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<h3>Job Description</h3>
Job Title: Head of Immunology Development Operations
Location: Cambridge, MA, Morristown, NJ
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress.&nbsp;
The Head of Immunology Development Operations will report directly to the Therapeutic Area Development Head of I&amp;I is a leadership role managing critical operational aspects of the TA, including resource planning, TA governance, leadership team meetings, town halls off-sites and core organization wide initiatives.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
<ul>
<li>
Member of the I&amp;I Therapeutic Leadership team providing direction for the portfolio and management group.
</li>
<li>
Responsible for management of the Therapeutic Area Review Committee (TARC) using&nbsp;knowledge of projects, timelines and deliverables, link scheduling and prioritization of topics to overall TA and Business Unit strategy.&nbsp;&nbsp;Maintain SharePoint site, serve as TARC Secretary keeping and distributing detailed minutes, coordinate with key functions including S&amp;BD and Research.
</li>
<li>
Responsible for coordination and execution of other key TA governance committees such as Protocol Review Committee (PRC) and TA Clinical Strategy Review meeting&nbsp;
</li>
<li>
Support the Development of Disease Area Strategy in cross-functional team workstream
</li>
<li>
Support the TA Development Head with preparations for major meetings (either internal or external)&nbsp;
</li>
<li>
Oversee TA communications including leading development of TA newsletter and I&amp;I Development Town Halls
</li>
<li>
Oversee development and execution of process and procedure improvement initiatives within TA.&nbsp;&nbsp;&nbsp;Assess, develop, and implement tools designed to facilitate operational excellence initiatives within TA.
</li>
<li>
Act as Resource for TA to advise and develop ad-hoc reports for project teams, functional leadership based on industry best practices.
</li>
<li>
Serve as liaison/interface to coordinate and potentially lead cross-functional projects with other critical functions (Commercial, Regulatory, Medical Affairs, Strategy and CSO) and Development.
</li>
<li>
Support preparation of business plans and requests for TA funding.
</li>
<li>
Partner with Global Project Heads/Regional Project Leads of Unit and business partners to ensure adequate resource allocation.
</li>
<li>
Contribute to the preparation of regular R&amp;D portfolio review process.
</li>
<li>
Lead capacity planning with TA members during planning process/cycle. Consolidate and follow-up TA budget and headcounts.
</li>
<li>
Prepare appropriate dashboards for TA leadership team.
</li>
<li>
Responsible for the effective implementation of projects and activities aiming to develop a culture of excellence, enhance knowledge and build skills across the TA.
</li>
<li>
Interface with Enabling Functions to ensure compliance of the TA with company’s standards.
</li>
<li>
Advise and assist with recruitment, training and people development.
</li>
</ul>
Key Shared accountabilities:
With Project Management and TA Operational Lead:
<ul>
<li>
Define project needs and resource allocation&nbsp;
</li>
</ul>
With Finance and Project Management:
<ul>
<li>
Define budget needs and allocation (sites/projects/T&amp;E/Training)
</li>
</ul>
With HR and TA Head:
<ul>
<li>
Elaborate recruitment and onboarding plans
</li>
<li>
Collaborate on people development and management activities
</li>
</ul>
With Purchasing &amp; Legal:
<ul>
<li>
Contracts, compliance and transparency&nbsp;
</li>
</ul>
About You
Qualifications
<ul>
<li>
Bachelor's degree with 10 + years international experience in pharmaceutical/life sciences industry, Master's with 7+ years /PhD/MD/PharmD with 5 + years of pharma/life science industry experience.
</li>
<li>
Prior Team Leader &amp; Managerial experience, both transversal and direct
</li>
</ul>
<ul>
<li>
Ideal candidate will have a mix of clinical or scientific experience, project management skills and financial/business background
</li>
<li>
Track record of accomplishments in keeping teams on track, in meeting goals and managing conflicts
</li>
<li>
Strong leadership &amp; communication, verbal and presentation skills
</li>
<li>
Open minded, critical thinker with strong analytical skills
</li>
<li>
Ability to navigate the management matrix; Negotiation skills
</li>
<li>
Knowledge of Product Development Process with broad cross-functional experience, insight, and ability to manage at both strategic and operational levels.
</li>
</ul>
<ul>
<li>
Demonstrated knowledge of the overall biologic/pharmaceutical product development process, stages of development, and role of different functional areas.
</li>
<li>
Requires an acceptance of potential ambiguity surrounding assumption-based analysis
</li>
<li>
Familiarity and comfort with budget reporting
</li>
<li>
Must be professional, dedicated, and detail-orientated and have the flexibility to travel domestically and internationally.
</li>
<li>
Excellent oral and written communication, interpersonal, analytical, and computer skills.
</li>
<li>
Effective problem solving and analytical skills to tackle and manage a broad range of issues and projects and deliver innovative solutions
</li>
<li>
Strong organizational skills required, including good time management skills.
</li>
<li>
Highly organized and able to work independently on multiple tasks in a fast-paced environment
</li>
</ul>
Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA ​ #LI-SA #LI-Onsite &nbsp;#vhd&nbsp;
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Head of Immunology Development Operations

