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job_organization_name

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<h3>Job Description</h3>
Job Description
Job Title: Spanish Language Instructor (Part Time)
General Responsibilities: Under the supervision of the Director of Educational Development, plans and facilitates beginner level Spanish language instructional sessions.
Major Duties:
<ul>
<li>Meets regularly with the Director of Educational Development</li>
<li>Plans and facilitates group and/or 1:1 beginner Spanish language instructional sessions</li>
<li>Assists students in the development of appropriate study skills, completion of homework and projects, and exploring topics of interest to the student</li>
<li>Maintains consistent communication the Director of Educational Development</li>
<li>Models appropriate academic and social behaviors</li>
<li>Performs other duties as assigned</li>
</ul>
Required Knowledge, Skills, and Abilities:
<ul>
<li>Ability to work with students of diverse ethnic backgrounds, academic profiles, and skill levels</li>
<li>Possess good interpersonal and organizational skills</li>
<li>Must demonstrate responsibility, a desire to help others, discretion, and flexibility</li>
<li>Knowledge of academic content and skills</li>
<li>Application of such knowledge and tools to help students access material</li>
<li>Ability to collect and analyze data to drive future instruction</li>
<li>Ability to work independently applying critical thinking skills and problem solving to various situations</li>
</ul>
Qualifications:
<ul>
<li>Must have extensive teaching and/or tutoring experience in Spanish and be able to provide proof of vaccination</li>
</ul>

Spanish Language Instructor (Part Time, In Person)

<h3>Job Description</h3>
Job DescriptionEnergy &amp; Natural Resources Associate – California
Regulatory • Administrative Litigation • Emerging Energy Issues 
Direct Counsel is partnering with a respected, full-service law firm to add an Energy &amp; Natural Resources Associate to its growing practice group. This is an exciting opportunity for an attorney who wants to work at the intersection of law, policy, and regulated industries—advising clients on some of the most complex and consequential energy and natural resources issues in California.
Why This Role Stands Out
This practice sits squarely at the center of California’s evolving energy landscape. You’ll work on high-impact matters involving utilities, renewable energy, natural resources, and regulatory policy, with meaningful responsibility and exposure early on. Attorneys with backgrounds in regulatory law, administrative litigation, civil litigation, or other regulated industries will find their skills highly transferable here.
What You’ll Do
<ul>
<li>
Research and analyze issues related to energy and natural resources law and policy
</li>
<li>
Represent clients in administrative proceedings and related litigation
</li>
<li>
Advise on matters involving electricity and natural gas utilities, renewable energy, oil &amp; gas, mining, and water rights
</li>
<li>
Draft and negotiate contracts, including leases, joint venture agreements, and purchase/sale agreements
</li>
<li>
Prepare legal memoranda assessing risk, strategy, and alternative problem-solving approaches
</li>
<li>
Assist in developing legal strategies, including analysis of proposed legislation and regulatory frameworks
</li>
<li>
Support administrative hearings, including pleadings, discovery, testimony preparation, witness prep, cross-examination, and oral argument
</li>
<li>
Collaborate with attorneys across practices to deliver comprehensive, business-minded legal advice
</li>
</ul>
Who They’re Looking For
<ul>
<li>
J.D. from an accredited law school
</li>
<li>
Active California Bar admission
</li>
<li>
2+ years of experience in regulatory law, administrative litigation, energy &amp; natural resources, or other regulated industries
</li>
<li>
Familiarity with federal and California energy and natural resources regulations
</li>
<li>
Strong research, writing, and analytical skills
</li>
<li>
Experience with or exposure to agencies such as the California Public Utilities Commission (CPUC) or California Energy Commission (CEC) is a plus
</li>
<li>
Comfortable managing multiple deadlines in a fast-paced environment
</li>
<li>
Strategic thinker who can translate complex regulatory issues into practical legal advice
</li>
</ul>
Compensation &amp; Benefits
<ul>
<li>
Base Salary Range: $190,000 – $245,000
</li>
<li>
Bonus Potential: Up to $112,500
</li>
<li>
Compensation will vary based on experience, expertise, and performance
</li>
<li>
Comprehensive benefits package provided
</li>
</ul>
The Big Picture
This is an excellent platform for attorneys who want to build a long-term practice in energy and natural resources, gain deep regulatory experience, and work on matters that directly affect infrastructure, sustainability, and public policy across California.
 About Direct Counsel
Direct Counsel partners with leading law firms and in-house legal departments nationwide to connect talented attorneys with outstanding opportunities. We take pride in matching professionals with roles that align with their expertise, values, and long-term career goals.
Apply confidentially by sending your resume to <a href="mailto:sagan@directcounsel.net" target="_blank">sagan@directcounsel.net</a>

