Research associate jobs in Davis, CA - 97 jobs

It's official. We're the #1 best place to work in Agriculture, Mining and Utilities awarded by @FinancialReview and @Inventium How can you grow with Nufarm? NuFarm delivers VALUE BEYOND YIELD through dedicated service, locally proven Canola, Carinata, Sorghum and Sunflower seed for farm customers and new plant-based solutions for end-use customers globally. Our industry leading Beyond Yield Carinata and Omega-3 Canola products provide a truly sustainable platform recognizing the ever-evolving environmental challenges our world is facing. All of this is core to our global commitment and what sets us apart. Over 3000 NuFarm employees work across our global locations, including three world-class NuFarm Innovation Centers. The Molecular Biologist is responsible for advancing molecular genotyping platforms and digital systems that enable seed product QAQC, marker discovery, and breeding applications. The role combines hands-on molecular biology, data analysis, and informatics with process innovation and cross-functional collaboration. This position supports global breeding, discovery, seed QAQC, and regulatory programs through the design, execution, and reporting of high-throughput molecular assays and through leadership of digital workflows such as the R&D LIMS. Be part of building a better Nufarm Lead marker validation and deployment across multiple crops, from early screening through assay optimization. Select and curate genetic materials and reference controls to support marker discovery, validation, and QC. Design and execute experiments for new trait markers, ensuring accuracy, reproducibility, and strong documentation. Own end-to-end Seed QAQC genotyping request support for a global supply chain stakeholder network. Manage the full QAQC workflow from sample receipt to traceable, accurate, and on-time report delivery. Investigate and resolve stakeholder inquiries by troubleshooting lab workflows, seed production methods, and genetic profiles. Execute genotyping workflows across KASP, qPCR, GBS, and WGS platforms using wet-lab techniques and automation. Build and manage projects in LGC Kraken LIMS, including sample layout design, controls, and genotype cluster scoring/verification. Analyze genotyping datasets using advanced Excel, R, and/or Python; diagnose data-quality issues and deliver clear stakeholder reports with final QAQC sign-off support. Lead GBS platform operations and improvement (high-throughput sequencing, library prep/indexing, pipeline optimization) while driving digital transformation via LIMS implementation, training, and reference genotype database development. Most importantly, you're positive, results driven, and you thrive off being empowered to own your own outcomes. If you want to be a part of a thriving, supportive environment and are inspired by the prospect of being a part of something bigger, we'd love to hear from you. Nufarm is proud to be recognised as an endorsed employer of choice for all woman by Work180 taking out the #6 spot in 2025!

Job Title: Research Associate, IPJob Description We are seeking a detail-oriented In-Vivo Research Associate to support preclinical studies involving laboratory animals. The ideal candidate will have hands-on experience in animal handling, randomization procedures, mortality tracking, and general animal husbandry. This role is critical to ensuring the integrity and welfare of in-vivo studies conducted in support of drug development and biomedical research. Responsibilities + Perform daily animal care and husbandry tasks, including feeding, cage cleaning, and health monitoring. + Execute study protocols involving animal dosing, sample collection, and behavioral observations. + Conduct randomization of animals into study groups using approved methods to ensure unbiased data collection. + Accurately record and report mortality counts and clinical observations in accordance with study protocols. + Maintain detailed and compliant documentation of all procedures and observations. + Collaborate with study directors and veterinary staff to ensure animal welfare and protocol adherence. + Assist in maintaining regulatory compliance and other relevant guidelines. + Participate in training and continuous improvement initiatives related to in-vivo techniques and animal care. Essential Skills + Bachelor's degree in biology, animal science, or a related field; or equivalent experience. + Minimum of 2 years of hands-on experience in in-vivo animal research, preferably in a GLP-compliant environment. + Proficiency in animal handling techniques for rodents (mice and rats). + Demonstrated experience with randomization procedures and mortality tracking. + Strong understanding of animal husbandry practices and ethical care standards. + Familiarity with electronic data capture systems and laboratory documentation. + Ability to work independently and collaboratively in a fast-paced research setting. Additional Skills & Qualifications + Experience with dosing techniques, IP preferred. + Knowledge of study design and statistical principles related to randomization. + Comfort with working in a regulated environment and following SOPs. Work Environment The position requires onsite presence 7 days a week, with the need to work during holidays and weekends until the end of the year. Shifts are structured into front-half and back-half schedules with rotating assignments. Job Type & Location This is a Permanent position based out of Hercules, CA. Pay and Benefits The pay range for this position is $80000.00 - $95000.00/yr. can be provided upon request Workplace Type This is a fully onsite position in Hercules,CA. Application Deadline This position is anticipated to close on Feb 2, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action. **Required Skills:** Research Scientist - CTRL Labs Responsibilities: 1. Research and develop Deep Learning or other computational models 2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets 3. Set technical direction for a project of 2-3 researchers and engineers 4. Help transition and deliver our work from research into product 5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU) **Minimum Qualifications:** Minimum Qualifications: 6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics 8. Experience with developing machine learning models at scale from inception to business impact 9. Programming experience in Python and hands-on experience with frameworks such as PyTorch 10. Exposure to architectural patterns of large scale software applications 11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment **Preferred Qualifications:** Preferred Qualifications: 12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP) 13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub) 14. Experience bringing machine learning-based products from research to production **Public Compensation:** $184,000/year to $257,000/year + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@meta.com.

