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Job DescriptionSalary: $26-$28 Hourly NURA is seeking a Quality Analyst to help our growing team. Primary responsibilities will be inspecting and testing raw materials to meet our quality standards to include maintaining our lab equipment, ensuring proper calibration and functionality. Other key responsibilities are listed below. The ideal candidate will demonstrate professionalism and tact and reacts well under pressure. Must adapt to changing work environments and able to deal with frequent changes, delays and unexpected events. Primary Responsibilities: • Prepare raw material samples for testing by following standard operating procedures for sample collection., • Inspect and test raw materials to ensure they meet quality standards and specifications., • Operate and maintain laboratory equipment, ensuring proper calibration and functionality., • Perform various physical testing and analyses on raw material, including but not limited to: FTIR, Bulk and Tapped Density, Particle Size, and Organoleptic analysis., • Prepare and send samples to external labs, ensuring proper documentation and adherence to submission guidelines., • Track and manage the status of third-party testing, including timelines, costs, and results., • Oversee the preparation and handling of samples for third party testing, ensuring proper labeling and storage., • Ensure that samples meet all criteria including but not limited to test method before being dispatched for outsource testing., • Document and maintain testing results accurately., • Review and interpret internal and third-party data against technical data, specifications, and/or related quality documents to maintain product quality and accelerate material qualification process., • Identify and report deviations from quality standards and recommend corrective actions., • Ensure all documentation complies with company policies and procedures., • Prepare and maintain standard operating procedures for quality control processes., • Assist in the development and validation of new test methods and procedures, • Maintain a clean and organized laboratory environment., • Perform routine maintenance and calibration of laboratory instruments and equipment., • Minimum Associate, Bachelors Degree (preferred) in the sciences relating to Chemistry, Biology, or Food Science, • Previous work experience in GMP regulated manufacturing facility, or laboratory preferred., • High attention to detail, and meticulous adherence to hygienic practices a must., • Efficiency with Microsoft Word and Excel a must., • Ethics: Treats people with respect and upholds organizational values., • Adaptability Adapts to changes in work environment; able to deal with frequent changes, delays, or unexpected events and handle multiple tasks simultaneously., • Initiative Volunteers readily, undertakes self-development activities, seeks increased responsibilities; asks for and offers help when needed, ensures key responsibilities are completed every day., • Professionalism Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration; follows through on commitments; self-sufficient and accountable.

Job Description Position Summary: The Biology Department at Concordia University Irvine seeks applicants for adjunct faculty positions in the area of Human Anatomy & Physiology. The department strives to develop wise and honorable citizens capable of excelling as witnesses of Christ through their various roles within the academic field and elsewhere. Pursuant to this mission, we seek faculty candidates who can articulate the interconnection between their Christian faith and their academic pursuits. Essential Duties and Responsibilities include: • Teaching in-person courses and labs in Human Anatomy and Physiology, Bio 246 & 247. See CUI Course Catalog for descriptions, • Conducting office hours, working with full-time faculty colleagues and attending department meetings as available, • Successful candidates must: 1) confess the Christian faith 2) demonstrate a commitment to a Lutheran liberal arts education and 3) demonstrate an excellence in teaching subject matter on Human Anatomy & Physiology, • Possess a doctorate or a master's degree in a relevant field Job Posted by ApplicantPro

Job DescriptionPosition Overview: We are seeking a passionate and knowledgeable Biology Instructor to join our academic team in a part-time on-site teaching role. The ideal candidate will have a strong foundation in the biological sciences and experience teaching high school or college-level Biology, including AP Biology. This role offers the flexibility to teach in-person, empowering students to engage with science through inquiry, experimentation, and real-world application. Key Responsibilities: • Deliver high-quality instruction in Biology—including General and AP Biology—through a combination of live teaching sessions and asynchronous content on platforms such as Canvas, • Implement provided curriculum materials and lesson plans, with thoughtful adaptations to support diverse learner needs and academic objectives, • Assess student understanding through quizzes, lab activities, tests, and projects; provide timely, constructive feedback to guide improvement, • Promote scientific thinking and inquiry through hands-on lab simulations, collaborative group work, and interactive class discussions, • Monitor student progress, attendance, and engagement; communicate proactively with students and academic staff regarding performance and support strategies, • Participate in professional development opportunities, instructional planning sessions, and classroom observation processes to enhance teaching practice, • Collaborate with faculty and academic support staff to align instruction with cross-disciplinary learning outcomes and school-wide goalsRequired:, • Bachelor’s degree or higher in Biology, Life Sciences, or a closely related field, • Minimum of two years of teaching experience in a U.S. high school or college setting, • Demonstrated experience teaching Biology or AP Biology in in-person, hybrid, or virtual formats, • Strong communication, instructional, and classroom management skills

Job DescriptionNRC Research Institute has been conducting clinical trials for pharmaceutical and biotech companies since 2004. We specialize in pharmaceutical clinical trials involving Central Nervous System disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism and numerous medical indications in Rheumatology and Vaccine development. We are looking for an energetic and experienced Clinical Research Coordinator (CRC) to join our team at our Orange location. The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments. Job Duties: • Perform study procedures in accordance with GCP and study protocols, • Coordinate protocol related research procedures, study visits, and follow-up care, • Organize and maintain paper and electronic study data in a complete and correct manner, • Work closely with recruitment and prescreening teams to meet study enrollment goals, • Adhere to an IRB approved protocol, • Participate in the informed consent process of study subjects, • Support the safety of clinical research patients/research participants, • Maintain study source documents, • Report adverse events, • Educate subjects and family on the protocol, study intervention, study drug, etc., • Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, • Complete case report forms (paper & electronic data capture) and address queries, • Facilitate study initiation, monitoring visits, and close out activities, • Retain records/archive documents after study close out, • Requires effective writing and communication, work as part of a team, ability to multitask, • Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals, • Document investigational product (drug/device) accountability Qualifications: • Minimum three year of comprehensive pharmaceutical clinical research coordinator experience, • Bachelor’s Degree and/or healthcare licensure/certification required; degree in Biology and/or Psychology field preferred, • Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population, • Must have ability to read and understand clinical trial protocols, • Must have attention to detail and the ability to handle multiple tasks with precision, • Must be adept with computers, • Must possess excellent critical thinking skill, • Must have excellent interpersonal and communication skills and be a hardworking team player, • Must possess strong data management skills, • Familiarity with medical terminology/environment required Compensation: min $75,000-$100,000 - DOE Health, dental, and vision insurance, 401(k), and other benefits are available for eligible full-time employees. This is a full-time onsite position (40 hrs/week). Hours are Mon-Fri, 8:30 am - 5:30 pm

Job Description QC Manager - Simply Biotech Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below. Immediate opening for a QC Manager in Anaheim, CA who possess: • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field. (MUST be able to pass education verification), • Minimum 5–7 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role., • Experience in a cGMP-compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred. Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards. Email resumes to or call 858.633.2357. FULL DESCRIPTION: The QA/QC Manager is responsible for overseeing the Quality Assurance and Quality Control functions across all manufacturing activities. This role ensures that products meet internal specifications, customer requirements, and regulatory standards. The QA/QC Manager will lead the implementation and continuous improvement of the Quality Management System (QMS), supervise quality staff, and serve as the primary contact for audits and compliance issues. The selected candidate will be responsible for: • Lead the QA and QC teams, including training, development, and performance management., • Develop, implement, and maintain a robust Quality Management System in compliance with GMP, FDA, ISO 22716, and customer standards., • Oversee all quality-related activities, including raw material testing, in-process checks, customer component AQL, finished goods inspection, and batch record review., • Investigate and resolve quality issues including non-conformances, deviations, customer complaints, CAPAs, and root cause analyses., • Ensure timely review and approval of production and laboratory documentation to support product release., • Manage internal audits, coordinate external audits (including customer and regulatory), and ensure timely resolution of findings., • Partner with R&D, Regulatory, Production, and Supply Chain to support product development, scale-up, and commercialization., • Maintain and report quality metrics (KPIs) and drive continuous improvement initiatives., • Ensure calibration and maintenance of lab equipment and oversee environmental monitoring and cleaning validation, if applicable., • Stay current with changes in regulatory requirements and ensure company compliance. The selected candidate will also possess: • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field., • Minimum 5–7 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role., • Experience in a cGMP-compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred., • Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards., • Strong leadership, problem-solving, and communication skills., • Experience with QMS platforms, LIMS, and document control systems preferred., • Ability to manage multiple priorities and thrive in a fast-paced, deadline-driven environment. Salary Range: $100k-120k/yr For immediate and confidential consideration, please email your resume to or call 858.633.2357. More information can be found at Company DescriptionSimply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2022, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, TalentZok is expanding to new markets and hiring additional staff in existing offices.Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2022, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, TalentZok is expanding to new markets and hiring additional staff in existing offices.