Energy & Natural Resources Associate

<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 Biologics CMC Development team at AbbVie has a long and rich history of biologics development. Now located in a new state of the art facility in South San Francisco, the team leverages its comprehensive end-to-end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing biologic therapies, such as monoclonal antibodies, bi-specifics and novel modalities, to human clinical studies and eventual licensure. This role will be imbedded in a team of highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel oncology drugs and successfully filed two BLAs.
The Cell Culture Development Group in South San Francisco, CA is seeking a Senior Scientist I to join a talented and collaborative team to develop and implement machine learning models for predicting optimal cell culture process performance. As a senior scientist, you will be responsible for all aspects of ML model development.
This position is an onsite role in a lab-based function. To be successful, candidates must enjoy and thrive in an onsite, highly collaborative lab environment with face-to-face cross-functional interactions between scientists.
In this position, you will perform cell culture process modeling, cell culture process development, scale-up, and technology transfer activities in a well-supported and dynamic environment to help advance novel biotherapeutics into human clinical studies.&nbsp;
KEY RESPONSIBILITIES:
<ul>
<li>Develop, implement, refine, and validate machine learning (ML) models for predicting cell culture process performance</li>
<li>Communicate model findings and suggest experimental strategy and/or workflow improvements to support early- and late-stage development</li>
<li>Actively seek out opportunities to optimize our platform or enhance our understanding of cell culture processes using ML models and wet lab experiments</li>
<li>Design and execute scalable ambr250, 2L, 50L, 200L and 500L single use bioreactors processes</li>
<li>Represent the cell culture development group in cross-functional meetings and collaborate closely with cell line, purification, analytical and formulation development leads to meet project deliverables and timelines</li>
<li>Publish or present scientific findings in peer-reviewed journals, internal or external conferences or consortia &nbsp;</li>
<li>Display effective organization, verbal written communication skills, and adherence to good documentation practices</li>
</ul>
Qualifications 
Basic Qualifications:&nbsp;
<ul>
<li>Scientific degree in computer science, statistics and applied mathematics, computational biology, bioinformatics, data science, chemical engineering, bioengineering, or a related field, with BS or equivalent education and&nbsp;10+ years of experience, OR MS or equivalent education and 8+ years of experience, OR PhD and 0+ years of experience</li>
<li>Must have industry or research experience in developing, implementing, and validating ML models</li>
<li>Must have a strong understanding of statistical methods, ML methodologies, and ML frameworks (e.g., Sci-kit Learn, TensorFlow, PyTorch)</li>
<li>Must demonstrate programming competency for model implementation in Python or equivalent</li>
<li>Must have experience in data visualization tools (e.g., Matplotlib, Plotly) to communicate model finding</li>
<li>Strong attention to detail; active and quick learner; able to change course quickly as needed; raises the bar and is never satisfied with the status quo; open to suggestions and embraces the ideas of others; collaborative actively builds relationships with others</li>
<li>Experienced in authoring peer-reviewed publications, technical reports, regulatory documents, and/or presentations at conferences</li>
<li>Proficient with Microsoft Office software and strong familiarity with statistical modelling software/tools (e.g., JMP, SIMCA, Minitab, Design Expert)</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Prior experience in developing and implementing ML models for biological data is highly desirable</li>
<li>Experience in implementing transfer learning is highly desirable</li>
<li>Expertise in programming (e.g., Python, Javascript, C++)</li>
<li>Experience in CMC cell culture process development is highly desirable</li>
<li>Demonstrated scientific aptitude through authorship of peer-reviewed publications&nbsp;</li>
<li>Strong understanding of design of experiments (DOE)</li>
<li>Proficient in aseptic technique</li>
<li>Basic understanding of mammalian cell and molecular biology and cell culture bioprocess engineering concepts</li>
<li>Experienced in developing and executing mammalian suspension cell culture processes in shake flasks, ambr250, and/or 2L bioreactors</li>
</ul>
<ul>
<li>Experienced in the tech transfer of cell culture and primary recovery processes to GMP manufacturing&nbsp;facilities in other locations</li>
</ul>
<ul>
<li>Experienced in authoring and reviewing technical reports, GMP campaign summary reports, and relevant sections in regulatory filings</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