Please note, the Water Boards do not participate in E-Verify. Please note: this is a re-advertisement. If you have previously applied for this vacancy, your application is being considered and you do not need to re-apply. Positions at the Water Boards may be eligible for telework with in-person attendance based on the operational needs of the position and might be expected to comply with Executive Order (EO) 22-25 after July 1, 2026. Salary Information - CalHR salary rules allow appointment at the entrance rate (Cal. Code Regs., tit. 2, § 599.673) of a classification. For classes with alternate ranges, placement is based on education/experience. Employees appointed to the Attorney or Water Resource Control Engineer classification will receive Recruitment Higher Above Minimum (HAM) rate in accordance with the approved Civil Service Pay Scales. In addition, note: Effective July 1, 2025, the State of California implemented the Personal Leave Program 2025 (PLP 2025) which reduces an employee's monthly salary in exchange for leave credits. Employees appointed to this classification will have their monthly salary reduced and will accrue hours of PLP 2025 on the first day of each pay period in accordance with the applicable bargaining contract. The salary range(s) included on this job posting do not reflect the reduction in pay. This position may be entitled to a $250.00 pay differential per month based on Bargaining Unit and/or work location if hired to report to the Richmond Office in Contra Costa County. Are you looking for an exciting and fulfilling career that is instrumental in the protection of the environment? The State of California is seeking a dedicated Research Scientist to join our dynamic team as a laboratory assessor. You will drive the enhancement of laboratory capabilities throughout the state, directly influencing the quality and reliability of environmental monitoring and protection. We offer a unique opportunity to apply your scientific expertise within a supportive and innovative team, dedicated to excellence and continuous improvement. Apply today and join us. The State Water Resources Control Board's Division of Drinking Water (DDW) has an opening for a Research Scientist I (Chemical Sciences) in the Environmental Laboratory Accreditation Program (ELAP) of DDW's Program Management Branch. The position may be filled at one of DDW's Field Office locations: * Redding - 364 Knollcrest Drive, Suite 101, Redding, CA 96002. * Sacramento - 1001 I Street, 17th Floor, Sacramento, CA 95814. * Santa Rosa - 50 D Street, Suite 200, Santa Rosa, CA 95404. * Richmond - 850 Marina Bay Parkway, Building P, 2nd Floor, Richmond, CA 94804. * Monterey - 1 Lower Ragsdale Drive, Building 1, Suite 120, Monterey, CA 93940. * Lodi - 3021 Reynolds Ranch Parkway, Suite 260, Lodi, CA 95240. * Fresno - 265 West Bullard Avenue, Suite 101, Fresno, CA 93704. * Carpinteria - 1180 Eugenia Place, Suite 200, Carpinteria, CA 93013. * Bakersfield - 4925 Commerce Drive, Suite 120, Bakersfield, CA 93309. * Glendale - 500 North Central Avenue, Suite 500, Glendale, CA 91203. * Santa Ana - 2 MacArthur Place, Suite 150, Santa Ana, CA 92707. * San Bernardino - 464 West 4th Street, Room 437, San Bernardino, CA 92401. * San Diego - 2375 Northside Drive, Suite 100, San Diego, CA 92108. Additional information: Candidates must possess essential personal qualifications including integrity, initiative, dependability, good judgment, the ability to work cooperatively with others, and the ability to perform the assigned duties of the class. If the position requires driving, you must possess a current and valid driver's license. Please Do Not include full Social Security Number, method of eligibility, and LEAP information in your application package. Please let us know how you heard about this position by taking this brief survey: Recruitment Survey. You will find additional information about the job in the Duty Statement. Minimum Requirements You will find the Minimum Requirements in the Class Specification. * RESEARCH SCIENTIST I (CHEMICAL SCIENCES) Additional Documents * Job Application Package Checklist * Duty Statement Position Details Job Code #: JC-482970 Position #(s): ************-XXX Working Title: Research Scientist I (Chemical Sciences) Classification: RESEARCH SCIENTIST I (CHEMICAL SCIENCES) $6,942.00 - $8,922.00 New to State candidates will be hired into the minimum salary of the classification or minimum of alternate range when applicable. # of Positions: 1 Work Location: United States Telework: Hybrid Job Type: Permanent, Full Time Facility: State Water Resources Control Board Department Information The State Water Resources Control Board (SWRCB) and the nine (9) Regional Water Quality Control Boards (RWQCB) (collectively the Water Boards) work to preserve, enhance, and restore the quality of California's water resources and drinking water for the protection of the environment, public health, and all beneficial uses, and to ensure proper water resource allocation and efficient use, for the benefit of present and future generations. The Water Boards value diversity, equity, and inclusion throughout the organization. We foster an environment where employees from a variety of backgrounds, cultures, and personal experiences are welcomed and can thrive. We believe the diversity of our employees is essential to inspiring innovative solutions. Together we further our mission to preserve, enhance, and restore the quality of California's water resources and drinking water for the protection of the environment, public health, and all beneficial uses, and to ensure proper water resource allocation and efficient use, for the benefit of present and future generations. Join the Water Boards to improve the lives of all Californians. Department Website: ******************************* Special Requirements In order to be considered for this position, you must include the following: * RPA# 24-410-009 in the "Examination or Job Title(s)" section of the State application when submitting a hardcopy application. * Photocopies of degree and official transcripts (if needed to establish eligibility). Must have Research Scientist I (Chemical Sciences) list, transfer, or reinstatement eligibility and be reachable on the certification list. Here is the link to the exam: ********************************************************************************* An applicant with a college degree obtained outside the United States that does meet accreditation standards must have education records evaluated by a credentials evaluation service. Evaluation of education records will be due during final minimum qualification evaluation of candidate(s). A link of accepted evaluation agencies can be found here: ****************************** Electronic submittal of applications and attachments through jobs.ca.gov is preferred. Emailed or faxed applications will not be accepted. You are required to complete employment history on the application form (STD. 678), including work experience, dates, hours worked, contact names and phone numbers of supervisors on the state application. Applicants who fail to submit a completed STD. 678 may be disqualified. In the hiring interview, the panel will consider education, experience, personal development, personal traits and fitness for the job. In appraising experience, more weight may be given to the breadth of pertinent experience and evidence of the candidate's ability to accept and fulfill increasing responsibilities than to the length of his/her experience. For additional information, you may refer to the class specification. Application Instructions Completed applications and all required documents must be received or postmarked by the Final Filing Date in order to be considered. Dates printed on Mobile Bar Codes, such as the Quick Response (QR) Codes available at the USPS, are not considered Postmark dates for the purpose of determining timely filing of an application. Final Filing Date: 2/5/2026 Who May Apply Individuals who are currently in the classification, eligible for lateral transfer, eligible for reinstatement, have list or LEAP eligibility, are in the process of obtaining list eligibility, or have SROA and/or Surplus eligibility (please attach your letter, if available). SROA and Surplus candidates are given priority; therefore, individuals with other eligibility may be considered in the event no SROA or Surplus candidates apply. Applications will be screened and only the most qualified applicants will be selected to move forward in the selection process. Applicants must meet the Minimum Qualifications stated in the Classification Specification(s). How To Apply Complete Application Packages (including your Examination/Employment Application (STD 678) and applicable or required documents) must be submitted to apply for this Job Posting. Application Packages may be submitted electronically through your CalCareer Account at ********************** When submitting your application in hard copy, a completed copy of the Application Package listing must be included. If you choose to not apply electronically, a hard copy application package may be submitted through an alternative method listed below: Address for Mailing Application Packages You may submit your application and any applicable or required documents to: State Water Resources Control Board Attn: Human Resources Branch - Katie Hill 1001 I Street, 18th Floor Sacramento, CA 95814 Address for Drop-Off Application Packages You may drop off your application and any applicable or required documents at: State Water Resources Control Board Human Resources Branch - Katie Hill 1001 I Street, 18th Floor Sacramento, CA 95814 08:00 AM - 05:00 PM Required Application Package Documents The following items are required to be submitted with your application. Applicants who do not submit the required items timely may not be considered for this job: * Current version of the State Examination/Employment Application STD Form 678 (when not applying electronically), or the Electronic State Employment Application through your Applicant Account at ********************** All Experience and Education relating to the Minimum Qualifications listed on the Classification Specification should be included to demonstrate how you meet the Minimum Qualifications for the position. * Resume is required and must be included. * Statement of Qualifications - Please see below for specific SOQ requirements. * Other - Cover Letter is required and must be included. Applicants requiring reasonable accommodations for the hiring interview process must request the necessary accommodations if scheduled for a hiring interview. The request should be made at the time of contact to schedule the interview. Questions regarding reasonable accommodations may be directed to the EEO contact listed on this job posting. Desirable Qualifications In addition to evaluating each candidate's relative ability, as demonstrated by quality and breadth of experience, the following factors will provide the basis for competitively evaluating each candidate: Knowledge of the fundamentals of a variety of scientific disciplines, general scientific concepts, and basic research principles. Knowledge of California Drinking Water related statues and regulations. Strong written and oral communication skills, strong organizational skills, and ability to work independently and as part of a team. Knowledge and experience with Microsoft computer software. Ability to organize and set priorities on assignments and meet deadlines. Excellent customer service skills. Benefits Water Board employees may be eligible for benefits. Health benefits and leave programs are available for most permanent, full-time employees, and some permanent, part-time employees. Benefit eligibility may depend on length of service and may be subject to collective bargaining agreements negotiated between the State of California and employee organizations that define wages, hours, and terms and conditions of employment. ******************************************************************************************** and Health Benefits | CalPERS Benefit information can be found on the CalHR website and the CalPERS website. Contact Information The Human Resources Contact is available to answer questions regarding the application process. The Hiring Unit Contact is available to answer questions regarding the position. Department Website: ******************************* Human Resources Contact: Katie Hill ************** ******************************** Hiring Unit Contact: Maria Friedman ************** ********************************* Please direct requests for Reasonable Accommodations to the interview scheduler at the time the interview is being scheduled. You may direct any additional questions regarding Reasonable Accommodations or Equal Employment Opportunity for this position(s) to the Department's EEO Office. EEO Contact: Shyla Hoffman ************** ******************************** California Relay Service: ************** (TTY), ************** (Voice) TTY is a Telecommunications Device for the Deaf, and is reachable only from phones equipped with a TTY Device. Statement of Qualifications A Statement of Qualifications (SOQ) must be submitted along with the State Application and serves as documentation of candidate's ability to present information clearly and concisely in writing. It should be typed, no more than two (2) pages in length, using Arial size 12 font, and normal margins. Please respond to the following statements/questions: 1. How many years of knowledge and/or experience do you have working in a commercial or governmental environmental testing laboratory? Describe your knowledge and/or experience and role(s). 2. How many years of knowledge and/or experience do you have writing quality manuals or Standard Operating Procedures (SOPs) for commercial or governmental environmental testing laboratories? Describe the documents involved. 3. How many years of knowledge and/or experience do you have with laboratory sample testing using published methods from the Environmental Protection Agency, Standard Methods, American Society for Testing and Materials, or other Voluntary Standards Consensus Body? Describe your knowledge and/or experience and role(s), including a description of the methods involved (including method number, where applicable). 4. How many years of knowledge and/or experience do you have with public speaking or interacting with the public in a professional setting? Describe the nature of your knowledge and/or experience. Applications received without the SOQ addressed as stated may not be considered. Note: Resumes, letters, and other materials will not be evaluated or considered as a response to the SOQ. Equal Opportunity Employer The State of California is an equal opportunity employer to all, regardless of age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (includes pregnancy, childbirth, breastfeeding and related medical conditions), and sexual orientation. It is an objective of the State of California to achieve a drug-free work place. Any applicant for state employment will be expected to behave in accordance with this objective because the use of illegal drugs is inconsistent with the law of the State, the rules governing Civil Service, and the special trust placed in public servants.

