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<h3>Job Description</h3>
Job Description
The research scientist will play an integral role in the organic growth strategy focused on the development of new materials for the organization. The primary responsibilities of this position include advancing the growth processes of novel single crystalline materials such as Ga2O3, ultimately contributing to new product sales. Additional responsibilities encompass identifying, testing, and managing raw material inventories for the research and development team; designing experiments and conducting growth trials for crystalline materials; modifying furnace designs to facilitate crystal growth and enhance performance; monitoring the performance characteristics of the produced crystals; and supporting the transition of research and development initiatives to the production team. The ideal candidate should possess knowledge of semiconducting materials and general crystallography, along with experience or familiarity with various high-temperature oxides such as sapphire and garnets, as well as several growth methods, including Czochralski, EFG, HEM, and Bridgman, among others.
Key Responsibilities 
<ul>
<li>Assist in the development of Ga2O3 single crystal growth processes, including the planning and carrying out of growth trials, and reporting on overall developments.</li>
<li> Provide support for characterization of Ga2O3 crystals, either those grown internally or sourced from external vendors or collaborators. This includes characterization of material in house, and management of material sent for analysis externally.</li>
<li>Assist in defect identification, analysis, material improvement and scale up of EFG grown oxides.</li>
<li>Stay abreast of and provide information to others at Luxium Solutions on technical advances in the field of functional materials with a focus on materials for power electronics. </li>
</ul>
Requirements
<ul>
<li>Bachelor of Science in Materials Science, Physics, or Chemistry</li>
<li>Ph.D. preferred</li>
<li>Minimum of 5 years of experience in the development of ceramic materials, including but not limited to crystal growth, processing, and characterization.</li>
<li>A minimum of 5 years of experience in crystal growth technologies.</li>
<li>Comprehensive understanding of solid-state physics and/or materials science.</li>
<li>Effective written and oral communication skills are necessary for interface with internal team members, other operations within Luxium Solutions, and outside experts.</li>
<li>Advises manufacturing, engineering and sales on technical specifics.</li>
<li>Proficient in utilizing computer software relevant to an industrial research and development environment.</li>
<li>Demonstrated experience in defect engineering of ceramic materials and devices.</li>
<li>Strong organizational, analytical, and problem solving skills using root cause analysis methods</li>
<li>Experience with crystal growth techniques, such as Czochralski and EFG, is highly desirable.</li>
<li>Familiarity with semiconducting materials and their applications in electronics, along with experience in modular instrumentation for materials testing and characterization, is preferred.. </li>
<li>As an employer, we operate as an ITAR-regulated site and must comply with U.S. export control laws, which may limit employment to U.S. Citizen as defined under ITAR regulations</li>
</ul>
Benefits
Luxium Solutions offers a goal-oriented team dedicated to Safety, Excellence, Agility and Respect. Come pursue your career within a niche business and learn something that you can’t find anywhere else! We have a great benefits package with:
<ul>
<li>ANNUAL BONUS</li>
<li>Salary: $90,000-$117,000</li>
<li>Paid Time Off available on day one (pro-rated for new hires)</li>
<li>Medical/Dental/Vision/Prescriptions available on day one</li>
<li>Employer Paid Life Insurance and AD&amp;D</li>
<li>Short/Long Term Disability </li>
<li>HSA/FSA</li>
<li>EAP</li>
<li>401(k) &amp; company match</li>
<li>Generous Tuition Reimbursement</li>
<li>6 week Paid Parental Leave</li>
<li>&amp; many more!</li>
</ul>

