field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionWhat it’s like to work with us:Craftwater is different. We empower and expect staff to create usable, actionable information through collaborative and innovative approaches that reflect their passion to impart much-needed environmental changes through engineering and science. We offer a flex work environment that combines remote and in-office time. California casual is our dress code of choice, unless we are headed to a client meeting or presentation. We take ourselves lightly, and our work seriously and cultivate a culture based around the desire to do things differently and better in every job we take on. Each of us has our own quirks, and we think we’re pretty hilarious. We genuinely like each other, and make time for “play,” and teambuilding, and try to push each other to find the next best approach to delivering the most well-founded and useful information to our clients in new and exciting ways. We are doing new big things and having an incredible time doing it.​Who we hire:Do you want to make a meaningful impact? &nbsp;Come join Craftwater and be on the cutting edge of resource planning and design including policy setting, water management, green infrastructure, scientific research, public education and outreach, environmental justice/equity, and more.&nbsp;You must be hard working, dynamic, an out-of-the-box thinker, and fun!&nbsp;Qualifications
<ul>
<li>Bachelor’s degree (Master’s Preferred) in environmental/civil engineering, environmental science, water resource management/policy, or related field, or a minimum of 8 years’ experience</li>
<li>Minimum 4 years in water resources or related field</li>
<li>Working knowledge of hydrology, water quality modeling, and geospatial analysis of hydrologic and related datasets</li>
<li>Working knowledge of ArcGIS tools and their application to planning and policy</li>
<li>Proven experience developing written communications for water resource management and policy decision-making</li>
<li>Understanding of stormwater management techniques including capture, green infrastructure, reuse, etc.</li>
<li>Proficient technical writing skills and ability to translate complex findings into graphics</li>
</ul>
If these attributes resonate with you, feel free to apply today.