Job DescriptionMolecular Matrix is pioneering innovative medical devices for tissue regeneration applications in multiple organ systems. We are seeking highly motivated, self-sufficient candidates who are interested in growing with our company in a fast-paced and exciting environment. About the role: Reporting to the Research & Development Lead, the Research Associate will use cell culture and molecular biology techniques to support the development of tissue engineering medical devices. The Research Associate works primarily in R&D to support advancements in bioprocessing, scaffolding, and large-scale tissue formation. About You: You are an experienced Bachelor's or Master's level cell biologist and/or molecular biologist who enjoys collaborating across disciplines in order to solve complex problems. You are good at communicating ideas, data, and bottle-necks to technical and non-technical audiences alike. You have knowledge or interest in tissue engineering and medical devices and are excited to bring your experience and enthusiasm to this nascent industry. You thrive in fast-paced environments. Responsibilities: Perform molecular cloning: PCR, restriction digest, DNA assembly Perform gene expression assays using RT-PCR Develop new cell lines by modifying growth factor signaling Develop assays to screen, isolate, and validate cell lines Reagent preparation, aliquoting, inventory management Collaborate with the preclinical team to support preclinical trials of novel technologies Contribute to various group efforts in research and development Identify, suggest, purchase and operate supplies and equipment through established processes to support this role Mentor junior members with technical skills, and experimental design Qualifications & Skills: Experienced in adherent mammalian cell culture Experience with molecular cloning and transfection including designing DNA constructs, producing plasmids, and delivering to cells using transfection or electroporation Cell line development: able to screen, isolate, and validate targeted cell populations Knowledge of basic cell biology with an ability to develop methods to manipulate We offer great benefits (health, vision, and dental insurance and a retirement plan) and challenging, impactful work. Join our growing team, work with smart and dedicated people, and help develop cutting-edge technologies that will positively impact the world. Job Type: Full-time Salary: From $64,480.00 per year Benefits: Dental insurance Health insurance Paid time off Retirement plan Vision insurance Schedule: 8 hour shift Weekend availability Ability to commute/relocate: Rancho Cordova, CA 95670: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Mammalian cell culture: 2 years (Required) Work Location: In person

POSITION DESCRIPTION: This position seeks a highly-skilled PhD-level scientist with expertise in Mass Spectrometry (MS) to conduct interdisciplinary metabolic research. The position includes: Core Lab Operations: Performing and overseeing sample analysis within the Mass Spectrometry Core Laboratory. This includes technical troubleshooting, data management, and data analysis. Research Design & Method Development: Developing and implementing new laboratory methods and participating in the preparation of grant proposals and manuscripts. Mentorship: Overseeing research projects for students in TUC's Master's and medical school programs. Responsibilities SPECIFIC RESPONSIBILITIES: Lead the processing and preparation of diverse biological and chemical samples for mass spectrometry analysis. Perform and optimize Gas Chromatography/Mass Spectrometry (GC/MS) methods. Provide direct technical and operational supervision for the wet laboratory (sample preparation), ensuring adherence to safety and quality standards. Analyze and interpret complex mass spectrometry data and prepare results for publication and presentation. Train and mentor student researchers (MS and DO students) on proper research methodologies, experimental design, and lab techniques. SUPERVISORY RESPONSIBILITIES (if applicable): Directly supervise the day-to-day work and performance of laboratory assistants and technicians. Oversee the scheduling, training, and quality assurance of wet laboratory activities. Qualifications Education & Experience A Ph.D. in Chemistry, Biochemistry, or a closely related field is required. Extensive hands-on experience operating and maintaining Mass Spectrometry instrumentation, particularly GC/MS. Skills & Abilities Demonstrated strong analytical and organizational skills with the ability to manage multiple projects simultaneously and meet strict deadlines. Advanced knowledge of biochemistry and organic chemistry principles relevant to sample preparation (e.g., TLC, derivatization). Ability to work independently with general guidance and collaboratively within an interdisciplinary team. Proficiency with general laboratory and data analysis software, including Microsoft Office Suite. CORE COMPETENCIES: Communication: Uses language effectively to gather information, clearly communicate technical results, and facilitate the exchange of complex scientific ideas. Professionalism & Collaboration: Exhibits respect and understanding for others, maintains strong professional relationships, and effectively contributes to a positive team environment. Technical Excellence: Maintains a high level of expertise in mass spectrometry and laboratory techniques, ensuring the reliability and quality of all research output Maximum Salary USD $86,305.63/Yr. Minimum Salary USD $73,359.79/Yr.

