field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionDaily Responsibilities/Job Description: 
<ul>
<li>Applies professional-level technical skill and judgment to provide non-routine technical support for computer/data center operations.</li>
<li>Installs, configures and troubleshoots server and non-desktop computer hardware, software, systems and other resources in a data center or other centralized computer network setting.</li>
<li>Maintains access control, data integrity and file system security for the computer/data center environment.</li>
<li>Monitors, tracks and records system performance and utilization metrics.</li>
<li>Communicates highly technical information to both technical and nontechnical personnel.</li>
<li>Recommends process, hardware and software solutions, including new acquisitions and upgrades, to improve computer/data center efficiency.</li>
<li>May participate in development of information technology and infrastructure projects. May be internal or external, client-focused, working in conjunction with Professional Services and outsourcing functions. May include company-wide, web-enabled solutions</li>
</ul>
Hours of Operation: 
<ul>
<li>Schedule would be either from 7am to 4pm OR 3pm to 12am Monday - Friday</li>
</ul>

Lab Computing Analyst

<h3>Job Description</h3>
Job Description
Position: Research Associate I - PK
FLSA Status: Non-Exempt
Location: San Diego, CA (ON-SITE)
Salary: The expected hourly range for this in San Diego, CA, is $24.00 to $28.00.
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our PK department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo pharmacokinetic studies. 
Primary responsibilities: 
This position requires a broad knowledge of anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing, and sampling techniques is required. 
Other important functions include: 
<ul>
<li>Experience in the administration of test substances by various basic methods (i.e., oral gavage, SQ, IV, dermal, etc.).</li>
<li>Manage and observe animals for general health, overall wellbeing, and normal Vitals.</li>
<li>Experience in the collection of biological specimens (i.e., blood from appropriate vessels from all species of laboratory animals at the site).</li>
<li>Able to perform study related activities in compliance with Good Laboratory Practice Regulations (GLPs), study protocols, and company policies and Standard Operating Procedures (SOPs).</li>
<li>Review documentation to ensure functions performed meet quality control requirements. </li>
<li>Handle, restrain, and provide care for all species of laboratory animals at the site.</li>
<li>Perform study preparation activities, including collection tube labeling and room setup.</li>
<li>Performed catheter placements in large animals.</li>
<li>Perform aseptic techniques.</li>
<li>Interface with different teams, including study director, principal investigator, QC/QA, and Account Managers/Sales.</li>
<li>Maintain accurate records in various internal databases. </li>
<li>Support internal research projects to optimize service offerings</li>
<li>Perform other duties as directed by management.</li>
</ul>
Candidate Requirements: 
<ul>
<li>HSD/GED with a minimum of 2 years relevant experience. </li>
<li>Associates degree (preferred) in veterinary technology with a minimum of 1-2 years relevant experience. </li>
<li>BS with 1-year relevant experience.</li>
<li>Education level requirements could be amended based on relevant years of experience.</li>
<li>Certification as a registered veterinarian technician (RVT) is a plus.</li>
<li>Background in lab animal (in vivo) research is a must. Working knowledge of preclinical techniques and modalities will be a plus.</li>
<li>Position requires good communication skills and attention to detail.</li>
<li>Strong work ethic, self-motivation, and ability to adapt in a dynamic team environment. </li>
</ul>
Benefits:
Pharmaron cares about our work community and offers a variety of benefits, allowing employees the opportunity to customize a benefits package that meets their personal needs. Company benefits include the following:
<ul>
<li>Medical, Dental &amp; Vision Insurance Plan with Employer Contribution</li>
<li>Health Reimbursement Account Funded by Employer</li>
<li>Healthcare &amp; Dependent Care Flexible Spending Accounts</li>
<li>Employee Life and AD&amp;D Insurance 100% Employer Paid</li>
<li>Voluntary Life and AD&amp;D Insurance for Employee, Spouse &amp; Child(ren)</li>
<li>Short and Long Term Disability 100% Employer Paid</li>
<li>401k with Employer Match</li>
<li>Employee Assistance Program</li>
</ul>
About Pharmaron 
Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&amp;D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&amp;D solutions to its partners in North America, Europe, Japan and China.
Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.
 
