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<h3>Job Description</h3>
Job Description
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow. 
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage— premiums either paid by Superior or highly subsidized—so you and your family can access great benefits with minimal cost. 
You’ll also join a supportive team, where experienced coworkers help you learn, grow, and succeed from day one. At Superior, you get more than a job—you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to team success.
We are currently seeking a Chemical Handler to work at our Louisville, KY location. The Chemical Handler is responsible for daily production, unloading raw materials, and completing paperwork, while maintaining a safe operation. 
This is a full-time, 1st shift position, working Monday through Friday, from 8:00 a.m. - 4:30 p.m. Additional hours may be required. 
What You’ll Do
<ul>
<li>Transfer products into and out of pails, drums, and totes utilizing transfer pumps and hoses.</li>
<li>Read detailed paperwork instructions regarding chemical amounts and blending instructions. </li>
<li>Pull product samples and submit to the Lab for quality control.</li>
<li>Label containers properly and secure to closure specifications.</li>
<li>Ensure all products are properly inspected, labeled, stored, and prepared for shipment.</li>
<li>Stage, load, and unload containers including; pails, drums, and totes.</li>
<li>Forklift operation.</li>
<li>Personal Protective Equipment (PPE) will be required in accordance with the potential hazard and potential for exposure.</li>
<li>Maintain a safe, orderly, clean operation of equipment and work area.</li>
<li>Must be able to lift and/or move 55 lbs.</li>
<li>May cross train in various positions including shipping/receiving, handling of bulk product, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventative plant maintenance, and/or yard truck spotting.</li>
</ul>
Candidates should possess:
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Must have effective verbal and written skills, enabling clear and strong interactions with co-workers, chemists, administrative staff, delivery personnel, and management.</li>
</ul>
Superior offers a competitive compensation package which includes Medical Insurance (HDHP 100% premium paid and a highly subsidized PPO option with very affordable premiums), Employee Stock Ownership Plan (ESOP), 401K, Flexible Spending, Paid Time Off, Paid Holidays, Life, Dental, Vision, STD and LTD.
We hire based on character as well as experience!
EOE including disability/veteran/drug free

Chemical Handler - Louisville, KY

<h3>Job Description</h3>
Job Description
We have an exciting opening for a Medical Physicist in sunny North Carolina! Don't miss this opportunity to join a dynamic team in a state-of-the-art facility! This is an excellent location with a low cost of living! Just around the corner from Lake Norman, a few minutes to the beach or mountains, 30 minutes to the city of Charlotte, NC. 
Equipment:
-TrueBeam
-Aria
-Eclipse
-Brachy, SBRT, IMRT, IGRT, SGRT
There is still a place that can elevate your mood, your sense of wonder, and your spirit. A charming place, Statesville, nestled in the brushy mountains of NC at the intersection of I-77 and I-40. A place you can kickstart your day in a historic downtown setting with locally roasted coffee and friendly smiles. A place where, if you're looking for a different speed, you'll find it with our many outdoor outfitters. Choose from lake activities, bike rentals, or recommendations for our area parks and trails.
Why Choose Rad Onc Solutions, LLC?
<ul>
<li>We have partnerships with some of the country's largest cancer care providers.</li>
</ul>
<ul>
<li>We will identify what you are looking for and where you dream of being, then put you in front of the people who matter.</li>
</ul>
<ul>
<li>No more applying for opportunities and waiting for months to hear whether you have been accepted or not.</li>
</ul>
<ul>
<li>Our team has over 40 years of combined experience in Clinical Radiation Oncology. We understand the dynamics within the clinic and how to create a perfect match.</li>
</ul>
<ul>
<li>Our main goal is Patient care. Whether you are a Radiation Therapist, Medical Dosimetrist, Medical Physicist, or Radiation Oncologist, you will have one point of contact who is heavily invested in your success.</li>
</ul>