Senior Scientist I (Machine Learning) - Biologics Cell Culture Development

<h3>Job Description</h3>
Job Description
We are looking for the best candidates to fill the position of full time Draft Technician for ACME dispensing service.
ACME dispensing service is the leader in draft maintenance, repair and installations in the Bay Area. We have been in operations since 2010 and service the most respected breweries, distributors, bars and restaurants in the Bay Area.
The draft technicians responsibilities are to complete a monthly maintenance route and occasional small repairs in the San Francisco area. We will train the right candidate for the position in the proper methods for draft maintenance and trouble shooting problems. The position is hourly with an incentive&nbsp;program to add additional income as well. The use of a personal vehicle and phone is required. A monthly reimbursement for phone and vehicle use is included along with fuel and parking ( a parking app account with company card is used for most parking)&nbsp;reimbursement.
Company DescriptionACME dispensing service has been the leader in draft maintenance, repair and installations for over 15 years. We were started with the intention of providing the best quality service to those who were being underserved in the craft beer community. Those people were independent distributors, craft breweries and bars/restaurants that wanted to serve true independent craft products without compromise. We continue to grow every year and look forward to adding people who share the same feelings for delivering quality service to the best customers in the Bay Area. 
<h3>Company Description</h3>
ACME dispensing service has been the leader in draft maintenance, repair and installations for over 15 years. We were started with the intention of providing the best quality service to those who were being underserved in the craft beer community. Those people were independent distributors, craft breweries and bars/restaurants that wanted to serve true independent craft products without compromise. We continue to grow every year and look forward to adding people who share the same feelings for delivering quality service to the best customers in the Bay Area.