#LI-ZS1

In Vivo Research Associate I, PK

<h3>Job Description</h3>
Job DescriptionDescription:
An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Therapeutic Medical Physicist at the G.V. Sonny Montgomery VAMC.
 
Therapeutic Medical Physicists (TMPs) work in Radiation Oncology and have responsibilities that include: protection of the patient and others from potentially harmful or excessive radiation; establishment of adequate protocols to ensure accurate patient dosimetry; the measurement and characterization of radiation used for radiotherapy; the performance and supervision of treatment planning; the determination of delivered dose; advancement of procedures necessary to ensure delivered dose integrity; the assessment and monitoring of image quality; development and direction of quality assurance programs; assistance to other health care professionals in optimizing the balance between the beneficial and deleterious effects of radiation; and compliance with applicable federal and state regulations. The advanced level TMP can perform the most complex of these tasks, and has the experience to commission and clinically implement novel technologies. 
Specific tasks include but are not limited to the following:
<ul>
<li>Recommending an optimal modality and treatment technique for the patient.</li>
<li>Evaluating the quality, safety, and accuracy of radiation treatments planned and delivered to patients, thus ensuring that radiation dose is carried out correctly and completely.</li>
<li>Safely operating all radiation planning and delivery devices.</li>
<li>Implementing radiation therapy of outstanding technical difficulty and responsibility, providing knowledge-based solutions to resolving issues where no rule-based solutions exist.</li>
<li>Planning and directing a specialized program encompassing all physics and clinical aspects of external beam and brachytherapy (if applicable) treatment procedures from treatment simulation to treatment planning to the actual treatment delivery.</li>
<li>Providing technical oversight for the work of entry level TMPs, medical dosimetrists and radiation therapists.</li>
<li>Overseeing radiation therapy treatment planning.</li>
<li>Designing and approving treatment plans.</li>
<li>Monitoring the accuracy of treatment data recorded in the patient's medical records.</li>
<li>Providing consultation to the radiation oncologist regarding difficult treatment cases.</li>
<li>Performing patient-specific treatment validation measurements.</li>
<li>Developing medical physics policies and procedures for the delivery and quality assessment of advanced treatment modalities such as intensity modulated radiation therapy, stereotactic body radiation therapy, and brachytherapy.</li>
<li>Developing, operating and fully documenting the medical physics quality assurance program and ensures regulatory compliance within the Radiation Safety Officer's radiation safety program.</li>
<li>Safely utilizing and properly operating all radiation oncology equipment, and is therefore qualified and responsible for educating radiation oncology team members including radiation oncologists, radiation therapists and dosimetrists in safety issues that relate to radiotherapy planning and delivery.</li>
<li>The employee performs the following actions to assist in the implementation of new equipment and processes:
<ul>
<li>Assesses radiation therapy equipment needs</li>
<li>Performs acceptance testing and commissioning of new radiation therapy equipment</li>
<li>Evaluates the adequacy of room shielding</li>
<li>Performs radiation surveys</li>
<li>Develops and implements treatment processes.</li>
</ul>
</li>
<li>The advanced level TMP will be a knowledgeable user and subject matter expert in the use of the Pinnacle, Eclipse and Cyberknife Precision treatment planning systems, Truebeam and Cyberknife delivery systems, and Sun Nuclear QA equipment and software.</li>
<li>The advanced level TMP will also be an expert in the following special procedures: stereotactic radiosurgery, stereotactic body radiation therapy, and surface-guided radiation therapy.</li>
<li>Provide support for clinical research trials, including submission of radiation plans, DICOM datasets as needed. </li>
</ul>
Requirements:
<ul>
<li>United States Citizenship: Non-citizens may only be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy.</li>
<li>Education: Master's degree or higher in a physics, science, or engineering discipline recognized by an accredited college or university with at least 30 semester hours in medical physics, health physics, radiological science, physics, engineering, chemistry, or biology; or an equivalent foreign degree and coursework substantiated by the National Association of Credential Evaluation Services.</li>
<li>Board Certification: Persons hired or reassigned to TMP positions in the VHA must be board certified in the field of therapeutic medical physics by an approved certifying body. The board certificate must be current and the applicant must abide by the certifying body's requirements for continuing education. Approved Certifying Bodies:
<ul>
<li>The American Board of Radiology (ABR) in any of the following field titles:
<ul>
<li>Therapeutic Medical Physics</li>
<li>Therapeutic Radiologic or Therapeutic Radiological Physics</li>
<li>Radiologic Physics or Radiological Physics</li>
</ul>
</li>
<li>The American Board of Medical Physics (ABMP) in the subfield of Radiation Oncology Physics.</li>
<li>The Canadian College of Physicists in Medicine (CCPM) in the subfield of Radiation Oncology Physics.</li>
</ul>
</li>
</ul>