<h3>Job Description</h3>
Job title: Senior Clinical Scientist
Location: Cambridge, MA
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.&nbsp;
Reporting to the Clinical Lead, the Senior Clinical Scientist is noted as the scientific expert for the execution of dedicated studies of assigned program. The role requires a well-organized, operationally focused, individual with good analytical skills and the ability deliver multiple operational tasks.
The role of the Senior Clinical Scientist is to:
<ul>
<li>
Provide scientific expertise to the clinical studies and/or registries (eg: protocol, Key Results, Clinical Study Report)
</li>
<li>
Support other clinical development activities (e.g. pressure test and cluster feasibility, medical review and validation of clinical data, study risk assessment)
</li>
</ul>
<ul>
<li>
Contribute to the Abbreviated Protocol, the final protocol and protocol amendments and the clinical study report for their project
</li>
</ul>
<ul>
<li>
Contribute to the clinical part of submission dossier for their projects: Common Technical Document for FDA &amp; EMA submission, filing in Japan and China and answers to questions from health authorities
</li>
<li>
Provide appropriate medical input &amp; support for all activities related to clinical studies such as medical training, feasibility, medical review of data, medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators
</li>
<li>
Be the clinical reference in the Clinical Study team related to clinical data
</li>
</ul>
Main Responsibilities:
<ul>
<li>
Ensure continuous medical review of aggregated data during clinical trial conduct (DRSR, safety, stat outputs of blinded data, listing, patient profile, etc) with operational support, bio statistics and global safety officer
</li>
<li>
Support the development of the abbreviated protocol
</li>
<li>
Support the development of the final protocol and protocol amendments
</li>
<li>
Author medical related study documents (pre-defined deviation list, the Informed Consent Form, Written Subject Information, study specific committee charter, etc)
</li>
<li>
Clinical support to clinical operation team during the clinical feasibility
</li>
<li>
Review and provide clinical input across different study documents (CRF, patient diary, central monitoring plan, QTL, deviation review, etc)
</li>
<li>
Clinical support to clinical operations team on study plans: CMP/MRP, DR &amp; DS review
</li>
<li>
Review/approve study-related documents (eg vendor specifications for centralized services, CRF, CRF completion guidance, patient diary, etc)
</li>
<li>
Participate in the elaboration of training material and presentations at the investigator meetings
</li>
<li>
Assist in the processing of responses to medical questions raised by EC/IRBs, sites
</li>
<li>
Support CRD trial master file documents readiness and availability, and mandatory trainings linked to the clinical function
</li>
</ul>
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Provide operational expertise to project clinical sub team, as needed
About You
Job requirements
<ul>
<li>
PhD in any biomedical discipline, post-doctoral studies in hematology / oncology is preferred; Pharm D with significant clinical data experience can apply
</li>
<li>
Must have at least 2+ years of experience in clinical development within pharmaceutical industry or CRO
</li>
<li>
Computer and MS application skills
</li>
<li>
Fluency in written and spoken English
</li>
<li>
Ability to work and interact within a matrix model
</li>
<li>
Open to work in an international and intercultural environment
</li>
<li>
Open-minded to apply and learn digital solutions
</li>
</ul>
Why Choose Us?
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA ​ #LI-SA #LI-Onsite &nbsp;#vhd&nbsp;
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Senior Clinical Scientist