Job Description Direct Counsel is partnering with a distinguished American international law firm to find a midlevel associate with 1–5 years of patent prosecution experience in biotechnology. The ideal candidate will have an advanced degree—preferably a Ph.D.—in a life sciences field such as molecular biology, immunology, biochemistry, or cell biology. This position involves working closely with emerging companies on patent prosecution and strategic IP counseling, particularly in cutting-edge areas like antibodies, DNA/RNA therapeutics, chemical biology, and gene-editing technologies. Qualifications: * 1–5 years of biotech patent prosecution experience * Advanced degree (Ph.D. preferred) in a life sciences discipline * USPTO Registration Number (Patent Bar membership) is required * Candidates must pass the patent bar exam either prior to joining or within the first 12 months of employment

Job DescriptionFirstCarbon Solutions (FCS), an ADEC Innovation, is focused on improving the world we live in by advancing sustainable practices globally. It's our goal to improve the lives of all the people we work with, whether they are clients, partners, or colleagues. We are seeking an Assistant Project Manager (CG04/CG05) who will assist managers with researching, writing, and preparing sections of environmental (CEQA/NEPA) and planning documents. This includes initial studies, environmental impact reports, environmental notices, and coordination through the environmental process. The Assistant Project Manager will also assist project managers with managing, processing, financial, and administrative functions, ensuring projects meet scopes, schedules, and budgets to client satisfaction. This position requires a minimum of three years of related experience. This role reports to the Project Manager Duties and Responsibilities • Assist project managers with the preparation of sections of initial studies, environmental impact reports, and other related CEQA/NEPA documents for both public and private clients., • Support project managers with team coordination including, but not limited to, internal meetings, client meetings, and public presentations and ensure that projects are completed on time and on budget., • Assist with the coordination of internal technical teams and sub-consultants., • Expand knowledge of environmental documentation through attendance at training sessions and courses, • Perform research, analysis, and writing of project conditions, impacts, and mitigation efficiently and present in a concise and professional manner, • Perform some coordination with public and private groups, • Conduct fieldwork, including site visits for environmental information and photos, • Assist in the preparation of proposals, statements of qualifications, as well as marketing materials, • Effective communication through written and oral methods, • Promote teamwork through interpersonal skills, • Demonstrate organizational skills, • Demonstrate proficiency in MS Office software applications, especially Word and Excel, as well as internet usage, • Bachelor's degree in Environmental Sciences, Planning, Geography, Biology, or a related field preferred, • 3+ years of related work experience, • Working knowledge of CEQA and its processing requirements, • General understanding of NEPA The position operates in either an in-office or remote home office environment. This role routinely uses standard office equipment. This position may require travel to attend meetings, briefings, hearings, and presentations. Compliance with all travel and in-person requirements is a must. Physical Demands The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. While performing the duties of this job, the employee may spend extended periods of time sitting in front of the computer. The position regularly requires talking and hearing, standing, stooping, walking, reaching with hands and arms, and hand/finger dexterity. Specific vision abilities required by this job include close vision, distance vision, and the ability to adjust focus. Compensation: $27.00 - $40.00 Hourly We offer competitive salaries based on location, experience, and education. Our comprehensive benefits also include personal and professional development opportunities for qualified employees. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply! Competitive, progressive benefits, including Example: Full-time, regular employee • Up to 100% employer paid premiums employee medical (with buy-up options) and up to 55% coverage for eligible dependent(s), • Up to 80% employer-paid dental and vision covered premiums for employees. Eligible dependent coverage also available., • Employer sponsored Group Life and AD&D insurance with discounted voluntary coverage also available, • Employer covered Short- & Long-Term Disability insurance, • Employee Assistance & Wellness Programs (EAP), • 401(k) & Roth retirement savings accounts (see HR department for details on contributions and exclusions), • Pet insurance discounts, • Volunteer programs, committees, and opportunities Information Security Adhering to all policies, guidelines, and procedures pertaining to the protection of information of the organization, employees must maintain confidentiality of all sensitive information to which they are given access. They are also responsible for reporting actual or suspected events or incidents, including vulnerabilities or breaches, that may affect the confidentiality, integrity, and availability of information to members of the Management Team. Mutual respect is fundamental. Fundamental to our teams. Fundamental to our clients. Fundamental to the communities we serve and live in. Fundamental to the landscapes we work within. We need you and your unique talents, history, and background to become the Company we aspire to be. We insist upon a culture of common respect, expect transparency, and celebrate the fundamental value and dignity of all individuals. Our mutual equality as humans is the path to innovative collaboration. We cultivate integrity, driving us to growth, and allowing us to achieve more together than we could ever hope to as individuals.

Job DescriptionBenefits: • Competitive salary, • Flexible schedule Position Overview: We are seeking an enthusiastic and experienced high school science teacher to join our dynamic faculty team. The ideal candidate should have a rich background in science, capable of teaching various courses including AP Physics 1: Algebra-Based, AP Physics 2: Algebra-Based, Physics, Honors Physics, AP Physics C: Mechanics, AP Physics C: Electricity and Magnetism, Biology, AP Biology, Chemistry, AP Chemistry, Environmental Studies, or AP Environmental Science. The candidate should demonstrate a commitment to fostering an inclusive and engaging learning environment while promoting critical thinking, analytical skills, and effective communication among students. Responsibilities: • Plan, prepare, and deliver engaging and challenging lessons aligned with the curriculum standards and objectives of the assigned science courses., • Establish a supportive and inclusive classroom environment, encouraging student participation, collaboration, and respect for diverse perspectives., • Meet the diverse learning needs and abilities of students, including those with special needs and English language learners, through various teaching methods., • Assess student learning through various forms of formative and summative assessments, providing timely and constructive feedback to support their academic growth., • Implement effective classroom management strategies, maintaining a positive and orderly learning environment conducive to student success., • Collaborate with colleagues to develop interdisciplinary units, share best practices, and align teaching strategies across grade levels and subject areas., • Stay updated on developments in the field of science education, including new teaching methods, educational technologies, and relevant research., • Participate in professional development opportunities, teacher meetings, and school activities., • Fulfill other duties and responsibilities assigned by the school administration.Qualifications:, • Bachelor's degree in Science, Education, or a related field; master's degree preferred., • Valid teaching certificate/license in secondary Science (or equivalent)., • At least two years of teaching experience at the high school level within the past two years, demonstrating effectiveness in teaching science., • Familiarity with various teaching strategies, assessment techniques, and educational technologies to support student learning and engagement., • Strong interpersonal and communication skills, able to collaborate effectively with colleagues, students, parents, and other stakeholders., • Commitment to diversity, equity, and inclusion in education, with the ability to create inclusive and supportive learning environments for all students., • Passion for science, education, and the teaching profession, genuinely aiming to inspire and empower students to become lifelong learners and critical thinkers., • Flexibility, adaptability, and willingness to embrace new challenges and opportunities for professional development., • Compliance with all relevant state and federal regulations regarding education and child welfare., • Salary: Starting at $40/hourly. Depending on experience.

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description The Principal Scientist I in the Tissue Materials Science group is responsible for directing research and/or project activities and professional development of a group of scientists within TMS by effectively mentoring, guiding and/or supervising scientific personnel. He/She/They independently conceive, execute and communicate novel multi-disciplinary research or development strategies that achieve project for the Fillers device franchise, including Juvéderm and Next Generation Dermal Fillers, pre-concept (early research) and new model development. The focus of such studies will be to evaluate the interaction of current and future medical devices with cells and tissues for purposes of establishing device proof of concept, completing regulatory submission-related studies (ISO 10993), performing life cycle compliance-related activities, and developing scientific messaging for advertising/promotional support. This individual is expected to be a team leader and engage key stakeholders, including global strategic marketing, medical affairs, regulatory affairs, clinical development, and publication planning to successfully achieve project goals. The individual serves as a lead scientist on his/her/their own project and contribute scientific insights into multiple other projects. The Principal Research Scientist I may mentor/supervise a team of one or more direct reports and evaluate the performance of those individuals. Additionally, the individual is accountable for the effective performance of the team/individuals. Key Duties / Responsibilities SCIENTIFIC LEADERSHIP • Function as a principle investigator/lead, generating original technical ideas and research or development strategies., • Represents TMS in cross functional teams to provide technical leadership for design, analysis and reporting for pre-concept or development programs and drive alignment with functional management., • Authors publications, presentations and/or primary inventor of patents., • Serve as a technical advisor and subject matter expert in his/her/their discipline., • May be required to mentor/train/manage junior staff in a matrix based organization or as part of a project team. SCIENTIFIC EXECUTION • Demonstrate creative “out of the box” thinking to solve difficult problems and champion new technologies to achieve project goals., • Develops and executes in vitro, in vivo and tissue processing methods to support development of novel medical device/tissue products., • Critically evaluate scientific or regulatory advances, competitive threats or business development opportunities. SCIENTIFIC COMMUNICATION • Serves as a technical advisor and subject matter expert in his/her/their discipline to management and internal customers, driving alignment with cross-functional Asset teams and management for activities and deliverables., • May contribute to publications, regulatory documents and inventions and present at external conferences., • Provides regular updates to manager and project teams, contributes and prepares technical reports for the department and management as needed. CROSS-FUNCTIONAL TEAM REPRESENTATION • Critical team member in Asset Strategy, involved in developing project strategy, • Serves as TMS representative on Asset teams, Strategy teams and product development subteams, providing expertise in areas of tissue responses to Fillers., • Supports Design Control activities as the non-clinical representative on development teams with minimal guidance., • Organizes, schedules, and participates in project team meetings to define and schedule project activities and review completed tasks., • Communicates project status to supervisor, project team leader, other research managers, and R&D committees as appropriate., • Prepares time and cost estimates of project activities for review by manager to achieve realistic project completion dates Qualifications Education and Experience • Ph.D. and a minimum of 6+ years of industry experience OR Master’s degree and 12+ years of industry experience OR BS and 14+ years of industry experience;. Degree in a related scientific or engineering discipline (cell biology, molecular biology, pharmacology, immunology, bioengineering, or similar), • Medical device experience or experience in a regulated environment is preferred., • Experience in a medical device, pharmaceutical, or related setting with a proven record of success in conducting R&D projects, • Experience and working knowledge of medical device, drug and/or biologics, and combination product regulations (21 CFR 820, 21 CFR 210/211, 21 CFR Part 4, Biologics, etc.), • Experience managing outsourced research activities, • Experience managing in vivo and in vitro research activities, • Working knowledge of biocompatibility testing requirements (ISO 10993), • Experience conducting/managing biocompatibility studies is a plus, • Technical report writing proficiency in support of regulatory submissions, • Expertise in small / large animal model study performance and imaging, • Creativity, strong verbal and written communication skills, strong scientific leadership skills, ability to work effectively in independent and team settings, and acute attention to detail are essential skills for this position, • Able to multitask and work within timelines., • Able to build strong relationships with peers and cross-functional partners to achieve higher performance. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. * This job is eligible to participate in our long-term incentive programs Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job Description JOB DESCRIPTION We are looking to hire an experienced Science instructor to provide instruction in science-related subjects ranging from Elementary School Science to High School AP Level Science. Your role is to provide instruction, create lesson plans, facilitate classroom discussions, evaluate student performance, and promote a positive learning environment. You will teach various science disciplines such as Biology, Chemistry, and Physics. JOB DUTIES: • Develop and implement engaging and comprehensive lesson plans, • Demonstrate adaptability in teaching both one-on-one and in small group settings., • Assess students progress through regular evaluations, including tests, assignments, and participation and provide constructive feedback to the students, • Communicate regularly with Masterprep Admin and Staff on student progress, • Prepare students for their AP Exams, • Provide homework help as needed, • Prepare students for science competitions QUALIFICATIONS: • Bachelor's degree in Science or related field from an accredited college or university (required), • Master's degree in Science or related field from an accredited college or university (preferred), • 2 years' experience as a Science instructor or tutor (required), • Knowledgeable with AP Science (Bio, Chem and Physics) content and tests, • Science competition knowledge (preferred), • Professional communication skills (both spoken and written), • Proven experience assisting students with essay review, • Competent in Microsoft Office products (Word, Excel, PowerPoint, etc.), • Able to work independently and collaborate with a team, • Enthusiastic about working with students and parents, • Able to maintain strict confidentiality, • Highly organized and detail-oriented (attention to detail and accuracy are imperative), • Ability to meet schedules and deadlines, • Good judgment and decision-making abilities, • Good problem-solving skills, • Good planning skills, • Highly responsive, • Highly proactive, • Highly reliable, • Integrity Possible shifts are between M-F 3pm - 8pm and Saturday 9am - 5pm