Research Scientist

<h3>Job Description</h3>
Shift:
Monday through Friday, 8:00AM - 5:00PM
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
Associate Scientist I
Pace Analytical Life Sciences, LLC is a premier Contract Research and Development Organization located just north of Cambridge, MA providing pharmaceutical development services for small molecules, biologics, oligonucleotide therapeutics, and other biopharmaceutical drug candidates.
Compensation: $28.00 per hour
Summary
We seek a motivated Associate Scientist with laboratory experience to conduct analytical testing and development experiments that support our client’s effort to develop oligonucleotide and mRNA therapeutics. Our clients include biotechnology and pharmaceutical companies from new startups to those with global operations. This individual will conduct analytical and bioanalytical testing of samples using written procedures and support the development of new methods. Competitive applicants will be able to demonstrate a knowledge of analytical methods for pharmaceuticals, creative problem solving, an ability to collaborate in a cross-functional team, and clearly communicate scientific results. This is an entry level, full-time bench scientist position in Woburn, MA suitable for a recent graduate or someone of limited pharmaceutical experience.
General Responsibilities:
<ul>
<li>Perform testing with good documentation practices using written methods and procedures</li>
<li>Execute development experiments, analyze data, write analytical test methods.</li>
<li>Present results and planned experiments clearly and concisely both verbally and in written reports.</li>
<li>Strive to meet agreed-upon timelines and regularly communicate progress to other stakeholders.</li>
<li>Follow standard operating procedures and other guidance documents as directed by management.</li>
<li>Maintain scientific instruments and troubleshoot problems as needed.</li>
<li>Maintain a clean and organized laboratory including shared benches, sample storage, etc.</li>
<li>Continuously improve technical skills and acquire knowledge specific to the pharmaceutical industry.</li>
</ul>
An Ideal Candidate will possess skills in one or more of the following areas:
<ul>
<li>Experience using analytical instruments such as chromatography (HPLC/UPLC), electrophoresis (PAGE, CE), spectrometry (LC-MS), and spectroscopy (UV/Vis).</li>
<li>Experience using or developing methods to determine the identity, purity, and assay of drug substance and product samples.</li>
<li>Knowledge of the physical and chemical properties of biological polymers (e.g., RNA, DNA, proteins)</li>
<li>Understand the scientific principles of new analytical techniques as well as the hardware and software needed to operate scientific instruments.</li>
</ul>

Required Education and/or Experience:
<ul>
<li>Education in chemistry, biochemistry, or closely related discipline and a B.S. with 0 – 2 year’s of industry experience performing routine testing or developing analytical methods for nucleic acid-based therapeutics.</li>
<li>Strong understanding of physical sciences at the undergraduate level.</li>
<li>Excellent written and oral communication skills.</li>
<li>Flexibility and outstanding time management skills.</li>
<li>Background maintaining and troubleshooting scientific instruments and equipment.</li>
</ul>
PHYSICAL/MENTAL REQUIREMENTS:
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.
WORKING ENVIRONMENT:
Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gasses, noxious odors and related items in a lab setting.
OFCCP Statement - Pace Analytical is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
Benefits When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Associate Scientist 1

<h3>Job Description</h3>
Job Description
Frontier Medicines is seeking a highly motivated individual to fill the position of Principal Scientist, Computational Chemistry. The successful candidate will play a leading role in developing medicinal chemistry optimization strategies for key drug discovery programs. This individual will review experimental results, develop SAR hypotheses for activity, selectivity, and properties, and make design suggestions to improve the profiles of small molecule drug candidates.
As a covalent drug discovery–focused company, there is the opportunity for method development within this evolving field, in addition to applying the full range of ligand-based and structure-based design approaches and leveraging data from chemoproteomics, AI and quantum mechanics.
This role is key to Frontier Medicines’ success and an opportunity to work in a highly collaborative and energetic environment with short communication lines across functions and departments, and regular interactions with senior leaders. As the senior computational chemist, there is furthermore an opportunity to build out the computational team in the future
Requirements
What will you be doing? 
<ul>
<li>Design, execute, and analyze computational chemistry studies using a wide range of ligand-based, structure-based, and physics-based modeling techniques.</li>
<li>Partner closely with medicinal chemists and biologists to develop and refine structure–activity relationships (SAR), optimize molecular properties, and guide design hypotheses.</li>
<li>Contribute to project strategy and decision-making across all discovery stages, including target assessment, hit identification, lead optimization, and development candidate nomination.</li>
<li>Champion innovative computational tools and workflows, identify and implement emerging technologies that enhance Frontier’s CADD capabilities – specifically with an eye to the applicability to the covalent domain.</li>
<li>Work closely and partner with the AI team to develop and integrate novel AI applications into daily drug design workflows</li>
<li>Communicate scientific results, design rationales, and strategic insights to multidisciplinary teams and senior leadership.</li>
</ul>
What are we looking for? 
<ul>
<li>Ph.D. in Computational/Theoretical Chemistry, Biophysics, or a related discipline with 5+ years of relevant industry experience in drug discovery (biotech or pharma).</li>
<li>Demonstrated expertise in applying computational chemistry to small molecule design and optimization.</li>
<li>Strong experience with leading computational chemistry tools, CCG tools including MOE is highly preferred</li>
<li>Basic knowledge of scripting and programming with Python preferred</li>
<li>Experience with quantum mechanics (QM) is highly preferred</li>
<li>Proven track record of scientific impact, as evidenced by publications, patents, and successful project contributions.</li>
<li>Solid understanding of medicinal chemistry principles, SAR analysis, and ADMET optimization.</li>
<li>Excellent communication, presentation, and cross-functional collaboration skills.</li>
<li>Ability to operate independently and as a scientific leader in a fast-paced, startup environment.</li>
<li>Legally authorized to work in the U.S.</li>
</ul>
Benefits
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
<li>Family Leave (Maternity, Paternity)</li>
<li>Short Term &amp; Long Term Disability</li>
<li>Training &amp; Development</li>
<li>Free Food &amp; Snacks</li>
<li>Wellness Resources</li>
<li>Stock Option Plan</li>
</ul>
At Frontier, we strive to build a diverse and equitable workplace. The salary range for this role is $175,000 - $231,000. Compensation for the role will depend on a number of factors, including candidates' qualifications, skills, competencies and experience. Frontier offers a competitive total rewards package which includes healthcare coverage, 401k and a broad range of other benefits. 
This compensation and benefits information is based on Frontier's knowledge as of the date of publication, and may be modified in the future.