<h3>Job Description</h3>
Job Title: Senior Scientist, Synthetic Enabling Technologies
Location: Cambridge, MA
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress.
The Process Chemistry team, part of the CMC Synthetics organization within Sanofi R&amp;D, is responsible for the design and preliminary process development of commercial manufacturing routes for drug substances undergoing clinical development. We strongly believe that innovation is an important driver to be successful and we focus a large part of our activity on developing new synthetic routes, concepts, and technologies to provide drug substances in the most efficient, robust, economical, environmentally benign, and intrinsically safe way.&nbsp;
We are looking for a highly motivated and collaborative individual with expertise in synthetic organic chemistry to join our Process Chemistry team. Under the direction of Process Chemistry leadership, the primary responsibility of this role is to perform and oversee multi-step route evaluation and route development activities, with the aim of establishing commercial drug substance manufacturing processes through management and execution of internal and outsourced laboratory activities. Depending on projects, this role may also oversee the activities of one or more collaborators.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
<ul>
<li>
Design novel synthetic pathway for drug substances in clinical development.
</li>
<li>
Conduct route scouting in laboratory to demonstrate synthetic viability.
</li>
<li>
Use all imaginable chemistry tools and methods to develop new synthetic pathways (photochemistry, biochemistry, flow chemistry, electrochemistry, on-line analysis, High Throughput Screening, structural analysis (NMR, UPLC/MS).
</li>
<li>
Analyze experimental data to drive synthetic experimental plans.
</li>
<li>
Assist in the design, planning and execution of multi-step experimental studies guided by risk assessment to deliver safe, efficient, robust and scalable drug substance manufacturing processes.
</li>
<li>
Investigate optimization and scale-up of reaction and purification unit operations.
</li>
<li>
Collaborate within project teams by working closely with analytical chemists, process engineers, pilot plant experts and project managers within the CMC Synthetics organization.
</li>
<li>
Communicate scientific results in a clear, concise, and accurate manner via electronic laboratory notebook documentation, development reports, project discussions and presentations.
</li>
<li>
Draft and review technical reports, external publications and patent applications.
</li>
<li>
May include management of outsourced laboratory activities: generating scope of work, supervising activities at CDMOs, validating reports for outsourced activities.
</li>
</ul>
About you
Qualifications &amp; Experience:
<ul>
<li>
Ph.D. in organic or synthetic chemistry.
</li>
<li>
Knowledge in at least one of the following areas: advanced analytics, flow chemistry, high throughput experimentation.
</li>
<li>
Experience in chemocatalysis or biocatalysis including characterization of catalytic processes and/or mechanistic analysis.
</li>
<li>
Computational capabilities and basic coding skills.
</li>
<li>
Strong publication record in peer-reviewed journals.
</li>
<li>
Excellent written and verbal communication skills.
</li>
<li>
Ability to operate with flexibility in a dynamic environment and with tight deadlines.
</li>
<li>
Post-doctoral experience.
</li>
<li>
Proficiency with Microsoft suite.
</li>
<li>
Familiarity with digital tools (e.g. Scifinder-n, and Reaxys) and advanced data analysis software (e.g. Spotfire).
</li>
<li>
Design of experiment, statistical and/or thermo-kinetic modeling.
</li>
<li>
Strategic and innovative thinker with a track record of fresh insightful thinking by developing creative approaches to processes and practices.
</li>
<li>
French language skills
</li>
</ul>
Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.​​
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.​​
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.​​
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.​
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.​
#GD-SA &nbsp;​ &nbsp;#LI-SA
#LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Senior Scientist, Synthetic Enabling Technologies

<h3>Job Description</h3>
Job Description
At Boston Fusion, we recognize diversity is the catalyst for limitless creativity.
 
As a Principal Research Scientist for Boston Fusion, you will have the opportunity to utilize your knowledge of scientific research and software engineering best practices to contribute and drive research efforts in development of systems core to the success of future Intelligence, Surveillance, and Reconnaissance (ISR) activities. This role will lead technical teams as a Principal Investigator, lead and contribute to proposal efforts, and collaborate with project teams to solve complex technical problems that support national security.
 
Every day, we go above and beyond to solve complex problems, making a difference for our nation. We do this by bringing together smart, curious people with diverse life experiences who collaborate creatively to achieve innovative technological breakthroughs. We are proudly building a work environment where you can bring your authentic self to work.
 
