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<h3>Job Description</h3>
Job DescriptionSalary: $60K-&amp;70K, DOE 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation.
 
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values:
 
<ul>
<li>Client Focused: We only succeed when our clients succeed.</li>
<li>Outstanding: We deliver meticulous results through outstanding performance.</li>
<li>Good: We act ethically and morally.</li>
<li>Employee-Centric: We honor and support our employees.</li>
<li>Nimble: We are prepared to adapt in an ever-changing industry.</li>
<li>Team-Oriented: We collaborate with each other and with our clients.</li>
</ul>
 
We currently have a role available for a Pharma Cell Biologist to join our San Diego based team.
 
Job duties include, but are not limited to, the following:
 Maintain and culture mammalian cells, including both adherent and suspension cell lines. Prepare, optimize, and maintain various cell culture media, supplements, and reagents. Perform routine cell passaging, counting, viability assessment, and cryopreservation.
<ul>
<li>Hands-on experience with mammalian cell culture, including adherent and suspension cells is a must.</li>
<li>Experience preparing and handling multiple types of cell culture media is required.</li>
</ul>
 Lyse cells and extract genomic DNA for downstream molecular biology applications.
<ul>
<li>Working knowledge of molecular biology techniques such as cell lysis, genomic DNA extraction, and PCR is required.</li>
</ul>
 Perform PCR and related molecular biology assays for genotyping or construct verification. Scale up plasmid DNA preparations for transfection and experimental use.
<ul>
<li> Experience with plasmid DNA preparation, including mid- to large-scale plasmid production is highly desirable.</li>
</ul>
 Support transfection and cell-based assays as needed.
<ul>
<li>Prior transfection experience is highly desirable.</li>
</ul>
 Prepare and maintain laboratory reagents, buffers, and consumables. Accurately document experimental procedures and results in lab notebooks or electronic systems. Work collaboratively with team members to support project timelines and experimental goals. Ensure compliance with laboratory safety, biosafety, and regulatory requirements. This position is a hands-on, lab-based role. 
Job requirements include, but are not limited to:
<ul>
<li>BS/MS degree in Cell/Molecular Biology (or related field) and at least 1 year laboratory experience in industry is required.</li>
<li>Team player mentality with strong written and verbal communication skills. Will be required to work collaboratively with cross-functional teams including structural biology, molecular biology, biochemistry, and biophysics.</li>
<li>The ideal candidate will be organized, comfortable with multi-tasking, enthusiastic, self-motivated and details oriented, with the skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.</li>
</ul>
 This job posting will close by March 31st 2026 or when candidates are identified, whichever comes first.

Pharma Cell Biologist

<h3>Job Description</h3>
Job Description
Job Title: Associate Research Scientist - Stability
Job Description
The Associate Research Scientist - Stability will provide scientific and technical support in the research and development of plasma-derived or recombinant proteins. This role supports the Stability Group by managing the stability program, ensuring compliance with regulatory standards, overseeing stability chambers, and maintaining product safety and quality for both licensed products and developmental projects.
Responsibilities
<ul>
<li>Maintain product inventory for active stability studies, ensuring accountability and compliance with all requirements.</li>
<li>Coordinate with Packaging to acquire samples for stability evaluation and ensure the accuracy of sample labeling and documentation.</li>
<li>Facilitate the delivery of stability samples for laboratory testing and resolve discrepancies in collaboration with QC Sample Specialists and stability supervisors.</li>
<li>Monitor and maintain label printers, ensuring they are in good working order for stability requests.</li>
<li>Track requests for additional samples and generate monthly pull schedules for stability testing.</li>
<li>Generate and manage work orders for maintenance and repairs of stability equipment to prevent product loss.</li>
<li>Ensure compliance with test request sheets and conduct investigations to resolve GMP discrepancies.</li>
<li>Enter test data into stability databases and assist with filing stability records.</li>
<li>Remove samples from inventory upon completion of stability studies and initiate purchase and work orders for the Stability Group.</li>
<li>Train staff on sample handling and inventory procedures, and perform daily assessments of stability incubators and freezers.</li>
<li>Investigate excursions outside validated temperature ranges and analyze chamber temperature and humidity trends.</li>
<li>Conduct reviews to ensure equipment compliance and address chamber concerns proactively.</li>
</ul>
Essential Skills
<ul>
<li>Understanding of ICH guidelines and GMP requirements for Stability product storage.</li>
<li>Excellent communication skills for generating clear, accurate reports and interacting with cross-functional teams.</li>
<li>Working knowledge of equipment and storage facility operations.</li>
<li>Ability to resolve chamber-related issues quickly and assess the impact of deviations.</li>
<li>Proficiency in ScienTek Stability System, labeling solutions software, Intermec printers, SAP, DeltaV Monitoring System, LabWatch, Maximo Management System, and TempTale Monitoring Devices.</li>
<li>Experience in visual inspection and vial integrity testing, as well as biological sample shipment.</li>
<li>Basic calculation skills, attention to detail, and effective verbal and written communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>MS Degree or BS with 1-2 years of experience, or no degree with 5 years of experience relevant to the role.</li>
<li>Education in a scientific field or experience in the regulated pharmaceutical industry.</li>
<li>Technical expertise in separations-based analytical techniques such as HPLC, Capillary Electrophoresis, and SDS-PAGE.</li>
<li>Working knowledge of Waters Empower and proficiency in method development and qualification based on ICH guidelines.</li>
</ul>
Work Environment
The work environment includes clinical and laboratory settings with exposure to biological fluids, potential infectious organisms, and chemicals. Personal protective equipment such as protective eyewear, garments, and gloves is required. The position involves frequent sitting and neck bending, occasional standing and waist twisting, and hand movements. Moderate lifting of 15-30 lbs. is required. The role demands precise coordinated movements and the ability to communicate complex information effectively. The work involves collaborating with diverse groups to address complex issues and performing tasks with variable demands.
Job Type &amp; Location
This is a Contract position based out of Durham, NC.
Pay and Benefits
The pay range for this position is $37.50 - $43.00/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 Durham,NC.
Application Deadline
This position is anticipated to close on Jan 20, 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.

