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<h3>Job Description</h3>
Job Description
RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better.
We don’t make MedTech. We make MedTech happen.
Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency.
Job Summary:
The Senior Chemist I is designed for an experienced, independent chemist and will perform laboratory analyses and support scientific data interpretation. This role will be responsible for conducting a variety of analyses, interpreting data, and developing technical reports for customer projects. The Senior Chemist I will leverage strong scientific knowledge and experience to ensure accurate and efficient testing while maintaining a focus on meeting client and internal standards. This role requires the ability to work autonomously with minimal supervision, while still collaborating effectively with laboratory teams and other departments to meet project goals.
Primary Responsibilities:
<ul>
<li>
Perform laboratory experiments to develop, optimize, and validate analytical methods (HPLC, GC, LCMS, GCMS). 
</li>
<li>
Prepare and analyze samples for routine testing, stability studies, and in-process controls, ensuring accuracy and reproducibility. 
</li>
<li>
Operate, calibrate, and maintain analytical instruments (e.g., HPLC, GC, LCMS, GCMS) and troubleshoot issues to minimize downtime. 
</li>
<li>
Support advanced analysis and writing of challenging, complex customer projects and related business needs. 
</li>
<li>
Collaborate with Laboratory Chemists, Study Directors, and Research &amp; Development teams to ensure alignment with project goals and timelines. 
</li>
<li>
Review and assess data for trends and discrepancies and suggest improvements where applicable. 
</li>
<li>
Ensure compliance with regulatory guidelines, laboratory safety protocols, and best practices during all laboratory activities. 
</li>
<li>
Maintain thorough documentation of experimental procedures, results, and data interpretations. 
</li>
<li>
Contribute to the development of laboratory methods and procedures. 
</li>
<li>
Provide technical support and mentorship to junior team members as needed. 
</li>
<li>
Act as support on primary review report writing process and finalization. 
</li>
<li>
Champion laboratory safety protocols, regulatory compliance, and adherence to industry best practices, continuously evaluating and improving safety measures in the lab. 
</li>
<li>
Keep up to date with the latest scientific literature, emerging technologies, and industry innovations, ensuring that the laboratory maintains a competitive edge in scientific advancements. 
</li>
<li>
Any other duties and tasks as directed by the supervisor. 
</li>
</ul>
Requirements:
<ul>
<li>
Bachelor’s Degree in relevant field with 7+ years’ experience; Masters 3+ years’ experience; Ph.D. 0-2 years’ experience. 
</li>
</ul>
<ul>
<li>
Proficiency in performing and interpreting laboratory experiments using techniques such as HPLC, GC, LCMS, GCMS. 
</li>
</ul>
<ul>
<li>
Advanced knowledge and understanding of analytical method development. 
</li>
<li>
Advanced knowledge and understanding of scientific report writing.
</li>
<li>
Advanced knowledge and understanding of investigative and regulatory techniques.
</li>
<li>
Advanced practitioner of all scientific methods and troubleshooting.
</li>
<li>
Advanced practitioner of all software with a deep understanding of settings and features.
</li>
<li>
Ability to be innovative and use the software to solve problems.
</li>
<li>
Ability to perform well under pressure and work with minimum supervision.
</li>
<li>
Demonstrate the ability to perform work accurately and efficiently
</li>
<li>
Computer proficiency and experience with all MS products
</li>
<li>
Computer skills proficiency and ability to learn new software.
</li>
<li>
Detail-oriented self-starter with ability to manage multiple projects, work independently, and learn new disciplines.
</li>
<li>
Excellent verbal and written communication skills.
</li>
<li>
Demonstrates the drive and energy to be effective.
</li>
</ul>
Behaviors: Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity &amp; Trust, Interpersonal Savvy, Planning
Supervisory Responsibilities:
This position will have no supervisory responsibilities. 
Work Environment/Physical Demands: This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers and filing cabinets. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift or move objects up to 10 pounds and occasionally lift or move objects up to 25 pounds.
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
Job Opportunity Verification
At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.