Due to the nature of our project work, we can only consider candidates with a current US Citizenship.
 Day to Day Responsibilities
 
 
<ul>
<li>Lead teams of two or more Scientists, Engineers, and Programmers, including identifying, assigning, and completing research and development tasks appropriate to each member of the team</li>
<li>Provide a strategic leadership role in working with a project / proposal team to identify the research approach, hypotheses to be tested, and program milestones to achieve all program objectives</li>
<li>Facilitate collaboration in large, complex teams to ensure resulting technology (algorithms, software, frameworks) achieves all research objectives</li>
<li>Select, improve, or design computational models</li>
<li>Identify relevant research approaches, hypotheses to be tested, and program milestones to achieve all program objectives with project and/or proposal teams</li>
<li>Provide scientific, technical and software design support to projects and proposals</li>
<li>Design statistically valid experiments to test and validate resulting computational models</li>
<li>Provide leadership and guidance in the analysis of results of the experiments using sound scientific principles</li>
<li>Design experiments to test and validate computational models</li>
<li>Establish and maintain a professional rapport with all project stakeholders (internal and external)</li>
<li>Additional project and proposal duties as assigned</li>
</ul>
 
Additional Responsibilities
<ul>
<li>Occasional travel to attend and present at customer meetings and essential industry conferences</li>
<li>Prepare technical briefing materials/summarize technical work and progress of projects</li>
<li>Collaborate with company leadership and senior technical staff to conduct proposal research and proposal writing</li>
<li>Publish technical reports based on original or improved algorithms created to solve the application challenges</li>
<li>Maintain high standards at work, continuously looking for solutions to improve processes and products</li>
<li>Develop, maintain, and strengthen partnerships with others inside and outside the organization to achieve Boston Fusion business goals</li>
<li>Demonstrate personal accountability, effective work habits, integrity, and ethical behavior that align with Boston Fusion corporate values</li>
<li>May perform other duties as required</li>
</ul>
 
This Job is Right for You if you Have:
 
<ul>
<li>Bachelor’s degree in computer science, engineering, mathematics, physics, or related field, with 15+ years of experience; Master’s degree with 13+ years of experience; PhD with 10+ years of experience</li>
<li>Excellent analytical and problem-solving skills</li>
<li>Ability to prioritize and manage time effectively</li>
<li>Excellent communication, writing and presentation skills</li>
<li>Ability to work both collaboratively and independently</li>
</ul>
 
Demonstrates strong competency in every category and a mastery of at least one category
<ul>
<li>Demonstrated competency in radar, signal processing, human-machine systems, computer vision, AI/ML, or other technical discipline</li>
<li>Experience implementing modeling and analysis techniques, including machine learning, operations research, optimization, control theory, probabilistic modeling, etc.</li>
<li>Understanding of mathematical principles which underlie these modeling methods</li>
<li>Experience in implementing algorithms in standard programming languages such as Python, Java, C++</li>
<li>Experience in using sound software development techniques, e.g., testing, documentation, source control</li>
</ul>
 
Preferred Technical Qualifications
<ul>
<li>Classical applied probabilistic, mathematical, and/or artificial intelligence methods (planning, searching, logic, uncertain knowledge, probabilistic reasoning, natural language processing)</li>
<li>Radar signal processing techniques</li>
<li>Machine learning frameworks (e.g., Scikit-learn, Tensorflow, PyTorch, Keras) and concepts (e.g., supervised, unsupervised, active, and reinforcement learning; neural networks; generative, discriminative models)</li>
</ul>
 
Preferred Domain Knowledge
<ul>
<li>6+ years of experience applying technology to US Department of Defense and/or Intelligence Community problems, including but not limited to the following: intelligence analysis, command and control, logistics, ISR, information operations, missile defense, operations in the cyber, space, or maritime domains</li>
<li>8+ years of experience in a research leadership role</li>
<li>Work Authorization/Security Clearance Requirements</li>
<li>U.S. citizenship and DoD security clearance (REQUIRED)</li>
</ul>
 