Associate Research Scientist - Stability

<h3>Job Description</h3>
Job DescriptionDescriptionKnowles Valencia is seeking reliable, detail-oriented, multi-area Cleanroom Operators to join our team on third shift.&nbsp; The Cleanroom Operator is responsible for executing manufacturing processes within a semi-automated system, rotating through multiple workstations in a controlled cleanroom environment. The ideal candidate will bring prior cleanroom experience, excellent manual dexterity, and a strong commitment to quality, safety, and precision. Key Responsibilities
<ul>
<li>Operate across various cleanroom workstations to support different stages of the manufacturing process.</li>
<li>Follow established protocols and safety standards to maintain product integrity and a sterile environment.</li>
<li>Monitor equipment and report any irregularities or malfunctions promptly to engineer.</li>
<li>Perform routine cleaning and maintenance of workstations and tools.</li>
<li>Accurately document production data and adhere to quality control procedures</li>
<li>Collaborate with team members to meet production goals and resolve workflow issues</li>
<li>Rotate across multiple workstations within the cleanroom to support various stages of the manufacturing process.</li>
<li>Lift and maneuver metal bars and components weighing up to 15 pounds safely and efficiently.</li>
<li>Read and interpret manufacturing procedures, work instructions, and technical documentation.</li>
<li>Demonstrate reliability by consistently following instructions, meeting deadlines, and taking ownership of assigned tasks.</li>
<li>Maintain cleanliness and organization of workstations in accordance with 5S principles.</li>
<li>Flexibly support multiple areas as required by production demands.</li>
</ul>
 Skills, Knowledge and Expertise
<ul>
<li>High School diploma or general education degree (GED) is required.</li>
<li>Demonstrate knowledge of manufacturing principles practices, and procedures.</li>
<li>Ability to read and comprehend simple instructions</li>
<li>Computer Skills: Basic knowledge in computers, accessing email, training, and documents via company network.</li>
<li>This position will be performed in a clean room production environment which requires certain preparation and gowning practices.</li>
<li>Will and able to work overtime as requested.</li>
<li>Must be able to work in a clean room setting wearing appropriate clean room attires, which includes but is not limited to, jumpsuit, shoe covers, hair covering, and glasses.</li>
<li>To maintain contamination control standards, employees are prohibited from wearing makeup, lotions, or other personal care products while working in the cleanroom. These substances can shed particles or emit vapors that compromise the cleanroom environment and product integrity. All personnel must ensure their face and exposed skin are free of such products prior to gowning and entry.</li>
<li>Complete repetitive movements for extensive periods.</li>
<li>Able to lift, push, pull, or otherwise move objects of up to 15 pounds.</li>
<li>Ability to stand/seat for long periods of time.</li>
</ul>
 BenefitsWhat’s in it for you on Day 1:
<ul>
<li>Medical, dental and vision insurance plans</li>
<li>Prescription Drug Plans</li>
<li>Basic Life Insurance&nbsp;</li>
<li>401k plan with company match</li>
<li>Tuition Reimbursement Program</li>
<li>Employee Referral Program&nbsp;</li>
<li>Vacation and Paid Sick Leave</li>
<li>Paid Holidays</li>
</ul>
Exciting Onsite Perks:&nbsp;
<ul>
<li>Free coffee available at our cafeteria</li>
<li>Employee Appreciation Events</li>
</ul>
&nbsp;Knowles is committed to providing a competitive and fair total compensation package for all employees. One element in our total compensation package is base pay.&nbsp; The pay rate for this role is targeted at $20.00 per hour plus a third shift differential.&nbsp; &nbsp;Individual compensation decisions are based on a number of factors, including but not limited to previous experience and skills acquired prior to joining Knowles, cost of living in the assigned work location, assigned schedule, and salaries of similarly situated peers at the company.&nbsp; It is to be expected that candidates will come to us with different sets of skills and experiences and therefore will be paid at different points in the stated range.&nbsp; We recognize that the person(s) we select for hire may be less experienced or more experienced than the role as posted; if this is the case, any updates to available salary ranges will be communicated with candidates during the recruitment process. &nbsp; &nbsp;Equal Opportunity Statement: Knowles Precision Devices prohibits pay discrimination and discrimination of any kind based on race, color, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation, or other legally protected status. Notice to Staffing Agencies, Search Firms and Recruitment Agencies: The recruitment process at Knowles is managed through the Human Resources department. Knowles does not accept resumes submitted from 3rd party agencies outside of our system. To submit resumes, 3rd party agencies will need to be a pre-approved vendor with a valid contract in place, be actively engaged by Knowles to recruit for a specific position and have agency log in credentials to submit candidates to our careers portal. Please do not submit resumes via e-mail, through our external website or directly to our employees. Any resumes submitted in this way become the property of Knowles and will not be eligible for any placement fee.

