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<h3>Job Description</h3>
The successful candidate will join the Genomic Medicine Drug Product Development group. This individual will be an integral part of a dynamic and growing group of scientists and engineers developing adeno-associated virus (AAV) based gene therapy products within the larger organization. This team member will execute studies for the development of AAV formulations, fill-finish processes, and clinical device compatibility to ensure clinical and commercial readiness.
 
You will be responsible for:
<ul>
<li>Execution of formulation studies and non-GMP stability studies for AAV-based drug candidates</li>
<li>Clinical administrative device compatibility and In-use studies for clinical dosing enablement</li>
<li>Supporting the development of GMP fill finish processes</li>
<li>Developing presentations for internal presentations</li>
<li>Technical report authoring and data verification.</li>
</ul>
 
You will need to have:
<ul>
<li>BS in Pharmaceutics, Biochemistry, Chemical Engineering, or relevant field with 2+ years, a MS with 1+ years of relevant experience</li>
<li>Hands on experience with biologic drug development</li>
<li>Understanding of protein chemistry, formulation, and degradation</li>
<li>Ability to work effectively in a cross-functional settings</li>
<li>Excellent interpersonal and communication skills</li>
</ul>
 
Highly Valued:
<ul>
<li>Experience developing stabilizing, clinically acceptable formulations, and fill finish processes for biologics.</li>
<li>Experience with biopharmaceutical assays (CE, SEC, SVP analysis, DLS, etc.).</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Job Description🧪 Quality Control Lab Analyst – Contract to Hire
📍&nbsp;Location: Hadley, MA
🕒&nbsp;Schedule: Monday–Friday, 8:30 AM–4:30 PM or 9:00 AM–5:00 PM
🔬&nbsp;Join a growing team in a cutting-edge lab environment
&amp;#x1F31F;&nbsp;Help Us Ensure Quality from Molecule to Market
Are you a hands-on chemist with a passion for precision and product safety? Join our expanding team as a&nbsp;Quality Control Lab Analyst&nbsp;and play a critical role in testing and validating the ingredients that power health and wellness products. You’ll work in a dynamic lab setting, using advanced instrumentation and wet chemistry techniques to ensure every batch meets the highest standards.
This is a fantastic opportunity for someone who thrives in a collaborative, science-driven environment and wants to grow with a company that values innovation and integrity.
💼&nbsp;What You’ll Do
<ul>
<li>Prepare and test samples using GC and wet chemistry methods (pH, titrations, LOD).</li>
<li>Run calibration curves and system suitability tests to ensure accuracy.</li>
<li>Perform first-line instrument care and basic troubleshooting (GC, HPLC).</li>
<li>Support method validation efforts (accuracy, precision, LOD, LOQ).</li>
<li>Maintain lab inventory, cleanliness, and documentation standards.</li>
<li>Draft and review SOPs and participate in notebook peer reviews.</li>
</ul>
✅&nbsp;What You Bring
<ul>
<li>Bachelor’s degree in Chemistry (Master’s preferred).</li>
<li>3–5 years of QC lab experience in food, supplements, or natural products.</li>
<li>Independent operation of&nbsp;GC and HPLC&nbsp;instruments.</li>
<li>Experience with lipid-rich or natural product matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with&nbsp;USP/AOAC methods&nbsp;and&nbsp;cGMP documentation.</li>
<li>Proficiency in chromatography software (OpenLab, ChemStation).</li>
<li>Strong lab safety mindset and attention to detail.</li>
</ul>
&nbsp;Why You’ll Love This Role
<ul>
<li>Work in a growing organization with room to influence lab operations.</li>
<li>Be part of a team that values scientific rigor and continuous improvement.</li>
<li>Enjoy a stable weekday schedule with flexibility in start time.</li>
<li>Opportunity to transition into a permanent role with long-term growth potential.</li>
</ul>
Ready to make your mark in quality control?
Apply today and help us deliver safe, effective products backed by science.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hadley,MA.
Application Deadline
This position is anticipated to close on Sep 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Qc Lab Analyst