PIbd12df9b44ff-25405-36297946

Principal Research Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Flex Image Operator Job Description
The Flex Image Operator is responsible for executing wet chemical tank and conveyor etching processes to meet customer specifications during the 2nd Shift, Monday through Friday, from 3:30 PM to 12:00 AM.
Responsibilities
<ul>
<li>Execute wet chemical tank and conveyor etching processes per standard work instructions to meet customer specifications, such as concentration, temperature, and dwell time.</li>
<li>Read, interpret, and apply special instructions or traveler notes for unique panel materials and custom etch depths.</li>
<li>Measure critical panel dimensions and surface conditions using specialized gauges and tools to verify conformance.</li>
<li>Accurately document measurements, process parameters, and trends on product control worksheets and traveler review sheets.</li>
<li>Fixture and process panels through various wet chemical tanks and conveyors using frames, leaders, and backboards to ensure parts are properly aligned and prevent defects.</li>
<li>Participate in cross-training for plating processes and support plating operations as needed.</li>
<li>Maintain a clean, organized workspace and equipment in compliance with prescribed safety regulations, including proper rinsing of stations, disposal of chemical waste, and keeping aisles clear.</li>
<li>Perform scheduled preventive maintenance on etch equipment per the operator process control checklist.</li>
<li>Complete daily tasks as directed by the production schedule with minimal supervision, consistently meeting or exceeding throughput targets.</li>
<li>Communicate process feedback, equipment issues, or material concerns to the department Lead or Supervisor in a timely manner.</li>
<li>Collaborate as a team member with peers and leadership to support production demands and continuous improvement initiatives.</li>
</ul>
Essential Skills
<ul>
<li>High school diploma or GED required.</li>
<li>At least 1 year of experience in wet chemical etching, plating, or related manufacturing environment preferred.</li>
<li>Ability to read written instructions clearly and write legibly for accurate documentation.</li>
<li>Quality-driven mindset with keen attention to detail.</li>
<li>Strong mechanical aptitude and desire to learn new processes.</li>
<li>Excellent time-management skills with the ability to multitask under tight deadlines.</li>
<li>Effective written and verbal communication skills.</li>
<li>Team-oriented attitude with a willingness to help peers and adapt to changing production needs.</li>
<li>Commitment to workplace safety and following all environmental, health, and safety protocols.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in production, cleanroom, assembly, machine operation, general labor, forklift operation, microscope usage, machine operating, packaging, general production, hand tool usage, blueprint reading, packing, inspection, medical device, and medical assembly.</li>
</ul>
Why Work Here?
Employees enjoy competitive pay with performance-based bonus opportunities, an Employee Stock Ownership Plan, generous paid time off, affordable health coverage, flexible spending accounts, a 401(k) with company match, a Wellness Incentive Program, and an Employee Assistance Program. We offer tuition assistance and career development pathways, as well as quarterly and individual performance bonuses.
Work Environment
This role operates within a fast-paced manufacturing environment, requiring adherence to safety regulations. The workspace involves working with wet chemical tanks and conveyors, with a focus on cleanliness and organization. Dress code complies with safety standards.
Job Type &amp; Location
This is a Contract to Hire position based out of Plymouth, Massachusetts.
Pay and Benefits
The pay range for this position is $17.50 - $25.00/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 Plymouth,MA.
Application Deadline
This position is anticipated to close on Jun 17, 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.

Flex Image Operator

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a Scientist&nbsp;with expertise in plate-based process impurity assays to support biologics programs. This role will focus on the development, qualification, troubleshooting, and transfer of ELISA-based assays for detecting Host Cell Proteins (HCP), residual Protein A, residual DNA, and other process-related impurities. The ideal candidate will have hands-on experience in assay development and validation, strong analytical problem-solving skills, and the ability to collaborate with cross-functional teams.
Key Responsibilities:
1. Assay Development &amp; Qualification (50%)
<ul>
<li>Develop, optimize, and qualify plate-based impurity assays (e.g., ELISA, qPCR, Western blot) for process impurity detection.</li>
<li>Evaluate assay performance, ensuring sensitivity, specificity, accuracy, and precision meet regulatory expectations.</li>
<li>Conduct method qualification and contribute to validation strategies in compliance with ICH and USP guidelines.</li>
<li>Support the development of custom and commercial HCP ELISAs, including reagent assessment and selection.</li>
</ul>
2. Assay Troubleshooting &amp; Remediation (30%)
<ul>
<li>Investigate assay variability, drift, and reagent stability issues to ensure robust impurity testing.</li>
<li>Work with internal teams and external vendors/CROs to assess critical reagents and optimize assay performance.</li>
<li>Provide technical expertise in resolving lot-to-lot variability issues in impurity assays.</li>
<li>Analyze and interpret assay data, preparing technical summaries and reports.</li>
</ul>
3. Technology Transfer &amp; Regulatory Support (20%)
<ul>
<li>Support the transfer of impurity assays to QC labs and external CRO/CDMO partners.</li>
<li>Prepare technical reports, regulatory submissions, and responses to health authority queries.</li>
<li>Participate in cross-functional meetings to ensure alignment on impurity assay strategies.</li>
</ul>
Qualifications 
Authorization to work in the United States indefinitely without restriction or sponsorship
<ul>
<li>MS with 2-4 years or BS with 4-6 years of experience in Biochemistry, Analytical Chemistry, or a related field.</li>
<li>Hands-on experience with ELISA-based impurity assays, including HCP, residual Protein A, and residual DNA detection.</li>
<li>Strong understanding of ligand-binding assay principles, including antibody-antigen interactions, signal detection, and assay robustness.</li>
<li>Experience troubleshooting plate-based assays and resolving reagent variability issues.</li>
<li>Knowledge of ICH/FDA regulatory guidelines for impurity testing in biologics.</li>
</ul>
Preferred Skills:
<ul>
<li>Familiarity with SoftMax Pro, JMP, or other data analysis tools.</li>
<li>Experience with custom antibody development for ELISA assays.</li>
<li>Knowledge of critical reagent lifecycle management for impurity assays.</li>
<li>Experience with method qualification and transfer in a GMP environment.</li>
</ul>
This role offers an exciting opportunity to work on business-critical impurity assays in a highly collaborative, cross-functional environment supporting late-stage and commercial biologics programs.
 Additional Information 
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;Lexington, 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.