Job Description Autonomous Medical Devices Incorporated (AMDI) is a California-based company employing a world class team of engineers, scientists, clinicians, manufacturing and quality/regulatory experts dedicated to the development and manufacture of best in class diagnostic devices using innovative technology, factory automation, and cloud connectivity. AMDI is headquartered in Santa Ana, CA where it manufactures the Fast PCR Mini Respiratory Panel in an ISO:13485 / MDSAP certified 110,000 square foot facility. Summary of Position Are you a curious and analytical professional with a passion for research and discovery? We're looking for a Research Associate to join our team! The Research Associate will be part of the Molecular Research and Development department as part of a collaborative team to assist in the development of new molecular diagnostic technologies and procedures. The candidate must be detail oriented to help plan, execute, and analyze basic molecular biology experiments including PCR, RT-PCR, and nucleic acid extraction. Location: This is an onsite position located at our Santa Ana, CA office. Candidates living within a 25 mile range preferred. Essential Duties and Responsibilities • Understanding of general practices and biohazards associated with performing molecular biology procedures in BSL-2 laboratories, • Ability to work in a fast-paced environment with deadline-driven workflows, • Prepares reagents and solutions as directed, using appropriate procedural and documentation methods, • Design of simple to moderate experiments (with assistance of experienced colleagues), • Execute various PCR-based experiments and analysis of raw data generated, • Provide written and/or oral updates to the team regarding data, progress, technical issues, etc., • Recording of experimental data in a lab notebook following good laboratory notebook practices to ensure proper traceability, • Coordinate and maintain inventory of critical lab reagents and supplies and laboratory equipment, • Assist other colleagues with additional laboratory work as needed, • Assist with other tasks as needed Qualifications Required for Position • Bachelor’s degree in Biology, Chemistry, Bioengineering, or equivalent degree, • Knowledge in Molecular Biology, Chemistry, or related field, • Minimum of 2 years experience in a biological or wet lab environment, preferably with industry experience in a molecular lab, • Hands-on experience with nucleic acid preparation, amplification and detection technologies using proper unidirectional molecular laboratory workflow., • Trained in Good Laboratory Practices (GLP) Desired skills and traits • Cooperative team player with a positive attitude and solid work ethic, • Sets specific goals and objectives to complete tasks on-time in an organized manner, • Effectively communicates in both written and oral presentations on data generated, • Excellent attention to detail, record keeping and a passion for accuracy and precision Work Environment • In-person position that requires working indoors in a BSL2 facility and testing laboratory environment. Autonomous Medical Device Incorporated offers a comprehensive compensation and benefits package to eligible employees including: • Company provided lunch to all employees when working at one of AMDI’s on-site locations., • 401(k) match, • Health insurance, 100% paid for by employer including: Medical, Dental, Vision & Life Insurance, • Competitive vacation, sick days & paid holidays, • Tuition reimbursement, • Casual dress code, • Employee discounts on activities such as theme parks, movie theaters, hotels, rental cars, etc., • Monthly company-wide socials and activities Autonomous Medical Devices Incorporated (AMDI) will not accept unsolicited resumes from any source other than directly from a candidate. An Agency must obtain advance written approval from AMDI’s internal Human Resources team to submit resumes only in conjunction with approved valid fully executed contracts. Our commitment to an inclusive workplace: We are an equal opportunity employer and encourage people from all backgrounds to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other protected characteristic under federal, state, or local law. Powered by JazzHR mkQLPEfcT7

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description • Manages the day to day operation of the microbiology department to insure smooth flow of samples and testing, • Provides laboratory operations leadership, • Hires, coaches, reviews, manages, and terminates assigned staff, • Prioritizes daily operational activities, • Ensures all quality control systems are operational and in force in all operations within scope, • Oversees the scheduling of microbiology staff to insure production schedules are met, • Maintains staffing to achieve workload goals by adjusting personnel to meet peak demands, • Ensures Key Performance Indicators (KPI's) are in place, relevant, and continually evaluated, • Prepares for and facilitates periodic customer or regulatory audits of all laboratories within scope, • Maintains current knowledge of industry standards and regulatory environment, • Reviews and approves SOPs, • Actively participates in strategic planning, • Provides method development leadership and oversight, • Builds and maintains positive client relationships, • Ensures client satisfaction, • Counsels microbiology staff with regard to problems encountered in daily operations, • Oversees the checking and transfer of microbiology data as necessary and takes steps to correct possibly inaccurate data prior to continued processing or release, • Oversees the orientation of new microbiology staff to their responsibilities and the function of the microbiology department, • Conducts timely investigations in coordination with Quality Assurance related to site quality events, including, but not limited to customer complaints, inquiries, non-conformances, corrective actions, and audit findings, • Identifies process improvements to better meet client expectations and company objectives, • Recommends new equipment for the microbiology department, • Compiles statistics, • Oversees the monitoring of inventory/ordering by establishing and maintaining par levels and re-stocking points for microbiology supplies and reagents, • Serves as a liaison for the department to outside vendors, • Assists in capital budgeting and execution, • Understands costs of testing and how to calculate them, • Initiates advances in methodology and/or technology use, • Interface with and represent laboratory operations to local, state, and federal regulators as required from time to time, • Performs duties in compliance with all applicable regulatory and accrediting agencies and cGMP expectations, including but not limited to: Facility and equipment maintenance, validation review and approval, training (internal, continuing education, proficiency testing, annual GMP, etc.), • Performs annual reviews and creates and maintains job plans, • Executes human resources management functions as required for laboratory staff within scopeQualifications The ideal candidate would possess: • Considerable knowledge of the methods, materials, equipment, and techniques used in microbiology testing, • Demonstrated success in improving operational, quality, and safety performance, • Strong problem solving skills, • Ability to organize, communicate, teach, and work with others in an effective manner, • Knowledge of federal, state, and local standards, regulations, guidelines and requirements effecting operations of a clinical reference laboratory, • Ability to manage and schedule the work of others, • Bachelors of Science degree in Biology or similar field required, • Minimum 5 years of experience in Microbiology, • Minimum 2 years in supervisory experience, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is Full-Time, Monday- Friday, 11am-7:30pm with additional hours/days, as needed. Candidates currently living in a commutable distance to Tustin, CA. are encouraged to apply. Pay Rate: $68,640k/Yr. - $78k/Yr. • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionBenefits: • 401(k), • Competitive salary, • Dental insurance, • Health insurance, • Paid time off Position Overview: We are seeking an enthusiastic and experienced high school science teacher to join our dynamic faculty team. The ideal candidate should have a rich background in science, capable of teaching various courses including AP Physics 1: Algebra-Based, AP Physics 2: Algebra-Based, Physics, Honors Physics, AP Physics C: Mechanics, AP Physics C: Electricity and Magnetism, Biology, AP Biology, Chemistry, AP Chemistry, Environmental Studies, or AP Environmental Science. The candidate should demonstrate a commitment to fostering an inclusive and engaging learning environment while promoting critical thinking, analytical skills, and effective communication among students. Responsibilities: • Plan, prepare, and deliver engaging and challenging lessons aligned with the curriculum standards and objectives of the assigned science courses., • Establish a supportive and inclusive classroom environment, encouraging student participation, collaboration, and respect for diverse perspectives., • Meet the diverse learning needs and abilities of students, including those with special needs and English language learners, through various teaching methods., • Assess student learning through various forms of formative and summative assessments, providing timely and constructive feedback to support their academic growth., • Implement effective classroom management strategies, maintaining a positive and orderly learning environment conducive to student success., • Collaborate with colleagues to develop interdisciplinary units, share best practices, and align teaching strategies across grade levels and subject areas., • Stay updated on developments in the field of science education, including new teaching methods, educational technologies, and relevant research., • Participate in professional development opportunities, teacher meetings, and school activities., • Fulfill other duties and responsibilities assigned by the school administration.Qualifications:, • Bachelor's degree in Science, Education, or a related field; master's degree preferred., • Valid teaching certificate/license in secondary Science (Preferred)., • At least two years of teaching experience at the high school level within the past two years, demonstrating effectiveness in teaching science(Preferred)., • Familiarity with various teaching strategies, assessment techniques, and educational technologies to support student learning and engagement., • Strong interpersonal and communication skills, able to collaborate effectively with colleagues, students, parents, and other stakeholders., • Commitment to diversity, equity, and inclusion in education, with the ability to create inclusive and supportive learning environments for all students., • Passion for science, education, and the teaching profession, genuinely aiming to inspire and empower students to become lifelong learners and critical thinkers.

