance standards</li>
<li>Responsible for general housekeeping in work area</li>
<li>Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems.</li>
<li>Works under close supervision using routine and standard methods.</li>
<li>Aliquots and weighs samples</li>
<li>Washes glassware</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
<ul>
<li>BS or BA in chemistry or related field. 3 years laboratory experience may substitute for degree.</li>
</ul>
Experience:
<ul>
<li>Laboratory experience helpful</li>
<li>Previous production-oriented work helpful (awareness and ability to meet deadlines)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li>
</ul>
 Additional Information 
This is a&nbsp;full-time&nbsp;position Monday to Friday&nbsp;8 am to 5 pm&nbsp;with overtime and weekends as needed. Candidates living within a commutable distance to Albuquerque, NM are encouraged to apply.&nbsp;
Salary Range: $20- $21 per hour.
Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/&amp;nbsp" target="_blank">https://careers.eurofins.com/&amp;nbsp</a>;
Company 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 :40 the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and&nbsp;agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Analyst I - Eurofins Environment Testing, Albuquerque, NM

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
Responsibilities:
<ul>
<li>Perform a wide range of analyses, both routine and non-routine, primarily in molecular biology, cell biology, and virology test areas of Biopharmaceutical Services</li>
<li>Conduct day-to-day activities in a laboratory setting under prescribed processes, including protocols, standard operating procedures, and methods</li>
<li>Review and evaluate raw data for acceptability, ensuring accuracy and reliability of results</li>
<li>Set up and validate new analytical or related processes used by the department</li>
<li>Learn and apply molecular biology technology to support ongoing research and development efforts</li>
<li>Design and execute experiments to investigate cellular and molecular mechanisms</li>
<li>Maintain detailed laboratory notebooks and electronic records of all experimental procedures and results</li>
<li>Analyze and interpret experimental data using appropriate statistical methods and software tools</li>
<li>Prepare technical reports, summaries, and presentations of research findings</li>
<li>Collaborate with cross-functional teams to support project goals and timelines</li>
<li>Troubleshoot and optimize experimental protocols to improve efficiency and reproducibility</li>
<li>Maintain and calibrate laboratory equipment to ensure optimal performance</li>
<li>Adhere to all safety protocols and regulatory guidelines in the laboratory environment</li>
<li>Contribute to the development of standard operating procedures (SOPs) and best practices</li>
<li>Participate in regular team meetings and scientific discussions to share knowledge and stay updated on project progress</li>
</ul>
Qualifications 
The ideal candidate would possess:
<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>
<li>PCR technique exposure/experience</li>
</ul>
Minimum Qualifications:
<ul>
<li>1-2 Full years of applied industry experience</li>
<li>Bachelor’s degree in biology, molecular or cell biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is full-time, working 8:00 AM-5:00 PM Monday-Friday. Candidates currently&nbsp;living within commutable distance to Lancaster, PA&nbsp;are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
<ul>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientist I - Cell and Molecular Biology

<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 
This role is for an advanced personnel who has in-depth knowledge of cell based and potency assays and are comfortable with troubleshooting. The Group Leader’s main technical responsibility will be to serve as SME for mRNA and gRNA potency assays to support several client programs.&nbsp;
Technical Responsibilities:
<ul>
<li>Optimize, technical transfer, qualification, and validation of potency assays used for lot release and characterization of cell and gene therapy products and critical materials.</li>
<li>Acting as an SME resource for potency assays.</li>
<li>Execution of complex GMP release and stability assays such as cell-based functional assays, flow cytometry methods, ddPCR, ELISA, and NGS assays.</li>
<li>Author and review SOPs and technical reports.</li>
<li>Work with cross-functional groups within the client environment to participate in various aspects of method development, transfer, process, and product characterization, comparability, and investigations.</li>
<li>Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance.</li>
</ul>
Leadership Responsibilities
<ul>
<li>Supports and monitors the performance of the team of employees</li>
<li>May participate in new hire interviews</li>
<li>Supports the on-boarding process of new employees</li>
<li>Disseminate administrative communications</li>
<li>Demonstrate and promote the company's vision</li>
<li>Ensure adherence to highest quality and efficiency standards in laboratory operations&nbsp;</li>
<li>Ensure coverage and performance for all shifts, and work duties&nbsp;</li>
<li>Performs administrative tasks for team member growth and development</li>
<li>Adeptly balance technical lab work with leadership responsibilities</li>
<li>Foster morale and teamwork&nbsp;</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s degree with 3-8 years of experience</li>
<li>Master’s degree with 2-5 years of experience</li>
<li>Must have experience with potency assay execution</li>
<li>Must have previous experience working in a GMP laboratory</li>
<li>Understanding of industry practices and standards is required</li>
<li>Laboratory supervisory experience&nbsp;is preferred</li>
<li>Team player with excellent oral and written communication skills</li>
<li>Independently motivated, detail-oriented, and excellent problem-solving abilities.</li>
</ul>
Differentiating qualifications:
<ul>
<li>Strong background in cell culture and experience working with cell lines and primary human cells.</li>
<li>Experience with functional, or potency assay transfer and execution in a GMP laboratory.</li>
<li>Broad experience with molecular biology, cellular, and immunoassay techniques including transfections/transductions, ddPCR/qPCR, flow cytometry, ELISA, and NGS.</li>
<li>Experience using data analysis software including JMP</li>
<li>Knowledge of ICH/USP guidelines.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute In Person Meeting&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins 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 clients’ 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.