ELISA Method Development Scientist

<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 DescriptionMaterials Scientist - Aerospace - Technical Ceramics- Relocation available! This Jobot Job is hosted by: Matt Swaneveld Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $150,000 per year 
A bit about us:
 We are a leader in manufacturing advanced materials and are known for our custom designed technical solutions. Due to growth, we are looking for a Materials Scientist to assist in our well structured engineering department. As a Materials Scientist, you will be responsible for developing and testing new materials, analyzing and improving existing materials, and ensuring that all materials meet our high standards of quality and performance. This is a challenging and exciting role that requires a deep understanding of ceramics, materials, raw material testing, and scientific principles. If you have a background in technical ceramics and are looking to take the next step in your career, please read on! 
Why join us?
 
<ul>
<li> We are an industry leader with an assortment of versatile advanced material products</li>
<li> Stable company with well over 50+ years behind us</li>
<li> Great starting salary </li>
<li> Comprehensive benefits package including health/dental/wellness/and more</li>
<li> 401K+ employee match </li>
<li> Relocation assistance package if needed</li>
</ul>
 
Job Details
 Qualifications: 
<ul>
<li> Bachelor's degree in Materials Science, Ceramics, or a related field (Master's / PhD preferred) </li>
<li> Industry experience with Aerospace/Defense/ITAR/Medical</li>
<li> 9+ years of experience in ceramics, materials, or a related field</li>
<li> Potential to obtain a government security clearance</li>
<li> Strong knowledge of scientific principles and research methods</li>
<li> Experience with raw material testing and analysis</li>
<li> Excellent problem-solving skills and attention to detail</li>
<li> Strong communication and collaboration skills</li>
<li> Ability to work independently and as part of a team</li>
<li> Experience with advanced scientific equipment and techniques</li>
<li> Ability to write technical reports and present findings to management and other stakeholders</li>
</ul>
 Responsibilities: 
<ul>
<li> Conduct research and development activities to create new materials that meet our specific needs and requirements</li>
<li> Analyze and improve existing materials to enhance their performance, durability, and reliability</li>
<li> Perform raw material testing to ensure that all materials meet our quality standards</li>
<li> Collaborate with other scientists and engineers to develop new products and improve existing ones</li>
<li> Use advanced scientific equipment and techniques to analyze and test materials</li>
<li> Keep up-to-date with the latest developments in materials science and technology</li>
<li> Write technical reports and present findings to management and other stakeholders</li>
</ul>
 If you are a skilled and experienced Materials Scientist with a passion for innovation and a commitment to quality, we want to hear from you. This is an exciting and rewarding opportunity to work in a dynamic and fast-paced environment, where you will have the opportunity to make a real impact on the manufacturing industry. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Senior Materials Scientist