Draft Beer/Wine/Cocktail Technician

<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 
Sr. Scientist I Cell/Molecular Biology
The Development Sciences Biologics CMC Drug Substance Cell Line Development Group in South San Francisco, CA is seeking a Senior Scientist to join a talented and collaborative team developing CHO cell lines for GMP applications. The successful candidate will have multi-faceted skills and experience across CHO cell line development and genetic characterization; Next Gen Sequencing methodologies (short- and long-read); cell engineering for gene knock-in/out/down; setting up automated workflows. &nbsp;
In this laboratory position, the candidate will design and perform hands-on studies in a well-supported and dynamic environment to help advance novel therapies to human clinical studies.&nbsp;&nbsp;The work will encompass cell and molecular studies relating to the generation and characterization of optimized CHO cell lines for production of our pipeline candidates. Additionally, the candidate will identify and evaluate new techniques, instrumentation and workflows to improve timelines, throughput and quality. The candidate will help set up automation of molecular biology workflows for NGS library preps and PCRs.&nbsp;
Key Responsibilities:
<ul>
<li>Design, test and optimize DNA vector constructs and vector workflows for protein expression (including monoclonal antibodies and antibody-like molecules) in CHO cells. Apply deep knowledge of expression vector design principles to optimize RNA expression levels and assembly of multi-chain biologics.</li>
<li>Design experiments and perform genetic characterization of CHO cell lines/banks using multiple methods (ddPCR, NGS by Illumina MiSeq and Nanopore PromethION 2, TLA, occasionally Southern/Northern blotting) to confirm identity, quality, and stability of transgene DNA and RNA. Manage and analyze all associated data, including NGS data.</li>
<li>Optimize genetic characterization workflows for technological advancement, efficiency and timeline improvement. Set up automation of wet lab and data analysis workflows.</li>
<li>Design and perform experiments for engineering gene knock-in/-out/-down in CHO cells.</li>
<li>Display effective organization, verbal and written communication skills, and adherence to good documentation practices, including real time entry of lab work into electronic lab notebook.</li>
<li>Author detailed technical reports that support regulatory filings at all stages from IND to BLA.</li>
<li>Present updates at team meetings and collaborate closely with others in the cell line development group.</li>
</ul>
Qualifications 
Qualifications
<ul>
<li>Bachelor’s Degree with 10 years of relevant experience, OR Master’s Degree with 8 years of relevant experience, OR PhD with no experience.</li>
<li>Proficiency with molecular biology techniques including complex molecular cloning; PCR, qPCR, ddPCR on DNA and RNA(RT); NGS (MiSeq and PromethION 2 preferred, both library prep and data analysis); gene editing technologies (CRISPR, ZFN, or other).</li>
<li>Hands-on experience using Illumina and Nanopore sequencers running DNA and RNA-seq workflows, from library prep, to instrument operation, to data analysis and data management.</li>
<li>Experience with NGS data analysis software, including genome browser (IGV) NGS data file formats, "FASTQC", Samtool, and other related tools to carry out basic NGS data analysis.</li>
<li>Familiarity with automated liquid handling work stations, such as Hamilton, Tecan, Biomek, or other. Familiarity with writing scripts to set up new automated workflows. Ability to troubleshoot software and hardware issues in collaboration with other specialists.</li>
<li>Deep understanding of cell and molecular biology concepts underpinning protein expression in CHO cells, including transfection and DNA integration; RNA transcription and its control; protein translation and its control; protein folding, glycosylation and secretion; mechanisms of genotypic instability in CHO cells.</li>
<li>Proficiency with sterile mammalian suspension cell culture; cell transfection; analytical flow cytometry.</li>
<li>Independently design experiments with proper controls, sample size and statistical analysis to reach sound conclusions. Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate strong data interpretation skills.</li>
<li>Excellent attention to detail and ability to keep detailed written records of protocols, raw materials, equipment, etc. in electronic lab notebook on a daily basis.</li>
<li>Proficiency with the following software: Microsoft Office, Geneious Prime, Spotfire, Sequencher, bioinformatics tools.</li>
<li>Proficiency in one or more programming/data science languages, such as R, Python, Java, C/C++ .&nbsp; Familiarity with Linux/Unix.</li>
<li>Ability to learn, understand, and execute new scientific techniques.</li>
<li>Ability to multi-task and work within timelines.</li>
<li>Ability to work collaboratively within and outside of group.</li>
<li>Strong communication skills – verbal, written, scientific data presentation.</li>
</ul>
Preferred:
<ul>
<li>Experience with synthetic biology screens</li>
<li>Familiarity with Chemistry, Manufacturing and Controls (CMC) and specifically CHO cell line development for GMP applications within biotech/pharma industry.&nbsp; Familiarity with relevant ICH guidelines.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

