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<h3>Job Description</h3>
Job DescriptionJob Description 
Strategic ACI is seeking a Senior GIS Application Developer to provide on-site support in designated Government workspaces primarily in the Washington, DC metropolitan and surrounding areas. Staff in this category work independently to develop GIS tools and applications, perform complex analyses, and develop multi- layered maps accomplished by using an appropriate combination of tools found in the GIS application suite and other programming environments.
Responsibilities:
<ul>
<li>Leads application development team.</li>
<li>Works with other members of a program team (i.e. infrastructure, security, etc.) to ensure applications meet Client IT requirements.</li>
<li>Design and implement data conversion procedures and perform software and database quality control.</li>
<li>Work closely with the GIS user community to determine specific application requirements and specifications.</li>
<li>Perform project planning, requirements analysis, database design and development, and quality assurance and quality control.</li>
</ul>
Qualifications:
Required:&nbsp;
<ul>
<li>US Citizen.</li>
<li>Active Secret Clearance.</li>
<li>Bachelor's Degree with at least 6 years of experience in GIS and related development.</li>
<li>Experience in GIS concepts, computer graphics fundamentals, and relational database fundamentals and concepts is essential.</li>
<li>Experience in the development of complex analysis and mapping projects.</li>
<li>Proficient in the coding of software and manipulating digital databases as well as using GIS programming languages, Internet markup languages, and other, pertinent technologies.</li>
<li>The ability to communicate technical information to non-technical computer users, both orally and in writing.</li>
</ul>
, About Strategic Alliance Consulting, Inc 
Strategic Alliance Consulting Inc. is an Equal Opportunity Employer.
It has been and will continue to be a fundamental policy of Strategic ACI not to discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This policy applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination. Applicants can learn more about the company’s status as an equal opportunity employer by viewing the federal EEO is the Law poster.
Why choose a career with Strategic ACI?
Strategic Alliance Consulting, Inc. believes that our greatest asset is our employees. Our goal is not to meet our staff’s expectations, but to exceed them. Competitive salaries, work-life balance, industry leading benefits packages, and family first values are at the core of Strategic ACI’s culture.
Where benefits meet your needs:
<ul>
<li>Competitive salary</li>
<li>100% benefits paid (Includes: Health, Dental, and Vision premiums) for all full-time employees, and their families</li>
<li>401(k) with 5% match vested at day one</li>
<li>PTO – 3 weeks and 3 days per year, increasing at 5 years service&nbsp;</li>
<li>11 Company Paid Holidays (aligned with Federal Government)</li>
<li>Long term/Short term disability</li>
<li>1.5x salary Life Insurance</li>
<li>$100 per month Cellular Device and IT Resource Benefit&nbsp;</li>
<li>$6,000 Cash in Lieu of Benefits per year, if employee is insured elsewhere</li>
<li>Tuition reimbursement of up to $5,250 per year for college or professional certifications</li>
<li>Retirement Savings 401(k) Contribution - Annually calculated as percentage of salary</li>
</ul>

Senior GIS Application Developer

<h3>Job Description</h3>
Job Description
We are seeking a Research Associate to become an integral part of our team! You will assist social scientists in educational research and data analysis. Looking to start ASAP Monday -Friday!!
Responsibilities:
<ul>
<li>Gather qualitative and quantitative social science data</li>
<li>Conduct statistical analysis on research data collected</li>
<li>Collaborate with others to identify research needs</li>
<li>Translate complex data into simple textual and visual representations</li>
<li>Summarize findings into presentations and reports</li>
<li>Molecular biology assays</li>
<li>Cell Culture</li>
<li>Manage sample inventory</li>
</ul>
Qualifications:
<ul>
<li>Previous experience in social sciences, educational research, or other related fields</li>
<li>Familiar with fundamental research practices</li>
<li>Deadline and detail-oriented</li>
<li>Excellent written and verbal communication skills</li>
<li>Bachelors' degree in Biology</li>
<li>Strong organizational skill with the ability to track multiple studies, manage inventory, and ensure smooth day-to-day laboratory operations.</li>
</ul>
Company DescriptionInfinity Staffing is a family owned organization whose mission is to provide "Service with a Smile". Our vision is to maintain a strong foundation in an ever changing and evolving marketplace through solid relationships with our clients and candidates. Our number one priority and commitment is to provide a service which enables our clients to attract and retain the very best people available, and our candidates to fulfill their career potential. We are committed to stand out among our competitors and be the one and only choice for staffing solutions. We approach all client projects to the highest ethical and professional level 
<h3>Company Description</h3>
Infinity Staffing is a family owned organization whose mission is to provide "Service with a Smile". \r\nOur vision is to maintain a strong foundation in an ever changing and evolving marketplace through solid relationships with our clients and candidates. Our number one priority and commitment is to provide a service which enables our clients to attract and retain the very best people available, and our candidates to fulfill their career potential. \r\nWe are committed to stand out among our competitors and be the one and only choice for staffing solutions. We approach all client projects to the highest ethical and professional level