Job Description About the Role Life IVF Center is seeking a motivated and capable Trainee Biologist / Andrologist to join our world-class IVF and Embryology Laboratory team. This is a high-impact role designed for candidates passionate about reproductive health, laboratory excellence, and long-term career growth in embryology and clinical science. You’ll work closely with our physicians, nurses, and scientists in one of the top IVF programs in California, gaining hands-on training in clinical embryology and andrology procedures. High-performing team members may be selected to advance to full embryology training. Why Join Life IVF Center • Comprehensive training program with long-term growth opportunities, • Work in a cutting-edge laboratory using advanced reproductive technologies, • Supportive and collaborative team culture focused on excellence and innovation Benefits • Health, dental, and vision insurance, • Paid time off and sick days, • 401(k) plan for tenured employees, • Company events, trips, and team banquets, • Leadership and professional development opportunities Qualifications • Minimum 1 year of experience in an embryology or related clinical laboratory (human preferred), • Bachelor’s degree in Biology, Biochemistry, or a related health science field (graduate degree preferred but not required), • Must be authorized to work in the U.S., • Seeking a long-term career in reproductive laboratory science, • Willingness to train primarily at our Irvine headquarters for several months, • Familiarity with EMR software and Microsoft Excel preferred Key Responsibilities • Assist embryologists in ART procedures including:, • Oocyte retrieval, • In-vitro fertilization (IVF) and ICSI, • Embryo culture, cryopreservation, thawing, and assisted hatching, • Embryo transfer preparation, • Perform andrology procedures such as:, • Sperm isolation (MESA/TESA) and semen washes for IVF/IUI, • Sperm motility analysis and proficiency testing (AAB), • Maintain quality control, safety, and compliance documentation, • Support laboratory operations including reagent preparation, equipment maintenance, and inventory management, • Ensure compliance with CLIA, OSHA, FDA, CAP, and Tissue Bank standards Core Laboratory Skillset • Sperm wash and all andrology duties, • Egg retrieval support, • Daily quality control and dish setup, • ICSI procedure assistance, • Embryo freezing and thawing Schedule • Full-time position, 5–6 days per week (Monday–Saturday), • Shorter daily hours compared to traditional full-time schedules, • Sundays off; occasional flexibility for five-day workweeks Ideal Candidate • Warm, professional demeanor and strong desire to help patients, • Detail-oriented and highly organized, • Fast learner with strong communication skills, • Team-oriented with a growth mindset, • Proactive, dependable, and committed to quality and precision Related Keywords Biologist, Clinical Biologist, Embryologist, Embryology, IVF Laboratory, Medical Laboratory Technician, Andrologist, Andrology, Reproductive Science, Sperm Wash Company DescriptionLife IVF Center is a nationally acclaimed fertility program, helping thousands build the family of their dreams. Located in Southern California, we specialize in Precision IVF®, offering our patients accessible treatment tailored to their needs and circumstances with high rates of success and reduced reliance on medication. We pride ourselves on our outstanding patient results, strong team atmosphere, and culture of continual improvement.Life IVF Center is a nationally acclaimed fertility program, helping thousands build the family of their dreams. Located in Southern California, we specialize in Precision IVF®, offering our patients accessible treatment tailored to their needs and circumstances with high rates of success and reduced reliance on medication. We pride ourselves on our outstanding patient results, strong team atmosphere, and culture of continual improvement.

Job Description Responsible for ensuring that the test(s) requested by physicians and facilities are performed in an accurate and timely manner and the Laboratory policies and procedures are followed and implemented correctly. • Follows the laboratory’s procedures for specimen handling and processing analysis, reporting and maintaining records of patient test results., • Ensuring that the patient’s name and specimen number are correctly identified., • Type of specimen and time drawn is correct for the test ordered., • Specimen integrity has been maintained from the initial draw / pick-up of specimen(s) until arrival and completion of test(s) requested., • Follows the laboratory’s procedures for handling potentially infectious materials., • Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient samples., • Adheres to the laboratory’s quality control policies, documents all quality control activities instrument and procedural calibrations and maintenance performed., • Follows the laboratory’s quality control policies whenever test systems are not within the laboratory’s established levels of performance., • Capable of identifying problems that may adversely affect test performance or reporting of test results., • Documents all corrective action taken when test systems deviate from the laboratory’s established performance specifications., • Documents all corrective action taken when test systems deviate from the laboratory’s established performance specifications., • Performs all routine and new test procedures that are complex and require professional judgment when assigned to a specific area., • Demonstrates knowledge of theory behind the test performed., • Recognized departure from the norm on adult and geriatric patients and be able to understand the scientific and theoretical reasons for such deviation., • Calibrates instruments and assess the accuracy of the equipment; performs equipment preventive and corrective maintenance., • Check and verify all the test results released by the laboratory. This includes accepting or rejecting results due to delta check inconsistencies, requesting redraw for verification, canceling results due to gross hemolysis, clots or QNS., • Reviews outgoing reports for technical and clerical errors., • Able to communicate with nurses and physicians, and ability to work well with others., • Assist the Lead CLS in maintaining adequate supplies and inventory levels., • Demonstrates the ability to prioritize work duties., • Recognizes the administrative changes in staffing and scheduling and adapt to these changes., • Assists in developing and installing quality control standards to ensure accuracy of test results., • Assists the Lead CLS in reviewing and solving quality control problems., • Initiates, suggests and if necessary, implements technical and administrative changes upon approval of the Laboratory Director. EXPERIENCE / SKILLS REQUIRED • Bachelor’s degree from an accredited college or university with major coursework in medical technology, microbiology, chemistry, biology or related field., • Possession of General Supervisor license issued by the State of California, • Must meet CLIA requirements for testing personnel for High Complexity Testing., • Ability to work independently and have good sound analytical judgment to function effectively under stress in certain situations., • Strong interpersonal skills sufficient to work closely with others on a team., • Possess the ability to work in a fast- paced environment, effectively interacting with physicians, facilities and laboratory personnel., • Possess speed, consistency and accuracy in tasks to meet the laboratory standards., • Customer service oriented, • Self- starter with a high initiative, a good problem and decision-maker., • Ability to demonstrate flexibility in work environment, performing a variety of changing tasks., • Commitment to tasks. Displaying a high level of cognitive, interpretive or judgment skills.