Potency Assay Scientist Group Leader

<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 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>
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>
RMA Northern California, part of the RMA Network of top fertility practices in the United States, is currently seeking a Senior Embryologist to join our growing San Francisco practice. Hours will be rotating Monday-Wednesday and Saturday - Wednesday 6am-3:30pm.
 
This position will be responsible for executing all laboratory procedures according to established policies as well as adhering to RMA’s quality assurance/control operating procedures. The ideal candidate will hone previous embryology experience and perform all aspects of clinical embryology independently and in accordance with RMA’s Laboratory Philosophy, Mission, and Performance Standards. 
 
Responsibilities:
<ul>
<li>Follow established policies for IVF procedures, specimen handling, and tissue storage</li>
<li>Maintain quality assurance, quality control, and operating guidelines for lab services</li>
<li>Adhere to quality control policies and documentation requirements</li>
<li>Follow OSHA requirements for safe lab operation</li>
<li>Obtain proficiency to perform all lab services efficiently and reliably on an independent basis</li>
<li>Participate in clinical and research lab operations as directed</li>
<li>Identify problems that may adversely affect patients and facilitate a solution</li>
<li>Participate in lab proficiency testing</li>
<li>Assist Laboratory Director in designing and implementing research protocols </li>
<li>Attend laboratory meetings as requested</li>
<li>Attend continuing education programs as requested</li>
</ul>
 
Requirements: 
<ul>
<li>Bachelor's of Science </li>
<li>4+ years embryology experience</li>
<li>Demonstrate an aptitude for performance of laboratory services</li>
<li>Aptitude to make appropriate judgments regarding clinical significance of laboratory data</li>
<li>Excellent work ethic and motivation to learn lab procedures</li>
<li>High level of listening and counseling skills </li>
<li>Aptitude to work independently and demonstrate good judgment</li>
<li>Ability to access, input, and retrieve information from a computer.</li>
<li>Knowledge of office procedure and office machines (i.e., computer, fax, copier, etc.)</li>
<li>Must be able to work weekends and some holidays.</li>
</ul>
 
IVI-RMA offers a comprehensive benefits package to all employees who work a minimum of 30 hours per week.
<ul>
<li>Medical, Dental, Vision Insurance Options</li>
<li>Retirement 401K Plan</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Company Paid: Life Insurance &amp; Long-Term Disability &amp; AD&amp;D</li>
<li>Flexible Spending Accounts</li>
<li>Employee Assistance Program</li>
<li>Tuition Reimbursement</li>
</ul>
 
About IVIRMA Global: 
IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: <a href="https://rmanetwork.com/" target="_blank">https://rmanetwork.com/</a> &amp; <a href="https://www.ivirma.com/" target="_blank">https://www.ivirma.com/</a> 
 
EEO
 “IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.”

Senior Embryologist

<h3>Job Description</h3>
We're seeking a skilled and dedicated Embryologist to join an innovative team in San Francisco. If you excel in a cutting-edge, fast-paced lab setting and are driven to support individuals and families on their fertility journey, this opportunity is for you.
 
What You’ll Do:
• Perform all aspects of IVF lab work: ICSI, embryo culture, cryopreservation, biopsies, AH, and more
&nbsp;• Collaborate with physicians and clinical staff to ensure outstanding patient care
&nbsp;• Maintain lab records, equipment, and QA processes with meticulous attention to detail
&nbsp;• Participate in research, meetings, and training initiatives
 
What You’ll Bring:
&nbsp;• Bachelor’s in Biological Sciences (Master’s preferred)
&nbsp;• 2–3+ years of clinical embryology experience
&nbsp;• Expertise in ICSI, embryo culture, and cryo techniques
&nbsp;• Team player with excellent communication and problem-solving skills
&nbsp;• Willingness to work occasional weekends/holidays
 
Perks &amp; Benefits:
&nbsp;• Competitive salary + sign-on + relocation
&nbsp;• Medical, dental, vision, 401(k) match
&nbsp;• Generous PTO and holidays
&nbsp;• Tuition assistance &amp; professional development
&nbsp;• The opportunity to help build families every single day
 
Compensation:
$150,000–$200,000 DOE + Sign-on Bonus + Relocation Assistance
 
To express interest or request more information, please submit your resume or CV via this job listing or email <a href="mailto:hr@ivfnomads.com" target="_blank">hr@ivfnomads.com</a>. Kindly include your availability for a brief introductory call.