Medical Physicist

<h3>Job Description</h3>
Job DescriptionJOB SUMMARY:The Geotechnical Department Manager will lead a team in coordinating and overseeing diverse geotechnical projects across industrial, commercial, and residential sectors. This role involves managing the geotechnical department, ensuring efficient operations, fostering teamwork, and promoting professional development. Responsibilities include client collaboration, project proposal development, and maintaining high quality standards. RESPONSIBILITIES:Strategic Planning &amp; Budgeting: Develops long-term goals and business plans for the department, manages the annual capital budget, and provides input on departmental budgets to align with overall business objectives. Participates in strategic planning initiatives and contributes to the overall growth and success of the organization. Business Development &amp; Networking: Collaborates with the Business Development department to create and execute the department’s annual business development plan, while networking to enhance the department’s and company’s reputation. Leads the development of project proposals and defines project tasks, schedules, and resource requirements. Department Management &amp; Performance: Monitors department chargeability targets, ensures staff understand both company-wide and departmental objectives, and oversees day-to-day operations, including quality of work environment and employee productivity. Provides leadership and management for the preparation of Geotechnical and CMT projects, conducting team meetings, evaluating project progress, and maintaining client satisfaction. Coordinates with project architects, civil engineers, structural engineers, and other technical staff to ensure successful project delivery. Policy &amp; Compliance Oversight: Develops, maintains, and enforces department-specific policies and procedures, ensuring compliance with company standards. Establishes project goals and ensures adherence to QA/QC standards, while developing and implementing departmental policies, procedures, and best practices to enhance efficiency and quality. Cross-Departmental Coordination: Works closely with the IT and HR departments to address department-specific technology and employee relations issues, providing input on hires and staff development. Collaborates with other department managers to optimize resource allocation and project scheduling. Financial Oversight: Reviews and approves weekly departmental invoices, including software, equipment, and other expenses. Manages project budgets, analyzes profitability, monitors revenue generation, prepares client billing information, manages collections, and identifies additional revenue opportunities. Workplace Culture &amp; Team Development: Fosters a positive work culture, maintains a professional workspace, and supports employee growth and relations. Mentors and develops staff within the geotechnical department to ensure ongoing professional growth. Client &amp; Contract Management: Consults with clients to determine site requirements, provides design information for geotechnical investigations, and maintains regular communication throughout the project lifecycle. Reviews and signs project contracts, handles change orders, and oversees project scope. Other Responsibilities: Leads special projects to support departmental operations or corporate goals. Performs additional duties as assigned to support department and company objectives QUALIFICATIONS:Bachelor’s Degree in Civil Engineering or equivalent Michigan P.E. License or ability to obtain 10 years of experience in the field of civil engineering, demonstrating increasing levels of responsibility. Working knowledge of typical computer software programs used for geotechnical engineering design and management (Microsoft Office, etc.) Working knowledge of codes, regulations, and standards applicable to the geotechnical design and construction of major site development projects in Michigan. Competencies and Personal Attributes:Demonstrated ability to manage staff and multi-disciplinary projects. Strong analytical and problem-solving skills, with the ability to resolve technical issues and address challenges encountered during geotechnical projects. Experience in mentoring and coaching junior geotechnical staff, providing guidance and support in their professional development. Proven track record of successful project delivery and client satisfaction, with a focus on delivering high-quality geotechnical services on time and within budget. Strong written and verbal communication skills. Self-motivated with the ability to motivate others. Sound understanding of financial management. Proficient in conflict resolution and client satisfaction. Physical Demands:The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work is performed mostly in office settings. Some outdoor work is required in the inspection of various land use developments, construction sites or public works facilities. Hand-eye coordination is necessary to operate drafting instruments, computers and various pieces of office equipment. While performing the duties of this job, the employee is occasionally required to stand; walk; use hands to handle, feel or operate objects, tools or controls; and reach with hands and arms. The employee is occasionally required to sit; climb or balance; stoop, kneel, crouch or crawl; talk or hear. The employee must occasionally lift and/or move objects up to 25 pounds. Availability:This is a full-time position. Days and hours of work are Monday through Friday, 8 a.m. to 5 p.m. and overtime as required. Travel:Travel will be required to respective job sites and is primarily local during the business day.

