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city

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<h3>Job Description</h3>
Job DescriptionOutstanding Benefits &amp; Hybrid Schedule | Collaborative &amp; Tenured Practice | Growth Track! This Jobot Job is hosted by: Christina Chariott Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $125,000 - $175,000 per year 
A bit about us:
 This full-service regional law firm has deep roots in New England and a longstanding reputation for client-focused legal work. The team values collaboration, integrity, and long-term relationships. Attorneys practice alongside like-minded professionals who care deeply about each other and their clients. The firm offers a supportive platform with full-time resources in IT, HR, accounting, legal writing, and business development -designed to help attorneys grow their practice and thrive. Currently expanding its Concord, NH office, the firm welcomes high-quality attorneys who want to be part of a collegial environment that prioritizes teamwork, professional growth, and meaningful client service. Apply now to learn more! 
Why join us?
 
<ul>
<li>Generous healthcare coverage: 90% paid by firm</li>
<li>Great tenure - most employees have been there 20+ years</li>
<li>Competitive compensation + bonuses + incentive compensation</li>
<li>Lots of growth and training opportunities</li>
<li>Established client base</li>
</ul>
 
Job Details
 Key Responsibilities: Advise high-net-worth individuals, families, and business owners on estate planning strategies and wealth transfer. Draft and review complex estate planning documents, including wills, trusts, powers of attorney, and healthcare directives. Handle probate and trust administration matters with precision and sensitivity. Provide guidance on gift, estate, and generation-skipping transfer tax issues. Collaborate with other attorneys across practice areas to deliver comprehensive client solutions. Maintain and grow client relationships through thoughtful, responsive service. Contribute to firm leadership and mentoring of junior attorneys, if desired. Qualifications: Juris Doctor (JD) from an accredited law school. Minimum of 10 years of experience in trusts and estates law. Admission to the New Hampshire Bar (or ability to waive in). Portable book of business of at least $275,000. Strong drafting, analytical, and communication skills. High ethical standards and professional integrity. Desire to work in a collaborative, team-oriented environment. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policyCompany DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Senior Trust & Estates Partner

<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 
We are seeking a highly skilled, passionate, and motivated scientist to join our Bioproduct Research and Development team. This position will play a key lab-based role in iPSC gene editing and will contribute to the development of next-generation islet cell therapies. Ideal candidates will have extensive hands-on experience with human iPSC culture, CRISPR-based gene editing, molecular biology, and assay development.&nbsp;
The successful candidate will be responsible for daily R&amp;D and GMP gene-editing operations, including iPSC culture, gene editing platform development and optimization, documentation preparation (SOP and batch record drafting and review), deviation investigation, raw material screening, clone characterization, and as well small-scale iPSC derived islet differentiation.
Key Responsibilities:
<ul>
<li>Lab-based role focused on advancing CRISPR-based iPSC gene editing and iPSC cell line generation to enable GMP readiness.</li>
<li>Develop and optimize gene-editing workflows, including gRNA design, RNP delivery, knock-in cargo design, clone genetic screening, and cell banking.</li>
<li>Characterize edited iPSC clones using DNA-based assays (PCR, qPCR, ddPCR), sequencing, flow cytometry, and next-generation sequencing (NGS).</li>
<li>Evaluate and implement iPSC culture media optimization and gene editing strategies to ensure genomic stability of iPSC lines.</li>
<li>Support and refine directed differentiation of iPSCs into islet cells and characterize resulting drug product attributes.</li>
<li>Perform hands-on iPSC gene editing within GMP settings to generate clinical-grade cell lines.</li>
<li>Draft, review, and execute SOPs and master batch records; ensure compliance with GMP, regulatory, and quality standards; support deviation investigations and maintain thorough documentation.</li>
<li>Participate in supplier qualification and sourcing of critical raw materials and consumables to ensure GMP readiness.</li>
<li>Demonstrate strong teamwork, communication, and organizational skills to manage multiple projects and timelines effectively.</li>
</ul>
Qualifications 
Minimum Required Qualifications:
<ul>
<li>Ph.D. in biology, bioengineering, or a related field with 0-1 years of relevant industry experience in iPSC gene editing and cell therapy.</li>
<li>Extensive experience with human iPSC culture, gene editing, and molecular biology techniques.</li>
<li>Proficiency in CRISPR gene editing, including optimization of protocols</li>
<li>Proficiency in gene editing workflows and molecular biology techniques including construct design, cell delivery methods, PCR, ddPCR, flow cytometry, and NGS.</li>
<li>Ability to troubleshoot and interpret experimental results and effectively present conclusions.</li>
<li>Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.</li>
<li>Strong organizational skills and diligent record keeping.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Hands-on GMP gene editing operational experience.</li>
<li>Experience in direct differentiation and scale-up of iPSC-derived cells.</li>
<li>Familiarity with electronic lab notebook (ELN) documentation.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process: 
<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 over Coffee for a Casual Discussion of the Role</li>
</ul>
The Position is full-time, Monday through Friday, 8am-5pm, with occasional weekends (on a rotational basis to support cell culture). Candidates currently living within a commutable distance of Boston, MA,&nbsp;are encouraged to apply.
What We Offer:
<ul>
<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>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
<li>Compensation is 84,000-91,000 anually&nbsp;</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.

