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<h3>Job Description</h3>
Job Description
Title: Research Scientist – Animal Studies Location: Marlborough, MA (Hybrid) Contract Length: 6-12 months with possibility for extension/conversion
General Description
<ul>
<li>Experience with benchtop models using phantoms.</li>
<li>Participation in preclinical investigations with tissue collection and biologic metrics.</li>
<li>Familiar with numerical models with finite element methods.</li>
<li>Skills on data collecting, analyzing, interpreting, and communicating experimental results to the team and organization.</li>
</ul>
Responsibilities and Duties
<ul>
<li>Collaborate with the research team to develop experimental methodologies in benchtop, numerical, and preclinical methodologies.</li>
<li>Execute benchtop and preclinical trial investigations, including collection, analysis, interpretation, and distribution of research findings.</li>
<li>Capacity to integrate research outcomes into meaningful technological advances.</li>
<li>Support regulatory submissions.</li>
<li>Generation of reviews supporting technical documentation and product development phases.</li>
<li>Contribute to the generation of intellectual property for the company.</li>
<li>Interaction with third-party service research providers.</li>
<li>Compilation and analysis of research data for scientific publications and technical writing.</li>
<li>Attendance at relevant scientific conferences and meetings.</li>
</ul>
Requirements
<ul>
<li>Advanced degree in Engineering, Biomedical Engineering, or a related scientific field. A PhD is highly valued.</li>
<li>Previous participation in a multidisciplinary project including benchtop, numerical, and preclinical. Experience pulsed electric fields and electroporation applications is highly valued.</li>
<li>Basic knowledge of electricity, mechanic, human anatomy and physiology.</li>
<li>Self-driven skills for execution and education.</li>
</ul>

Research Scientist- Animal Studies

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery department based in Cambridge MA.
</li>
<li>
The candidate will focus on generating biology data packages to help advance target identification and validation within GI immunology.
</li>
<li>
The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery.
</li>
<li>
The scientist will focus on developing and optimizing cellular/molecular assays to generate reliable and reproducible data in a timely manner.
</li>
<li>
The scientist is expected to read and adapt scientific literature and internal protocols to accomplish assignments and demonstrate broad and versatile technical expertise within immunology.
</li>
<li>
Develop and execute cell-based functional assays using cell lines and mammalian tissue primary cells, for key readouts including cell activation, differentiation and effector molecule secretion
</li>
<li>
Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF)
</li>
<li>
Isolate and culture immune cells (T cells, myeloid cells) from human and mouse tissues
</li>
<li>
Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need
</li>
<li>
Implement and innovate new experimental protocols/techniques as needed
</li>
<li>
Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings
</li>
<li>
Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment
</li>
<li>
Impact projects mostly through lab-based activities
</li>
</ul>
Qualifications:
<ul>
<li>
Master's degree in Biological Science or related field with 2-3 years of experience in biotech or pharma set up.
</li>
<li>
Experience in in vitro cell culture (sterile techniques, handling challenging cell types) and cell-based assays development is required.
</li>
<li>
Experience with human PBMC functional assays and/or immune cells (T cells and myeloid cells) is required.
</li>
<li>
Experience in immunoassays including multi-color flow cytometry and ELISA (or MSD, HTRF) is required.
</li>
<li>
Experience with mouse tissue processing for immune profiling (not direct mouse handling) is a plus but not required.
</li>
<li>
Knowledge of DNA/RNA handling and other molecular biology techniques like PCR and qPCR is a plus but not required.
</li>
<li>
Ability to learn new skills and apply them in a fast-paced research environment.
</li>
<li>
Creativity, problem-solving, and attention to details.
</li>
<li>
Excellent oral and written communication and collaboration skills.
</li>
<li>
Ability to work independently as well as in a team.
</li>
<li>
Proven flexibility to deal with changing timelines and shifting work priorities.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist, Immunology Discovery

<h3>Job Description</h3>
Job DescriptionCompany Description 
Why Join Eurofins?