Cleanroom Operator - Third Shift 11:30 PM - 7:00 AM

<h3>Job Description</h3>
Job DescriptionThis general submission posting is an opportunity to submit your resume for future consideration only; not for an existing opening. We anticipate this role may be open in the near future. If you wish to be considered for this potential opportunity, please submit your resume. When a position becomes available, you may be contacted by our Talent Acquisition team. The Company will only contact applicants who are selected for further consideration about potential future opportunities.&nbsp; Business Unit: Curated Position: Compositor, Sr Location: New York, NY (Remote) *Pay Range: $59.23 - $88.85 USD hourly POSITION SUMMARY: The Senior Compositor role requires creativity and high technical abilities. They will take direction from the VFX and Compositing Supervisors and will also be expected to work autonomously in a fast paced environment to deliver an extremely high level of work. The Compositor is often given the most complex and demanding shots to complete. They are expected to be comp generalists who can handle a wide range of comp tasks from start to finish including but not limited to compositing live action and CG, blue/green screen keying, camera tracking, photoreal CG integration, set extensions with matte painting projections, complicated removals, beauty work, and paint/rotoscoping. MAIN DUTIES: The Senior Compositor will take instruction and direction from Leads and VFX Supervisors to execute assigned shots in the most efficient and fastest way possible. They will balance&nbsp;the creative and technical aspects of each shot. They will meet&nbsp;task schedules and show deadlines. Other duties include:
<ul>
<li>Have an excellent understanding of the broader VFX pipeline including color space, workflow and industry-standard script layouts.</li>
<li>Ongoing communication with Production and Leads regarding schedules and deadlines.</li>
<li>Taking responsibility for own workload, time management and notes/feedback actions required by Supervisors.</li>
</ul>
 WHAT YOU BRING: The ideal candidate will&nbsp;be an expert in all aspects of compositing in Nuke, integrating 2D, 3D and live-action elements to a high-end visual effects standard. They will be a&nbsp;team player with a great attitude and an independent problem solver. They will take feedback and direction well with ability to understand and apply notes. They&nbsp;will bring experience with sound aesthetic with a good understanding of color, light and photography. The ideal candidate will also bring the following:
<ul>
<li>Clean and efficient script organization / dependable and flexible.</li>
<li>A strong creative eye, artistic and problem-solving skills&nbsp;/ extreme attention for detail.</li>
<li>Thorough understanding of compositing techniques.</li>
<li>Excellent people and communication skills.</li>
<li>Participate in creative and technical discussions.</li>
<li>Experience using Shotgrid.</li>
<li>Ability to work under tight deadlines.</li>
<li>Advanced knowledge of CG rendering and compositing multi-channel EXRs.</li>
<li>Excellent understanding of 2D and 3D tracking.</li>
<li>Highly proficient in using IBK, Primatte or Keylight.</li>
<li>Excellent knowledge of Nuke's 3D system.</li>
<li>Strong understanding of colorspace pipelines.</li>
<li>Experience with mocha, photoshop, other photo editing software is a plus.</li>
<li>Experience with Python scripting preferred.</li>
</ul>
 ABOUT THE COMPANY: Company 3, including its various business units and family of brands, provides a full range of Creative Services for content creators, including conceptual design, pre-vis, look development, ideation and rapid prototyping, 3D animation/CGI, motion graphics/designers, matte painting, compositing, dailies and production services, color grading, post-production finishing, marketing/trailers, live-action production, experiences, and more. Diversity and Inclusion at Company 3: Creativity has diversity at its core. We celebrate the value of each unique experience by being dedicated to fostering the most diverse, equitable, and inclusive culture where every employee feels empowered and safe to show up to work as their full self. It is our policy to provide equal employment opportunities to all applicants and employees. Please inform the Company's HR representative if you need assistance completing any forms or otherwise need any accommodation or support in order to participate in the application process. *The listed pay range represents the lowest to highest range that we in good faith believe we would pay for this role at the time of this posting. This range may be modified in the future. An employee’s pay position within the range may be based on several factors including, but limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, local currency exchange rates, performance, shift, travel requirements, sales or revenue-based metrics, applicable law, and business or organizational needs.&nbsp; The benefits for eligible part-time employees working 25 or more hours per week and full-time employees in the US include a comprehensive package of health, retirement, and insurance benefits and paid time off. The benefits for eligible project hires and part-time employees working less than 25 hours per week in the US include retirement, select insurance benefits, and where required by law, health benefits. For roles filled in Canada and other territories, local benefits plan offerings as adopted and amended from time to time will apply. The above compensation and benefits information is provided in accordance with various state, provincial, and local pay transparency laws. The Company’s recruitment processes will also be conducted in accordance with applicable law as adopted and amended from time to time. Both external and internal candidates can apply for this general submission posting through the Company’s Career Page.
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Compositor, Sr (General Submission)