Lead Water Resources Policy & Regulatory Compliance Planner/Scientist

<h3>Job Description</h3>
Job DescriptionDescription:
Lead Scientist, Electrophysiology (In Vitro / Ex Vivo)
Palo Alto, CA 
About GondolaBio
GondolaBio is a clinical-stage biopharmaceutical company focused on developing breakthrough therapeutics for genetic diseases. GondolaBio is an independent sister company to BridgeBio, originally carved out in 2024 after securing $300M in private financing from external investors. GondolaBio aims to leverage cutting-edge biological research to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases. 
Who You Are
We’re seeking an entrepreneurial scientific leader with deep expertise in in vitro and ex vivo electrophysiology to advance GondolaBio’s rare disease pipeline. You will serve as the scientific lead for multiple preclinical programs where electrophysiology plays a critical role in understanding target biology and driving drug discovery. You will design, execute, and interpret electrophysiology experiments that guide compound optimization and translational strategy. 
This role offers the opportunity to shape research strategy, build electrophysiology capabilities, and mentor junior scientists while contributing to a growing interdisciplinary team. You will thrive in an environment where scientific rigor, creativity, and collaboration are valued equally, and where your work directly informs the development of transformative medicines for patients. 
Key?Responsibilities
<ul>
<li>Lead the design, execution, and interpretation of in vitro and ex vivo electrophysiology studies to characterize ion channels, transporters, and other excitable membrane proteins </li>
<li>Apply advanced electrophysiology techniques (e.g., patch-clamp, multi-electrode arrays, automated electrophysiology platforms) to study compound mechanism of action, potency, selectivity, and safety liabilities </li>
<li>Develop and validate electrophysiology assays to support drug discovery, including primary cell and tissue slice preparations </li>
<li>Oversee external collaborations with CROs and academic partners to ensure high-quality and timely data delivery </li>
<li>Communicate findings effectively with medicinal chemistry and biology colleagues to guide compound design and optimization </li>
<li>Supervise and mentor junior scientists, building expertise within the team </li>
<li>Stay current with emerging electrophysiology and ion channel drug discovery advances; represent GondolaBio at external meetings and in publications </li>
<li>Contribute to the development of research strategy and integration of electrophysiology insights into broader discovery and translational programs </li>
</ul>
Preferred Education?&amp;?Experience
<ul>
<li>PhD in neuroscience, pharmacology, physiology, or a related field with 2+ years of laboratory experience (postdoc + industry/academic) </li>
<li>Strong track record applying patch-clamp electrophysiology (manual and automated) or related ex vivo techniques in drug discovery or advanced academic research </li>
<li>Demonstrated experience with ion channels, transporters, or excitable cells/tissues (neurons, cardiomyocytes, muscle fibers, etc.) </li>
<li>Hands-on expertise in designing, executing, and interpreting electrophysiological assays for compound evaluation </li>
<li>Experience managing projects, collaborating cross-functionally, and directing CROs or external partners </li>
<li>Strong problem-solving skills and ability to integrate electrophysiology with other discovery disciplines (structural biology, pharmacology, computational modeling) </li>
</ul>
Nice-to-Haves
<ul>
<li>2+ years of industry drug discovery experience highly valued, especially collaborations with medicinal chemistry teams to inform SAR </li>
<li>Experience with tissue slice electrophysiology, synaptic physiology, or stem cell–derived excitable cell models </li>
<li>Familiarity with assay automation, high-throughput electrophysiology platforms, and data analysis pipelines </li>
<li>Broader understanding of preclinical drug discovery disciplines, including cellular disease models, target engagement assays, pharmacology, and PK/PD </li>
<li>Experience mentoring and building an electrophysiology team in an industry setting </li>
</ul>
No matter your role at GondolaBio, successful team members are
<ul>
<li>Patient Champions, who put patients first and uphold strict ethical standards </li>
<li>Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset </li>
<li>Truth Seekers, who are detailed, rational, and humble problem solvers </li>
<li>Individuals Who Inspire Excellence in themselves and those around them </li>
<li>High-quality executors, who execute against goals and milestones with quality, precision, and speed </li>
</ul>
What We Offer
<ul>
<li>Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts </li>
<li>A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak </li>
<li>An unyielding commitment to always putting patients first. </li>
<li>A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science </li>
<li>A place where you own the vision – both for your program and your own career path </li>
<li>A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game </li>
<li>Access to learning and development resources to help you get in the best professional shape of your life </li>
<li>Robust and market-competitive compensation &amp; benefits package (Base, Performance Bonus, Equity, health, welfare &amp; retirement programs) </li>
<li>Flexible PTO </li>
<li>Rapid career advancement for strong performers </li>
<li>Potential ability to work on multiple GondolaBio programs across multiple therapeutic areas over time </li>
<li>Partnerships with leading institutions</li>
<li>Commitment to Diversity, Equity &amp; Inclusion </li>
</ul>
The base pay range for this position is $150,000 to $200,000 per year. The actual compensation offered will be determined based on a number of job-related factors, including experience, skills, qualifications, and location. A bonus plan and equity will also be offered. 
Requirements:

Lead Scientist, Electrophysiology (In Vitro / Ex Vivo)