Senior Scientist I, Cell/Molecular Biology - Cell Line Development

<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 
This role is field-based, and candidates must live in one of the San Francisco bay area cities, Santa Rosa, Oakland or Sacramento.
This individual will be responsible for developing and maintaining strategic business relationships with Oncology departments and practices consisting of interactions with Oncologists, Hematologists, Pharmacists, Nurses, Executive level personnel, Department heads and Managers,&nbsp;and various other support staff. Business relationships will be focused on increasing education on product benefits/risks consistent with approved label, developing new business, improving resource utilization, and growing sales and market share by achieving sales plan for the assigned Oncology product and indications.
Key Responsibilities Include:
<ul>
<li>Uses opportunities to understand and address customer needs. Builds strong relationships that provide market intelligence and support development of compliant and innovative programs and initiatives. Builds and maintains relationships across accounts that result in opportunities to benefit patients, physicians, and other HCPs within the geography.</li>
<li>Consistently partners with in-house and/or cross-franchise leaders, and collaborates with such partners to identify, design and/or adapt appropriate approaches and tactics demonstrating resources within geography.</li>
<li>Delivers effective on-label technical and scientific presentations utilizing approved data,&nbsp; to appropriately highlight the benefits and risks of the product resulting in sales quota achievement.</li>
<li>Serve as lead US Commercial contact with targeted accounts in assigned geography and collaborate with all AbbVie and any co-promotion Counterparts including Brand and Strategic Marketing, GPO team, Thought Leader Liaisons, MSLs, and contracted SPPs to provide excellent customer support for physicians to the benefit of their patients. Such support should include site support and addressing any potential customer issues.</li>
<li>Build, implement, communicate, and regularly update strategic and tactical business plans for targeted accounts. In collaboration with sales leadership and other appropriate AbbVie or Co-Promote partners, facilitate site physician/treatment team training on approved and safe use of AbbVie’s products. Monitor and report sales progress. Provide routine communications to all internal and external (as applicable) partners.</li>
<li>Act as AbbVie key point of contact to each account. Respond to or direct customer to the appropriate service or point of contact for their questions or requests and actively follow-up. Take lead in coordinating and ensuring any needed or requested support is delivered in a timely manner and to the satisfaction of the account by the best person withing AbbVie or copromote partner.</li>
<li>Attend and actively participate in local societies, and other HCP&nbsp; meetings when appropriate. Represent AbbVie and assigned products at such venues, build/improve new/existing relationships. Channel key information, developments or findings to internal partners/stakeholders. All communications in these forums are on-label.</li>
<li>Remain current on all clinical, market, and payer developments, trends, and issues specific to oncology and disease areas.</li>
<li>Complete all AbbVie required training and maintain adherence to all company policies and OEC/Legal procedures.</li>
<li>Within assigned accounts and geography, seeks out important information and articulate implications to our business and to our customers’ business’.</li>
<li>Transfers knowledge to appropriate internal partners and integrate standard methodologies that have tangible value for customers and patients across assigned indications/brands to benefit the geography and AbbVie Oncology.</li>
<li>Establishes and maintains a complete understanding of approved product label and disease state knowledge for impactful use with customers.</li>
<li>Optimizes both external and internal data, resources, and tools to identify sales opportunities and program strategy for customers in assigned territories.</li>
<li>With the approval of legal/OEC, actively participates in relevant organizational programs in local markets.</li>
<li>Develops a strong command of available selling resources and tools; fully demonstrates those resources to support selling strategies and maximize impact.</li>
<li>An essential requirement of the position is to meet health care industry representative credentialing requirements to gain entry into facilities and organizations that are in assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.</li>
</ul>
Qualifications 
<ul>
<li>Business savvy: analytical ability to analyze diverse sets of data using multiple tools and define account/program strategies that drive business objectives.</li>
<li>Ability to demonstrate an understanding of how to effectively meet customer needs in a complex environment through forward-thinking, innovative strategies that align with the company and customer objectives.</li>
<li>Excellent communication and presentation skills</li>
<li>Persistency and grit with strong track record of succeeding in a challenging environment.</li>
<li>Travel: 40% travel, depending on residence location</li>
<li>Valid driver’s license: Ability to pass a pre-employment drug screening test and meet safe driving requirements</li>
</ul>
Preferred:
<ul>
<li>Oncology, Specialty, or other pharma experience</li>
<li>Bachelor’s degree</li>
<li>Account Management experience in any industry</li>
<li>Healthcare industry experience</li>
<li>MBA or other advanced degree</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>