Principal Scientist, Computational Chemistry

<h3>Job Description</h3>
Job DescriptionJob Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Overview:
We’re seeking a detail-oriented and experienced Bench Chemist to join our team. This role is ideal for someone with a strong background in analytical chemistry who thrives in a fast-paced lab environment. You’ll be responsible for performing chemical analyses on raw materials, in-process samples, and finished products using advanced instrumentation and wet chemistry techniques.
Key Responsibilities:
<ul>
<li>Perform LC and GC testing on various sample types, including raw materials and finished goods.</li>
<li>Prepare samples, run calibration curves, and conduct system suitability and integration reviews.</li>
<li>Execute wet chemistry procedures such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance (e.g., column care, leak checks, pump seal replacement) in compliance with IQ/OQ/PQ standards.</li>
<li>Troubleshoot and maintain lab instruments to ensure optimal performance.</li>
<li>Support method validation efforts, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Assist with lab operations including inventory, cleanliness, and peer review of lab notebooks.</li>
<li>Draft and review SOPs to support quality and compliance.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Proficient in operating HPLC and GC systems independently.</li>
<li>Experience with small molecule testing in complex matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Skilled in chromatography software (OpenLab, ChemStation).</li>
<li>Strong commitment to lab safety and quality standards.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in wet chemistry, organic chemistry, formulation, or R&amp;D.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, MA.
Pay and Benefits
The pay range for this position is $40.00 - $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 Nov 17, 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.

Bench Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Overview:
We’re seeking a detail-oriented and experienced Bench Chemist to join our team. This role is ideal for someone with a strong background in analytical chemistry who thrives in a fast-paced lab environment. You’ll be responsible for performing chemical analyses on raw materials, in-process samples, and finished products using advanced instrumentation and wet chemistry techniques.
Key Responsibilities:
<ul>
<li>Perform LC and GC testing on various sample types, including raw materials and finished goods.</li>
<li>Prepare samples, run calibration curves, and conduct system suitability and integration reviews.</li>
<li>Execute wet chemistry procedures such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance (e.g., column care, leak checks, pump seal replacement) in compliance with IQ/OQ/PQ standards.</li>
<li>Troubleshoot and maintain lab instruments to ensure optimal performance.</li>
<li>Support method validation efforts, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Assist with lab operations including inventory, cleanliness, and peer review of lab notebooks.</li>
<li>Draft and review SOPs to support quality and compliance.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Proficient in operating HPLC and GC systems independently.</li>
<li>Experience with small molecule testing in complex matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Skilled in chromatography software (OpenLab, ChemStation).</li>
<li>Strong commitment to lab safety and quality standards.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in wet chemistry, organic chemistry, formulation, or R&amp;D.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, MA.
Pay and Benefits
The pay range for this position is $40.00 - $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 Nov 14, 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.

