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<h3>Job Description</h3>
Applied Research II
At Capital One, we are creating trustworthy and reliable AI systems, changing banking for good. For years, Capital One has been leading the industry in using machine learning to create real-time, intelligent, automated customer experiences. From informing customers about unusual charges to answering their questions in real time, our applications of AI &amp; ML are bringing humanity and simplicity to banking. We are committed to building world-class applied science and engineering teams and continue our industry leading capabilities with breakthrough product experiences and scalable, high-performance AI infrastructure. At Capital One, you will help bring the transformative power of emerging AI capabilities to reimagine how we serve our customers and businesses who have come to love the products and services we build.
Team Description:
The AI Foundations team is at the center of bringing our vision for AI at Capital One to life. Our work touches every aspect of the research life cycle, from partnering with Academia to building production systems. We work with product, technology and business leaders to apply the state of the art in AI to our business. &nbsp;
In this role, you will:&nbsp;
<ul>
<li>
Partner with a cross-functional team of data scientists, software engineers, machine learning engineers and product managers to deliver AI-powered products that change how customers interact with their money.
</li>
</ul>
<ul>
<li>
Leverage a broad stack of technologies — Pytorch, AWS Ultraclusters, Huggingface, Lightning, VectorDBs, and more — to reveal the insights hidden within huge volumes of numeric and textual data.
</li>
</ul>
<ul>
<li>
Build AI foundation models through all phases of development, from design through training, evaluation, validation, and implementation.
</li>
</ul>
<ul>
<li>
Engage in high impact applied research to take the latest AI developments and push them into the next generation of customer experiences.
</li>
</ul>
<ul>
<li>
Flex your interpersonal skills to translate the complexity of your work into tangible business goals.
</li>
</ul>
The Ideal Candidate:
<ul>
<li>
You love the process of analyzing and creating, but also share our passion to do the right thing. You know at the end of the day it’s about making the right decision for our customers.
</li>
</ul>
<ul>
<li>
Innovative. You continually research and evaluate emerging technologies. You stay current on published state-of-the-art methods, technologies, and applications and seek out opportunities to apply them.
</li>
</ul>
<ul>
<li>
Creative. You thrive on bringing definition to big, undefined problems. You love asking questions and pushing hard to find answers. You’re not afraid to share a new idea.
</li>
</ul>
<ul>
<li>
A leader. You challenge conventional thinking and work with stakeholders to identify and improve the status quo. You’re passionate about talent development for your own team and beyond.
</li>
</ul>
<ul>
<li>
Technical. You’re comfortable with open-source languages and are passionate about developing further. You have hands-on experience developing AI foundation models and solutions using open-source tools and cloud computing platforms.
</li>
</ul>
<ul>
<li>
Has a deep understanding of the foundations of AI methodologies.&nbsp;
</li>
</ul>
<ul>
<li>
Experience building large deep learning models, whether on language, images, events, or graphs, as well as expertise in one or more of the following: training optimization, self-supervised learning, robustness, explainability, RLHF.
</li>
</ul>
<ul>
<li>
An engineering mindset as shown by a track record of delivering models at scale both in terms of training data and inference volumes.
</li>
</ul>
<ul>
<li>
Experience in delivering libraries, platform level code or solution level code to existing products.
</li>
</ul>
<ul>
<li>
A professional with a track record of coming up with new ideas or improving upon existing ideas in machine learning, demonstrated by accomplishments such as first author publications or projects.
</li>
</ul>
<ul>
<li>
Possess the ability to own and pursue a research agenda, including choosing impactful research problems and autonomously carrying out long-running projects.
</li>
</ul>
Basic Qualifications:
<ul>
<li>
Currently has, or is in the process of obtaining, PhD in Electrical Engineering, Computer Engineering, Computer Science, AI, Mathematics, or related fields, with an exception that required degree will be obtained on or before the scheduled start date plus 2 years of experience in Applied Research or M.S. in Electrical Engineering, Computer Engineering, Computer Science, AI, Mathematics, or related fields plus 4 years of experience in Applied Research
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
PhD in Computer Science, Machine Learning, Computer Engineering, Applied Mathematics, Electrical Engineering or related fields
</li>
<li>
LLM
<ul>
<li>
PhD focus on NLP or Masters with 5 years of industrial NLP research experience
</li>
<li>
Multiple publications on topics related to the pre-training of large language models (e.g. technical reports of pre-trained LLMs, SSL techniques, model pre-training optimization)
</li>
<li>
Member of team that has trained a large language model from scratch (10B + parameters, 500B+ tokens)&nbsp;
</li>
<li>
Publications in deep learning theory&nbsp;
</li>
<li>
Publications at ACL, NAACL and EMNLP, Neurips, ICML or ICLR
</li>
</ul>
</li>
<li>
Optimization (Training &amp; Inference)
<ul>
<li>
PhD focused on topics related to optimizing training of very large deep learning models&nbsp;
</li>
<li>
Multiple years of experience and/or publications on one of the following topics: Model Sparsification, Quantization, Training Parallelism/Partitioning Design, Gradient Checkpointing, Model Compression&nbsp;
</li>
<li>
Experience optimizing training for a 10B+ model&nbsp;
</li>
<li>
Deep knowledge of deep learning algorithmic and/or optimizer design&nbsp;
</li>
<li>
Experience with compiler design
</li>
</ul>
</li>
<li>
Finetuning
<ul>
<li>
PhD focused on topics related to guiding LLMs with further tasks (Supervised Finetuning, Instruction-Tuning, Dialogue-Finetuning, Parameter Tuning)&nbsp;
</li>
<li>
Demonstrated knowledge of principles of transfer learning, model adaptation and model guidance
</li>
<li>
Experience deploying a fine-tuned large language model&nbsp;
</li>
</ul>
</li>
</ul>
Capital One will consider sponsoring a new qualified applicant for employment authorization for this position.
The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked.
Cambridge, MA: $257,300 - $293,700 for Applied Researcher II
 &nbsp;
McLean, VA: $257,300 - $293,700 for Applied Researcher II
 &nbsp;
New York, NY: $280,700 - $320,400 for Applied Researcher II
 &nbsp;
San Francisco, CA: $280,700 - $320,400 for Applied Researcher II
 &nbsp;
San Jose, CA: $280,700 - $320,400 for Applied Researcher II
 &nbsp;
 &nbsp;
 &nbsp;
 &nbsp;
 &nbsp;
 &nbsp;
Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate’s offer letter.
This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan.
Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the&nbsp;Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level.
This role is expected to accept applications for a minimum of 5 business days.No agencies please. Capital One is an equal opportunity employer (EOE, including disability/vet) committed to non-discrimination in compliance with applicable federal, state, and local laws. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City’s Fair Chance Act; Philadelphia’s Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries.
If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at 1-800-304-9102 or via email at <a href="mailto:RecruitingAccommodation@capitalone.com" target="_blank">RecruitingAccommodation@capitalone.com</a>. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations.
For technical support or questions about Capital One's recruiting process, please send an email to <a href="mailto:Careers@capitalone.com" target="_blank">Careers@capitalone.com</a>
Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site.
Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).