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job Description
Position Purpose:The primary purpose of this position is to prepare samples and perform data collection activities using physics and X-ray based instrumentation at the Transportation Security Laboratory (TSL).
Essential Duties &amp; Responsibilities:
- Performs material characterization (e.g. microscope imaging, density measurements, rheological and mechanical properties). - Prepares test samples for analyses. - Operates explosive detection systems (EDS) as well as analytical physics instrumentation (computed tomography, x-ray fluorescence, x-ray diffraction, etc.) for data collection. - Performs troubleshooting, maintenance, and method development on EDS and analytical instrumentation. - Safely handles explosive and other hazardous materials. - Assembles test articles and bags per test specifications. - Develops and uses code (MATLAB, Python, R) for data analysis. - Analyzes, compiles, and reports data collection results for research and development and quality control testing events. - Composes and reviews technical reports and standard operating procedures. - Composes, reviews, and executes test plans. - Performs literature reviews. - Sources materials and submits purchase requests. - Other duties as assigned.
Required Knowledge, Skills and Abilities:
 - Good interpersonal, verbal, and written communication skills. - Good listening skills. - Good working knowledge of scientific and analytical techniques. - Good working skills of software and tools necessary for job functions including Microsoft Office suite, MATLAB, Python.
Education/Experience:
Incumbent should have a minimum of a bachelor's degree in chemistry, engineering, physics, or other core science and up to five years of experience.
Working Conditions/Experience:
The incumbent is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%.
 Powered by ExactHire:160579

Entry Level Physical Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
<ul>
<li>Perform biochemical testing on proteins and antibodies including, but not limited to,&nbsp;CE, HPLC, SEC, IEX, UV, Purity Analysis, and/or Bioassays</li>
<li>Enter data into LIMS</li>
<li>Participate in conducting investigations</li>
<li>Document test results in notebooks and reports</li>
<li>Supervise others in performing client’s service requirements</li>
<li>Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements</li>
<li>Foster motivation and morale</li>
<li>Coordinate workflow and perform daily monitoring to meet TAT</li>
<li>Prepare and review job plans, conduct semiannual performance reviews, interview applicants, keep training records up to date for assigned employees, perform succession planning in preparation for growth</li>
<li>Coach and develop individuals and team to maximize performance</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in biochemistry 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 a related major)</li>
<li>At least four years’ experience working in a biochemistry role in industry&nbsp;</li>
<li>At least 1-2 years of supervisory experience</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>Position is&nbsp;Monday- Friday 8:00 am-5:00 pm. Overtime as needed.&nbsp; Candidates currently living within a commutable distance of&nbsp;&nbsp;Indianapolis, IN&nbsp;are encouraged to apply.&nbsp;</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
#LI-EB1
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Chemist Supervisor