Job DescriptionJOB DESCRIPTION We are looking to hire an experienced Science instructor to provide instruction in science-related subjects ranging from Elementary School Science to High School AP Level Science. Your role is to provide instruction, create lesson plans, facilitate classroom discussions, evaluate student performance, and promote a positive learning environment. You will teach various science disciplines such as Biology, Chemistry, and Physics. JOB DUTIES: • Develop and implement engaging and comprehensive lesson plans, • Demonstrate adaptability in teaching both one-on-one and in small group settings., • Assess students progress through regular evaluations, including tests, assignments, and participation and provide constructive feedback to the students, • Communicate regularly with Masterprep Admin and Staff on student progress, • Prepare students for their AP Exams, • Provide homework help as needed, • Prepare students for science competitionsQUALIFICATIONS:, • Bachelor's degree in Science or related field from an accredited college or university (required), • Master's degree in Science or related field from an accredited college or university (preferred), • 2 years' experience as a Science instructor or tutor (required), • Knowledgeable with AP Science (Bio, Chem, and/or Physics) content and tests, • Science competition knowledge (preferred), • Professional communication skills (both spoken and written), • Proven experience assisting students with essay review, • Competent in Microsoft Office products (Word, Excel, PowerPoint, etc.), • Able to work independently and collaborate with a team, • Enthusiastic about working with students and parents, • Able to maintain strict confidentiality, • Highly organized and detail-oriented (attention to detail and accuracy are imperative), • Ability to meet schedules and deadlines, • Good judgment and decision-making abilities, • Good problem-solving skills, • Good planning skills, • Highly responsive, • Highly proactive, • Highly reliable, • IntegrityPossible shifts are between M-F 3pm - 8pm and Saturday 9am - 5pm

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description Purpose: The Senior Manager is responsible for leading the sustainment, improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices and combination products. The role serves as Deputy Person Responsible for Regulatory Compliance for assigned Device Legal Manufacturer under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, demonstrating AbbVie quality management system compliance to external regulators, and leading continuous process improvement & globalization initiatives with other cross-functional AbbVie team members. Responsibilities: • Serves as the Deputy Person Responsible for Regulatory Compliance for assigned Device Legal Manufacturer under EU MDR 2017/745, supporting quality management supervision under the direction of the Management Representative., • Hosts External Audits primarily in the US region, demonstrating AbbVie quality management system compliance to external regulators for ISO 13485 and other country-specific device audits under MDSAP., • Conducts Internal Audits to assess the compliance of AbbVie quality management system in accordance with ISO 13485 and other country-specific device regulations under MDSAP., • Leads root cause investigation and corrective action planning in response to external and internal audit observations, in collaboration with departmental process owners and subject matter experts., • Maintains expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products., • Performs regulatory compliance assessments to support the decision-making in critical business decisions, including Market Actions., • Analyzes & interprets quality system performance metrics, presenting to Top Management as part of Management Reviews., • Program manages initiatives intended to improve and globalize the AbbVie quality management system. Qualifications Qualifications • Bachelor’s degree, preferably in engineering, physical science (e.g. Chemistry), life science(e.g. Microbiology or Biology) or pharmacy and a minimum of 8 years of industry experience in a GXP regulated environment, with a minimum 3 years in Quality Assurance Operations Management. A strong technical background is required because the scope of responsibilities is broad and requires the ability to communicate, understand and direct individuals in highly specialized technical fields., • ISO 13485 Lead Auditor certification by a professional body is required. Additional accreditation by a professional body is desirable; examples include American Society of Quality (ASQ) Certified Manager of Quality & Operational Excellence (CMQ-OE), Six Sigma Black Belt Certification, or Project Management Professional (PMP) Certification., • The role operates with a high degree of autonomy & accountability, making independent quality & compliance decisions timely and demonstrating the ability to manage multiple commitments while delivering on-time., • The role also demonstrates an enterprise mindset, being able to influence without direct authority and apply past learnings to novel situations., • Quality Assurance, Quality Control, Regulatory, Manufacturing, Laboratory or Validation background in a GXP regulated environment is required., • Thorough, documented understanding/knowledge of GXP regulations. · Regulatory inspection experience preferably with direct agency inspector interaction., • Must have understanding and ability to anticipate and manage the sensitive nature of proprietary information., • Strong project management skills are essential., • Excellent oral and written communication skills required with the capability of clearly presenting and justifying quality requirements. External Manufacturing Business Relationships, Operations, Third Party Manufacturers Business Alliance, Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, Research and Development. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. * This job is eligible to participate in our long-term incentive programs Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job Description JOB DESCRIPTION We are looking to hire an experienced Science Instructor to be responsible for developing and implementing effective strategies to enhance students' mathematical proficiency. Your expertise will be vital in creating engaging and innovative mathematics curricula, promoting problem-solving skills, and supporting students' academic growth. Science subjects include: High School Biology, Chemistry, and Physics up to AP Levels. This is an exciting opportunity for a passionate and experienced Science Instructor to make a positive impact on our students and their learning goals. This is a Flexible, Part-Time opportunity. JOB DUTIES: • Develop and implement engaging and comprehensive lesson plans, • Demonstrate adaptability in teaching both one-on-one and in small group settings., • Assess students progress through regular evaluations, including tests, assignments, and participation and provide constructive feedback to the students, • Communicate regularly with Masterprep Admin and Staff on student progress, • Prepare students for the AP exam, • Provide homework help as neededQUALIFICATIONS:, • Bachelors degree in Science or any related field (required), • Master's degree in Science or related field from an accredited college or university (preferred), • 1 year experience as a Science instructor or tutor (required), • Successful track record of developing students knowledge in learning Science(required), • Professional communication skills (both spoken and written), • Competent in Microsoft Office products (Word, Excel, PowerPoint, etc.), • Able to work independently and collaborate with a team, • Enthusiastic about working with students and parents, • Able to maintain strict confidentiality, • Highly organized and detail-oriented (attention to detail and accuracy are imperative), • Ability to meet schedules and deadlines, • Good judgment and decision-making abilities, • Good problem-solving skills, • Good planning skills, • Highly responsive, • Highly proactive, • Highly reliable Job Type: Part-time

Job DescriptionCompany Overview: GATC Health is an innovative TechBio company at the forefront of revolutionizing pharmaceutical discovery and accelerating their development through the integration of artificial intelligence (AI), science and finance. Our company is dedicated to advancing therapeutic discoveries and improving human health by leveraging the power of technology and interdisciplinary collaboration. Position Overview: We are seeking a talented Bioinformatics Analyst to join our dynamic, multi-disciplinary team that is responsible for implementing and aiding in design and analysis software and informatics pipelines for primary, secondary, and tertiary analysis of data generated from transcriptional, proteomic, and mult-omic assays. As a Bioinformatics Scientist, you will innovate, develop and implement novel analysis methods for different data types from sparse to large and complex datasets to support the internal development and validation of new pharmaceutical assets and the development of end-user, customer-facing data analysis and visualization for biotech customers and stakeholders. A highly motivated scientist with broad expertise and experience in bioinformatics, computational biology, transcriptomics, proteomics and multi-omics would be an ideal fit for this position. Roles and Responsibilities • Prep and Process data through GATC platform based on customer or internal end user requirements., • Implement primary and secondary analysis tools for GATC’s assays., • Work with cross-disciplinary R&D teams to develop and implement new discovery and risk assessment product applications., • Aid in Development and implementation processes and algorithms for multi-modal datasets, scalable to very large numbers of samples., • Engage with external collaborators on the evaluation of beta version products and analysis of novel data.Role Requirements, • Degree in computational biology, bioinformatics, computer science or similar., • Experience analyzing complex multi-omic datasets, including human or single cell data., • Experience implementing, and evaluating novel bioinformatics algorithms and pipelines., • Experience in programming in scripting (Python or similar) and interpreted languages (R, etc)., • Demonstrated ability to become proficient in new fields and work with interdisciplinary teams., • Excellent verbal/written communication and interpersonal skills with scientist and non-scientists.Role Preferences, • Experience using or interfacing with machine learning algorithms., • Experience analyzing and interpreting large-scale human or single cell datasets., • Experience with professional software development methods and tools in a team environment., • Experience in programming in scripting (Python), interpreted (R ) and compiled languages (C++ / Rust / Java)., • Experience working with collaborators, including lab scientists on multi-omic method development., • Experience visualizing scientific datasets and results., • Experience using cloud computing environments., • Computational biology and bioinformatics innovation.Why Join Us:• Opportunity to work at the intersection of technology and science, driving innovation in pharmaceutical discovery.• Collaborative and inclusive work culture that values diversity, creativity, and continuous learning.• Competitive compensation package, including salary, benefits, and opportunities for professional development.• Chance to make a meaningful impact on human health and contribute to groundbreaking research and development projects. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description Position Summary: The Natural Sciences Department at Concordia University Irvine seeks applicants for adjunct faculty positions in the area of general Biology & Biochemistry. The department strives to develop wise, honorable & cultivated citizens capable of excelling both as effective educators in their field and as witnesses of Christ through their various roles within the academic field and elsewhere. In line with this mission, we are seeking faculty candidates who are knowledgeable and articulate in Biology and Biochemistry, and who are eager to explore the connections between their Christian faith and their academic pursuits alongside colleagues and students. Essential Duties and Responsibilities include: • Teaching introductory and/or upper-division courses in general Biology and Biochemistry such as General Biology I, Biochemistry I and Biochemistry II (See CUI Catalog for details), • Conducting office hours, and working with full-time faculty colleagues, • Successful candidates must confess the Christian faith, demonstrate a commitment to a Lutheran liberal arts education and possess teaching excellence., • Candidates should have earned a doctorate or a master's degree in a relevant field Job Posted by ApplicantPro

Job Description Terra Universal is a leading US manufacturer and supplier of cleanroom and laboratory equipment. We help our customers in high-tech research and manufacturing to transform the world with innovative solutions that improve health, safety and performance. Terra Universal’s diversified customer base includes biotechnology researchers, pharmaceutical manufacturers, semiconductor fabricators, aerospace firms, universities and government entities. Position Overview: This is a business to business inside sales and product specialist position. The Sales Representative develops and manages relationships with our clients and prospects. The individual is responsible for achieving specified sales targets, following up on orders, and prospecting and developing sales towards industries such as life science, biotechnology, pharmaceutical, semi-conductor, aerospace and academic sectors. Responsibilities: • Ensure client retention via responsive and proactive account management support, • Develop knowledge and thorough understanding of all products and services, and apply knowledge to provide appropriate recommendations/ solutions that meets client's business requirements., • Establish and maintain executive level relationships in major functional areas of the customer organization. Utilize the relationships to develop strong revenue growth initiatives., • Manage renewal sales process for existing customer base, including setting of expectations, changing needs assessments, negotiating contracts and processing of contracts via relevant internal systems., • Follow up on all inbound client inquiries to uncover new and expanding sales opportunities., • Bachelor's Degree Required. Science degree preferred (Engineering, Chemistry, Biology). Copy of transcripts and diploma will be requested as part of job application., • Excellent verbal and written communication skills., • Self-motivated with positive attitude., • Ability to work with diverse population and all levels of personnel professionally and effectively., • Must possess organizational, analytical, time management, and problem-solving skills., • Must be detail-oriented and possess the ability to handle multiple tasks simultaneously., • Ability to perform simple algebra/calculations., • Ability to maintain professionalism and confidentiality at all times., • Basic skills in negotiating with clients., • Basic skills with Microsoft Windows, Word, Excel, and Outlook., • Salary depends on experience/qualifications, • Company-subsidized affordable health/dental/vision plans, • Annually, the company provides one week of paid vacation, one week of sick leave (which may be added to vacation time), two floating holidays and 10 paid holidays. Staff members become eligible for these benefits after twelve months of employment.

