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Job Description Location(s): Portland, OR Practice/Department: Emerging Regions Internal Title: As-Needed Biologist Work Environment: Field with up to 20% office work Compensation: $25-35/hourly * Dudek’s journey began in 1980 with a vision to serve Southern California’s water and wastewater agencies. Today, we are a 100% employee-owned firm supporting clients nationwide and delivering projects that improve and protect the built and natural environments of communities throughout the United States. Our work has been recognized by leading industry organizations, and we’ve been honored with multiple national Top Workplace Awards. Our employee-owners are unified by a singular commitment to supporting projects that address key societal issues, such as the transition to renewable energy, infrastructure hardening and repair, environmental protection, and community resilience. Learn more about our award-winning culture, the benefits and perks of being a Dudekian, and the projects you will have the opportunity to shape. Who You Are As an employee-owner, you embrace accountability, working safely, and collaboration while thinking resourcefully and independently. Like all Dudekians, you are curious and solution-oriented, with the ability to adapt quickly to changes and approach challenges with a spirit of innovation. How You’ll Make an Impact Dudek is seeking field biologists and botanists to provide as-needed field support for projects in Oregon and Washington. This position will provide biologists with 2-6+ years of of experience to support a variety of projects in the Pacific Northwest, including projects related to utility infrastructure upgrades and renewable energy generation and storage. Strong candidates will have extensive outdoor experience, particularly through agencies, volunteering, or graduate schoolwork. Candidates with strong writing skills and a desire to assist with reporting will be given the chance to do so. Duties and Responsibilities • Conduct site assessments, surveys, and habitat evaluations for common and special-status plant and wildlife species and map vegetation communities, • Conduct wetland delineations pursuant to federal and state requirements, • Record and take notes on a mobile device, • Follow all Dudek and project site safety protocols, • Hike long distances in potentially inclement weather, heat, and rough terrain, • Bachelor’s degree in biology, environmental science, or other related field; OR a minimum of 1-3 years demonstrated field experience in biological resource management and surveying, • Knowledge of and ability to identify Oregon and Washington wildlife and/or plant species, • 2-6+ years of experience in environmental field settings in Oregon and Washington, • Understanding of and familiarity with environmental regulations and permits, • Strong botanical knowledge including experience identifying common and rare plant species and/or using dichotomous keys to identify Pacific Northwest plants., • Experience executing species-specific survey protocols, e.g., marbled murrelet, western toad, northern spotted owl, northwestern pond turtle., • 4-wheel-drive experience Working Conditions: Environment • This job operates in a remote or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc., • Working on a computer, sitting, or standing for long periods of time in an office or remote office setting., • Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees)., • Attending meetings, both in person and virtually, and speaking on the phone with peers, clients, etc. Dudek is genuinely committed to equal employment opportunities within our company and on our project teams. Dudek is also committed to compliance with all applicable laws providing equal employment opportunities. This commitment applies to all persons involved in Dudek’s operations and prohibits unlawful discrimination by any employee of Dudek, including supervisors and coworkers. Equal employment opportunities will be extended to all persons (including those with disability and veteran status) in all aspects of the employment relationship, including recruitment, hiring, training, promotion, transfer, compensation, benefits, discipline, layoff, recall, and termination. Any employee who violates this policy and Dudek’s commitment to equal employment opportunities will be subject to disciplinary action. Dudek is a U.S.-based employer. All positions are based in the United States and require U.S. work authorization Powered by JazzHR HVGIh82rKT

Job DescriptionAbout use184 is a biotechnology research company advancing in vitro gametogenesis to transform reproductive medicine. We're developing integrated platforms that combine cellular reprogramming, machine learning-guided optimization, multi-omics analysis, and automated experimental workflows to enable gamete development for individuals facing reproductive challenges. We're assembling interdisciplinary teams across cell and molecular engineering, synthetic biology, epigenetic editing, bioinformatics and computational biology to tackle one of biology's most impactful problems - returning the fundamental right to procreate. Role overviewAs a Bioinformatics Scientist specializing in genomic foundation models, you will lead computational analysis of multi-modal genomics data (scRNA-seq, ATAC-seq) to identify transcription factor combinations driving desired cell state conversion. This role bridges classical gene regulatory network inference and modern foundation model approaches, requiring deep expertise in single-cell genomics analysis, transcriptional regulation biology, and demonstrated interest in applying transformer-based methods to cellular reprogramming problems. You will work on traditional multi-platform genomics analysis and on integrating and fine-tuning foundation models, collaborating closely with wet lab teams to translate computational predictions into experimental designs for our cell fate engineering platform.Primary responsibilities • Perform genomics analysis across scRNA-seq and ATAC-seq data from human, NHP, and mouse gametogenesis to identify transcription factors governing cell state trajectory, • Integrate classical and modern approaches by combining GRN inference methods with transformer-based models to create hybrid TF ranking systems, leveraging both motif-guided statistical learning and self-supervised deep learning representations, • Build version-controlled data platforms harmonizing gametogenesis datasets across multiple modalities and sequencing platforms, preparing integrated datasets for both traditional analysis and foundation model fine-tuning, • Develop trajectory inference workflows using RNA velocity, pseudotime analysis, and optimal transport models to map cellular transitions, identifying critical commitment points where TF interventions are most effective, • Apply chromatin accessibility analysis and TF motif enrichment to decode regulatory grammar at key transition junctions, identifying synergistic TF combinations and repressive factors required for cell fate conversion, • Collaborate with experimental teams on screen design and interpretation, translating computational predictions into biologically interpretable experimental plans specifying which TF combinations to test and validation strategies, • Establish automated feedback loops for ingestion of screening NGS data, implementing active learning strategies that prioritize informative experiments and building retraining pipelines that continuously improve prediction accuracy, • Build computational infrastructure for reproducible bioinformatics workflows and foundation model fine-tuningRequired qualifications, • PhD in Bioinformatics, Computational Biology, or related quantitative field (or MS with 5+ years relevant industry experience), • Multi-platform single-cell RNA-seq expertise: hands-on analysis of data from at least two different platforms, including platform-specific troubleshooting and quality control, • Multi-modal genomics proficiency: experience with ChIP-seq, CUT&RUN, or ATAC-seq analysis including peak calling, differential accessibility, and TF motif enrichment, • Computational TF identification background: applied computational methods (GRN inference, chromatin accessibility, perturbation screens, ML) to identify transcription factors for cell fate conversion beyond literature-curated lists, • Cellular reprogramming knowledge: prior research experience (computational or experimental) in cell fate conversion, direct reprogramming, transdifferentiation, iPSCs, or differentiation systems with deep understanding of transcriptional regulation, • Strong programming skills: Python and R with proficiency in Scanpy/Seurat, standard genomics toolkits, and statistical analysis for high-dimensional data, • Foundation model interest: familiarity with transformer architectures in genomics through coursework/self-study/application, OR strong demonstrated interest with clear learning approach, • Strong publication record and demonstrated cross-functional collaboration with experimental biologistsPreferred qualifications, • Experience fine-tuning or applying genomic foundation models with demonstrable results, or contributions to bioinformatics tools incorporating transformer architectures, • Prior computational research in cellular reprogramming; extensive experience with multiple GRN inference methods and perturbation response modeling, • Background in trajectory inference beyond basic pseudotime, GRN for biological networks, or Bayesian approaches to genomics, • GPU cluster experience for model training, multi-omics integration methods, and cross-species genomics analysisWhat we offer, • On-site work in the US Pacific Northwest in state-of-the-art facility, • Unique opportunity at early-stage biotech startup where you'll shape computational strategy from the beginning, build infrastructure from scratch, and have direct impact on our computational approaches for years to come, • Autonomy and ownership to design analysis frameworks, choose methodologies, and pioneer novel approaches without bureaucratic constraints, with competitive compensation including equity participation, • Mission-driven impact developing novel technologies for fertility medicine