Applied Research II

<h3>Job Description</h3>
Job Description
Scientific Marketing Manager / Director - in vivo Pharmacology
Location: Remote, USA
Salary: $120,000 - $160,000
 
Combine your passion for science with creativity in scientific marketing.
Join our dynamic marketing team at Pharmaron as a Scientific Marketing Manager. We are seeking an individual who is passionate about drug discovery and preclinical development with experience in drug efficacy testing in disease models. Become part of our team to help us elevate our brand and drive sales.
 
Your Key Responsibilities:
<ul>
<li>Craft compelling narratives: Translate complex scientific concepts into engaging stories that resonate with our audience.</li>
<li>Create new content: Partner with our scientists to create engaging content that showcases our expertise such as brochures, white papers, flyers, webpage content, etc.</li>
<li>Lead marketing campaigns: Develop and execute multi-channel campaigns that increase brand awareness and generate leads.</li>
<li>Analyze and optimize: Track marketing performance, identify trends, and refine our strategies for maximum impact.</li>
<li>Represent our brand: Manage our presence at industry conferences and events.</li>
</ul>
 Your Profile:
<ul>
<li>Location: Remote, the applicant must be located in Europe or North America.</li>
<li>Scientific background: A degree in biology, pharmacology, veterinary medicine or a related field is essential.</li>
<li>Experience: Minimum of 5 years of industry experience related to animal disease models in drug discovery or drug development.</li>
<li>Exceptional communication skills: A passion for writing and the ability to convey complex scientific ideas to diverse audiences.</li>
<li>Passion for learning: A desire to stay updated on industry trends and best practices.</li>
<li>Collaborative spirit: Enjoy working with cross-functional teams and external partners with a willingness to travel as needed.</li>
</ul>
 