<h3>Job Description</h3>
Job Description
Desired Experience: 
<ul>
<li>Formulating or compounding resins</li>
<li>Hands on laboratory experience in SMC, BMC, or Pultrusion molding processes.</li>
<li>Experience in formulation and compounding of unsaturated polyester and epoxy vinyl ester resins</li>
<li>Graduate research in polymer science (synthesis, compounding, or materials science)</li>
</ul>
Required Skills:
<ul>
<li>Excellent knowledge in resin chemistry formulations and compounding</li>
<li>Hands-on laboratory skills</li>
<li>Knowledge of physical testing and mechanical properties</li>
<li>Excellent organizational and project management skills</li>
<li>Strong written and oral communication skills</li>
<li>Interpersonal skills for customer and colleague collaboration</li>
<li>Microsoft Office</li>
</ul>
Additional Desired Skills and Characteristics:
<ul>
<li>Proven track record in product development, ability to recite and quantify these successes</li>
<li>Creativity, curiosity, mechanically inclined, problem solving, time management, ability to seek out and find new opportunities for composites, business acumen.</li>
</ul>
Required Qualifications:
<ul>
<li>M.S. in Polymer Science, Material Science, Chemistry, Chemical Engineering, Composites Engineering or related field. (Ph.D. candidates will be considered).</li>
</ul>
Other:
<ul>
<li>Minimal travel, up to 10%</li>
<li>Applicants must be currently authorized to work in the US on a full-time basis. This position is not eligible for immigration sponsorship.</li>
</ul>
 

Job Description:
The Scientist, Structural Composite Molding Formulations at AOC will be based in Valparaiso, Indiana. The main responsibilities are product development of AOC products for composite applications that are using sheet molding compound, bulk molding compound and pultrusion. Examples of end uses are construction, automotive and infrastructure. The position is hands on with formulating, compounding and molding. The candidate should be mechanically inclined as well as have excellent chemical formulation knowledge, specifically with unsaturated polyester and epoxy vinyl ester chemistries. The individual will support the product leaders and the technical manager in design of experiments, formula development, preparing samples with hands on laboratory work, maintaining equipment, molding, and authoring technical reports. Organization and project management skills are important as well as business acumen. Salary is negotiable and commensurate with experience. Individuals with experience and skills far exceeding those in this job descriptions will be eligible for a senior material scientist role.

Material Scientist, Composite Molding Formula

<h3>Job Description</h3>
Job Description
Position Purpose: 
We are seeking an experienced subject matter expert in molecular biology and/or microbiology to provide technical support to Signature Science’s quality assurance (QA) contracts for national and homeland security programs, with a focus on CBRNe collection and analysis efforts. The successful candidate will also support internal Signature Science quality programs, including the Signature Science ISO 17043 accredited Proficiency Testing Program, through auditing, quality management system document development and QA laboratory support