Job Description Beeflow is looking for a strategic and driven Regional Manager to lead our growth across North America. This role is responsible for the region’s commercial success (P&L ownership), leading the US team and expanding into Canada, Mexico, and new crop opportunities. You’ll shape the business strategy, build client relationships, and drive sales while ensuring operational excellence. This role requires a strong agribusiness background, leadership skills, experience driving commercial growth, and established grower relationships—particularly in almonds and/or blueberries. This position reports to the CEO. This role may be based in Central Valley, CA, or in the PNW region. Key Responsibilities • Strategy & Growth – Develop and execute business plans, identify market opportunities, and expand Beeflow’s presence., • Sales & Business Development – Build client relationships, drive sales, and manage a strong pipeline., • Client Management – Ensure customer satisfaction by delivering high-quality pollination solutions., • Financial Oversight – Manage budgets, forecasts, and financial performance., • Team Leadership – Hire, train, and mentor a high-performing team., • Bachelor’s in Business, Agriculture, or related field (MBA preferred)., • 5+ years in commercial or business development roles in agribusiness., • Strong network in the almonds and/or blueberries industry., • Experience in startups or building operations from scratch., • Proven sales and business growth success., • Strong leadership, negotiation, and communication skills., • Market analysis and strategic planning expertise., • Fluent/Advanced Spanish., • Willingness to travel (up to 50%). Most importantly, you could be a good fit if you share our values: • Collaboration – We are one team: we respect each other, learn from our differences, and work together to find the best solutions., • Transparency – We communicate assertively, acting with openness and honesty., • Excellence – We focus on achieving exceptional results, exploring new ways to do things better. $130,000 - $150,000 base salary + up to 100% bonus Beeflow reserves the ability to adjust the compensation range based on the final candidate’s experience, skillset, and geography. In addition to on target earnings, we offer stock options as we believe that every employee should have a stake in the company’s growth. In addition, we offer: • Medical, Vision and Dental Insurance for the employee and their dependents., • 401k., • A generous PTO schedule: 15 working days of vacation + a week off between Christmas and New Year’s., • Family Leave: 4 weeks of paid leave for the pregnant and nonpregnant parent + Soft Landing options to return to work after the leave both for pregnant and nonpregnant person., • In-company Spanish lessons., • Learning & Development budget + 3 days off per year to attend conferences, industry events, courses, etc. About Beeflow Beeflow is a biotechnology company revolutionizing how farmers manage crop pollination. By combining deep expertise in plant science, bee biology, and proprietary technologies—including bee-training molecules and a plant-based diet that boosts colony strength—we deliver professional pollination services that increase yield potential and fruit quality. Our platform enables growers to better manage the critical bloom period through data-driven insights and more consistent bee activity, even under suboptimal conditions. Founded in 2016, Beeflow is headquartered in California with growing operations across the U.S. and Latin America. Backed by leading investors such as Ospraie Ag Sciences, Future Ventures, Vectr Ventures, Jeff Wilke, SOSV, and GridX, our global team of scientists, agronomists, beekeepers, and business professionals is committed to building the future of sustainable agriculture. For more information, please visit beeflow.com

Job DescriptionAbout use184 is a biotechnology research company advancing in vitro gametogenesis to transform reproductive medicine. We're developing integrated platforms that combine cellular reprogramming, machine learning-guided optimization, multi-omics analysis, and automated experimental workflows to enable gamete development for individuals facing reproductive challenges. We're assembling interdisciplinary teams across cell and molecular engineering, synthetic biology, epigenetic editing, bioinformatics and computational biology to tackle one of biology's most impactful problems - returning the fundamental right to procreate. Role overviewWe are seeking a Science Team Lead to drive our innovative research program developing advanced epigenetic editing technologies for therapeutic applications. This is a leadership position reporting directly to the Chief Scientific Officer (CSO). The successful candidate will guide scientific planning, supervise project execution, contribute to team building, and shape the long-term R&D roadmap.This is a hands-on role: in addition to team leadership and project management, the candidate will be directly involved in designing and conducting experiments, especially in early stages of the program.What you will do • Lead a focused research team of 4-6 scientists and report directly to the CSODesign and personally conduct experiments in DNA methylation editor optimization and validation, • Develop guide RNA libraries targeting chromatin regulatory regions, • Establish protocols for targeted methylation editing with persistence validation through cell divisions, • Create delivery strategies for enhanced efficiency in challenging cell types, • Execute single and multiplex editing approaches with maintained specificity across targets, • Drive progression from cell culture proof-of-concept to functional validation in mammalian models, • Define research approaches and priorities aligned with company objectives, • Drive scientific output, IP development, and milestone achievement within established timelinesRequired qualifications, • PhD in Molecular Biology, Epigenetics, Developmental Biology, or related field, • Minimum 5 years postdoctoral or industry experience in epigenetic editing, chromatin modification, or CRISPR-based technologies, • Proven expertise developing DNA methylation editors including fusion protein design and optimization, • Hands-on experience with guide RNA design and validation for chromatin targets, • Advanced skills in DNA methylation and chromatin modification analysis, • Knowledge of chromatin biology, gene regulation, and epigenetic inheritance mechanisms, • Experience with allele-specific epigenetic editing approaches, • Track record of integrating innovative experimental and computational approaches in epigenetic editing with publications in high-impact journals and experience in IP development, • Familiarity with mammalian reproduction models and developmental biology applicationsWhat we offer, • On-site work in the US Pacific Northwest in state-of-the-art facility, • Competitive compensation, equity participation, and comprehensive benefits, • Collaborative and supportive culture with mission-driven colleagues focused on breakthrough discoveries

Job Description Cramer Fish Sciences (CFS) is seeking an experienced SENIOR FISHERIES SCIENTIST to join our team in Portland, OR. The Senior Fisheries Scientist will lead and manage scientific studies on salmon ecology, fish habitat, fish-forestry interactions, and habitat restoration ensuring accurate data analysis and effective implementation of objectives, tasks, supervision of staff, and budgets. This position will contribute to developing innovative initiatives and large-scale projects that advance CFS's mission to deliver impactful, science-based solutions for fisheries, forestry, and natural resource management. INTERESTED IN APPLYING? Please submit your resume and cover letter in a single file on our website at ESSENTIAL RESPONSIBILITIES: • Provide specialized technical analysis and counsel directly to clients., • Lead and oversee all aspects of project work, including scoping, implementation, data analysis, and reporting., • Develop new project opportunities with existing and new funding sources (clients)., • Foster business development by maintaining and expanding client relationships to secure profitable projects staffed by CFS personnel., • Manage project budgets and communicate regularly with administrative staff and clients., • Oversee and review project tasks of scientists and specialists., • Supervise junior staff including biologists, foresters, and technicians., • Representing CFS at scientific conferences, delivering presentations to increase awareness of our mission and activities., • Master's degree in fisheries, biology, or a related science field required, PhD in a science-related discipline preferred., • At least 15 years of experience in designing, implementing, managing, completing and multiple applied studies related to Pacific salmon and steelhead and their freshwater or estuarine habitats post master's degree., • Extensive knowledge and expertise in fisheries science and/or aquatic restoration, steam and estuarine ecology with the versatility to manage a variety of relevant projects., • Experience collaborating with State, Federal, Tribal, and Industry partners., • Ability to write grants/proposals to obtain funding fisheries, habitat, or restoration projects., • Demonstrated ability to acquire and lead complex, dynamic fisheries projects., • Published co-author of peer-reviewed articles on fisheries or aquatic science issues., • Strong organizational, delegation, and communication skills, with a focus on transparency and accountability., • Ability to balance scientific expertise with management and business acumen to deliver practical, cutting-edge solutions., • Proven ability to mentor, manage and develop team members, leveraging individual strengths, experience working in a collaborative Employee Stock Ownership Plan (ESOP) culture is a plus., • Proficiency in Microsoft Office 365., • Proficiency in clear verbal, written, and electronic communication with internal and external stakeholders., • Ability to work on a computer for prolonged periods of time., • Ability to work in aquatic environment including working from a boat platform, swimming and wading in rivers and streams., • Ability to work effectively in inclement weather, including hot, cold, rainy, and fog conditions, including ability to drive in such conditions. Salary: $110,000 - $170,000 (depending on experience) Benefits: CFS is committed to supporting our employees with a competitive benefits package, including: • 100% employer-paid medical, dental, and vision coverage for our base employee-only plan and 80% employer-paid coverage for dependents (with additional plans options available), • FSA or HSA through medical plan options, • Company Provided basic life insurance and long-term disability coverage, • Paid time off (PTO) and company holidays, • Employee Assistant Program (EAP) access, • Gym/Wellness Reimbursement benefit ABOUT: The mission of Cramer Fish Sciences is to provide quality, expert science which supports wise policy decisions and advances the field of natural resource management. We help clients in the Pacific Northwest and California find innovative and practical solutions to challenges with fisheries, riparian, and aquatic ecology. Cramer Fish Sciences is an Affirmative Action/Equal Opportunity Employer. We welcome and consider all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. We are committed to fostering diversity, equity, and inclusion throughout our profession.

