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<h3>Job Description</h3>
Job DescriptionBoston Materials produces advanced materials with enhanced energy transfer properties using its patented Z-axis Carbon Fiber technology. The Company's products solve critical performance bottlenecks in applications spanning thermal, electrical, and structural use cases. Its breakthrough Liquid Metal ZRT thermal interface material is designed for the most demanding AI Infrastructure. Boston Materials is committed to expanding high-volume manufacturing in the United States. For more information, visit&nbsp;<a href="https://www.bomaterials.com/&amp;nbsp" target="_blank">https://www.bomaterials.com/&amp;nbsp</a>; ABOUT THE OPPORTUNITYNot often in one’s career do we get the chance to— Get close to the mission. Getting a real sense of what the business does and how our work directly affects the outcome. Where everyone is involved with the company’s success. No layers, no silos, no bureaucracy. Just the opportunity to make the greatest impact with the most responsibility.Move faster. Adapting to changes in the market at record speed. No multi-layer signoffs and approvals. Instead, the latitude needed to get a new idea, product, or process off the ground quickly. Where we can experiment and test new ideas— and are encouraged to do so. We create solutions to problems that our customers truly care about, and we understand that customers won’t wait for us to figure them out.Branch beyond the role. We’re not defined by past experiences or confined by our current job description. Every day offers opportunities to have influence and be challenged with new projects and tasks. Working shoulder-to-shoulder with some of the top talent in the industry, we’re able to showcase our talents, expand our knowledge, develop new skills, and take ownership and act. All while contributing to the overall success of the organization.Create critical solutions. Join us to solve the most critical challenges facing the Advanced Semiconductor, AI Infrastructure, and Advanced Materials industries.&nbsp;Opportunity knocks at Boston Materials. Will you answer the call? Solve one of the most critical challenges facing the Semiconductor and Electronics Industry – thermal management! Join the Boston Materials team to help unlock the full potential of Z-axis Fiber™ technology and pave the way for groundbreaking advancements powering AI. The Role We are seeking an experienced and motivated Senior Chemist to join our dynamic Liquid Metal Thermal Interface Materials Team. In this role, you will play a crucial part in the development of novel TIMs designed to enhance the performance and cooling efficiency of advanced electronics. Your expertise will contribute to the creation of state-of-the-art solutions that meet the demands of cutting-edge AI and datacenter technologies. Your Responsibilities
<ul>
<li>Lead and execute in R&amp;D programs focused on organic/inorganic interface engineering&nbsp; relating to TIM products.</li>
<li>Design and conduct experiments to explore novel organic and inorganic compounds for thermal management applications.</li>
<li>Collaborate with cross-functional teams to integrate thermal interface materials into electronic devices.</li>
<li>Analyze and interpret experimental data to optimize material properties and performance.</li>
<li>Develop and implement testing protocols to assess the reliability and efficiency of thermal interface materials.</li>
<li>Prepare technical reports, presentations, and documentation to communicate findings and progress.</li>
<li>Stay up-to-date with advancements in chemistry, materials science, and the electronics industry to drive innovation.</li>
</ul>
Your Skills and Expertise
<ul>
<li>Ph.D. or M.Sc. in Chemistry, Materials Science, or a related field.</li>
<li>Strong understanding of organic/inorganic interfacial engineering.</li>
<li>Experience with materials development for the electronics industry is highly preferred.</li>
<li>Proven track record in the research and development of thermal interface materials or related technologies.</li>
<li>Proficiency in designing and conducting experiments, data analysis, and material characterization.</li>
<li>Excellent problem-solving skills and the ability to work independently and collaboratively.</li>
<li>Strong communication skills, both written and verbal.</li>
<li>Passion for innovation and staying abreast of industry trends.</li>
</ul>
Summary of Benefits
<ul>
<li>Health, Vision &amp; Dental – Boston Materials pays 75% of Health, Vision and Dental Care coverage for employee and dependents</li>
<li>401(k) plan</li>
<li>4 weeks of supplemental Paid Parental and Family Leave</li>
<li>Unlimited Paid Time Off</li>
<li>Holidays: 14 days/year</li>
</ul>
Boston Materials is an EOE and at the forefront of materials innovation, the key to which is diverse teams with unique backgrounds and experiences. We are committed to employing a diverse workforce with equal employment opportunities regardless of race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, marital status, veteran status, or disability. Applicants must be currently authorized to work in the US on a full-time basis.