Essential Duties and Responsibilities:
<ul>
<li>Provide subject matter expertise in the areas of molecular biology and/or microbiology as they pertain to quality assurance of collection or analytical activities</li>
<li>Serve as a Lead Auditor for external audits of client laboratories and/or sample collection teams, providing on-site identification of audit findings, interacting directly with management of auditee organization, delivering an oral out-brief summary of audit findings, and overseeing the development of the written audit report.</li>
<li>Provide feedback on auditee corrective actions</li>
<li>Assist client laboratories in preparing for external ISO 17025 accreditation assessments and attend assessments as an advocate for the client laboratory.</li>
<li>Perform internal audits of Signature Science systems and procedures against relevant internal or external standards, including audits of the Signature Science Proficiency Test Program against the requirements of ISO/IEC 17043 and internal policies and procedures.</li>
<li>Review and summarize quality assurance and/or proficiency test data, provide input and review of technical reports, identify data trends and other issues.</li>
<li>Contribute to the development and revision of project quality documents based on the ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and Clinical Laboratory Improvement Program (CLIP) standards, as applicable.</li>
<li>Provide ISO 17025 (or other quality topics) training to clients</li>
<li>Other activities may include:</li>
<li>Perform proficiency test sample preparation laboratory activities, including sample spiking, microbiological analysis, nucleic acid extraction, PCR analysis, immunoassay analysis, and packaging samples for shipment. o Lead or assist with the validation and/or verification of new methods o Communicate with external laboratory staff to help resolve QA, PT, or other quality-related issues o Serve as a task leader on one or more projects</li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li>Knowledge of PCR, immunoassay, and/or microbiological laboratory methods.</li>
<li>General quality management experience and familiarity with ISO/IEC 17025 and ISO/IEC 17043 standards.</li>
<li>Analytical laboratory auditing experience;</li>
<li>Ability to lead small teams and ensure accurate and timely submission of project deliverables</li>
<li>Proficiency in MS Word, MS Excel, and MS PowerPoint</li>
<li>Strong written and verbal communication skills</li>
<li>Proactive, self-starter</li>
</ul>

Education/Experience:
<ul>
<li>Bachelor degree (or higher) in biology or related field</li>
<li>5-10 years of experience performing molecular biology and/or microbiological laboratory methods and/or providing quality assurance support to molecular biology and/or microbiological analytical programs</li>
</ul>
 

Certificates and Licenses:
Certified Quality Auditor (CQA) certification required. This certification must be obtained within 6 months from date of hire.
 
Clearance:
Candidate must be able to obtain a Secret level security clearance.

Supervisory Responsibilities:
N/A
 
Working Conditions/ Equipment:
<ul>
<li>Ability to work in varying conditions to include: traditional office environments with sedentary extended periods required for voluminous data analysis via office automation;</li>
<li>Climate controlled laboratory environments requiring extended periods of standing when performing laboratory analyses, or during audits and SOP observation;</li>
<li>Mobile laboratories, subject to wide ranges of temperature and humidity requiring extended periods of standing, stooping or kneeling in confined spaces; conference, classrooms or theaters that involve extended periods of standing for training delivery or command briefings; and outdoors in various weather and lighting conditions including heat, humidity, cold, snow, bright sun, and dark night.</li>
<li>Exposure to various chemical and biological materials associated with an analytical lab or facility.</li>
<li>Ability to wear required personal protective equipment (PPE) including gloves, coats or gowns, shoe cover, tyvek coveralls, safety glasses, respirators, and/or PAPRs.</li>
<li>Subject to medical monitoring based on lab functions.</li>
</ul>

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.
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QA Biologist

<h3>Job Description</h3>
Job Description The Air-Conditioning, Heating, and Refrigeration Institute (AHRI) is one of the largest trade associations in the nation, representing more than 300 heating, ventilation, air-conditioning (HVAC), water heating, and commercial refrigeration manufacturers from all parts of the world. Ensuring human comfort, productivity, and safety while practicing environmental stewardship is the mission of AHRI. Through our certification program, standards, advocacy, and other activities, we strive to help save energy, improve productivity, and ensure a better environment. AHRI’s internship program is approximately 8 weeks long, beginning in early June. Interns will have the opportunity to contribute to professional projects and in turn, develop their skills in problem solving, research, and communication while working in a team-oriented environment. This internship is based in our main office in Arlington, VA. Join us and see how AHRI strives to Make Life Better. We are looking for an enthusiastic and motivated intern for our Advocacy Team! The ideal candidate is pursuing a degree in Mechanical Engineering, but a general engineering major is acceptable as well. Your internship experience will include:
<ul>
<li>Evaluate the current project tracking and management system and identify sticking points or opportunities for improvement. Create brief reports that cover problems, opportunities, and possible new features that would improve the workflow.</li>
<li>Complete a literature review of recent AHRI and AHRTI projects, including project charters, contracts, and proposals. Consult with Research staff on current statuses and key points. </li>
<li>Complete a full meeting cycle around a specific project, including planning, agenda development, approval processes, meeting operation, and minutes. Learn proper formatting, writing style, and organizational practices.</li>
<li>Compile a list of current issues and trends in the HVACR (heating, ventilation, air-conditioning, and refrigeration) world. Issues can be within the realm of policy, regulatory, technical issues/advancements, or research trends. </li>
<li>Attend various meetings and webinars both within and outside the organization to learn about these issues and gain an understanding of how the public and private sectors interact and coordinate. &nbsp;</li>
</ul>
Qualifications: Actively pursuing a degree from an accredited college or university. Consideration will be given to recent graduates (no more than 6 months since graduation date). Skills: Microsoft Office skills, basic research skills. Compensation: This is a part-time paid internship at $20/hour, up to 28 hours/week. AHRI does not offer any housing assistance; if you are applying from out-of-state and have any questions about housing, please contact Nicole Rich at <a href="mailto:nrich@ahrinet.org" target="_blank">nrich@ahrinet.org</a>. Application deadline: applications must be received by March 13, 2026. To apply, please visit our website. A full application includes a cover letter, resume, 1 letter of recommendation, and a school transcript. Please consolidate documents into 1 PDF file. AHRI does not discriminate and will not tolerate discrimination on the basis of race, color, national origin, military service, ethnic origin, sex, sexual orientation, age, handicap, or differing ability as those terms are defined under applicable law in its selection, recruitment, or employment practices. This position does not offer employment-based visa sponsorship and/or assistance to include H1B, F1- OPT or F1-CPT visas. &nbsp;
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Intern - Advocacy - Research

