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<h3>Job Description</h3>
Job Description
Required:
<ul>
<li>Must have a BA or BS degree in Chemistry or closely related science.</li>
<li>Minimum of 1-year relevant experience preferred.</li>
<li>Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE).</li>
<li>Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.</li>
</ul>
Responsibilities:
<ul>
<li>Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures.</li>
</ul>
Primary Responsibilities
<ul>
<li>Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.</li>
<li>Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.</li>
<li>Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.</li>
<li>Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.</li>
<li>Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency.</li>
<li>Aid other group members as required.</li>
<li>Ensure that equipment and working areas are maintained with good safety and housekeeping practices.</li>
<li>Re-stock chemicals and consumables used in analysis.</li>
<li>Performs other related assignments and duties as required and assigned.</li>
</ul>
<ul>
<li>Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels.</li>
<li>Equipment and parts could weigh up to 20 pounds.</li>
<li>Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required.</li>
</ul>
Company DescriptionHired by Matrix believes in the human touch and starts every partnership with an in-depth conversation. By talking with our clients about their hiring needs and listening to job seekers describe their career goals, we build an understanding of what they are looking for and work hard to make it happen. 
<h3>Company Description</h3>
Hired by Matrix believes in the human touch and starts every partnership with an in-depth conversation. By talking with our clients about their hiring needs and listening to job seekers describe their career goals, we build an understanding of what they are looking for and work hard to make it happen.

Chemist

<h3>Job Description</h3>
Job Description
The Methods Development Chemist ensures the establishment and continual improvement of analytical test methods required to verify the quality, safety, and efficacy of all products produced by Tower Laboratories. The position directly supports all Quality Control equipment and personnel by providing technical expertise in the acquisition, troubleshooting, and proper use of all instrumentation and analytical apparatus, through the establishment and review of Standard Operating Procedures. The position supports Quality Assurance in the investigation and resolution of quality concerns related to Quality Control testing identified from internal and external audits, or non-conformances.
Ideal candidate will be proficient in developing and validating new analytical methods with minimal supervision, as well as performing all phases of chemical testing of raw materials, in-process samples, and finished products for full integration and support of Tower Laboratories’ business and operations.
This position may be based either in our Centerbrook, CT or Montague, MI facilities.
Essential Functions:
<ol>
<li>In collaboration with the QC department, Develop and conduct validation studies for all test methods for all products as applicable.</li>
<li>Support the implementation of new testing strategies and methods to improve accuracy, cost-effectiveness, and productivity.</li>
<li>Adhere to the Method validation master plan when developing new validation studies.</li>
<li>Report all observations and data promptly, meeting specified deadlines. </li>
<li>Adhere to cGMP, Good Laboratory Practices, and all quality and safety requirements while maintaining an orderly working environment.</li>
<li>Support and assist in investigations, audits, and customer concerns regarding analytical data as needed.</li>
<li>Assist in the creation, review, and approval of Tower’s various QC and technical documents regarding SOPs, validations, operations, and other QC/R&amp;D studies as needed.</li>
<li>Assist in the instruction and training of QC personnel as needed.</li>
</ol>
Qualifications:
<ul>
<li>Minimum 3 yrs. of proven success in developing and writing procedures and methodology and performing methods development and validation.</li>
<li>Experience/knowledge in identifying, sourcing, and coordinating implementation of appropriate analytical instrumentation as part of the method development process.</li>
<li>Excellent analytical and wet chemical techniques in support of chemical and manufacturing operations;</li>
<li>Demonstrated proficiency with HPLC</li>
<li>Demonstrated self-starter and independent worker with strong commitment to Quality and Compliance.</li>
<li>Strong writing skills</li>
<li>Good interpersonal skills; ability to communicate effectively with all levels of plant personnel.</li>
<li>Strong team player, demonstrated team attitude and behaviors.</li>
<li>BS in Chemistry with Lab specialization highly preferred.</li>
</ul>
Tower Laboratories is the premier effervescent product manufacturer in the U.S. We develop and manufacture over-the-counter medications, prescription pharmaceuticals, dietary supplements, personal care, beverage and household products. The company has been expanding over the last few years and prospects for continued growth are excellent with several new and interesting products currently in the development stages right now. Please visit our website: <a href="http://www.towerlabs.com" target="_blank">www.towerlabs.com</a>.
This medium sized company offers a friendly, dynamic working environment with a competitive benefit package including 401(k) with company match. 
Tower Labs is a Socially Responsible employer and a great place to work!
Apply and start the conversation today!