Senior Chemist I

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
<ul>
<li>Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.</li>
<li>Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.</li>
<li>Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.</li>
<li>Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure compliance with international regulations such as FDA and EMA.</li>
<li>Work collaboratively with R&amp;D and production teams to support product development and release.</li>
<li>Provide technical support and training to junior team members or other departments.</li>
</ul>
Essential Skills
<ul>
<li>3-7 years of routine testing experience using HPLC and dissolution techniques.</li>
<li>Proficiency in working with solid oral dosage forms, raw materials, and finished products.</li>
<li>Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.</li>
<li>Strong understanding of Pharma GMP practices.</li>
<li>Competence in laboratory applications including wet chemistry, titration, and chromatography.</li>
<li>Basic computer skills in MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>Ability to document and record analytical experiments and results as per cGMP guidelines.</li>
<li>Strong problem-solving skills and attention to detail.</li>
<li>Knowledge of regulatory guidelines such as GMP and GLP.</li>
</ul>
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type &amp; Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $35.00/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 East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 2026.
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.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Job Description

POSITION SUMMARY The Microbiology Supervisor is responsible for the operation of Microbiology section of the clinical laboratory.&nbsp; The Microbiology Supervisor facilitates the implementation of hospital and laboratory policies and procedures.&nbsp; Responsible for assisting in training new employees, supervising both Clinical Laboratory Scientists and laboratory phlebotomist’s workload organization, and monitoring daily maintenance and quality control. This person will report to the Lab Manager Implements good public relations by representing the laboratory directly to patients, physicians and hospital staff at all times.
ESSENTIAL DUTIES AND RESPONSIBILITIES
<ul>
<li>Responsible for assisting with the selection of methodology and instrumentation to perform laboratory tests appropriate for the patient population served.&nbsp; Responsible for the validation and implementation of new instrumentation.&nbsp; Ensures the standardization of tests methodologies, procedures, instrumentation, and reference ranges.</li>
<li>Verifies test procedures performed and established the laboratory’s test performance characteristics, including, but not limited to the linearity, precision and accuracy of each test and test system.</li>
<li>Ensures participation in and successful completion of a quality control and approved proficiency testing program commensurate with the services offered.&nbsp; Troubleshoots any problems with the proficiency testing program.&nbsp; Establishes parameters for acceptable level of analytic performance.&nbsp; Ensures that quality is maintained throughout entire testing process from order entry through results reporting.</li>
<li>Reviews the work of others to ensure that tests are performed in accordance with prescribed standards.</li>
<li>Assists in maintaining and optimizing work standards to assure a reasonable turnaround time of test results.</li>
<li>Troubleshoots equipment problems.</li>
<li>Maintains inventory control of supplies and reagents in his/her section(s).</li>
<li>Schedules, organizes and delineates duties of personnel.</li>
<li>Assists manager in performance evaluations of the employees in his/her sections.</li>
<li>Responsible for the operation of the Microbiology department.</li>
<li>Works closely with the Laboratory Manager to meet the administrative and financial goals of the department</li>
<li>Responsible for meeting the service and quality goals of the department. Assumes responsibility for daily operations and meets CLIA requirements for microbiology</li>
<li>Provides clinical microbiology consultations to medical and hospital staff</li>
<li>Present micro data reports clearly and concisely to management, including QC performance metrics and trends</li>
<li>Proactively identifies and implements improvements and lean initiatives</li>
<li>Responsible for the technical and scientific oversight of the department including assisting in hiring of personnel, training/competency assessment and input for performance review of the staff in their designated area.</li>
<li>Responsible for making clinical/technical decisions in the resolution of testing/reporting issues, maintenance of the quality and security of department instrumentation, quality control documentation and meeting hospital goals to ensure accurate and timely patient care.</li>
<li>Responsible for maintaining procedure manuals for all testing performed and the documentation required for regulatory and licensing organizations</li>
<li>Oversee and manage team schedule of staff and PTO request.&nbsp;</li>
<li>Work collaboratively with other department leaders to have a more efficient workflow for the Clinical laboratory.&nbsp;</li>
<li>Responsible for ensuring staff compliance with hospital policies and meeting regulatory requirements within their assigned areas (e.g. coordinate meal breaks, corrected reports, attendance, overtime and punctuality)</li>
<li>Setting an example- must always be conscious of how his / her words and actions will be perceived.</li>
<li>Attend minimum of three (3) leadership seminar/workshop annually</li>
<li>Performs additional duties as directed by the by the Laboratory Director or Manager which are necessary for the efficient operation of the laboratory.</li>
</ul>
Job Requirements