Why Pharmaron?
Pharmaron is a premier 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 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental &amp; Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare &amp; Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&amp;D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
 
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
 
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
 
#LI-EH1

Scientific Marketing Manager / Director - in vivo Pharmacology / Toxicology

<h3>Job Description</h3>
Job Description
Head of Biologics MSAT
<ul>
<li>Can be based in Philadephlia or Boston</li>
</ul>
Position Summary: The head of Biologics MSAT will lead the strategic and operational oversight of the Manufacturing Science and Technology function for biologics DS and/or DP manufacturing. This role is responsible for ensuring robust technology transfer, process validation, lifecycle management, and continuous improvement of biologics manufacturing processes across internal and external manufacturing global sites. The ideal candidate will bring deep technical expertise in biologics (e.g., monoclonal antibodies, ADCs, dAbs, fusion proteins), strong leadership capabilities, and a proven track record of cross-functional collaboration.
Key Responsibilities:
<ul>
<li>Lead and develop a high-performing MSAT team supporting clinical and commercial biologics manufacturing.</li>
<li>Oversee technology transfer of biologics processes from development to manufacturing, ensuring scalability, robustness, and compliance.</li>
<li>Drive global process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH).</li>
<li>Provide technical leadership for troubleshooting, deviation investigations, and CAPA implementation.</li>
<li>Partner with Quality, Regulatory, Development, and Manufacturing to ensure seamless product lifecycle management.</li>
<li>Lead initiatives for process optimization, cost reduction, and implementation of new technologies (e.g., PAT, automation, single-use systems).</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Serve as a subject matter expert during regulatory inspections and audits.</li>
<li>Develop and manage MSAT budgets, resource planning, and strategic initiatives.</li>
<li>Foster a culture of innovation, scientific excellence, and continuous improvement.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. or M.S. in Biochemical Engineering, Biotechnology, or related field; Ph.D. preferred.</li>
<li>15+ years of experience in biologics manufacturing, with at least 7 years in a leadership role within MSAT or Technical Operations.</li>
<li>Deep understanding of scale-up, upstream &amp; downstream biologics processes, tech transfers, and regulatory requirements.</li>
<li>Experience with CMO/CRO management and global manufacturing networks.</li>
<li>Demonstrated success in leading cross-functional teams and managing complex projects.</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Extensive experience in structured technical troubleshooting, RCA and CAPA effectiveness</li>
<li>Excellent communication, leadership, and strategic thinking skills.</li>
</ul>
Preferred Experience:
<ul>
<li>Experience with advanced biologics modalities (e.g., bispecifics, fusion proteins, ADCs, monoclonal antibodies).</li>
<li>Familiarity with digital tools for process monitoring and data analytics.</li>
<li>Prior experience in a fast-paced biotech or a global pharmaceutical environment.</li>
</ul>
Company DescriptionA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints. Job Responsibilities: •\tConducting Post Market Activities and Post Market Surveillance •\tManaging Customer and Product Complaint Investigation programs Education and Experience: •\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry •\tBachelor's degree •\tComputer proficiency 
<h3>Company Description</h3>
A top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints.\r\nJob Responsibilities:\r\n•\tConducting Post Market Activities and Post Market Surveillance\r\n•\tManaging Customer and Product Complaint Investigation programs\r\nEducation and Experience:\r\n•\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry\r\n•\tBachelor's degree\r\n•\tComputer proficiency