Oncology Account Executive - San Francisco

<h3>Job Description</h3>
Job DescriptionWe are a well-established national litigation firm looking to expand our Litigation team across our California office locations. The team is looking to bring aboard a few attorneys with 2-8+ years of defense litigation experience in one or all practices: General Liability, Products Liability, and/or Toxic Tort/Asbestos/Silica Liability. These roles offer a collaborative culture, diverse casework, and the flexibility of a hybrid or fully remote work arrangement.BRIEF OVERVIEW
<ul>
<li>Manage an independent litigation caseload across general liability, product liability, toxic tort, or complex matters</li>
<li>Handle local and national accounts, including case strategy and direct client communication</li>
<li>Conduct and defend depositions (plaintiff, fact, and expert) and prepare witnesses for deposition or trial</li>
<li>Draft and respond to discovery, pleadings, and motions; analyze complex request.</li>
<li>Prepare court filings (including e-filing) and support all phases of trial preparation</li>
</ul>
QUALIFICATIONS
<ul>
<li>2-8+ years of Defense Litigation experience in one or all practices: General Liability, Products Liability, and/or Toxic Tort, Asbestos, Silica.</li>
<li>JD from an accredited law school &amp; admitted to practice in the state of CA</li>
<li>Handle discovery, motion practice, depositions, and trial preparation</li>
<li>Prepare pleadings, briefs, and discovery responses</li>
<li>Engage directly with clients and senior attorneys on complex matters</li>
</ul>
WHY JOIN?
<ul>
<li>Collaborative, collegial environment where associates work closely with senior attorneys and clients.</li>
<li>Competitive compensation and comprehensive benefits package (medical, dental, vision, life, disability, 401(k)).</li>
<li>Hybrid work structure with flexibility for remote work.</li>
<li>Exposure to sophisticated litigation and opportunities for professional growth.</li>
<li>Inclusive culture that values diversity and promotes professional development.</li>
</ul>

Litigation Associate Attorney

<h3>Job Description</h3>
IMMIX Biopharma, Inc.
 
Our 3 Core Values 
<ul>
<li>Intelligence</li>
<li>Integrity</li>
<li>Initiative</li>
</ul>
 
What You'll Do 
The Clinical GCP Quality lead will provide Quality oversight of clinical development programs to ensure compliance with ICH GCP and FDA regulatory requirements. The role will actively support clinical operations team, vendor oversight, clinical site readiness, and inspection preparedness for clinical trials.
 
Key Responsibilities
<ul>
<li>Provide QA oversight for CROs, clinical sites, and service providers to ensure compliance with GCP.</li>
<li>Actively support clinical vendor management initiatives, including qualification, monitoring, and performance management.</li>
<li>Coordinate clinical site readiness for inspections and sponsor audits.</li>
<li>Manage TMF readiness, conduct TMF audits, and oversee ongoing TMF periodic reviews.</li>
<li>Perform on-site and remote clinical site audits to evaluate investigator site compliance with protocols, GCP, and applicable regulations.</li>
<li>Review and provide QA input on clinical trial documentation (protocols, ICFs, monitoring plans).</li>
<li>Support inspection readiness activities, including mock inspections, CAPA tracking, and documentation control.</li>
<li>Support Supplier Quality Manager with establishment and maintenance of vendor quality agreements.</li>
<li>Provide GCP training to clinical operations and cross-functional teams.</li>
<li>Ability to support BIMO Inspections.</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor’s degree in Life Sciences, Nursing, or related field; advanced degree preferred.</li>
<li>5–7 years of Clinical Quality Assurance (CQA) experience in pharma/biotech.</li>
<li>In-depth knowledge of ICH E6 (R2/R3), FDA 21 CFR Part 312 guidelines.</li>
<li>Demonstrated experience in clinical site audits, TMF audits, and vendor oversight.</li>
<li>Strong interpersonal, communication, and influencing skills.</li>
<li>Willingness to travel (30–40%) for site/vendor audits.</li>
</ul>
 
About IMMIX Biopharma, Inc.
Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a global leader in relapsed/refractory AL Amyloidosis. AL Amyloidosis is a devastating disease where the immune system, that’s supposed to protect, instead produces toxic light chains, clogging up the heart, kidney and liver, causing organ failure and death. Our lead candidate is sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201 with a “digital filter” that is designed to filter out non-specific activation. NXC-201 teaches the immune system to recognize and eliminate the source of the toxic light chains. NXC-201 is being evaluated in the U.S. multi-center study for relapsed/refractory AL Amyloidosis NEXICART-2 (NCT06097832), with a registrational design. NXC-201 has been awarded Regenerative Medicine Advanced Therapy (RMAT) by the US FDA and Orphan Drug Designation (ODD) by FDA and in the EU by the EMA.