POSITION REQUIREMENTS
A.&nbsp; &nbsp;Education
<ul>
<li>Bachelor’s degree – Science</li>
</ul>
B.&nbsp; Qualifications/Experience
<ul>
<li>2-5 years Microbiology Clinical Laboratory Experience</li>
<li>CA Clinical Laboratory Scientist License or Clinical Microbiologist Scientist License</li>
<li>2 years leadership experience in an acute care setting required</li>
</ul>
C.&nbsp; &nbsp;Special Skills/Knowledge
<ul>
<li>Strong interpersonal and organizational skills.&nbsp; Proficient with computer.</li>
</ul>
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#LI-AJ1

Microbiology Supervisor - Full Time Days

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical EngineerJob Description
We are seeking a skilled Chemical Engineer to perform all chemical process functions related to chemical batching. This role involves conducting root cause analysis (RCA) to troubleshoot batching issues and implementing corrective and preventive actions (CAPAs) for both internal and external challenges. You will be responsible for scaling up and commercializing new formulas, adjusting existing formulas, and validating all manufacturing and quality processes and specifications. Additionally, you will perform in-process batch adjustments, support production scaling to meet product specifications, and analyze production and laboratory data to optimize processes and reduce costs.
Responsibilities
<ul>
<li>Conduct root cause analysis for customer complaints and internal production issues.</li>
<li>Ensure all batch adjustments are executed accurately when raw materials or formulas change.</li>
<li>Scale up and commercialize new formulas and products, ensuring correct implementation.</li>
<li>Analyze production data and quality data to identify optimization and cost reduction opportunities.</li>
<li>Participate in the disposition of non-conforming materials and support deviation management.</li>
<li>Mentor and coach fellow engineers and quality and production personnel in continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>1-5 years of experience in chemical engineering or chemical process engineering.</li>
<li>Ability to diagnose and resolve customer complaints and internal production issues.</li>
<li>Experience with root cause analysis and implementation of CAPA.</li>
<li>Expertise in chemical manufacturing, quality control, and process engineering.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Degree in Chemical Engineering or a related field.</li>
<li>Experience in scale-up and commercialization processes.</li>
<li>Familiarity with chemical equipment and laboratory practices.</li>
<li>Knowledge of new product development and chemical processing.</li>
</ul>
Work Environment
This position operates in a chemical manufacturing environment, working across offices, laboratories, production areas, and production labs. The role follows a first shift schedule from Monday through Friday, with flexible working hours typically ranging from 40 to 45 hours per week, extending to 50 hours during major projects or issues. You will collaborate with various organizational levels, including R&amp;D, Quality, Production, Maintenance, Customers, Sales, and leadership roles.
Job Type &amp; Location
This is a Permanent position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
This company offers health insurance, dental insurance, vision insurance, 401k match, bonuses, etc. They also provide paid vacation and paid holiday.
Workplace Type
This is a fully onsite position in Germantown,WI.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
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 Engineer