Head of Biologics MSAT

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJoin a team where science meets purpose!
We’re looking for a detail-oriented and driven Analytical Chemist to support critical testing operations in a fast-paced pharmaceutical environment. If you're passionate about precision, thrive in a collaborative setting, and are ready to make an immediate impact, we want to hear from you.
What You’ll Do
<ul>
<li>Perform routine and advanced chemical testing using cutting-edge techniques and instruments.</li>
<li>Operate and maintain specialized lab equipment including HPLC, GC, ICP, and more.</li>
<li>Lead and support investigations to troubleshoot and resolve analytical issues.</li>
<li>Ensure strict adherence to cGMP standards, data integrity, and documentation practices.</li>
<li>Collaborate with cross-functional teams to support raw material testing and product release.</li>
</ul>
What You Bring
<ul>
<li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li>
<li>Hands-on experience in the pharmaceutical or biotechnology industry.</li>
<li>Proficiency with analytical instruments such as HPLC, GC, and ICP.</li>
<li>A strong understanding of regulatory compliance and quality standards.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a mission-driven organization focused on improving patient outcomes.</li>
<li>Work in a collaborative, innovation-focused environment.</li>
<li>Gain exposure to advanced technologies and industry-leading practices.</li>
</ul>
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
Health Vision 401 K Dental Relocation Assistant
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Jun 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
esponsibilities:
<ul>
<li>Perform routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability under supervision, following established SOPs</li>
<li>Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations</li>
<li>Accurately record experimental data and observations in compliance with GxP standards.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. Seeking a recent graduate with Coop/Internship experience.</li>
<li>0 to 2 years of experience in a GMP/GLP regulated laboratory environment, with exposure to pharmaceutical or biotechnology industries preferred</li>
<li>Understanding of analytical techniques and their application in raw materials, in-process testing, release, and stability studies is preferred</li>
<li>Experience in HPLC, GC, MS or wet/analytical chemistry</li>
</ul>
Why Choose R&amp;D Partners?
As an employee, you have access to a comprehensive benefits package including:
<ul>
<li>Medical insurance – PPO, HMO &amp; HSA</li>
<li>Dental &amp; Vision insurance</li>
<li>401k plan</li>
<li>Employee Assistance Program</li>
<li>Long-term disability</li>
<li>Weekly payroll</li>
<li>Expense reimbursement</li>
<li>Online timecard approval</li>
</ul>
Pay Scale:
$62,400/annually
R&amp;D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research &amp; engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&amp;D Partners is an equal-opportunity employer.
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

QC Chemist I

<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.
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 
We are seeking a motivated and detail-oriented Research Associate – Analytical R&amp;D to join our team. This role supports ongoing research and development efforts by performing routine analytical testing, assisting with data analysis and documentation, and operating advanced laboratory instrumentation. The ideal candidate is eager to learn, technically skilled, and committed to maintaining quality and safety in a collaborative lab environment.
Key Responsibilities:
<ul>
<li>Perform routine analytical tests independently, following established protocols and procedures.</li>
<li>Support activities related to Corrective and Preventive Actions (CAPA), System Suitability Testing (SST), and Analytical Quality Management (AQM).</li>
<li>Prepare samples and mobile phases using techniques such as solid-phase extraction (SPE), liquid–liquid extraction (LLE), and supported liquid extraction (SLE).</li>
<li>Operate and assist in the maintenance and troubleshooting of advanced laboratory instruments, including:
<ul>
<li>Agilent: UPLC, SQ, TOF, QTOF</li>
<li>Thermo: UPLC, Duo LC, Orbitrap</li>
</ul>
</li>
<li>Analyze and interpret data with guidance, applying foundational knowledge of method parameters and system performance.</li>
<li>Assist in method development and sample preparation experiments under the direction of senior scientists.</li>
<li>Document all lab activities accurately and in a timely manner using electronic laboratory notebooks and internal systems.</li>
<li>Contribute to lab operations by helping maintain equipment, supplies, and shared responsibilities for cleanliness, organization, and compliance.</li>
<li>Collaborate effectively with team members to support ongoing projects, safety standards, and data integrity.</li>
<li>Actively participate in training opportunities and expand technical skills through hands-on learning.</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related scientific discipline</li>
<li>3–4 years of industry experience in an analytical or bioanalytical laboratory setting</li>
<li>Hands-on experience operating, troubleshooting, and maintaining LC-MS systems, including HPLC, UPLC, and LCMS platforms</li>
<li>Proficiency with Agilent UPLC instrumentation and OpenLab ChemStation software</li>
<li>Familiarity with mobile phase preparation and common sample preparation techniques</li>
<li>Understanding of Automated Quality Management (AQM) systems and basic statistical analysis</li>
<li>Experience performing System Suitability Testing (SST) and interpreting results</li>
<li>Strong collaboration and communication skills; able to work effectively in cross-functional team environments</li>
<li>Ability to manage multiple tasks and adapt in fast-paced, changing environments</li>
<li>Demonstrated problem-solving skills, willingness to learn, and attention to detail</li>
<li>Commitment to laboratory safety protocols and data integrity</li>
<li>Must be authorized to work in the United States without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with advanced LC-MS instruments, including:
<ul>
<li>Agilent: SQ, TOF, QTOF</li>
<li>Thermo: UPLC, Duo LC, Orbitrap</li>
</ul>
</li>
<li>Familiarity with software platforms such as MassHunter, Xcalibur, or Chromeleon</li>
<li>Prior experience supporting or executing:
<ul>
<li>CAPA investigations (Corrective and Preventive Actions)</li>
<li>Method development and validation</li>
<li>RNA and oligonucleotide analysis</li>
</ul>
</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 Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly 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 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.