Job Description We are currently seeking resumes from qualified, responsible, self-sufficient, energetic West Coast Natural Resources Group Manager’s for our Irvine, California office. The ideal candidate will be motivated to develop and build their personal knowledge and skills to assist with the growth and success of the office. We offer a friendly, professional atmosphere with excellent benefits and a salary commensurate with experience. Job Description: As the West Coast Natural Resources Group Manager, this position is to develop and manage natural resource projects from the pursuit and proposal phase through deliverable completion and close-out while mentoring, hiring, and training staff. Along with mentoring and training, this position will monitor staff workloads and progress on assigned projects to ensure that project goals and objectives are accomplished to both internal and external quality expectations. This position will work as a project manager and/or provide technical support on large and small-scale federal, state, and local infrastructure and development and regulatory compliance projects. Projects will require management of NRS staff, inter-discipline coordination, coordination with various engineering disciplines, but may also require management of technical leads in-house and sub-consultants. As a project manager this position plans, directs, manages, primary and reviewer of technical analysis and recommendation documents, oversees and conducts fieldwork (as needed), and provides oversight of projects to ensure that project goals and objectives are accomplished within prescribed schedule and budget parameters. Group Manager Responsibilities: • Manages and completes project tasks, including staff oversight, fieldwork, and deliverables, within schedule and budget constraints, • Foster and maintain good working relationships with state and federal agency staff and clients, • Take initiative and be proactive to resolve problems and implement improved procedures to assure tasks are completed effectively, • Coordinate and obtain permitting and adhere to agency guidelines/policies, • Remain current with agency protocol for conducting natural resources work, • Manage natural resources staff workloads, task assignments, training, hiring, and performance evaluations, • Approves natural resources staff timesheets and expense reports, • Assist and lead marketing and business development tasks to achieve company goals and objectives, as necessary Technical Lead Responsibilities: • Coordinate staff for fieldwork, including survey, and monitoring. This position may require fieldwork participation as well as oversight and coordination of staff., • Prepare and review technical assessments/evaluations, reports, and writing deliverables, • Perform research and synthesize findings into technical reports and permit documentation, • Effectively communicates with management, technical staff, and clients, • Provides effective and professional internal and external coordination and collaboration with clients, project partners and stakeholders, • Interface with clients, and Federal, Local and State government contacts, • Develop proposals, hour estimates, scopes of work, and project schedules, • Review design plans for compliance with environmental and/or permit requirements, • Direct staff and subs to ensure that project scope is accomplished within schedule and budget parameters Job Qualifications (Education, Experience, and Skills): • Minimum of a bachelor’s degree in biology, botany, wildlife, ecology, environmental sciences, or related degree, • Minimum of fifteen years of experience in natural resources management, related fieldwork and document preparation., • Demonstrated experience in managing and completing projects on time, and within budget, • Demonstrated knowledge of of federal, state, and local regulations pertaining to natural resources including but not limited to Endangered Species Act, Clean Water Act, California Environmental Quality Act, and National Environmental Policy Act, • Experience with federal and state agency consultations for listed species, • Experience with preparing environmental regulatory compliance documents and conducting fieldwork for biological assessments/evaluations, jurisdictional delineations including wetlands, and water permit applications, • Experience with desktop analysis for determination of field survey needs for projects, • Knowledge of Western US flora and fauna, • Excellent written and oral communication skills, • Strong technical writing, analytical, fieldwork, problem solving, and data management skills, • General computer hardware and software skills, • Ability to work independently and take the initiative expected given years of experience and knowledge., • Ability to work closely with fellow employees and clients, • Ability to foster a positive work environment and organize and handle multiple assignments, • Ability to pass a background check, • Project Specific Requirements may include, but not limited to, additional background checks and/or drug testing prior to and during work on the project, • Ability to work in harsh outdoor conditions (heat, cold, dust, wind, and rough terrain), • Ability to climb stairs without assistance, • Ability to lift and carry 30 pounds of equipment for at least 1 hour, • Ability to drive to project locations or meetings as needed., • Ability to use a computer while sitting for extended periods on a daily basis, • Ability to work in both office and work-from-home environment Competencies (To perform the job successfully, an individual should demonstrate the following competencies): • Communicative – interacts openly with others; can maintain relationships, works well independently or with a team., • Consultative - Consults with other disciplines as needed; tolerates different perspectives or opinions., • Decisive & Action Oriented - Has a high level of energy and stamina; gets things done; makes sound educated but rapid decisions even when short of information; enjoys managing challenging projects and works well in fast-paced and pressure environments. Self-motivated and proactive, • Flexible - Adapts to new challenges and circumstances; able to multi-task; thrives on variety and frequently changing environments; creative problem solver. Resourcefulness, with minimal direction., • Analytical – Uses sound data, and procedures, and follows all laws, rules, and regulations but is a solutionist or problem-solver., • Conscientious and Organized – Believes professional integrity is paramount; understands the importance of project records; responsive to clients and deadline oriented; quality oriented. Working Conditions and Environment: Will need the ability to establish rapport quickly with others working on the same project, and be able to promote a positive team environment. Working knowledge of dealing with a diverse population while using tact, diplomacy, and respect. AZTEC Culture: • Action oriented and flexible, • Zealous supporter of clients and teammates, • Thinking toward future and personal growth, • Equitable, inclusive, and diverse, • Collaborative comradery AZTEC Benefits: AZTEC offers competitive salaries and a comprehensive benefits package, including medical, dental, life insurance, short and long-term disability, flexible spending accounts, Paid-time-Off, and a 401(k) plan. AZTEC Overview: AZTEC Engineering Group, Inc. (AZTEC) is headquartered in Phoenix, Arizona, and provides diversified technical and consulting services to clients in the United States. AZTEC is part of the TYPSA Group, an international consulting engineering firm with over 3,700 employees and more than 50 offices worldwide providing multidisciplinary consulting services in the fields of civil engineering, architecture, and environment. AZTEC has a diverse culture that focuses on providing rich opportunities for its employees. AZTEC is an Equal Opportunity Employer committed to affirmative action planning and encourages diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, disability, marital status, veteran status, housing status, or any other non-job-related characteristic under applicable law. Please apply online at .

Job Title: Regulatory Affairs Specialist II Location: Hybrid – Core onsite days are Tuesday and Thursday; third onsite day is flexible Duration: 1 Year Contract - possible extension Pay Range: $45–$50/hour Position Overview Join our client's Regulatory Affairs team to support the transition to the EU’s In Vitro Diagnostic Regulation (IVDR), impacting all CE-marked IVD products. This role plays a critical part in ensuring regulatory compliance by revising technical documentation, updating labeling, and coordinating regional notifications. Key Responsibilities • Technical File Management:, • Revise assigned technical files using the latest templates., • Ensure each file clearly presents product details, performance expectations, and supporting evidence of conformity., • Incorporate updated technical reports, validations, and test documentation., • Complete each file within defined timelines and participate in weekly project meetings to report progress and resolve issues., • Labeling Compliance:, • Support IVDR labeling conversion efforts through cross-functional collaboration., • Maintain and update the labeling conversion tracking log based on manufacturing schedules, product fill dates, lot numbers, and change request references., • Revise labeling specifications to meet IVDR requirements., • Product De-Registration:, • Assist in un-CE marking selected products., • Track progress until final labeling reflects required changes per specification documents., • Regulatory Coordination:, • Update the technical file tracking log., • Notify and track RA Regional updates related to labeling changes., • Bachelor’s degree in Biochemistry, Biology, Medical Technology, or a related field., • 3–5 years of experience in Regulatory Affairs, Quality Assurance, R&D, Manufacturing, or Project Management within the IVD industry., • Familiarity with FDA and CE marking requirements for IVD products is preferred., • Strong ability to work independently and collaboratively across teams., • Excellent communication skills, including negotiation and persuasion., • Proficient in analytical thinking, problem solving, and computer-based documentation., • Deep understanding of regulatory policies, procedures, and best practices.

