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<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 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 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>.

Geotechnical Project Manager

<h3>Job Description</h3>
Job DescriptionJob Title: Biologist Location: Boston, MA 02210 Duration: 12 Months+ Shift: Standard shift Pay range: $38 - $41/ hr. on W2 Job Description:
<ul>
<li>Perform cell-based and molecular biology assays, including cell viability, ELISA, immunofluorescence, flow cytometry, and functional assays. </li>
<li>Make observations, evaluate data, interpret results, and maintain good written records of laboratory procedures, results, and conclusions.</li>
<li>Comply with standard laboratory practices and company policies.</li>
</ul>
 Qualification/ Requirements:
<ul>
<li>B.S in biology, molecular biology, biotechnology, or related field</li>
<li>Basic laboratory skills and aseptic technique.</li>
<li>Prior experience with tissue culture and cell-based and molecular biology assays. Experience with ELISAs, immunofluorescence, and cry sectioning is a plus. </li>
<li>Outstanding interpersonal skills and established collaborative working habits.</li>
<li>Excellent oral and written communication skills.</li>
</ul>
 #sczr2

Biologist

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Identifies and validates molecular targets that play a key role in a particular disease process.
</li>
<li>
Studies origin, relationship, development, anatomy, functions, and chemical processes of living organisms.
</li>
<li>
Analyzes materials to determine their toxic or nontoxic properties, binding and efficacy. Isolates or purifies analyses, and identifies hormones,minerals, proteins, and/or cultures of microorganisms to determine their biological properties.
</li>
<li>
Examines and conducts research on chemical aspects chemistry of cells andcell division.
</li>
<li>
May identify and produce small quantities of new drugs, pharmaceutical compounds and/or nutrients.
</li>
<li>
May develop an assay which employs in-vitro and/or in-vivo biological and immunological systems.
</li>
<li>
May experiment with animals and tissue to determine the effect of new drug compound entities utilizing in-vivo, in-vitro and ex-vivomodels on cells, tissues and whole animal systems.
</li>
<li>
Performs experiments and procedures demonstrating proficiency with a broad range of scientific or technology techniques; executes high-quality experiments and delivers and interprets data with colleagues and/or project teams.
</li>
<li>
Executes experiments and procedures requiring specific scientific or technical knowledge and laboratory techniques; delivers high-quality data to impact drug discovery, technology, and/or early development projects.
</li>
<li>
Generates hypotheses to test, troubleshoots issues and designs and executes the next set of experiments with some input from senior lab members/manager.
</li>
<li>
Approaches work with urgency, manages basic research activities in parallel.
</li>
<li>
Provides basic data analysis to interpret own experiments - assesses whether experimental hypothesis was appropriately tested and answered.
</li>
<li>
Works collaboratively across teams and trains other members of team in areas of technical expertise as needed.
</li>
<li>
Participates constructively in working teams and at lab meetings.
</li>
<li>
Steps in to support general lab responsibilities.
</li>
<li>
Generates hypotheses, independently executes experiments, and uses results to assist in the design of the next experiment.
</li>
<li>
Recognizes problems and provides input on solutions; suggests new approaches to established procedures to progress key drug discovery, technology, and/or early development projects.
</li>
<li>
Works collaboratively across lab with all members.
</li>
<li>
Expected to be an excellent lab citizen.
</li>
<li>
Uses understanding of experimental hypothesis and works with manager and colleagues to troubleshoot issues and help design and execute next experiment.
</li>
<li>
Experimental results support progression of drug discovery, technology, and/or early development projects.
</li>
<li>
Distribution of marketing samples (where applicable)
</li>
</ul>
Work Experience:
<ul>
<li>
PhD is required
</li>
<li>
Requires an understanding of one or more of the following: molecular biology, biochemistry, microbiology, cell biology, biophysics, virology and/or immunology.
</li>
<li>
The successful candidate will be proficient:
<ul>
<li>
expressing and purifying recombinant proteins from bacteria, insect and mammalian cells,
</li>
<li>
the ability to characterize small molecule and protein-protein interactions using biophysical techniques including SPR, DSF, SEC-MALLS, analytical ultracentrifugation and ITC and
</li>
<li>
previous experience solving protein structures using x-ray crystallography and cryoEM microscopy.
</li>
</ul>
</li>
<li>
Functional Breadth.
</li>
<li>
Collaborating across boundaries.
</li>
<li>
Skills:
</li>
<li>
Algorithms.
</li>
<li>
Analytical Skill.
</li>
<li>
Analytical Thinking.
</li>
<li>
Chemical Biology.
</li>
<li>
Clinical Research.
</li>
<li>
Clinical Trials.
</li>
<li>
Collaboration.
</li>
<li>
Communication Skills.
</li>
<li>
Curiosity.
</li>
<li>
Data.
</li>
<li>
Data Analysis.
</li>
<li>
Design Of Experiments.
</li>
<li>
Detail Oriented.
</li>
<li>
Diversity &amp; Inclusion.
</li>
<li>
Drug Discovery.
</li>
<li>
Ethics.
</li>
<li>
Hypothesis Testing.
</li>
<li>
Immunology.
</li>
<li>
Laboratory.
</li>
<li>
Lifesciences.
</li>
<li>
Mammalian Cell Culture.
</li>
<li>
Medical Research.
</li>
<li>
Molecular Biology.
</li>
<li>
Organization.
</li>
<li>
Problem Solving Skills.
</li>
<li>
Project Teams.
</li>
<li>
Reports Writing.
</li>
<li>
Research.
</li>
<li>
Science.
</li>
<li>
SOP (Standard Operating Procedure).
</li>
<li>
Time Management Skills.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Research Associate

<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.

Senior Materials Scientist

<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.

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