At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits.
Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries—from food and water to pharmaceuticals and advanced materials. We help the world’s top companies ensure their products are safe, authentic, and accurately labeled.
Why Relocate to Rensselaer, NY?
<ul>
<li>Be part of a thriving biopharma and life sciences hub.</li>
<li>Enjoy a lower cost of living compared to Boston and other major metro areas.</li>
<li>Benefit from relocation assistance and onboarding support for a smooth transition.</li>
</ul>
Job Description 
We’re seeking a Microbiology Operations Supervisor to lead second-shift operations in a GMP-regulated environment at our Rensselaer, NY site. This is a full-time leadership role with relocation support provided.
What You’ll Do
<ul>
<li>Oversee environmental monitoring (EM) activities, including sampling of cleanrooms, compressed gases, and water systems.</li>
<li>Conduct microbial identification and acceptance testing of microbiological culture media.</li>
<li>Maintain microbiology productivity databases and generate trend reports.</li>
<li>Lead investigations into microbiological deviations and prepare detailed reports.</li>
<li>Ensure calibration and maintenance of lab equipment and compliance with GMP standards.</li>
<li>Supervise and mentor microbiology analysts and group leaders.</li>
<li>Manage onboarding, training, and scheduling for second-shift operations.</li>
<li>Apply Lean principles to optimize workflows and drive continuous improvement.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Microbiology, Life Sciences, or related field.</li>
<li>Minimum 3 years of microbiology lab experience, including EM in a GMP setting.</li>
<li>At least 3 years of leadership experience in technical or lab environments.</li>
<li>Strong understanding of microbiological testing, EM protocols, and compliance standards.</li>
<li>Proven ability to coach and develop staff while managing operations.</li>
<li>Authorized to work in the U.S. without restriction or sponsorship.</li>
<li>Willingness to relocate to Rensselaer – relocation support is available.</li>
</ul>
 Additional Information 
<ul>
<li>Full-time, onsite position based on second-shift schedule (Mon–Fri, 2:30pm–11:00pm), with occasional weekends and overtime as needed.</li>
<li>Candidates within a commutable distance to Rensselaer, NY, are strongly encouraged to apply.</li>
<li>Relocation assistance may be available for qualified candidates seeking to relocate.</li>
</ul>
Benefits include:
<ul>
<li>Comprehensive medical, dental, and vision coverage</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly pay ranges from&nbsp;$33–$38/hour + 10% shift differential</li>
</ul>
Ready to make an impact? Join a team where your scientific skills matter and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS!
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Microbiology Operations Supervisor - Relocation to Rensselaer, NY Provided!

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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, a place to call home, apply with us today!
Job Description 
This scientist will develop formulations for oral solid dosage forms (tablets and capsules) on high-priority programs with accelerated timelines. Key responsibilities include designing and executing formulation and process development experiments, interpreting scientific data, and communicating findings to stakeholders. The role requires close coordination with cross-functional teams to meet tight project deliverables and authoring technical reports and CMC sections for regulatory submissions.
Position Responsibilities:
<ul>
<li>Understand project timelines and deliverables and plans/coordinates project work accordingly with stakeholders.</li>
<li>Contribute significantly and independently to project work which may include multiple projects within functional area.</li>
<li>Review, interpret and communicate data within project teams. &nbsp;</li>
<li>Plan and implement resolutions to technical problems/issues.</li>
<li>Independently design and execute experiments and report results.</li>
<li>Proactively analyze manufacturing issues and coordinate potential resolution with the drug substance team.</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>A degree in chemistry, biology, pharmacy, engineering, or a related pharmaceutical science with at least 4 years of formulation development experience</li>
<li>BS with at least 6 years of industry experience, MS with at least 4 years of industry experience, or PhD with at least 6 months of industry experience in formulation development</li>
<li>Must have experience specificially with oral solid dosage formulation development</li>
<li>Strong knowledge of CMC pharmaceutical development, including hands-on operation manufacturing equipment and laboratory instruments (compression, wet/dry granulation, capsule filling, etc.)</li>
<li>Sound knowledge of current Good Manufacturing Practices</li>
<li>Technical writing experience</li>
<li>Experienced working in a multi-disciplinary team environment</li>
<li>Must be eligible to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday – Friday, 8am-5pm with overtime as needed.&nbsp;Candidates currently living within a commutable distance of&nbsp;Cambridge, MAare 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 holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
<li>Base Compensation: $90,000 to $99,000 per year based on experience and education</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Formulation Development Scientist - Oral Solid Dosage

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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, a place to call home, apply with us today!