<h3>Job Description</h3>
Job Description
Position: Supervisor, Senior Scientist – In Vivo Pharmacokinetics
Salary Range: $120,000 - $135,000 / yr
Location: Boston, MA
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit <a href="http://www.pharmaron.com" target="_blank">www.pharmaron.com</a>.
Job Overview:
We are seeking a Supervisor, Senior Scientist with deep expertise in In Vivo Pharmacokinetics (PK) studies to lead and contribute to our DMPK team. This role combines hands-on scientific work with leadership responsibilities, including supervising technical staff, overseeing rodent PK study design and execution, and ensuring compliance with AAALAC and IACUC guidelines.
Key Responsibilities
<ul>
<li>Establish, train and provide scientific direction, oversight, and guidance to the technical staff that support in vivo studies.</li>
<li>Design, supervise, and conduct rodent PK studies, ensuring compliance with AAALAC and IACUC guidelines.</li>
<li>Draft, review, and interpret study protocols, data, and reports with scientific rigor and accuracy.</li>
<li>Ensure efficient scheduling of studies and staff to optimize capacity and deliver high-quality results on time.</li>
<li>Partner with project management, business development, and bioanalysis teams to ensure seamless client interactions and study execution.</li>
<li>Act as a technical representative in sales discussions with new and prospective clients.</li>
<li>Implement harmonized processes, best practices, and state-of-the-art methodologies for PK studies.</li>
<li>Recommend and implement strategies to improve productivity, increase efficiency, and maintain scientific excellence.</li>
</ul>
What We're Looking For:
<ul>
<li>PhD, MS, or BS in Pharmacokinetics, Chemistry, Biochemistry, or related discipline.</li>
<li>5+ years of laboratory experience in a CRO environment.</li>
<li>3+ years of management experience, including staff development and budget oversight.</li>
<li>Strong expertise in rodent PK studies, including dosing, sampling, and tissue collection/processing.</li>
<li>Proficiency with noncompartmental analysis (Phoenix WinNonlin) is required.</li>
<li>Proven ability to manage multiple projects while maintaining attention to detail and high-quality standards.</li>
<li>Excellent written and verbal communication skills, with a client-focused mindset.</li>
</ul>
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
<ul>
<li>Insurance including Medical, Dental &amp; Vision with significant employer contributions</li>
<li>Employer-funded Health Reimbursement Account</li>
<li>Healthcare &amp; Dependent Care Flexible Spending Accounts</li>
<li>100% Employer-paid Employee Life and AD&amp;D Insurance, Short- and Long-Term Disability Insurance</li>
<li>401k plan with generous employer match</li>
<li>Access to an Employee Assistance Program</li>
</ul>
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-MC1

Supervisor, Senior Scientist - In Vivo Pharmacokinetics

<h3>Job Description</h3>
Job DescriptionHiring for a Quality Control Lab Analyst in Hadley!
Job Description
We are seeking a dedicated Quality Control Lab Analyst to join our growing team. This role involves conducting GC testing of raw materials, in-process samples, and finished goods. The successful candidate will play a key role in ensuring the quality and safety of our products.
Responsibilities
<ul>
<li>Prepare samples across various matrices and run calibration curves and system suitability tests.</li>
<li>Perform wet chemistry tests, including pH, titrations, and loss on drying (LOD).</li>
<li>Provide first-line instrument care, such as column maintenance and addressing leaks and pump seals, following IQ/OQ/PQ guidelines.</li>
<li>Conduct basic troubleshooting and maintenance of laboratory instruments.</li>
<li>Support method validation work, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Flexibly support lab needs, including inventory management, lab cleanup, and notebook peer review.</li>
<li>Draft and review Standard Operating Procedures (SOPs).</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry is necessary; a Master's degree in Chemistry or Analytical Chemistry is preferred.</li>
<li>3-5 years of experience in a QC lab within the food or supplement industry.</li>
<li>Demonstrated independent operation of HPLC and GC.</li>
<li>Experience with natural product or lipid-rich matrices, including small molecule testing like vitamins, fats, emulsifiers, and actives.</li>
<li>Working knowledge of USP/AOAC methods and cGMP documentation.</li>
<li>Proficiency in chromatography software such as OpenLab and ChemStation.</li>
<li>Strong lab safety mindset and approach to work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience as a bench lab analyst or chemist.</li>
<li>Proficiency in titration and wet chemistry.</li>
<li>Experience with ICP-MS.</li>
</ul>
Work Environment
The position is based in a laboratory/manufacturing setting. The work schedule is Monday through Friday, with working hours from 8:30 am to 4:30 pm or 9 am to 5 pm. As a smaller organization looking to expand, this role offers significant opportunities for growth and influence in the day-to-day operations of the lab.
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, Massachusetts.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hadley,MA.
Application Deadline
This position is anticipated to close on Sep 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
We are seeking a Scientist to join our client’s Manufacturing Sciences &amp; Technology team in Devens, MA. This role supports the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing.
You will collaborate closely with Manufacturing, Quality Assurance, Quality Control, Supply Chain, and Procurement on cross-functional teams to ensure GMP compliance and continuity of supply.
Key responsibilities include:
<ul>
<li> Qualify alternative raw material suppliers and partner with Procurement to identify new options. </li>
<li> Recommend and lead necessary testing to qualify materials for GMP manufacturing. </li>
<li> Author technical equivalency assessments, specification comparisons, material characterization reports, and change controls. </li>
<li> Support material and consumable manufacturing investigations. </li>
<li> Manage supplier change notifications and evaluate risks to maintain GMP compliance. </li>
<li> Contribute to risk assessments and material specification development. </li>
<li> Partner with cross-functional teams to deliver results in a fast-paced, matrixed environment.</li>
</ul>
Requirements
Bachelor’s or Master’s degree in Material Science Engineering, Chemistry, or related field with 2+ years of industry experience, or a PhD. 
 Strong technical writing skills and ability to author GMP documentation. 
 Experience in cross-matrix team environments and stakeholder collaboration. 
 Proven ability to manage multiple projects in a fast-paced setting. 
 Independent contributor with strong communication and interpersonal skills. 
 Experience with GMP change controls and investigations preferred. 
 Familiarity with analytical techniques (FTIR, SEM-EDS, etc.) and data trending/analysis a plus. 
 Awareness of cGMP regulations and compliance requirements.
Benefits
Competitive hourly rate: $67.20 – $75.20/hr (W-2 only, no C2C)
 Hybrid schedule (50% onsite Tue–Thu; full onsite during the first month) 
 12-month contract with possible extension 
 Health benefits, holiday pay, and 401(k) program 
 Paid time off (UTO) and professional development support 
 Employee referral bonus program 
 Opportunity to contribute to high-impact projects with a leading biopharma company