<h3>Job Description</h3>
Job Description
Senior Blaster JOB SUMMARY: To manage location assets and personnel at the customer site to meet established customer requirements in support of the location's strategic plan. Must be certified by APC to blast.
ESSENTIAL FUNCTIONS, DUTIES, AND RESPONSIBILITIES:
Must satisfactorily perform each of the essential functions, duties, and responsibilities listed below. •Maintains a safe and healthy work environment by complying with MSHA, OSHA, ATF, •DOT regulations within the work area. •Performs all necessary duties to prepare designated area for blasting including verification of •blast shelter, blast equipment, drill pattern stemming, face, and blast area. •Supervises personnel at the customer site/blast area. •Assists in training and development of employees. •Builds and sustains rapport with the current customer base to increase market share and •ensure growth, including pricing or budget controls. •Coordinates the handling of all complaints and/or incidents of customers with appropriate •personnel. •Communicates regularly with sales representative regarding customer accounts.
MARGINAL FUNCTIONS, DUTIES, AND RESPONSIBILITIES:
May perform any of the marginal functions, duties, and responsibilities listed below on a limited basis in the event that a subordinate is unavailable or unable to perform their functions, duties, and responsibilities. •Assist or perform the duties of any location position (as qualified).
DECISION MAKING AND ACCOUNTABILITY: Has overall authority and responsibility for the following as defined by corporate policies, procedures, and guidelines. •Personnel in blast area. •Customer satisfaction. •Regulatory compliance.
ERGONOMIC CONDITIONS:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. •Outdoor climate and terrain. Exposure to dust, noise, oils, greases, and other debris. •Work outdoors year-round on surfaces that may be dry, wet, slippery/slick, or uneven, on rock, in water, or snow. •While performing the duties of this job the employee is frequently required to walk, stand; sit; use hands to finger, handle, or feel objects, tools, or controls, reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk and hear.
QUALIFICATIONS: •Must be 21 as required by ATF. •High school or equivalent (GED) degree. •Must possess upon hire or acquire within 12 months of hire the following certification: Austin Powder Company Blasting Certification - State Blaster's License. •Minimum 5 years certified blasting experience. •Must be technically capable to blast any quarry or mine serviced by the location. •MSHA Safety and First Aid Certification.
SKILLS/KNOWLEDGE: •Must demonstrate competency and proficiency in the following skills and/or abilities. •Interpersonal skills. •Product/technical knowledge including: Proficient in EBR. Intermediate knowledge of ABS. •2D Profiling, seismograph operation and blast site security proficient. •Global Position System proficient. •Monitoring and implementing compliance measures. •Knowledge of applicable regulations. •Time and priority management skills. •Basic computer skills.
 Job Posted by ApplicantPro

Senior Blaster

<h3>Job Description</h3>
Job DescriptionDescription:
Title: Senior Peer Mentor - Transportation Services
Department: Behavioral Health
Reports To: Transportation Services Coordinator
Location: 56 Bay Street, 1st Floor, Staten Island, NY 10301
Position Status: Part Time (20 hours per week)
FLSA Status: Non-Exempt
Pay &amp; Benefits: The pay range for this role is generally $17.79- 19.00 per hour, commensurate with relevant experience and qualifications and in alignment with internal equity.
 
Community Health Action of Staten Island (CHASI) drives dramatic improvements in the health of New Yorkers by feeding people who are hungry, healing families broken apart by violence, and bridging the gaps between people and the compassionate health care they deserve. CHASI provides outreach, education, prevention, and direct support services for populations most affected by health disparities – people with low or no income, low-income people with chronic illnesses, people with criminal justice involvement, people who use drugs, domestic violence survivors, people of color, and the LGBTQ community.
 
POSITION SUMMARY:
The Senior Peer Mentor (SPM) will support the Transportation Coordinator in managing a grant-funded rideshare transportation program for individuals with a history of substance use disorder. The SPM will be responsible for documenting all transportation services utilized on a weekly and monthly basis and escorting participants to necessary locations across Staten Island when warranted. This role is ideal for a compassionate and detail-oriented individual committed to supporting people in recovery by ensuring they have reliable access to essential services.
 