JOB SUMMARY: The Farm Technician works in cooperation with the Farm Manager and the Research Trials Manager to improve the growing conditions of the research crops. Farm Technician is primarily responsible for supporting daily farm operations and assisting with irrigation and pesticide applications. Manage equipment and working closely with the crew to keep operations running efficiently on the Research Station. ESSENTIAL DUTIES AND RESPONSIBILITIES*: · Responsible for assisting farming crops and maintaining greenhouses. Assists the Farm Manager with the maintenance of the research farm. · Responsible for recording seasonal data relating to crop maps, fertilizer, irrigation, and overall growing season performance for each crop. · Responsible for irrigation management including that the irrigation systems are maintained and operated correctly. · Responsible for spraying and maintaining (as needed) on-farm research and demonstration plots. · Responsible for pesticide applications including completing required documentation and posting requirements. · Assists in monitoring and guiding the farming activities to achieve desired results. · Coordinate with Farm Manager and Breeder Assistants regarding chemical applications in the field and greenhouses. REQUIRED KNOWLEDGE/SKILLS/ABILITIES: · Must be able to operate and maintain farm equipment such as irrigation pumps, tractors, pickups, disks, sprayers, levelers, fertilizer spreaders, bed presses, mulch machines, pesticide applicators, etc. · Must have general knowledge of farm operations and farm management principles. · Bi-lingual English/Spanish ability is highly desirable but not required. · Ability to handle stress especially when encountering necessary projects, deadlines and/or high workload. · Must be able to work under strict time constraints and requirements. · Computer experience with Microsoft Office software desired. EDUCATIONAL REQUIREMENTS: · B.S. in agriculture or related subject, or equivalent knowledge and experience as determined by Sakata EXPERIENCE AND BACKGROUND: · Farm management experience highly desirable. · Must have and maintain a current pesticide applicator's license. WORKING CONDITIONS/PHYSICAL DEMANDS: · Must be able to work with chemicals and other irritating substances. · Must be able to wear personal protective equipment when required. · Must be able to work under different weather conditions such as extremes of temperature, dampness, rain and sun exposure. · Must be able to work in dusty conditions. · Must be able to walk and stand for long periods of time. · Must be able to work long and irregular hours. BENEFITS: Medical, Dental & Vision Insurance coverage for employees and their families Basic Life & AD&D Insurance 401k program with company match Profit Sharing program (via 401k) Holiday & Performance Incentive Bonus program Paid Vacation: 10 days per year to start, increases with tenure Sick Leave: 1 hour accrued per 30 hours worked for first 30 days, 6.67 hours per month after. 14 paid company holidays, 2 floating holidays & birthday off Paid Family Leave: 15 days after 12 months of service for FMLA qualifying events * To perform this job successfully, an individual must be able to perform each essential duty (as described above) satisfactorily. Reasonable accommodations may be made to enable Individuals with disabilities to perform these essential functions.

River Partners' helps local communities reconnect and revitalize floodplains and river landscapes across the state of California. We are a private, non-profit organization with offices in Chico, Sacramento, Turlock, and San Diego. As a project-focused company, we believe in the power of demonstrating environmental improvement through large-scale river restoration and empowering others through partnership and collaboration. Job Description Position Description: River Partners' Turlock office is looking for a qualified Restoration Ecologist to help us on our habitat restoration projects on the San Joaquin River. The Restoration Ecologist works with River Partners' biology, field implementation, and development teams to identify, develop and execute riparian habitat restoration projects. Here are some of the essential functions and responsibilities of this position: • Managing complex large-scale restoration projects • Developing and building good rapport with external partners • Writing quality plans, reports, and articles • Managing multi-million-dollar budgets for restoration, mitigation and consulting projects • Assisting in the development of new restoration projects • Providing recommendation for problematic soil conditions on existing projects • Evaluating soil conditions for new projects to assist in project planning • Managing the Enterprise geographic information system (GIS) • Proactively communicating with team members to improve habitat restoration and implementation techniques • Securing permits from local, state and federal agencies • Conducting vegetation and biological monitoring and studies • Training and supervising entry-level biologists and interns • Meeting multiple and competing deadlines and providing outstanding customer relations • Developing and delivering presentations to the scientific community, government agencies and the public • Attending public events, fairs and meetings to promote the organization and its mission • Working independently in a fast-paced, dynamic environment • May involve travel and/or long hours and weekends in a variety of field conditions. • Other duties as assigned. Essential Knowledge Skills and Abilities: • Possess the enthusiasm and drive to assist River Partners in fulfilling its mission • Enjoy working with diverse people and organizations to get things done • Creatively solve problems and delight in learning new skills • Effectively communicate complicated soil science findings orally and in writing • Possess knowledge of and experience with basic irrigation techniques and a knowledge of soil chemistry, physics and plant science • Possess advanced knowledge of California native plants, riparian ecology, and river hydrology • Proven ability to work effectively with a team and independently • Possess an understanding of statistics, experimental design and data collection • Experience collecting, organizing, and analyzing field data • Demonstrate good organizational skills, ability to work under multiple deadlines, and flexibility to handle changing priorities • Be able to remain dedicated and focused on multiple tasks • Advanced skills in Microsoft Word, Excel, Access, and other programs Qualifications Qualifications: • M.S or equivalent work experience in ecology, plant biology, soil science, agriculture or natural resource science or related science and • Three to five years of appropriate work experience • Successful candidates must possess a valid driver's license with no restrictions Additional Information To apply email your resume, cover letter and 3 references to: Jobs AT riverpartners.org Or send an application via mail to: River Partners Attn: Turlock Ecologist 580 Vallombrosa Ave Chico CA 95926 Please no calls on this position.