<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 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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We're looking for someone to support routine lab testing and help maintain a well-organized QC environment. This role involves working with various instruments, preparing samples, and following established procedures. A great fit would be someone detail-oriented, eager to learn, and comfortable working in a team setting.
Job Duties Include:&nbsp;
<ul>
<li>Perform routine testing of pharmaceutical samples by following analytical compendial methods (pH, osmolality, concentration, break-loose extrusion force, etc.)</li>
<li>Prepare standards and samples for analysis</li>
<li>Monitoring and replenishing lab reagents and solutions</li>
<li>Maintain, calibrate, and operate instrumentation in the QC laboratory</li>
<li>Document work as required for GMP compliance</li>
<li>Execute work in accordance with standard operating procedures, with attention to detail, and with strong organizational skills</li>
<li>Interact effectively with peers and leaders as part of a multi-disciplinary team</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry or other science related degree concentration</li>
<li>0-2 years of QC analytical experience</li>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</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 Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>30 Minute Virtual Interview with Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, first shift, Monday-Friday from 8 am-5 pm. Candidates must be flexible to adapt to schedule&nbsp;changes requiring shift changes and/or weekend work, and overtime may be required as needed.&nbsp;Candidates living within a commutable distance of Andover, MA&nbsp;are encouraged to apply.&nbsp;&nbsp;
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 holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</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.

QC Analytical Chemist

<h3>Job Description</h3>
Job Description
Department:Research and Clinical Development Position Title: Research Intern Reports To: Senior Director, RCD Company Location: Irving, TX Location of Position: Irving, TX (Hybrid) Preferred
Company Background
Revision Skincare®, based in Irving, TX, partners with dermatologists, plastic surgeons, and medical spas to deliver clinically proven, high-performing skincare products. Our collection, formulated with premium quality ingredients, provides targeted solutions for enhancing skin’s long-term health through innovative and visible results.

Scope of Position
As a Research Intern, you will engage in one to two key research projects supporting new product development and ongoing business growth. You will delve into the science behind our proprietary and licensed technologies. This role involves collaboration within the department and with marketing and regulatory teams.

Key Responsibilities
<ul>
<li>Lead and Complete In Vitro Study Design:
<ul>
<li>Identify optimal testing facilities to design studies that achieve product claims.</li>
<li>Review and present testing and cost proposals to the team.</li>
<li>Write or review study documentation, including protocols and final reports.</li>
<li>Evaluate and present study results to the department, marketing, and regulatory</li>
</ul>
</li>
<li>Conduct Literature Reviews:
<ul>
<li>Substantiate the efficacy of highlighted ingredients through scientific literature.</li>
<li>Assist in publishing clinical studies in reputable, peer-reviewed journals.</li>
<li>Research competitor products and ingredients.</li>
</ul>
</li>
</ul>
Leadership Competencies
<ul>
<li>High Standards: Demonstrates a commitment to excellence.</li>
<li>Results-Oriented: Focuses on achieving the right outcomes.</li>
<li>Collaborative: Works effectively across functions.</li>
<li>Adaptable: Learns and adjusts quickly in a dynamic environment.</li>
</ul>
Requirements
<ul>
<li>Passion for Research: Enthusiasm for clinical testing, publications, and literature reviews.</li>
<li>Communication Skills: Strong verbal and written communication abilities.</li>
<li>Positive Attitude: Ability to thrive in a fast-paced environment.</li>
<li>Educational Background: Pursuing a bachelor’s degree in Biochemistry, Chemical Engineering, Cellular Biology, Molecular Biology, or Biomedical Engineering.</li>
<li>Detail-Oriented: Keen attention to detail.</li>
<li>Team Player: Ability to collaborate effectively in a team setting.</li>
<li>Eligibility: Must be authorized to work in the U.S.</li>
</ul>

Key Development Opportunities: 
<ol>
<li>Professional Development Opportunities: Opportunity to connect with cosmetic industry subject matter experts including physicians, aestheticians, and physician assistants. One on One mentorship meetings with executive leadership to learn more about company dynamics. Attendance at August Sales meeting in Dallas. </li>
<li>Impact and Contribution: Opportunity to be a co-author on a peer-reviewed publication, poster or white paper. This directly contributes to the success of the company. </li>
<li>Company Culture: Team of empathetic, humble, innovative, and quality driven individuals focused on doing right for Revision Skincare and our customers.</li>
<li>Career Path:This internship will assist in future opportunities in the field of cosmetic sciences, dermatology, and longevity sciences. </li>
</ol>