Job DescriptionAbout use184 is a biotechnology research company advancing in vitro gametogenesis to transform reproductive medicine. We're developing integrated platforms that combine cellular reprogramming, machine learning-guided optimization, multi-omics analysis, and automated experimental workflows to enable gamete development for individuals facing reproductive challenges. We're assembling interdisciplinary teams across cell and molecular engineering, synthetic biology, epigenetic editing, bioinformatics and computational biology to tackle one of biology's most impactful problems - returning the fundamental right to procreate. Role overviewWe are seeking an expert Bioinformatician to lead computational analysis for our cellular reprogramming research program. This position will support critical objectives in high-throughput screening analysis, single-cell multi-omics, and predictive modeling for transcription factor-mediated cell fate conversion, working directly with the experimental team to guide screening strategies. Primary responsibilities • Build and maintain version-controlled repositories harmonizing publicly available datasets (scRNA-seq, bulk RNA-seq, ChIP-seq, CUT&RUN, ATAC-seq), • Establish and manage AWS cloud computing infrastructure from scratch for large-scale data processing, • Analyze single-cell and single-nucleus RNA-seq/ATAC-seq data from raw reads through biological interpretation, • Process and analyze barcoded screening datasets from CRISPRa/i and other libraries for factor identification, • Perform trajectory inference, RNA velocity, and gene regulatory network analysis for cellular state transitions, • Contribute to developing predictive models for transcription factor combinations using multi-omics integration, • Create automated analysis pipelines and quality control frameworks for high-throughput experimentsBuild data visualization and reporting systems for cross-functional collaboration, • Analyze Perturb-seq and pooled screening data with barcode deconvolutionRequired qualifications, • PhD in Bioinformatics, Computational Biology, or other quantitative field with 3+ years relevant experience, • Demonstrated expertise analyzing scRNA-seq and scATAC-seq from raw reads (FASTQ to biological interpretation), • Proven experience building and maintaining version-controlled multi-dataset repositories, • Strong proficiency in R and Python with experience in single-cell analysis frameworks (Seurat, Scanpy), • Hands-on experience establishing AWS cloud computing environments from scratch, • Experience building automated analysis pipelines using workflow management systems (Nextflow, Snakemake), • Expertise with trajectory inference tools (Monocle, RNA velocity) and gene regulatory network analysis (SCENIC, CellOracle), • Experience with Perturb-seq analysis and pooled screening data deconvolution, • Familiarity with multiple scRNA-seq platforms beyond 10XPreferred qualifications, • Track record of novel computational method development, • Experience with chromatin accessibility analysis and transcription factor motif enrichment methods, • Background in predictive modeling for cellular reprogramming applicationsWhat we offer, • Competitive compensation, equity participation, and comprehensive benefits, • Collaborative and supportive culture with mission-driven colleagues working on high-impact cellular engineering challenges

Job Description Rebound is looking for a full-time Physical Therapist to join our team at our Cascade Park Physical Therapy clinic. Our Physical Therapists are responsible for rehabilitating people with physical disabilities and/or injuries. Patients include post surgical, accident victims and individuals with disabling conditions such as back pain, arthritis, heart disease, fractures, head injuries, and neurological conditions such as multiple sclerosis and post surgical patients. The ideal candidate may specialize in pediatrics, geriatrics, orthopedics, sports medicine, neurology, or cardiopulmonary physical therapy. The candidate will also possess excellent interpersonal skills, a superior commitment to patient care, and the ability to work closely with patients and physicians. New PT Graduates are encouraged to apply! Responsibilities: • Support an environment that reinforces Rebound’s mission and Core Values of Superior Service, Teamwork, Integrity, Innovation, Quality and Recognition., • Help to restore physical function, improve mobility, relieve pain, and prevent permanent disability. Assist in restoring, maintaining, and promoting overall fitness and health., • Examine patient medical histories. Test and measure patients’ strength, range of motion, balance and coordination, posture, muscle performance, respiration, and motor function., • Determine patients’ ability to be independent and reintegrate into the workplace or community after injury or illness., • Develop plans describing a treatment strategy, its purposes, and its anticipated outcome. Plan often includes exercise regimens at the clinic and at home to increase flexibility, strength, or endurance. May use electrical stimulation, hot packs, cold compresses, and ultrasound to relieve pain and reduce swelling., • Teach patients how to use assistive and adaptive devices such as crutches, prostheses, and wheelchairs., • Document patient progress, conduct periodic examinations, and modify treatments with emphasis on identification of areas requiring more/less attention., • May participate in supervising physical therapy students, assistants and aides., • Maintain a high degree of confidentiality and abide by all HIPAA rules and regulations., • Bachelor's degree in physical therapy from accredited program; successful completion of clinical internship. Master's or Doctorate degree in physical therapy preferred., • Current state physical therapist license., • Current BLS certificate., • Must have previous outpatient orthopedics experience, clinical internships considered., • Knowledge of basic science including biology, chemistry, and physics as well as biomechanics, neuroanatomy, and disease manifestations., • Knowledge of medical practice policies/procedures, regulations, safety/injection control, and quality assurance requirements., • Knowledge of examination techniques and therapeutic procedures., • Skill in appropriate evaluation and treatment of patients including hands-on procedures such as deep-tissue massage., • Skill in using physical therapy equipment by consistently using devices appropriately to improve patient health status. Skill in effectively maintaining equipment; successful completion of related, • competency testing., • Ability to effectively communicate interpersonally in order to educate patients about their physical therapy treatments., • Ability to demonstrate compassion and desire to help patients., • Medical/Vision/Rx, • Dental, • 401(K) Retirement Plan, including discretionary profit sharing, • Company paid Life Insurance/AD&D, • Voluntary Life insurance/AD&D, • Company paid short and long-term disability, • Flexible Spending and Health Saving Accounts, • Employee Assistance Program, • Paid Time Off accrued at up to 24 days in your first year based on FTE, • Continuing education and professional due reimbursement