<h3>Job Description</h3>
Job DescriptionAbout the Institute of Foundation ModelsWe are a dedicated research lab for building, understanding, using, and risk-managing foundation models. Our mandate is to advance research, nurture the next generation of AI builders, and drive transformative contributions to a knowledge-driven economy.As part of our team, you’ll have the opportunity to work on the core of cutting-edge foundation model training, alongside world-class researchers, data scientists, and engineers, tackling the most fundamental and impactful challenges in AI development. You will participate in the development of groundbreaking AI solutions that have the potential to reshape entire industries.&nbsp;Strategic and innovative problem-solving skills will be instrumental in establishing MBZUAI as a global hub for&nbsp;high-performance computing in deep learning, driving impactful discoveries that inspire the next generation of AI&nbsp;pioneers. Position SummaryAs a member of the Agents team, you will tackle research and engineering challenges to train advanced agentic language models that are adept at using reasoning and tool use to complete tasks on a computer. These challenges range from building high-quality training datasets and robust evaluations to innovative reinforcement learning infrastructure, algorithms and environments. The team aims to recruit candidates across the research-engineering spectrum, from algorithmic and empirical research to large-scale systems and optimization, reflecting the breadth of interesting problems we aim to solve. We value depth in any subset of these areas; there is no single “right” background. Key Responsibilities·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Propose, prototype, and scale algorithms/systems to support agentic learning·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Develop new paradigms for agentic behavior that go beyond current practices·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Contribute to technical reports, research publications, and open-source software·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Collaborate with other teams to produce state-of-the-art foundation models&nbsp;Academic&nbsp;Qualifications•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; BS, MS, or PhD degree (or equivalent experience) in Computer Science, Machine Learning, or related fields&nbsp;Professional&nbsp;ExperienceMinimum·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 2 years of experience working in one of the following or related areas: LLM training/fine-tuning, evaluations, reinforcement learning, LLM inference, distributed machine learning systems·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Python and PyTorch development experience·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in using LLM agents for your personal or professional use·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in designing and implementing algorithms from scratch (for algorithms focus)·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in dataset curation and generation (for data focus)·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in building or contributing to training/serving infrastructure (for systems focus)·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in designing and deep diving into evaluations (for evals focus)&nbsp;Preferred Skills·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Expertise in one or more of PyTorch, Ray, Triton, CUDA C++·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong knowledge of literature on RL, LLM reasoning, and tool use·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in training or using LLM agents for SWE tasks·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Deep understanding of reinforcement learning principles·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience implementing distributed learning algorithms·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Contributions to published research and/or open-source ML softwareVisa SponsorshipThis position is eligible for visa sponsorship. Benefits Include*Comprehensive medical, dental, and vision benefits&nbsp;&nbsp;*Bonus*401K Plan*Generous paid time off, sick leave and holidays*Paid Parental Leave*Employee Assistance Program*Life insurance and disability

Research Scientist - Agents

<h3>Job Description</h3>
Job Description
About the Team:
The Sensors Division specializes in the development of advanced sensor systems, with a particular focus on airborne and surface-based radar, space-based sensing, electronic warfare, and underwater acoustics. This position is within the Space Missions and Sensing (SMS) Sector of the Sensors Division. In this sector, we develop and deliver technology to advance space-based sensing, space control, and counter-sensing missions.
The Role:
The SMS Sector is seeking a Senior RF signal processing scientist to support algorithm development in a Research &amp; Development environment. In this role, you will be an integral part of a team developing a cutting-edge space-based radar system. Your responsibilities will include utilizing and advancing existing signal processing algorithms and analytics tools. This position offers significant opportunities for career growth within a fast-paced and rapidly expanding company.
What you will do:
<ul>
<li>Design signal processing and data exploitation algorithms that support day to day satellite operations</li>
<li>Conduct performance analysis through simulations and real-world testing to validate system performance</li>
<li>Communicate effectively with internal teams and stakeholders to convey technical concepts and project updates</li>
</ul>
Who you are:
<ul>
<li>Active Security Clearance at the Secret (S) level</li>
<li>BS or MS in Physics, Applied Mathematics, Electrical Engineering</li>
<li>3-5+ years of experience depending on degree</li>
<li>Radar signal processing, statistical signal processing background (detection, estimation)</li>
<li>Proficiency in MATLAB and/or Python programming languages</li>
</ul>
Even Better:
<ul>
<li>Past experience in space-based remote sensing (e.g. SAR, signal exploitation)</li>
<li>Expertise in linear algebra, mathematical optimization a plus</li>
<li>PhD in Applied Mathematics, Electrical Engineering with research background related to radar, radar signal processing in lieu of experience</li>
</ul>
Pay Information Full-Time Salary Range: $134,000 - $184,000
The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate's experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions.
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Senior RF Signal Processing Scientist