Methods Development Chemist

<h3>Job Description</h3>
Job DescriptionChemical Operator
Job Description
We are seeking an experienced Chemical Operator who can work independently and efficiently. The successful candidate will communicate ideas effectively, request actions, and formulate plans or policies under supervision. This role involves developing, monitoring, interpreting, and understanding policies and procedures to ensure alignment with organizational strategies and objectives. The Chemical Operator will organize, prioritize, and oversee activities to meet business objectives and apply safe systems of work. The role also involves creating and reviewing reports, motivating employees, managing risks in production processes, and ensuring compliance with regulations.
Responsibilities
<ul>
<li>Develop, monitor, interpret, and understand policies and procedures.</li>
<li>Plan, organize, prioritize, and oversee activities to efficiently meet business objectives.</li>
<li>Manage and apply safe systems of work.</li>
<li>Create and review relevant reports.</li>
<li>Motivate employees to learn, grow, and develop.</li>
<li>Identify, assess, prioritize, and manage risks in production processes.</li>
<li>Achieve compliance with applicable rules and regulations.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemical mixing, compounding, and GMP.</li>
<li>Basic equipment operation.</li>
<li>Ability to carry out routine tasks and follow strict, detailed instructions.</li>
<li>Knowledge of chemistry.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Ability to carry out operational tasks following established processes.</li>
<li>Experience in installing and maintaining equipment.</li>
<li>Support the quality function by adhering to strict quality standards.</li>
<li>Follow mandatory work instructions, including the use of personal protective equipment.</li>
</ul>
Work Environment
The work environment operates on a quarterly swing shift, alternating between day and night shifts every three months. The company is based in Germany and is committed to employee retention, offering opportunities for cross-training and internal promotions.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Birmingham,AL.
Application Deadline
This position is anticipated to close on Sep 22, 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.

Chemical Operator

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking a highly motivated and skilled Microbiologist to join our Quality Control team at Medivant Healthcare. The ideal candidate will have a strong background in microbiological testing, laboratory techniques, environmental monitoring, and personnel monitoring, all focused on ensuring the safety and quality of healthcare products. The Microbiologist will be responsible for conducting routine and non-routine microbiological tests, performing environmental and personnel monitoring, identifying pathogens, and ensuring compliance with industry standards and regulations. This role is essential in maintaining the highest quality standards and supporting the production of safe and effective pharmaceutical products.
 
Key Responsibilities:
<ul>
<li>Perform microbiological testing of raw materials, finished products, and environmental samples to ensure quality and safety.</li>
<li>Conduct routine microbiological assays including sterility testing, endotoxin testing, microbial limit testing, environmental monitoring, and personnel monitoring.</li>
<li>Interpret test results, analyze data, and document findings in a clear and concise manner.</li>
<li>Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and relevant regulatory standards.</li>
<li>Maintain laboratory equipment and perform calibration, maintenance, and troubleshooting as needed.</li>
<li>Assist in the development and validation of microbiological testing methods and protocols.</li>
<li>Participate in investigations of out-of-specification (OOS) results and provide support for corrective actions.</li>
<li>Collaborate with cross-functional teams, including R&amp;D, production, and quality assurance, to support product development and ensure compliance with regulatory requirements.</li>
<li>Ensure proper documentation and reporting of test results and assist with regulatory audits and inspections as needed.</li>
<li>Stay current with industry trends, regulatory updates, and advancements in microbiological testing technologies.</li>
</ul>
Qualifications:
<ul>
<li>Education: Bachelor’s degree in microbiology, Biology, or a related field. Master’s degree is a plus.</li>
<li>Experience: Minimum of 2 years of experience in microbiological testing, preferably within the pharmaceutical or healthcare industry.</li>
<li>Skills:
<ul>
<li>Strong knowledge of microbiological testing methods and laboratory equipment.</li>
<li>Experience with microbiological techniques such as PCR, ELISA, and sterility testing.</li>
<li>Familiarity with GMP, GLP, FDA, USP, and other regulatory guidelines.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Strong attention to detail and accuracy in laboratory practices.</li>
<li>Ability to work independently and as part of a team in a fast-paced environment.</li>
</ul>
</li>
</ul>