DUTIES &amp; RESPONSIBILITIES:
Transportation Support &amp; Documentation:
<ul>
<li>Maintain accurate records of all rides provided through the program, including dates, times, destinations, and participant details.</li>
<li>Prepare and submit weekly and monthly transportation utilization reports to the Transportation Coordinator.</li>
<li>Assist with tracking program performance and identifying trends in transportation needs.</li>
<li>Communicate with participants about their scheduled rides, ensuring they understand pickup times and locations.</li>
</ul>
Peer Support &amp; Escorting Services:
<ul>
<li>Provide in-person escort services for participants who require additional support traveling to appointments, treatment programs, or other essential locations across Staten Island.</li>
<li>Offer peer-based support and encouragement during transit, helping participants navigate barriers to accessing care.</li>
<li>Act as a liaison between participants, transportation providers, and the program team to ensure smooth service delivery.</li>
</ul>
Collaboration &amp; Advocacy:
<ul>
<li>Work closely with the Transportation Coordinator and case management staff to address transportation-related concerns.</li>
<li>Advocate for participant needs and provide feedback on ways to improve the program’s accessibility and effectiveness.</li>
<li>Uphold confidentiality and ethical standards while supporting individuals in their recovery journey.</li>
<li>Perform all functions in alignment with CHASI’s Mission, Vision, and Core Values.</li>
</ul>
Requirements:
QUALIFICATIONS:
<ul>
<li>New York State Certified Recovery Peer Advocate-Provisional (CRPA-P), at minimum.</li>
<li>Prior experience in peer support, case management, or human services preferred.</li>
<li>Strong attention to detail with the ability to maintain accurate records and reports.</li>
<li>Excellent interpersonal skills with the ability to engage and support individuals in recovery.</li>
<li>Must be dependable and able to meet participants at designated locations on time.</li>
<li>Familiarity with Microsoft Office (Excel, Word) or Google Docs/Sheets for reporting.</li>
</ul>
PREFERRED:
<ul>
<li>Experience working with individuals in recovery and/or navigating transportation challenges.</li>
<li>Knowledge of Staten Island’s public transit system and local recovery resources.</li>
<li>Valid driver’s license and reliable transportation (not required but a plus).</li>
</ul>
COMPETENCIES:
<ul>
<li>Works independently following receipt of instructions on a task, demonstrating the ability to understand and execute the task with minimal supervision.?</li>
<li>Takes initiative on future tasks by identifying potential areas for improvement and proactively addressing them.?</li>
<li>Ability to work independently, establish priorities, and handle multiple tasks simultaneously.</li>
<li>Models ethics and integrity?</li>
<li>Manages and accepts change to ensure successful growth and changes within the organization.</li>
<li>Evaluates obstacles and contributes alternative solutions. ?</li>
<li>Demonstrates strategic, conceptual, and critical thinking skills.</li>
</ul>
CHASI is an equal opportunity employer and is committed to hiring and supporting a diverse staff. All qualified applicants will be afforded equal employment opportunities without discrimination because of race, religion, color, national origin, sex, sexual orientation, gender identity, age, genetic information, disability or marital status.

Senior Peer Mentor - Transportation Services

<h3>Job Description</h3>
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for two Post Doctorate in our Bioanalytical (GBA) department. GBA is comprised of four laboratory operation units: Small Molecules, Oligonucleotides, Proteins, and Support Functions. This is a two-year temporary position with the potential for a permanent position at another QPS site in the US. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support biomarker quantitation. 
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
 
Please visit our website (<a href="http://www.qps.com" target="_blank">www.qps.com</a>) for more information and to see all current openings.
The Job
<ul>
<li>Independently manage one or more method development/validation studies at the same time with minimum supervision.</li>
<li>Prepare, and/or review and understand study protocols.</li>
<li>Evaluate the significance of data and report findings. </li>
<li>Prepare Study summaries and/or reports.</li>
<li>Set-up, utilize, and maintain complex instrumentation</li>
<li>Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.</li>
<li>Maintain schedule of projects and timelines.</li>
<li>Develop, validate and run sensitive, reliable and efficient LC-(HR)MS/MS assays for TK/PK/Biomarker assessment.</li>
<li>Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.</li>
</ul>
Work Location
<ul>
<li>This job will be 100% QPS-office/facility based</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Analytical Chemistry, Biochemistry, Microbiology, Pharmacology, Food Science, Plant Science or related scientific discipline with hands-on experience in mass spectrometry.</li>
</ul>
Why You Should Apply
<ul>
<li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li>
<li>Structured Career Ladders that provide excellent growth based on your personal aspirations.</li>
<li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li>
<li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li>
<li>Park-like setting in Newark, Delaware</li>
<li>Internal committees designed with the needs and enjoyment of QPS employees in mind.</li>
</ul>
QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Post Doctorate Scientist