<h3>Job Description</h3>
Job Description
Join an exciting, multidisciplinary PhD program that offers hands-on training from day one, bridging cutting-edge laboratory science with clinical research. We are seeking motivated and dedicated doctoral students for the Neuroscience Ph.D. program at the Roskamp Institute, which currently has openings for a 4-year Ph.D. project in Traumatic Brain Injury (TBI) research. 
Roskamp Institute projects are all focused on translational research, with analysis of clinical samples to define the conditions under investigation, and extensive characterization of relevant preclinical models in order to identify and develop diagnostic strategies and therapeutic targets. 
This PhD student will join our translational team investigating a brain-penetrant bioactive neurotherapeutic, as an anti-inflammatory treatment for traumatic brain injury (TBI). Our research integrates PK/PD modeling, dose optimization, therapeutic time-window analysis and acute-to-chronic efficacy studies in a mouse model of TBI, complemented by cell-based systems that model inducible inflammatory signaling.
Techniques associated with this Roskamp Ph.D. project include:
<ul>
<li>Analysis of rodent and human TBI tissue samples </li>
<li>Cell- and tissue-specific isolation and culturing</li>
<li>Cre-LoxP and inducible mouse models and CRISPR/Cas9 editing of glial cell cultures</li>
<li>Antibody-based analytical approaches - Immunoblotting, ELISA, transactivation assays</li>
<li>Rodent manipulation including TBI surgeries, behavioral testing and therapeutic studies. </li>
<li>Neuropathological analyses – Microscopy, Immunohistochemistry</li>
<li>Mass spectrometry analyses – Kp, uu drug concentration levels in the brain </li>
<li>Spatial transcriptomics and proteomics approaches </li>
<li>Pharmacokinetics, pharmacodynamics and physiologically based pharmacokinetic modeling</li>
</ul>
The Roskamp Institute is a leader in the field of neuroscience, with a strong reputation for developing novel therapies for conditions such as traumatic brain injury (TBI), Alzheimer’s disease and Gulf War Illness. The Institute’s cutting-edge research environment offers unmatched opportunities for multidisciplinary training and hands-on experience, working with experts in translational neuroscience. Sarasota, Florida, is known for its beautiful, pristine beaches and pleasant weather year-round, making it an ideal place to live and work. As part of the Roskamp Institute, you will not only advance your career but also enjoy the benefits of living in a vibrant coastal community. Qualifications Required ·Master’s degree in a scientific field, or a Bachelor’s degree with demonstrated scientific laboratory experience.
Please visit The Roskamp Institute – About Us – Ph.D. Program section of the website located at the following weblink, and select the Blue ‘Download Application form’: <a href="https://www.roskampinstitute.org/ph-d-program/" target="_blank">https://www.roskampinstitute.org/ph-d-program/</a>. 
The deadline for submission of applications is January 31st, 2026

