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city

state

<h3>Job Description</h3>
Job Description
Job Summary
<ul>
<li>Member of the production team that operates machinery and works within the production process. </li>
<li>Operators typically are involved in cleaning, preparing, and monitoring the heavy machines used to mix and process chemicals. They mix and handle chemicals, record information and observations relating to the mixing process, troubleshoot issues with equipment, and assist in process improvement initiatives and the work plan development process.</li>
</ul>

Essential Functions / General Accountabilities
<ul>
<li>Package and transfer chemicals safely. </li>
<li>Perform packaging operations into various sized containers.</li>
<li>Load and unload bulk tank trailers.</li>
<li>Operate forklifts and material moving equipment.</li>
<li>Process chemicals by following guidelines and instructions on equipment such as reactors, distillation systems, etc. </li>
<li>Follow a strict blend sheet and mix chemicals for drumming.</li>
<li>Complete all necessary paperwork, including packing sheets, checklists.</li>
<li>Conduct all tasks in a safe manner and utilize appropriate personal protective equipment per site policies.</li>
<li>Complete janitorial duties and general laborer work as directed, including housekeeping activities.</li>
<li>*The company reserves the right to add or change duties at any time.</li>
</ul>
Job Qualifications
<ul>
<li>Education: High school diploma or equivalent</li>
<li>Experience: 1-2 years of related experience in manufacturing (preferred)</li>
<li>Forklift Certified (preferred)</li>
</ul>
Skills
<ul>
<li>Understanding of chemical process.</li>
<li>Basic computer skills.</li>
<li>Verbal and written communication skills.</li>
<li>A desire to work with team members to improve processes and product quality in a fast-paced, physically demanding environment.</li>
<li>Willingness to comply with safety and quality regulations, including wearing protective gear when necessary.</li>
</ul>
 
Work Environment
<ul>
<li>Outdoors</li>
<li>Warehouse</li>
</ul>
Physical Demands
 
<ul>
<li>Physical requirements of the position, including walking, standing, or sitting for extended periods, lifting heavy objects, climbing, crouching, operating tools, and wearing safety gear.</li>
<li>Ability to lift 50lbs or more.</li>
</ul>
 
*This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.
 Monday - Friday, 8 AM to 4 PM.

Drumming and Blending Chemical Operator

<h3>Job Description</h3>
Job Description
Position: Research Associate - Preclinical Research
Pay: $22.73 - $36.00 per hour (based on level and experience)
Contract: Contract hire, full-time
Description: The Research Associate supports preclinical research operations within the Large Animal team (primates and beagles). This role involves performing technical procedures, collecting data, and supporting toxicology and pharmacology studies while ensuring compliance with GLP standards. A strong interest in animal care and drug development science is essential.
Key Responsibilities:
<ul>
<li>Prepare and conduct technical procedures (blood collection, IV administration, injections, anesthesia, dosing).</li>
<li>Handle, restrain, and provide clinical care to animals (primates 2-5kg, beagles).</li>
<li>Accurately document and collect study data in compliance with SOPs and GLP standards.</li>
<li>Operate laboratory equipment (glucometer, pumps, thermometers).</li>
<li>Monitor and report changes in animal health, behavior, or housing conditions.</li>
<li>Maintain veterinary instruments, study ancillaries, and facility organization.</li>
<li>Participate in large and small molecule toxicology studies (50-100 studies running concurrently).</li>
<li>Support study directors and supervisors with sample and data collection.</li>
<li>Cross-train across departments and engage in continuous learning.</li>
</ul>
Schedule/Shift:
<ul>
<li>Training period (2-3 months): Monday-Friday, 8:00 AM - 4:00 PM.</li>
<li>Post-training: Tuesday-Saturday OR Sunday-Thursday, 8:00 AM - 4:00 PM.</li>
<li>Overtime, rotating holidays, and occasional weekend coverage are required.</li>
</ul>
Requirements:
<ul>
<li>High school diploma required; Bachelor's degree in science preferred.</li>
<li>Preclinical technical skills: blood collection, IV administration, injections.</li>
<li>Animal research experience (internship, academic lab, or CRO) strongly preferred.</li>
<li>Experience from companies such as Covance, NPI, or Charles River is a plus.</li>
<li>Willingness to work overtime and adapt to shifting schedules.</li>
</ul>
Nice-to-Have Skills:
<ul>
<li>Veterinary assistant experience.</li>
<li>Clinical procedures (injections, IV administration, surgery support, necropsy, or euthanasia exposure).</li>
</ul>
uthanasia exposure).
For California Applicants:
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).
This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
Company DescriptionHere at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine. Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us? 
<h3>Company Description</h3>
Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.\r\n\r\nOur commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?