Research Associate

<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
Chemist in the Process Development Chemistry Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates.
Responsibilities
<ul>
<li>Work closely with senior chemists on development of new synthetic approaches to desired compounds with an eye toward large-scale synthesis</li>
<li>Cooperate with other chemists in the group in preparation of complex organic constructs</li>
<li>Perform solid-phase synthesis and purification of oligonucleotide drug candidates</li>
<li>Analyze small-molecule and macromolecular targets using standard methods</li>
<li>Maintain a well-documented laboratory notebook</li>
<li>Prepare documentation for transfer of new technologies to the Manufacturing group</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and issues to management, including presentation of findings at team meetings</li>
<li>Coordinate delivery of materials both internally and externally</li>
</ul>
Requirements:
<ul>
<li>BS or MS in chemistry or biochemistry with an excellent understanding of organic and analytical chemistry</li>
<li>Excellent verbal and written communication skills</li>
<li>Strong problem-solving skills</li>
<li>Eagerness to learn new techniques</li>
<li>Experience with synthetic organic chemistry in a laboratory setting</li>
<li>Experience with small-molecule and macromolecule analytical techniques (e.g., HPLC, UV-Vis spectrophotometry, mass spectrometry, NMR, etc.)</li>
</ul>
Preferred: 
<ul>
<li>Experience working with both small molecule or large molecule synthetic targets either in an academic or industrial setting</li>
<li>Experience with solid phase synthesis of oligonucleotides or peptides</li>
<li>Basic familiarity with GLP/GMP regulations</li>
</ul>
Wisconsin pay range $57,000—$70,000 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 I, CMC Process Development

