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<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins 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 
<ul>
<li>Perform routine testing of pharmaceutical samples by following analytical compendial methods (pH, appearance, osmolality, concentration, break-loose extrusion force testing, etc.)</li>
<li>Prepare standards and samples for analysis</li>
<li>Monitoring and replenishing lab reagents and solutions</li>
<li>Maintain, calibrate, and operate instrumentation in the QC laboratory</li>
<li>Document work as required for GMP compliance</li>
<li>Execute work in accordance with standard operating procedures, with attention to detail, and with strong organizational skills</li>
<li>Interact effectively with peers and leaders as part of a multi-disciplinary team</li>
<li>Experience operating an HPLC utilizing Empower software and Capillary Gel Electrophoresis (CGE) are both a plus</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry or other science related degree concentration</li>
<li>0-2 years of QC analytical experience</li>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite to Meet the Team</li>
</ul>
Additional Details:&nbsp;
The position is permanent, on-site and full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Andover, MA, and the surrounding areas are encouraged to apply.&nbsp;
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</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.

QC Analytical Chemist

<h3>Job Description</h3>
Job Description
Summary: The Quality Control (QC) Chemist is responsible for performing complex chemical and physical analyses of raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements. This role involves method development and validation, data analysis, troubleshooting, and collaboration with cross-functional teams to support manufacturing processes.
 Essential Duties and Responsibilities include the following. Other duties may be assigned.
<ul>
<li>Analytical Testing:
<ul>
<li>Perform complex chemical and physical analyses using advanced laboratory techniques and instrumentation.</li>
<li>Develop, validate, and implement new analytical methods as needed.</li>
</ul>
</li>
<li>Data Analysis and Reporting:
<ul>
<li>Interpret analytical data to assess product quality and identify trends or anomalies.</li>
<li>Prepare detailed reports and documentation in compliance with regulatory standards.</li>
</ul>
</li>
<li>Method Development and Validation:
<ul>
<li>Develop and validate analytical methods to support new product development and process improvements.</li>
<li>Ensure methods are robust, reproducible, and compliant with industry standards.</li>
</ul>
</li>
<li>Troubleshooting and Problem-Solving:
<ul>
<li>Investigate and resolve analytical issues, non-conformances, and out-of-specification results.</li>
<li>Collaborate with production and quality teams to implement corrective actions.</li>
</ul>
</li>
<li>Compliance and Documentation:
<ul>
<li>Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory requirements.</li>
<li>Maintain accurate and complete records of all analyses, calibrations, and maintenance activities.</li>
</ul>
</li>
</ul>
Location:
Must be commutable within 25 miles of Derry, NH. Local applicants considered only.
Education/Experience:
Bachelor's degree from four-year college or university, preferably in Microbiology, Chemistry, Biology or a related field. Experience with microbiology is preferred. Four plus years of laboratory experience, including internships or academic lab work; or equivalent combination of education and experience is a plus. Basic understanding of chemical analysis techniques and laboratory equipment is also preferred.
Language Ability:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
Qualifications:
<ul>
<li>Proficiency in advanced analytical techniques and instrumentation (e.g., HPLC, GC, FTIR, UV-Vis).</li>
<li>Strong problem-solving and troubleshooting abilities.</li>
<li>Excellent attention to detail and organizational skills.</li>
<li>Effective communication and interpersonal skills.</li>
<li>Ability to work independently and as part of a team</li>
</ul>