Bench Chemist - Food Industry

<h3>Job Description</h3>
Job DescriptionCompany Description 
Are you ready to take the next step in your career and join a company that truly values your contributions? At Eurofins PSS, we offer more than just a job—we provide a rewarding, enriching, and fulfilling career path with opportunities for growth and advancement.
As part of our team, you’ll work in state-of-the-art laboratories alongside passionate professionals dedicated to the testing, development, and advancement of life-saving drug products. Together, we’re making the world a healthier and happier place to live.
Eurofins PSS is a global leader in life sciences, delivering a unique range of analytical testing services that help ensure the safety, authenticity, and accuracy of products and their ingredients. We partner with some of the world’s largest companies to make life and our environment safer, healthier, and more sustainable.
Our people are our chemistry—and we’re looking for talented individuals like you to join us in making a difference.
Job Description 
Advance your scientific career in&nbsp;Indianapolis, a thriving center for pharmaceutical and biotech innovation. We’re seeking a&nbsp;Metrologist Group Leader&nbsp;to oversee equipment maintenance, qualification, and team development in a GMP-regulated lab environment. This is a full-time leadership role with&nbsp;relocation assistance provided&nbsp;to support your move.
&nbsp;Why Relocate to Indianapolis?
<ul>
<li>Affordable cost of living with vibrant urban and suburban options</li>
<li>Expanding life sciences and pharmaceutical ecosystem</li>
<li>Relocation support and onboarding assistance to help you settle in smoothly</li>
</ul>
&nbsp;What You’ll Do
<ul>
<li>Lead equipment maintenance and qualification activities across lab operations</li>
<li>Troubleshoot technical issues and serve as a subject matter expert on lab instrumentation</li>
<li>Collaborate cross-functionally with internal teams, vendors, and global quality groups</li>
<li>Recommend and implement process improvements to enhance lab efficiency</li>
<li>Supervise and mentor team members, manage workflow, and conduct performance reviews</li>
<li>Ensure compliance with GMP standards and maintain accurate documentation</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in physical sciences (e.g., chemistry, physics)</li>
<li>4+ years of&nbsp;industry lab experience, including leadership responsibilities</li>
<li>Strong troubleshooting skills and familiarity with CMMS systems</li>
<li>Excellent communication, organizational, and team leadership abilities</li>
<li>Authorization to work in the U.S. indefinitely without sponsorship</li>
<li>Willingness to relocate to Indianapolis –&nbsp;relocation support is available</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&nbsp;</li>
<li>Position is located in downtown Indianapolis, IN.&nbsp;</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Metrologist Group Leader - Relocation Opportunity to Indianapolis

<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 DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care.
Position Overview:
AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department in Cambridge, MA. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies.
Responsibilities:
<ul>
<li>Lead research efforts within a cross-functional team to advance new extrahepatic therapeutic targets for siRNA -based drug discovery.</li>
<li>Design and execute in vitro and in vivo proof-of-concept studies to assess target engagement, validate biological pathways and therapeutic benefits.</li>
<li>Develop and optimize assays and tools to evaluate siRNA library for their delivery, efficacy, and off-target risks.</li>
<li>Contribute scientific leadership and expertise in target biology, target selection and pipeline development.</li>
<li>Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor.</li>
<li>Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions.</li>
<li>Collaborate and effectively communicate results with key stakeholders and cross-functional teams throughout the organization.</li>
<li>Contribute as a primary author to scientific publications, presentations, and/or as a primary inventor of patent applications.</li>
<li>Mentor and support junior scientists within the team.</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>BS, MS, or PhD in cell biology, molecular biology, biochemistry, pharmacology or related field with typically 10+ (BS), 8+ (MS), or 0-3 (PhD) years of experience.</li>
<li>Demonstrated expertise in siRNA library design and screening for discovery programs.</li>
<li>Demonstrated experience in assay development, optimization, troubleshooting and high-throughput implementation for target identification and validation, mechanism of action studies, siRNA efficacy/biodistribution/stability assessments, and biomarker analysis.</li>
<li>Extensive hands-on experience and techniques for in vitro and in vivo sample process and analysis, including cell culture, RNA extraction, RNA quantification (RT-PCR, qPCR, ddPCR), next-generation sequencing (NGS) library preparation, protein assays (ELISA, Western Blot, JESS) and flow cytometry.</li>
<li>Proven capability to interpret complex biological data and derive mechanistic insights that guide program decisions for discovery programs.</li>
<li>Familiarity with immunological disease models, antibody-oligo-conjugates (AOCs), and multi omics approaches is highly desirable.</li>
<li>Highly self-motivated and capable of thriving in a fast-paced, collaborative team environment.</li>
<li>Strong written and verbal communication skills, with experience contributing to technical reports, publications, or regulatory documentation.</li>
</ul>
Why AbbVie?
AbbVie is a global biopharmaceutical company committed to bringing innovative medicines to patients in need. We offer a collaborative work environment, opportunities for professional growth, and the ability to make an impact on the future of healthcare. Join us and be part of a team that is transforming the landscape of genetic medicine.
How to Apply:
If you are passionate about advancing RNA-based therapeutics and have a track record of success in cell and molecular biology, we encourage you to apply! Please submit your resume and a cover letter outlining your relevant experience and why you would be a great fit for this position.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist I - siRNA, Pipeline Development

<h3>Job Description</h3>
Job Description
Harrison Gray Search has partnered with a prominent Boston-based multi-family office and investment advisory firm.
 