<h3>Job Description</h3>
Job Description
Laboratory Toxicology Supervisor Rocky Mountain Laboratories – Draper, Utah
About Us Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting-edge technology and a customer-focused approach.
Position
The&nbsp;Laboratory Toxicology Supervisor&nbsp;is responsible for leading day-to-day operations within the toxicology department, with a strong focus on&nbsp;clinical accuracy, regulatory compliance, and operational efficiency. This role combines hands-on technical expertise with supervisory leadership in a&nbsp;high-complexity clinical toxicology laboratory.
The successful candidate will oversee&nbsp;LC-MS/MS instrumentation, method validation, quality control processes, and staff training while ensuring compliance with&nbsp;CLIA, CAP, OSHA, and other applicable regulatory standards. This position serves as the primary technical and operational lead for toxicology testing and acts as the department representative in the absence of the Lab Manager.
Schedule: Full-time, onsite in Draper, Utah Monday to Friday 0800 to 1630 with some flexibility
Responsibilities:
<ul>
<li>Supervise daily operations of the toxicology laboratory to ensure accurate, timely, and compliant testing</li>
<li>Oversee&nbsp;LC-MS/MS and mass spectrometry instrumentation, including calibration, maintenance, troubleshooting, and method optimization</li>
<li>Develop, implement, and maintain&nbsp;Standard Operating Procedures (SOPs)&nbsp;for validations, clinical testing, and regulatory compliance</li>
<li>Review, interpret, and release patient test results in accordance with laboratory policies and regulatory requirements</li>
<li>Manage&nbsp;quality control (QC) and quality assurance (QA)&nbsp;programs; investigate out-of-range results and implement corrective actions</li>
<li>Monitor workflow, prioritize testing, and allocate staff resources to meet turnaround time expectations</li>
<li>Conduct internal laboratory inspections, audits, and regulatory readiness activities</li>
<li>Ensure compliance with&nbsp;CLIA high-complexity testing, CAP standards, OSHA safety requirements, and other applicable regulations</li>
<li>Train, mentor, and evaluate laboratory staff; provide ongoing technical guidance and performance feedback</li>
<li>Collaborate cross-functionally with Chemistry, Molecular, Client Services, and other departments to resolve operational or testing issues</li>
<li>Ensure proper handling, storage, and disposal of hazardous and toxic materials</li>
<li>Drive continuous improvement initiatives related to workflow efficiency, cost control, and quality outcomes</li>
<li>Serve as acting leader for the toxicology department in the absence of the Lab Manager</li>
<li>Perform other duties as assigned</li>
</ul>
Required Qualifications:
<ul>
<li>Minimum&nbsp;2 years of documented clinical toxicology experience&nbsp;in a regulated laboratory environment</li>
<li>Hands-on experience with&nbsp;LC-MS/MS instrumentation, including sample preparation and data analysis</li>
<li>Strong knowledge of&nbsp;quality assurance and quality control&nbsp;principles</li>
<li>Demonstrated ability to follow and enforce regulatory standards (CLIA, CAP, OSHA)</li>
<li>Excellent organizational, analytical, and problem-solving skills</li>
<li>Strong written and verbal communication skills</li>
<li>Ability to manage multiple priorities while maintaining accuracy and compliance</li>
</ul>
Preferred Qualifications: 
<ul>
<li>3–5+ years&nbsp;of clinical toxicology laboratory experience, including&nbsp;at least 1 year in a supervisory or lead role</li>
<li>Clinical toxicology experience in&nbsp;pain management, drugs of abuse, or therapeutic drug monitoring</li>
<li>Hands-on experience with&nbsp;triple quadrupole mass spectrometry</li>
<li>Proficiency with&nbsp;Agilent 6460,&nbsp;MassHunter software, and&nbsp;Beckman AU 480/680 analyzers</li>
<li>Experience validating new assays and troubleshooting complex LC-MS/MS methods</li>
<li>Familiarity with&nbsp;Laboratory Information Systems (LIS)&nbsp;and electronic reporting workflows</li>
<li>Experience supporting laboratory audits and regulatory inspections</li>
<li>Ability to design and deliver technical training programs</li>
<li>Master’s degree in chemistry, toxicology, clinical laboratory science, or a related field</li>
</ul>
Education: Bachelor of Science or higher in chemistry, biology, clinical laboratory science, or related field
Job Type:&nbsp;Full-time Salary:&nbsp;$95,000 – $120,000 annually, including bonus opportunities
Benefits for full-time W2 Team Members: Benefits begin 60 days after the first full month of full-time employment.
<ul>
<li>Health, Dental, and Vision Insurance</li>
<li>Paid Time Off (21 days annually for full-time team members)</li>
<li>7 Paid Holidays</li>
<li>401(k) with 50% Company Match up to 6% ***</li>
<li>Health Savings Account (HSA)</li>
<li>Short-Term &amp; Long-Term Disability (RML covers 60% of STD premium) ***</li>
<li>Voluntary Life and AD&amp;D Insurance</li>
<li>100% Company-Funded Employee Assistance Program (EAP) ***</li>
</ul>
Ability to commute/relocate: Draper, UT: Reliably commute or plan to relocate before starting work (Required)
Ideal start date:&nbsp;When the right candidate is found Application Deadline:&nbsp;Applications are reviewed on a rolling basis, and the position may be filled before any stated deadline
If you meet the above qualifications and are interested in joining our team, please submit your resume for consideration. We look forward to hearing from you!
At Rocky Mountain Laboratories, we prioritize the care and well-being of our team members.
Equal Opportunity Employer Statement Rocky Mountain Laboratories is an Equal Opportunity Employer committed to diversity in its workforce. We comply with all applicable federal and state laws and prohibit discrimination based on race, ethnicity, religion, color, national origin, sex, age, sexual orientation, gender identity or expression, veteran status, disability, or genetic information. We also comply with the Americans with Disabilities Act (ADA) and provide reasonable accommodations to qualified individuals with disabilities.
Pre-Employment Notice &amp; E-Verify Rocky Mountain Laboratories participates in E-Verify. Employment is contingent upon successful completion of a background check and other pre-employment screenings, as required.
Employment with Rocky Mountain Laboratories is at-will. This means either the Team Member or the company may end the employment relationship at any time, with or without cause or notice, in accordance with applicable laws. Nothing in this posting or in future communications alters that relationship.
While we appreciate interest from staffing agencies, Rocky Mountain Laboratories does not currently partner with external agencies. Resumes submitted unsolicited will not be considered, and no fees will be paid.
Please only reference our LinkedIn and Indeed pages for current openings:
<ul>
<li><a href="http://www.linkedin.com/company/rocky-mountain-laboratories" target="_blank">www.linkedin.com/company/rocky-mountain-laboratories</a></li>
<li><a href="http://www.indeed.com/cmp/Rocky-Mountain-Laboratories" target="_blank">www.indeed.com/cmp/Rocky-Mountain-Laboratories</a></li>
<li><a href="http://www.rockylabs.com/" target="_blank">www.rockylabs.com/</a></li>
</ul>
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Laboratory Supervisor (Clinical Toxicology, LC-MS/MS)