Research Technician - Analytical R&D

<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.
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 
This role involves performing routine analytical testing, supporting data analysis and documentation, operating advanced lab instruments, and collaborating with the team to maintain quality and safety standards.
Responsibilities include:&nbsp;
<ul>
<li>Independently perform assigned analytical tasks under minimal supervision, including support for Corrective and Preventive Actions (CAPA), System Suitability Testing (SST), and Analytical Quality Management (AQM) activities.</li>
<li>Conduct routine analytical activities, including but not limited to sample and mobile phase preparation, using a variety of techniques such as solid-phase extraction (SPE), liquid–liquid extraction (LLE), and supported liquid extraction (SLE), in accordance with established protocols.</li>
<li>Operate and perform complex troubleshooting on laboratory instrumentation, such as Agilent UPLC, SQ, TOF, and QTOF systems as well as Thermo UPLC, Duo LC, and Orbitrap platforms.</li>
<li>Execute data analysis and reporting, applying foundational knowledge of parameters needed for accurate data processing and reduction.</li>
<li>Support and execute experiments for method development and sample preparation studies by following protocols and documenting results in collaboration with senior team members.</li>
<li>Contribute to the improvement of standard procedures, including preparation protocols and basic sample quality control techniques.</li>
<li>Maintain accurate and timely documentation of laboratory activities, including experiments, results, and observations, in electronic laboratory notebooks and systems.</li>
<li>Collaborate with team members to support daily lab operations and quality initiatives, including compliance with safety, data integrity, and lab standards.</li>
<li>Proactively identify technical training needs to enhance skills and actively participate in hands-on learning of analytical techniques and laboratory best practices</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field with 3-4 years of industry experience&nbsp;</li>
<li>Hands-on expertise in troubleshooting and maintaining LC-MS systems.</li>
<li>Experience troubleshooting and maintaining&nbsp;LC systems: HPLC, UPLC, LCMS</li>
<li>Hands-on experience with&nbsp;Agilent UPLC&nbsp;instruments</li>
<li>Proficiency with&nbsp;OpenLab ChemStation&nbsp;software</li>
<li>Familiarity with&nbsp;mobile phase preparation&nbsp;techniques</li>
<li>Knowledge of&nbsp;Automated Quality Management (AQM)&nbsp;and related statistical analysis</li>
<li>Experience performing&nbsp;System Suitability Testing (SST)&nbsp;and interpreting associated statistics</li>
<li>Strong collaboration skills with cross-functional teams.</li>
<li>Ability to manage multiple priorities and adapt in dynamic environments.</li>
<li>Demonstrated scientific problem-solving, learning agility, and effective communication (written and verbal).</li>
<li>Strong adherence to safety protocols.</li>
<li>Authorized to work in the U.S. without restriction or sponsorship.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with instruments:
<ul>
<li>Agilent: SQ, TOF, QTOF systems</li>
<li>Thermo: UPLC, Duo LC, Orbitrap platforms</li>
</ul>
</li>
<li>Experience with software:
<ul>
<li>MassHunter,&nbsp;Xcalibur,&nbsp;Chromeleon</li>
</ul>
</li>
<li>Experience with methods:
<ul>
<li>CAPA&nbsp;(Corrective and Preventative Actions)</li>
<li>Method development and validation</li>
<li>RNA analysis</li>
<li>Oligonucleotide analysis</li>
</ul>
</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 Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly 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 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.

