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<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Statistical Genetics &amp; Human Biobanks Intern will support Translational Genetics research at Arrowhead Pharmaceuticals by developing AI-augmented workflows that integrate large-scale global human biobank data to identify disease-relevant genes for RNAi target discovery. This internship offers hands-on experience applying statistical genetics, functional genomics, and causal inference methods to real-world therapeutic discovery challenges. The intern will collaborate closely with computational and translational scientists to generate high-confidence, genetically supported hypotheses that inform target prioritization and decision-making.
This is an 11-week Summer Internship Program paying $27.00 per hour and this role requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Support analysis of large-scale genetic and biomedical datasets to help identify disease-relevant signals.</li>
<li>Assist in developing and applying analytical and AI-enabled workflows for data integration, interpretation, and reporting.</li>
<li>Contribute to evidence synthesis and data summarization to support research and target evaluation efforts.</li>
<li>Help assess consistency and robustness of findings across multiple datasets or sources.</li>
<li>Prepare clear summaries, visualizations, or reports to communicate results to the project team.</li>
<li>Present updates and findings during team meetings and participate in scientific discussions.</li>
<li>Collaborate with scientists and computational team members on research projects and special initiatives.</li>
</ul>
Requirements
<ul>
<li>Currently pursuing a PhD in Statistical Genetics, Human Genetics, Computational Biology, Bioinformatics, Biostatistics, or a closely related field.</li>
<li>Hands-on experience analyzing data from at least one major human biobank.</li>
<li>Proficiency in Python and/or R for statistical genetics and data analysis workflows.</li>
<li>Familiarity with GWAS summary statistics, rare variant interpretation (pLoF/GoF), and functional genomics datasets such as eQTL and pQTL.</li>
<li>Strong understanding of population genetics, genetic architecture, and variant-to-gene mapping.</li>
<li>Ability to translate genetic association evidence into actionable therapeutic hypotheses.</li>
<li>Excellent verbal and written communication skills and ability to collaborate in a cross-functional research environment.</li>
</ul>
Preferred 
<ul>
<li>Proficiency with statistical genetics and functional genomics tools such as REGENIE, SAIGE, TWAS frameworks, Mendelian randomization packages, and colocalization methods.</li>
<li>Demonstrated ability to interpret pLoF/GoF variants and integrate eQTL/pQTL data with GWAS findings to identify causal genes and pathways.</li>
<li>Experience developing AI- or LLM-assisted analytics for evidence synthesis, automation, or variant-to-gene mapping.</li>
<li>Strong interest in translational genetics, RNAi therapeutics, and data-driven target discovery.</li>
</ul>
California pay range $11,440—$11,440 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Statistical Genetics & Human Biobanks

<h3>Job Description</h3>
Job DescriptionSalary: $18.96 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Fisheries Observer!!

A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is recruitingReef Fish and ShrimpFisheries Observersto work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Southeast Fisheries Science Center (SEFCS) aboard commercial fishing vessels.

The primary goals of the governments shrimp and reef fish observer programs are to provide quantitative biological, vessel, and gear-selectivity information for the southeastern shrimp fishery and Gulf of Mexico reef fish fishery. Observers deploy on commercial shrimp and reef fish vessels operating in the Gulf of Mexico and South Atlantic.If you ever wanted to make a difference, this is how.

Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between the fishing industry and fisheries scientists like yourself. In order to facilitate cooperation, fisheries observers collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen.Commit to the journey!

Click toLearn More about Becoming a Fisheries Observer

Observers record detailed information on the gear and fishing activity of the vessels. Observers work on deck on vessels ranging from 30 to 90 on trips roughly ranging from 1 to 45 days collecting data on fish catch and bycatch, and incidental takes such as marine mammals, seabirds and marine turtles. After attending a 3-week paid training in-person training in Galveston, TX observers are deployed from ports throughout the Gulf of Mexico and southern Atlantic states. Gear types assessed include but are not limited to shrimp trawl, bottom longline, modified buoy gear, bandit reel, and handline. Training projected for end of March/ April timeframe.

Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.