Scientist - iPSC Gene Editing

<h3>Job Description</h3>
Job DescriptionTitle : Biologist Location : Boston MA Duration -12 months Pay :$35-$45/hr on w2 We are seeking a highly motivated Contractor – Purification Scientist to join our Downstream Process Development team. The successful candidate will contribute to the purification and characterization of viral vectors, biologics, or recombinant proteins to support process development and manufacturing activities. The ideal candidate has hands-on experience in ion-exchange chromatography, affinity purification, and tangential flow filtration (TFF), with a strong understanding of purification principles and data analysis. Key Responsibilities
<ul>
<li>Execute purification processes including affinity chromatography (e.g., AVB, Capture Select), ion-exchange chromatography (AEX, CEX), and other polishing steps.</li>
<li>Operate AKTA systems (Avant, Pure, or Pilot) for small- to large-scale purification runs.</li>
<li>Perform TFF operations for buffer exchange and concentration of intermediate or final products.</li>
<li>Support experimental design, data collection, and documentation following established procedures and GMP/GLP best practices.</li>
<li>Assist in troubleshooting and optimization of purification processes.</li>
<li>Analyze in-process and purified samples using relevant analytical methods (e.g., UV, SDS-PAGE, ddPCR, ELISA, or HPLC).</li>
<li>Collaborate cross-functionally with upstream, analytical, and manufacturing teams.</li>
<li>Maintain lab equipment, manage buffers and column inventory, and ensure compliance with safety and documentation standards.</li>
</ul>
 Quals--
<ul>
<li>Education: Master’s degree in Biochemistry, Chemical Engineering, Biotechnology, or related field.</li>
<li>Experience: Minimum 2 years of hands-on purification experience in an academic or industry setting.</li>
</ul>
 Technical Skills:
<ul>
<li>Strong knowledge and practical experience with ion-exchange and affinity chromatography.</li>
<li>Familiarity with buffer preparation.</li>
<li>Understanding of basic analytical methods for product characterization.</li>
</ul>
 Soft Skills:
<ul>
<li>Strong attention to detail and excellent documentation habits.</li>
<li>Effective communication and teamwork skills.</li>
<li>Ability to manage multiple tasks and meet project timelines.</li>
</ul>
 Preferred Qualifications
<ul>
<li>Experience in AAV or other viral vector purification.</li>
<li>Experience with AKTA systems and Unicorn software.</li>
</ul>
#sczr2