Job DescriptionBenefits: • Supplemental Health Insurance, • 401(k) matching, • Flexible schedule Other Info and Desired Personality/Skills: Able to work IN-PERSON the morning and/or afternoon for about 2-6 hours/day between 9am-6pm, up to 5 days per week, during regular seasons. Able to work IN-PERSON 4-8 hours per day for up to 5 days during summer season. Need to work occasionally on weekends for event hosting or marketing event for 2-5 hours. We need people who love working with kids, reliable, organized, flexible, eager to learn, team player, and have good communication skills. Requires travel to different cities in Orange County. Must have a reliable transportation. Need to pass a background/fingerprint check, drug, and TB tests. Paid hourly, approximately up to 30 hours a week, depending on your availability and registration numbers. Able to earn working hours from home when assisting in different departments we have (Administration, Marketing, and Curriculum Team). Employee Benefits when qualified: Simple IRA Aflac Supplemental Insurance and Coverage credit (including Dental and Vision)

Job DescriptionBenefits: • 401(k) IvyMax Academy is a leading education service provider that prepares students exceptionally well for admission to top-tier universities and beyond. Since 2004, IvyMax has been delivering industry-best results, having helped thousands of students ace tests, develop strong leadership intelligence, and get admitted to great schools. The strength of IvyMaxs reputation and brand name is directly attributable to the quality and breadth of its products and services. We are excited to see the continued commitment from IvyMaxs management team to devote significant resources to enhancing IvyMaxs current offerings and developing new high-quality programs, products, and services that are responsive to the evolving market needs. IvyMax courses focus on quality instruction and test-taking strategies and techniques designed to help students achieve high scores on the tests and build strong fundamentals. IvyMax continuously recruits experienced teachers who generally teach in classes ranging from 5 to 20 students at the learning centers. Responsibilities and Duties In-depth knowledge of AP Biology experience Initiate, facilitate, and moderate classroom discussions. Prepare course materials, such as syllabus, homework assignments, and handouts. Plan, evaluate, and revise curricula, course content, course materials, and methods of instruction. Maintain regularly scheduled office hours to advise and assist students. Select and obtain materials such as textbooks, with the help of center staff members and the management team. Collaborate with colleagues to address teaching issues. Positively reinforce student self-confidence and self-esteem Be organized and well-prepared for every lecture Qualifications and Skills 4-year undergraduate degree (BA, BS) or higher related to the subject 2+ year(s) of direct teaching/tutoring experience Must have reliable transportation Available weekday afternoons, evenings, and weekends Work Location: IvyMax Learning Centers Job Type: Part-time

Job DescriptionBenefits: • Flexible schedule, • Training & development, • 401(k) IvyMax Academy is a leading education service provider that prepares students exceptionally well for admission to top-tier universities and beyond. Since 2004, IvyMax has been delivering industry-best results, having helped thousands of students ace tests, develop strong leadership intelligence, and get admitted to great schools. The strength of IvyMaxs reputation and brand name is directly attributable to the quality and breadth of its products and services. We are excited to see the continued commitment from IvyMaxs management team to devote significant resources to enhancing IvyMaxs current offerings and developing new high-quality programs, products, and services that are responsive to the evolving market needs. IvyMax courses focus on quality instruction and test-taking strategies and techniques designed to help students achieve high scores on the tests and build strong fundamentals. IvyMax continuously recruits experienced teachers who generally teach in classes ranging from 5 to 20 students at the learning centers. Responsibilities and Duties In-depth knowledge of AP Biology experience Initiate, facilitate, and moderate classroom discussions. Prepare course materials, such as syllabus, homework assignments, and handouts. Plan, evaluate, and revise curricula, course content, course materials, and methods of instruction. Maintain regularly scheduled office hours to advise and assist students. Select and obtain materials such as textbooks, with the help of center staff members and the management team. Collaborate with colleagues to address teaching issues. Positively reinforce student self-confidence and self-esteem Be organized and well-prepared for every lecture Qualifications and Skills 4-year undergraduate degree (BA, BS) or higher related to the subject 2+ year(s) of direct teaching/tutoring experience Must have reliable transportation Available weekday afternoons, evenings, and weekends Work Location: IvyMax Learning Centers Job Type: Part-time

Job DescriptionDescription: Biology and Chemistry Instructor FLEX College Prep is seeking dynamic individuals with strong communication skills to join our pool of instructors and teach both Biology and Chemistry to middle and high school students. Teaching experience in these subjects is preferred, but for those of you who are new to our industry, training is provided! This position is a non-exempt, part-time role that is on demand depending on business needs. It is a perfect position for candidates looking to earn extra on the side or looking to get started in their career in education. The compensation range for this position is $30-45 an hour depending on experience. Why FLEX? We at FLEX know that teaching and consulting are opportunities to build relationships. Our team understands that each student has a unique background and a unique set of challenges and goals; we work closely with families to help every student overcome those challenges and achieve those goals. In an increasingly crowded industry, FLEX leads through integrity. FLEX has provided admissions consulting, standardized test prep, tutoring and enrichment services for pre-collegiate students since 2001. Our team members offer a nuanced understanding of colleges and their admissions philosophies and give thorough, step-by-step guidance in all areas of the application process. They provide personalized instruction to raise grades and scores and expand students’ knowledge beyond what’s covered in a typical textbook or classroom. What you’ll do: • Academic Instructors assist students individually and in small groups with academic coursework, standardized test prep, and enrichment courses., • They develop and customize lesson plans and curriculum to provide students with targeted, individualized academic support and they maintain comprehensive reports of sessions to track progress and adapt to students’ needs., • FLEX Irvine, • Most sessions occur in-center. In-home sessions are only scheduled with prior consent of instructors and are compensated at a higher rate., • Bachelor's degree in Biology or similar required (U.S. Top 50 college or university strongly preferred), • Strong communication skills to establish rapport with students and co-workers, • Passion for education, • Experience teaching or tutoring High School students, • Availability to work at least some evenings and Saturdays, • Formal experience and/or training in education, • Ability to teach multiple subjects in the sciences highly preferred (AP Physics, AP Chemistry, etc.), • Familiarity with standardized tests (AP, SAT II, SAT, ACT, etc.) in your subjects

Job DescriptionCompany Overview: GATC Health is an innovative TechBio company at the forefront of revolutionizing pharmaceutical discovery and accelerating their development through the integration of artificial intelligence (AI), scientific and finance. Our company is dedicated to advancing therapeutic discoveries and improving human health by leveraging the power of technology and interdisciplinary collaboration. Position Overview: We are seeking a skilled and dynamic mid-level Project Manager to join our growing team. In this role, you will be responsible for coordinating and managing various therapeutic discovery projects, working closely with technical and scientific teams, including chemists, biologists, and engineers. The ideal candidate will possess strong project management skills, excellent communication abilities, and a passion for driving innovation in the biotech industry.Key Responsibilities • Collaborate with cross-functional teams to plan, execute, and deliver therapeutic discovery projects within defined timelines and budget constraints., • Serve as the primary point of contact for project stakeholders, providing regular updates, addressing inquiries, and ensuring alignment with project goals., • Develop comprehensive project plans, including scope, objectives, timelines, resources, and risk assessments., • Coordinate activities among internal teams and external partners to ensure smooth project execution., • Facilitate regular team meetings, including kick-off, status update, and post-mortem meetings, to track progress, identify issues, and drive solutions., • Manage project budgets, track expenses, and report financial performance to stakeholders as needed., • Implement project management best practices, tools, and methodologies to optimize project outcomes and streamline processes., • Proactively identify risks and issues, develop mitigation strategies, and escalate concerns to senior management as necessary., • Foster a collaborative and innovative work environment that encourages knowledge sharing, continuous learning, and professional growth.Qualifications, • Bachelor's degree in a relevant field such as project management, life sciences, engineering, or related discipline. Master's degree preferred., • 3+ years of experience in project management, preferably within the biotech, pharmaceutical, or healthcare industry., • Demonstrated experience managing cross-functional teams and complex projects from initiation to completion., • Strong understanding of scientific and technical concepts related to pharmaceutical discovery and development, including AI, chemistry, biology, and engineering., • Proficiency in project management tools and software (e.g., Microsoft Project, Jira, Asana) and familiarity with Agile methodologies., • Excellent communication, interpersonal, and leadership skills, with the ability to influence stakeholders and build consensus., • Proven ability to prioritize tasks, manage multiple projects simultaneously, and adapt to changing priorities in a fast-paced environment.

Job DescriptionBenefits: • Supplemental Health Insurance, • 401(k) matching, • Flexible schedule Other Info and Desired Personality/Skills: Able to work IN-PERSON the morning and/or afternoon for about 2-6 hours/day between 9am-6pm, up to 5 days per week, during regular seasons. Able to work IN-PERSON 4-8 hours per day for up to 5 days during summer season. Need to work occasionally on weekends for event hosting or marketing event for 2-5 hours. We need people who love working with kids, reliable, organized, flexible, eager to learn, team player, and have good communication skills. Requires travel to different cities in Orange County. Must have a reliable transportation. Need to pass a background/fingerprint check, drug, and TB tests. Paid hourly, approximately up to 30 hours a week, depending on your availability and registration numbers. Able to earn working hours from home when assisting in different departments we have (Administration, Marketing, and Curriculum Team).