Cramer Fish Sciences (CFS) is seeking a GENETICIST/MOLECULAR BIOLOGIST to join our Genidaqs team in West Sacramento! The Geneticist/Molecular Biologist will work with the Director of Laboratory Services and Business Development Group to lead research and development in genetic research, using techniques such as metabarcoding, qPCR, microsatellites, and NGS. This role provides technical leadership on complex, multi-partner projects in genetics, molecular ecology, and environmental modeling, and is responsible for developing bioinformatic pipelines and procedural workflows. This individual will also be trained in business development and client communication. INTERESTED IN APPLYING? Please submit your resume and cover letter at: ************************************************* ESSENTIAL RESPONSIBILITIES: Lead, train, supervise, and support field crews and technicians across multiple projects, including hands-on work with laboratory techniques aligned with project protocols. Design and implement rigorous scientific studies; test hypotheses, collect and analyze data, and troubleshoot issues as needed. Collaborate with project managers to develop project scopes and budgets that align with client needs. Manage genetic data workflows, including acquisition, analysis, interpretation, and visualization; maintain databases and generate scripts in R, Python, or other languages to curate datasets. Apply statistical methods to support genetic and molecular ecological studies and communicate findings through reports, manuscripts, and conferences. Represent Genidaqs-CFS at scientific conferences and contribute to the field through presentations and peer-reviewed publications. Provide technical direction to key staff and collaborate with peers and leadership to meet project objectives. Lead the development and implementation of new initiatives and large-scale projects. Travel to the Genidaqs lab as needed for training and business development. Perform other duties as assigned. EDUCATION REQUIREMENTS: Bachelor's or Master's degree in the Biological Sciences or a related field, with an emphasis in molecular/evolutionary biology or population genetics. WORKING CONDITIONS/PHYSICAL DEMANDS: Prolonged periods of sitting or standing at a laboratory bench or computer Ability to comfortably use standard laboratory equipment, including pipettes, centrifuges, and PCR machines Ability to lift up to 30 lbs. Occasional work outdoors in variable weather conditions and remote locations during field visits or project support. Travel to the Genidaqs lab in West Sacramento or other locations may be required for training, collaboration, or business development. COMPENSATION & BENEFITS: $80,000 - $100,000 per year, depending upon experience. 401(k) has a 3% match and full vesting after one year. The annual cash bonus has a 3% target. The benefit package includes medical, dental, vision, basic life, long-term disability, flexible spending accounts, employee assistance programs, paid time off, paid company holidays, and other various voluntary benefits. ESOP: CFS is a 100% employee-owned company. Our employee stock option plan (ESOP) is a qualified defined contribution plan. Our target ESOP contribution is 5%. Eligibility is after one year of service with an entry date of Jan 1 or July 1. ABOUT CRAMER FISH SCIENCES: We are a fisheries research consulting firm operating throughout the Pacific States and Idaho. As a growing, employee-owned company, our mission is to rigorously apply the scientific method to provide innovative, scientifically robust solutions to a variety of fisheries and environmental challenges. We do this through effective and unbiased data collection, insightful analysis, and clear communication, including publishing results in scientific journals. ABOUT GENEDAQS: The Genidaqs Lab is a business unit within Cramer Fish Sciences that provides clients with access to cutting-edge genetic and molecular ecology techniques for solving today's natural resource management challenges. AFFIRMATIVE ACTION: Cramer Fish Sciences is an Affirmative Action/Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Dr. Stephen Huppert is seeking an Associate Dentist to join his practice. We have more than 40 high quality independent dental practices in Northern California that make up the Mosaic Dental Collective. Our multi-specialty partnership focuses on clinical excellence and patient outcomes. Working in a Mosaic Dental Collective office assures you the best of both worlds - be part of an independent office team but have the support of a dynamic partnership. Every Mosaic office has a long-standing reputation in the Sacramento dental community and operates independently, but by sharing the "best of the best practices" we're truly better together! * Daily guarantee and % of production * Equity and a Path to Partnership * Sign-on bonus and relocation reimbursement * Reimbursement for CE, license, malpractice, association dues, etc. * Medical/Dental/Vision/401K Inquiries and CV's can be sent to Nathalie La Chance: ************************************ Requirements * Doctor of Dental Medicine (DMD), Doctor of Dental Surgery (DDS) * License/credentials applicable to the state of California * CPR/BLS Certification * Evidence Based Dental Practices

Dr. Stephen Huppert is seeking an Associate Dentist to join his practice. We have more than 40 high quality independent dental practices in Northern California that make up the Mosaic Dental Collective. Our multi-specialty partnership focuses on clinical excellence and patient outcomes. Working in a Mosaic Dental Collective office assures you the best of both worlds - be part of an independent office team but have the support of a dynamic partnership. Every Mosaic office has a long-standing reputation in the Sacramento dental community and operates independently, but by sharing the “best of the best practices” we're truly better together! Daily guarantee and % of production Equity and a Path to Partnership Sign-on bonus and relocation reimbursement Reimbursement for CE, license, malpractice, association dues, etc. Medical/Dental/Vision/401K Inquiries and CV's can be sent to Nathalie La Chance: ************************************ Requirements Doctor of Dental Medicine (DMD), Doctor of Dental Surgery (DDS) License/credentials applicable to the state of California CPR/BLS Certification Evidence Based Dental Practices

About Us Sequoia Ecological Consulting, Inc. (Sequoia) is a small, woman-owned environmental consulting firm that specializes in environmental planning, wildlife and fish biology, botanical, and arboricultural services from the planning stages through permitting and compliance during project implementation. We serve federal, state, and local public agencies, as well as private clients throughout California. Sequoia's team develops creative solutions to complex projects through proactive planning, collaboration, and attention to detail. Summary Description You're Excited about this Opportunity Because… You share our values. You will thrive supporting environmental permitting and compliance projects based in our Walnut Creek office. You will leverage your understanding of biology, state and federal regulations, and project management to lead moderately complex projects or programs located throughout California for a variety of clients. We are looking for a dynamic individual who enjoys working independently and with teams. You are experienced in project management and coordination, deliverable oversight and QAQC, business development, field survey coordination, impacts analysis, permit assessments, and report preparation for biological work. This individual will be a member of the Sequoia supervisory team and will supervise 2-4 team members. Travel may be necessary, with mostly day trips within the Sacramento and/or San Francisco Bay areas. Occasional overnight travel will also be expected. Key Responsibilities Act as field lead on projects, including supporting Staff Biologists and Field Techs Interpret compliance packages, permits and project scopes to ensure compliance in the field Prepare Biological resources technical reports and/or habitat restoration plans for moderately complex projects. Participate in field mapping of existing biological resources for large and/or complex projects Write sound Biological Constraints Analyses. Consistently show thoughtful reasoning on impacts, impact avoidance measures, and recommendations. Assess potential constraints to development and construction based on documented conditions and applicable laws/regulations protecting biological resources (such as Endangered Species Act and Clean Water Act) and assess potential effects on biological resources of proposed developments or actions. Prepare documents that are consistently free of glaring or repeated technical and grammatical errors. Interact/Coordinate with clients on a weekly basis Support permit applications through completion of the application, project descriptions and species accounts. Perform protocol-level and/or focused surveys for sensitive (e.g., federally listed Threatened or Endangered) plant or animal species. Develop cost estimates and scopes of work for complex construction compliance projects, under the direct supervision of a Principal Assist with marketing proposals Attend site walk-downs and pre-bid meetings Create and perform biological trainings for construction and/or operation crews. May act as a Project Coordinator to coordinate complex projects, resources and schedule Function as an Associate Biologist (Bio II) as needed Consistently comply with all company administrative and technical policies and procedures, including time and expense reporting, standard operating procedures and other company directives. We're Excited about You Because You… Have these minimum qualifications and knowledge: Bachelor's degree in marketing, English, business administration, engineering, or a related field Demonstrated success working as an Associate Biologist (Bio II) Lead projects independently with minimal supervision Bachelor's Degree in Biology or related field The equivalent of a minimum of 3 to 6 years of full-time wildlife fieldwork and technical report writing experience and at least 3 of those in California. Master's Degree may substitute up to 2 years of experience, depending on degree and thesis work. Specialized federal 10(a)1(A) recovery permits and/or state MOUs relevant to Sequoia work may provide an additional year to count towards experience. Working understanding of California flora/fauna and regulatory environment Demonstrated verbal and written communication skills Proficient in MS Office Suite Familiar with GIS Mapping tools and able to navigate existing tools Approvable as a Project or Designated Biologist level by regulatory agencies for at least one species Valid Driver's License Able to work long field days Able to traverse difficult terrain An insured vehicle in a condition so that it does not leak fluids Ability to work long field days and drive long distance Must be able to perform fieldwork and/or travel up to 60-75% of time Overnight stays up to 25-50% of the time, depending on projects assigned. Why You'll Love Working at Sequoia Ecological Consulting, Inc. We provide a collaborative, employee-forward working environment. Do you enjoy creating, building, and maintaining long-term relationships in your work and find satisfaction in making a lasting impact in protecting our biodiversity, while also protecting your community? Sequoia is looking for a self-motivated individual who is eager to steer the direction of their career in a company that promotes and supports professional development. We don't hire candidates to suit the job; we find the work that fulfills our employees and helps them meet their professional goals. Our Commitment to Equality, Diversity, Inclusion, and Belonging At Sequoia, we create a “safe space” culture focused on fostering employee well-being, job satisfaction, and productivity. We are committed to a more inclusive and diverse workforce, where each employee can reach their full potential without the burden of discrimination or harassment. We strive to maintain a strong culture built upon our shared core values of Respect, Excellence, Passion, Integrity, and Teamwork. Sequoia is an equal opportunity employer. We understand that diversity, including human diversity, is the key to the success of all healthy ecosystems. We are a forest of remarkable individuals, standing tall as our authentic selves and as one. At Sequoia, we grow together to form a stable community that is diverse in character and content.