Biologist

<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 
Eurofins is seeking motivated individuals to join our team as Biochemistry Laboratory Associates supporting the development of a novel drug delivery platform. This full-time role offers hands-on experience in a dynamic, multidisciplinary environment. You will contribute to IND-enabling formulation activities and gain exposure to cutting-edge biopharmaceutical processes.
Key Responsibilities
<ul>
<li>Perform biochemical and microbiological assays</li>
<li>Conduct characterization and release testing of drug products using qualified methods</li>
<li>Maintain accurate records in electronic laboratory notebooks (ELN)</li>
<li>Assist with laboratory upkeep and instrument maintenance</li>
<li>Support technology transfer of biochemistry and microbiology methods to CDMO</li>
<li>Troubleshoot and resolve testing-related issues</li>
<li>Participate in internal and external audits</li>
<li>Stay current with industry developments and regulatory requirements</li>
</ul>
Qualifications 
<ul>
<li>Education: Bachelor’s degree in biochemistry, chemistry, biology, or related field</li>
<li>Experience: 0–2 years of relevant laboratory experience</li>
<li>Familiarity with techniques such as liquid chromatography (SEC, IEX, ProA, HIC), UV-vis spectroscopy, and capillary electrophoresis (CE-SDS, cIEF)</li>
<li>Knowledge of endotoxin/LAL testing and bioassays is a plus</li>
<li>Experience with aseptic techniques and sterilization processes desirable</li>
<li>Understanding of cGMP, GLP, and regulatory requirements preferred</li>
<li>Strong attention to detail and ability to document work accurately</li>
<li>Proficiency with MS Office, Teams, and SharePoint</li>
<li>Ability to work in a fast-paced, collaborative environment</li>
<li>Must be authorized to work in the U.S. without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday-Friday, First Shift.&nbsp;Candidates currently living within a commutable distance of&nbsp;Boston, MA&nbsp;are encouraged to apply
Excellent full-time benefits include:&nbsp;
<ul>
<li>Medical Coverage:&nbsp;Comprehensive medical insurance options</li>
<li>Dental &amp; Vision:&nbsp;Full dental and vision coverage available</li>
<li>Life &amp; Disability Insurance:&nbsp;Employer-sponsored plans</li>
<li>Retirement:&nbsp;401(k) plan with company match</li>
<li>Paid Time Off:&nbsp;Vacation days, paid holidays, and additional PTO options</li>
<li>Compensation: $24.00-$29.00 per hour</li>
</ul>
Ready to Start Your Career in Biopharmaceuticals?
Apply today and take the first step toward building your future with Eurofins!
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Biochemistry Laboratory Associate