This is a challenging job, and candidates must be mentally prepared to be away from home without access to internet or cellular telephone signal for multiple days and often weeks at a time. Candidates must be physically able to handle heavy lifting, working odd hours, and spending long days in rough seas. Many crews speak limited English compounding the effects of loneliness and isolation on long trips. Observing provides an excellent career in marine biology, as observers are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.

Compensation:Observersstarting pay is $18.96/hour. Dependent on enrollment in our H&amp;W benefit, observers may also be eligible for anadditional $4.93/hourfor the first 40 hours worked on each calendar week for a total of$23.89 hour. This is a fulltime position with benefits.Annually, observers earn between $35K - $55K a yeardependent on their availability to deploy offshore and their personal sea day accomplishments. Observers will be paid a minimum of 8 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.

AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.

Travel is reimbursedin accordance with federal travel guidelines at an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.

Minimum Qualifications:
<ul>
<li>A bachelor's degree from an accredited college or university with a major in one of the natural sciences and a minimum of 30 semester hours or equivalent in the biological sciences</li>
<li>At least one undergraduate course in math or statistics.</li>
<li>All relevant course work must have been performed at a level acceptable for credit at the candidates academic institution.</li>
<li>Experience with data entry on computers.</li>
<li>Observer candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
</ul>

Preferred Qualifications:
<ul>
<li>At-sea experience</li>
<li>The ability to work independently and live in close quarters with little to no communication for purposes other than safety status check-ins for up to 8 weeks. (phone, internet, email and other amenities are unavailable at-sea)</li>
<li>Coursework with dichotomous keys</li>
</ul>

Homeport:
Applicants must be currently living, or be willing to live within 50 miles of either Myrtle Beach or Charleston, SC

Contact:
If you would like to apply for one of these exciting new openings, please click the following linkCareers Pageto submit the following information.

<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts.</li>
</ul>

All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to theTalent Teamor 774-770-5833

An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

Reef Fish and Shrimp Fisheries Observer - South Carolina

<h3>Job Description</h3>
Job DescriptionCompany Description
We are Olsson. We engineer and design solutions that improve the world around us. As a company, we promise to always be responsive, transparent, and focused on results – for our people, our clients, and our company.
We're a people-centric firm, so it's no surprise our greatest asset is our people. The impact this creates is an environment that encourages our people to grow and be creative with their talents. This approach builds a culture that is uniquely Olsson. It allows us to grow our people as we grow our business. This, in turn, creates a lasting impact on the world around us.
Job Description
As one of our student interns on the Geotechnical team you will perform meaningful, hands-on, real-world work that will transform your classroom experience and help you envision your future career. Your experience will involve assisting our geotechnical engineering staff putting together geotechnical reports and appendices. You'll get an introduction to Olsson's culture that will help you evaluate our firm as a career choice. This position may occasionally assist with working in the lab and in the field performing various types of testing and reporting.
Freshman and sophomores are encouraged to apply. 

Qualifications
You are passionate about:
<ul>
<li>Working collaboratively with others</li>
<li>Having ownership in the work you do</li>
<li>Using your talents to positively affect communities</li>
</ul>
You bring to the team:
<ul>
<li>Strong communication skills.</li>
<li>Ability to contribute and work well on a team.</li>
<li>Proficiency in Microsoft Excel, Word, and Outlook.</li>
<li>Problem-solving and decision-making skills.</li>
<li>The ability to work in a constant state of alertness and safe manner.</li>
<li>The ability to work during the school year in addition to the summer.</li>
</ul>

#LI-DNI



Additional Information
Olsson specializes in engineering and design, client advisory services, planning, field services, and environmental. Improving the world has been our mindset from the very beginning, back when Olsson first opened for business in 1956. And it will be our mindset for years to come.
As an Olsson employee, you will:
<ul>
<li>Receive a competitive 401(k) match</li>
<li>Be empowered to build your career with tailored development paths</li>
<li>Have the possibility for flexible work arrangements</li>
<li>Engage in work that has a positive impact on communities</li>
<li>Participate in a wellness program promoting balanced lifestyles</li>
</ul>
In addition, full-time employees will receive our traditional benefits package (health care, vision, dental, paid time off, etc.) and the opportunity to participate in a bonus system that rewards performance.