Research Intern

<h3>Job Description</h3>
Job DescriptionCompany Description 
The Bosch Research and Technology Center North America with offices in Sunnyvale, California, Pittsburgh, Pennsylvania and Cambridge, Massachusetts is a part of the global Bosch Group /home/bou1pi/workspace/active-learning-toolchain/actlearn/training/config/model/frontend/gabor.yaml (<a href="http://www.bosch.com" target="_blank">www.bosch.com</a>), a company with over 90 billion euro revenue, 400,000 employees worldwide, a very diverse product portfolio, and a history spanning over 125 years. The Research and Technology Center North America provides technologies and system solutions for various Bosch business fields, primarily in the field of artificial intelligence (for example, human-assisted AI, natural language processing, robotics, 3D perception, and AI platform), energy technologies, internet technologies, circuit design, semiconductors and wireless, as well as advanced MEMS design.
The Bosch Research and Technology Center in Pittsburgh, PA is focused on the research and development of cutting-edge AI and sensing technologies that will shape the future of the company's products. This position is part of an ambitious effort to design and develop intelligent multi-modal sensing at the intersection of deep learning and signal processing, with diverse application domains ranging from physical security to intelligent and connected vehicles.
Job Description 
Originating from Bosch AI research in Pittsburgh, we are responsible for pushing the boundaries of signal sensing and multimodal models through key innovations to solve complex industry problems and shape the future of Bosch products and services for both internal and external users. We work with internal partners of different Bosch business units to transfer our solutions into future products. We also actively collaborate with leading groups in academia and industry to promote research ideas and publish research findings in internationally renowned conferences and journals.
In this position, you are expected to:
<ul>
<li>Develop and lead research projects focusing on multi-sensor data fusion, including acoustic, vibration, radar, lidar, image, Wi-Fi, time series, and ultrasound data, to improve sensing capabilities in autonomous driving vehicles, predictive maintenance in manufacturing processes, and next generation smart home devices, leading to enhanced safety, efficiency, and user experience.</li>
<li>Design, build, train, evaluate multi-modal deep-learning models that leverage sensor signals, and work together with several business units within Bosch to transfer research artifacts into products and processes.</li>
<li>Offer expert insights to the management team in relevant technology sectors, aiding in strategic planning, R&amp;D trajectory, and investment decisions.</li>
<li>Stay abreast of the latest technological innovations, document and disseminate research findings through high-caliber publications and/or patent submissions.</li>
</ul>
Qualifications 
Basic Qualifications
<ul>
<li>Ph.D. in Computer Science, Electrical Engineering, Information Technology or a related discipline</li>
<li>In-depth experience in signal processing for sensor data and their integration with deep-learning methods.</li>
<li>Proficiency in Python, PyTorch (including libraries such as torchaudio, torchvision, torchmetrics), familiarity with PyTorch Lightning.</li>
<li>A strong publication record in relevant venues such as&nbsp;ICASSP, InterSpeech, WASPAA, SenSys, IPSN, ICCPS, ICML, ICLR, ICRA, CVPR, ICCV, ECCV, NeurIPS, or equivalent contributions to the field such as patents or significant open-source projects.</li>
<li>Strong interpersonal, communication, and teamwork capabilities.</li>
</ul>
Preferred Qualifications
<ul>
<li>3+ years of experience in industrial research.</li>
<li>Proficiency with version control systems (Git), integrated development environment (VSCode or PyCharm) and experience with experiment tracking tools (MLFlow).</li>
<li>Familiarity with high-performance computing (HPC) systems and job schedulers (Slurm, LSF).</li>
<li>Hands-on experience in product development in the above-mentioned areas for consumer/enterprise markets.</li>
<li>Experience leading projects with small teams, demonstrating the ability to mentor junior researchers and interns, manage project timelines, and deliver results within time constraints.</li>
</ul>
 Additional Information 
Equal Opportunity Employer, including disability / veterans.  
*Bosch adheres to Federal, State, and Local laws regarding drug-testing. Employment is contingent upon the successful completion of a drug screen and background check. Candidates who have been offered the position must pass both screenings before their start date.&nbsp;