<h3>Job Description</h3>
Job Description
Organization Overview
The National Institute for Children’s Health Quality (NICHQ) is a mission-driven nonprofit dedicated to driving dramatic and sustainable improvements in the complex issues facing children’s health. We provide deep expertise in building and managing effective change strategies that align partners and engage participants to achieve better outcomes for children’s health. 
Position Overview 
The Senior Analyst brings knowledge of and experience in applied research and evaluation and applies that knowledge to lead the successful design, execution and management of projects in the context of NICHQ’s maternal child health work. The Senior Analyst works closely and collaboratively with the Senior leadership in Programs and in the Department of Applied Research and Evaluation (DARE), project leads, Quality Improvement Advisors, expert faculty members, funders, and project teams to design and execute applied research and evaluation work that provides high-quality, relevant data analysis and recommendations across the lifecycle of projects. The Senior Analyst plays an integral and leadership role on NICHQ’s Applied Research and Evaluation team, guiding the department’s work (under the supervision of the Associate Director and senior leadership in DARE), as well as in the team’s work to capture, develop, and spread innovative approaches. The Senior Analyst may provide additional research consulting services and assist in elevating NICHQ’s standing in the scientific community by driving strategic planning for publications and conference presentations. 
Summary 
Career Level: Experienced 
Status: Full-Time, Exempt Employee, US Based Remote
Education: Master’s degree required; doctoral degree in relevant discipline preferred 
Reports to: Principal Analyst Department of Applied Research and Evaluation (DARE) 
Salary: $84,000 
Responsibilities 
<ul>
<ul>
<li>Applied research and evaluation tasks including
<ul>
<li>Planning
<ul>
<li>Create and implement plans for data management and analytic file creation</li>
<li>Collaborate with program staff to meet project deliverables on schedule</li>
</ul>
</li>
<li>Data collection and management
<ul>
<li>Design, build and maintain REDCap databases to support research data collection efforts</li>
<li>Create and optimize data collection instruments ensuring alignment with research objectives and reporting requirements</li>
<li>Develop and implement data collection protocols, including date entry guidelines, access controls and validation rules</li>
<li>Establish and maintain quality assurance and quality control systems</li>
<li>Perform data validation checks and produce reports for internal teams and external stakeholders</li>
<li>Investigate, track, and resolve data queries, support extant data transfer efforts</li>
<li>Lead data harmonization efforts across data sources</li>
<li>Provide technical guidance and support on REDCap functionalities and best practices to project teams</li>
</ul>
</li>
<li>Data analysis
<ul>
<li>Clean, transform, and validate data to ensure accuracy and readiness for analysis</li>
<li>Conduct descriptive and inferential analysis using statistical software such are SAS to inform research findings</li>
<li>Utilize knowledge of statistical methodology to inform study design and operations.</li>
<li>Provide consultation to other project teams on statistical analysis techniques (e.g., sampling, random assignment, application scoring and weighting), as needed</li>
<li>Keep abreast of current trends in statistical methods and program evaluation</li>
</ul>
</li>
<li>Reporting and dissemination
<ul>
<li>Prepare comprehensive summaries and graphic representations of statistical findings across different formats</li>
<li>Review abstracts for professional conferences and manuscripts for peer-reviewed publications</li>
<li>Provide consultation to project teams in their development of reports and other materials that include research data</li>
</ul>
</li>
</ul>
</li>
<li>Identifies and appropriately brings complex project insights, concerns, and potential solutions in a timely manner to project and DARE lead(s) and collaborates to implement solutions</li>
<li>May be responsible for the supervision and development of individuals working in applied research and evaluation</li>
<li>Represents the Applied Research and Evaluation team on projects in a collaborative and supportive manner and participates in other activities of the applied research and evaluation team as needed</li>
</ul>
</ul>
Skills and Knowledge
<ul>
<li>Demonstrates subject matter expertise in data management, biostatistics and/or epidemiology</li>
<li>Synthesizes complex information into usable formats</li>
<li>Works independently, capable of making decisions with limited oversight</li>
<li>Ability to manage multiple projects and meet deadlines with minimal support from supervisor while working remotely</li>
<li>Strong communications skills (both verbal and written)</li>
</ul>
 Qualifications and Characteristics
<ul>
<li>Master’s degree or MPH in biostatistics or epidemiology; at least 3 years’ work experience in a health services, social science, or clinical research setting doing quantitative research</li>
<li>Experience designing, building and maintaining REDCap databases</li>
<li>Extensive experience and strong programming skills in statistical software programs (e.g. SAS and R)</li>
<li>Proficient in Microsoft Office, visualization software and database management; adept at quickly learning new technologies</li>
<li>Detail-oriented “achiever” who takes initiative</li>
</ul>
Benefits 
We offer a generous benefits package for employees including competitive compensation; US based remote work; paid time off including vacation, sick and holidays; insurance including medical, dental, vision, disability and life; flexible spending accounts; employee assistance programs; paid parental leave and professional development benefits.
NICHQ is committed to increasing the representation of people from culturally and linguistically diverse backgrounds in our workforce and to value and embrace their skills, perspectives and experiences for the benefit of our mission. NICHQ is an equal opportunity employer; all qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender or gender expression, sexual orientation, age marital status or disability. NICHQ strongly encourages applications from candidates who identify as BIPOC, LGBTQIA+, or from any other minoritized group.
To Apply 
To apply for this employment opportunity, please complete and submit an online application at NICHQ.org.

Senior Analyst, Applied Research and Evaluation

<h3>Job Description</h3>
Job Title: Principal Research Scientist VI
Pay rate: $120-140/hr on w2 
Duration: 12 Months (possible opportunity to convert to perm after contract term)
Location: Lexington, MA
 
About the Role
We are seeking an experienced DMPK Project Representative to provide scientific leadership in the discovery and optimization of small-molecule drug candidates. This role leads DMPK strategy across multiple therapeutic areas and collaborates closely with cross-functional scientific teams.
The ideal candidate is an ADME or PK/PD subject matter expert with a strong project-facing background and a track record of impactful scientific contributions.
 