<h3>Job Description</h3>
Job DescriptionAbout Us
Connected International, Inc. (Connected Cannabis Co.) is a leading vertically integrated cannabis company based in Sacramento and operating in California, Arizona, and Florida. With over 11 years experience, Connected specializes in breeding, growing, manufacturing, and distributing top-shelf cannabis through its state-of-the-art facilities and proprietary genetics. 
With over 250 employees across the United States, Connected maintains a strong presence in the industry across multiple markets. The company has recently expanded into Arizona and Florida with ambitious national expansion plans underway. Connected's mission has always been to breed, grow, and sell the best cannabis in the world, setting high standards for its products, people, and partners wherever we go.
About the Job
The Cultivation Technician performs labor to assist in the upkeep, stocking, and fulfillment of growing cannabis, including, but not limited to; watering, feeding, flushing, pruning, washing, cloning, transplanting, harvesting, and facility maintenance under the supervision of the Cultivation General Manager. Attention to detail is extremely important. NOTE: This is a 90 day temp to hire position. 
What You Will Do
<ul>
<li>Perform all tasks in the indoor harvest grow</li>
<li>Mother plant maintenance, cloning, transplanting, nutrients and pH management, water management, positive airflow, temperature and humidity control, pest and disease control, IPM program implementation, plant transfer from veg to flowering.</li>
<li>Manage plant scheduling and organization to precisely project all plant needs on a daily, weekly, and monthly basis to produce the best results for maximum plant yield.</li>
<li>Cataloguing and maintaining organization of plants, tags, and pruning biomass</li>
<li>Knowledge of pest and disease control management a plus. </li>
<li>Maintain and follow the cultivation department policies and procedures.</li>
<li>Wash and sanitize all equipment. Scout all equipment, ensuring all tools are free of pests, viruses or disease.</li>
<li>Must be able to adapt to various strains, styles and types of cannabis they are cultivating; adjusting techniques to maintain a steady pace and quality.</li>
<li>Breakdown flowers off stem and stalk of plant to separate unusable waste from useable product; employee must track the amount of unusable waste for each batch.</li>
<li>Demonstrate accurately and thoroughly in a timely manner to meet production standards.</li>
<li>Work in a timely manner and strive to increase productivity.</li>
<li>Maintain organization and cleanliness of the cultivation facility while performing job duties.</li>
<li>Exhibit competency in basic organizational, tracking and communication skills.</li>
<li>Works in a timely manner to efficiently meet goals while consistently producing quality product.</li>
<li>Employee must be able to follow basic instructions and take constructive feedback from their managers to maintain quality standards and production goals.</li>
<li>Employee must show up on time for work every day ready to work.</li>
<li>Employee must exhibit personal hygiene and follow the health guidelines set forth by the company and the state while processing patient medicine.</li>
<li>Cultivation staff is responsible for clean-up of all processing areas and equipment at the end of every shift. </li>
</ul>
What We Are Looking For
<ul>
<li>Minimum age of 21 years or older and pass a criminal background check</li>
<li>High school or equivalent</li>
<li>May require working rotating shifts with varied hours/day, including evenings, weekends, holidays, and special events</li>
<li>Previous agricultural/warehouse/manufacturing/laborer experience preferred.</li>
<li>Adhere to company mission statement, while maintaining high ethical standards and professionalism.</li>
<li>Ability to be flexible and work in various sectors of the department as needed an/or requested by their direct supervisor; this may include but is not limited to, helping grow staff with small tasks, cleaning and/or moving supplies and equipment and/or helping the packaging department or working at other locations as needed.</li>
<li>Must be able to identify various problems with any strain/product and communicate with direct supervisors as necessary.</li>
<li>Have a basic understanding of cannabis laws, rules and regulations set forth by the state; a pursuit to further their understanding and knowledge of the industry and the laws is appreciated and commendable.</li>
<li>Must work well with others and ability to adapt quickly to changes in policy, procedure, methods and technique. Frequent contact with supervisor via face-to-face discussions</li>
<li>Use of independent judgment regarding product processing, keeping quality, projections and goals in mind.</li>
<li>Help create a proactive and positive environment; a positive attitude and self-motivation to help produce high quality manicured product, while meeting and/or exceeding personal and/or company goals.</li>
<li>Ability to work with, help, guide, challenge and motivate other team members to create a cohesive unit.</li>
<li>Must manage their time during work efficiently to meet goals while consistently producing quality product.</li>
<li>Must be able to follow basic instructions and ability to take constructive criticism from their managers to maintain quality standards and production goals.</li>
<li>Must understand and implement the rules, regulations, policies, and procedures of the company and the cultivation department.</li>
<li>Fundamental knowledge, as well as the ability to be taught and guided in areas related to cultivation with other areas being taught as the employee shows interest while still maintaining their capabilities as a cultivation technician.</li>
<li>Skill in analyzing potential problems with a plant or the product being processed.</li>
<li>Shows self-motivation/innovation and the ability to work well with all members of their staff and the company, as well as with their direct supervisor.</li>
<li>Ability to listen well and communicate effectively various audiences, especially with the direct supervisors and other co-workers.</li>
<li>Other duties as assigned</li>
</ul>
Physical Requirements/Work Environment
<ul>
<li>Must be able to lift up to a maximum of 50 lbs. occasionally without assistance or 100 lbs. with assistance.</li>
<li>Regularly required to perform carrying, grasping, lifting, walking, standing, some bending/crouching, stooping, stretching, talking, hearing, seeing and repetitive motions.</li>
<li>Must be able to stand for extended periods of time while maintaining focus.</li>
<li>Able to be in varying temperature and humidity environmental conditions</li>
<li>Must not be allergic to or have a fear of insects.</li>
</ul>
Work is performed in a fast-paced cannabis grow location. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Why Connected?
Connected is an exciting and innovative workplace with a highly engaged workforce brought together by a shared passion to be the best in the business. We are on a mission to breed, grow and sell the best cannabis in the world! This is a super unique opportunity to be part of the start-up stage of the booming cannabis industry. We are looking for exceptional people to join our team as we transition into the next phase of our business ventures and become a leader in the cannabis space. 
<ul>
<li>Competitive Pay</li>
<li>401(k), Medical, Dental, Vision, Life Insurance</li>
<li>Paid Vacation Time</li>
<li>Career Growth and Internal Advancement Opportunities</li>
<li>Chance to work in an exciting new start-up industry with awesome people!</li>
</ul>