Job Description OMIC USA, Inc. is an international Analytical Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients. MISSION OF THE ROLE: The Laboratory Assistant in the Chemistry Laboratory performs an essential role of our high quality testing services by supporting continuous sample flow through providing a reliable supply of clean labware, calibration and verification of laboratory support equipment as directed and proposing improvements in their area to achieve the Company’s mission and objectives. RESPONSIBILITIES: Other duties may be assigned. Laboratory Glassware • Performs accountabilities as Laboratory Assistant as per documented methods, Standard Operating Procedures (SOPs), or other laboratory procedures., • Wash and clean the glassware used in the laboratory and keep the work areas neat and clean to avoid cross contamination., • Ensure sufficient supply of reusable sample storage containers that are clean and ready for use., • Coordinate and provide labware cleaning and associated equipment training for Chemists and Laboratory Assistants as necessary., • Directly train Chemists and others in various glassware and labware cleaning techniques and associated equipment., • Direct work of Chemists and others supporting glassware and labware cleaning to ensure glassware and labware is available for use in a timely manner., • Perform internal calibration and verification of laboratory support equipment (pipette performance, temperature accuracy, etc.) as directed/scheduled by the Quality Assurance Unit (QAU), • Communicate non-conformities to QAU for course of action and/or data impact assessments., • Assist sample preparation supervisor with any activities in this area as needed and directed (such as but not limited to performing backup task for sample preparation including Brix dilution and/or grinding)., • Maintain, verify, and calibrate general laboratory equipment associated with daily work activities. Indicate when maintenance has been performed in logbooks as needed. Troubleshoot equipment problems and performs minor repairs; notify supervisor of issues that require external repair. This role has no supervisory responsibilities. SKILLS AND EXPERIENCE: EDUCATION High school diploma; or equivalent combination of education and experience. CERTIFICATES, LICENSES, REGISTRATIONS None SKILLS & EXPERIENCE • Improvement initiatives, • Learning initiatives, • Ability to handle multiple priorities and deadlines, • Problem-solving skills, • High Emotional Intelligence, • Good cultural awareness and communication with people who have diverse backgrounds, • Quality of Work, • Communication, • Adaptability, • Teamwork, • Time Management, • Knowledge and Skills, • Initiative Ability to read, analyze, and interpret technical procedures and governmental regulations. Ability to write Standard Operating Procedures and additional laboratory documentation. MATHEMATICAL SKILLS Ability to apply mathematical operations to tasks applicable to the position. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Page Break EDUCATION Bachelor's degree (B.S.) in Biology, Chemistry, or related science from a four-year college or university; or equivalent combination of education and experience. SKILLS & EXPERIENCE • Experience with food and agricultural sample preparation and troubleshooting, • Knowledge of other relevant technologies and markets, • Familiar with the laboratory business environment TRAINING REQUIREMENTS OJT in understanding company operating systems, including the maintenance and operation of equipment. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. The employee regularly lifts and/or moves items averaging 20 pounds, and occasionally up to 50 pounds. 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. WORK ENVIRONMENT Works in a laboratory using general laboratory equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Job Description Salary, Benefits and Hiring level: $95,488 – $128,689 starting, DOE; (promotion potential to GS-13 step 10, equivalent to $147,615 in 2025) . In addition, the Pacific Council offers generously competitive insurance and retirement benefits. Organizational Culture At the Pacific Council, we value respect, integrity, curiosity, and collaboration. Our team is mission-driven and supportive, combining analytical rigor with a genuine commitment to sustainable fisheries and fishing communities. We work together in a transparent, collegial environment that celebrates teamwork, innovation, and diverse perspectives. Summary The Pacific Fishery Management Council (Pacific Council) is one of eight regional councils established under the Magnuson–Stevens Fishery Conservation and Management Act. The Council manages fisheries in federal waters off Washington, Oregon, and California through transparent, science-based decision-making that sustains fish populations and the communities that depend on them. Our work covers groundfish, salmon, highly migratory species, and coastal pelagic species, and increasingly addresses issues such as climate change, offshore wind energy, and aquaculture. Council staff support this mission by conducting analyses, coordinating advisory bodies, and ensuring open, inclusive public processes in collaboration with stakeholders as well as state, tribal, and federal partners. Position Overview The Pacific Council is seeking a Fisheries Scientist (Staff Officer) with a Ph.D. or equivalent experience in fisheries science, marine biology, oceanography, ecology, or a related discipline. This position plays a central role in the development of scientific processes, the review of scientific analyses, and providing recommendations and insights for informing Council decisions. The successful candidate will apply strong analytical and problem-solving skills to complex fishery management issues, work collaboratively with diverse experts and stakeholders, and communicate scientific information clearly to policymakers and the public. Key Responsibilities • Lead or contribute to scientific analyses, reports, and discussion papers supporting Fishery Management Plans, plan amendments, and regulatory actions., • Conduct or review biological, oceanographic, and ecological analyses relevant to fisheries management decisions., • Integrate information from stock assessments, ecosystem models, and monitoring programs into management advice., • Foster evidence-based decision making via the development and application of peer review processes., • Coordinate with state, tribal, and federal scientists to ensure analytical rigor and consistency across disciplines., • Facilitate and coordinate the meetings and agendas of Council advisory bodies and scientific review panels., • Present complex scientific information clearly and objectively to decision-makers, advisory bodies, and the public. Desired Minimums • Ph.D. (or equivalent experience) in fisheries science, marine biology, oceanography, ecology, or a closely related field., • Demonstrated ability to design, conduct, or synthesize scientific analyses related to living marine resources., • Excellent writing and verbal communication skills, including the ability to convey complex concepts to non-technical audiences., • Strong organizational, analytical, and problem-solving skills., • Ability to work collaboratively with individuals from diverse scientific and technical backgrounds., • Familiarity with West Coast fisheries and the Council’s management process., • Experience contributing to peer review, stock assessments, or ecosystem-based management., • Experience leading or supporting multidisciplinary or interagency projects. Staff Officers operate at the intersection of science, policy, and public engagement. The position requires occasional travel throughout the West Coast (typically 4–8 days per trip) and occasional international travel. A primarily remote work arrangement is not available. Work Environment The work is primarily in an office environment. Frequent use of a keyboard and other computer hardware is required, often for lengthy periods of time. Use of other typical office equipment may also be required. Extended periods of continuous work beyond eight hours per day is often required. Lifting of light to moderately heavy boxes and equipment and unloading and loading boxes and equipment into and from vehicles, may be required. Hiring Requirements Employment will be contingent upon successful completion of a background check. Applications will be accepted until position is filled.