Senior Chemist, Interfacial Engineering

<h3>Job Description</h3>
Job DescriptionPsivant Therapeutics is seeking a computational medicinal chemist with expertise in drug discovery, molecular simulations and AI/ML to join our dynamic, multidisciplinary team. &nbsp;Our science, our team, and our mission are focused on applying advanced computational technologies to progress a pipeline of innovative medicines for patients.&nbsp; We are looking for a self-motivated individual who thrives in a fast-paced, highly collaborative environment that integrates computational and wet lab capabilities to drive our programs to the clinic. &nbsp;The ideal candidate will utilize advanced computational strategies across all stages of drug discovery, including hit identification, hit-to-lead and lead optimization. &nbsp;In addition, a successful candidate will have a demonstrable pharma/biotech industry record using computational methods to advance drug discovery projects, analyze simulation and AI/ML results, derive actionable hypotheses and effectively communicate findings to the team. &nbsp;This individual will report to the Senior Director of CADD and collaborate closely across functions including experimental medicinal chemistry, structural biology, and application engineering teams to provide actionable insights and strategic guidance.Key Responsibilities
<ul>
<li>Design small molecule (and related modality) therapeutics using structural/simulation/ML/assay data, ensuring alignment with the requirements and timelines of our drug discovery projects, and leading computational analysis and design activities on cross-functional projects.</li>
<li>Integrate knowledge of relevant computational tools and approaches, as well as key aspects of medicinal chemistry and compound property optimization, for all project stages from target selection and druggability analysis to clinical candidate nomination.</li>
<li>Collaborate with the computational development team to align priorities between platform application development and R&amp;D projects.</li>
<li>Develop modifications and drive improvements in internal applications, building on our internal physics-based simulation capabilities and assessment of fidelity and accuracy of calculations.</li>
<li>Train and mentor team members across the organization to build understanding of modeling and AI/ML concepts and how they address project team needs.</li>
</ul>
Requirements
<ul>
<li>PhD in computational chemistry, organic or physical chemistry, physics, or a closely related field</li>
<li>Minimum of 5 years computer-aided drug design (CADD) or related biotech/pharma experience, with expertise accelerating small molecule drug discovery projects from target tractability and hit identification, through lead optimization (demonstrated by peer reviewed publications and inventorship status on patent applications)</li>
<li>Demonstrated experience and understanding of physics-based, AI/ML, and generative computational approaches to drug discovery</li>
<li>Excellent communication and collaboration skills, with the ability to work well in a multidisciplinary environment</li>
<li>Excellent organizational skills and attention to detail, with a strong passion for learning new concepts and technologies</li>
</ul>
Additional Qualifications
<ul>
<li>Proficiency in scientific programming (e.g. Python, R, C++)</li>
<li>Proficiency in molecular simulation packages (e.g. AMBER, OpenMM, NAMD, Gromacs)</li>
<li>Proficiency in data science and machine learning tools (e.g. scikit-learn, pytorch)</li>
<li>Experience mentoring interns, co-ops, and junior scientists</li>
</ul>
Psivant offers a competitive base salary plus discretionary annual bonus and company ownership through stock options. We also support employees with subsidized medical/dental/vision insurance, 20 days vacation, and a 401k match. Salary for this opportunity will be commensurate with experience.About Psivant TherapeuticsPsivant Therapeutics is creating better therapeutics through an integrated molecular design paradigm that leverages best-in-class physics-based and AI technologies honed through decades of research and innovation. &nbsp;Our focus is first-in-class inflammation and immunology (I&amp;I) small molecule therapeutics. We have assembled a diverse team with extensive experience across disciplines ranging from physics and computer science to chemistry, biology, biochemistry, and structural biology. &nbsp;This continuum of complementary skills drives our scientific vision to deliver meaningful therapeutics to patients in need. &nbsp;We are patient-inspired, perseverant, synergistic, supportive, intrepid, and inclusive. &nbsp;If you’re passionate about advancing medicine in a fast-paced, innovative environment, and eager to contribute to a team that blends advanced computation with drug discovery, Psivant might be the perfect fit for you.&nbsp;At Psivant, we are a lean, high-performing team dedicated to pushing boundaries and achieving growth—both personally and scientifically. &nbsp;We seek individuals who are smart, collaborative, and thrive in a dynamic, early-stage biotech environment. Read More About Us·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Our Story: &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <a href="https://psivant.com/company/our-story/" target="_blank">https://psivant.com/company/our-story/</a>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Vision &amp; Values: &nbsp; <a href="https://psivant.com/company/vision-and-values/" target="_blank">https://psivant.com/company/vision-and-values/</a>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Team: &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <a href="https://psivant.com/company/team/" target="_blank">https://psivant.com/company/team/</a> Psivant Therapeutics is proud to be an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. We comply with all applicable laws and regulations, ensuring that all qualified applicants receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, genetic information, or any other legally protected status.Please note that we do not accept unsolicited resumes and kindly request that recruiters do not contact our team regarding this job posting. If a resume is submitted without a prior agreement, we will not be obligated to pay any referral or placement fees. Thank you for your understanding!&nbsp;
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Principal Scientist, Computer-Aided Drug Design (CADD)