Senior Chemist - Quality Control

<h3>Job Description</h3>
Job Description
Company Overview 
1910 Genetics is a Series A stage biotechnology company that is pioneering a novel Input-Transform-Output (ITO™) platform as the first ever horizontal AI infrastructure for drug discovery. 
In a crowded space with hundreds of AI drug discovery companies, 1910's ITO™ platform is differentiated by: 
<ul>
<li>Modality agnostic drug discovery: our platform is capable of designing both small molecule and large molecule therapeutics across all disease areas, with an initial focus on neuroscience, oncology, and autoimmune diseases.</li>
<li>Proprietary massive multimodal data, which overcomes the data scarcity problem that prevents frontier AI models from being utilized for drug discovery.</li>
<li>Multi-AI agent systems that include a robust collection of frontier AI/ML models, each of which works in a task-oriented manner to achieve the multi-parameter optimization problem of drug discovery and development.</li>
<li>A state-of-the-art (SOTA) fully-automated, high throughput wet laboratory in the premier Boston Seaport District for both data generation for AI model training as well as validation of the safety and efficacy of drug candidates that are outputted by our frontier AI models.</li>
<li>An unprecedented partnership with Microsoft, which positions 1910 as the only biotech/pharma company leveraging Azure Quantum Elements, a groundbreaking, AI-driven, high performance computing (HPC) cloud architecture for advanced AI.</li>
<li>Bespoke conversational AI chatbots that provide a customer friendly UI/UX to access our platform for specific drug discovery tasks.</li>
<li>Being the only biotech company helping pharma companies integrate 6 core areas of AI infrastructure.</li>
</ul>
1910 Genetics is looking for an In Vitro Pharmacology Assay Scientist to design, develop and execute assays to measure the activity of small molecules on specific biological targets, such as proteins or cells. This position requires a strong background in molecular biology and biochemistry, along with experience in laboratory techniques and data analysis. The ideal candidate will have experience in small molecule discovery and characterization. 
Role Responsibilities 
<ul>
<li>Design, develop and execute in vitro biological assays to measure the activity of small molecules on specific biological targets, such as proteins or cells </li>
</ul>
<ul>
<li>Adapt and validate assays to apply laboratory automation to test libraries of small molecules quickly, reliably and efficiently </li>
</ul>
<ul>
<li>Perform data analysis and interpretation of assay results to identify promising molecules for further development </li>
</ul>
<ul>
<li>Collaborate with cross-disciplinary scientists to refine assays to deliver program objectives </li>
</ul>
<ul>
<li>Maintain detailed records of experimental procedures and results in electronic lab notebook </li>
</ul>
<ul>
<li>Present experimental results/progress in timely manner and contribute to scientific discussion in group meetings </li>
</ul>
<ul>
<li>Collaborate with cross-functional teams, including AI Research and Computational Chemistry to discuss project updates as well as ensure the project milestones and timelines are met </li>
</ul>
<ul>
<li>Assist laboratory operations, including maintenance of equipment, reagent tracking and monthly inspections for safety equipment </li>
</ul>
<ul>
<li>Develop and execute standard operating procedures and best practices to enhance lab efficiency and productivity </li>
</ul>
<ul>
<li>Contribute to the preparation of scientific reports, presentations, and publications. </li>
</ul>
<ul>
<li>Stay current with scientific literature and emerging technologies in the fields of large and small molecule research </li>
</ul>
Qualifications 
<ul>
<li>PhD in Biology with a focus on Molecular Biology, Biochemistry, Cell Biology, In Vitro Pharmacology, Biomedical Sciences or a related field </li>
</ul>
<ul>
<li>Postdoctoral experience or relevant industry experience in drug discovery or In Vitro Pharmacology </li>
</ul>
<ul>
<li>Strong understanding of molecular biology, biochemical, and cell-based assays and their applications in drug development </li>
</ul>
<ul>
<li>Familiarity with signal transduction pathways in relevant therapeutic areas such as Immunology &amp; Inflammation, neuroscience, oncology, and cardiometabolic diseases </li>
</ul>
<ul>
<li>Experience in immune cell isolation and cell-line engineering and assay development </li>
</ul>
<ul>
<li>Excellent problem-solving, critical thinking, and data analysis skills </li>
</ul>
<ul>
<li>Ability to work independently and as part of a collaborative team in a fast-paced and dynamic research environment </li>
</ul>
<ul>
<li>Strong track record of research accomplishments, as evidenced by publications in scientific journals </li>
</ul>
#LI-Onsite
Diversity and Inclusion (1910's Promise) 
At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. 
Benefits and Perks 
<ul>
<li>Competitive compensation package </li>
<li>Above market benefits </li>
<li>Generous vacation and parental leave </li>
<li>Super cool team building activities </li>
<li>Great colleagues </li>
</ul>

Scientist I, Small Molecule Assay Development (Biochemistry / Cell Biology)