Scientist - GMP Quality & Technical Writing (Hybrid, Devens MA)

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Analytical Chemist – Method Development &amp; Validation
Location:&nbsp;Tewkesbury, MA
Employment Type:&nbsp;Full Time - Permanent 
Experience Level:&nbsp;Intermediate
Overview:
We are seeking a highly skilled&nbsp;Analytical Chemist&nbsp;to join our team in supporting the development, validation, and implementation of analytical methods for pharmaceutical products. This role involves hands-on testing using advanced instrumentation, troubleshooting analytical issues, and ensuring compliance with GMP standards. The ideal candidate will have a strong experience in analytical chemistry and experience with a wide range of techniques and equipment.
Key Responsibilities:
<ul>
<li>Develop and optimize new analytical methods and techniques for product release.</li>
<li>Validate and verify analytical methods in accordance with regulatory and internal standards.</li>
<li>Investigate out-of-specification (OOS) results, out-of-trend (OOT) data, and equipment failures.</li>
<li>Analyze and present trending data to support method development and validation efforts.</li>
<li>Perform analytical testing of organic and inorganic compounds using FTIR, HPLC, NMR, LCMS, GCMS, ICP-MS, GC, and wet chemistry techniques.</li>
<li>Author test procedures and provide analytical support for research and development projects.</li>
<li>Follow GMP guidelines and contribute to continuous improvement initiatives.</li>
<li>Train and mentor junior team members as needed.</li>
</ul>
Required Skills &amp; Expertise:
<ul>
<li>Strong proficiency in analytical techniques including NMR, GCMS, HPLC, FTIR, LCMS, ICP-MS, and wet chemistry.</li>
<li>Deep understanding of GMP regulations and quality systems.</li>
<li>Experience conducting method development, validation, and troubleshooting.</li>
<li>Ability to work independently and collaboratively in a fast-paced environment.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree (MS) in Chemistry or Biochemistry with 3–5 years of relevant experience, or</li>
<li>Bachelor’s degree (BS) in Chemistry or Biochemistry with 5–7 years of experience.</li>
<li>Proven experience working with advanced analytical instrumentation in a pharmaceutical setting.</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $75000.00 - $85000.00/yr.
Company provides holiday, vacation, and 401k benefits. They will be able to gain bonuses past on company and personal performance.
Workplace Type
This is a fully onsite position in Tewksbury,MA.
Application Deadline
This position is anticipated to close on Sep 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a detail-oriented and motivated&nbsp;QC Microbiologist II to support microbiological testing and laboratory operations in a&nbsp;GMP-regulated environment. This role is critical to ensuring the quality and safety of pharmaceutical products through sterility, endotoxin, and bioburden testing, as well as general lab support and data review.
Key Responsibilities
<ul>
<li>Perform&nbsp;endotoxin and bioburden testing&nbsp;using standard microbiological methods (e.g., membrane filtration, LAL)</li>
<li>Conduct&nbsp;sterility testing&nbsp;and support microbial challenge recovery of drug substances and raw materials</li>
<li>Prepare microbial cultures for&nbsp;validation protocols,&nbsp;developmental studies, and&nbsp;growth promotion testing</li>
<li>Perform&nbsp;growth promotion,&nbsp;mold spore suspension, and&nbsp;water activity testing</li>
<li>Read and interpret microbial plates and document results accurately</li>
<li>Maintain lab cleanliness and organization, including&nbsp;cold room 5S, stocking supplies, and general housekeeping</li>
<li>Review and verify data for accuracy and compliance with cGMP standards</li>
<li>Utilize&nbsp;LIMS&nbsp;and&nbsp;electronic laboratory notebooks&nbsp;for data entry and tracking</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Microbiology, Biology, or a related scientific field</li>
<li>1–2 years of relevant experience in a&nbsp;Quality Control Microbiology&nbsp;or similar laboratory setting</li>
<li>Hands-on experience with:
<ul>
<li>Bioburden testing&nbsp;(membrane filtration)</li>
<li>Endotoxin testing&nbsp;(LAL)</li>
<li>Sterility testing&nbsp;(preferred)</li>
<li>Aseptic techniques and microbial culture preparation</li>
</ul>
</li>
<li>Familiarity with&nbsp;cGMP guidelines&nbsp;and regulatory compliance</li>
<li>Proficiency in&nbsp;Microsoft Word and Excel</li>
<li>Strong understanding of&nbsp;experimental design, data interpretation, and scientific methodology</li>
<li>Authorized to work in the United States 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 Onsite Meeting with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, first shift, Monday-Friday from 8 am-5 pm. Candidates must be flexible to adapt to schedule&nbsp;changes requiring shift changes and/or weekend work, and overtime may be required as needed.&nbsp;Candidates living within a commutable distance of Andover, MA,&nbsp;are encouraged to apply.&nbsp;&nbsp;
Benefits
<ul>
<li>Comprehensive&nbsp;medical, dental, and vision&nbsp;coverage</li>
<li>Life and disability insurance</li>
<li>401(k)&nbsp;with company match</li>
<li>Paid vacation and holidays</li>
<li>Annual goal-based bonus&nbsp;and&nbsp;merit-based increases</li>
<li>$27–$30/hour (based on education and experience)</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