Olsson is an Equal Opportunity Employer. We encourage qualified minority, female, veteran, and disabled candidates to apply and be considered for open positions. We do not discriminate against any applicant for employment or any employee because of race, color, religion, national origin, sex, sexual orientation, gender identity, gender, disability, age, military status, or other protected status.
Olsson understands the importance of privacy and is committed to protecting job applicants' personal information. Pursuant to the California Consumer Privacy Act, as amended by the California Privacy Rights Act (collectively, the "CCPA"), this notice explains Olsson's practices regarding the collection, use, and disclosure of personal information for job applicants residing in California. Please read this Notice carefully to understand our privacy practices.
For more information about the types of information we collect and how we use it in connection with your general access and use of our website, please review our general California Privacy Notice here.

Student Internship - Geotechnical

<h3>Job Description</h3>
Job Description
Field Scientist / Field Geologist – Environmental Remediation 
Location: Carlsbad, New Mexico
Employment Type: Full-Time
About the Role We are seeking a motivated Field Scientist / Field Geologist to support environmental remediation projects throughout New Mexico’s oilfield regions. Based in Carlsbad, this role is field-focused and central to the investigation and cleanup of soil and groundwater contamination. You will apply technical expertise, regulatory knowledge, and field leadership to ensure compliance with New Mexico Environment Department (NMED) requirements while contributing to environmental restoration efforts that matter to both the community and industry. This is a great opportunity for someone to get their foot in the door and grow within the environmental consulting industry.
Key Responsibilities
<ul>
<li>Conduct field investigations including soil, groundwater, surface water, and vapor sampling in accordance with NMED/EPA standards.</li>
<li>Oversee remediation activities including excavation monitoring, confirmatory sampling, and adaptive in-field decision-making.</li>
<li>Supervise drilling operations (direct-push, auger, and monitoring well installations) and ensure proper chain-of-custody and documentation.</li>
<li>Lead environmental site assessments (Phase I &amp; II ESAs), spill response, and post-cleanup verification.</li>
<li>Operate field instruments such as PID/FID meters, water-quality probes, GPS units, and GIS software.</li>
<li>Prepare accurate daily field logs, sampling documentation, and regulatory-ready reports.</li>
<li>Coordinate with subcontractors, drilling crews, clients, and project managers to ensure smooth field operations and effective remediation strategies.</li>
<li>Adhere strictly to health and safety plans (HAZWOPER, HASP) in active oilfield environments.</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor’s degree in Geology, Environmental Science, Earth Sciences, or related field.</li>
<li>2–4 years of field experience in environmental consulting or remediation.</li>
<li>Demonstrated experience working on New Mexico environmental sites with knowledge of NMED regulations and reporting requirements.</li>
<li>Strong technical writing and reporting skills; proficiency in Microsoft Office.</li>
<li>Valid driver’s license with clean record.</li>
<li>OSHA 40-hour HAZWOPER (or ability to obtain).</li>
</ul>
Preferred Qualifications
<ul>
<li>Oilfield remediation experience (spill response, soil excavation, groundwater recovery).</li>
<li>Familiarity with regulatory communications to NMED.</li>
<li>Experience with ISNetworld or Veriforce compliance systems.</li>
<li>GIS mapping or digital field data platforms.</li>
<li>First Aid/CPR certification and mechanical troubleshooting ability.</li>
</ul>
Working Conditions
<ul>
<li>Primarily outdoor work in oilfield and remote environments under varying weather conditions.</li>
<li>Frequent travel to regional project sites, with occasional overnight stays.</li>
<li>Physical requirements include lifting up to 50 lbs., standing for long periods, and navigating uneven terrain.</li>
</ul>
Why Join Us
<ul>
<li>Full benefits: health insurance, 401(k) with company match, paid time off, and training.</li>
<li>Diverse project exposure across all phases of environmental remediation—from investigation to site closure.</li>
<li>Opportunity to directly contribute to environmental restoration in one of the nation’s most active oilfield regions.</li>
<li>Supportive culture built on safety, technical expertise, and professional growth.</li>
<li>A career-building role for those ready to learn, grow, and advance.</li>
</ul>
Please Note:
<ul>
<li>Candidates must be authorized to work in the U.S, no sponsorship is available. </li>
<li>Relocation reimbursement is not available.</li>
<li>Must live within commuting distance of Carlsbad, NM.</li>
<li>Must be available to start within 2–3 weeks of offer.</li>
</ul>