Associate Director / Sr.Manager - Clinical GCP Quality

<h3>Job Description</h3>
Job Description
Job Summary
X2nSat seeks a highly skilled and experienced Senior Network Architect to design, implement, and maintain our Layer 2/3 network. Our company is a service provider specializing in satellite and cellular technologies. You will be responsible for the overall network architecture, ensuring high availability, performance, and security across our infrastructure.
Responsibilities
<ul>
<li>Design and architect a scalable and robust Layer 2/3 network infrastructure, ensuring fault tolerance.</li>
<li>Develop network diagrams, documentation, and standard operating procedures (SOPs).</li>
<li>Implement and configure Cisco and Ubiquiti switches and routers.</li>
<li>Troubleshoot complex network issues and provide expert-level support.</li>
<li>Ensure network security and compliance with industry best practices.</li>
<li>Monitor network performance and optimize configurations for efficiency.</li>
<li>Plan and execute network upgrades and expansions.</li>
<li>Collaborate with other IT teams to integrate network services.</li>
<li>Lead the end-to-end lifecycle of network solutions, from conceptualization and planning to implementation and optimization.</li>
<li>Evaluate emerging technologies and make recommendations to support evolving business needs.</li>
<li>Perform capacity planning and network performance tuning for both core and edge systems.</li>
</ul>
Requirements
<ul>
<li>Valid CCNA and CCNP certifications are highly preferred.</li>
<li>Valid CCIE certification is a nice-to-have.</li>
<li>Extensive experience in designing and maintaining Layer 2/3 networks.</li>
<li>Proficiency in configuring and troubleshooting Cisco and Ubiquiti equipment.</li>
<li>Strong understanding of networking protocols (e.g., BGP, OSPF, MPLS).</li>
<li>Proven experience with network monitoring and management tools (e.g., OpManager, NetFlow, SNMP).</li>
<li>Knowledge of cloud networking (AWS, Azure, GCP, etc.) and hybrid-cloud connectivity.</li>
<li>Familiarity with automation tools and scripting (e.g., Python, Ansible) for network configuration and monitoring.</li>
<li>Experience with network security best practices and firewalls.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Strong communication and documentation skills.</li>
</ul>
Current Network Infrastructure
The current network infrastructure comprises approximately 100 switches and routers distributed across three locations. The technology deployed includes Cisco and Ubiquiti equipment.
Here is a summary of the current network status:
Attribute - Details
Total Devices - ~100 Switches/Routers
Equipment Vendors - Cisco, Ubiquiti
Locations - 3
Layer - Layer 2/3
Service Provided - Satellite and Cellular Technologies
Preferred Qualifications
<ul>
<li>Experience in a service provider environment.</li>
<li>Knowledge of satellite and cellular communication technologies.</li>
<li>Experience with network automation and scripting.</li>
</ul>
Company DescriptionX2nSat is leading the way into the future of satellite communications with the most reliable connections and data capacities anywhere in North America and beyond. Providing reliable, wireless network solutions for over 20 years, we are the satellite communications arm of your organization, committed to superior service. 
<h3>Company Description</h3>
X2nSat is leading the way into the future of satellite communications with the most reliable connections and data capacities anywhere in North America and beyond. Providing reliable, wireless network solutions for over 20 years, we are the satellite communications arm of your organization, committed to superior service.