<h3>Job Description</h3>
Job Description
Company Overview 
1910 Genetics is a Series A stage biotechnology company that is pioneering a novel Input-Transform-Output (ITO™) platform as the first ever horizontal AI infrastructure for drug discovery. 
In a crowded space with hundreds of AI drug discovery companies, 1910's ITO™ platform is differentiated by: 
<ul>
<li>Modality agnostic drug discovery: our platform is capable of designing both small molecule and large molecule therapeutics across all disease areas, with an initial focus on neuroscience, oncology, and autoimmune diseases.</li>
<li>Proprietary massive multimodal data, which overcomes the data scarcity problem that prevents frontier AI models from being utilized for drug discovery.</li>
<li>Multi-AI agent systems that include a robust collection of frontier AI/ML models, each of which works in a task-oriented manner to achieve the multi-parameter optimization problem of drug discovery and development.</li>
<li>A state-of-the-art (SOTA) fully-automated, high throughput wet laboratory in the premier Boston Seaport District for both data generation for AI model training as well as validation of the safety and efficacy of drug candidates that are outputted by our frontier AI models.</li>
<li>An unprecedented partnership with Microsoft, which positions 1910 as the only biotech/pharma company leveraging Azure Quantum Elements, a groundbreaking, AI-driven, high performance computing (HPC) cloud architecture for advanced AI.</li>
<li>Bespoke conversational AI chatbots that provide a customer friendly UI/UX to access our platform for specific drug discovery tasks.</li>
<li>Being the only biotech company helping pharma companies integrate 6 core areas of AI infrastructure.</li>
</ul>
1910 Genetics is looking for an In Vitro Pharmacology Assay Scientist to work closely with our biologists in the discovery of antibodies. An expert in biochemical characterization of biological drug molecules, the ideal candidate will have experience in antibody drug discovery and characterization of a variety of molecular types. 
Role Responsibilities 
<ul>
<li>Validate target material in functional biochemical assays prior to the start of antibody discovery. </li>
</ul>
<ul>
<li>Design, validate and execute in vitro biochemical assays for the screening of molecules from 1910 Genetics' AI-driven large molecule therapeutics platform </li>
</ul>
<ul>
<li>Develop, validate and execute assays for the biophysical characterization of antibodies in various formats and for various modalities </li>
</ul>
<ul>
<li>Work closely with 1910 scientists to refine assays to help drive delivery of program objectives </li>
</ul>
<ul>
<li>Maintain detailed records of experimental procedures and results in electronic lab notebook </li>
</ul>
<ul>
<li>Present experimental results/progress in a timely manner and contribute to scientific discussion in group meetings </li>
</ul>
<ul>
<li>Collaborate with cross-functional teams, including AI Research and Computational Chemistry to discuss project updates as well as ensure the project milestones and timelines are met </li>
</ul>
<ul>
<li>Assist laboratory operations, including maintenance of equipment, reagent tracking and monthly inspections for safety equipment </li>
</ul>
<ul>
<li>Develop and execute standard operating procedures and best practices to enhance lab efficiency and productivity </li>
</ul>
<ul>
<li>Contribute to the preparation of scientific reports, presentations, and publications. </li>
</ul>
<ul>
<li>Provide intellectual input into small molecule projects when required </li>
</ul>
<ul>
<li>Stay current with scientific literature and emerging technologies in the fields of large and small molecule research </li>
</ul>
Qualifications
<ul>
<li>PhD in Biology with a focus on Biochemistry, Cell Biology, In Vitro Pharmacology, Biomedical Sciences or a related field </li>
</ul>
<ul>
<li>Postdoctoral experience or relevant industry experience in drug discovery or In Vitro Pharmacology </li>
</ul>
<ul>
<li>Experience in developing, validating and implementing biology, biochemical, and cell-based assays </li>
</ul>
<ul>
<li>Familiarity with signal transduction pathways in relevant therapeutic areas such as Immunology &amp; Inflammation, neuroscience, oncology, and cardiomedabolic diseases </li>
</ul>
<ul>
<li>Experience with immune cell isolation and assay development </li>
</ul>
<ul>
<li>Experience using analytical techniques/instrumentation for characterization and quantification of large molecules, including chromatographic techniques such as HIC (Hydrophobic Interaction Chromatography) and RP (Reverse Phase), SEC (Size Exclusion Chromatography), SDS-PAGE, UV-Vis, etc. </li>
</ul>
<ul>
<li>Familiarity with conjugation, purification and characterization of antibody drug conjugates </li>
</ul>
<ul>
<li>Excellent problem-solving, critical thinking, and data analysis skills </li>
</ul>
<ul>
<li>Ability to work independently and as part of a collaborative team in a fast-paced and dynamic research environment </li>
</ul>
<ul>
<li>Strong track record of research accomplishments, as evidenced by publications in scientific journals </li>
</ul>
#LI-Onsite
Diversity and Inclusion (1910's Promise) 
At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. 
Benefits and Perks 
<ul>
<li>Competitive compensation package </li>
<li>Above market benefits </li>
<li>Generous vacation and parental leave </li>
<li>Super cool team building activities </li>
<li>Great colleagues </li>
</ul>