Microbiologist

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

Research Associate

<h3>Job Description</h3>
Job DescriptionABOUT STRM.BIO STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genentic medicines that target the bone marrow. We’re a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We’re here to do great science and build a company we’re proud of. THE OPPORTUNITY We’re looking for a Senior Scientist to help lead and grow our research engine. You’ll work shoulder-to-shoulder with the VP of R&amp;D and Director of Research to drive key programs forward and manage external collaborations. This is a hands-on, highly cross-functional role ideal for someone who’s ready to lead and execute in equal measure. This is a full-time, on-site role. WHAT YOU’LL DO (Key Responsibilities)&nbsp;
<ul>
<li>Lead day-to-day scientific execution across internal teams and CRO/academic partners</li>
<li>Own program timelines and technical plans; troubleshoot and drive decisions to keep progress on track</li>
<li>Design, run, and refine experiments, hands-on and alongside junior team members</li>
<li>Coordinate with collaborators, ensure data integrity, and maintain clean documentation across projects</li>
<li>Contribute to company strategy through project planning, milestone tracking, and resource scoping</li>
<li>Present internally and externally, including pitch decks, grant applications, and scientific meetings</li>
<li>Stay sharp on emerging EV, gene therapy, and CAR-T technologies to shape R&amp;D direction</li>
<li>Pitch in on lab ops, team culture, and whatever else it takes to get the job done</li>
</ul>
WHAT YOU BRING (Required Qualifications)
<ul>
<li>Ph.D. + 5 years’ postdoc or industry experience in gene therapy/genetic medicines, CAR-T, or related areas</li>
<li>Deep expertise in in vivo gene delivery platforms (viral vectors, LNPs, EVs)</li>
<li>Strong bench skills in molecular/cell biology, including flow cytometry, qPCR, Western, microscopy, NGS</li>
<li>Experience developing ex vivo and in vivo CAR-T or other T-cell based therapies</li>
<li>Solid working knowledge of genome editing tools (CRISPR, Cre-lox, etc.)</li>
<li>Experience managing external partners (CROs, academic labs)</li>
<li>Comfortable navigating ambiguity, shifting priorities, and high ownership environments</li>
<li>Excellent communicator, highly organized, strong attention to detail</li>
<li>Bonus: experience with startup ops, grant writing, or early product development</li>
</ul>
KEY POSITION DETAILS
<ul>
<li>100% on-site in Cambridge, MA</li>
<li>Full time with competitive compensation
<ul>
<li>The salary range for this position is $140,000 to $160,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. &nbsp;</li>
</ul>
</li>
</ul>
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Senior Scientist

<h3>Job Description</h3>
Job Description
Chemistry Lab Analyst
Location: Sunnyvale, CA
Why Ascend?
Come work for a company that is transforming the industry!
We are Eurofins Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment.
Job Summary
The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing.
Responsibilities:
<ul>
<li>Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures</li>
<li>Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines</li>
<li>Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens</li>
<li>Instrument daily, weekly, and monthly maintenance</li>
<li>Troubleshooting instruments</li>
<li>Instrument validation</li>
<li>Attends and completes advance training for department instrumentations</li>
<li>Capable of assisting in sample processing and preparation in high complex test environments</li>
<li>Actively participates in facility's Quality Assurance program</li>
<li>Assists in orientation and training of new staff members, as directed by management</li>
<li>Assumes responsibility for special projects, as directed by management</li>
<li>Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed</li>
</ul>
Qualifications:
<ul>
<li>College degree, science related preferred or equivalent number of years of relevant job experience</li>
<li>2-4 years of experience</li>
<li>Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments</li>
<li>Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC</li>
<li>Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely</li>
</ul>
Compensation:
<ul>
<li>$25-35/hr</li>
<li>Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role</li>
</ul>
Benefits: As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Eurofins Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law.&nbsp; The company’s policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status.
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t09VLs1XEi