Cultivation Technician I

<h3>Job Description</h3>
Job Description
Associate Restoration Scientist

Position Title : Associate Restoration Scientist
Location: Sacramento Valley, CA
Status: Full-time, Non-Exempt Reports to: Restoration Ecologist
Pays Scale: $26.20-$33.00
A thriving future for California’s environment and communities requires bold vision, creative problem-solving, and relentless determination. This is a critical decade for action and River Partners is growing our team of talented, tenacious change-makers to meet the challenge head on. Join us! 

Who We Are
River Partners brings life back to California rivers. We’ve revitalized more habitat along impaired California rivers than any other entity in the western U.S., having led hundreds of projects across nearly 20,000 acres throughout California. We restore thriving native forests and ecosystems that support imperiled wildlife, improve flood safety, boost the state’s climate resilience, replenish and improve freshwater resources, create open space for communities, and build stronger local economies. Since 1998, we have pioneered an innovative, entrepreneurial approach to conservation, combining modern farming, cutting-edge science, and diverse partnerships.   
Position Description
The Restoration Science Associate collaborates with River Partners’ larger Restoration Team to identify, evaluate, implement, and complete restoration activities. This position reports to a Restoration Science Manager and regularly works in outdoor conditions to conduct field monitoring and data collection, providing essential insights for project planning and data-driven decision-making. The Restoration Science Associate also ensures the effective communication of findings to team members and external partners. 
Essential Functions and Responsibilities
(10%) Project and Team Collaboration
<ul>
<li>Participate with the Restoration Science Team to deliver large-scale ecological restoration projects on time, within the budget, and with the highest standards of project performance. </li>
<li>Participate in developing workplans, training plans, performance appraisal, timesheets, and expense reports. </li>
<li>Maintain a personal 70-20-10 plan in partnership with supervisor, and share with peers.</li>
<li>Ensure compliance with workplace regulations in collaboration with the Safety &amp; Office Manager. </li>
<li>Exercise sound judgement in elevating issues for support or review by senior leadership.</li>
<li>Maintain and support good working relationships with clients and vendors. </li>
<li>Fulfill project monitoring obligations while contributing to organizational outcomes such as organization-wide impact tracking, seed collections, and developing restoration science partnerships. </li>
<li>Regularly travel to project sites and regional offices to complete job duties and collaborate with the larger Restoration Science Team. </li>
<li>Foster positive working relationships amongst Restoration Science, Field Restoration and Administrative teams to support excellent project delivery.</li>
</ul>
(70%) Project Planning, Monitoring, and Development
<ul>
<li>Conduct data collection and analysis to support site evaluation and conception scoping.</li>
<li>Participate in writing and analysis to assist in project planning and design, cost-estimation, budgeting, partnership cultivation, and work planning to support the Restoration Team in delivering excellent restoration projects and the Development team in securing new restoration projects (grants and contracts).</li>
<li>Support the Restoration Team to:</li>
<li>Ensure timely and budget-complaint agreement deliverables. </li>
<li>Proactively monitor budgets and schedules, revise workplans, troubleshoot project obstacles, and manage productive relationships with clients and regulators.</li>
<li>Collect field data and perform literature review and synthesis to inform and monitor restoration projects using data-drive approaches. </li>
<li>Cleary communicate project developments, constraints, and opportunities to peers, external partners, and the Leadership team. </li>