Scientist I, Assay Development for Small Molecule & Antibody Discovery (Biochemistry / Cell Biology)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, a place to call home, apply with us today
Job Description 
<ul>
<li>Meticulously prepare complex media at various scales to support cell culture for various iPSC differentiation workflows, ensuring timely and accurate execution of requested formulations.</li>
<li>Read, review, and execute SOPs for preparation of reagents, stock solutions, and media handling and formulation.</li>
<li>Track expiry of corresponding stock solutions and complete complex media.</li>
<li>Maintain an updated media inventory database for forecasting, tracking raw material use &amp; stock, lot usage, and overall material performance.</li>
<li>Maintain accurate and meticulous record keeping with internal ELN system, independent data analysis, and reporting of data in written and oral formats.</li>
<li>Perform work in full compliance with safety policies and technical protocols and complete all required training activities in the timeframe specified.</li>
<li>Perform complex algebraic mathematical calculations with high accuracy to determine critical parameters such as molarity, molality, and percentages.</li>
<li>Precisely calculate volumes of solution components based on intricate mathematical formulas, ensuring exact proportions for experimental and manufacturing processes.</li>
<li>Troubleshoot media preparation challenges and deviations when necessary.</li>
<li>Collaborate with process development scientists to support high throughput optimization of media formulations for scale-up, reproducibility, and cost-efficiency.</li>
<li>Operate automation platforms (e.g., liquid handlers, automated dispensers, robotic mixing systems) to support streamlined media preparation, increasing throughput, reproducibility, and data traceability.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>B.S. and/or M.S. in biological or biochemical sciences (or a related field). B.S., 1-2 years of experience or M.S., less than 1 year of experience.</li>
<li>Demonstrated proficiency in aseptic technique and reagent, stock solution, and complex cell culture media preparations.</li>
<li>Advanced skills in algebraic calculations: molarity, percentages, solution component volumes.</li>
<li>Unwavering commitment to safety protocols and procedures</li>
<li>Proven capacity to ensure work product quality and understand the impact on downstream processes.</li>
<li>Work within a team-oriented lab environment and work within cross-functional project teams.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Exposure to automated systems (e.g., liquid handlers, automated dispensers, robotic mixing systems).</li>
<li>Track record of working in or supporting high-throughput or high-volume laboratory environments. &nbsp;</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</li>
</ul>
Additional Details:&nbsp;
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (once every 1-2 months) to support cell culture.Candidates currently living within a commutable distance of Boston, MA 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 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.