Chemistry Lab Analyst

<h3>Job Description</h3>
Job Description
🧪 Lab Technician – Chemical Analysis &amp; Quality Support
📍&nbsp;Location: Hadley, MA
🕒&nbsp;Schedule: Monday–Friday | 10-Hour Shifts + Overtime Available
🔁&nbsp;Contract-to-Hire Opportunity
We are seeking a dedicated Lab Technician to perform chemical analysis of plating baths and process solutions using titration, spectrophotometry, and other methods. The ideal candidate will play a vital role in ensuring the quality and compliance of our processes with industry standards.
Responsibilities
<ul>
<li>Conduct chemical analysis of plating baths and process solutions using titration, spectrophotometry, and other methods.</li>
<li>Prepare and maintain standard solutions, reagents, and laboratory equipment.</li>
<li>Monitor bath chemistry to ensure compliance with internal specifications and industry standards.</li>
<li>Assist in maintaining records of analysis, solution concentrations, and corrective actions.</li>
<li>Support environmental testing and wastewater treatment monitoring.</li>
<li>Collaborate with production teams to troubleshoot quality issues or solution variances.</li>
<li>Maintain a clean, safe, and organized laboratory workspace.</li>
<li>Adhere to all safety and environmental protocols.</li>
</ul>
Essential Skills
<ul>
<li>Quality control</li>
<li>Laboratory experience</li>
<li>Titration expertise</li>
<li>Experience with metal finishing</li>
<li>Chemistry knowledge</li>
<li>GMP (Good Manufacturing Practice)</li>
<li>Quality control and assurance</li>
</ul>
Must Haves:
<ul>
<li>Hands-on experience in a lab setting (no degree required).</li>
<li>Strong skills in titration and wet chemistry.</li>
<li>Familiarity with metal finishing processes (preferred).</li>
<li>Understanding of GMP and quality control practices.</li>
<li>Motivated, reliable, and safety-conscious mindset.</li>
</ul>
Work Environment The position is based in a laboratory environment. The work schedule is Monday through Friday, with 10-hour workdays and the possibility of 10-15 hours of overtime per week.
Pay and Benefits
The pay range for this position is $25.00 - $27.00/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 Springfield,MA.
Application Deadline
This position is anticipated to close on Sep 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Plating Lab Technician

<h3>Job Description</h3>
Job Description
About Cleerly
We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. 
Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. 
At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. 
About the Opportunity
We are seeking a highly skilled Staff Scientist to lead the design, development, validation of innovative clinical workflow that can directly impact the diagnosis and treatment for heart disease. In this senior-level role, you are responsible for architecting a cutting-edge product that integrates our existing technologies while pushing the boundary of innovation in cardiac vascular imaging. You will also represent the company in strategic research collaborations with leading academic and clinical institutions, driving innovation at the intersection of AI and cardiovascular health.
TTC*:
NY: $270,000 - $310,000 CO: $265,000 - $305,000
*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.). We hire employees anywhere within the United States and account for geography when determining base salary.
Responsibilities
<ul>
<li>Research and develop state-of-the-art AI and non-AI algorithms for coronary CT/fluoroscopy imaging applications.</li>
<li>Implement efficient and robust image processing pipeline to solve challenging problems in low latency environments.</li>
<li>Translate product and clinical requirements into algorithmic specifications in collaboration with Product and Clinical teams.</li>
<li>Partner with Regulatory Affairs to support regulatory submissions (e.g., 510(k), De Novo, PCCP), including generating evidence and documentation.</li>
<li>Collaborate with engineering teams to deploy AI and non-AI based solutions in clinical practice.</li>
<li>Communicate findings and strategy to internal stakeholders and leadership through clear technical documentation, presentations, and demos.</li>
<li>Contribute to intellectual property development through patents and scientific publications.</li>
<li>Mentor junior scientists and foster a culture of technical excellence and scientific rigor.</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Computer Science, Data Science, Biomedical Engineering, Biomedical Imaging, or a related technical field, with 5+ years combined postdoc and/or industry experience; OR an M.S. with 8+ years of relevant experience.</li>
<li>R&amp;D experience in medical image processing, including classical image processing algorithm, optical flow analysis, 2D&amp;3D rigid/deformable image registration</li>
<li>Proven track record of publications in top-tier medical imaging or computer vision conferences and journals (e.g., MICCAI, IEEE TMI, CVPR, Medical Image Analysis).</li>
<li>Strong experience in C++ and Python.</li>
<li>Experience of developing and applying graph processing or GNN(graph neural network) </li>
<li>Prior experience with ITK, OpenCV, VTK, CMake, Slicer is a plus</li>
<li>Prior experience with cardiac motion modelling or tracking is a plus</li>
<li>Excellent interpersonal, cross-functional, and cross-cultural collaboration skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>5+ years of industry experience in AI-based medical device development or clinical deployment.</li>
<li>Experience supporting FDA regulatory submissions for ML-based software, including familiarity with De Novo, 510(k), and PCCP pathways.</li>
<li>Deep domain knowledge in cardiovascular imaging and CT interpretation workflows.</li>
</ul>
Working at Cleerly takes HEART. Discover our Core Values:
<ul>
<li>H: Humility- be a servant leader</li>
<li>E: Excellence- deliver world-changing results</li>
<li>A: Accountability- do what you say; expect the same from others</li>
<li>R: Remarkable- inspire &amp; innovate with impact</li>
<li>T: Teamwork- together we win</li>
</ul>
Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.
OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.
By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (<a href="https://cleerlyhealth.com/privacy-policy" target="_blank">https://cleerlyhealth.com/privacy-policy</a>). All official emails will come from @cleerlyhealth.com email accounts. 
#Cleerly