Job Description 
The individual will join a team of scientists and engineers focused on developing and optimizing mammalian cell culture processes for recombinant proteins and biologics for early-phase and late-phase clinical trials. He or she will be responsible for executing mammalian cell culture experiments in bench-top bioreactors and associated scale-down equipment with the goal of developing robust, scalable, high productivity processes that produce therapeutic proteins with the appropriate product quality attributes for use in treating human disease. The work will also involve working with clinical production facilities to ensure accurate technology transfer and successful large-scale production.
Responsibilities
<ul>
<li>Plan and execute experiments in shake flasks and bench-top bioreactors.</li>
<li>Ensures timely, effective, and high-quality documentation in electronic laboratory notebooks.</li>
<li>Communicate results and findings to stakeholders on a regular basis; presents data/strategy to colleagues and management as appropriate.</li>
<li>Work collaboratively with colleagues both within the group and cross-functionally contributes to maintaining and improving upon our safe, effective, and efficient lab operations.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree with 2–5 years of relevant experience, OR</li>
<li>Master’s degree with 0–2 years of relevant experience in Biotechnology, Microbiology, Cell Biology, Chemical/Biochemical Engineering, or a related field.</li>
<li>Strong aseptic laboratory technique (required)</li>
<li>Exceptional attention to detail</li>
<li>Excellent organizational skills</li>
<li>Clear and effective oral and written communication</li>
<li>A collaborative, team-oriented mindset</li>
<li>Must be authorized to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting to Meet the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule Monday through Friday, with overtime required as needed. Candidates located within a commutable distance to&nbsp;Andover, MA,&nbsp;are strongly encouraged to apply.&nbsp;
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly rate is between $26.00-$30.00,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Ready to take the next step in your career? Apply today and join a team that’s making a difference in science every day.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Upstream Process Development Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics:&nbsp;
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face. About Fapon Biotech:
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
Key Responsibilities:
We are seeking a scientific contributor to lead and execute novel LNP formulation process development activity for the delivery of circular RNA therapeutic at scale. This role will spearhead LNP process development/scale up activity and would be responsible for designing and executing DOE-based formulation process optimization. They would engineer and functionalize LNPs, develop analytics for formulation quality control, and develop processes to improve formulation at scale. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams, plan and run animal studies with a cross-functional group of scientists, and support the growth and career development of junior scientists. The ideal candidate is a chemical engineer/pharmaceutical major with strong LNP formulation, optimization, and process development experience, who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
<ul>
<li>Establish, execute and document protocols for preparation and characterization of targeted LNP formulations with nucleic acid cargo for in vitro and in vivo studies</li>
<li>Design and execute DOE-driven studies for LNP composition, mixing parameters and process optimization to improve formulation quality, stability, delivery efficiency and functional activity</li>
<li>Develop cell and molecular biology assays to assess the delivery efficiency of RNA cargo in mammalian primary cells to facilitate development of therapeutics drugs pipelines</li>
<li>Assist in the buildout of formulation and analytical capabilities with focus on delivery with nanoparticle technology, lyophilization and process development for scale up/production</li>
<li>Contribute to patent applications related to the delivery technology</li>