Analytical Chemist - R&D

<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 detail-oriented In Vivo Research Associate to support preclinical neuroscience studies through specialized rodent procedures, including CNS-targeted surgeries and drug delivery techniques. This role is hands-on and highly technical, involving stereotaxic surgery, tissue dissection, and injection methods such as ICV and IT, with a strong emphasis on precision, animal welfare, and accurate data documentation
Key Responsibilities:
<ul>
<li>Conduct rodent surgical and technical procedures, including intravenous (IV), subcutaneous (SC), intraperitoneal (IP), intracerebroventricular (ICV), and intrathecal (IT) injections.</li>
<li>Perform precise stereotaxic and microsurgical procedures targeting the central nervous system (CNS).</li>
<li>Dissect CNS and peripheral tissues with accuracy and care for downstream analysis.</li>
<li>Carry out blood collection and processing, including centrifugation of whole blood and plasma isolation via pipetting.</li>
<li>Troubleshoot, optimize, and refine in vivo techniques according to protocol requirements.</li>
<li>Maintain thorough and accurate records of experimental procedures and results in an electronic laboratory notebook (ELN), preferably Benchling.</li>
<li>Work independently and collaboratively in a fast-paced, team-oriented research environment.</li>
<li>Ensure full compliance with institutional animal care and use policies, standard operating procedures, and best laboratory practices.</li>
</ul>
Physical Requirements:
<ul>
<li>Frequent use of fine motor skills and steady hand-eye coordination for detailed surgical procedures.</li>
<li>Regular repetitive motion involving hands, wrists, and arms.</li>
<li>Ability to walk between research buildings, climb stairs, and transport laboratory materials and supplies as needed.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s Degree (B.S.) in Neuroscience, Biology, or a related field, with at least 5 years of relevant industry experience in in vivo pharmacology.</li>
<li>Master’s Degree (M.S.) in Neuroscience, Biology, or a related field, with at least 3 years of relevant industry experience in in vivo pharmacology.
<ul>
<li>Proven skill and proficiency in microscopic CNS surgery and fine CNS dissection techniques, with the ability to validate these skills following established protocols.</li>
</ul>
</li>
<li>Comfortable working in a laboratory animal research environment within the industry.</li>
<li>Experienced in rodent dosing techniques, including intravenous (IV), subcutaneous (SC), and intraperitoneal (IP) administration.</li>
<li>Proficient in stereotactic injections, with demonstrated validation against established protocols.</li>
<li>Strong knowledge of brain and spinal cord anatomy.</li>
<li>Experience with electronic laboratory notebook (ELN) entry, preferably using Benchling.</li>
<li>Demonstrated attention to detail, independence, accountability, and responsibility for own work.</li>
<li>Excellent organizational skills and ability to manage multiple tasks simultaneously.</li>
<li>Ability to follow standard operating procedures (SOPs) and maintain good documentation practices.</li>
<li>Commitment to safety and strict adherence to animal welfare policies.</li>
<li>Authorization to work in the United States indefinitely without restrictions or sponsorship.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience performing intracerebroventricular (ICV) injections in mice and intrathecal (IT) injections in rats.</li>
<li>Familiarity with neuroscience-relevant in vivo models and assays supporting drug discovery programs.</li>
<li>Strong interest in expanding scientific knowledge and developing surgical and technical skills related to CNS research.</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 Onsite Meeting with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 7:00 AM to 3:00 PM), with occasional weekends and overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly 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&nbsp;</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.