QC Microbiologist II

<h3>Job Description</h3>
Job DescriptionJob Title: Scientist IV Location: Cambridge, MA 02141 Duration: 12 Months+ (Possible Extension) Shift: Standard shift Pay Range: $100 - $111/ hr. on W2 Must have experience: 
<ul>
<li>PHD or Master’s degree Molecular Biology, Cellular Biology, Genomics, or a related field. </li>
<li>Minimum of 1+ years of dedicated single cell and Next gen sequencing experience with demonstrated expertise in transcriptomics and spatial biology. </li>
<li>scRNA-seq and snRNA-seq, Bulk RNA-seq, Next-Gen Sequencing (NGS) </li>
<li>Preferred qualifications: 3-5 years of related of dedicated single cell and Next gen sequencing experience with demonstrated expertise in transcriptomics and spatial biology. </li>
<li>scRNA-seq and snRNA-seq o Spatial transcriptomics platforms (e.g., 10x Genomics Visium and/or Xenium, NanoString GeoMx). </li>
<li>Spatial proteomics technologies (e.g., Akoya CODEX/Phenocycler-Fusion) </li>
<li>Proficiency in tissue handling, imaging, and histological techniques. </li>
<li>Familiarity with bioinformatics tools and pipelines for omics data analysis. </li>
<li>Fully onsite role</li>
<li>Position is 100% lab-based</li>
</ul>
 Job Description: 
<ul>
<li>We are looking for a highly motivated and innovative scientist to join the Target, Disease &amp; Systems Biology (TDSB) department at Client as a Scientist. In this role, you will collaborate with the Pre-clinical Omics research team to investigate disease biology, uncover Client pathways and mechanisms, and identify strategies to address unmet medical needs across a range of therapeutic areas.</li>
<li>This position offers the opportunity to apply cutting-edge molecular biology and spatial technologies to advance our therapeutic discovery efforts. The ideal candidate will bring strong technical expertise in bulk RNA-seq, single-cell/single-nucleus RNA-seq (sc/snRNA-seq), spatial transcriptomics, and spatial proteomics to support a broad Product of research initiatives.</li>
</ul>
<ul>
<li>We are seeking someone who can lead and execute scientific research, analyze and present complex data, and communicate effectively with both expert and non-expert audiences. Strong organizational skills—including meticulous record keeping, planning and scheduling, and maintaining laboratory equipment—are essential. The successful candidate will be curious, Product, and creative in exploring new scientific directions and proposing innovative experimental approaches.</li>
<li>At Client, we are an innovative global healthcare company driven by a singular purpose: to chase the miracles of science to improve people’s lives. We offer a dynamic environment where you can thrive professionally, build meaningful connections, and push the boundaries of scientific discovery. Ready to begin your journey?</li>
</ul>
 Responsibilities:
<ul>
<li>Experimental Design &amp; Execution
<ul>
<li>Design and perform experiments using bulk RNA-seq, single-cell/single-nucleus RNA-seq (sc/snRNA-seq), NGS and spatial assays (GeoMx, Visium, Xenium, Phenocycler-Fusion) on human and non-human biological samples.</li>
<li>Optimize and troubleshoot protocols for molecular and spatial assays.</li>
</ul>
</li>
<li>Data Analysis &amp; Interpretation
<ul>
<li>Collaborate with bioinformatics teams to analyze high-dimensional omics data.</li>
<li>Interpret results to guide therapeutic target identification and validation.</li>
</ul>
</li>
<li>Technology Development &amp; Innovation
<ul>
<li>Evaluate and implement emerging molecular biology and spatial technologies.</li>