Field Geologist / Scientist - Earth Systems R&R

<h3>Job Description</h3>
Job DescriptionSublime is advancing a breakthrough, clean, efficient, low-waste process for manufacturing cement, the essential ingredient in the most-consumed human-made material on Earth: concrete. Replacing 200-year-old manufacturing methods that are reliant on kilns running hotter than lava, our near-ambient-temperature, electrochemical technology manufactures industry-accepted cement and critical minerals. We’re partnering with leading general contractors, concrete producers, developers, and technology hyperscalers to deploy our clean, durable, beautiful Sublime Cement® in infrastructure that is defining the future of clean construction. Backed by some of the world’s largest cement producers, leading private investors, and the U.S. Department of Energy, we are assembling a talented, collaborative team that is "amped about cement" (pun intended) and committed to operating on the frontiers of material science, manufacturing, industry, construction, and commercial partnerships, to advance cement innovation that will endure for the next millennium. &nbsp;Sublime is seeking a&nbsp;Managing Scientist&nbsp;to&nbsp;join the product&nbsp;R&amp;D team and&nbsp;contribute to the development of&nbsp;the next generation of&nbsp;our decarbonized cement. &nbsp;Ideal candidates&nbsp;will&nbsp;bring&nbsp;strong&nbsp;expertise&nbsp;in&nbsp;one or more&nbsp;of&nbsp;following&nbsp;areas:&nbsp;mineral&nbsp;processing&nbsp;(grinding)&nbsp;and&nbsp;particle technology, and/or&nbsp;suspension&nbsp;rheology.&nbsp;This&nbsp;Managing&nbsp;Scientist&nbsp;will&nbsp;be responsible for&nbsp;managing&nbsp;projects,&nbsp;conducting&nbsp;research&nbsp;and leading cross&nbsp;functional efforts&nbsp;to improve the performance of&nbsp;Sublime Cement through literature reviews, designing experiments, performing hand-on&nbsp;characterization&nbsp;and testing in lab, analyzing and interpreting data, and communicating results. This&nbsp;Scientist will&nbsp;also&nbsp;utilize&nbsp;their&nbsp;expertise&nbsp;to help set technical priorities and research strategy, plan and prioritize experiments, and contribute to the successful operation of our shared laboratory.  &nbsp;&nbsp;This&nbsp;Managing Scientist will manage a team of 2-5 people&nbsp;with significant cross-functional&nbsp;responsibilities&nbsp;that will report to Sublime’s&nbsp;Director&nbsp;of&nbsp;Product&nbsp;R&amp;D. This position is&nbsp;in-person&nbsp;at Sublime’s headquarters in Somerville, MA, with occasional flexibility to work from home as&nbsp;appropriate based&nbsp;on team and project needs. &nbsp;Responsibilities for this role will include:
<ul>
<li>Provide technical leadership in the development, validation, and optimization of cement formulations, with emphasis on mineral processing, milling, particle technology, and&nbsp;suspension&nbsp;rheology.&nbsp;</li>
<li>Lead&nbsp;team&nbsp;and coordinate multiple R&amp;D workstreams simultaneously, ensuring alignment with product development priorities and timelines.&nbsp;Provide guidance,&nbsp;mentorship,&nbsp;and technical oversight to other scientists and engineers.&nbsp;</li>
<li>Partner closely with&nbsp;Pilot /&nbsp;Process R&amp;D&nbsp;and other cross-functional teams to&nbsp;establish&nbsp;tight feedback loops between laboratory results, process constraints, and scale-up learnings.&nbsp;</li>
<li>Design, execute, and interpret experimental programs involving milling and grinding, rheology, and cement property measurements; analyze data and clearly communicate results and implications.&nbsp;</li>