<h3>Job Description</h3>
Job DescriptionSenior Relativity Archiving AnalystEmployment Type: Full-Time, ExperiencedDepartment:&nbsp;Information Technology CGS is seeking a Senior Relativity Archiving Analyst, who will be responsible for vetting Relativity workspaces and file share folders and archiving or purging them. File shares will be moved to archive locations. Relativity workspaces will be archived using both Relativity ARM and a flat format which can be fully restored in Relativity or another system. CGS brings motivated, highly skilled, and creative people together to solve the government’s most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities. Skills and attributes for success- Collaborating with DOJ management, lead attorneys, and Section Chiefs on the disposition of data/files- Archiving older file shares- Archiving full Relativity workspaces using ARM- Archiving images, natives, text,- Archiving in flat format the metadata, coding fields, choices/tags- Documenting user interface- Documenting the archiving process for approval by the Senior IT Manager.- Evaluating and resolving any archiving issues. Qualifications- At least 3 years of hands-on experience with backend Relativity 2022 and prior.- At least 3 years of hands-on experience with archiving Relativity workspaces.- At least 3 years of hands-on experience with restoring Relativity archives workspaces.- Knowledge of Windows permissions and file transfer utilities.- Excellent written and oral communication skills required.- Experience working in a collaborative environment.- Must be a US Citizen- Must be able to obtain a Public Trust security clearance Ideally, you will also have- An undergraduate degree is strongly preferred; preferably in the computer science or management information/technology disciplines.- Experience in storage technology planning, performance capacity planning, and modeling, applications Our CommitmentContact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client’s specific needs. We are committed to solving the most challenging and dynamic problems. For the past seven years, we’ve been growing our government contracting portfolio, and along the way, we’ve created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work. Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come. We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Join our team and become part of meaningful government innovation!Explore additional job opportunities with CGS on our Job Board:<a href="https://cgsfederal.com/join-our-team/For" target="_blank">https://cgsfederal.com/join-our-team/For</a> more information about CGS please visit <a href="https://www.cgsfederal.com" target="_blank">https://www.cgsfederal.com</a> or contact:Email:&nbsp;<a href="mailto:info@cgsfederal.com" target="_blank">info@cgsfederal.com</a> #CJ
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior Relativity Archiving Analyst