RESEARCH ASSOCIATE/STUDENT

<h3>Job Description</h3>
Job Description

Position: Research Associate II - Myers Lab
Job Type: Full-Time
INSTITUTE OVERVIEW
The HudsonAlpha Institute for Biotechnology (<a href="http://www.hudsonalpha.org" target="_blank">www.hudsonalpha.org</a>) is a non-profit organization with the mission to use biotechnology and basic biological research to make important discoveries, improve human health, stimulate economic development, inspire young people to seek careers in science and teach members of the public the importance of science in their everyday lives. Located in Cummings Research Park in Huntsville, Alabama, one of the world's leading science and technology parks, HudsonAlpha's campus contains state-of-the-art laboratories for biological research and development, as well as education, in the areas of genomics, genetics and personalized medicine.
DEPARTMENT OVERVIEW
Dr. Richard M. Myers is a Faculty Investigator and Chief Scientific Officer of the HudsonAlpha Institute for Biotechnology. His laboratory uses genomic, genetic, molecular biology, and cell biology approaches to study problems in human neurobiology and gene regulation on a genome-wide level. We especially seek to understand how germline and somatic DNA sequence variation, epigenetics, and the environment affect the levels of transcription of genes in cell-type specific manners in the human nervous system. We focus on normal, healthy brain function as well as diseases, including Huntington disease, Alzheimer disease, Parkinson disease, psychiatric disorders, and amyotrophic lateral sclerosis, often in the context of differential responses to therapeutic agents. In addition, we work on neuropsychiatric disorders, and with Dr. Greg Cooper's lab at HudsonAlpha, on understanding the causes and mechanisms of unexplained diseases in children. Our experimental and computational work include genome-scale analysis of cis-acting regulatory sequences, DNA binding proteins and epigenetic action involved in human gene regulation and disease, as well as the development of molecular biomarkers for early detection and monitoring of diseases relevant to neuroscience.
While not required, subject area familiarity and/or interest in genetics, genomics, neuroscience, neuropsychiatric diseases, and/or neurodegenerative diseases is desirable. Project areas include study of gene regulation for genes implicated in normal human biology as well as disease, novel analysis approaches for associating genetic variation with gene expression, and genome-wide approaches relevant to disease as well as genome function in the brain more broadly.
POSITION SUMMARY
This Research Associate (RA) position is in the Myers Lab supporting genomics research projects in a variety of basic and applied areas, including global genomic assays and functional characterization. The activities of the RA include: molecular techniques including restriction digests, ligations, annealing, gel electrophoresis, quantification of nucleic acids, bacterial cloning, nucleic acid extractions; mammalian cell culture using fully consented cell lines; preparation of samples for next-generation sequencing; and other cellular and molecular biology protocols. This position requires exacting attention to detail, strong organizational skills, and the ability to work as part of a team as well as independently.
The Research Associate carries out research protocols as determined by the Principal Investigator. The Associate follows procedures exactly as outlined, ensuring the consistency of research practices and, ultimately, helping ensure the consistency and integrity of project outcomes. The Associate also provides feedback in the case that procedures are not producing expected results.
The Research Associate must understand laboratory procedure and safety. In addition to a general knowledge of the overall objectives of the research project, the Associate must have an understanding of the tactical methodology in particular. The Associate works under the direction of a graduate student, postdoctoral fellow, research assistant with supervisory responsibilities, senior scientist, or the lab Principal Investigator, communicating progress and advising of any issues that arise. The Associate must be able to adapt to modifications in protocol, changes in equipment or upgrades in software, as well as adjustments to the scope of research projects.
JOB SPECIFIC TASKS
<ul>
<li>Hands-on laboratory work, executing research assignments according to existing protocols </li>
<li>Communicates with lab colleagues regarding shared equipment and reagent usage, experimental results, and any potential troubleshooting</li>
<li>This position will periodically require limited weekend hours for performance of mammalian cell culture and/or molecular cloning procedures but will not exceed 40 total hours per week</li>