Job Description OMIC USA, Inc., Oregon Job Description Position Title: Quality Assurance Associate Department: Quality Assurance Unit Position Number: JD-023 Reports To: Quality Assurance Manager FLSA Status: Non-Exempt Prepared Date: Position Start or Revision of Current Duties OMIC USA, Inc. is an international Analytical Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients. MISSION OF THE ROLE: The Quality Assurance Associate position supports the Quality Assurance Manager in the tasks required to verify regulatory compliance of all operations associated with the laboratory (e.g. sample receipt, processing, analytical, reporting, sales and human resources, etc.) with accreditation standards. (e.g. ISO/IEC 17025:2017) and contributes to the on-going development of the laboratory’s quality management system. Based on experience, the Associate can take self-directed ownership for some QA tasks and contribute to quality management system continuous improvement. Serves as QA Manager’s backup as directed. RESPONSIBILITIES: Other duties may be assigned. • Perform in-depth Internal Audits, • Continuous improvement, and implementation of systems for compliance, • Proactive document control to ensure all documents are within the system, • Proficiency Testing; scheduling, reporting & follow up, • Supplier qualification, and traceability, • Perform internal audits of the quality management system to ensure compliance to the appropriate standards and accreditation programs and identify areas of non-conformance and/or areas for improvement., • Perform procedural audits of methods conducted in the laboratory against the appropriate SOPs and LABs to ensure accuracy of procedural documentation and adherence to laboratory procedures in the areas of analytical technique, QC and quality system compliance, including:, • reference material/solution tracking, reagents & solutions tracking, equip verification logs, instrument logbooks, training records, document control, and data package compliance., • Report audit details (observations, findings, non-compliances and non-conformances) to the Quality Assurance Manager and assist with resolution as applicable., • Supports the Quality Assurance Manager and assists in external audit activities as needed, including implementation of corrective action and improvements the Laboratory receives, as they relate to the quality management system., • Promote QAU information and QA training to laboratory staff, in meetings and as needed., • Periodically reconcile database records of Suppliers of externally provided products and services to the laboratory, to ensure qualification records are kept up to date; maintain supporting documentation and traceability in LIMS., • Records new laboratory equipment information in LIMS for unique identification and tracking purposes. Work with laboratory staff to ensure routine maintenance documentation is in place before use., • Coordinate and oversee internal & external calibration and verification of laboratory support equipment (pipette performance, temperature accuracy, etc.) The actual calibration/verification tasks may be performed by this position or other assigned laboratory personnel, • Coordinate external calibration and/or repair of equipment as needed. Communicate non-conformities to Quality Assurance Manager for course of action and/or data impact assessments., • Maintain documentation of support equipment calibration both internal and external (hard copy, electronic and data base)., • Ensure training of new lab personnel on operation and best practices for pipette use and handling, when applicable., • The actual training tasks may be performed by this position or other assigned laboratory personnel, however this position is responsible for being a back-up trainer., • Assists the Quality Assurance Manager and laboratory staff by reviewing new or revised documentation for overall conformity with our internal policies and procedures as well as regulatory compliance, when applicable, prior to inclusion in the Document Control systems., • Ensure that routine maintenance/consumable replacement for residue water purification systems and on-site technician visits are scheduled as needed. Audit electronic water quality/use logs and records to ensure they are being maintained as needed. Ensure new personnel are trained in operation and best practices; serve as back-up trainer., • Periodically reconcile database records of reference materials and solutions to ensure that records are complete and accurate; maintain documentation of notification for corrections to be made by Chemists and traceability of completion. Ensure disposal of expired solutions (and neat as applicable). Periodically check physical neat standards and stock solutions for compliance (correct labeling, assigned physical locations, etc.) and maintain records of non-compliance. This role has no supervisory responsibilities. SKILLS AND EXPERIENCE: EDUCATION Bachelor's degree (B.S.) in Chemistry, Biology or related science from a four-year college or university and two years relevant QA experience working in a regulated laboratory; or equivalent combination of education and experience. CERTIFICATES, LICENSES, REGISTRATIONS None SKILLS & EXPERIENCE • Working knowledge of common laboratory equipment types, test methods, and regulations/ standards (preferably ISO 17025 or similar), • Improvement initiatives, • Learning initiatives, • Ability to handle multiple priorities and deadlines, • Analytical and problem-solving skills, • High emotional Intelligence, • Good cultural awareness and communication with people who have diverse backgrounds, • Experienced user of MS Office and Adobe Acrobat PERFORMANCE FACTORS Page Break • Quality of Work, • Communication, • Adaptability, • Teamwork, • Time Management, • Knowledge and Skills, • Initiative, • Dependability Page Break LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write Standard Operating Procedures, analytical methods, reports, business correspondences, and additional laboratory documentation. Ability to perform standard quality assurance / quality control evaluation procedures, including audits. Technical writing for preparing manuals and documentation. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, and quadratic equations. Ability to apply mathematical operations to tasks such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. SKILLS & EXPERIENCE • Familiar with the laboratory business environment TRAINING REQUIREMENTS OJT in understanding company operating systems, including the maintenance and operation of extraction and analytical equipment, and passing the Initial Demonstration of Capability (IDOC) for existing SOPs. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. 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. WORK ENVIRONMENT Works in a laboratory using analytical equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Management reserves the right to add, modify, change, or remove work assignments. This job description is designed to outline primary duties, qualifications, and job scope, but not limit the employee nor the company to just the work identified. It is OMIC USA Inc.’s expectation that each employee will offer their services wherever and whenever necessary to ensure the success of the Company and that each employee is adhering to the Company’s policy set up in the Company’s Employee Handbook.

Job DescriptionSalary: Title: Restoration Engineer Location: Portland Oregon Job Type: Regular Full-time Whats the Opportunity? Anchor QEA is seeking a full-time senior-level engineer and project manager to support Anchor QEA in the delivery of innovative projects across the Pacific Northwest and nationwide, including marsh and estuary restoration, coastal restoration, riverine and stream restoration, compensatory mitigation, fish passage, living shorelines and engineering with nature and nature-based solutions. The applicant will have 8 or more years of experience providing restoration-related field assessments, data collection and analysis, hydraulic and hydrologic modeling, geomorphic and habitat assessment support, fish passage and restoration design, and construction and project management. We are committed to investing in the right person and to providing support to foster your professional success and long-term impact. Responsibilities: As a senior engineer and project manager, youll lead restoration projects from concept to construction, collaborating closely with clients, partners, and interdisciplinary teams. Your work will include: • Leading hydrologic, hydraulic, and geomorphic analyses to support estuarine, river, stream, coastal, and/or floodplain restoration., • Designing fish passage solutions, engineered log jams, channel realignments, habitat and floodplain enhancement projects., • Preparing detailed design plans, specifications, cost estimates, and construction documents., • Managing project teams, budgets, scopes, and schedules for complex, multi-stakeholder projects., • Assisting with the development of competitive proposals., • Providing field oversight during construction, including adaptive design and troubleshooting., • Mentoring junior engineers and contributing to technical review and quality assurance., • Engaging directly with tribes, state and federal agencies, conservation districts, and non-profits to deliver high-impact restoration outcomes. What Are We Looking For? Were seeking a collaborative, solutions-oriented engineer whos ready to step into a leadership role. The ideal candidate will have: • B.S. or M.S. degree in civil, hydraulic, water resources engineering, or related discipline., • 8 or more years experience in river, stream, floodplain, or fish passage restoration design with a minimum of 3 years of project management experience., • Professional Engineer (PE) license in Washington or Oregon (or ability to obtain within one year)., • Proven ability to lead projects, including client engagement, scope and task management, budget oversight, and schedule coordination, • Proven skills in hydraulic, hydrologic and sediment transport modeling of riverine or coastal systems (e.g., HEC-RAS 1D/2D, SRH-2D) and geomorphic assessments., • Proficiency in AutoCAD Civil 3D, ArcGIS, and related design tools., • Experience with construction observation, field data collection, and field engineering., • Willingness to travel seasonally for field work and construction projects for up to 2 weeks at a time., • Strong communication skills and the ability to work across disciplines and with diverse stakeholders. Bonus experience includes: • Experience with large wood design, sediment transport analysis, or drone-based field surveying., • Familiarity with Pacific Northwest fisheries biology and environmental regulatory frameworks., • Experience supporting proposal development and business growth initiatives. What Can You Expect? A collaborative work environment where we encourage everyone to bring their authentic self. We offer competitive compensation and benefits which are detailed below. Who Are We? Anchor QEA provides environmental planning, science, and engineering consulting services with the mission of transforming our environment and communities with integrity and vibe. With more than 500 people in offices across the United States, our collective vision is to be an inclusive, sustainable, and growing environmental innovator making generational impacts. By embodying our core values, we strive to be our clients first choice for solving their most challenging problems and to be our employees reason to be excited about going to work each morning. Learn more about Anchor QEA at . How to Apply? Apply online through Anchor QEAs Open Positions page at . Veterans are encouraged to apply. Applicants with a disability, who require a reasonable accommodation for any part of the application or hiring process, may e-mail their request to Additional Information We work hard to embrace diversity and inclusion. As an equal opportunity employer, Anchor QEA is committed to a diverse, multi-cultural work environment. Anchor QEA does not discriminate in employment based on age, race, creed, gender, religion, marital status, veterans status, national origin, disability or sexual orientation. Employment is contingent upon satisfactory results of a comprehensive background check. Salary and Other Compensation: • Annual Bonus, • Other potential bonus types: Billable Time Bonus, Spot Bonus, Milestone Anniversary Bonus, Receiving Professional License/Certification Bonus, Peer-reviewed Publication Bonus, Employee Referral Bonus. Base Level Benefits for Regular Full-Time Positions: • Healthcare: Medical, dental, vision, basic life and AD&D insurance, short- and long-term disability programs., • Paid Company and Floating Holidays: 7 paid company and 2 floating holidays annually, • Vacation: 2 weeks accrued paid vacation based on length of service. Vacation may vary by level., • Sick and Safe Time: 80 hours annually, • Retirement Plan: 401k plan with an employer match Further information on benefits:

Job Description Job Title: Medical Laboratory Technician - Inpatient Lab SHIFT: The schedule includes 1st shift hours from 6am-2:30pm or 7am-3:30pm with rotating weekends MUST HAVE • Associate degree in Biology, Chemistry, Clinical Laboratory Science, or Medical Technology., • ASCP or AMT certification as a Medical Lab Technician., • Experience in clinical laboratory testing., • Proficiency in laboratory information systems., • Attention to detail and strong communication skills., • Experience in Chemistry Hospital Lab/Clinical Chemistry., • Experience in hematology, clinical chemistry, coagulation, urinalysis, or microscopy., • Ability to operate and maintain laboratory instruments. We are seeking a dedicated Medical Laboratory Technician to join our fast-paced inpatient lab team. The role involves determining the acceptability of specimens for testing, performing both routine and complex technical procedures, and ensuring the proper functionality of laboratory instrumentation. You will contribute to quality patient care by delivering accurate and timely test results. Responsibilities • Determine the acceptability of specimens for testing according to established criteria., • Perform routine and complex technical procedures according to departmental SOPs., • Monitor, operate, and troubleshoot laboratory instrumentation., • Make technical decisions regarding testing and problem-solving., • Prepare, test, and evaluate new reagents or controls., • Report accurate and timely test results., • Perform and document preventive maintenance and quality control procedures., • Maintain and replenish testing bench supplies as necessary., • Assist with the processing of specimens when needed. The position is located at a large hospital lab, serving as the central lab for all inpatient samples. It is a fast-paced, high-throughput environment with a variety of samples and tests conducted. The schedule includes 1st shift hours from 6am-2:30pm or 7am-3:30pm with rotating weekends. The contract duration is initially set for 3 months, with the potential for extension. The role offers a strong team environment and opportunities for growth and movement into different departments. #LI-SC1 Job Type & Location This is a Contract position based out of Portland, OR. Pay and Benefits The pay range for this position is $25.00 - $30.15/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Portland,OR. Application Deadline This position is anticipated to close on Jan 9, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Our client is an analytical laboratory dedicated to global food health and safety. They support their clients through comprehensive analytical testing services and a robust commitment to quality and accreditation standards. MISSION OF THE ROLE The Quality Assurance Associate supports the Quality Assurance Manager by ensuring regulatory compliance across all laboratory operations—including sample receipt, processing, analysis, reporting, sales, and human resources—under accreditation standards such as ISO/IEC 17025:2017. This role also contributes to the development and continuous improvement of the Quality Management System (QMS) and may assume ownership of certain QA tasks depending on experience. Serves as the backup to the QA Manager as assigned. KEY RESPONSIBILITIES Quality Management System Support • Assist in maintaining and improving the Quality Management System (QMS), • Contribute to:, • Internal audits, • Continuous improvement initiatives, • Document control, • Proficiency testing (scheduling, reporting, follow-up), • Conduct in-depth internal audits to ensure compliance with standards and accreditation requirements, • Perform procedural audits to verify method accuracy and adherence to SOPs and laboratory procedures, including:, • Reference materials and solutions tracking, • Reagents and solutions, • Equipment verification logs and instrument logbooks, • Training records, • Document control, • Data package compliance, • Assist the QA Manager in preparing for and participating in external audits, • Promote QA information to staff during meetings and training sessions, • Train new personnel in proper pipette handling and best practices (or serve as backup trainer), • Reconcile supplier qualification records and maintain documentation within LIMS, • Record and track new laboratory equipment in LIMS, • Coordinate internal and external calibration/verification of laboratory support equipment, • Review new or revised documentation for compliance with internal policies and regulatory standards prior to Document Control inclusion, • Support maintenance of quality records across all formats (hard copy, electronic, database), • Reconcile database records for reference materials and solutions, • Maintain documentation for corrective actions Other duties may be assigned in all areas JOB REQUIREMENTS Education • Bachelor’s degree (BS) in Chemistry, Biology, or related science, plus two years of relevant QA experience in a regulated laboratory;, • Working knowledge of laboratory equipment, analytical methods, and standards (preferably ISO 17025 or similar), • Ability to manage multiple priorities and deadlines, • Strong analytical and problem-solving skills, • High emotional intelligence; ability to work effectively with diverse teams, • Proficiency with Microsoft Office and Adobe Acrobat, • Ability to interpret technical procedures, manuals, and regulations, • Strong technical writing skills for SOPs, analytical methods, reports, and other documentation, • Ability to apply advanced mathematical concepts (exponents, logarithms, quadratic equations), • Experience with statistical and analytical methods such as:, • Frequency distribution, • Reliability and validity assessments, • ANOVA, • Correlation techniques, • Sampling theory, • Ability to define problems, collect data, and form valid conclusions, • Experience in a laboratory business environment, • On-the-job training in company operating systems, • Training in the use of extraction and analytical equipment, • Ability to hear instructions clearly, • Ability to perform repetitive hand and wrist movements, • Work performed in a laboratory setting with exposure to analytical equipment and potentially hazardous chemicals, • Reasonable accommodations may be made for individuals with disabilities JOB BENEFITS Medical/vision insurance (company covers 100% of EE premium and 90% of dependent and HSA- company covers 100% of premium and contributes to HSA every month), dental insurance, LTD, FSA, supplemental insurance, LegalShield/IDShield, 401(k), PTO, 13 paid holidays, and partnership with Adidas and Columbia employee store Company DescriptionReal People. Real Connections. Real Results. That's the Messina Talent Advantage. For more than 40 years, Messina's Talent practice has continuously evolved to meet the needs of our clients. We not only help our clients fill roles and build their teams, but we also help them better understand their workforce and develop strategic talent initiatives that drive value for their organizations. Messina Talent Advisors, a Messina Group Company, has the network, proven processes, and all the latest technologies to connect the right candidates with the right jobs - faster.Real People. Real Connections. Real Results.\r\n\r\nThat's the Messina Talent Advantage.\r\n\r\nFor more than 40 years, Messina's Talent practice has continuously evolved to meet the needs of our clients. We not only help our clients fill roles and build their teams, but we also help them better understand their workforce and develop strategic talent initiatives that drive value for their organizations.\r\n\r\nMessina Talent Advisors, a Messina Group Company, has the network, proven processes, and all the latest technologies to connect the right candidates with the right jobs - faster.