Research Associate II - Large Animals

<h3>Job Description</h3>
Job Description 
Position Summary:
The Electroless Cuposit Operator plays a key role in the application and maintenance of the Electroless Cuposit process, a specialized chemical plating method used to deposit a uniform, conductive copper layer on non-conductive surfaces in printed circuit board (PCB) manufacturing. This process is essential for forming interconnects through vias and drilled holes prior to electrolytic copper plating.
This position is responsible for preparing panels, managing the chemical bath parameters, analyzing process performance, and ensuring the Electroless Cuposit process meets production, quality, and reliability standards. 
Qualifications: To perform this job successfully, an individual must have a minimum of four (4) years’ in the printed circuit board industry and must be able to perform each essential duty satisfactory. The requirements listed below are representative of the knowledge, skill and/or ability required.
 
Responsibilities:
<ul>
<li>Operate and monitor the electroless copper plating line according to process specifications and safety protocols.</li>
<li>Prepare and load PCB panels into cuposit racks.</li>
<li>Handle and prepare chemical solutions safely and accurately.</li>
<li>Inspect boards for defects or process issues before and after electroless plating.</li>
<li>Clean and maintain equipment, tanks, and work areas in accordance with safety and quality standards.</li>
<li>Coordinate with Quality Assurance to ensure product conformance to specification.</li>
<li>Report equipment malfunctions or process deviations to maintenance or supervision.</li>
<li>Follow all environmental, health, and safety regulations including proper handling and disposal of hazardous materials.</li>
</ul>

Required Skills: 
<ul>
<li>Basic understanding of chemistry and plating processes preferred.</li>
<li>Strong attention to detail and commitment to quality.</li>
<li>Ability to read and interpret work instructions and production travelers.</li>
<li>Ability to work in a fast-paced manufacturing environment.</li>
<li>Good communication and teamwork skills.</li>
</ul>

Education/Experience:
<ul>
<li>High School Diploma or equivalent</li>
<li>Minimum four (4) years experience in the printed circuit industry, and three (3) years in copper plating.</li>
</ul>

Physical Requirements:
<ul>
<li>Ability to lift up to 50 lbs.</li>
<li>Standing, walking, and reaching for extended periods.</li>
<li>Use of PPE including gloves and goggles.</li>
</ul>
 
ITAR Compliance Notice
This position requires compliance with the International Traffic in Arms Regulations (ITAR). Under ITAR, candidates must be a U.S. citizen, U.S. lawful permanent resident (e.g., "Green Card" holder), asylee, or refugee as defined by 8 U.S.C. 1324b(a)(3). Applicants who do not meet this requirement may not be eligible for employment in this position.
Summit Interconnect is an Equal Opportunity Employer We are committed to fostering an inclusive and diverse workplace where everyone is valued and respected. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic.

Electroless Cuposit Operator (Grave Shift)