<li>Develop and execute rheological testing strategies to characterize flow behavior, thixotropy, structuration,&nbsp;particle&nbsp;interactions&nbsp;and&nbsp;additive/admixture compatibility in cementitious systems.&nbsp;</li>
<li>Evaluate and optimize grinding and classification parameters to control particle size distribution, surface area, and morphology in support of fresh and hardened cement performance.&nbsp;</li>
<li>Contribute to&nbsp;cement performance and&nbsp;technology development through literature review,&nbsp;balancing chemistry/processing/manufacturability consideration,&nbsp;competitive analysis, and engagement with external experts, suppliers, and industry partners.&nbsp;</li>
<li>Develop,&nbsp;validate, and implement new test methodologies to characterize cement performance, processing behavior, and scale-up risks.&nbsp;</li>
<li>Maintain, calibrate, and expand laboratory capabilities, particularly in rheology and particle&nbsp;engineering.&nbsp;</li>
<li>Author technical white papers, internal reports, and patent applications to document and protect Sublime’s innovations.&nbsp;</li>
<li>Champion safety and responsible laboratory practices, particularly when developing new experimental methods and processes.&nbsp;</li>
<li>Foster a collaborative, inclusive, and innovative team culture, setting expectations for rigor, accountability, and continuous learning.&nbsp;</li>
</ul>
Requirements Include:
<ul>
<li>Ph.D. in Materials Science &amp; Engineering, Chemical Engineering, Civil Engineering, or&nbsp;related discipline.&nbsp;</li>
<li>2+ years of industry experience in research and development,&nbsp;materials&nbsp;engineering.&nbsp;</li>
<li>Strong technical foundation in inorganic materials and particle-based systems, with&nbsp;demonstrated&nbsp;expertise&nbsp;in: Mineral processing and milling, Particle technology&nbsp;and PSD control,&nbsp;Suspension rheology and&nbsp;rheometry.&nbsp;</li>
<li>Proven ability to develop and interpret structure–property relationships for cementitious&nbsp;systems&nbsp;to guide material design and performance optimization.&nbsp;</li>
<li>Hands-on experience with characterization techniques such as laser diffraction, TGA, XRF, XRD, BET, optical microscopy, and/or SEM.&nbsp;</li>
<li>Experience&nbsp;in&nbsp;leading research projects involving hypothesis-driven experimentation, DOE, and statistical data analysis&nbsp;to measure physical and chemical properties relevant to cementitious materials.&nbsp;</li>
<li>Demonstrated&nbsp;leadership and project management skills, including the ability to prioritize work,&nbsp;develop and&nbsp;manage&nbsp;complex workflows, and drive progress across multiple R&amp;D initiatives.&nbsp;</li>
<li>Strong written and verbal communication skills, with the ability to present technical findings clearly to diverse audiences&nbsp;and build effective cross-functional relationships&nbsp;across disciplines and organizational boundaries.&nbsp;</li>
<li>Strong attention to detail and data quality, paired with the ability to&nbsp;maintain&nbsp;a system-level, strategic perspective.&nbsp;</li>
<li>Ability to thrive in a&nbsp;dynamic,&nbsp;collaborative&nbsp;and inclusive&nbsp;startup environment&nbsp;with&nbsp;adaptability,&nbsp;professionalism,&nbsp;and&nbsp;a&nbsp;positive&nbsp;“can-do"&nbsp;attitude.</li>
</ul>
Sublime Systems is proud to be an Equal Opportunity EmployerAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law. Your Right to WorkIn compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Notice of E-VerifySublime Systems use E-Verify to confirm the identity and employment eligibility of all new hires.
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.