Senior Network Architect

<h3>Job Description</h3>
Job Description
About Us
One Medical is a primary care solution challenging the industry status quo by making quality care more affordable, accessible and enjoyable. But this isn't your average doctor's office. We're on a mission to transform healthcare, which means improving the experience for everyone involved - from patients and providers to employers and health networks. Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years.
In February 2023 we marked a milestone when One Medical joined Amazon. Together, we look to deliver exceptional health care to more consumers, employers, care team members, and health networks to achieve better health outcomes. As we continue to grow and seek to impact more lives, we're building a diverse, driven and empathetic team, while working hard to cultivate an environment where everyone can thrive.
Employment type:
<ul>
<li>Full time</li>
</ul>
What you'll do:
<ul>
<li>Provide care for acute medical concerns as well as offering same-day and next-day access to patients with time-sensitive needs–without having your own patient panel</li>
<li>Work flexible hours, including evenings (after 5 p.m.) and weekends, as our clinics operate 7 days a week from 8 a.m. to 9 p.m. 365 days per year</li>
<li>Address a broad range of concerns such as chest pain, shortness of breath, abdominal pain, headaches, URIs, UTIs, STI testing/treatment, laceration repair, I&amp;Ds, wound care, musculoskeletal injuries, short-term medication refills, acute mental health triage, and time-sensitive post-hospital follow-ups; Successful applicants will be comfortable with initial management of acute changes in chronic conditions</li>
<li>Stay up to date on evidence-based urgent care practices and maintain working knowledge of common primary care issues (e.g., hypertension, diabetes, depression/anxiety)</li>
<li>Complete thorough documentation for all patient encounters including procedures</li>
</ul>
You'll be set up for success if you have:
<ul>
<li>The desire to be an integral part of a rapidly growing team of clinicians dedicated to changing healthcare delivery </li>
<li>An interest in using technology to deliver high quality, evidence-based care</li>
<li>Excellent clinical and communication skills </li>
<li>Practiced at least 2 of the last 5 years in an outpatient primary or urgent care setting seeing all ages (0+)</li>
<li>At least one year of experience caring for pediatric patients including newborns</li>
<li>The ability to work a flexible schedule including weekends and evenings</li>
<li>The ability to work at least 3 major holidays a year</li>
<li>The ability to work two full weekends per month (4 shifts)</li>
<li>The ability to work between the hours of 8am-9pm</li>
<li>State licensing in California, obtained by your One Medical start date</li>
</ul>
This is full-time role based in Mill Valley, CA.
One Medical is committed to fair and equitable compensation practices.
The base salary range for this role is $178,000 - $189,520 based on a full-time schedule. Final determination of starting pay may vary based on factors such as practice experience and patient care schedule. Additional pay may be determined for those candidates that exceed these specified qualifications and requirements. For more information, visit <a href="https://www.onemedical.com/careers/" target="_blank">https://www.onemedical.com/careers/</a>.
One Medical is an equal opportunity employer, and we encourage qualified applicants of every background, ability, and life experience to contact us about appropriate employment opportunities.
One Medical offers a robust benefits package designed to aid your health and wellness. All regular team members working 24+ hours per week and their dependents are eligible for benefits starting on the team member's date of hire:
Taking care of you today
<ul>
<li>Paid sabbatical for every five years of service</li>
<li>Free One Medical memberships for yourself, your friends and family</li>
<li>Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues</li>
<li>Competitive Medical, Dental and Vision plans</li>
<li>Pre-Tax commuter benefits</li>
<li>PTO cash outs - Option to cash out up to 40 accrued hours per year</li>
</ul>
Protecting your future for you and your family
<ul>
<li>401K match</li>
<li>Credit towards emergency childcare</li>
<li>Company paid maternity and paternity leave</li>
<li>Paid Life Insurance - One Medical pays 100% of the cost of Basic Life Insurance</li>
<li>Disability insurance - One Medical pays 100% of the cost of Short Term and Long Term Disability Insurance</li>
</ul>
In addition to the comprehensive benefits package outlined above, practicing clinicians also receive
<ul>
<li>Malpractice Insurance - Malpractice fees to insure your practice at One Medical is covered 100%.</li>
<li>UpToDate Subscription - An evidence-based clinical research tool</li>
<li>Continuing Medical Education (CME) - Receive an annual stipend for continuing medical education</li>
<li>Rounds - Providers end patient care one hour early each week to participate in this shared learning experience</li>
<li>Discounted rate to attend One Medical's Annual REAL primary care conference</li>
</ul>
One Medical is an equal opportunity employer, and we encourage qualified applicants of every background, ability, and life experience to contact us about appropriate employment opportunities. One Medical participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Please refer to the E-Verification Poster and Right to Work Poster for additional information.

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