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<h3>Job Description</h3>
Yoh presents an excellent long-term&nbsp;Internal Laboratory Testing Coordinator&nbsp;opportunity with a trusted, long-term client located in Waltham, MA. Scientist/Sr. Research Associate -ESI&nbsp;Multiplex assays/Flow Cytometry Scientist/Sr. Research Associate The Yoh resource is expected to apply expertise across several areas in support of Sanofi Vaccines R&amp;D Global Immunology function developing innovative vaccine solutions for infectious diseases. Key Responsibilities:
<ul>
<li>Design and execute complex immunological experiments to evaluate vaccine candidates</li>
<li>Analyze immune responses using state-of-the-art techniques including multiparameter flow cytometry, ligand-binding, and cell-based assays</li>
<li>Support optimization of the automation of protocols and testing of the samples in automated immune assays as needed</li>
<li>Develop novel immunological assays to support vaccine development programs</li>
<li>Generate, analyze, visualize, and interpret scientific data sets, record experimental procedures and raw and analyzed data in electronic laboratory notebook</li>
<li>Author technical reports, SOPs, and contribute to regulatory submissions as required</li>
<li>Prepare and present findings to internal stakeholders</li>
<li>Provide technical guidance to junior team members as required</li>
<li>Collaborate within immunology and cross-functional teams across R&amp;D</li>
<li>Comply with the company HSE policies and minimize risk to self, others, and the environment, consistent with the community and industry standards.</li>
</ul>
Required Responsibilities:
<ul>
<li>Expertise in cellular and molecular immunology techniques</li>
<li>Proven experience with:</li>
<li>Spectral flow cytometry or flow cytometry with primary mammalian cells</li>
<li>Primary cells isolation and culture</li>
<li>Immunological assays development and implementation (ligand binding, multiplex (Luminex, MSD), cell-based)</li>
<li>Data visualization and analysis</li>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent documentation and record-keeping abilities</li>
<li>Proficiency in standard laboratory software and data analysis tools</li>
<li>Strong written and verbal communication skills</li>
</ul>
Preferred Responsibilities:
<ul>
<li>Experience with vaccine development or infectious disease research</li>
<li>Working knowledge of Good Research Practices (GRP) and electronic note booking</li>
<li>Proficiency in advanced data analysis tools (FlowJo, OMIQ, GraphPad Prism, &amp; other)</li>
<li>Experience with automated/semi-automated platforms/ liquid handlers</li>
</ul>
Education Experience:
<ul>
<li>Data Review</li>
<li>Training</li>
<li>Scheduling</li>
<li>GDP</li>
<li>GRP, compliance requirements for clinical trial samples</li>
<li>Master's degree in Immunology, Microbiology, or related field with 2+ years of relevant industry or academia experience</li>
<li>Bachelor's degree with 4+ years of relevant experience</li>
<li>Experience in pharmaceutical or biotechnology industry preferred. </li>
</ul>
 Estimated Min Rate: $31.50 Estimated Max Rate: $45.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities </li>
</ul>
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:&nbsp;<a href="https://www.yoh.com/privacy-notice" target="_blank">https://www.yoh.com/privacy-notice</a>

Scientist/Sr. Research Associate-ESI Multiplex assays/Flow Cytometry

<h3>Job Description</h3>
Central Processing Supervisor, Core Laboratory - Evening Shift
Location: Boston Teaching Hospital
 
<ul>
<li>Evening Shift: 3p – 11:30p ($3/hr evening diff).</li>
<li>Must be ASCP certified (or equivalent).</li>
<li>Sign-on bonus eligible.</li>
</ul>
 
Responsibilities:
<ul>
<li>Responsible for coordinating the daily operation of the front office of the core laboratory.</li>
<li>Oversees all Pre and Post analytic activity on the evening shift, in close conjunction with the day shift MT Operations Coordinator, reference lab staff, and other individuals who oversee areas that have an overlapping operating relationship with Central Processing.</li>
<li>Ensures that all activities, processes and policies are carried out in strict compliance with governmental regulations, licensing agency standards, and hospital policies and procedures.</li>
<li>Responsible for day-to-day general management including staffing, schedules, payroll, performance management, training, education, development of policy and protocol, compliance, and safety.</li>
<li>FTE's: 25+/-.</li>
<li>Reports to the Technical Director of Pre/Post Analytics in the Core Laboratory.</li>
</ul>
 
Qualifications:
<ul>
<li>MT (ASCP) or equivalent.</li>
<li>Bachelor’s Degree in Medical Technology or physical sciences.</li>
<li>4+ years of hospital laboratory experience, including knowledge of &amp;/or experience with pre/post analytics &amp;/or central processing.</li>
<li>1+ years of leadership experience.</li>
<li>Preferred: experience overseeing non-exempt hourly staff.</li>
</ul>

Central Processing Supervisor, Core Laboratory

<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
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>
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 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 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>
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.
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Sr Scientist I R&D

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
Direct the development and establishment of processes in Process Development. This individual is accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. The individual will provide technical expertise and leadership in science &amp; technology and requires close collaboration with internal stakeholders.
JOB RESPONSIBILITIES
<ul>
<li>Design and execute upstream process development activities and identify opportunities to improve process yield, product safety, and product quality.</li>
<li>Writes and reviews experimental protocols, batch production records, experimental reports.</li>
<li>Analyze, review, and communicate data to senior management and team members.</li>
<li>Be accountable for supporting the establishment of upstream gene therapy drug substance development platform from small scale through intermediate scale (50L) for adeno-associated virus, lentiviral and retroviral vector processes.</li>
<li>Train and mentor research associates.</li>
<li>Maintain open communication via one-on-one and team meetings.</li>
<li>Stay current with relevant technologies and need to be adept at identifying new approaches.</li>
<li>Responsible for the process transfer activities from/to clients and to in-house manufacturing team(s), such as creation of bill of materials and sampling plan, generation of process description documents, technology transfer reports.Provide process training to MSAT and manufacturing teams and assist with process troubleshooting and deviations during GMP production.</li>
<li>Maintain external technical relationships and collaborate with equipment and material suppliers.</li>
<li>Serve as process SME for client-facing and internal programs.</li>
<li>Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the assigned functional area.</li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS or MS in biochemistry, chemical engineering
Desired
ON-THE-JOB EXPERIENCE

4-8+ years of relevant industry experience
Essential
Experience with cell culture technologies, molecular biology, upstream processing, and aseptic processing
Essential
Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations
Desired
Solid foundation in the fundamentals of biochemical engineering, virology and cell biology
Essential
Entrepreneurial experience dealing with customers in product development
Desired
SKILLS / ABILITIES

Working knowledge of Upstream process (Cell culture, Aseptic Technique, bioreactor operations).
Essential
Hands-on experience on complex biologics e.g. gene therapy, transient transfection, baculovirus infection
Desired
Working knowledge of Upstream process (process design and bioreactor scale up, cGMP manufacturing). 
Desired
Ability to interface successfully with multi-disciplined teams
Desired
Extremely detail-oriented with strong technical skills &amp; mechanically inclined/knowledge of hand tools
Desired
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning.</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities.</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock.</li>
<li>Occasionally exposed to extremely loud noise levels</li>
<li>Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required.</li>
</ul>
Movement
<ul>
<li>Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms.</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl.</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 10 pounds.</li>
<li>Occasionally lift and/or move up to 25 pounds.</li>
</ul>
Vision 
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
Pay Range: The annual salary range for this position is $100,000-$120,000.
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Scientist II, Upstream Process Development

<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.

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