Managing Scientist- Product

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Head of Mariana Research
 
Description: 
We are seeking an experienced Head of Chemistry to join and lead Marianas Chemistry organization, advancing personalized medicine and radiopharmaceuticals.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Lead, mentor, and develop a growing team of chemistry professionals, fostering a collaborative and innovative environment.</li>
<li>Set the strategic direction for the chemistry function, ensuring alignment with the companys overall scientific and business objectives.</li>
<li>Drive the design, synthesis, and optimization of novel radiopharmaceutical drug candidates, ensuring they meet preclinical requirements for potency, selectivity, and ADME properties.</li>
<li>Provide scientific and strategic guidance to cross-functional teams (including biology, radiopharmacology, preclinical development, imaging, and clinical development) to advance projects through discovery and development.</li>
<li>Evaluate assay and instrument performance, ability to troubleshoot issues.</li>
<li>Collaborate with internal and external partners to integrate cutting-edge technologies and methodologies (e.g., structure-based design, computational chemistry, medicinal chemistry) to accelerate drug discovery.</li>
<li>Stay ahead of emerging trends and innovations in medicinal chemistry and oncology to ensure the company remains at the forefront of the field.</li>
<li>Lead the timely delivery of key milestones in the drug discovery process, from hit identification through lead optimization; support preclinical development, translational, and clinical activities.</li>
<li>Promote professional development opportunities for team members through mentorship, training, and career advancement.</li>
<li>Effectively manage the teams workload and distribution to ensure proper load management and optimize each programs chance for success based on each individuals strengths.</li>
<li>Oversee effective CRO management for external vendors to optimize value, efficiency, and speed.</li>
<li>Partner with senior leadership to shape the company's R&amp;D pipeline and identify new opportunities to address critical oncology challenges.</li>
</ul>
 
Requirements/Skills:
<ul>
<li>Ph.D. in Chemistry (Medicinal Chemistry, Organic Chemistry, or related field) with a strong record of achievement in oncology drug discovery.</li>
<li>12+ years of experience in the pharmaceutical or biotechnology industry, with at least 5 years in a leadership role.</li>
<li>Proven track record of success in leading chemistry teams and advancing oncology drug candidates to development candidates and beyond.</li>
<li>Strong leadership and management skills, with a demonstrated ability to inspire and guide cross-functional teams.</li>
<li>In-depth knowledge of medicinal chemistry principles, drug design strategies, and preclinical drug development.</li>
<li>Expertise in synthetic organic chemistry, structure-based drug design, and/or computational chemistry is highly desirable.</li>
<li>Experience in peptides is highly preferred. </li>
<li>Experience in targeted radiopharmaceuticals is preferred but not required.</li>
<li>Demonstrated track record of success in oncology is required.</li>
<li>Strong problem-solving, analytical, and decision-making skills.</li>
<li>Excellent communication and presentation skills, with the ability to articulate complex scientific concepts to both technical and non-technical stakeholders.</li>
<li>Strategic thinker with the ability to manage multiple priorities in a fast-paced, dynamic environment.</li>
</ul>
 
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>
 
 
Mariana Oncology Compensation Summary:
The salary for this position is expected to range between $189,420.00 and $351,000.00 per year. Your compensation will also include a performance-based cash incentive.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and will be reviewed periodically upon joining Mariana Oncology. Mariana may change the published salary range based on company and market factors.

US-based eligible employees will receive a comprehensive benefits package that includes a strong health insurance package, life insurance, disability benefits, a 401(k) with company contribution and match, tuition reimbursement, and a variety of other benefits. In addition, employees are eligible for a generous flexible time off program.