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The&nbsp;Associate Director, Statistics - Oncology&nbsp;provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients.
This role will work a hybrid schedule in one of the AbbVie locations:
<ul>
<li>Lake County, IL</li>
<li>South San Francisco, CA</li>
</ul>
Responsibilities
<ul>
<li>Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission.</li>
<li>Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans.</li>
<li>Represent function/department on project team(s) to provide statistical input to compound/drug development and drive alignment with functional management. Partner with other functions (Clinical, Regulatory, Patient Safety, and GMA, etc.) to create development strategies for assigned projects.</li>
<li>Demonstrate extensive understanding of statistical concepts and methodology. Propose novel statistical methodological approaches to design of scientific studies. Provide sufficient detail to allow programming implementation. Ensure that all statistical analyses specified in scientific protocols and analysis plans are conducted appropriately.</li>
<li>Train and mentor staff on statistical methodology and operations. May supervise contract statisticians or junior statisticians. Gain expertise in innovative statistical methods. Assist functional leaders in recruiting qualified personnel and arranging training opportunities for professional development of staff.</li>
<li>Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.</li>
<li>Act as the liaison for statistical issues on AbbVie collaborative studies with CROs, academic institutions, government agencies, steering and/or data monitoring committees, joint ventures or licensing collaborators. Build external scientific connections which foster professional development and promote the reputation of the Statistics Department.</li>
<li>Ensure that all applicable regulatory requirements for work processes are met. Critically review regulatory submission documents. Participate in discussions with regulatory agencies as needed. Validate external statistical software to ensure compliance with SOPs and regulatory requirements</li>
<li>Significant Work Activities:&nbsp;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</li>
</ul>
Qualifications 
<ul>
<li>MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics, Biostatistics, or a highly related field.</li>
<li>High degree of technical competence and excellent communication skills, both oral and written</li>
<li>Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others</li>
<li>Able to manage project timeline and quality of deliverables</li>
<li>Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo</li>
<li>Have strong leadership skills and experience in working/managing cross-cultural or oversea teams</li>
<li>Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment.</li>
<li>(SSG) Experience leading safety-related projects (eg, ISS, benefit-risk assessment, signal detection)</li>
<li>(GMA Stat) Competence in experimental and RWE study design, descriptive statistics, inferential statistics, statistical modeling, and statistical programming. Knowledge of methodologies for confounding control and bias minimization in observational studies preferred.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Director, Statistics

<h3>Job Description</h3>
Job Description
<ul>
<li>We are hiring immediately for full time CLEANROOM TECHNICIAN positions.</li>
<li>Location: Amgen - 4130 Friendship Road, Apex, NC 27502. Note: online applications accepted only.</li>
<li>Schedule: Full time; Days and hours may vary. 10 to 12-hour shifts. More details upon interview.</li>
<li>Requirements: Prior cleanroom experience is preferred. Prior janitorial experience in a commercial building is preferred.</li>
<li>Pay Range: $21.00 per hour to $23.00 per hour.</li>
</ul>
&nbsp;
ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the International WELL Building Institute (IWBI).&nbsp;
&nbsp;
We Make Applying Easy!&nbsp;Want to apply to this job via text messaging? Text JOB&nbsp;to 75000&nbsp;and search requisition ID number&nbsp;1489094.