<li>Advance the science of Restoration Ecology through management of research partnerships, site studies, field trials, and demonstrations using River Partners' projects as living laboratories.</li>
<li>Adhere to sensitivity and permit compliance requirements. </li>
<li>Use projects and project partner relationships to maintain and grow restoration project adaptation, learning, and improvement.</li>
<li>Support the Development Team to: </li>
<li>Develop realistic project outcomes, workplans, and schedules for proposals. </li>
<li>Generate technical language for grant proposals as requested. </li>
<li>Support Advancement Director to secure private funding for projects and initiatives: </li>
<li>Prepare materials and represent River Partners at site tours and pitch meetings as requested.</li>
<li>Regularly share stories, project outcomes, photos, and other pertinent information from the field with River Partners leadership and team members.</li>
<li>Support Heritage Growers:</li>
<li>Regularly scope and forecast seed and plant requirements for restoration projects.</li>
<li>Scout and participate in wildland seed collections.</li>
<li>Collaborate with Heritage Growers to pilot and test new ecotypes in restoration projects. </li>
</ul>
(10%) Communications – Internal and External
<ul>
<li>Share project and team issues with appropriate team leads and senior leadership at River Partners.</li>
<li>Serve as an organizational ambassador for conferences, site tours and project visits with vendors, partners, and clients. </li>
<li>Know and coach staff and peers from Field Restoration Team to know the specific details of project implementation and outcomes including:
<ol>
<li>Timeline, tasks, and budget.</li>
<li>Special regulatory permit conditions and sensitivities (for example cultural resources). </li>
<li>Conceptual site model and intended measurable outcomes. </li>
<li>Strategic partners and regional importance of project. </li>
</ol>
</li>
<li>Inspect project sites and collaborate with Safety &amp; Office Manager, CFO, Senior Director of Field Restoration, and Director of Communications to highlight successes and outcomes, correct errors and respond to challenges. </li>
<li>Cultivate collaboration amongst Field Restoration and Restoration Science teams to ensure project compliance with permitting conditions, restoration plans and best available science. </li>
</ul>
Required Knowledge, Skills, and Abilities
<ul>
<li>Working knowledge of California plants, riparian ecology, hydrology, soils, and wildlife.</li>
<li>Familiarity with California and Federal environmental permitting including NEPA/CEQA, ESA, CDFW Code, California Water Code, and Clean Water Act Section 404/401.</li>
<li>Ability to collaborate with diverse team members and community partners with poise, vision, and respect. </li>
<li>Working understanding of statistics and experimental design.</li>
<li>Intermediate skills in collecting, organizing, and analyzing field data, including spatial data and maps. </li>
<li>Excellent verbal, analytical, organizational, and written skills, including data visualization to technical and non-technical audiences.</li>
<li>Integrity and ethics beyond reproach. </li>
</ul>
Qualifications
<ul>
<li>BS and a minimum of 1 year of experience in Ecology, Wildlife Management, Restoration, or a related field. Relevant experience may substitute for education. </li>
<li>Experience working with GPS/GIS applications. </li>
<li>Experience in ecological monitoring and program-building in ecological assessment. </li>
<li>Proficiency in working with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook), and SharePoint.</li>
<li>Valid California driver’s license with no restrictions.</li>
<li>Ability to communicate in Spanish (preferred). </li>
<li>Commitment and enthusiasm to carry out River Partners’ mission. </li>
</ul>
Compensation Salary is commensurate with experience, anticipated to range between $26.20 to $33.00 hourly. River Partners offers a generous benefits package including ample holidays and paid time off, an alternative work week schedule, flexible location and hours, medical insurance, and up to 4% 401(k) match on your contribution. 