Head of Chemistry

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
As a Quality Control Chemist, you will be responsible for performing routine analysis of raw materials, in-process, and finished products. This includes conducting tests such as titrations, FTIR, GC, HPLC, Color, and using a viscometer. Your role involves performing calculations for batch tests in a lab environment using instrumentation and physical test methods. You will follow setup procedures and work instructions for laboratory equipment while adhering to customer and company quality standards. Safety is paramount, so you must follow all safety rules and regulations, including the use of appropriate PPE at all times.
Responsibilities
<ul>
<li>Conduct routine analysis of raw materials, in-process, and finished products.</li>
<li>Perform tests including titrations, FTIR, GC, HPLC, Color, and viscometer.</li>
<li>Carry out calculations for batch tests using lab instrumentation and physical test methods.</li>
<li>Set up and operate laboratory equipment according to established procedures.</li>
<li>Ensure compliance with customer and company quality standards.</li>
<li>Follow all safety rules and regulations, using appropriate PPE at all times.</li>
</ul>
Essential Skills
<ul>
<li>Minimum 1 year of industry experience in analytical testing, troubleshooting, and quality assurance.</li>
<li>Proficiency in gas chromatography (GC), high-performance liquid chromatography (HPLC), and FTIR.</li>
<li>Strong understanding of quality control processes in chemical manufacturing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Chemistry or other Sciences preferred; AS in Chemistry is acceptable.</li>
<li>Experience in chemical manufacturing is preferred.</li>
<li>Familiarity with basic laboratory equipment (GC/LC/FTIR) and techniques (titration, liquid-liquid partition).</li>
</ul>
Work Environment
You will work independently on the night shifts in the lab, handling chemical products. The lab is equipped with newer equipment to assist with testing. The work schedule is a 12-hour night shift, following a 2/2/3 non-rotating pattern in a 7-day x 24-hour chemical operation, from 7PM to 7AM. The role offers opportunities for cross-training and education in certifications, contributing to employee development and career growth.
Job Type &amp; Location
This is a Contract to Hire position based out of High Point, NC.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 High Point,NC.
Application Deadline
This position is anticipated to close on Jan 16, 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 Title: Research Associate - Formulations
Job Description
The Research Associate in Formulation Sciences plays a crucial role in advancing scientific experiments and research to support pre-clinical and clinical formulation development programs. This position requires designing, executing, and analyzing complex experiments using Quality-by-Design approaches. The focus is on supporting intravenous and subcutaneous formulation development and stability characterization for regulatory submissions. The role involves maintaining rigorous documentation and adhering to quality standards to ensure reproducibility and compliance. Ultimately, this position drives the generation of high-quality data that informs strategic formulation decisions and accelerates the development of products.
Responsibilities
<ul>
<li>Design and conduct advanced experiments in formulation development and drug stability according to ICH, FDA, and EMA standards.</li>
<li>Prepare and maintain accurate records of experimental procedures, observations, and results in laboratory notebooks and electronic databases.</li>
<li>Analyze and interpret DoE experimental data using statistical and modeling tools.</li>
<li>Collaborate with interdisciplinary teams to develop research strategies and troubleshoot technical challenges.</li>
<li>Prepare detailed reports, scientific manuscripts, and presentations to communicate findings to internal and external stakeholders.</li>
<li>Mentor and train junior research staff to enhance laboratory skills and ensure adherence to best practices and safety standards.</li>
</ul>
Essential Skills
<ul>
<li>Strong foundation in protein-based formulation development with 3+ years of industry experience.</li>
<li>Highly skilled in hands-on laboratory work and familiar with analytical equipment.</li>
<li>Capable of designing and executing formulation studies for intravenous and subcutaneous routes.</li>
<li>Solid understanding of FDA stability requirements and attention to detail.</li>
<li>Experience with biophysical characterization techniques and plate-based assays.</li>
<li>Strong analytical and documentation skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Biotechnology, Molecular Biology, Biochemistry, Chemical/Biochemical Engineering, or a related field with at least 3 years of experience, or a Master’s degree or higher in a relevant scientific discipline.</li>
<li>Strong experimental skills with standard laboratory techniques, including weighing of excipients, pipetting, solution and buffer preparation.</li>
<li>Familiarity with common lab instruments such as pH meters, balances, UV-Vis spectrophotometers, automated liquid handlers, and osmometers.</li>
<li>Ability to learn new skills and techniques as relevant.</li>
<li>Experience with formulation development for pharmaceutical products is a plus.</li>
<li>Experience with biophysical instrument techniques such as dynamic light scattering, circular dichroism, differential scanning calorimetry, particle analysis via membrane imaging, and viscometry is a plus.</li>
</ul>
Work Environment
The role operates under standard business hours and involves collaboration with interdisciplinary teams. The environment is supportive of learning and development, with opportunities for mentoring and skill enhancement.
Job Type &amp; Location
This is a Contract position based out of Durham, NC.
Pay and Benefits
The pay range for this position is $38.00 - $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 26, 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.