<li>Immediately reviews initial outcomes for quality and consistency, and participates in team discussions regarding short-term and long-term goals</li>
<li>Maintains an accurate and up-to-date laboratory notebook and tracks work as required by the project or supervisor</li>
<li>Participates in general lab maintenance such as cleaning freezers, shared lab space and equipment, and stocking and/or ordering shared reagents and consumables</li>
<li>Other duties as assigned</li>
</ul>
EDUCATION AND REQUIRED SKILLS EXPERIENCE
<ul>
<li>Master's degree in a life or physical science field requiring hands-on laboratory work with 5 years experience, or a bachelor's degree in a life or physical science field requiring hands-on laboratory work and 7 years experience</li>
<li>Meticulous attention to detail, both in actual laboratory practice and in documentation</li>
<li>Excellent laboratory skills, including proficiency in pipetting, documentation, and procedure (clinical, sterile, or molecular, depending on the needs of the laboratory)</li>
<li>Ability to accurately convert measurements as required</li>
<li>Ability to understand protocols, clarify as needed, and perform protocols with consistency, as demonstrated through previous laboratory experience</li>
<li>Ability to operate basic equipment (thermal cycler, gel electrophoresis, tabletop centrifuge, etc.) and troubleshoot basic problems</li>
<li>While not required, experience with mammalian cell culture is preferred</li>
</ul>
Physical Demands/Environmental Factors/Mental Functions
ADA Requirements – The physical demands, work environment factors, and mental functions described below are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Disclaimer - All job requirements are subject to possible revision to reflect changes in the position requirements or to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a threat or risk to the health and safety of themselves or other employees. This job description in no way states or implies that these are the only duties which will be required in this position. Employees will be required to follow other job-related duties as requested by their supervisor/manager (within guidelines and compliance with Federal and State Laws). Continued employment remains on an "at-will" basis.
Physical Demands
<ul>
<li>Must be able to remain in a stationary position (sit or stand) for prolonged periods (50% of the time).</li>
<li>Frequently moving between work areas.</li>
<li>Frequently moving, transporting, and positioning materials up to 30 pounds.</li>
<li>Vision abilities required by this job include close vision, distance vision, and depth perception.</li>
<li>Frequent operation of common office equipment (e.g. computers, mobile devices, calculators, copiers, scanners) and laboratory equipment.</li>
<li>Frequently position self (e.g. stoop, crouch, crawl, bend) and pull/push, grasp/squeeze, wrist flexion/extension, reach to operate and maintain laboratory equipment.</li>
</ul>
Environmental Factors
<ul>
<li>Exposure to chemical, mechanical and electrical hazards, and hazardous physical substances and fumes, and airborne particles.</li>
<li>Noise level in the work environment is usually moderate.</li>
</ul>
Mental Functions
<ul>
<li>Continuous mental and visual attention, requiring sustained attention and observation.</li>
<li>Excellent fine motor skills and hand control in order to pipette accurately. </li>
<li>Ability to sustain focus during research procedures (to maintain protocol such as order of operations). </li>
<li>Ability to visually observe results and record outcomes on lab logs and/or PC.</li>
<li>Extensive documentation skills, good attention to detail, and exceptional organizational skills are required.</li>
<li>Communicate effectively, both orally and in writing, in the English language.</li>
<li>Requires the ability to adapt to change efficiently.</li>
<li>Ability to independently lead and conduct research, and to evaluate, interpret and present complex scientific data.</li>
<li>Capacity to work productively within functionally diverse teams as well as collaborate with external investigators and partners in academic and industrial settings.</li>
<li>Ability to prioritize issues and use sound judgment to recognize when additional consultation and/or help is needed.</li>
<li>Comfortable working on multiple projects at one time.</li>
<li>Strong logical thinking and deduction skills.</li>
<li>Ability to effectively present ideas and information in a variety of formats to a wide range of audiences.</li>
<li>Positive, flexible, and professional attitude.</li>
</ul>
It is the policy of HudsonAlpha Institute for Biotechnology, in accordance with all applicable laws, to recruit, hire, train, and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, disability, genetic information, sexual orientation, veteran status, or any other basis prohibited by applicable law.
 Job Posted by ApplicantPro