To learn more about River Partners leading approach to restoring California ecosystems, please visit our website: <a href="http://riverpartners.org" target="_blank">http://riverpartners.org</a>
To Apply
Please submit a cover letter, resume, and contact information for three references to the link below
Careers at River Partners


 

River Partners is an Equal Opportunity Employer.
River Partners is an Equal Opportunity/Affirmative Action (EEO/AA) Employer. All qualified applicants will receive consideration without regard to race, color, national origin, sex, sexual orientation, genetic information, gender identity, religion, age, status as a protected veteran, status as an individual with disability, or any other protected group status or non-job related characteristic as directed by law.

Associate Restoration Scientist

<h3>Job Description</h3>
Job Description
Summary:
The Chemical Operator will apply various technologies to test and modify manufacturing machinery and equipment. Additionally, they will be required to operate chemical packaging and/or processing equipment, such as the production of Cyanoacrylate adhesives, photopolymer resins, and various other chemical blending. In addition, the successful candidate will start at the basic level of operations as a chemical operator and can progress based on skill set and ability to perform at the different levels of the chemical operator position.
Key Duties and Responsibilities:
<ul>
<li>Showing good personal safety practices are followed on Chemence property, including but not limited to FDA, OSHA, and EPA. </li>
<li>Understanding how to obtain safety information on various chemicals.</li>
<li>Responsible for daily lab manufacturing activities which include setup, in process, and post process handling and monitoring of all reaction’s intermediates, and products. Includes but not limited to following routers and written/verbal instructions.</li>
<li>Demonstrates cGMP, GLP, and FDA requirements are being followed. Includes recording and verifying accurate information is reported on all documentation. </li>
<li>Makes suggestions for improvements to routers, work practices, and areas.</li>
<li>Keeping equipment and glassware fit and ready for use in a timely manner.</li>
<li>Reporting chemical and supply inventory shortages in a timely manner. </li>
<li>Handling, transferring, and confirming all inventory items.</li>
<li>Proper handling of all waste materials. Understanding the differences between various types of waste, storage locations, and personal protection requirements. Instructing other departments about safety and handling when required.</li>
<li>Proper handling of all chemicals presents on the Chemence property. </li>
<li>Instructing other departments about safety and handling when required.</li>
<li>Able to handle and participate in special projects when assigned.</li>
<li>Willing to be self-motivated in the continual improvement of the work environment and personal performance.</li>
<li>Other duties as assigned. </li>
</ul>
Qualifications, Education and/or Experience Required:
<ul>
<li>At least 3-years’ experience in Manufacturing or Production experience. </li>
<li>High School education or equivalent.</li>
<li>Basic math skills with the ability to learn intermediate level math.</li>
<li>Must pass a respirator fit test and online medical exam in accordance with OSHA regulations; compliance is required prior to employment and as a condition of continued assignment.</li>
</ul>
Language Skills:
<ul>
<li>English required; Spanish is a plus.</li>
</ul>
Physical Demands: 
<ul>
<li>Position requires walking, standing for prolonged periods, occasionally required to sit, climb, or balance, stoop, kneel, crouch or crawl. May frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.</li>
<li>All employees must successfully complete and pass a respirator fit test and online medical exam in compliance with applicable OSHA standards as a condition of employment. This qualification is mandatory for performing essential job functions safely and effectively. </li>
</ul>
Other Duties:
<ul>
<li>Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.</li>
</ul>
AAP/EEO Statement:
<ul>
<li>CHEMENCE® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.</li>
<li>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</li>
</ul>

Chemical Operator

<h3>Job Description</h3>
Job DescriptionTumor Ex-vivo Research Associate (6 month contract role) Position Summary We are seeking a highly motivated Research Associate on a 6 month contract basis to join the Primary Cell Platform (PCP) Team within the Immunology and Pharmacology Department at PIRC. The candidate will be part of a collaborative and fast-paced team driving preclinical research focused on human tumor biology and immune function. The role offers the opportunity to work with clinically relevant human samples and contribute to translational research efforts that support early-stage therapeutic discovery. A strong candidate will have a background in immunology and/or cell biology, with prior hands-on experience in cellular assays, tissue culture, or immunoassays. The ability to work effectively within multidisciplinary teams, follow complex protocols, and deliver high-quality experimental data is essential. This is an excellent opportunity to gain experience in advanced tumor modeling and immunoprofiling techniques while supporting impactful, real-world research. This is a 6 month contract with potential to transition to a full-time permanent role based on performance and project success. Upon conversion, the employee will be eligible for our full benefits package. &nbsp;Main Responsibilities
<ul>
<li>Perform in vitro and ex vivo experiments focused on tumor-immune interactions using primary human models</li>
<li>Support the culture and maintenance of primary tumor tissues, including tumor slice assays, spheroids/organoids, and immune co-cultures</li>
<li>Process tumor/blood specimens: e.g. tissue dissociation, PBMC isolations from whole blood, viability assessment, and assay preparation</li>
<li>Execute immunological assays such as:
<ul>
<li>Flow cytometry, ELISA, MSD, cytokine profiling</li>
<li>T cell activation, proliferation, and cytotoxicity assays</li>
</ul>
</li>
<li>Culture primary human immune cells (e.g., PBMCs, T cells, macrophages)</li>
<li>Analyze and interpret experimental data and present findings to the team</li>
<li>Maintain detailed, timely, and compliant documentation using an electronic lab notebook (ELN)</li>
<li>Follow lab safety and quality standards</li>
<li>Be available for occasional after-hours work to support time-sensitive tumor sample processing</li>
</ul>
Basic Qualifications
<ul>
<li>Bachelors/Masters degree in Immunology, Cell Biology, Biomedical Sciences, or a related life science field with 2-3 years of industrial experience</li>
<li>Available to work full-time, onsite for the 6 months duration without needed work authorization/sponsorship from the company</li>
</ul>
Preferred Qualifications
<ul>
<li>Previous relevant laboratory experience is highly preferred</li>
<li>Skilled in aseptic technique and primary human cell culture</li>
<li>Experience with tumor tissue handling, 3D culture systems, or ex vivo tumor models</li>
<li>Familiarity with flow cytometry, immunoassays, and related technologies</li>
<li>Experience using an electronic lab notebook for experimental documentation</li>
<li>Excellent communication, time management, and organizational abilities</li>
<li>Collaborative, flexible, and motivated to work in a fast-paced translational research environment</li>
</ul>
 &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Tumor Ex-vivo Research Associate (6 month contract role)