Senior Embryologist - Brand New Facility

<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 
AbbVie Precision Medicine Pathology organization is committed to driving tissue based translational and biomarker efforts for our pre-clinical and clinical stage programs. We are seeking a highly motivated ML/AI scientist to join our expanding computational pathology group to revolutionize digital pathology and precision medicine. Candidates for this senior position should have several years of experience in the field, a passion for research, and a track record of productivity and accomplishments. They should enjoy working in a fast-paced, dynamic and highly interactive environment. Their scientific leadership will enable them to independently and expertly guide teams in their approaches to quantitative image derived data generation and interpretation.
The ideal candidate will apply their expertise in computer vision and AI to analyze complex microscopy image and spatial-omics datasets, enabling breakthroughs in companion diagnostics, biomarker discovery, and personalized treatment strategies. As a computational pathology scientist, you will be embedded in our small but evolving organization that works closely with colleagues in the various pathology laboratories as well as with the research pathologists. You will provide scientific leadership to our team as you interface with investigators in discovery and late-stage research across our spectrum of disease areas which ranges from oncology, cancer immunotherapy, immunology, to neuroscience.
Key Responsibilities:
<ul>
<li>Lead the design, development, and deployment of state-of-the-art machine learning algorithms such as deep learning, representation learning, and self-supervised learning to solve key challenges in tissue image analysis, segmentation, and classification.</li>
<li>Develop interpretable AI approaches by integrating attention mechanisms or explainable AI (XAI) techniques for clinical validation and adoption.</li>
<li>Evaluate large-scale histopathology and spatial omics datasets to identify biomarkers that inform patient stratification and companion diagnostics.</li>
<li>Collaborate cross-functionally with pathologists, biologists, statisticians, data analysts, and fellow scientists to ensure seamless integration of ML/AI solutions into workflows and pipelines.</li>
<li>Manage external collaborations with research partners to enhance project outcomes and foster innovation.</li>
<li>Mentor and guide junior AI scientists and engineers in the team, fostering a collaborative and innovative environment.</li>
<li>Publish research findings in top-tier journals and conferences and present your work to internal and external stakeholders.</li>
<li>Stay at the forefront of advancements in AI, computer vision, and digital pathology to continuously refine and expand the impact of your work.</li>
</ul>
Qualifications 
Required Qualifications:
<ul>
<li>Ph.D. in Computer Science, Electrical Engineering, Computational Biology, Bioinformatics, or related field with an emphasis on computer vision or machine learning with 6+ years of relevant industry experience; or M.S. with 12+ years of relevant industry experience; or BS or equivalent education and extensive, Typically, 14+ years of experience</li>
<li>Demonstrated expertise in developing, validating, and deploying advanced computer vision and deep learning algorithms, evidenced by the successful release of products.</li>
<li>Proficiency in programming with Python, C++, and experience using computer vision libraries such as OpenCV and ML frameworks like TensorFlow and PyTorch.</li>
<li>Strong experience in image analysis and techniques such as segmentation, object detection, and classification, preferably in the field of digital pathology (e.g., histopathology or tissue imaging) and/or spatial omics.</li>
<li>Experience with MLOps practices, including deployment, monitoring, and lifecycle management of machine learning models in production environments.</li>
<li>Knowledge of cloud computing platforms and scalable AI/ML pipelines (e.g., AWS, Azure, GCP).</li>
<li>Excellent communication skills, with the ability to convey complex technical concepts to non-technical stakeholders. Proven ability in scientific writing.</li>
<li>Strong problem-solving skills and demonstrated creative approaches to overcoming challenges.</li>
<li>Excellent organizational skills and the capability to manage multiple projects simultaneously.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience handling large-scale heterogeneous biomedical data with a focus on image processing and associated clinical data integration.</li>
<li>Experience with spatial omics datasets and integration of molecular data with image analysis.</li>
<li>Understanding of precision medicine applications, including biomarker discovery, patient stratification, and personalized treatment strategies.</li>
<li>Demonstrated desire and ability to learn, understand and master new techniques or technologies.</li>
<li>Familiarity with cell and molecular biology concepts relevant to immunology, cancer immunotherapy, or oncology, or a strong willingness to learn about these areas.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;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>

Principal Research Scientist I

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Assembler Responsibilities
<ul>
<li>Cleanroom assembly</li>
<li>Ability to read work instruction</li>
<li>Assemble torque wrenches</li>
<li>Install screws to complete the assembly process using a screw down machine</li>
<li>Adjust torque on wrenches using a torque tester</li>
<li>Install caps</li>
<li>Perform final cleaning and packaging of completed wrenches</li>
</ul>
Essential Skills
<ul>
<li>Experience in production</li>
<li>Assembly skills</li>
<li>Understanding of Good Manufacturing Practices (GMP)</li>
<li>Ability to work in a clean room environment</li>
</ul>
Must have 2nd shift availability. This position is in Newbury Park, CA.Pay and Benefits
The pay range for this position is $20.00 - $22.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Newbury Park,CA.
Application Deadline
This position is anticipated to close on May 13, 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.

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