<h3>Job Description</h3>
Job Description
RESPONSIBILITIES:
R&amp;D Technical Execution:
<ul>
<li>Conduct hand, laboratory, and pilot-scale trials for new and reformulated products, generating precise and accurate data reports.</li>
<li>Obtain raw materials, perform weighing, and execute product development trials, including pilot and clinical batches.</li>
<li>Perform product development equipment set-up, operation, and clean-up.</li>
<li>Perform visual inspection and physical testing on intermediates and finished trial products.</li>
<li>Maintain all documentation for trial batches in compliance with GMP standards.</li>
</ul>
Project Management &amp; Site Expansion Support:
<ul>
<li>Play a key role in site expansion and facility build-out projects by providing critical operational and technical input.</li>
<li>Serve as a primary R&amp;D liaison for third-party contractors, vendors, and equipment suppliers to ensure project alignment with technical requirements and timelines.</li>
<li>Support the timely execution of capital projects by coordinating R&amp;D activities with construction and installation schedules.</li>
<li>Assist in the commissioning and qualification (C&amp;Q) of new R&amp;D and pilot plant equipment.</li>
</ul>
Facility &amp; Operational Management:
<ul>
<li>Support facility management activities for the R&amp;D and pilot plant areas, including coordinating maintenance, calibrations, and repairs.</li>
<li>Assist in managing site services and infrastructure relevant to the R&amp;D operations to ensure minimal downtime.</li>
<li>Identify and implement process improvements to enhance operational efficiency, safety, and compliance within the R&amp;D facilities.</li>
<li>Act as lead to R&amp;D Technicians, assigning tasks and prioritizing workloads based on project and operational demands.</li>
</ul>
Additional Duties:
<ul>
<li>Perform other related duties as required to support the strategic and operational goals of the department and site.</li>
</ul>