<li>Support technology transfer to CDMOs and Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed) to formulate, characterize, develop, and support assessment of efficacy</li>
<li>Plan and coordinate animal studies with in vivo team</li>
<li>Author technical documents, including SOPs for formulation processes and analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in chemical engineering, chemistry, pharmaceutical sciences, or related field, preferably with industry experience of 2-5 years for MS or 5-8 years for BS candidates.</li>
<li>Strong track record of productivity in nanoparticle research with an understanding of key challenges in nanoparticle/formulation scale-up and translation</li>
<li>Prior experience in developing lyophilization protocols for nanoparticle formulation, and stability testing is a plus</li>
<li>Technical proficiency with LNP formulation of RNA and analytical assays for particle characterization</li>
<li>Technical proficiency in developing cell and molecular biology assays to support drug product development</li>
<li>A minimum of 3-4 years of experience working with lipid nanoparticles for RNA delivery in any capacity</li>
</ul>
Preferred Qualifications:
<ul>
<li>Demonstrated capability in LNP formulation for nucleic acid delivery is must</li>
<li>LNP process development and scale-up experience is desired</li>
<li>Experience with tissue-specific targeted delivery of LNP-nucleic acid formulation is a plus</li>
<li>Demonstrated ability to present complex technical topics to a wide range of audiences with varying technical depth</li>
<li>Demonstrated proficiency in record keeping and documentations to support SOP generation, technology transfer and preferably regulatory filings</li>
</ul>
 Additional Information 
What We Offer: 
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior/Principal Research Associate, LNP Discovery/PD

<h3>Job Description</h3>
Job Description
At the Center for Health Information and Analysis (CHIA), we serve as stewards of Massachusetts health data, employing multifaceted datasets and&nbsp;cutting-edge&nbsp;analytics to ensure transparency in our health care system. By joining CHIA,&nbsp;you'll&nbsp;dive into health care data, revealing invaluable trends and insights, and play a pivotal role in evidence-based decision-making.   &nbsp;
Our work directly&nbsp;impacts&nbsp;the health care system, supporting the development of data-driven policies that aim to improve the quality and equity of care, while keeping costs affordable for Massachusetts families. We foster a flexible, collaborative environment, offering a hybrid model that balances in-person and remote work. Our hybrid approach allows you to work alongside your colleagues in our vibrant Boston office at 501 Boylston Street for at least two designated days per week, with the flexibility to work remotely on others.   &nbsp;
Join us at CHIA and be a driving force&nbsp;in&nbsp;health policy impact! We&nbsp;are seeking&nbsp;a&nbsp;Research Analyst&nbsp;to&nbsp;contribute to&nbsp;our growing research projects within the dynamic Strategy and Research team.   &nbsp;
The Research&nbsp;Analyst&nbsp;will work closely with the research team and other colleagues at CHIA, vendors,&nbsp;and stakeholders such as sister agencies,&nbsp;providers,&nbsp;payers etc.&nbsp;The Research&nbsp;Analyst&nbsp;will help lead and support&nbsp;analytic work and product development&nbsp;in addressing ongoing and emerging health care information and data gaps, particularly in areas such as health care&nbsp;workforce, health care&nbsp;utilization,&nbsp;and emerging issues.&nbsp;&nbsp;
As a&nbsp;Research Analyst, you will have the opportunity to: &nbsp;
<ol>
<li>
Drive Data-Backed Insights: Seize the opportunity to work with an extensive range of data on health care&nbsp;utilization, access, and&nbsp;equity&nbsp;related issues. You will be at the forefront of producing and reviewing clear and comprehensive written analyses, graphics,&nbsp;tables&nbsp;and presentations using CHIA's rich data sources to unearth crucial insights that will inform and shape health care policies and initiatives.  &nbsp;
</li>
</ol>
<ol>
<li>