Job DescriptionAbout use184 is a biotechnology research company advancing in vitro gametogenesis to transform reproductive medicine. We're developing integrated platforms that combine cellular reprogramming, machine learning-guided optimization, multi-omics analysis, and automated experimental workflows to enable gamete development for individuals facing reproductive challenges. We're assembling interdisciplinary teams across cell and molecular engineering, synthetic biology, epigenetic editing, bioinformatics and computational biology to tackle one of biology's most impactful problems - returning the fundamental right to procreate. Role overviewMost research associate positions involve executing protocols someone else designed, in systems someone else built, following SOPs someone else wrote. This role is not that. You'll work directly alongside our CSO/co-founder and Science Team Leads helping build something from scratch. You'll have input on procurement decisions, equipment choices, lab layout, and operational systems. When we design our new facility, you'll be part of those conversations. You'll see how a biotech startup actually works - the business development, the strategic decisions about what experiments to prioritize and why. This exposure is nearly impossible to get in academic labs or established companies. You'll wear multiple hats and develop a broad skill set. One day you're troubleshooting iPSC culture protocols, the next you're evaluating vendors for cell culture reagents, and the following week you're helping write SOPs for our quality management system. This breadth accelerates your professional development in ways that narrowly-focused positions cannot. You'll contribute to cutting-edge science in stem cell biology, working on technologies that could fundamentally change reproductive medicine. Your work will directly enable experiments that move us toward clinical applications. This isn't a 9-to-5 job. It's startup life - sometimes chaotic, always demanding, occasionally uncertain. But if you're at a stage in your career where learning and growth matter, this is a rare opportunity.Primary responsibilities - Cell culture operations (50-60% of your time) • Perform primary cell derivations and maintain mammalian cell cultures, • Conduct iPSC reprogramming, culture, characterization, and banking, • Develop and validate reporter cell lines using knock-in techniques, • Maintain detailed experimental records and documentation, • Troubleshoot culture conditions and optimize protocols, • Weekend cell culture maintenanceLab Operations & Management (40-50% of your time), • Assist with vendor evaluation and procurement of lab supplies and equipment, • Help establish and document standard operating procedures, • Maintain lab organization, inventory management, and quality standards, • Contribute to lab setup and design decisions for our upcoming facility expansion, • Support regulatory compliance and documentation requirements, • What this actually looks like day-to-day: Expect extended periods of hands-on lab work. Cell culture doesn't accommodate a traditional schedule - cells need attention when they need it, including weekends. You'll need to be adaptable when priorities shift (they will), detail-oriented when documenting experiments (always), and comfortable working independently while also communicating proactively about challenges and progress.Required qualifications, • Bachelor's degree in Biology, Biotechnology, Cell or Molecular Biology, or related field, • 2-3 years of research experience (academic or industry), • Hands-on laboratory experience with mammalian cell culture, • Strong organizational skills and attention to detail, • Ability to work independently with minimal supervision, • Comfortable with weekend responsibilities for cell culture maintenance, • Physical ability to handle extended periods of laboratory work, • Genuine excitement about startup environment and mission-driven sciencePreferred qualifications, • iPSC culture and characterization experience, • Molecular biology techniques (DNA/RNA extraction, PCR, qPCR, libraries preparation), • CRISPR/Cas9 experience (or strong desire to learn), • Previous startup or fast-paced environment experienceWho we´re looking for, • You're someone who gets energized by building things, not just maintaining them, • You're comfortable with ambiguity and can make good decisions without perfect information, • You ask questions, suggest improvements, and take ownership of problems, • You're self-aware about what you don't know and proactive about learning, • You value being part of something meaningful, • You're at a career stage where growth opportunities matter the mostWhat we offer, • Competitive compensation, equity participation, and comprehensive benefits, • Direct mentorship from CSO and Science Team Leads, • Early employee status and ability to grow with the company, • Broad exposure across scientific, operational, and business functions, • Real input on decisions that shape the company, • Experience building a biotech company from the ground up - invaluable if you have entrepreneurial interests, • More autonomy, more diverse responsibilities, and more direct impact than you'd have almost anywhere else at this career stage

Please no C2C or Sponsorship Staff Regulatory Engineer: The Staff Regulatory Engineer is responsible for ensuring safety, performance, and regulatory requirements applicable to ensure our products are met for global markets. This position plans, schedules, and leads the regulatory aspects of project assignments requiring independent judgement and a deep technical understanding of the applicable regulatory requirements. The incumbent is also responsible for providing deep technical regulatory support and guidance on product software, cybersecurity, and wireless compliance topics throughout the company. We value diversity in the workplace and encourage women, minorities, and veterans to apply. Thank you! Type: direct hire Location: Hybrid Job Duties And Responsibilities: • Provides deep technical interpretation, guidance, and training on regulatory requirements to various areas including executive leadership, management, and cross-functional teams regarding design, development, evaluation, or marketing of products to ensure regulatory requirements are met., • Independently identifies regulatory requirements, develops regulatory strategy, and executes regulatory deliverables to meet project objectives and timelines; partners with Engineering for in-house and/or external testing, when necessary; and maintains documentation., • Researches and analyzes state of the art regulatory requirements. Integrates learning through strong collaboration into our product technology design and standard processes to ensure ongoing compliance in this dynamic arena., • Supports the design engineering teams to ensure robust and consistent application of regulatory requirements in new designs., • Creates deep technical regulatory deliverables to demonstrate product meets applicable regulatory requirements throughout the product lifecycle., • Leads regulatory & risk management evaluations on new and existing products to identify risks and review product changes for compliance to regulatory requirements., • Manages risk analyses for products and documents the results in a risk management file., • Prepares regulatory submissions as appropriate for approval of new or modified products. Ensures submissions are prepared and submitted accurately, completely and in a timely manner to meet business objectives, consulting with regulatory agencies as appropriate for clarification., • Supports product approvals by providing requested documentation, resolving open issues, and answering questions, in addition to resolving compliance issues with products in the field., • Contributes to the accomplishment of the Regulatory team objectives through effective communication and teamwork, and by providing advanced technical assistance as needed., • Remains aware and informed on the global regulatory changes and updates via industry affiliations and third-party collaboration as it relates to software and cybersecurity regulatory compliance (FDA, EU, global). Works with respective teams to ensure we remain compliant to upcoming regulations and executes plans/changes towards compliance., • Creates, reviews, and/or approves procedures related to regulatory compliance., • Mentors and trains junior regulatory professionals and provides work direction on projects of large scale with significant business impact., • In depth knowledge of applicable regulations and requirements (e.g. ISO 13485, global medical device requirements, IEC 60601-1, ISO 14971, ISO 10993, ISO 17664, ISO 62366, and relevant global guidance)., • Strong interpersonal skills to build strong rapport with internal and external customers (e.g. cross-functional project team members and leaders, regulatory agencies)., • Deep technical understanding of the purpose, requirements, and trends of regulations for medical device regulatory compliance, with the ability to read, analyze, and interpret common scientific and technical journals and legal documents, and train others regarding regulatory requirements., • Demonstrates intermediate project management skills and experience with the ability to manage regulatory projects effectively., • Demonstrates the ability to represent the department and to direct the work of engineers and designers and to provide consulting advice to designers and engineers., • Demonstrates ability to work independently with minimal supervision and in a team environment., • Demonstrates ability to communicate effectively in oral, written, and illustration form., • Previous experience in the medical device industry., • Regulatory Affairs Professional Certification (RAC)

Remote contract for PhDs in Biology, Biotechnology, Biochemistry, or related fields. Work on cutting-edge projects with top AI labs while earning up to $50+/hour, fully remote, with flexible weekly hours. No AI experience required. Role Overview: Help fine-tune large language models (like ChatGPT) using your biology knowledge. You’ll design problems, check how well AI solves them, and work with researchers to build better benchmarks. Responsibilities: • Design advanced biology questions to test AI performance., • Develop clear, step-by-step solutions with rigorous logic., • Evaluate AI outputs for accuracy and quality of reasoning., • Collaborate with researchers to refine benchmarks across undergraduate to PhD-level biology topics. Requirements: • PhD (pursuing or completed) in Biology, Biotechnology, Biochemistry, or a related field., • Strong biology reasoning and problem-solving skills across advanced domains., • Ability to communicate complex ideas clearly in writing and provide structured feedback., • No AI experience required Perks: • Fully remote, flexible work., • Work on cutting-edge AI projects with leading LLM companies. Offer Details: • Pay rate: $50+/hour (depends on role and candidate expertise)., • Assessment: Shortlisted experts complete an evaluation before selection., • Assignments: Contract roles with defined start/end dates; up to 40 hrs/week. About Turing: Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L. After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile. Know amazing talent? Refer them at ___, and earn money from your network.