Geotechnical Manager with Michigan P.E. license

<h3>Job Description</h3>
Job Description
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
THE ROLE:
This is a contracted position requiring 40 hours per week for a 12-month term. The Research Associate / Senior Research Associate will primarily be responsible for the development and conduct of in vivo, ex vivo, as well as in vitro studies in Disease Biology and Translational Sciences to support the advancement of Septerna's small molecule drug discovery pipeline. They will work independently and collaboratively in an inter-disciplinary setting to design and execute experiments in preclinical models to understand in vivo pharmacology, establish PK/PD relationships, and inform the efficacy of Septerna's therapeutic candidates. They will help generate and analyze functional in vitro, in vivo, and ex vivo data to determine the therapeutic mechanism of action, and rank candidates for preclinical development. They may also engage in biomarker discovery efforts by utilizing a variety of in vitro, in vivo and ex vivo models to enable and inform effective therapeutic development. This role is expected to be primarily in the lab with some desk work. 
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will help move therapies through preclinical development, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team on the frontlines of innovative therapeutic development.
The position is based in South San Francisco, CA.
*Title commensurate with experience
Key Responsibilities include but are not limited to: 
<ul>
<li>Design and execute in vivo pharmacology studies to understand therapeutic mechanism in relevant disease models</li>
<li>Generate, analyze, document, and help interpret data to establish functional PK/PD relationships</li>
<li>Work collaboratively to determine the mechanism of action of drug candidates in in vivo, in vitro and ex vivo models</li>
<li>Be a member of multiple project teams and present results in lab, team and department meetings</li>
<li>Perform in literature searches, read and interpret papers to help design and trouble-shoot in vivo and in vitro experiments</li>
<li>Help in authoring in vivo pharmacology study designs, protocols, and reports to support regulatory filings</li>
<li>Follow all company policies/practices, and maintain accurate records and notebooks</li>
</ul>
REQUIRED EDUCATION, SKILLS &amp; EXPERIENCE 
<ul>
<li>BSc or MSc in Pharmacology, Toxicology, or related biological science</li>
<li>2- 4 years of direct full-time hands-on experience with in vivo studies or disease models in academia or the biotechnology and pharmaceutical industries</li>
<li>Demonstrated ability to be hands on and work directly with rodent models (mice and rats), including multiple routes of administration (e.g. oral, subcutaneous, intraperitoneal, intravenous, intramuscular) and sample collection (e.g. submandibular bleed, tail vein bleed, cardiac puncture, etc).</li>
<li>Experience working with other scientists to analyze, interpret, and present data</li>
<li>Ability to collaborate in writing protocols and trouble-shooting biological experiments</li>
<li>Detail-oriented and organized, with strong interpersonal skills for clear and effective communication – ability to proactively engage and collaboration with colleagues</li>
</ul>
PREFERRED SKILLS &amp; EXPERIENCE
<ul>
<li>Experience working with protein and RNA/DNA (e.g. ELISA, qPCR)</li>
<li>Experience working with primary cells or ex vivo models or in vivo species</li>
<li>Experience measuring and interpreting rodent behavior</li>
<li>Experience working with generation of surgical models in rodents</li>
<li>Previous work on therapeutic discovery and development programs in the field of endocrine, inflammatory, neuroscience or metabolic diseases</li>
<li>Experience working with vendors and CROs to execute studies, analyze data, and generate reports</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $37.00/hr - $45.00/hr. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Research Associate / Senior Research Associate, In Vivo Pharmacology (Contract)