Associate Media Preparation 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 
The Molecular Profiling and Drug Delivery (MPDD) function within the Small Molecule CMC organization is accountable for a broad range of deliverables across various stages of drug discovery and development. During virtual screening/lead generation/optimization and through candidate selection, MPDD scientists utilize state of the art automation and computational tools supported by expertise in biopharmaceutics, drug delivery, and solid-state chemistry to collaboratively&nbsp;design and progress candidates with higher probability of success into&nbsp;development and advise clinical formulation strategy. From candidate selection through clinical proof of concept and product launch, MPDD scientists&nbsp;work in cross functional teams to identify the commercial solid form of the active pharmaceutical ingredient (API) and establish structure-property-performance correlations to help deliver robust commercial processes and align control strategies across drug substance and product. They also transition drug substance isolation processes and relevant physical characterization methods to commercial manufacturing sites and work within teams to ensure successful regulatory submissions.
Computational chemists within AbbVie's MPPD organization work collaboratively&nbsp;with other functions within Development Sciences and Discovery Sciences across two focus areas: Molecular design and profiling, and formulation design across modalities, including small molecules, peptides, and large molecules, towards the design and progression of compounds and formulations with optimal developability properties, towards the overall vision of advancing first-in-class and best-in-class clinical candidates.&nbsp; Computational chemists focus on developing hierarchical modeling approaches, including physics-based atomistic modeling, encompassing Molecular Dynamics (MD) and Quantum Mechanics (QM), Machine learning (ML)/Artificial Intelligence (AI) and hybrid models based on Physics-ML/AI approaches. Computational chemists also collaborate seamlessly with medicinal chemists, data scientists, material scientists, and molecular modelers to incorporate these models in project screening funnels and medicinal chemistry design cycle.&nbsp;
Job Description
AbbVie's MPDD organization is seeking a highly motivated, talented, and creative scientist with experience and expertise in computational chemistry for a Senior Scientist position. This person will make key contributions towards enablement of our modeling vision. Specifically, the person will be working collaboratively with discovery colleagues to develop stage-appropriate computational models using advanced computational techniques to enable design and optimization of oral and developable macrocyclic peptides. &nbsp;The ideal candidate should possess an advanced degree in computational chemistry with a strong background in the area such as quantum mechanics, atomistic molecular simulations (molecular dynamics) and AI/machine learning.
Responsibilities 
<ul>
<li>In collaboration with Discovery Research and Development Sciences project teams, utilize advanced computational tools towards the design, optimization, and profiling of macrocyclic peptides, large and small molecule drug candidates</li>
<li>Advance our peptide and large molecule computational chemistry capabilities through innovation and implementation of new methodologies and workflows towards capturing key developability properties such as permeability, stability, and solubility. Examples include, but are not limited to, utilization of molecular simulations/QM approaches, coupled with AI/ML approaches, to predict dynamic molecular conformations and stability from macrocyclization and residue modifications, towards their impact on Absorption, Distribution, Metabolism, and Excretion (ADME) properties and Chemistry, Manufacturing and Controls (CMC) properties.</li>
<li>Serve as a lead computational scientist on project teams and drive the development and implementation of appropriate computational models within projects to support various aspects of drug discovery and drug development.</li>
<li>Generate hypotheses for compound property improvement and apply them to new compound design</li>
<li>Contribute to the development of computational infrastructure by identification of novel tools and techniques</li>
<li>Play a strong team player in a cross functional collaborative environment</li>
<li>Demonstrate excellent communication skills and specifically
<ul>
<li>Illustrate strong oral and written technical communications</li>
<li>Promote design-driven and predict-first culture</li>
<li>Educate and train colleagues on various computational tools and techniques</li>
</ul>
</li>
</ul>
Qualifications 
<ul>
<li>Bachelors, Masters, or PhD with 8+ (BS), 5+ (MS), and 0-3 (PhD) years of experience in computational chemistry, computer science, biophysics, chemical engineering, or related field</li>
<li>Knowledge in one or more areas of the computational chemistry discipline, such as quantum mechanics, molecular dynamics, structure-based design, ligand-based design, structure property relationship modeling, physicochemical property prediction</li>
<li>Advanced user of QM or MD software packages.&nbsp; This may include open-source codes (GROMACS, OpenMM, LAMMPS) or commercial software (Schrodinger, OpenEye, MOE, etc).</li>
<li>Ability to build and integrate computational models through combining different workflows while also modifying or improving workflow source codes as needed.</li>
<li>Familiarity with machine learning or neural network packages including but not limited to Scikit-learn, Pytorch,</li>
<li>Well versed in writing codes in Python, R, C/C++ etc.</li>
</ul>
Key Competencies
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance.</li>
<li>Learns fast, grasps the "essence" and can change course quickly where indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Copy of Senior Scientist I Computational Chemistry