In Vivo Research Associate - CNS Focus

<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 
<ul>
<li>Perform rodent surgical and technical procedures, including intravenous IV), subcutaneous (SC), intraperitoneal (IP), intracerebroventricular (ICV), and intrathecal (IT) injections.</li>
<li>Perform central nervous system (CNS) and peripheral tissue dissection</li>
<li>Perform stereotactic and microscopic surgeries.</li>
<li>Perform blood collection and processing (i.e., centrifuging whole blood, pipetting plasma)</li>
<li>Troubleshoot and refine in vivo techniques.</li>
<li>Maintain precise and organized documentation of experimental procedures and results in an electronic laboratory notebook (ELN).</li>
<li>Work independently as well as within a flexible team-oriented environment.</li>
<li>Ensure adherence to animal welfare policies, research protocols, and laboratory best practices.</li>
</ul>
Additional Physical Requirements:
<ul>
<li>Requires fine motor skills and dexterity of fingers, hands, wrists, and arms.</li>
<li>Frequently required to use repetitive hand/wrist/arm motion.</li>
<li>Walking, climbing stairs, and moving materials and supplies between research buildings.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s Degree (B.S.)&nbsp;in Neuroscience, Biology, or related field:
<ul>
<li>Minimum&nbsp;5+ years of relevant industry experience&nbsp;in&nbsp;in vivo pharmacology</li>
<li>Skilled and proficient&nbsp;in&nbsp;microscopic CNS surgery&nbsp;and&nbsp;fine CNS dissection techniques
<ul>
<li>Must be able to&nbsp;validate skills using established protocols</li>
</ul>
</li>
</ul>
</li>
<li>Master’s Degree (M.S.)&nbsp;in Neuroscience, Biology, or related field:
<ul>
<li>Minimum&nbsp;3+ years of relevant industry experience&nbsp;in&nbsp;in vivo pharmacology</li>
<li>Skilled and proficient&nbsp;in&nbsp;microscopic CNS surgery&nbsp;and&nbsp;fine CNS dissection techniques
<ul>
<li>Must be able to&nbsp;validate skills using established protocols</li>
</ul>
</li>
</ul>
</li>
<li>Comfortable working in an industry laboratory animal research environment.</li>
<li>Skilled and proficient with rat and mouse dosing (IV, SC, IP routes).</li>
<li>Skilled and proficient with stereotactic injections (validation with established protocols will be required).</li>
<li>Expertise in brain and spinal cord anatomy.</li>
<li>Experience with ELN entry (Benchling is preferred).</li>
<li>Demonstrated attention to detail, independence, accountability and responsibility for own work.</li>
<li>Exceptional organizational skills and performing multiple tasks simultaneously.</li>
<li>Ability to follow standard operating procedures and good documentation practices.</li>
<li>Unwavering commitment to safety and animal welfare policies.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with ICV (mouse) and IT (rat) injections.</li>
<li>Experience working with neuroscience-relevant in vivo models and assays to support drug discovery programs.</li>
<li>Interest to expand scientific knowledge and surgical and technical procedure portfolio.</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 Onsite Meeting with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 7:00 AM to 3:00 PM), with occasional weekends and overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly 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&nbsp;</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.

Scientist - In Vivo Pharmacology

<h3>Job Description</h3>
Job DescriptionInnovative Chemical Products Group (ICP Group) is a leading formulator and manufacturer of specialty coatings, adhesives, and sealants serving the construction and industrial end markets. ICP Group is comprised of market leading brands known for innovation, quality, and performance. Founded in 2015 and supported by a lean corporate team, ICP Group has scaled rapidly through organic and acquisition growth into one of the largest coatings, adhesives, and sealants companies in North America. ICP Group is headquartered in Andover, MA and has manufacturing and distribution sites throughout North America, Latin America, UK, Europe and the Asia Pacific region. ICP Group is looking to hire a Lab Technician to support the R&amp;D facility in Andover, MA. Andover specializes in water-based coating manufacturing with the majority of its volume made up of tennis court coatings and architectural coatings. You will work in a supporting role with R&amp;D Chemists to accomplish project-related tasks and report directly to the Technical Director. In this role you will be responsible for the following:
<ul>
<li>Supporting Chemists on projects</li>
<li>Accurate and reliable lab batch manufacturing: water and solvent-based</li>
<li>Testing and application of coatings</li>
<li>Ability to learn color matching</li>
<li>Ability to organize testing data to present information to team</li>
</ul>
Requirements:
<ul>
<li>Preferred BS in Chemistry, Biology, Engineering, or related field</li>
<li>Paint experience preferred but not required</li>
<li>Product manufacturing, application and testing can involve physical activity. Prefer ability to lift 50lbs.</li>
<li>Proficient with Microsoft Office </li>
<li>Self-motivated and organized</li>
</ul>
 ICP Group is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, or religion or other legally protected status. &nbsp;
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