<h3>Job Description</h3>
Description
The Multi Domain Solutions Division at Leidos has an opening for a 24/7 RF Signals Analyst. The successful candidate has strong analytical skills and is a problem solver. The candidate will be required to understand collections, platform capabilities, signal processing dataflows, and analytic methodologies.
Primary Responsibilities
<ul>
<li>Acquire complex data for critical analysis, explore new sources of data, and combine data from disparate sources to validate information and extract new meaning</li>
<li>Execute and refine the process and procedure of instrumentation Signals Analysis operations in a purpose-built enterprise environment throughout the lifecycle of operations&nbsp;</li>
<li>Become an authority in the mission area and provide time-critical recommendations</li>
<li>Interact with collection managers, operators, and analysts on new methods, technologies, and collection strategies</li>
<li>Collaborate with national and tactical collection elements to advance target development efforts, recommend collection strategies, and support strategic and operational requirements</li>
<li>Create processing models and scripts and report technical characteristics</li>
<li>Search for new and unusual signal activity associated with events and forward this information to the designated community entities as necessary</li>
<li>Troubleshoot technical issues and provide effective solutions</li>
</ul>
Basic Qualifications
<ul>
<li>Requires a Bachelors degree or equivalent experience and 2-4 years of prior relevant experience in digital signals collection, real-time operations, or signals analysis or a Masters degree with &lt;2 years of prior relevant experience</li>
<li>Active TS/SCI with Polygraph and US Citizenship</li>
<li>Proven experience and proficiency with RF Signals Intelligence collection tools and techniques</li>
<li>Knowledge of Doppler effects on RF transmissions</li>
<li>Ability to work a 24/7 shift rotation</li>
<li>Excellent verbal and written communication skills and detail oriented</li>
<li>Ability to work collaboratively and constructively with leaders across the site</li>
<li>Ability to work in a fast-paced team environment</li>
</ul>
Preferred Qualifications
<ul>
<li>Proficiency in multiple types of SIGINT collection&nbsp;or&nbsp;technical work at customer sites</li>
<li>Experience with Measurement and Signatures and other specialized IC SIGINT tasking, collection, exploitation, analysis, and mapping tools</li>
<li>Knowledge of specific customer requirements and intelligence oversight&nbsp;policies&nbsp;</li>
<li>Ability to evaluate and document system inaccuracies and identify improvements</li>
</ul>
If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo — because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 — and moving faster than anyone else dares.
Original Posting:December 12, 2025
For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.
Pay Range:Pay Range $59,150.00 - $106,925.00
The Leidos pay range for this job level is a general guideline only&nbsp;and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
About Leidos
Leidos is an industry and technology leader serving government and commercial customers with smarter, more efficient digital and mission innovations. Headquartered in Reston, Virginia, with 47,000 global employees, Leidos reported annual revenues of approximately $16.7 billion for the fiscal year ended January 3, 2025. For more information, visit <a href="http://www.Leidos.com" target="_blank">www.Leidos.com</a>.
Pay and Benefits
Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available at <a href="http://www.leidos.com/careers/pay-benefits" target="_blank">www.leidos.com/careers/pay-benefits</a>.
Securing Your Data
Beware of fake employment opportunities using Leidos’ name. Leidos will never ask you to provide payment-related information during any part of the employment application process (i.e., ask you for money), nor will Leidos ever advance money as part of the hiring process (i.e., send you a check or money order before doing any work). Further, Leidos will only communicate with you through emails that are generated by the Leidos.com automated system – never from free commercial services (e.g., Gmail, Yahoo, Hotmail) or via WhatsApp, Telegram, etc. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at <a href="mailto:LeidosCareersFraud@leidos.com" target="_blank">LeidosCareersFraud@leidos.com</a>.
If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the U.S. Federal Trade Commission.
Commitment to Non-Discrimination
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.
#Featuredjob

RF Signals Analyst 24x7

<h3>Job Description</h3>
Job Description
Title: Forensic Chemist I/II (Multiple Openings) 
Department: IFS-DFW
Job Type: Regular Full-Time
Location: Grand Prairie, TX
Functional Area: Forensic Laboratory Testing
Shift: 1st
Schedule: Monday-Friday, 7:00am to 3:30pm
Company Overview:
NMS Labs has developed an extensive menu of more than 2,500 tests to support clients in forensic, criminalistic, public health and clinical fields. For over 50 years, our clients have relied on NMS Labs for unique testing solutions that demonstrate our company core values of Quality, Integrity, Service, Innovation and Engagement. As we work to increase the company’s positive impact on public health and public safety, we are seeking talented professionals to join us for the journey! We invite you to learn more about our company by visiting NMSLabs.com. 
Job Description:
NMS Labs is hiring a Forensic Chemist for our Grand Prairie, TX location! The Forensic Chemist will perform chemical and analytical testing including the isolation and identification of chemical substances in forensic casework samples. This person is responsible for specimen processing, test performance, reporting of test results, and the quality assurance and documentation of analytical processes.
 Other duties include:
<ul>
<li>Handling and sampling of forensic casework samples</li>
<li>Maintaining the appropriate chain of custody of evidence</li>
<li>Independently performing analysis of chemical substances utilizing chemical, microscopic, TLC, and instrumental methods to include GCMS</li>
<li>Generating, interpreting, reviewing, and releasing results</li>
<li>Performing routine maintenance and basic troubleshooting of analytical instrumentation</li>
<li>Providing expert testimony</li>
<li>Performing and maintaining appropriate quality assurance and quality control procedures</li>
<li>Effectively communicating scientific findings to internal and external clients</li>
</ul>
The Forensic Chemist must have working knowledge of analytical procedures including a basic understanding of analytical terminology, methods, and theory, and should be able to apply these to forensic cases. A high level of integrity is required, as well as good organizational, interpersonal, and communication skills. The Forensic Chemist must have the ability to follow SOPs, as well as compliance standards and safety practices. 
Requirements:
A minimum of a Bachelor's degree is required; 6 months lab related experience is strongly preferred.
<ul>
<li>Degree must be in a chemical, physical, biological science, or forensic science from an accredited university</li>
<li>Minimum of 16 semester credit hours in college-level chemistry coursework above General Chemistry</li>
<li>MUST HAVE coursework and labs in General Chemistry, Organic Chemistry and Analytical (Instrumental) Chemistry</li>
<li>MUST HAVE 3 college-level semester credit hours in Statistics or be willing to take and pass a statistics course within one year of employment</li>
<li>Licensed by the Texas Forensic Science Commission within 1 year of hire, as applicable</li>
</ul>
Preferred:
<ul>
<li>ABC certified</li>
<li>Court testimony experience</li>
</ul>
Physical Demands:
<ul>
<li>Ability to hear</li>
<li>Vision (with correction) including color, distance, peripheral vision, depth perception, and the ability to adjust focus</li>
<li>Standing, reaching with hands and arms, and using hands and fingers to manipulate instruments or equipment controls, computer keyboard, office equipment, objects or tools</li>
<li>Movement from one work location to another</li>
<li>Sitting and standing, sometimes for extended periods of time</li>
<li>Lifting objects up to 20 lbs.</li>
<li>Ability to travel as needed for court testimony.</li>
<li>Exposure to intermittent or constant sounds generated by equipment</li>
<li>Exposure to fumes, noxious odors and dust</li>
<li>Handling of biological material and blood-borne pathogens</li>
<li>Handling of toxic or caustic chemicals</li>
<li>Proximity to moving parts</li>
</ul>
Offers of employment are made contingent upon a nationwide background investigation and urine drug screen with results satisfactory to standards of employment at NMS.
To be considered for this position, please submit a cover letter, resume and official or unofficial transcripts and apply at <a href="http://www.nmslabs.com/careers" target="_blank">http://www.nmslabs.com/careers</a> 
We are an equal opportunity employer and will not discriminate against any employee or applicant for employment because of race, creed, sexual orientation, color, religion, sex, national origin, age, marital status, citizenship status, otherwise qualified disability, or protected veteran status (disabled Armed Forces Service medal, recently separated, active duty or campaign badge), domestic violence victim status, arrest record, or predisposing genetic characteristics.v