<h3>Job Description</h3>
Job Description
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
The Role:
We are seeking passionate and creative individuals who want to contribute to Septerna's mission to utilize innovative drug discovery technologies for GPCR targets. The ideal candidate will have a strong background in protein biochemistry, including expression, purification, and characterization of proteins from mammalian, bacterial, and insect cells at a variety of scales. The chosen candidate will be working in a collaborative team contributing to improvements in protein expression and purification to support production and characterization of proteins for use in structural biology, biophysics, and small molecule drug discovery. This position offers the unique opportunity to join an innovative well-funded biotechnology company and to contribute to its long-term success. 
The position is based in South San Franscisco, CA. Title and compensation commensurate with experience.
Responsibilities
<ul>
<li>Perform as a hands-on protein scientist to help fully enable Septerna's Native Complex™ </li>
<li>Design and implement workflows to express, purify and characterize soluble and membrane proteins from mammalian, bacterial, and insect cells. </li>
<li>Develop and deploy platforms for parallel mid-scale screening of protein production constructs to enable optimization of protein quality and yield.</li>
<li>Closely collaborate with protein sciences team to automate and streamline current protein production workflows. </li>
<li>Responsibilities will include expression construct design, protein engineering, eukaryotic cell culture, automated column chromatography (FPLC/HPLC), and protein QC.</li>
<li>Work in a collaborative environment to support discovery, biophysics, and structural biology efforts for internal drug discovery programs. </li>
<li>Independently design, execute, and interpret biochemical workflows</li>
<li>Data analysis, documentation, and presentation in group and project team meetings</li>
</ul>
Qualifications
<ul>
<li>PhD with a minimum of 5+ years, or BS/MS with 10+ years, of relevant experience in a biotechnology or pharmaceutical setting.</li>
<li>Proficiency in protein engineering, cell culture, and protein expression in bacterial, insect, and mammalian systems is required.</li>
<li>Expertise in design of protein expression constructs focused on parallel exploration of promoters, tags, and other elements to improve protein yield and quality.</li>
<li>Required hands-on experience with small-scale multi-parallel expression and purification.</li>
<li>Strong experience in protein purification using FPLC-based column chromatography including affinity, ion exchange, and size exclusion. </li>
<li>Experience with purification and characterization of membrane proteins, particularly GPCRs, using detergents, nanodiscs, amphipols, and other stabilization technologies considered a plus.</li>
<li>Knowledge of protein characterization techniques including multi-angle light scattering (MALS), Differential Scanning Fluorimetry (DSF), analytical size exclusion (AnSEC), etc. </li>
<li>Familiarity with automation and data analysis/reporting software is highly desired. </li>
<li>Demonstrated experience building strong partnerships across the organization; ability to work collaboratively in a team-oriented environment while also working independently on experimental planning, data analysis and interpretation</li>
<li>Clear and effective verbal and written communication skills</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $135,000 - $155,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Senior Scientist/Staff Scientist, Protein Science (industry experience required)