HudsonAlpha - Research Associate II - Myers Lab

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist OperatorJob Description
The Chemist Operator will be responsible for producing Active Pharmaceutical Ingredients using chemical reactors. This role requires following specific Batch Records to ensure the production of a consistent product.
Responsibilities
<ul>
<li>Handle various unit operations, such as reactions, filtration, distillation, drying, and milling, on raw materials and various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document instructions per batch sheet to produce products in accordance with all cGMP guidelines.</li>
<li>Set up equipment, including vessels, tanks, centrifuges, and dryers, for proper processing. Clean and verify equipment and vessels.</li>
<li>Record observations of operating conditions.</li>
<li>Drive and operate a fork truck.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in Chemical Operation or Batching, 1-5 years preferred.</li>
<li>Knowledge of GMP guidelines from food, chemical, or pharmaceutical industries.</li>
<li>Understanding of Analytical Chemistry and Chemical Operating.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma with experience, or an Associate's or Bachelor's degree in Sciences, preferably in Chemical Technology or Chemistry.</li>
<li>Experience in GC and Batching processes.</li>
</ul>
Work Environment
The work environment is a clean laboratory and production setting. Initial training will be on the first shift for 3-6 months, after which the role will transition to a permanent shift from 6 p.m. to 6:30 a.m., following a 2-2-3 schedule, including working every other weekend. The company is expanding its innovation hub, offering growth opportunities into leadership positions for those who excel.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $24.00 - $26.50/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 Grafton,WI.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
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.

Chemist Operator

<h3>Job Description</h3>
Job Description
Senior Machine Learning Scientist sf, ca
Senior Machine Learning Scientist, you will play a leading role in designing the next generation of foundation models of gene regulatory networks powered by Tahoe's large scale single-cell datasets such as Tahoe-100M and beyond. This role is well-suited for someone with a strong background in machine learning and statistics, and an interest in applying cutting-edge breakthroughs in ML to meaningful problems in drug discovery. We are looking for non-incremental thinkers with the skills to help build models that can make a real impact on drug discovery.
Qualifications - Essential
PhD or equivalent practical experience in a technical field.
A proven track record of developing and applying deep learning methods, including experience with modern architectures such as transformers, state-space models, graph neural networks or diffusion-based generative models.
Proficiency with modern ML frameworks (e.g., PyTorch, JAX, or TensorFlow) and core scientific computing libraries (e.g., NumPy, SciPy, Pandas).
A genuine enthusiasm for applying cutting-edge ML research to real-world biological problems and a bias towards action. Qualifications - Nice to have
Prior experience with ML applied to problems in biology or chemistry.
Familiarity with multimodal modeling, contrastive learning or self-supervised learning.
Experience with large scale distributed ML techniques (e.g., FSDP, TP, dMoE, flash attention) Key Responsibilities
Develop and apply machine learning techniques towards building multimodal foundation models that bridge the chemical and biological domains, i.e.: integrate models of chemical structure, target protein sequence and whole transcriptome scRNAseq.
Stay at the forefront of ML and computational biology research and rapidly adopt state-of-the-art techniques to our problems and datasets.
Collaborate with our team of biologists and engineers in cross-functional pods to test novel ML-driven hypotheses. Benefits
Unlimited Paid Time Off (PTO).
Monthly Lunch budget.
One-time Office set up budget.
US Employees: HMO Kaiser Platinum and PPO Anthem Gold medical as well as vision and dental plans for both the employee and dependents.
$200,000 - $275,000 a year
This position requires on-site presence at our South San Francisco office a minimum of three days per week.
We welcome applicants who require visa sponsorship and provide work authorization support for qualified candidates.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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