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<h3>Job Description</h3>
Job DescriptionAbout Commonwealth Fusion Systems:&nbsp; Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy. Combining decades of research, top talent, and new technologies, we’re designing and building commercially viable fusion power plants. And working with policymakers and suppliers to build the energy industry of the future.&nbsp; We’re in the best position to make it happen. Since 2018, we’ve raised nearly $3 billion in capital, making us the largest and leading private fusion company in the world. Now we’re looking for more thinkers, doers, builders, and makers to join us. People who’ll bring new perspectives, solve tough problems, and thrive as part of a team.&nbsp; If that’s you and this role fits, we want to hear from you. Join the power movement as a Computational Materials Scientist The Materials and Processing (M&amp;P) Department at CFS supports design engineers, supply chain, and manufacturing by selecting materials, unambiguously defining materials and processing routes, validating and measuring those materials and their properties, and conducting R&amp;D to develop new materials and processes to enable fusion power deployment. M&amp;P at CFS is organized around three primary thrusts: engineering, test and characterization, and development programs. The work is undertaken in support of delivering SPARC, the net energy tokamak under construction in Devens, MA, and ultimately in designing the ARC fusion power plant. These devices pose unique materials challenges including neutron fluxes produced by deuterium-tritium fusion, high heat loads, molten salt coolant systems, complex component topologies, high magnetic fields, and high mechanical loading in cryogenic conditions.&nbsp;&nbsp;To support this mission, the CFS Materials Department is seeking a Computational Materials Engineer with expertise in process-structure-properties relationships, physics informed modeling, and materials in extreme environments. The ideal candidate would have a background in both computational materials simulation methods, and materials science and/or physical chemistry. The responsibilities will include physics-based modeling, synthetic data generation, and first-principles modeling and simulation to support development of CFS materials. They will collaborate with other engineers and subject matter experts to identify highest sensitivity parameters and prioritize experimental work for greatest impact to decreasing uncertainty.What you'll do:
<ul>
<li>Use and build computational toolsets to generate predicted material properties in extreme environments including temperature, radiation, and magnetic field with uncertainty bounds informed by physical mechanisms</li>
<li>In collaboration with design and analysis engineers, develop material design curves methodology capable of determining statistically significant minimum properties for tokamak applications such as low and high cycle fatigue, dielectric breakdown, radiation effects.</li>
<li>Identify gaps in knowledge and experimental capability which can be filled via simulation or model building</li>
<li>Assist in benchmarking and creating metrics for material property variability and sources of variability in manufacturing processes</li>
<li>Collaborate with other M&amp;P Engineers to create workflows to enable the appropriate capture, storage, data visualization and analysis of data generated within the materials domain</li>
<li>Support writing materials standard specifications</li>
<li>Stay current with the evolving technology and modeling techniques</li>
</ul>
What we’re looking for:
<ul>
<li>MS in Materials Science Engineering, Applied Physics, Physical Chemistry, or related field</li>
<li>Minimum of 3+ years’ experience in experimental or computational materials science</li>
<li>Implementation and/or authorship of codes for calculation and analyses of material properties</li>
<li>Building predictive models for material properties in extreme environments</li>
<li>Validation of models with experimental data or physical mechanism bounds</li>
<li>Process failure modes or physical mechanism driven hypothesis formulation and design of experiments</li>
<li>Understanding process-structure-properties-performance principles and fundamental mechanisms responsible for property changes in extreme environments</li>
<li>Understanding of the underlying models that enable materials simulation methods across length scales including; Atomistic, molecular dynamics, density functional theory, Monte Carlo, phase field, crystal plasticity, dislocation dynamics, and computational thermodynamics</li>
<li>Understanding of the sensitivity to uncertainty in the inputs and outputs of those models</li>
<li>Demonstrated ability to work effectively cross-functionally</li>
<li>Excellent organizational skills including prioritization of multiple concurrent projects</li>
<li>Ability to break down complex problems into smaller deliverables that add value</li>
</ul>
Bonus points for:
<ul>
<li>Experience using computational materials science tools and integrated computational materials engineering (ICME) tools to answer specific scientific questions, ideally across length scales</li>
<li>Experience displaying complex quantitative data in a simple, intuitive format and presenting findings clearly and concisely</li>
<li>Experience making and justifying decisions in fast paced engineering settings</li>
<li>Written and verbal communication with technical teams</li>
<li>Taking under-defined problems and driving them to a state of completion</li>
<li>Operating in a flexible, service-oriented engineering domain team</li>
</ul>
Must-have Requirements:
<ul>
<li>Perform activities such as typing or sitting for extended periods of time</li>
<li>Work in a facility that contains industrial hazards including heat, cold, noise, fumes, strong magnets, lead (Pb), high voltage, high current, pressure systems, and cryogenics</li>
<li>••Willingness to travel or work required nights/weekends/on-call occasionally</li>
</ul>
Salary range for this full-time position + equity + benefits.&nbsp;The actual salary will depend on level, location, qualifications, and experience. The range displayed on each job posting reflects new hire salaries for the position across all US locations. Benefits include:•&nbsp; Competitive compensation with equity•&nbsp; 12.5 Company-wide Holidays•&nbsp; Flexible vacation days•&nbsp; 10 sick days•&nbsp; Generous parental leave policy•&nbsp; Health, dental, and vision insurance•&nbsp; 401(k) with employer matching•&nbsp; Professional growth opportunities•&nbsp; Team-building activities#LI-Hybrid At CFS, we excel in fast-paced environments, driven by our values of integrity, execution, impact, and self-critique. As we grow, we’re eager to bring on mission-driven folks who offer diverse perspectives and fresh ways to tackle challenges. We value diversity deeply and are proud to be an equal opportunity employer by choice. We consider all qualified applicants equally, regardless of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law. This role requires compliance with U.S. laws concerning the export of controlled or protected technologies or information (collectively, “Export Control Laws"). Any offer of employment will be contingent on the need for compliance with such Export Control Laws.