Senior Research Associate - Formulations

<h3>Job Description</h3>
Job DescriptionLCMS Lead Scientist
Job Description
As a LC-MS Lead Scientist, you will play a pivotal role in overseeing bioanalytical studies, ensuring that all methods meet regulatory and client requirements. You will not be working directly in the lab but will be responsible for reviewing data, signing off on reports, and acting as the primary scientific point of contact. Your expertise will guide the bioanalytical study work, and you will coordinate with regulators and stakeholders, both internally and externally.
Responsibilities
<ul>
<li>Oversee studies and ensure all methods are prepared, validated, executed, and documented to meet regulatory and client requirements.</li>
<li>Sign off on reports and approve raw data.</li>
<li>Act as the primary scientific point of contact for studies.</li>
<li>Coach and indirectly guide a team of up to 20 members.</li>
<li>Coordinate across internal and external stakeholders, including discussions with regulators for clinical or pre-clinical studies.</li>
<li>Travel up to 10% for cross-site or client visits.</li>
</ul>
Required Skills
<ul>
<li>B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.).</li>
<li>2-3 years of LCMS experience.</li>
<li>Experience as a Lead Scientist with 1-5 years (LS1) or 7-9 years (LS2) of experience.</li>
<li>Must have experience as a Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector (GLP or GCP regulations).</li>
<li>Full responsibility over the study, with experience in BioA CRO regulated space.</li>
<li>LBA (Ligand Binding Assay) experience, including data review/approval, protocol/sample analysis plan development, and method validation readiness.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with Sciex Mass Spec and analysis software.</li>
<li>Familiarity with LIMS, Nautilus, and Analyst software.</li>
<li>Knowledge of ICH or 28BMV regulatory guidance protocols and FDA internal standards.</li>
</ul>
Work Environment
The role is based in a lab setting within the Bioanalytical team, consisting of approximately 100 employees, including 60 chemists. This is a hybrid position, requiring 2-3 days onsite per week, with flexibility on the days but consistency each week. The role involves indirect reporting from method development chemists, validation chemists, sample analysis, and report writing. The work is workload-based rather than project-based, with a varying number of projects depending on client needs. The team is expanding, with current plans to increase from 16 to 18 members in Madison. Travel is limited, with a maximum of 10% required for client visits or conferences.
Job Type &amp; Location
This is a Permanent position based out of Madison, WI.
Pay and Benefits
The pay range for this position is $85000.00 - $110000.00/yr.
Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&amp;D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&amp;D Employee Stock Purchase Plan (ESPP)
Workplace Type
This is a hybrid position in Madison,WI.
Application Deadline
This position is anticipated to close on Jan 16, 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.

LCMS Lead Scientist

<h3>Job Description</h3>
Job Description???? Now Hiring: Chemical Operator | Join Our Team and Power the Process!
???? Location: Rock Hill, SC. ???? Schedule: Full-Time | 8-, 10-, or 12-hour shifts (Overtime &amp; Weekend Opportunities!) ???? Pay Type: Hourly | Non-Exempt
Are you ready to get hands-on in a fast-paced, safety-first manufacturing environment? We're looking for a Chemical Operator to join our operations team and play a key role in producing high-quality chemical products that make a difference. If you’re dependable, detail-oriented, and thrive in a production setting, this is your chance to grow your career in industrial manufacturing!
???? What You’ll Do:
✅ Operate and monitor a variety of process equipment including reactors, pumps, centrifuges, filters, and more ✅ Load/unload raw materials and finished goods safely and efficiently ✅ Monitor gauges and instruments, record data, and adjust valves and controls to ensure safe operations ✅ Troubleshoot and report mechanical/process issues as they arise ✅ Perform basic equipment maintenance and keep your work area clean and orderly ✅ Wear PPE and follow all HSEQ (Health, Safety, Environment &amp; Quality) protocols ✅ Communicate clearly with team members and participate in shift handovers
???? What You Bring:
✔️ High School Diploma or GED required ✔️ At least 1 year of experience in a manufacturing or chemical plant environment ✔️ Forklift experience (or willing to be trained) ✔️ Strong attention to detail and commitment to safety ✔️ Ability to work flexible hours, including overtime and weekends as needed
???? Bonus if you have: • WorkKeys Certification (SC) • 2+ years of relevant industry experience
???? Why You’ll Love Working Here:
???? Career growth potential ???? Team-oriented environment ???? On-the-job training ????️ Opportunity to work with cutting-edge equipment ???? Make a real impact in production
Ready to operate with purpose? ???? Apply today and bring your skills to a team that values your work and keeps safety at the core of everything we do.
Click below to schedule a conversation today: ???? Book a time here
or email me at: <a href="mailto:cwhitehead@qworksgroup.com" target="_blank">cwhitehead@qworksgroup.com</a>
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