Remote contract for PhDs in Biology, Biotechnology, Biochemistry, or related fields. Work on cutting-edge projects with top AI labs while earning up to $50+/hour, fully remote, with flexible weekly hours. No AI experience required. Role Overview: Help fine-tune large language models (like ChatGPT) using your biology knowledge. You’ll design problems, check how well AI solves them, and work with researchers to build better benchmarks. Responsibilities: • Design advanced biology questions to test AI performance., • Develop clear, step-by-step solutions with rigorous logic., • Evaluate AI outputs for accuracy and quality of reasoning., • Collaborate with researchers to refine benchmarks across undergraduate to PhD-level biology topics. Requirements: • PhD (pursuing or completed) in Biology, Biotechnology, Biochemistry, or a related field., • Strong biology reasoning and problem-solving skills across advanced domains., • Ability to communicate complex ideas clearly in writing and provide structured feedback., • No AI experience required Perks: • Fully remote, flexible work., • Work on cutting-edge AI projects with leading LLM companies. Offer Details: • Pay rate: $50+/hour (depends on role and candidate expertise)., • Assessment: Shortlisted experts complete an evaluation before selection., • Assignments: Contract roles with defined start/end dates; up to 40 hrs/week. About Turing: Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L. After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile. Know amazing talent? Refer them at ___, and earn money from your network.

Remote contract for PhDs in Biology, Biotechnology, Biochemistry, or related fields. Work on cutting-edge projects with top AI labs while earning up to $50+/hour, fully remote, with flexible weekly hours. No AI experience required. Role Overview: Help fine-tune large language models (like ChatGPT) using your biology knowledge. You’ll design problems, check how well AI solves them, and work with researchers to build better benchmarks. Responsibilities: • Design advanced biology questions to test AI performance., • Develop clear, step-by-step solutions with rigorous logic., • Evaluate AI outputs for accuracy and quality of reasoning., • Collaborate with researchers to refine benchmarks across undergraduate to PhD-level biology topics. Requirements: • PhD (pursuing or completed) in Biology, Biotechnology, Biochemistry, or a related field., • Strong biology reasoning and problem-solving skills across advanced domains., • Ability to communicate complex ideas clearly in writing and provide structured feedback., • No AI experience required Perks: • Fully remote, flexible work., • Work on cutting-edge AI projects with leading LLM companies. Offer Details: • Pay rate: $50+/hour (depends on role and candidate expertise)., • Assessment: Shortlisted experts complete an evaluation before selection., • Assignments: Contract roles with defined start/end dates; up to 40 hrs/week. About Turing: Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L. After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile. Know amazing talent? Refer them at ___, and earn money from your network.

Job DescriptionSalary: Title: Senior Biologist / Project Manager Location: Portland, OR Job Type: Regular Full-time Whats the Opportunity? Anchor QEA is seeking an experienced Senior Biologist / Project Manager to lead and deliver high-impact ecological and restoration projects across the Pacific Northwest, with a strong focus on Washington State and Puget Sound ecosystems. The successful candidate will leverage their established relationships with municipalities, state and federal agencies, tribal members, non-governmental entities and funding bodies to position Anchor QEA and our clients for success on competitive projects, including those supported by Floodplains by Design and Salmon Recovery Fund grants. Anchor QEA delivers innovative projects across Washington and nationwide, including marsh and estuary restoration, riverine and stream restoration, compensatory mitigation, fish passage, living shorelines and engineering with nature and nature-based solutions. The ideal candidate will bring more than 10 years of experience in both desktop and field habitat assessment, habitat restoration design, and project delivery. Youll lead multidisciplinary teams, mentor staff, build strong client relationships, and develop innovative solutions for restoration, regulatory, and habitat enhancement challenges. We are committed to investing in the right person and to providing support to foster your professional success and long-term impact. Responsibilities: • Lead complex biological and ecological studies in freshwater, estuarine, marine, and riparian environments including habitat assessments, species surveys, and biological evaluations., • Plan and manage large-scale restoration projects, from initial identification of limiting factors to alternatives development and feasibility studies through final design, permitting, construction oversight, and adaptive management., • Develop and implement mitigation strategies, and represent clients in consultation with agencies such as NOAA, USFWS, USACE, Ecology, and WDFW and tribes., • Manage project scope, schedule, and budget, including QA/QC review of technical deliverables, oversight of field teams, and coordination of subcontractors., • Mentor and support junior staff, fostering a culture of quality, collaboration, and professional growth., • Contribute to business development efforts, including positioning for and winning multi-disciplinary projects with a focus on resilient restoration solutions either as part of a larger team or as the prime contractor. This would be accomplished through leveraging existing relationships, serving as a visible leader in professional organizations, developing new clients, identifying project opportunities, leading proposal efforts, and capturing new work. What Are We Looking For? The ideal candidates will have the following: • Bachelors degree (minimum) in biology, ecology, natural resources, or a related field., • 10+ years of professional experience in biology, habitat restoration, or related field., • Deep knowledge of Pacific Northwest ecosystems, including Puget Sound and western Washington watersheds., • Expertise in restoration design and implementation, including floodplains, riparian zones, estuaries, rivers, streams, and fish passage improvements., • Experience in local, state, and federal permitting or coordination/communication/facilitation with agencies and tribes, • Proven experience in managing complex projects, including familiarity with project management tools and experience in developing and managing scopes, detailed schedules, budgets, and subconsultants., • Proven leadership in business development activities., • Ability to work collaboratively within multidisciplinary teams and foster a positive work environment., • Excellent written and verbal communication skills, with the ability to convey complex technical information to diverse audiences What Can You Expect? A collaborative work environment where we encourage everyone to bring their authentic self. We offer competitive compensation and benefits. Benefits detailed below. Who Are We? Anchor QEA provides environmental planning, science, and engineering consulting services with the mission of transforming our environment and communities with integrity and vibe. With more than 500 people in offices across the United States, our collective vision is to be an inclusive, sustainable, and growing environmental innovator making generational impacts. By embodying our core values, we strive to be our clients first choice for solving their most challenging problems and to be our employees reason to be excited about going to work each morning. Learn more about Anchor QEA at . How to Apply? Apply online through Anchor QEAs Open Positions page at . Veterans are encouraged to apply. Applicants with a disability, who require a reasonable accommodation for any part of the application or hiring process, may e-mail their request to Additional Information We work hard to embrace diversity and inclusion. As an equal opportunity employer, Anchor QEA is committed to a diverse, multi-cultural work environment. Anchor QEA does not discriminate in employment based on age, race, creed, gender, religion, marital status, veterans status, national origin, disability or sexual orientation. Employment is contingent upon satisfactory results of a comprehensive background check. Salary and Other Compensation: • Annual Bonus, • Other potential bonus types: Billable Time Bonus, Spot Bonus, Milestone Anniversary Bonus, Receiving Professional License/Certification Bonus, Peer-reviewed Publication Bonus, Employee Referral Bonus. Base Level Benefits for Regular Full-Time Positions: • Healthcare: Medical, dental, vision, basic life and AD&D insurance, • Paid Company and Floating Holidays: 7 paid company and 2 floating holidays annually, • Vacation: 2 weeks accrued paid vacation based on length of service. Vacation may vary by level., • Sick and Safe Time: 80 hours annually