<li>Contribute to the development of Client workflows and platforms.</li>
</ul>
</li>
<li>Cross-functional Collaboration
<ul>
<li>Work closely with scientists across biology, chemistry, and computational disciplines.</li>
<li>Present findings in internal meetings and contribute to strategic research discussions.</li>
</ul>
</li>
<li>Documentation &amp; Reporting
<ul>
<li>Maintain detailed experimental records.</li>
<li>Prepare technical reports and presentations</li>
</ul>
</li>
</ul>
 Qualifications: Master’s degree or Ph.D. in Molecular Biology, Cellular Biology, Genomics, or a related field. 3–5 years of relevant experience in academia or industry, with demonstrated expertise in transcriptomics and spatial biology. Required qualifications:
<ul>
<li>scRNA-seq and snRNA-seq</li>
<li>Bulk RNA-seq</li>
<li>Next-Gen Sequencing (NGS)</li>
</ul>
<ul>
<li>Preferred qualifications:</li>
<li>Spatial transcriptomics platforms (e.g., 10x Genomics Visium and/or Xenium, NanoString GeoMx).</li>
<li>Spatial proteomics technologies (e.g., Akoya CODEX/Phenocycler-Fusion)</li>
<li>Proficiency in tissue handling, imaging, and histological techniques.</li>
<li>Familiarity with bioinformatics tools and pipelines for omics data analysis.</li>
<li>Strong problem-solving skills and ability to work independently and collaboratively.</li>
<li>Excellent communication and organizational skills.</li>
</ul>
 #sczr2

Scientist IV

<h3>Job Description</h3>
Job Description
Nanopath is a well-funded Series A-stage company working to develop a first-in-class in vitro diagnostics platform to revolutionize the way we diagnose disease. Nanopath works to disrupt existing lengthy molecular testing methodologies by bringing them closer to the patient. We aim to improve the lives of patients, starting with women, using our purpose-built tool that provides actionable information within a single office visit.
The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. As a company, we are committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social - is at the forefront of our decision making.
About the Role
<ul>
<li>Support and manage a variety of assay development tasks. We are happy to tailor key responsibilities to the candidate ranging from molecular biology, cell culture, biomanufacturing, and bioinformatics. </li>
<li>Participate in critical team discussions, meetings, and presentations. Our co-ops are given critical and important projects!</li>
<li>Work directly with our tight-knit team of scientists and engineers to drive our product forward.</li>
<li>Learn more about cutting edge biophysics and interdisciplinary medtech development.</li>
</ul>
Qualifications:
<ul>
<li>Ability to commit to 15+ weeks of full-time and onsite work in Cambridge, MA</li>
<li>Sophomore or above with demonstrated experience through past internships or research projects</li>
<li>Excellent communication and presentation skills, highly organized with demonstrated curiosity, scientific rigor and creative problem-solving</li>
<li>Proactive self-starter with eagerness to adapt to a fast-paced, dynamic startup environment</li>
<li>Passion for technology translation and willingness to shape Nanopath's future</li>
<li>Current enrollment in a relevant academic program - we are open to undergraduate and graduate degree opportunities</li>
</ul>
This is a full-time onsite role in Cambridge, MA starting in early January, lasting no less than 5 months.
Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles!
Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

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