ERM is hiring Field Biologists to conduct surveys and monitoring for large construction projects in Fresno/Tulare/Shaver Lake, California. Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills. This is a full-time (40+ hours/week), limited-term role with a duration of 9 months, with the possibility of extension. RESPONSIBILITIES: Field biologist position to conduct pre-construction special status species surveys across the client's project area. Work locations are remote and require Biologist to work independently. Electronic data collection. Daily reporting and survey report compilation. Other duties as assigned or required. Compliance with ERM's rigorous safety program. REQUIREMENTS: A bachelor's degree in Environmental Science, Biology or related discipline. Be able to demonstrate familiarity with nesting bird survey protocols and/or general bird identification skills. A minimum of 2 years of Field Biology with experience in vegetation ecology, rare plant identification, and amphibians. Ability to work safely outdoors in variable weather conditions and on challenging terrain. Must have a strong attention to detail in the documentation of work. Must have strong organizational and communication skills. Desire to work in the field for an extended period and maintain a positive attitude. Willingness and ability to travel with overnight stays possible. Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project. Demonstrated independent and effective problem-solving and decision-making skills. Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area. Fluency in English and Spanish is highly preferred. For the Field Biologist position, the anticipated hourly base pay is $35.97-$46.58 (USD). Actual pay will depend on factors such as education, experience, skills, location, performance, and business needs. In some cases, pay may fall outside this range. This role may be eligible for bonus pay (casual and fixed term/flex force employees are not bonus eligible). We offer a comprehensive benefits package, including paid time off, parental leave, medical, dental, vision, life, disability, AD&D insurance, 401(k) or RRSP/DPSP, and other applicable benefits to eligible employees. Note: Bonuses, commissions, and other forms of additional compensation are not guaranteed and subject to the sole discretion of ERM and its policies and procedures. Who We Are: As the largest global pure play sustainability consultancy, we partner with the world's leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations. At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career. We also see our diversity as a strength that helps us create better solutions for our clients. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues. We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level. Please submit your resume and brief cover letter. ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes. ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. Thank you for your interest in ERM! #LI-JN1 #LI-Onsite

Pay Range: $18.00 - $19.00 Hourly We're seeking a steward to maintain operational functions in the restaurant, provide clean tableware for all hotel dining areas and functions, clean and sanitize all pots and pans used by the kitchen staff, and maintain a clean, safe, and comfortable work area for the kitchen and food service staffs. Dr. Wilkinson's Dr. Wilkinson's Backyard Resort and Mineral Springs is an iconic resort and spa destination located in the heart of the charming town of Calistoga, offering time-honored mud bath and spa treatments, healing mineral pool soaks, and the best of Calistoga right outside its doors. The transformed resort honors its iconic past while looking toward the future with a new mid-century inspired design, 50 completely refreshed guestrooms, a brand-new restaurant with indoor and outdoor seating, a completely re-imagined spa, and the same proven mud bath treatments first shared with the world over 65 years ago. Best-in-class yet playful and approachable, the spa will make the art of mud bathing accessible for all. Who We Are Recognized as a Top Workplace in The Washington Post and Philadelphia Inquirer. Passionate - about hospitality and fostering an environment where associates will thrive. Culture driven - dedicated to respect, teamwork, an entrepreneurial spirit, and the drive to succeed. Unique - we encourage our associates to express themselves and their individual talents. We celebrate diversity and are committed to equity and inclusion. Innovators - we are a lifestyle hotel management company that is constantly evolving. We are open minded individuals who embrace change. A growing team looking to expand with authentic and genuine individuals who recognize the importance of team engagement. A company that has a culture of promoting from within. What You Will Be Doing Perform routine pre-service tasks as directed, including transporting china, glassware, and silver; making sure service plates are hot and ready to be used. Attend to food service lines throughout service, including maintaining an adequate supply of clean dishes and utensils; refilling plate warmers as needed; and providing a constant supply of hot dishes and platters. Sweep, clean, and de-grease all kitchen floors on a daily basis. Follow all specifications to properly presoak, clean, and store all china, glassware, and silverware. Tear down dish-washing machine at end of each shift and thoroughly wash baskets, tanks, sprayers, and all parts, in preparation for the next shift. Follow all specified procedures to wash, disinfect, and store pots, pans, and fryers. Maintain the cleanliness of all sinks in the back of the kitchen, keeping them free of pots and pans. Retrieve fry pans from the line cooks, and clean and return them as soon as possible. Satisfactorily perform routine cleaning tasks in the kitchen as directed, including: o Sweeping ,cleaning, and mopping in various areas, including inside and out of all walk-in refrigerators and freezers o Cleaning tasks in the kitchen as directed, o Cleaning all machines, sinks, shelves, and working tables; o Keeping dumpster area clean and orderly at all times; o Cleaning dish and food warmers; o Cleaning Chef's office; o Keeping coffee machine area clean; o Cleaning and mopping employee dining' lounge area. Empty, wash, and reline all trash cans in back of kitchen, as soon as they are filled. Remove dirty towels from kitchen collection areas as they are filled, and replenish supply of clean linens and towels as needed. Maintain the banquet silver utensils storage area in an orderly manner, at all times. Set tables and empty trash containers in the employee lounge as needed, prior to and during service hours. Follow all company policies and procedures. Immediately report all suspicious occurrences and hazardous conditions. Maintain the cleanliness and safety of work areas at all times. Follow all company safety standards, including proper equipment handling to avoid injury to yourself and others. What We're Looking For Must be detail oriented, organized and efficient. A courteous, professional and friendly manner. A quick learner and able to work productively with little supervision. Open availability required. Must be prepared to work various shifts (for example: 7-3pm, 3-11pm, weekdays, weekends, holidays). What's In It for You Access to free virtual fitness classes and discounted in-person memberships Paid holidays Paid Parental Leave Tuition reimbursement opportunities - when you grow, we grow! Non-Negotiables (Our Core Values) SERVE OTHERS. LIVE 360. BUILD A POSITIVE TEAM. COMMUNICATE. BE WILDLY PASSIONATE. TAKE OWNERSHIP. LEARN + INNOVATE. EMBRACE CHANGE As part of an organizational culture that embraces change and progress, this job description does not seek to limit the tasks and responsibilities of the position. Rather, it acts as a springboard for future career and personal development within the property team and entire Modus Hotels' community. We are an equal opportunity employer. We actively respect the right of any qualified individual who performs to Modus standards to work. Discrimination based on gender, age, race, religion, national origin, marital status, sexual orientation, disability, or any other characteristic not related. Modus by PM Hotel Group will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. This description is subject to change, at the sole discretion of the Company, and in no way creates an employment contract, implied or otherwise; each associate remains, at all times, an “at will” associate. This position is non-exempt and will require standing and moving at least 75% of the time.