<h3>Job Description</h3>
Job Description
Location: Redwood City, CA &nbsp; &nbsp;
Company Overview: &nbsp;
ImmunEdge is a biopharmaceutical company committed to developing novel therapeutics for patients with serious or life-threatening diseases. With a highly experienced team of experts in immunology and drug development, we are pioneering innovative approaches to target and modulate key molecular pathways that regulate the immune response.  &nbsp;
At ImmunEdge, we are driven by a shared commitment to improving human health through innovative science. We are building a culture based on kindness, collaboration, and a deep passion for advancing science. As an early joiner to the company, you will help cultivate an environment where every team member is encouraged to challenge ideas, think critically, and contribute their unique perspectives. We value openness, transparency, and continuous learning, and want to empower our employees to take ownership of their work while fostering a sense of community and teamwork. Whether you’re working in the lab, the office, or across functional teams, you will find an inclusive space where your contributions matter and your professional growth is supported. &nbsp;
Join us in shaping the future of biotechnology. Together, we can change lives. &nbsp; &nbsp;
Position: &nbsp;
ImmunEdge has an exciting opportunity for a Scientist to join our Translational Science &amp; Biomarkers team. This person will contribute to preclinical and clinical programs by developing and validating biomarkers for clinical trials. Strong candidates will be highly collaborative, strategically organized, and passionate about drug discovery and precision medicine. Expertise in immunology, tumor biology, and biomarker assays are highly desirable, and candidates should have experience working with human clinical samples.&nbsp;&nbsp; &nbsp;
Key Responsibilities: &nbsp;
<ul>
<li>
Design and implement innovative in vivo and ex vivo studies to identify novel biomarkers and investigate the mechanisms of action of ImmuneEdge’s therapeutic candidates&nbsp;
</li>
</ul>
<ul>
<li>
Conduct a range of assays – including biochemical, molecular, cellular, immunological, in vivo and ex vivo – using mouse and human-derived samples to support preclinical and clinical research&nbsp;
</li>
</ul>
<ul>
<li>
Support the identification and assessment of emerging biomarker technologies to determine their clinical/scientific relevance and technical performance&nbsp;
</li>
</ul>
<ul>
<li>
Analyze biomarker data from preclinical experiments and present the data clearly and effectively&nbsp;
</li>
</ul>
<ul>
<li>
Contribute to scientific strategy by proposing new hypotheses and supporting the advancement of ImmunEdge’s research and development pipeline&nbsp;
</li>
</ul>
<ul>
<li>
Maintain accurate, well-organized records while supporting a safe and compliant lab environment  &nbsp; &nbsp;
</li>
</ul>
Qualifications: &nbsp;
<ul>
<li>
Ph.D. in Immunology, Molecular and Cellular Biology, or a related field&nbsp;
</li>
</ul>
<ul>
<li>
2+ years of industry experience in oncology or immunology drug development is preferred, with a track record of hands-on experimental success &nbsp;
</li>
</ul>
<ul>
<li>
Strong technical expertise in immunology-relevant lab techniques, including flow cytometry, ELISA, primary cell culture, in vitro functional assays, immunohistochemistry (IHC), RNA isolation/sequencing, ddPCR / qPCR&nbsp;
</li>
</ul>
<ul>
<li>
Ability to independently oversee scientific activities and rigorously analyze and interpret scientific data&nbsp;
</li>
</ul>
<ul>
<li>
Ability to work effectively and collaboratively in a supportive, but dynamic, start-up environment&nbsp;
</li>
</ul>
<ul>
<li>
Excellent communication, technical writing, and organizational skills&nbsp;
</li>
</ul>
<ul>
<li>
Experience with PEAs (e.g. Olink), MSD, bead-based cytokine arrays, WGS, cfDNA analysis, Incucyte, MIBI, ISH, automated IHC instruments (e.g. Leica Bond), spatial genomics, and/or PK assay development would be a plus&nbsp;
</li>
</ul>
<ul>
<li>
Ability to perform bioinformatic analysis of gene expression and other high-dimensional datasets (R, Python, etc.) would be a plus&nbsp;
</li>
</ul>
This is a position that requires working in a laboratory environment with biological and chemical hazards. Protective clothing, gloves and safety glasses are required while working in the laboratory. This position requires the ability to lift containers or instruments up to 25 pounds and working standing at a fume hood or lab bench for extended periods. &nbsp; &nbsp;
Expected Salary Range: $127,000 - $142,000&nbsp; &nbsp;
We encourage candidates of all levels to apply as there is sometimes flexibility on job level and responsibilities. Compensation will be based on a variety of factors, including experience, qualifications, internal equity, and location.  &nbsp;
ImmunEdge offers a competitive employment package that includes an annual bonus plan, equity, and a generous benefits package including comprehensive health (medical, dental, and vision) insurance for our employees and their families, a 401k plan, FSA plans (medical, dependent), an Employee Assistance Plan, and a holiday and paid time off plan. &nbsp;
At ImmunEdge, we believe that a diverse, open, and inclusive environment and culture is key to our success.  We will not be influenced in recruiting, hiring, promoting or any other employment practices by race, color, citizenship status, national origin, ancestry, sex, sexual orientation, gender identity/expression, age, religion, physical or mental disability, medical or genetic condition, marital status, veteran status, or any other characteristics protected under applicable federal, state and local laws. ImmunEdge will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable laws. &nbsp;
Note to External Recruiters: Submission of unsolicited resumes prior to an agreement set in place does not create any implied obligation. &nbsp;
Powered by JazzHR
dZiOrxfCAz