Top Skills
<ul>
<li>3+ years in a project-facing scientific leadership role</li>
<li>Expertise in ADME and/or PK/PD modeling</li>
<li>Strong publication/abstract history in metabolism, drug interactions, or PK/PD modeling</li>
</ul>
 
 Key Responsibilities
<ul>
<li>Serve as the DMPK representative on global, cross-functional small-molecule project teams</li>
<li>Provide expert guidance on experimental strategy, data interpretation, and DMPK strategy</li>
<li>Lead internal and external research efforts supporting drug discovery</li>
<li>Work closely with pharmacology, medicinal chemistry, and CRO teams</li>
<li>Design, troubleshoot, and interpret complex DMPK experiments (in vitro, in vivo, in silico)</li>
<li>Analyze sophisticated datasets and communicate findings to project stakeholders</li>
<li>Ensure accurate documentation and contribute to scientific reports, manuscripts, and milestone documents</li>
<li>Build collaborations with external scientific partners</li>
<li>Represent the organization as a subject matter expert at scientific conferences</li>
</ul>
 
 Qualifications
<ul>
<li>Bachelor’s degree with 18+ years experience,</li>
<li> OR Master’s degree with 12+ years,</li>
<li> OR Doctoral degree with 6+ years relevant post-doc/industry experience</li>
<li>Deep understanding of ADME principles; PK/PD modeling or biotransformation experience preferred</li>
<li>Experience working with outsourced or hybrid ADME models is a plus</li>
<li>Strong communication skills—verbal, written, and cross-functional</li>
</ul>
 
 Ideal Candidate
You thrive in a scientifically complex, highly collaborative environment and enjoy integrating DMPK strategy to advance drug discovery programs. You’re comfortable leading projects, influencing cross-functional teams, and representing DMPK expertise internally and externally.

Senior DMPK 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
Eurofins is seeking a highly motivated and detail-oriented lab associate who will be responsible for qualifying and performing analytical methods to support particulate testing of drug products. This role will begin in&nbsp;January 2026. This individual will work directly on a client site in Boston, MA, supporting a multidisciplinary team of scientists and engineers. The candidate will contribute to a variety of CMC activities in a fast-paced, agile, and highly collaborative environment.
Key Responsibilities:
<ul>
<li>Routinely perform batch and stability testing of drug products using qualified methods.</li>
<li>Troubleshoot and resolve testing-related issues.</li>
<li>Maintain accurate records and documentation of test results.</li>
<li>Regularly perform analytical data review and reporting of results.</li>
<li>Participate in internal and external audits.</li>
<li>Stay current with the latest industry developments and regulatory requirements.</li>
<li>Aid in the development and qualification of particulate assays.</li>
<li>Support the technology transfer of analytical methods to external parties.</li>
<li>Maintain safe laboratory working conditions following GLP and EHS guidelines.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree with 0-2 years of industry experience, in Chemistry or a related field.</li>
<li>Hands-on experience with microscopy techniques such as: Flow Imaging Microscopy (FIM), Scanning Electron Microscopy (SEM), Fluorescent Microscopy preferred.</li>
<li>Experience with other methods for particle characterization (e.g. Raman) and counting (e.g. light obscuration) is also desirable.</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for biotech and pharmaceutical industries is highly desirable.</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN) is a must.</li>
<li>Experience performing analytical data review and historical data evaluations.</li>
<li>Experience with writing SOPs and technical documents.</li>
<li>Familiarity with standard office software (MS Office, Teams, SharePoint).</li>
<li>Ability to work in a fast-paced, agile and highly collaborative environment is essential.</li>
</ul>
 Additional Information 
Position is full-time, Monday - Friday, 8:00 am - 5:00 pm.&nbsp; Candidates currently living within a commutable distance of Cambridge, MA, are encouraged to apply.
<ul>
<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>
<li>Compensation is between 23.00-29.00 per hour, depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Particulates Lab Associate