The advertised program is a conversational recruiting assistant that helps you apply to jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help. Terms and conditions: <a href="http://olivia.paradox.ai/moSkg" target="_blank">http://olivia.paradox.ai/moSkg</a>
Rooted in hospitality, ESFM elevates the workplace experience as the single source of innovative FM solutions that ensure a safe, healthy, and sustainable environment. ESFM’s clients include many household names from Life Science, Technology, Oil &amp; Gas and Manufacturing markets.
&nbsp;
ESFM self-performs 80% of all IFM solutions provided to clients. Their portfolio of service categories includes Environment, Health &amp; Safety, Facilities Maintenance &amp; Engineering, Sustainability, Janitorial &amp; Industrial Cleaning, Laboratory Support and Workplace solutions.&nbsp;&nbsp;This self-performance model creates a consistent hospitality experience for clients, resulting in higher engagement and productivity from their employees.
&nbsp;
In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA).
&nbsp;
Job Summary
Summary: Maintains a sterile environment in the clean room, by garbing, cleaning the room, and behaving according to clean room procedures that align with the facilities practices or guidelines. 
Essential Duties and Responsibilities: 
<ul>
<li>Practices efficient use of cleaning techniques, solutions preparation, equipment and tool operation.</li>
<li>Performs all decontamination cleaning and project assignments within area of responsibility or as directed by supervisor with high level of consistency, accuracy and reliability. This also includes executing cleanroom cleaning SOP’s.</li>
<li>Maintains documentation on all activities and frequent (often daily) quality control testing and verifies the efficiency of the work performed.</li>
<li>Monitor and maintain the stock of cleanroom garments and cleaning materials when applicable.</li>
<li>Monitor and manage contamination sources within the cleanroom environment including materials and personnel.</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications: 
<ul>
<li>High School Diploma, GED preferred or equivalent combination of education and experience</li>
<li>1-2 years housekeeping or cleaning service experience preferred </li>
<li>Strong verbal and written communication skills.</li>
<li>Ability to read and comprehend Standard Operating Procedure Documents (SOPs)</li>
</ul>
Work Environment: 
<ul>
<li>Exposure to chemicals on a constant basis requiring special clothing and/or safety equipment. </li>
</ul>
Associates at ESFM are offered many fantastic benefits.
Full-time and part-time positions offer&nbsp;the following benefits to associates:&nbsp;Retirement Plan,&nbsp;Associate Shopping Program,&nbsp;Health and Wellness Programs,&nbsp;Discount Marketplace,&nbsp;Identity Theft Protection,&nbsp;Pet Insurance,&nbsp;Voluntary Benefits, including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program
Full-time positions also offer&nbsp;the following benefits to associates:&nbsp;Medical,&nbsp;Dental,&nbsp;Vision,&nbsp;Life Insurance/AD,&nbsp;Disability Insurance,&nbsp;Commuter Benefits,&nbsp;Employee Assistance Program,&nbsp;Flexible Spending Accounts (FSAs)
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws.&nbsp;For positions in Washington State, Maryland, or to be performed Remotely, click here or copy/paste the link below for paid time off benefits information.
<a href="https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTransparency_ESFM.pdf" target="_blank">https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTranspa…</a>
About Compass Group: Achieving leadership in the foodservice and facility management industry
&nbsp;
Compass Group is an equal opportunity employer.&nbsp; At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
&nbsp;
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation.&nbsp;Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity.&nbsp;
Applications are accepted on an ongoing basis.
ESFM maintains a drug-free workplace.
ESFM&nbsp;