Shape&nbsp;Data Management and Analysis:&nbsp;Take an active role in shaping data projects&nbsp;by&nbsp;implementing&nbsp;data management&nbsp;tasks for&nbsp;large datasets such as&nbsp;the&nbsp;All&nbsp;Payer Claims&nbsp;Database&nbsp;(APCD),&nbsp;hospital discharge data&nbsp;(Case&nbsp;Mix),&nbsp;and other&nbsp;data&nbsp;assets&nbsp;to facilitate and deliver&nbsp;insightful analyses that drive real change in Massachusetts health care, all while expanding your skills in a dynamic, mission-driven environment.&nbsp;
</li>
</ol>
<ol>
<li>
Champion Data Integrity:&nbsp;Participate&nbsp;in quality assurance (QA) and documentation processes to ensure that reported data is reliable and&nbsp;accurate. Work both independently and collaboratively with team members in developing analytical plans&nbsp;and documentation&nbsp;appropriate for&nbsp;each project.&nbsp;
</li>
</ol>
<ol>
<li>
Become&nbsp;a Technical and Subject Matter Expert: Provide technical support to&nbsp;the&nbsp;research&nbsp;team in programming and data analytics using&nbsp;APCD,&nbsp;Case Mix, and other&nbsp;data&nbsp;assets. Use your critical thinking skills to conduct literature searches and synthesize findings&nbsp;on topics of interest.&nbsp;&nbsp;
</li>
</ol>
Here are the important qualifications we are looking for:  &nbsp;
<ol>
<li>
Data&nbsp;Programming and Visualization&nbsp;Expertise:&nbsp;At least&nbsp;1&nbsp;year of experience&nbsp;and knowledge of&nbsp;data management and analysis using SAS, R, STATA, and/or any other major statistical packages.&nbsp;Knowledge of/experience with&nbsp;PowerBI,&nbsp;Tableau for data visualization&nbsp;preferred&nbsp;
</li>
</ol>
<ol>
<li>
Research Background: Knowledge of and experience with research methods&nbsp;and processes&nbsp;
</li>
</ol>
<ol>
<li>
Health Care Knowledge: Experience working with&nbsp;hospital&nbsp;discharge&nbsp;data and&nbsp;previous&nbsp;experience working with&nbsp;health&nbsp;care claims&nbsp;data strongly&nbsp;preferred.&nbsp;&nbsp;
</li>
</ol>
<ol>
<li>
Effective Communication: Demonstrate&nbsp;excellent written and verbal communication skills, with an ability to articulate complex technical issues clearly and persuasively.  &nbsp;
</li>
</ol>
<ol>
<li>
Educational Background:&nbsp;Bachelor’s degree in social sciences, public policy, public health, or quantitative field&nbsp;required;&nbsp;Advanced degree in health services research, statistics, epidemiology, or related&nbsp;field&nbsp;strongly&nbsp;preferred.&nbsp;&nbsp;
</li>
</ol>
Minimum Entrance Requirements:&nbsp; &nbsp; Analyst I: Applicants must have at least (A) two years of full-time, or equivalent part-time professional experience in business administration, health care planning or administration, public health policy or administration, human services policy analysis or administration or economics, the major duties of which included financial analysis of costs, expenses and revenue and/or the development, implementation and monitoring of financial reimbursement systems, or (B) any equivalent combination of the required experience and the substitutions below.&nbsp; &nbsp; Substitutions:&nbsp; I. A&nbsp;Bachelor's&nbsp;or higher degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public&nbsp;administration&nbsp;or economics may be substituted for the required experience.&nbsp; &nbsp; Analyst II: Applicant must have at least (A) three years of full-time, or equivalent part-time professional experience in business administration, finance, accounting, health care planning or administration, public health policy or administration, human services policy analyses or administration, economics, or a similar field; or (B) any equivalent combination of the required experience and the substitutions below.&nbsp;
Substitutions:&nbsp;
I. A Bachelor's degree with a major in health care administration, hospital administration, public health or health services administration, finance, accounting, business administration, business management, public policy, public administration, economics, or similar degree may be substituted for a maximum of two years of the required&nbsp;experience.*&nbsp;
II. A graduate degree with a major in health care administration, hospital administration, public health or health services administration, finance, accounting, business administration, business management, public policy, public administration, economics, or a similar degree may be substituted for a maximum of three years of the required&nbsp;experience.*&nbsp;