<h3>Job Description</h3>
Job DescriptionDEKA Research &amp; Development has an immediate opening for a Biocompatibility &amp; Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role will work directly with Research &amp; Development, Regulatory &amp; Clinical Affairs and Quality Engineering to formulate and execute biocompatibility and toxicological evaluation strategies that support development objectives and world-wide regulatory approvals.&nbsp; How you will make a difference as a&nbsp;Biocompatibility &amp; Toxicology Senior Scientist:
<ul>
<li>Work in close association with customers and development teams to define and execute biocompatibility/toxicology evaluations, including establishing requirements for biological safety of medical devices and combination products</li>
<li>Lead the preparation and conduct of biocompatibility/toxicology test programs</li>
<li>Lead interactions with external consultants and contract laboratories including in-person meetings, teleconferences, and other communications as needed to support program objectives</li>
<li>Develop and deploy mechanisms to continually maintain state of the art knowledge and understanding related to biocompatibility and toxicological safety of medical devices, including relevant standards and test methods.&nbsp; Insure processes and procedures maximize resource efficiency and minimize time to market</li>
<li>Insure the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through monitoring regulatory authority and industry resources</li>
<li>Coach and mentor internal and external partners on effective strategies and tactics</li>
<li>Interface with customers on biocompatibility and toxicology issues</li>
</ul>
Skills you will need to be successful:
<ul>
<li>MS in a technically related field (toxicology, materials science, chemical engineering, biomedical engineering or related).</li>
<li>Minimum of 7 years direct work experience in a medical device and/or combination product development role with demonstrated success in planning and conducting biocompatibility and toxicological evaluations</li>
<li>Expertise in U.S. and international medical device biocompatibility requirements including ISO 10993 standards, Good Laboratory Practices, and guidance from regulatory authorities</li>
<li>Demonstrated practical knowledge of the laboratory methods and analytical techniques associated with medical device and/or combination product biocompatibility and chemical characterization evaluations</li>
<li>Demonstrated ability to establish consensus and work collaboratively across functions and development teams</li>
<li>Excellent written and verbal communication skills including the ability to effectively communicate at all levels of the organization and with external partners</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
 &nbsp;
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Biocompatibility & Toxicology Senior Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
This role supports analytical method development and data generation to inform product development, with cross-functional collaboration and a strong emphasis on scientific rigor, safety, and continuous improvement.
Responsibilites Include:&nbsp;
<ul>
<li>Engage with scientists across Development and Manufacturing organizations to develop, evaluate, and implement robust analytical methods/technologies and control strategies to advance current analytical capabilities.</li>
<li>Independently generate data to inform development activities through the use of HPLC, UHPLC, and LCMS.</li>
<li>Help to develop and perform robust analytical methods (e.g., HPLC purity, potency) and collaborate with other functions to enable the successful transfer and implementation of those methods.</li>
<li>Direct or facilitate material testing activities conducted by specialized characterization groups</li>
<li>Perform laboratory activities with a strong emphasis on safety and technical rigor, while adhering to policies and procedures.</li>
<li>Identify and exploit new scientific concepts, exhibit strong problem-solving skills, and be self-motivated to contribute across multiple projects.</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field</li>
<li>(B.S. with 3–4 years of industry experience; M.S. with less than 1 year required)</li>
<li>Strong hands-on experience with liquid chromatography (HPLC, UPLC, LC-MS)</li>
<li>Familiarity with additional analytical techniques, including FTIR, NMR, UV-Vis, KF, ICP, DSC, TGA, and XRPD</li>
<li>Solid understanding of method characterization (e.g., linearity, precision, LOD/LOQ)</li>
<li>Experience with analytical instrumentation: Waters I-Class, Thermo Vanquish Flex, AKTA Pure 150 M</li>
<li>Proficiency in relevant software: Empower, Xcalibur, Unicorn, BioPharma Finder</li>
<li>Working knowledge of IPRP, AEX/IEX, and HILIC chromatography</li>
<li>Proven ability to troubleshoot and maintain analytical instrumentation</li>
<li>Strong communication, scientific problem-solving skills, and learning agility</li>
<li>Effective collaborator who can manage multiple priorities and thrive in dynamic environments</li>
<li>Commitment to safety and compliance</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with mass spectrometry, including oligonucleotide and RNA analysis</li>
<li>Hands-on experience with RNA workflows and techniques related to RNA purification, quantification, and stability</li>
<li>Familiarity with oligonucleotide characterization and analytical methods</li>
<li>Knowledge of 5S or lean methodologies in laboratory settings</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly rate is between $38&nbsp;- $43,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development.&nbsp;
We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects.&nbsp;
Job Responsibilities and Requirements:&nbsp;
<ul>
<li>Experience with protein chemistry, protein analytics, and bioprocess technology is required&nbsp;</li>
<li>Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process&nbsp;</li>
<li>Hands on experience and working knowledge on techniques including but not limited to&nbsp; liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet&nbsp;</li>
<li>Hands on experience with SDS-PAGE, ELISA, and&nbsp;experience with protein purification/chromatography at the lab scale is a plus&nbsp;</li>
<li>A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred&nbsp;</li>
<li>Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data&nbsp;</li>
<li>Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices&nbsp;</li>
<li>Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline&nbsp;</li>
<li>BS 2-4&nbsp;years or MS +0-2 years of relevant experience&nbsp;</li>
<li>Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet&nbsp;</li>
</ul>
<ul>
<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 
<ul>
<li>Position is full-time, on-site Monday-Friday 8AM-5PM.&nbsp;</li>
<li>Pay range: $27.00 - $31.00 based on degree level and years of relevant experience with the skills utilized in the role.&nbsp;</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioprocess Analytical Chemist (Purification Process Support)