Job Description About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to the core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals Inc., Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Research Chemist (E&L) We are seeking an experienced Research Chemist (E&L) with a minimum of 3-5 years of pharmaceutical industry experience. Responsibilities: Maintain, operate, and troubleshoot LC-MS and GC-MS, GC-FID, and ICP-MS Systems. Perform extraction, analysis, and characterization of extractables and leachables from polymeric materials associated with container closure systems of pharmaceutical drug products as per USP, PQRI, ICH and other regulatory guidelines. Develop and optimize sample preparation techniques for analysis on GC-MS, LC-MS, and ICP-MS systems. Develop and validate LC-MS, GC-MS, and ICP-MS methods for finished product and raw material characterization as well as extractable/leachable testing. Unknown impurity identifications using GC-MS, LC-MS, and LC-MS/MS or other suitable techniques. Interpret complex spectral data and fragmentation patterns. Routine stability testing of API, finished product samples for assay and impurities using various instrumental techniques as suited, and prepare stability data summaries. Generate study designs, write protocols, methods, Datasheets and reports. Provide support in the critical review of analytical data, reports and protocols. Write Instrument-related SOPs and provide training on the instrument and related software. Train new recruits in the lab and support the team as needed. Participate in internal meetings and conferences. Provide support during technical transfer between R&D and QC. Whenever needed, attend SOP, Safety, and scientific trainings to remain current with cGMP regulations, safety standards, and development technologies. Preparation and review of analytical methods, method validation, and related study reports for ANDA/ NDA submissions and support, document preparation for ANDA/ NDA submissions. Any other activities as directed by the supervisor. Qualifications: Education/Experience: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. Knowledge, Skills, and Abilities: Familiarity with the characterization and isolation of impurities. Strong foundation in organic chemistry and structural elucidation, with expertise in small molecule pharmaceutical drug development and peptides, including computational techniques. Proficiency in using standard laboratory equipment, including pipettes, graduated cylinders, and balances. Skilled in laboratory techniques for measuring, weighing, and handling samples. Hands-on experience with HPLC (highly preferred). Knowledge of chemical handling procedures, including safety precautions and documentation such as Safety Data Sheets (SDS). Competency in Microsoft Office applications. Experience or familiarity with current Good Manufacturing Practices (cGMP) is preferred. Requirements: Must live or be willing to move to the Sacramento Metropolitan Region (Approximately 40 miles' radius) Benefits: Pay range $70,000 - $85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401 (k) savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment o retaliation based on any of these factors.

Who We Are Machinify is a leading healthcare intelligence company with expertise across the payment continuum, delivering unmatched value, transparency, and efficiency to health plan clients across the country. Deployed by over 60 health plans, including many of the top 20, and representing more than 160 million lives, Machinify brings together a fully configurable and content-rich, AI-powered platform along with best-in-class expertise. We're constantly reimagining what's possible in our industry, creating disruptively simple, powerfully clear ways to maximize financial outcomes and drive down healthcare costs. Location: This position is full remote and working hours are 11am - 8pm EST. About the Opportunity At Machinify, we're constantly reimagining what's possible in our industry-creating disruptively simple, powerfully clear ways to maximize our clients' financial outcomes today and drive down healthcare costs tomorrow. As part of the Data Mining Group, the Research and Creation Team Specialist (RCT) is an integral part of a dynamic team, supporting and facilitating the recovery of healthcare payments. RCT Specialists handle inbound calls, initiating new files, and identifying potential Subrogation claims. This role requires strong communication, analytical thinking, and attention to detail to ensure accurate file setup, effective documentation, and early recognition of recovery potential. What you'll do Answer inbound ACD call line and provide prompt, professional customer service to members and insurance companies. Create new claim files with accurate and complete information. Regularly accesses client systems to gather information used to create inventory. Uses multiple computer systems to review claim data and work efficiently. What experience you bring (Role Requirements) High School diploma, GED, or equivalent combination of education and experience in the health insurance, legal, property and casualty or related fields is preferred. Professional communication skills, fluent in Spanish and English Strong analytical skills, attention to detail and ability to adapt to new tasks Strong organizational skills Excellent written and verbal communication skills Word and Excel proficiency required What Success Looks Like… After 3 months You will have a strong understanding of the role. You begin building relationships and collaborating with peers. You develop effective time and priorities management. You receive initial feedback about your performance and are using it to improve. You've gained confidence in your abilities and are starting to feel more comfortable in your role. After 1 year You have mastered the tasks and responsibilities of the position, executing them with confidence and efficiency. You have established a strong network of internal relationships and are recognized as a key collaborator. You've been entrusted with greater responsibility indicating the company's confidence in your abilities. You see opportunities for career progression and personal development. Pay range: This is a non-exempt position at $25.00/hour. What's in it for you PTO, Paid Holidays, and Volunteer Days Eligibility for health, vision and dental coverage, 401(k) plan participation with company match, and flexible spending accounts Tuition Reimbursement Eligibility for company-paid benefits including life insurance, short-term disability, and parental leave. Remote and hybrid work options At Machinify, we're reimagining a simpler way forward. This begins with our employees. We are innovators who value integrity, teamwork, accuracy, and flexibility. We do the right thing, and we listen to the needs of our clients and their members. As tenured experts with unmatched experience, we champion diverse perspectives that help us to better understand and serve our clients. Our values come to life through our culture. We embrace flexible working arrangements that allow our employees to bring innovation to life in the way that best suits their productivity. We work cross-functionally, abandoning silos, to bring innovative and accurate solutions to market. We invest in each other through ongoing education and team celebrations, and we give back to our communities through dedicating days for volunteering. Together, Machinify is making healthcare work better for everyone, and we're passionate about a future with better outcomes for all. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace. Machinify is an employment at will employer. We participate in E-Verify as required by applicable law. In accordance with applicable state laws, we do not inquire about salary history during the recruitment process. If you require a reasonable accommodation to complete any part of the application or recruitment process, please contact our People Operations team at machinify_*********************. See our Candidate Privacy Notice at: ***************************************************