Scientist I/II, Translational Science & Biomarkers

<h3>Job Description</h3>
Job Description
Senior Port Captain&nbsp;Job Summary: We are seeking an experienced Senior Port Captain specializing in tanker operations to provide leadership and expert support for marine activities at our facilities. This shore-based role is critical in ensuring the safe, compliant, and efficient handling of tankers and barges involved in crude oil refining and distribution. The ideal candidate will bring a strong maritime background, regulatory knowledge, and leadership capabilities to support operations, emergency response, and marine assurance functions.
Senior Port Captain&nbsp;Responsibilities:
<ul>
<li>Oversee and support marine operations involving tankers and barges, ensuring adherence to U.S. Coast Guard and international maritime regulations.</li>
<li>Provide technical guidance on marine measurement, loss control, and interface issues with facility operations.</li>
<li>Ensure compliance with terminal operational standards and safety regulations, including dangerous cargo handling.</li>
<li>Assist in developing and executing emergency response procedures and plans.</li>
<li>Support marine assurance activities by liaising with facility management and regulatory agencies to maintain regulatory compliance and safety standards.</li>
<li>Maintain operational oversight with a strong focus on safety, compliance, and best practices.</li>
</ul>
Senior Port Captain Position Requirements:
<ul>
<li>Bachelor’s Degree from a recognized Maritime Academy or equivalent maritime experience.</li>
<li>Master Mariner License with Dangerous Cargo Endorsement (OIL) preferred.</li>
<li>A minimum of 8 years of marine-related experience, including time at sea on tankers or shoreside management roles.</li>
<li>Strong understanding of tanker operations, marine measurement, loss control, and regulatory compliance.</li>
<li>Proven computer literacy skills and familiarity with marine software tools.</li>
<li>Excellent communication, leadership, and collaboration skills, with the ability to coordinate effectively with facility teams and regulatory authorities.</li>
</ul>
#LI-OnsitePandologic. Keywords: Sailor, Location: Sulphur, LA - 70664 , PL: 601142990

Senior Port Captain ( Tankers )

<h3>Job Description</h3>
Job DescriptionExpress Employment of Covina, CA is seeking a&nbsp;Clean Room Assembler&nbsp;for our client located in&nbsp;Irwindale.&nbsp;Clean room Assembler: $17.00hr Shift&nbsp;Hours:&nbsp;Mon-Fri 7AM- 3:30PM&nbsp;The Role you will play
<ul>
<li>Assembling components and product in a clean room environment.</li>
<li>Conducts, visual inspections and measurements to determine product conformance. focusing on scratches or damages to inbound product.</li>
<li>Detect problems and notify appropriate personnel of item non-conformance. Perform product containment on suspect ware. Properly tags all non-conforming and suspect material and/or parts. Assist with the investigation of line failures. Audit product after sort/rework and report&nbsp;results.</li>
<li>Maintains documentation (drawings, procedures, forms, reports, etc.) utilized for inspection and assures that they are current, accurate and complete. Complete and maintain all QA documentation in accordance with established procedures and work practices. Closes out OTC Orders.</li>
<li>Analyze QA data and provide summarization reports.</li>
<li>Deliver samples and support line trials and product validations as needed</li>
</ul>
&nbsp;Background Profile:&nbsp;
<ul>
<li>High school diploma and minimum of one-year related experience and/or training; or equivalent combination of education and experience</li>
<li>Ability to work well with others</li>
<li>Must be able to read and write proficiently.</li>
<li>Ability to work with minimal supervision</li>
</ul>
&nbsp;About us:Impacting people. One Job at a time. Our positions vary from permanent, temporary, and evaluation hire. We look forward to matching you to a position that fits your experience and thank you for your interest in Express Employment Professionals Covina.&nbsp;We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with state and local laws including the City of Los Angeles Fair Chance Initiative Hiring Ordinance #Covina&nbsp;&nbsp;PandoLogic. Keywords: Assembler, Location: IRWINDALE, CA - 91702 , PL: 601433571