<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 is seeking an experienced and highly motivated in vivo electrophysiologist to join our Circuit Biology team within Discovery Psychiatry. This pivotal role involves&nbsp;facilitating electrophysiological insights of circuit dysfunction in psychiatric disorders and treatment. This is an excellent opportunity to work at the forefront of psychiatry drug discovery research, contributing to target validation and compound profiling studies within a dynamic and collaborative team.
Responsibilities
<ul>
<li>Independently conceive, execute, and communicate original technical ideas and novel multi-disciplinary research that achieves project and area goals</li>
<li>Drive internal in vivo electrophysiology efforts by developing and optimizing recording strategies from disease-relevant circuits</li>
<li>Develop and maintain in vivo electrophysiology technology, methodology, and utility in psychiatric drug discovery</li>
<li>Generate, through lab-based activities, multi-unit electrophysiology, local field potential and/or EEG data to support projects</li>
<li>Ensure alignment of electrophysiology efforts with the broader goals of cross-functional teams</li>
<li>Present findings to internal teams and external collaborators or conferences</li>
<li>Contribute to strategic decision-making in psychiatry drug discovery</li>
<li>Provide scientific guidance and training to junior scientists and research associates</li>
<li>Serve as a lead scientist on projects and contribute scientific insights across multiple other project teams</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in neuroscience, or related field, with typically 12+ (BS), 10+ (MS), or 4+ (PhD) years of experience</li>
<li>Extensive experience in unanesthetized, in vivo multi-unit electrophysiology</li>
<li>Extensive experience using large-scale neural recording with single cell resolution with strong analytical skills</li>
<li>Experience with local field potentials and EEG recordings and analyses</li>
<li>Demonstrated expertise in the design and execution of hypothesis-driven studies related to synaptic and circuit function</li>
<li>Ability to process and interpret large datasets using appropriate software tools</li>
<li>Strong ability to work in cross-functional teams and effectively communicate scientific findings</li>
</ul>
Desired Qualifications
<ul>
<li>Previous industry experience within early discovery, preferably within psychiatry research</li>
<li>Expertise in AI/ML methodology for signal analysis</li>
<li>Recognized and sought out as an expert in field or discipline</li>
<li>Track record of impactful publications&nbsp;</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>

Senior Scientist II, In Vivo Electrophysiology

<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 is seeking an experienced and highly motivated electrophysiologist to join our Circuit Biology team within Discovery Psychiatry. This pivotal role involves&nbsp;facilitating in vitro and ex vivo electrophysiological insights of circuit biology to drive our understanding of synaptic and circuit dysfunction in psychiatric disorders and treatment. This is an excellent opportunity to work at the forefront of psychiatry drug discovery research, contributing to target validation and compound profiling studies within a dynamic and collaborative team.
Key Responsibilities
<ul>
<li>Independently conceive, execute, and communicate original technical ideas and novel multi-disciplinary research that achieves project and area goals</li>
<li>Drive internal electrophysiology efforts by developing and optimizing disease-relevant in vitro and&nbsp;ex-vivo experiments to investigate synaptic and circuit function</li>
<li>Develop and maintain slice electrophysiology technology, methodology, and utility in psychiatric drug discovery</li>
<li>Generate, through lab-based activities, slice electrophysiology data to support projects</li>
<li>Ensure alignment of electrophysiology efforts with the broader goals of cross-functional teams</li>
<li>Present findings to internal teams and external collaborators or conferences</li>
<li>Contribute to strategic decision-making in psychiatry drug discovery</li>
<li>Provide scientific guidance and training to junior scientists and research associates</li>
<li>Serve as a lead scientist on projects and contribute scientific insights across multiple other project teams</li>
</ul>
Qualifications 
<ul>
<li>PhD, MS, or BS in neuroscience, or related field, with typically 4+ (PhD), 10+ (MS) or 12+ (BS) years of experience</li>
<li>Extensive experience in whole-cell patch-clamp electrophysiology in acute brain slices, in vitro and ex vivo slice electrophysiology</li>
<li>Extensive experience using slice electrophysiology to study intact circuitry from striatal, cortical and hippocampal networks</li>
<li>Demonstrated expertise in the design and execution of hypothesis-driven studies related to synaptic and circuit function</li>
<li>Ability to process and interpret large datasets using appropriate software tools</li>
<li>Strong ability to work in cross-functional teams and effectively communicate scientific findings</li>
</ul>
Desired Qualifications
<ul>
<li>Previous industry experience within early discovery, preferably within psychiatry research</li>
<li>Expertise in ion channel drug discovery</li>
<li>Recognized and sought out as an expert in field or discipline</li>
<li>Track record of impactful publications&nbsp;</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>

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