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are seeking a highly motivated Senior Scientist I to join our Analytical Development team in the Product Development Science and Technology, Biologics Development Launch division. Our team is responsible for the development, qualification, and execution of analytical methods to provide product and process understanding for biological entities from discovery through commercial stages.
The successful candidate will be a part of the Biomolecular Interaction Group which is mainly focused on method development and implementation of various immunoassays to monitor process impurities and to assess potency of AbbVie’s Biologics to support product and process development for early-phase, late-phase, and commercial programs.&nbsp; Some of the techniques/methods utilized in the group include 1) ELISAs to monitor and detect process related impurities; 2) surface plasmon resonance using Biacore for assessment of antigen binding and binding of antibody Fc receptors; and 3) qPCR to measure levels of residual DNA and mycoplasma. The role will &nbsp;involves managing all analytical aspects of biologics products on the market, overseeing commercial methods throughout their lifecycle - from method transfer, performance monitoring, troubleshooting, to method enhancement. The individual will also play a key role in establishing commercial product specifications, stability programs, and regulatory filings. Collaboration with other analytical teams, process development, global QC, and manufacturing science and technology groups is a crucial part of this role to meet business objectives and program milestones.
Responsibilities:
<ul>
<li>Partner with Analytical Development groups to achieve commercial method readiness using traditional and advanced analytical techniques, including but not limited to ELISA, bioassays, spectrophotometric and compendial methods.</li>
<li>Participate in cross-functional, multi-site, global meetings / projects and oversee commercial analytical method transfer between sites, product/process investigations, method performance monitoring and troubleshooting.</li>
<li>Establish scientifically sound, analytical lifecycle strategies, including methods, stability, specification and change management that meet Health Authority best practices and expectations.</li>
<li>Participate in the preparation and review of technical documents to ensure global compliance - including validation protocols and reports, reference standard qualification reports and analytical test procedures.</li>
<li>Author regulatory submissions, support regulatory inspections and provide scientifically sound responses to agency deficiency letters.</li>
<li>Conduct periodic review of methods and work with program leads to design, execute remediation experiments, and implement changes to new or existing commercial methods when necessary.</li>
</ul>
Qualifications 
<ul>
<li>BS or equivalent education in Biology, Biochemistry, Engineering or related discipline and 8+ years of experience in the biopharmaceutical industry; MS and 6+ years experience; PhD and 3+ years experience.</li>
<li>Industry experience in method development, qualification, validation, and method transfer in support of development and/or commercialization of biological products. &nbsp;</li>
<li>Methods including but not limited to ELISA, western blot, qPCR, ddPCR, SPR and automation</li>
<li>Ability to lead and manage projects/teams of significant scope and complexity, while meeting all deliverables and timelines.</li>
<li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</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- Analytical Development ( On-site-Worcester, MA)

<h3>Job Description</h3>
Job DescriptionSalary: $1,615 - $1,793/week based on experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Boylston, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