<h3>Job Description</h3>
Job Description
 
Title: Scientist 
Location: Hayward, CA 
Reports To: Group Leader
Company
Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Position/Job Summary We are seeking a highly motivated and experienced Scientist specializing in LC-MS/MS to join our dynamic team. This individual will play a pivotal role in quantitative bioanalysis and the characterization and identification of drug metabolites, contributing to our understanding of DMPK (Drug Metabolism and Pharmacokinetics) and its impact on drug safety and efficacy.
 
Roles &amp; Responsibilities
<ul>
<li>Develop and optimize sample preparation and analytical methodology for quantitative measurement of drugs in a variety of modalities and metabolite profiling/identification using state-of-the-art LC-MS/MS and high-resolution mass spectrometry (HRMS).</li>
<li>Lead and execute LC-MS/MS-based projects in a timely and high-quality manner.Interact with clients to provide actionable insights on method development and sample analysis-related challenges.</li>
<li>Operate, maintain, and troubleshooting LC-MS/MS instruments; serve as instrument lead as needed.</li>
<li>Prepare and review scientific reports, presentations, and regulatory documents to ensure accuracy and compliance with industry standards.</li>
<li>Stay updated on advancements in LC-MS/MS technologies and methodologies.</li>
<li>Collaborate with cross-functional teams and provide technical guidance when needed.</li>
<li>Mentor and train junior lab staff.</li>
</ul>
Education, Experience &amp; Skills Required
<ul>
<li>Ph.D. in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.</li>
<li>Solid hands-on experience with LC-MS/MS-based bioanalytical method development including sample preparation, instrument operation and data processing.</li>
<li>Proven track record operating LC-MS/MS systems in a bioanalytical lab</li>
<li>Strong expertise in drug metabolism and biotransformation, with hands-on experience in metabolite identification using LC-MS/MS and HRMS.</li>
<li>Demonstrated ability to analyze and interpret complex mass spectrometry data and provide detailed reports.</li>
<li>Excellent communication skills and ability to work both independently and collaboratively in a cross-functional team environment.</li>
<li>Experience in pharma or biotech environment is a plus</li>
</ul>
Salary and Benefits:
Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Scientist

<h3>Job Description</h3>
Job DescriptionSenior/Principal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated and experienced senior or principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond. In this position, you will utilize your expertise in pharmacokinetics, pharmacodynamics, and biomarker discovery to guide drug development and biomarker strategies, optimize dosing regimens, and ensure the safety and efficacy of investigational drugs. You will also contribute to translational activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms. These efforts include indication expansion, novel combinations, and refining/improving biomarker approaches to guide dosing and patient selection. Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities:
<ul>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Further Exploration of BESREMi: Collaborate with clinical development team to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally and be involved in investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Regulatory Interaction: Work with regulatory affairs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, new drug applications (NDAs), and marketing authorization applications (MAAs). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>3+ (for senior scientist) or 8+ (for principal scientist) years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via contract research organizations and academic collaborations.</li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism of action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models is preferred.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials is strongly desirable.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Experience working closely with academic collaborators via sponsored research agreements or IITs is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
Conclusion: As a Senior/Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward and ultimately improving patient outcomes at PIRC.
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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