Computational Materials Scientist

<h3>Job Description</h3>
Job DescriptionParallel Squared Technology Institute&nbsp;(PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Why?&nbsp;Protein dysfunctions directly cause many diseases, such as Alzheimer’s disease. Yet, proteins remain understudied because of technological hurdles. How?&nbsp;To resolve these limitations, PTI will develop mass tags enabling a new&nbsp;framework&nbsp;for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at:&nbsp;parallelsq.org. New career opportunitiesMembers of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals.&nbsp;&nbsp; Summary of PositionWe are looking for an individual contributor with previous experience in ‘omics data interpretation,&nbsp; who will lead the design and development of new computational analysis pipelines. This position will involve analyses of mass spectrometry proteomics data in order to infer biological mechanisms at play in either the Alzheimer’s Disease or Immuno-Proteome Aging projects at PTI. The successful candidate will work in a highly interdisciplinary team environment with other scientists. In order to be seriously considered for this position, we require a cover letter as part of the candidate’s application.Responsibilities:
<ul>
<li>Develop and adapt pre-processing algorithms for mitigation of data collection artifacts</li>
<li>Work with biological project leads to define hypotheses and apply appropriate statistical framework</li>
<li>Design and develop optimized analysis pipelines for large ‘omics datasets</li>
<li>Perform deep and detailed analyses for data-intensive experiments with team members and communicate interpretable results</li>
<li>Hands-on development of interactive tools for data interpretation of high throughput proteomics datasets for other team members using RShiny, Python, D3, or other tools</li>
<li>Curate large-scale datasets for internal and external usage</li>
<li>Mentor scientists and research associates</li>
<li>Prepare internal reports and manuscripts as well as present results at internal or external scientific meetings as appropriate</li>
<li>Demonstrate a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others</li>
<li>Other duties as assigned</li>
</ul>
Qualifications:
<ul>
<li>Advanced degree in Statistics, Mathematics, Bioengineering, Computer Science, or other computational science.&nbsp;</li>
<li>Demonstrable professional or PhD experience working with professional biologists on single cell ‘omics questions</li>
<li>Strong understanding of generalized linear models and nonparametric regression, hypothesis testing, optimization, dimension reduction techniques, and machine learning algorithms</li>
<li>Advanced proficiency in R and/or Python</li>
<li>Demonstrable experience with data set alignment, batch correction, cell type assignment, differential abundance testing, and gene ontology mapping</li>
<li>Experience handling terabyte-scale biological data</li>
<li>Demonstrable experience with model validation: cross validation, bootstrapping, posterior predictive, or simulation-based model checking</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with proteomics spectral library prediction</li>
<li>Must have single cell 'omics experience OR experience working with mass spectrometry data</li>
</ul>
We offer:
<ul>
<li>An opportunity to change the world and work with some of the smartest and the most talented experts from different fields.</li>
<li>Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from.</li>
<li>Company-paid group life, AD&amp;D, long- and short-term disability insurance</li>
<li>15 days PTO + 10 sick days per year</li>
<li>18 company holidays + your birthday off</li>
<li>$5,000 per year educational reimbursement</li>
<li>Up to 16 weeks paid parental leave</li>
</ul>
We aim to help fill a structural gap in today's R&amp;D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&amp;D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations.&nbsp;We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind.
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.

Computational Scientist - Single-Cell Algorithms

<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.&nbsp;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;

Scientist/Senior Engineer I, Platform Research

<h3>Job Description</h3>
Job Description
Job Title: Clean Room Assembler
Job Description
The Mechanical Assembler will be responsible for assembling high quality medical devices while working within a controlled (clean, sterile, medical grade) manufacturing area.
Shift : 3:30pm-11:30pm, $22/hour+
Responsibilities
<ul>
<li>Assembling small medical devices</li>
<li>Inspection of medical devices</li>
<li>High attention to detail, hand dexterity</li>
<li>Using a microscope and hand tools to perform assembly</li>
<li>Using a computer for documentation</li>
<li>Working in a cleanroom, wearing PPE</li>
</ul>
Pay and Benefits
The pay range for this position is $20.00 - $24.20/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Danvers,MA.
Application Deadline
This position is anticipated to close on Oct 20, 2025.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

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