Project Geotechnical Engineer - Boylston

<h3>Job Description</h3>
Job Description
Job Title: Chemist II – Stability Testing (Quality Control) Job Location: Fall River, MA (On-site) Schedule: 8:00 AM – 5:00 PM (May vary based on business needs) Classification: Full-Time, Exempt Relocation Assistance: Up to $6,000 available Work Authorization: US Citizen, Green Card, H1B Transfer, TN Visa, OPT-EAD
About the Role:
We are seeking a QC Chemist II – Stability Testing to join our Quality Control Department. The selected candidate will be responsible for performing and overseeing stability testing for pharmaceutical formulations under various environmental conditions, ensuring data integrity, and compliance with cGMP guidelines.
Key Responsibilities:
<ul>
<li>
Conduct routine and advanced stability testing in a laboratory setting.
</li>
<li>
Operate and maintain instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers.
</li>
<li>
Perform raw material testing and release.
</li>
<li>
Lead investigations into out-of-specification (OOS) or deviations and document findings.
</li>
<li>
Ensure adherence to cGMP, Good Documentation Practices (GDP), and data integrity principles.
</li>
<li>
Prepare and review documentation, including lab notebooks and reports.
</li>
<li>
Participate in audits and ensure inspection readiness.
</li>
<li>
Collaborate with cross-functional teams, including QA and manufacturing.
</li>
<li>
Support training and mentoring of junior team members.
</li>
<li>
Execute additional duties as assigned by departmental leadership.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Bachelor’s degree (BS/BA) in Chemistry or a related physical science.
</li>
<li>
Minimum 3 years of experience in formulation stability testing in a pharmaceutical setting.
</li>
<li>
Working knowledge of analytical instruments including HPLC, GC, ICP, Karl Fischer, and particle size analyzers.
</li>
<li>
Familiarity with MDI (Metered Dose Inhaler) testing is a strong plus.
</li>
<li>
Experience with various dosage forms (liquid, solid, tablets, capsules) is desirable.
</li>
<li>
Strong command of English – spoken and written.
</li>
<li>
Proficiency with Microsoft Office and scientific software.
</li>
<li>
Excellent analytical, documentation, and communication skills.
</li>
<li>
Must be authorized to work in the United States and be available to work on-site full-time.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience working with inhalation products (MDIs).
</li>
<li>
Previous work in a fast-paced, regulated pharmaceutical QC lab environment.
</li>
<li>
Experience leading or contributing to laboratory investigations.
</li>
</ul>
Work Environment Physical Requirements:
<ul>
<li>
Work in a cGMP laboratory or manufacturing environment requiring the use of personal protective equipment (PPE).
</li>
<li>
Regular exposure to solvents, powders, and chemical substances.
</li>
<li>
Must be able to stand or walk for 75% or more of an 8-hour shift.
</li>
<li>
Must be able to lift up to 10 kg unassisted.
</li>
<li>
Must be able to sit and work at a computer for extended periods.
</li>
</ul>
Compensation Benefits:
<ul>
<li>
Competitive salary based on experience ($75K–$105K)
</li>
<li>
Bi-weekly pay
</li>
<li>
Paid Time Off (PTO)
</li>
<li>
Health Insurance (Medical, Dental, Vision) – starts on Day 1
</li>
<li>
Disability Insurance
</li>
<li>
Overtime and shift differential as applicable
</li>
<li>
401(k) with company match
</li>
<li>
Career advancement opportunities and ongoing training
</li>
<li>
Company-sponsored events
</li>
</ul>
Important Notes:
<ul>
<li>
Candidates must have prior pharmaceutical (not biopharma) experience.
</li>
<li>
Chemistry background is highly preferred.
</li>
<li>
Candidates should clearly indicate experience with formulations including MDI, liquid, solid, tablets, and capsules in their resume.
</li>
<li>
No Green Card sponsorship available; H1B transfers are acceptable.
</li>
</ul>

QC Chemist II

<h3>Job Description</h3>
Job DescriptionWe are looking for a skilled, resourceful, and collaborative Senior Geotechnical Project Manager to join our client's team in Burlington, Vermont. The Senior Geotechnical Project Manager will work closely with a team of staff engineers and scientists on challenging and exciting projects largely in urban environments. This is a fast-paced and dynamic position, with opportunities to be challenged, contribute to project outcomes, interact routinely with project Principals and clients, and is designed to support your professional growth. Essential Functions – What You Will DoTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Develop new business opportunities. Manage and grow client relationships. Prepare proposals and project budgets. Manage project budgets and prepare invoices. Manage and supervise staff engineers. Set technical strategy and oversee production of technical work products. Plan and coordinate field investigation programs. Interpret and analyze field and laboratory data. Coordinate and oversee construction administration for development projects. Manage preparation of reports, design plans, data tables, specifications, and other deliverables. Formulate conclusions, recommendations, and geotechnical strategies for development projects.Qualifications Minimum of ten years relevant experience and a BS in Civil Engineering (Geotechnical Focus) or seven years relevant experience and a MS in Civil Engineering (Geotechnical Focus). Possess Professional Engineering Licensure. Strong attention to detail and understanding of geotechnical engineering. Experience with geotechnical field work and construction earthwork. Strong organizational and time management skills combined with the flexibility to work with shifting priorities. Desire and affinity for networking and business development. Awareness and general understanding of environmental considerations (i.e., contaminated soil and groundwater management during construction). Client-service orientation with the ability to anticipate needs and deliver to meet expectations. Excellent verbal and written communication skills. Work well as a team member, with a collaborative communication style.If you meet these requirements and qualifications, please apply or reach out to <a href="mailto:mforde@aectac.com" target="_blank">mforde@aectac.com</a>.

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