Staff Scientist, Imaging Systems

<h3>Job Description</h3>
Job Description
Who We Are:
Do you want to work for a company named to the Best Places to Work in Rubber and Plastics in 2024? If so, Zeon Chemicals’ Emerging Student Talent Program (ESTP) is the place for you! Our co-op program provides students with hands on experience, workforce training and education, networking opportunities, and countless other benefits; all while working for our industry leading company. We strive to develop the next workforce generation into motivated, capable, and responsible individuals who are equipped to make a difference.
First rotation schedules to begin in January of 2026. This is a paid position and housing assistance may be provided for qualifying applicants based on ZEON’s relocation policy.
 
Purpose:
This position is a developmental role, providing college level students an opportunity to practically employ and supplement their course work in a plant environment. Typically, the co-op arrangement is established in the Sophomore year of college and alternates semesters thereafter for three co-op experiences of increasing responsibility.
Job Functions/Accountabilities (Essential &amp; Marginal):
<ul>
<li>Support one or more experienced engineers in performance of assignments, spend time shadowing actual operations, and have unique assignments that support larger projects as well as experience the day-to-day workings of engineering.</li>
<li>Perform daily review of NBR and ACM reactions and maintain comprehensive record of polymerization conversion and charge Mooney.</li>
<li>Investigate polymerization irregularities and failed charges daily. Document off-specification and aborted charges.</li>
<li>Monitor plant utilities and issue usage report to management team daily. Issue summary total usage report at month end.</li>
<li>Execute small projects at the direction of the Plant Manager, coordinating work with multi-discipline projects team.</li>
<li>Assist with scanning and saving project documents for capital project folders.</li>
<li>Perform drawing reviews to verify field installation versus P&amp;IDs and equipment drawings.</li>
<li>Assist in ongoing migration of historical documents to electronic records.</li>
<li>Assist in redefining pipe and equipment labeling strategy and implementation.</li>
<li>Participate in process management of change (MOC) activities and attend meetings bi-weekly.</li>
<li>Participate on environmental improvement team and attend bi-weekly meetings.</li>
<li>Participate in review of new engineering specifications and assist in adoption.</li>
</ul>
Qualifications:
Education:
Enrolled in a four (4) year or more college degree program in with Chemical Engineering major.
Skills and Abilities:
<ul>
<li>Ability to communicate effectively with a diverse range of audiences.</li>
<li>Ability to identify, formulate, and solve complex engineering problems by applying principles of engineering, science, and mathematics.</li>
<li>Positive attitude with ability to function effectively on a team.</li>
<li>Skilled in use of Microsoft applications, including Excel, Outlook, and Word.</li>
<li>Ability to prioritize tasks to meet schedules/deadlines and complete assignments accurately.</li>
</ul>

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