<h3>Job Description</h3>
Job Description
Grow with Welch's! 
Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary!
At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you.
Position Summary:
We're looking for an R&amp;D Technician to join our team of technicians, scientists, and engineers who are committed to transforming science into commercial reality.
WHAT YOU'LL DO:
<ul>
<li>Learn to operate &amp; troubleshoot lab instruments (e.g. pH meters, refractometers, titrators, etc.) and pilot plant equipment (e.g. pasteurizer, carbonator, filter press, etc.) to produce reliable results.</li>
<li>Learn the fundamentals of development software to create batch sheets, record test results and applicable notes.</li>
<li>General support of R&amp;D including equipment maintenance and calibration, receiving, restocking inventory, and labeling and packing samples.</li>
<li>Lead equipment cleaning activities in accordance with GMPs.</li>
<li>Manage stocking of lab supplies and ingredients, coordinating orders and deliveries as necessary to ensure lab and pilot plant are fully stocked.</li>
<li>Cross train in facilities for shipping, receiving, and building operations.</li>
<li>Work with scientists and engineers to create experiments, execute work and manage recording of analytical data.</li>
<li>Deliver results during product testing, batching, production runs, sensory studies and document the testing results.</li>
<li>Conduct batching, production, and testing of food and beverage products on the lab bench or in the pilot plant to meet project objectives and in accordance with HACCP and GMP requirements.</li>
</ul>
WHO YOU ARE:
An ideal candidate:
<ul>
<li>Interest in packaging and running packaging studies</li>
<li>Is familiar with set up, operation, and shutdown of processing equipment and relevant analytical instruments including refractometers, titrators, and pH meters.</li>
<li>Has a good working knowledge of laboratory best practices and safety measures including appropriate PPE usage, chemical handling skills, and GMPs. HACCP experience a plus.</li>
<li>Able to adhere to guidelines and follow processing equipment operating procedures.</li>
<li>Able to solve machine / mechanical problems.</li>
<li>Strong communication and interpersonal skills.</li>
<li>Able to manage time well and work independently.</li>
<li>Able to collaborate with internal partners.</li>
<li>Demonstrate precise, autonomous, organized, detailed and efficient work.</li>
<li>Able to adhere to guidelines, follow procedures and utilize resources to find information.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Monday – Friday primarily onsite</li>
<li>1+ years of lab experience in a relevant technical field (pharmaceutical, biotech, life sciences, chemical / engineering). Experience in food &amp; beverage preferred.</li>
<li>Associate's degree in a relevant technical field preferred.</li>
<li>Proficiency in Microsoft Outlook, Excel, Word, and Teams.</li>
<li>Ability to operate and maintain equipment safely.</li>
<li>Must be able to lift 50 lbs.</li>
<li>Ability to stand for an extended period of time.</li>
</ul>
What You'll Enjoy:
<ul>
<li>Organization with a bold, clear purpose &amp; vision for the future</li>
<li>Inclusive Culture: Be a part of an inclusive workplace where you not only belong but also have the opportunity to be the best version of yourself</li>
<li>Passionate Community: You are encouraged to have a voice, share your opinions, and have individual impact on the success of the business</li>
<li>Hybrid work model: Flexible &amp; collaborative work environment to maximize well-being &amp; success</li>
<li>Paid Time Off and Holidays: Available immediately for you to enjoy time away from the office to rest and recharge</li>
<li>Paid Volunteer Time Off: 40 hours of paid volunteer time for all non-union employees</li>
<li>Development &amp; Advancement: Access to LinkedIn Learning as well as both formal and informal opportunities to develop and grow your career</li>
<li>Compensation Package Consisting of Competitive Base Salary and Annual Incentive Plan (Bonus)</li>
<li>401K plan with Generous Company Match</li>
<li>Flexible Benefits from your first day: Choose the benefits that meet your needs and preferences
<ul>
<li>Health, Dental &amp; Vision Insurance </li>
<li>Health Savings Accounts </li>
<li>Life and accident insurance </li>
<li>Employee Assistance Programs </li>
<li>Tuition reimbursement program </li>
<li>Additional benefits available through Perks at Work </li>
</ul>
</li>
<li>Paid parental (and adoption) leave – Available after 12 months of employment </li>
</ul>
The anticipated hiring base salary range for this position is $65,000 - $75,000 non-exempt, annually for US-based employees. This range reflects the minimum and maximum for the position across all US locations, is based on a full-time work schedule, and is Welch's good faith estimate as of the date of this posting. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. In addition to base salary, this role is eligible for participation in a bonus plan.
#LI-OnSite
Welch's is an Equal Employment Opportunity Employer. We are committed to the prevention of employment discrimination based on race, religion, color, sex, gender identity, national origin, age, marital status, disability and/or military or veteran status, sexual orientation or any other action covered by federal or applicable state/local laws.
Welch's offers more than just a job - it's an opportunity to grow, innovate, and make a global impact with a passionate community.