Research Scientist - Multi-modal Sensing AI

<h3>Job Description</h3>
Job Description
Glendora Employment Agency, Inc. is a boutique agency located in the foothills of the San Gabriel Valley. We specialize in connecting local employers with local talent. We are currently seeking a Cleanroom Technician for a precision cleaning company in Irwindale, CA.
 JOB DESCRIPTION: Duties for this position include, but are not limited to: •Work in a class 10,000 cleanroom inspecting and packaging parts according to customer specifications. •Identify and report any defects or non-conforming issues (scratches, dents, etc.). •Precision clean parts per spec and traveler instructions. •Collaborate with the team to address any quality assurance issues.
•Inspect finished and packaged products for foreign object debris (FOD). •Package product and review labels for accuracy. •Wear personal protective equipment required to perform job duties. •Keep workstation and equipment/tools clean. •Other related duties as assigned.
 MINIMUM QUALIFICATIONS: Ideal candidates should possess the following skills/qualifications demonstrated through previous work experience: •High school diploma required. •Prior experience working in a cleanroom environment highly preferred. •Strong attention to detail. •Proficient computer and data entry skills. •Ability to work independently, as well as part of a team. •Great written and verbal communication skills.
DRESS CODE: **No outside debris is allowed in the cleanroom** •Jeans (no ripped or distressed jeans allowed), slip resistant shoes, and an appropriate shirt/top. •No sandals or open toed shoes allowed. •No makeup, perfumes/colognes, hair products, scented lotions, etc. allowed. •Nails must be short enough to not puncture gloves. •Hair must be in a ponytail or bun. •Leggings are allowed on Friday’s if they are not see-through.
Position Type: Temp-to-Hire Schedule: Monday – Friday from 7:00am – 3:30pm Salary: $17/hour
Company DescriptionGlendora Employment Agency, Inc. is a boutique staffing firm located in the foothills of the San Gabriel Valley. Glendora Employment Agency, Inc. specializes in bringing local job seekers together with local employers. Benefits offered by client once successful candidate goes is hired by client. GEA, Inc. - Bringing People and Business Together Since 1956 
<h3>Company Description</h3>
Glendora Employment Agency, Inc. is a boutique staffing firm located in the foothills of the San Gabriel Valley. Glendora Employment Agency, Inc. specializes in bringing local job seekers together with local employers. Benefits offered by client once successful candidate goes is hired by client.\r\n\r\nGEA, Inc. - Bringing People and Business Together Since 1956

Cleanroom Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today!
Job Description 
Position Overview:
The Non-Regulated Bioanalytical Scientist will work in a team environment conducting bioanalytical assay development and&nbsp;in vivo&nbsp;study support in a non-regulated environment with fit-for-purpose assays.
Position Responsibilities:
<ul>
<li>Sample (blood, plasma, bio-fluid, and bio-tissue) preparation (protein precipitation, SLE, SPE, or other appropriate sample clean up techniques)</li>
<li>Conduct LC-MS/MS analysis and assay troubleshooting</li>
<li>Process data and&nbsp;report generation</li>
</ul>
Qualifications 
Basic Minimum Requirements:
<ul>
<li>BS degree in biology or related discipline</li>
<li>Must have effective oral and written communication and be able to work effectively in a team environment</li>
<li>Must be proficient and/or familiar in computer systems such as Watson LIMS or Sciex OS, or be willing to learn</li>
<li>This role requires full-time on site work during core business hours of Monday-Friday, 9am-3pm at a minimum</li>
<li>Must be eligable to work in the United States indefinitely without sponsorship.</li>
</ul>
 Additional Information 
Position is full-time&nbsp;Monday-Friday, 8am-5pm&nbsp;with overtime as needed; core hours are 9am-3pm.Candidates currently living within a commutable distance of Groton, CTare encouraged to apply.
What we offer:
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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