CLEANROOM TECHNICIAN (FULL TIME)

<h3>Job Description</h3>
Job Description
The Development Scientist will support microbiological lab activities for antimicrobial susceptibility testing (AST). The incumbent performs experiments as defined and planned by supervisor; reviews test results for experimental error and determines if repeats are required. Updating project lead(s) with data and any issues will be required, as well as an ability to work in cross-functional teams. Position Requirements: Bachelor's degree in a Life Science or related field with 1+ years experience in laboratory experience. Strong communication skills with the ability to work in a multidisciplinary team environment. Ability to problem solve is a must. Knowledge of aseptic lab techniques, pipetting, good laboratory practice (GLP), good documentation practices (GDP), and general wet bench experience. Ability to be flexible and work in a rapidly changing task environment and with variety of tasks. Familiarity with Excel and data analysis is desired.
Company DescriptionNicman Group is a consulting company that has a blend of internal and external projects. This isn't a staffing augmentation position, but rather one where you will be joining an existing NIcman team on a long-term project. 
<h3>Company Description</h3>
Nicman Group is a consulting company that has a blend of internal and external projects. This isn't a staffing augmentation position, but rather one where you will be joining an existing NIcman team on a long-term project.

Development Scientist I

<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 Pharmacovigilance Systems Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to laboratory projects that strengthen experimental capabilities and support program progress. This internship offers hands-on experience working with biological assays, data analysis, and scientific collaboration in a research environment. The intern will work alongside experienced scientists and gain exposure to laboratory workflows that help advance understanding of RNA biology.
This is an 11-week Summer Internship Program paying $26.00/hour and requires full-time, on-site work five days per week.
Responsibilities
<ul>
<li>Develop an understanding of the scientific background and workflow for RNA isolation assays and related experimental approaches.</li>
<li>Under supervision, establish and optimize assay parameters and conditions for isolating RNA from specific cellular compartments.</li>
<li>Perform experimental readouts using multiple methods to confirm assay performance and results.</li>
<li>Analyze experimental data and organize results using appropriate analytical tools.</li>
<li>Maintain accurate and well-organized experimental records.</li>
<li>Communicate findings and present results to the project team during meetings.</li>
<li>Collaborate with scientists to support continued assay refinement and project progression.</li>
</ul>
Requirements
<ul>
<li>Currently enrolled student in an accredited university Master's degree program in Biology or a related field.</li>
<li>Familiarity with RNA-related techniques.</li>
<li>Hands-on experience with biological laboratory techniques.</li>
<li>Strong verbal and written communication skills.</li>
<li>Excellent problem-solving and analytical skills.</li>
<li>Excellent verbal and written communication skills, including comfort presenting in group settings.</li>
<li>Strong problem-solving and organizational skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
</ul>
Preferred
<ul>
<li>Previous experience with RNA isolation techniques.</li>
<li>Familiarity with Microsoft Excel and GraphPad Prism.</li>
<li>Strong interest in RNA biology, assay development, or discovery research.</li>
<li>Attention to detail and enthusiasm for learning new experimental approaches.</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, Bioassays

<h3>Job Description</h3>
Job DescriptionJob at a Glance
Title:&nbsp;Statistical Data Analyst Location:&nbsp;Columbia, SC (hybrid model)&nbsp; Contract:&nbsp;6&nbsp;month contract + extensions/conversion Pay:&nbsp;$40-$46/hour + optional medical, dental, vision, 401(k) match
Overview
This role involves developing complex statistical analyses, reports, and data visualizations for the Medicare Statistical Analysis Department. The candidate will support data integrity, create ad hoc reports, and assist in transitioning from SAS to Python for data programming tasks.
Key Responsibilities
<ul>
<li>Develops difficult statistical analysis using standard reporting, ad hoc reporting, and data mining tools to identify patterns and trends. Prepares charts, illustrations, and narrative reports to explain data findings.</li>
<li>Develops, maintains, and executes complex database programs for data extraction and presentation, creating supporting documentation.</li>
<li>Develops complex sampling design and/or execution methodology for sample selection.</li>
<li>Provides sophisticated data interpretation, compilation, and verification to guide departmental efforts.</li>
<li>Participates in writing articles for internal/external publication, potentially assuming a leadership role.</li>
<li>Assists in developing project plans, performing quality checks on relational database tables, and developing focused end-user applications.</li>
<li>Participates in development of change requests and testing plans for database modifications, researching new data sources, and providing feedback to management.</li>
</ul>
Required Skills
<ul>
<li>4 years of statistical programming or interpretation experience</li>
<li>5 years experience with statistical software and relational databases</li>
<li>Proficiency in SAS and/or Python</li>
<li>Experience converting SAS to Python (strongly desired)</li>
<li>Knowledge of SQL and data visualization tools</li>
<li>Strong communication skills, including ability to communicate with non-technical audiences</li>
<li>Ability to create clear, detailed documentation</li>
<li>Deep understanding of statistical analysis within a healthcare/Medicare context</li>
<li>Ability to adapt quickly to new environments and systems</li>
<li>Self-motivated and confident in tackling challenging problems with limited guidance</li>
</ul>
Preferred Skills
<ul>
<li>Master’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or related field</li>
<li>Experience with data visualization, dashboarding, and modeling</li>
<li>Familiarity with Databricks</li>
<li>Experience working with Medicare or healthcare data</li>
</ul>
Call to Action
Candidates who are motivated to work on impactful healthcare data projects and possess the required technical skills are encouraged to apply. Join us to contribute to meaningful healthcare analytics and advance your career in a dynamic environment.
About CEI
As a trusted technology partner, CEI delivers solutions that help our customers transform their business and achieve meaningful results. From strategy and custom application development through application management - our technology and digital experience services are tailored to meet each unique need of our customers. Our staffing solutions bring specialized skills to complement our customers' workforce and project requirements.
#ZR #INDGEN

Statistical Data Analyst

<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 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 the Bayou La Batre, AL

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

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