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Engineer Science into Impact
At EmergingDx Inc, we are reimagining diagnostics at the edge of science, engineering, and innovation. As an institution for integrated innovation, we fuse biology, technology, and systems design to build transformative diagnostic tools that improve human health and empower clinicians, patients, and communities.
We’re looking for an In Vitro Diagnostics (IVD) Scientist/Engineer to join our mission-driven team. You’ll help architect, prototype, and validate next-generation diagnostic platforms—from rapid point-of-care assays to integrated microfluidic systems for disease monitoring and early detection.
This role is ideal for someone who thrives at the intersection of biological insight and engineering ingenuity, and who wants to shape the future of healthcare from the bench to the field.
Responsibilities (What You’ll Do)
<ul>
<li>Design, develop, and optimize IVD assays (immunoassays, molecular diagnostics, or clinical chemistry) for lab-on-chip and point-of-care platforms</li>
<li>Collaborate with cross-functional teams to integrate biological assays with microfluidic, optical, and electronic systems</li>
<li>Lead analytical validation studies including sensitivity, specificity, reproducibility, and regulatory performance metrics</li>
<li>Prototype, test, and troubleshoot diagnostic systems across wet lab and hardware environments</li>
<li>Contribute to product development processes including documentation, risk analysis, quality systems (ISO 13485), and FDA regulatory pathways</li>
<li>Apply systems thinking to challenges in sample preparation, biomarker detection, signal amplification, and data analysis</li>
<li>Effectively communicate results and technical insights to clients and stakeholders through both written reports and oral presentations</li>
<li>Develop and manage fast-paced project timelines while proactively identifying and mitigating risks</li>
<li>Stay current on scientific literature, emerging technologies, and clinical needs in diagnostics</li>
<li>Craft and deliver clear, compelling narratives—both written and oral—conveying technical project progress and proposed initiatives</li>
</ul>
Qualifications (What You Bring)
<ul>
<li>PhD in Bioengineering, Molecular Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or related field</li>
<li>7+ years of experience in vitro diagnostics, medical devices, genetics, microbiology, synthetic biology, translational research</li>
<li>Strong knowledge of assay formats: ELISA, lateral flow, qPCR, CRISPR-based diagnostics, isothermal amplification, or electrochemical detection</li>
<li>Experience with fluidic handling systems (manual and automated), sample matrices (blood, saliva, urine), and surface functionalization</li>
<li>Familiarity with data acquisition and analysis, including use of MATLAB, Python, or other statistical tools</li>
<li>Comfortable working across disciplines with engineers, designers, and clinicians</li>
<li>Adaptability in fast-paced environments</li>
<li>Detail-oriented, systems-focused, and passionate about delivering health impact through innovation</li>
<li>Proven track record of leading R&amp;D programs to deliver innovative, high-quality outcomes on schedule, aligned with stakeholder expectations and technical goals</li>
<li>Excellent verbal and written communication skills</li>
<li>Bonus: Experience in microfabrication, biosensor integration, point-of-care regulatory submissions, or multiplexed assay development</li>
</ul>
Why EmergingDx
<ul>
<li>You’ll work on products, platforms, and ventures — not just features</li>
<li>You’ll gain ownership, mentorship, and momentum</li>
<li>You’ll be part of something bigger: a community shaping what’s next</li>
<li>We offer a competitive salary with full benefits package.</li>
</ul>
Ready to redefine diagnostics? Send your resume to <a href="mailto:careers@emergingdx.com" target="_blank">careers@emergingdx.com</a>
Subject: In Vitro Diagnostics Scientist/Engineer – [Your Name]
Due to the nature of our business and information associated with this position, interested candidates must be US Citizens or Permanent Resident.
At EmergingDx Inc, we are proud to be an Equal Opportunity Employer committed to building and sustaining a talented, inclusive, and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, marital status, national origin, age, veteran status, disability, or any other legally protected status.
Note to recruiters: We are not seeking assistance for this position. Please do not contact us via phone or email regarding this opening.
As a U.S. Government contractor, we are required to collect certain applicant information for federal reporting purposes.

12,232 Science Jobs