Research and Development Technician

<h3>Job Description</h3>
Industry: Pharmaceuticals
Title: Associate Scientist II
Job ID: CAMB000068
Location: Cambridge, MA
Duration: 06+ months contract (+Possibility of extension)
 
Overview
The Research Department at Client is seeking a motivated research associate to join our team to support the biology group in research including CNS and emerging tissues. We are seeking a highly organized individual that can work quickly and efficiently in a fast-paced laboratory setting. This ideal candidate will be a strong team player, capable of coordinating tasks with various stakeholders to meet deadlines. This is a full-time, onsite role based in Cambridge MA location, with a requirement to be onsite five days per week.
 
Summary of Key Responsibilities
<ul>
<li>Contribute to the design and execution of studies to characterize molecules for RNAi therapeutic programs, including rodent disease models.</li>
<li>Support animal tissue processing protocols through grinding, homogenization, RNA extraction, and more.</li>
<li>Conduct assays such as qPCR, western blot, ELISA, that support in vivo studies.</li>
<li>Analyze and report scientific data to manager.</li>
<li>Diligently follow SOPs/protocols.</li>
<li>Track samples in databases including but not limited to Electronic Laboratory Notebook (ELN), Laboratory Information Management System (LIMS), Smart Refrigeration systems, Smartsheet's and other proprietary databases.</li>
<li>Adapt quickly to changing priorities in a dynamic work environment.</li>
<li>Communicate openly and directly with lab groups to provide sufficient solutions that will work for all team members.</li>
</ul>
 