<h3>Job Description</h3>
Job Description
Senior Chemical Process Engineer Tewksbury, MA Direct Hire |
Summary
We are seeking a Senior Chemical Process Engineer with experience in process development, design, and construction of industrial facilities. This role will lead engineering efforts for complex process-facility projects, including new plant design, facility upgrades, and rehabilitation of high-hazard environments. The Senior Engineer will work closely with clients, vendors, contractors, and internal teams to deliver projects successfully.
Qualifications
<ul>
<li>B.S. in Chemical Engineering (minimum)</li>
<li>10+ years’ experience in chemical process engineering</li>
<li>Experience in process development, design, and construction</li>
<li>Ability to manage multiple projects and shifting priorities</li>
<li>Strong time management and leadership skills</li>
<li>Comfortable supervising junior engineers and collaborating with multidisciplinary teams</li>
<li>Background in chemical processing or related industries</li>
<li>Capital project management experience is a plus</li>
</ul>
Responsibilities
<ul>
<li>Lead and support engineering design for process-facility projects</li>
<li>Supervise and mentor engineering team members</li>
<li>Develop material &amp; energy balances and process flow diagrams (PFDs)</li>
<li>Prepare piping &amp; instrumentation diagrams (P&amp;IDs)</li>
<li>Size, specify, and procure equipment</li>
<li>Provide equipment and piping layout design support</li>
<li>Perform process and utility calculations</li>
<li>Support construction activities and process startups</li>
<li>Coordinate closely with vendors and clients to ensure requirements are met</li>
</ul>
Preferred Experience
<ul>
<li>Project management of capital projects</li>
<li>Construction support and startup/commissioning</li>
</ul>
Company DescriptionWhy Join · Collaborative, experienced engineering team. · Competitive salary &amp; full benefits. · Opportunity to deliver impactful next-generation products. 
<h3>Company Description</h3>
Why Join\r\n· Collaborative, experienced engineering team.\r\n· Competitive salary &amp; full benefits.\r\n· Opportunity to deliver impactful next-generation products.

Senior Chemical Process Engineer

<h3>Job Description</h3>
Job DescriptionCompany Summary:&nbsp;Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro’s lead program is Alpha-1 Antitrypsin Deficiency (AATD). Korro is based in Cambridge, Massachusetts. We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health. Position Summary: Korro Bio&nbsp;is&nbsp;seeking an analytical scientist to join the growing CMC team. You will focus on management of CMO analytical labs as well as development of analytical methods, characterization of impurities, degradation pathways, and transfer, qualification/validation of analytical methods for RNA-based therapies. This role will support and manage - the quality and stability of drug substances and drug products throughout the development lifecycle. You will work closely with cross-functional teams and external partners to ensure that analytical data supports regulatory filings and clinical trial progression.Key Responsibilities:
<ul>
<li>Serve as SME for RNA-based drug substance and drug product release and characterization assays including assay develop and optimize analytical methods as needed.</li>
<li>Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards.</li>
<li>Collaborate with the Process Development teams to ensure seamless integration of analytical methods into DS and DP manufacturing workflows.</li>
<li>Analyze, interpret, and present complex data to cross-functional teams and senior management.</li>
<li>Author and review technical reports, protocols, SOPs, and sections of regulatory filings (IND, IMPD etc.).</li>
<li>Assist in managing external analytical collaborations with CROs and CMOs, ensuring data quality and timelines are met.</li>
<li>Stay current with emerging analytical technologies and apply innovative solutions to improve method robustness and efficiency.</li>
<li>Support investigations and root cause analyses for any out-of-specification (OOS) results, deviations, or process failures.</li>
</ul>
Required Qualifications:
<ul>
<li>PhD in Analytical Chemistry, Biochemistry, Molecular Biology, or related field with 2+ years’ experience; or MS with 7+ years or BS with 9+ years of relevant industry experience.</li>
<li>3+ years of hands-on experience in analytical method development for biologics, with experience in RNA therapeutics preferred.</li>
<li>Expertise in chromatographic (e.g., UPLC -UV, and UPLC-MS) and spectroscopic techniques (e.g., UV-Vis), with a strong understanding of method validation requirements. </li>
<li>Familiarity with cGMP and ICH guidelines for analytical development and quality control of small molecules and/or biologics.</li>
<li>Experience with supporting design and management of stability studies, impurity profiling, and degradation pathways.</li>
<li>Expertise with managing primary and working reference standard qualification, aliquoting, and long-term management across all end users of the material.</li>
<li>Managed transfer, qualification, and ideally validation of methods.&nbsp; </li>
<li>Supported batch disposition, OOS, OOT, and investigations.</li>
<li>Excellent written and verbal communication skills, with experience drafting technical reports and regulatory documents.</li>
<li>Ability to work collaboratively in a fast-paced environment and manage multiple projects simultaneously.</li>
</ul>
Benefits:&nbsp; Korro offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior Scientist, Analytical Sciences