Analyst III: Applicant must have at least (A) four years of full-time, or equivalent part-time professional experience in business administration, health care planning or administration, public health policy or administration, human services policy analyses or administration, economics, the major duties of which included financial analysis of costs, expenses and revenue and/or the development, implementation and monitoring of the health care service delivery system and pricing methods. In addition, applicant must have a working knowledge of CHIA’s administration of nursing and residential care facility rate setting operations, including&nbsp;determining&nbsp;revised capital rates, setting rates for existing and new facilities, ownership changes, realty and management companies, and CHIA’s systems used to&nbsp;maintain&nbsp;nursing and residential care facility operations and rates.&nbsp;
Substitutions:&nbsp;
I. A Bachelor's degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public administration, economics, or similar degree may be substituted for a maximum of two years of the required&nbsp;experience.*&nbsp;
II. A graduate degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public administration, economics, or a similar degree may be substituted for a maximum of three years of the required&nbsp;experience.*&nbsp;
*Education toward such a degree will be prorated&nbsp;on the basis of&nbsp;the proportion of the requirements&nbsp;actually completed.&nbsp;
NAGE: Reimbursement Systems Analyst I (RSA I) and Reimbursement Systems Analyst II (RSA II)&nbsp;
The full&nbsp;salary band: &nbsp;
Analyst I/&nbsp;RSA I: $61,551.88&nbsp;- $87,921.34&nbsp;annually.&nbsp; Analyst II/&nbsp;RSA II: $70,757.18&nbsp;- $102,269.96&nbsp;annually.
Analyst II/&nbsp;RSA III: $81,166.28&nbsp;- $118,145.56 annually. &nbsp;
Total Compensation: &nbsp;
We value the talent and&nbsp;expertise&nbsp;you bring to the table. We offer a competitive salary range&nbsp;of $61,551.88 - $118,145.56&nbsp;annually&nbsp;for this position. Salary is&nbsp;commensurate&nbsp;with experience. CHIA may adjust title, responsibilities, and salary depending on the experience and&nbsp;expertise&nbsp;of the individual selected.  &nbsp;
Comprehensive Benefits  &nbsp;
When you embark on a career with the Commonwealth, you are offered an outstanding suite of employee benefits that add to the overall value of your compensation package. We take pride in providing&nbsp;a work&nbsp;experience that supports you, your loved ones, and your future.  &nbsp;
Want the specifics? Explore our Employee Benefits and Rewards!  &nbsp;
Together,&nbsp;let's&nbsp;embark on a journey of meaningful impact&nbsp;in&nbsp;healthcare. We invite you to&nbsp;join CHIA, where your&nbsp;expertise&nbsp;will shape the future of healthcare in Massachusetts. Likewise,&nbsp;we're&nbsp;eager to take a chance on you - to welcome a dedicated professional who shares our passion for making a difference. Join us in this collaborative endeavor, where&nbsp;we'll&nbsp;forge new paths, innovate, and lead the way toward a healthier Commonwealth. &nbsp;
Apply now and be part of our transformative journey at CHIA! &nbsp;
An Equal Opportunity / Affirmative Action Employer. Females, minorities, veterans, and persons with disabilities are strongly encouraged to apply.
The Commonwealth is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, disability, national origin, veteran status, or any other basis covered by appropriate law. Research suggests that qualified women, Black, Indigenous, and Persons of Color (BIPOC) may self-select out of opportunities if they don't meet 100% of the job requirements. We encourage individuals who believe they have the skills necessary to thrive to apply for this role.
Information submitted by applicants is collected through the JazzHR Platform, your submission of application materials constitutes your express consent for this information to be provided to JazzHR for processing. Please do not include any personally identifiable information with your application materials other than that specifically requested by CHIA. CHIA requests basic information such as name, address, telephone number, and email address. You may also self-identify with your race/ethnicity, gender, disability and/or veteran status. However, you should not provide more detailed personal information such as your date of birth or Social Security Number with your application materials.