Qualifications
 
<ul>
<li>Minimum B.S. degree in a life sciences-related discipline such as Molecular Biology, Cell Biology, or Genetics</li>
<li>Must be flexible, open to new tasks and challenges and able to work on tight deadlines.</li>
<li>Exceptional interpersonal skills and the ability to function at a high capacity within a fast-paced team environment.</li>
<li>Excellent attention to detail, organizational skills, eagerness to learn, and the ability to follow written and verbal instruction.</li>
<li>Working knowledge of standard Microsoft Office applications including Excel, GraphPAD, Outlook, PowerPoint, and Word.</li>
<li>Familiarity with laboratory automation and liquid handling systems is a plus.</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Biologist II – in vitro primary cellular assays (FACS, MSD, and qPCR) Onsite in Worcester MA Length of assignment: 1 year to start Hourly Rate: $37-40/hr (medical benefits available at a cost) Schedule: M-F 40hrs/week (limited flexibility with schedule/hours). 100% onsite/lab position. &nbsp; Key Responsibilities Include: 
<ul>
<li>Perform in vitro primary cellular assays to evaluate target biology using technologies like FACS, MSD, and qPCR</li>
<li>Analyze biological samples by flow cytometry, including tissue processing and preparation, staining cells, acquiring data, and analyzing results</li>
<li>Experience processing human or large animal lab species tissues</li>
<li>Generate data in a timely fashion</li>
<li>Inventory control of study samples and reagents</li>
<li>Effectively and accurately record and report experiment results </li>
</ul>
Qualification / Requirements: 
<ul>
<li>Bachelors with 3-5 years or Masters in cellular biology, immunology, or a related discipline with at least 0-3 years of relevant experience</li>
<li>Experience in performing flow cytometry assays, cell culture, and sterile technique</li>
<li>Excellent communication, interpersonal, organization skills desired </li>
</ul>
Preferred: 
<ul>
<li>Experience in handling human or large animal lab species ex vivo samples</li>
<li>Experience in flow cytometry panel design</li>
<li>Proficiency in data reporting and FlowJo analysis software</li>
<li>Experience working in a team environment to achieve goals and timelines</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>
&nbsp; Our role in supporting&nbsp;diversity&nbsp;and&nbsp;inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

Biologist II - in vitro primary cellular assays (FACS, MSD, and qPCR)

<h3>Job Description</h3>
Location:&nbsp;Woburn, MA
 
Vaxess is developing next generation medicines on our novel microneedle array patch (MAP) platform. The platform combines high temperature stability with simple self-application and only a five-minute wear time to dramatically alter the way that drugs are delivered. We are committed to enabling products that are not only more effective, but also more accessible to patients around the world. 
 
Research &amp; development at Vaxess is cross-disciplinary, integrating science and engineering across biology, chemistry, materials, and mechanics to address important unmet medical needs in biologics delivery. We are seeking a talented, collaborative, and highly motivated individual with a background in formulation and materials characterization to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging startup bringing innovative technology to the global market. 
 
Responsibilities 
<ul>
<li>Design and execute studies to identify novel candidates for development on the MAP platform, build platform flexibility and utility to support pipeline product development. </li>
<li>Develop platform and product formulations enabling room-temperature distribution and storage of MAPs. </li>
<li>Serve as subject matter expert and lead on materials characterization for the Platform Research team.</li>
<li>Document and analyze experimental results, effectively communicate research results through technical presentations and written reports. </li>
<li>Develop and document test methods to characterize MAP formulations and functional device performance.</li>
<li>Collaborate closely with analytical, MAP manufacturing, and preclinical colleagues to generate proof of concept with new molecules, materials; support early collaborations with strategic partners. </li>
<li>Provide technical guidance to and mentor junior scientists/engineers as needed. </li>
<li>Contribute to intellectual property filings and regulatory submissions. </li>
</ul>
 
Qualifications 
<ul>
<li>PhD in Biological/Chemical Engineering, Materials Science, Chemistry, or related discipline with at least 2 years of relevant experience; or BS/MS with at least 7 years of relevant experience. </li>
<li>Experience with development of protein/peptide formulations and materials characterization in the context of polymer drug delivery platforms is ideal. </li>
<li>Experience with physical properties characterization of liquid formulations and solid phase matrices (e.g. surface tension, viscosity, mechanical strength) is preferred. </li>
<li>Experience with analytical characterization of materials related to structure and moisture (e.g. spectroscopic, thermal analysis methods) is preferred. </li>
<li>Experience with GxP and familiarity with regulatory guidelines is a plus.</li>
<li>Strong attention to detail, with excellent verbal and written communication skills. </li>
<li>Demonstrated abilities to learn new skills and fields, solve challenging technical problems, think independently, and work collaboratively in cross-functional teams. </li>
<li>Entrepreneurial spirit and drive to positively impact public health. </li>
</ul>
 
Vaxess, a venture-backed biotech company, is building a team of exceptional people to rapidly advance products on its microneedle array patch platform. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you’re interested in joining the Vaxess team, please submit your CV/resume to <a href="mailto:careers@vaxess.com" target="_blank">careers@vaxess.com</a>.&nbsp;

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