<h3>Job Description</h3>
Job Description
Why Join Us?
Parabilis Medicines, Inc is a biopharmaceutical company pioneering the discovery and development of Helicon™ peptide therapeutics; these ultra diverse alpha-helical peptides are capable of efficient cell entry and modulation of both protein-protein and protein-DNA interactions. Through Helicon therapeutics, Parabilis is poised to revolutionize the medical possibilities for patients by precisely drugging intracellular targets long understood to be significant drivers of disease but never before drugged due to the limitations of existing drug modalities to act within the cell. FOG-001, the company's first-in-class TCF-blocking β-catenin inhibitor, is being evaluated in a Phase 1/2 study for patients with advanced solid tumors, including desmoid tumors and colorectal cancer. Parabilis is fully leveraging the unprecedented potential Helicons present by deploying proprietary, custom-built machine learning and computational methods as part of its discovery and development process. Parabilis Medicines has raised more than $500 million to date from leading life sciences investors. Parabilis is headquartered in Cambridge, Mass.
What's the opportunity?
As a senior scientist at Parabilis and a biology lead for a preclinical oncology program, you'll help drive the biological strategy through candidate selection and IND-enabling studies, integrating mechanistic insight and in vitro/in vivo pharmacology for our one of our novel HeliconTM peptide programs. We're looking for a highly motivated Senior Scientist with significant experience in cell and molecular biology to report to the Sr. Director, Biology. 
Key Responsibilities: 
<ul>
<li>Independently design, execute, and interpret in vitro assays (e.g., viability, degradation, CRISPR/RNAi perturbation).</li>
<li>Work closely with pharmacology and chemistry colleagues to support in vivo validation studies and SAR decision making.</li>
<li>Oversee external work with CROs: write SOWs, ensure scientific rigor, timelines, and budget adherence. Work onsite with limited travel to oversee CROs.</li>
<li>Sit on a core team as the Biology Lead to hep drive go/ no-go recommendations. In partnership with the Program Lead, drive the biology strategy for a preclinical oncology program; define key hypotheses, decision points, and a data driven plan from hit to lead through IND enabling.</li>
<li>Mentor junior scientists and foster high standards for experimental design, documentation (ELN), and reproducibility.</li>
<li>Communicate clearly across levels: crisp slides, data packages, experimental plans, and narrative that link results to program decisions.</li>
</ul>
What you'll need to be successful:
<ul>
<li>Ph.D. and 5+ years of industry experience in cancer biology as a biology lead.</li>
<li>Experience in drug discovery, hit-to-lead process, degrader programs, and matrixed teams</li>
<li>Innovative, creative, inquisitive, motivated researcher with strong problem-solving skills.</li>
<li>Proficiency in a broad range of molecular and cellular techniques including: NanoBRET and HiBiT assays, western blotting, qPCR. transfection, immunofluorescence, flow cytometry, cell-based functional assays.</li>
<li>Experience in managing relationships with collaborators and/or CROs.</li>
<li>Excellent written and oral communication skills, and a track record of cross-functional collaboration</li>
<li>Proficiency in data analysis and statistics (e.g., GraphPad Prism, FlowJo; familiarity with R/Python or Spotfire is a plus).</li>
</ul>
Preferred but not required:
<ul>
<li>Biotech experience with ADC programs. </li>
<li>People management experience.</li>
<li>Publication/patent record that demonstrates depth in oncology or molecular/cell biology.</li>
<li>Familiarity with functional genomics (CRISP screens), multi-omics (RNAseq/singlecell/spatial), and imaging based pharmacodynamic readouts.</li>
<li>Prior contribution to IND submissions or regulatory interactions for nonclinical pharmacology.</li>
</ul>
Core Values
Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.
<ul>
<li>Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.</li>
<li>In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.</li>
<li>Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.</li>
<li>All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.</li>
</ul>
The base salary range for this position is $135,000-$165,000, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitivebenefits designed to support our employees' overall well-being.
As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
30 Acorn Park Drive | Cambridge, MA 02140 | <a href="http://www.parabilismed.com" target="_blank">www.parabilismed.com</a>

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