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QtHTmBP6d8

Research Analyst

<h3>Job Description</h3>
Job DescriptionABOUT STRM.BIO STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genetic medicines that target the bone marrow. We’re a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We’re here to do great science and build a company we’re proud of. THE OPPORTUNITY We’re looking for Research Associates to help grow our research engine. You’ll work shoulder-to-shoulder with the Director of Research and a team of Scientists to support key programs and facilitate external collaborations. This is a hands-on, highly cross-functional role ideal for someone who’s ready to dive in and execute in equal measure. This is a full-time, on-site role. WHAT YOU’LL DO (Key Responsibilities)&nbsp;
<ul>
<li>Support the Research Team in efforts across multiple collaborative research programs &nbsp;</li>
<li>Contribute to R&amp;D efforts to meet project milestones, maintaining the standards of scientific rigor and adhering to ethical standards &nbsp;</li>
<li>Maintain standards consistent with company culture and values &nbsp;</li>
<li>Work closely with team members to maintain project development, implementation and troubleshooting of experiments &nbsp;</li>
<li>Generate, analyze, and share experimental results and ensure that all protocols, reagents, data, and analyses are documented following data integrity principles and prepared and made available in a timely manner &nbsp;</li>
<li>Attend team meetings to discuss results, future plans and experiments, with a keenness to help achieve company milestones &nbsp;</li>
<li>Maintain comprehensive and up-to-date knowledge of molecular and cellular biology techniques &nbsp;</li>
<li>Perform other duties as assigned, including all those associated with facilitating the smooth operation of a wet lab environment &nbsp;</li>
<li>Maintain accurate records in electronic lab notebooks (ELNs) and contribute to documentation for internal reports and regulatory filings &nbsp;</li>
<li>Attend regular EHS meetings and maintain accurate biologic and chemical records</li>
</ul>
WHAT YOU BRING (Required Qualifications)
<ul>
<li>B.S. or M.S. in biology, immunology, bioengineering, or related field</li>
<li>Some prior industry experience is strongly preferred</li>
<li>Academic or industry experience working with T cells in a research setting&nbsp;</li>
<li>Familiarity with gene-editing technologies (e.g., CRISPR, TALEN, ZFNs) and delivery platforms (e.g., viral vectors, LNPs, exosomes)</li>
<li>Previous involvement in in vivo studies or willingness to learn animal handling and vivarium protocols</li>
<li>Strong organizational and communication skills, with comfort operating in interdisciplinary project teams</li>
<li>Prior experience with CRO collaboration or CMC workflows is a bonus</li>
</ul>
KEY POSITION DETAILS
<ul>
<li>100% on-site in Cambridge, MA</li>
<li>Full time with competitive compensation
<ul>
<li>The salary range for this position is $70,000 to $90,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. &nbsp;</li>
</ul>
</li>
</ul>
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4Ulhi74kGw

Research Associate

<h3>Job Description</h3>
Job DescriptionSenior Product Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a Senior Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing new platform technologies for environmental protection and implementing at our customers around the world. A master’s or doctorate in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop functional materials, test methods, and implementation solutions for the environmental protection of automotive and consumer electronics.</li>
<li>Maintain project plans, timelines, and deliverables related to product launch strategy.</li>
<li>Communicate technical advances and project strategy to a global team of technical and sales personnel.</li>
<li>Work autonomously on open-ended projects, from new coating development to novel application techniques.</li>
<li>Expand actnano’s IP portfolio by innovating on coatings and application technology.</li>
<li>Serve as the subject matter expert on coatings and participate in developing customer implementation strategies.</li>
<li>Collaborate with cross-functional teams and maintain project plans, timelines, and deliverables for product launches.</li>
<li>Mentor technicians and co-ops on conducting experiments for coating development.</li>
<li>International and domestic travel is required.</li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $115,000 – $125,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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T2HGUzK02S

Senior Product Development Engineer / Scientist

<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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