QUALIFICATIONS:
Education &amp; Experience:
<ul>
<li>Bachelor’s degree in engineering, Science, or a related field is preferred; equivalent combination of education and significant relevant experience will be considered.</li>
<li>5+ years of experience in a pharmaceutical manufacturing or R&amp;D environment, with a demonstrated ability to handle increasing responsibility.</li>
<li>Proven experience in supporting facility projects, working effectively with third-party contractors, and managing timelines is highly desired.</li>
<li>Technical &amp; Professional Skills:</li>
<li>Able to apply concepts of basic algebra and geometry for calculations and layout planning.</li>
<li>Proficient in MS Word, Excel, and Project (or similar project management software).</li>
<li>Able to read and interpret technical procedures, SOPs, GMPs, construction plans, and equipment manuals.</li>
<li>Strong communication, coordination, and interpersonal skills for effective collaboration with internal teams and external parties.</li>
<li>Strong attention to detail and able to manage multiple complex tasks simultaneously.</li>
</ul>

Physical Requirements:
<ul>
<li>Able to regularly lift up to 25 pounds and navigate active construction or facility expansion sites as needed.</li>
</ul>
 
At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

SENIOR R&D TECHNICIAN SPECIALIST

<h3>Job Description</h3>
Job DescriptionAbout Becoming
Becoming is building Developmental Intelligence: AI for predicting how organisms change over time.
Most existing models work in short-horizon or static regimes. They fail when systems become long-horizon, nonlinear, and context-dependent — exactly where development, biology, and many real-world systems live.
We are building a new modeling primitive for reasoning about complex dynamics over time, starting with developmental biology and extending to other domains where prediction fundamentally breaks.

The Role
We are hiring a Research Scientist to help verify, validate, and shape a new modeling primitive designed for complex, time-evolving systems.
This role is not about incremental model improvements or benchmark chasing. Your responsibility is to rigorously evaluate whether this primitive works, where it works, where it fails, and why. You will help define its scope, limits, and evolution through careful analysis, experimentation, and comparison to existing approaches.
Your work will directly influence how the platform develops and how broadly it can be applied.

What You’ll Own
<ul>
<li>Validation of a new AI modeling primitive for long-horizon dynamical systems</li>
<li>Design of experiments and benchmarks that test stability, generalization, and predictive fidelity over time</li>
<li>Comparative evaluation against existing modeling approaches</li>
<li>Identification of failure modes, assumptions, and edge cases</li>
<li>Clear articulation of why the model succeeds or fails in different regimes</li>
<li>Translation of findings into guidance for future architecture and system design</li>
<li>Exploration of applicability across multiple domains with complex dynamics, not just biology </li>
</ul>

Who You Are
You are someone who:
<ul>
<li>Operates with high agency — you identify problems, define solutions, and execute</li>
<li>Brings high energy to complex, ambiguous engineering challenges</li>
<li>Acts with high integrity — you are honest about tradeoffs, risks, and failure modes</li>
<li>Communicates directly and clearly, especially when something won’t work</li>
<li>Is self-aware about your strengths and gaps, and proactively fills them</li>
<li>Thinks naturally in terms of dynamics, stability, and generalization</li>
<li>Enjoys stress-testing models to understand their limits</li>
<li>Is comfortable working on foundational problems with ambiguous answers</li>
</ul>
Requirements
Required
<ul>
<li>PhD or equivalent experience in applied mathematics, physics, computer science, machine learning, or a related field</li>
<li>At least 1 year of industry or applied research experience working on real modeling systems</li>
<li>Strong grounding in dynamical systems, time-series modeling, control, or sequence modeling</li>
<li>Experience evaluating models where ground truth is partial, delayed, or noisy</li>
<li>Ability to design validation strategies when standard benchmarks are insufficient</li>
<li>Comfort working with first-of-its-kind architectures and open-ended questions </li>
</ul>
Strong Signals
<ul>
<li>Experience with state-space models, world models, neural ODEs, diffusion over time, or hybrid approaches</li>
<li>Prior work on systems where prediction degrades over long horizons</li>
<li>Exposure to biological, physical, or other real-world dynamical systems</li>
<li>Track record of identifying why models fail — not just improving metrics</li>
</ul>
Benefits
<ul>
<li>Competitive salary and meaningful equity</li>
<li>Full benefits</li>
<li>High-trust, high-ownership environment</li>
<li>Rapid growth in scope and responsibility</li>
</ul>

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