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Responsibilities: The Scientist - TSMS PAR will initially focus on the delivery of parenteral operations, specifically regarding technical transfer and process validation. TSMS PAR Scientists will support one of either formulation, filling, or visual inspection (VI), although may support multiple areas during start-up phase. Upon the start of commercial production, this role's objectives include maintaining the validated state of applicable processes, establishing and monitoring metrics/methods to ensure a state of capability and control, harmonization of control strategies across process teams, evaluate process improvement, and serving as an escalation point for day-to-day operations issues. The role will also author and execute protocols as well as conduct root cause investigations. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to parenteral manufacturing. Key Objectives/Deliverables: * Support the assigned Process Team (formulation, filling, or VI) as TSMS representative. • (Associate/Senior) Serve as floor-level support and technical interface for manufacturing components, equipment, and operations for the TSMS team. * Represent Concord TSMS team for internal and external communications on a regular basis * Lead risk management activities as it pertains to product/process * Provide technical support to non-routine (e.g., deviation, complaint) investigations, including consultation on quality and stability issues * Prepare and Review or approve, as required, relevant technical documents such as: Annual Product Reviews, Change Controls, Regulatory Submissions, Deviations, Validations, Procedures, PFDs, PFMEAs, etc. * Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability * Identify opportunities and lead technical projects to improve process control and/or productivity * Serve as interface with upstream suppliers and parenteral product networks * Drive stability strategy for Concord products * Provide Audit support as needed * Identify opportunities and participate in projects to improve process control and/or productivity Basic Qualifications: * Bachelor's degree or higher an engineering, packaging science, or related field Additional Skills/Preferences: * Pharmaceutical and/or medical device manufacturing experience * Root Cause Investigation Experience * Proficiency with computer systems including Microsoft Office products, Veeva Vault, TrackWise, electronic batch records, and SAP * Demonstrated successful leadership of cross-functional teams * Strong interpersonal and teamwork skills * Strong self-management and organizational skills Additional Information: * Role is Monday through Friday. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and /or off-hour work may be required. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Job Description TITLE: Seasonal Research Technician REPORTS TO: R&D Manager SUPERVISORY RESPONSIBILITIES: DIRECT: None INDIRECT: None EXEMPT ( ) NON-EXEMPT ( x ) Domain HWH, a family winegrowing endeavor built to last for generations, is part of Pacific Union Co. The Domain has evolved through the decades and comprises three Napa Valley properties that form its pillars: Harlan Estate, founded in 1984; BOND, founded in 1996; and Promontory, founded in 2008. The Mascot- a wine made from the younger vines of the three estates-was established in 2012. Each of these undertakings is dedicated to the understanding of our land, and to faithfully translating the respective characters of the individual properties into their wines. ABOUT THE ROLE The Research Technician supports the R&D department by preparing, processing, and analyzing vineyard samples for laboratory testing under established protocols. The role focuses on routine molecular diagnostics, laboratory accuracy, and reliable data recording to support vineyard health monitoring and viticulture research programs. This position is suited for individuals interested in viticulture, plant science, or agricultural research who are comfortable working in both laboratory and field environments and following structured sampling, testing, and data protocols. ESSENTIAL DUTIES AND RESPONSIBILITIES: Prepare and process plant tissue samples according to established laboratory protocols and standard operating procedures. Perform loop mediated isothermal amplification (LAMP) assays for vineyard pathogen detection. Maintain a clean, organized, and contamination-controlled laboratory workspace. Conduct routine laboratory analyses, as assigned. Handle, label, store, and dispose samples and reagents in accordance with laboratory requirements. Accurately record test results and associated metadata to ensure traceability and data integrity. Assist with data entry, basic summaries, and organization of analytical results. Support ongoing R&D and viticulture research activities as needed. QUALIFICATION REQUIREMENTS: Basic laboratory skills Ability to work in a laboratory environment and follow established safety practices. Strong attention to detail and organizational skills. Proficient in Microsoft Word and Excel. Basic analytical, mathematical, and problem-solving skills. Ability to manage multiple tasks and meet deadlines. Valid driver's license and insurance WILLINGNESS AND ABILITY TO: Stand and walk on uneven, sloped terrain and hillside for extended periods. Grasp, stoop, carry and crouch. Ability to accurately distinguish colors. Lift and handle materials weighing up to 50 pounds. Work overtime, as needed, pre-dawn or late hours. Pay Transparency Disclosure: The pay scale for this position is $22-$22 hourly. These figures represent what we reasonably expect to pay for this position, but the actual compensation offered will depend upon numerous job-related factors, including but not limited to candidate qualifications, skills, experience, education, location, and alignment with market data. The Company reserves the right to modify the range in the future. Bonus Pay Disclosure: In addition to the base pay of $22.00 per hour, employees hired for this seasonal position will be eligible to earn a $1.00 per hour bonus for each day worked (anticipated up to 100 days), provided the employee meets performance expectations and remains an active employee at the time of bonus payout; this bonus will be paid in accordance with the Domain Services payroll practices following completion of the assignment. Domain HWH is proud to be an Equal Opportunity Employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. Employment with Domain HWH is at-will, meaning either the employee or employer may terminate the relationship at any time with or without cause and with or without notice, except as provided by law. If you require an accommodation to apply for or interview for a position, please contact our Human Resources Department at ************ **********************************

About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to the core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals Inc., Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Research Chemist (E&L) We are seeking an experienced Research Chemist (E&L) with a minimum of 3-5 years of pharmaceutical industry experience. Responsibilities: Maintain, operate, and troubleshoot LC-MS and GC-MS, GC-FID, and ICP-MS Systems. Perform extraction, analysis, and characterization of extractables and leachables from polymeric materials associated with container closure systems of pharmaceutical drug products as per USP, PQRI, ICH and other regulatory guidelines. Develop and optimize sample preparation techniques for analysis on GC-MS, LC-MS, and ICP-MS systems. Develop and validate LC-MS, GC-MS, and ICP-MS methods for finished product and raw material characterization as well as extractable/leachable testing. Unknown impurity identifications using GC-MS, LC-MS, and LC-MS/MS or other suitable techniques. Interpret complex spectral data and fragmentation patterns. Routine stability testing of API, finished product samples for assay and impurities using various instrumental techniques as suited, and prepare stability data summaries. Generate study designs, write protocols, methods, Datasheets and reports. Provide support in the critical review of analytical data, reports and protocols. Write Instrument-related SOPs and provide training on the instrument and related software. Train new recruits in the lab and support the team as needed. Participate in internal meetings and conferences. Provide support during technical transfer between R&D and QC. Whenever needed, attend SOP, Safety, and scientific trainings to remain current with cGMP regulations, safety standards, and development technologies. Preparation and review of analytical methods, method validation, and related study reports for ANDA/ NDA submissions and support, document preparation for ANDA/ NDA submissions. Any other activities as directed by the supervisor. Qualifications: Education/Experience: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. Knowledge, Skills, and Abilities: Familiarity with the characterization and isolation of impurities. Strong foundation in organic chemistry and structural elucidation, with expertise in small molecule pharmaceutical drug development and peptides, including computational techniques. Proficiency in using standard laboratory equipment, including pipettes, graduated cylinders, and balances. Skilled in laboratory techniques for measuring, weighing, and handling samples. Hands-on experience with HPLC (highly preferred). Knowledge of chemical handling procedures, including safety precautions and documentation such as Safety Data Sheets (SDS). Competency in Microsoft Office applications. Experience or familiarity with current Good Manufacturing Practices (cGMP) is preferred. Requirements: Must live or be willing to move to the Sacramento Metropolitan Region (Approximately 40 miles' radius) Benefits: Pay range $70,000 - $85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401 (k) savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment o retaliation based on any of these factors.