Job Description
 
The Associate role reports to the Managing Director of Investment Research and works in conjunction with the Portfolio Advisory and Family Office Management groups. The successful candidate will have some knowledge of financial markets and third-party managers, including traditional and alternative investments, as well as programming and database management experience.
 
Primary Responsibilities
 
The responsibilities are equally split, focusing on core investment research and crucial engineering/automation tasks.
 
Investment Research (~50%)
<ul>
<li>Maintain, update, and QA the research and manager databases, ensuring completeness, timeliness, and integrity of documents and data.</li>
<li>Source, screen, and monitor third-party managers/funds across traditional and alternative strategies (SMAs, mutual funds, ETFs, LPs).</li>
<li>Support thematic research aligned with the firm's macro views; draft concise research notes and contribute to Due Diligence Memoranda.</li>
<li>Participate in weekly research meetings; assist Portfolio Advisory with portfolio analysis and client-facing materials.</li>
</ul>
 
Engineering, Data &amp; Automation (~50%)
<ul>
<li>Build research tools, including scripts, notebooks, and lightweight apps that automate data intake, validation, transformation, and reporting.</li>
<li>Create reusable models and analytics, including screeners, factor/peer comps, performance/attribution and risk dashboards with clear documentation and an easy UI.</li>
<li>Systematize processes and codify recurring workflows (intake to diligence to approval to monitoring) and reduce manual steps via automation.</li>
<li>Produce dashboards and templates for investment memos, DD checklists, KPI trackers, and monitoring reports.</li>
</ul>
 
Qualifications
<ul>
<li>1-3 years of experience in investment research, manager due diligence, data analytics, or a related role (buy-side, allocator, consultant, data/research engineering).</li>
<li>Strong coding ability in Python, or similar, and SQL or comparable database management skills.</li>
<li>Proficiency in Excel (advanced formulas; Power Query or VBA a plus).</li>
<li>Experience building simple tools/dashboards (e.g., Power BI/Tableau or Python-based).</li>
<li>Familiarity with APIs, CSV/XLSX/PDF ingestion, and basic data QA/validation practices.</li>
<li>Solid grasp of investment concepts (returns, risk, factor exposures, benchmark construction, fees, share classes, liquidity terms), or willingness to take the time to learn.</li>
<li>Detail-orientation, strong organization, and the ability to own projects end-to-end.</li>
<li>Ability to write and present technical topics in a clear and effective manner.</li>
<li>Exposure to alternative investments and investment diligence a plus, but not required.</li>
<li>Experience with Bloomberg, FactSet, or CapIQ a plus, but not required.</li>
<li>Basic systems architecture and cloud literacy a plus, but not required.</li>
<li>Progress or interest toward CFA or CAIA.</li>
</ul>

Associate Investment Research Analyst

<h3>Job Description</h3>
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
This position is part of the R&amp;D department located in Waltham, MA and will be on-site. At Aldevron, we combine best-in-class products and service&nbsp;with the ideal operating environment to lay the groundwork&nbsp;for vital new discoveries worldwide. You will be a part of the cell-free DNA team and report to the Associate Director responsible for DNA and New Platforms. 
In this role, you will have the opportunity to:
<ul>
<li>Lead a small team to develop innovation to progress the strategy of the cell-free DNA platform</li>
<li>Manage project resourcing and timelines to deliver results</li>
<li>Perform experiments to improve quality or processes related to production of cell-free DNA</li>
<li>Establish new site operations including preparation of laboratory, installation of equipment, development of SOPs, etc.</li>
<li>Creating detailed project summary reports and presenting findings and recommendations to senior management.</li>
</ul>
The essential requirements of the job include:
<ul>
<li>PhD in biology, molecular biology, biochemistry, chemistry, or related discipline with 3+ years of experience, MS with 5+ years of experience, or BS with 8+ years of experience in related industry</li>
<li>At least 3+ years of experience (additional with educational achievement outlined above) in an industry R&amp;D setting with leadership responsibilities</li>
<li>Proven track record of developing novel assays/techniques to achieve molecular biology goals</li>
<li>Experience related to production, amplification, or modification of nucleic acids; purification of nucleic acids; and analytics related to nucleic acids</li>
<li>Experience in mammalian cell culture techniques including expression-based assays, flow cytometry, and cell viability assays</li>
</ul>
Travel, Motor Vehicle Record &amp; Physical/Environment Requirements:
<ul>
<li>Some travel may be required</li>
</ul>
It would be a plus if you also possess previous experience in:
<ul>
<li>Isothermal amplification of nucleic acids including rolling circle amplification (RCA)</li>
<li>Analytical methods using HPLC</li>
</ul>
Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

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