Forensic Chemists I/II - Multiple Openings

<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
Arrowhead is seeking a highly motivated molecular biologist to join our growing Bioassays team at our Madison site. The Molecular Biology team supports R&amp;D projects across all sites. The ideal candidate should have 1-2 years of cloning experience with the ability to independently work on multiple constructs simultaneously.
Responsibilities
<ul>
<li>Support in vitro, ex vivo and/or in vivo studies to facilitate drug discovery and development with some independence</li>
<li>Propose methods and ways to optimize cloning</li>
<li>Occasionally present research findings to project teams</li>
<li>Occasionally read relevant scientific literature and propose applications to projects to troubleshoot and solve problems</li>
<li>Maintain a high level of productivity and quality in the lab</li>
<li>Perform critical experiments </li>
<li>Primary Molecular Biology Responsibilities:
<ul>
<li>Clone plasmid constructs by various methods (Digest/ligation, IVA)</li>
</ul>
</li>
<ul>
<li>Perform large-scale plasmid preps</li>
<li>Autoclave glassware and media</li>
<li>Manage lab inventory and assist in ordering</li>
<li>Project documentation</li>
<li>Work with a small team of scientists, while working closely with other research groups and senior managers</li>
</ul>
</ul>
Requirements
<ul>
<li>Bachelor of Science in Biology or related field</li>
<li>3+ years of experience in cell biology, molecular biology, immunology, pharmacology or a related field of biology</li>
<li>2+ years experience with methods and technologies involving plasmid cloning, AAV packaging, protein expression vectors</li>
<li>Experience in standard cellular and molecular biology techniques (PCR, Digestion, Ligation, Transformation, DNA isolation)</li>
<li>Experience in standard microbiology techniques (Bacterial cultures, Autoclaving, Preparing Media)</li>
<li>Experience with Benchling and Snapgene</li>
<li>Demonstrated innovation, creativity and resilience in problem solving</li>
<li>Excellent oral and written communication skills</li>
<li>Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment</li>
</ul>
Wisconsin pay range $70,000—$80,000 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

Associate Scientist II, Bioassays (Plasmid Cloning)

<h3>Job Description</h3>
Job Description
Bio-statistician is required to conduct statistical analysis, modelling, and reporting activities in pharmaceutical industry.

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