Job DescriptionSalary: Company Overview: At Acorn Biolabs, we are pioneering the future of health through cutting-edge cellular preservation and regenerative medicine. By empowering individuals to bank their healthy, younger cells today, we provide access to tomorrows advancements in personalized healthcare and age-related treatments. Our dynamic team is composed of leading experts passionate about driving innovation and transforming the way we approach long-term health and longevity. Join us in making an impact on the future of medicine and improving lives globally. Key Responsibilities: Topical product creation & HA Production • Retrieve biological samples from liquid nitrogen (LN2) storage tanks or dewars., • Plate hair follicle samples within ISO-7 and ISO-5 cleanrooms, following all Standard Operating Procedures (SOPs) and Good Laboratory Practice (GLP) guidelines., • Monitor cell cultures routinely and harvest cell-conditioned media., • Prepare hyaluronic acid (HA) diluent, then seal and crimp vials., • Perform aseptic filtration and filling of product vials; conduct visual inspections, sealing, and crimping., • Maintain accurate batch records, complete required forms, and enter data into the laboratory information system (LIS)., • Label and package vials for shipment, ensuring quality and compliance. Hair Follicle Biobanking • Collect, analyze, and cryopreserve human biological samples within ISO-7 and ISO-5 cleanrooms, adhering to Standard Operating Procedures (SOPs) and Good Laboratory Practice (GLP) guidelines., • Facilitate the transfer of biological samples into and out of liquid nitrogen tanks., • Maintain liquid nitrogen supply through coordination with Liquid Nitrogen Supplier, • Maintain precise documentation to track all stages of the biobanking and manufacturing workflow., • Perform routine data entry in batch records, forms, and logs., • Identify and report any deviations to the immediate supervisor, ensuring proper documentation of deviation records., • Contribute to quality control improvements by assisting in SOP development and maintaining thorough documentation. Commercial Laboratory Operations • Manage inbound sample receipt, inventory tracking, and dispensing of collection kits., • Handle biohazardous waste disposal, uphold lab cleanliness, and coordinate the recycling of reusable instruments., • Monitor and maintain lab supply inventory, reporting shortages to the operations manager. Education • Bachelors degree in Biology, Biotechnology, Biomedical Sciences, or a related field (or equivalent laboratory experience) or equivalent lab diploma (medical lab technologists) Experience Level • Entry-Level: 02 years of experience in a biobank, laboratory, or cleanroom environment (suitable for recent graduates with relevant hands-on experience)., • Mid-Level: 25 years of experience in biobanking, cell culture, or biospecimen processing (preferred). Technical Skills • Experience handling biological samples, ideally including cryopreservation and liquid nitrogen storage., • Familiarity with ISO-7 and ISO-5 cleanroom environments and SOP/GLP compliance., • Knowledge of biobanking workflows, sample tracking, and data documentation., • Experience in inventory management, shipping logistics, and equipment maintenance., • Ability to follow quality control procedures and assist in SOP development. Preferred but Not Required • Experience working in a regulated environment (e.g., GMP, CLIA, or FDA-compliant labs)., • Previous work in commercial laboratory operations, biomanufacturing, or regenerative medicine., • Familiarity with FedEx shipment coordination for biological samples., • Experience in a startup environment is a plus. Schedule • Tuesday to Saturday, subject to change based on business needs. Whats in it for you: • We offer a competitive salary, benefits package, and additional perks that reward your hard work and dedication., • You will get to be part of a forward-thinking team at the forefront of regenerative medicine and cellular preservation., • You will play a key role in shaping the future of healthcare, making a tangible difference in the lives of our clients and society., • You will have opportunities for professional development and advancement as we continue to expand and innovate., • You will be joining a passionate, diverse team that values creativity, collaboration, and knowledge-sharing., • You will work with the latest advancements in biotech and gain exposure to groundbreaking research and applications. Why Join Acorn: This is more than just a jobits an opportunity to be part of a company revolutionizing healthcare. At Acorn, we value teamwork, adaptability, and a passion for growth. Our sales team thrives on collaboration, sharing wins and challenges, and pushing forward together to shape the future of regenerative medicine. At Acorn, our values are important to us and define our companys culture. Integrity First. In our science, with our clients and with each other. Always. Collaborate. Be kind, supportive, respectful, and inclusive. Be humble and grateful. Show up. Take pride in your work. Be dependable, accountable, and disciplined. Strive for excellence - and be agile. Add value. Be curious. Ask why. Constantly learn. Create. Innovate.

Job Description Job Title: Production Chemist (Immediate Need) Production Chemist Pay Range: $31.00 Production Chemist Schedule: 7:00 am-3:30pm Monday-Friday Production Chemist Start Date: ASAP We are seeking a Production Chemist for a contract opportunity with a global life sciences organization in Orange County! The Production Chemist will be responsible to formulate products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications. The Production Chemist Responsibilities: • Responsible for bulk formulating products of low complexity including intermediates in accordance with approved written procedures and policies, • Perform data entry and inventory control utilizing the ERP database, • Responsible for completing production documentation and maintaining quality records to GDP/GMP standards, • Coordinate prioritize and plan lab tasks to meet strict deadlines, • Follows controlled Standard Operation Procedures/ documents, • Monitors manufacturing processes and performs adjustments when necessary to meet required yields, • May participate in the initiation of Quality Notifications and Material Review Board process, • Understands the basics of lean practices, • Able to generate Quality Notifications and perform preliminary investigations, • Performs necessary SAP transactions in a Production Environment The Production Chemist Qualifications: • 1-3 years working in a general manufacturing environment formulating products in the areas of biological sciences, life sciences, or an equivalent, • BA degree within Life Sciences, Chemistry, Biology, • Experience working in a GMP manufacturing environment preferred., • Must be comfortable working with infectious disease materials, • Understanding of Good Manufacturing Practices and Good Laboratory Practices., • Strong working knowledge of Microsoft Office tools- Excel and Word., • Strong working knowledge of laboratory environment, materials, and equipment., • PPE provided, • Must have non slip safety shoes

These individuals will serve a number of program priorities in our undergraduate and graduate degree programs, which include: Biological Sciences, Ecology and Evolutionary Biology, Exercise Science, Biology/Education, and Conservation and Restoration Science. UC Anti-Discrimination Policy for Employ

Job DescriptionSalary: $50,000 - $55,000 per year DOE Ideal Candidate Profile Do you fit this profile? • Wants to start a CAREER / not just another "job", • Wants to make a difference, • High Moral Standards & Values, • Positive, • Helpful, • Team Player, • Professional, • Wants to be the best of the best, • Is Ready Envirocheck is a growing company and has exciting opportunities for A players on our team. Job Summary Our environmental field technicians / consultants (Level 1) provide clients with advice regarding potential contaminant presence in a variety of settings including residential, commercial, and industrial buildings. An ideal candidate should be an individual who is self-motivated, this hands-on position requires strong analytical and communication skills to identify a potential issue and convey the said issue to a client with remedial solutions when necessary. Through on-the-job training and certification courses, field technicians gain knowledge regarding state and federal regulations and in turn conduct surveys and produce reports as a knowledgeable party. Responsibilities and Duties • Conduct on-site inspections, which includes documentation of site conditions, sampling, and in-person consultation, • Produce professional survey reports based on inspection notes and sample data with remedial recommendations as necessary, • Coordinate with multiple parties regarding inspections while keeping all parties best interests in mind, • Adhere to all applicable state and federal laws and regulations and communicate that information to clients in a professional manner Qualifications and Skills • No experience required - will train., • High school diploma is required., • Prefer individuals with a bachelor's of science degree in construction management, biology, chemistry, environmental science, and/or a related science., • Valid Driver's License, • We are hiring for all levels! Certified asbestos consultants (CAC), certified site surveillance technicians (CSST), Lead sampling technicians, or CA DHS lead inspector/assessors are encouraged to apply. Benefits • Health Insurance options, • 401K with matching, • Company vehicle & iPhone & gas card provided, • Paid Training & Field-Related Education

Job DescriptionAutonomous Medical Devices Incorporated (AMDI) is a California-based company employing a world class team of engineers, scientists, clinicians, manufacturing and quality/regulatory experts dedicated to the development and manufacture of best in class diagnostic devices using innovative technology, factory automation, and cloud connectivity. AMDI is headquartered in Santa Ana, CA where it manufactures the Fast PCR Mini Respiratory Panel in an ISO:13485 / MDSAP certified 110,000 square foot facility. Our lead product, the Fast PCR System, delivers molecular respiratory results (Flu A, Flu B, RSV, and COVID) in under 10 minutes, purpose-built for urgent care and office labs. The product pipeline includes assays for STIs and Strep A, designed specifically for CLIA-waived environments, underscoring AMDI’s mission to deliver accurate results at the time of care. Why join AMDI? At AMDI, you’ll work on breakthrough technology that redefines what’s possible at the point of care. From 10-minute PCR results to a growing pipeline of CLIA-waived assays, your work directly impacts patient care and empowers urgent care and office labs with tools that save time and improve outcomes. Compensation: $150,000 - $250,000 base Location: Santa Ana, CA Perks & Benefits • Enjoy 13 company-paid holidays, along with generous vacation and sick days, • Daily onsite free lunch, snacks, and drinks, • 100% employer-paid Medical, Dental, Vision & Life Insurance, • 401(k) matching, • Education assistance, • Monthly socials and employee events, • Casual dress code, • Sales Strategy & Execution, • Execute the sales execution for AMDI Fast PCR System launch and through that initial launch experience and develop strategies to prioritize wins within urgent care systems and drive adoption among primary care physicians., • Using Salesforce to build scalable sales processes and implement tools for efficient lead generation, conversion, and customer retention., • Establish, monitor, and exceed sales targets for the Sales team, while personally owning and driving quota attainment in the Southern California region to accelerate adoption near company corporate headquarters., • Team Building & Leadership, • Recruit, train, and establish a high-caliber sales team., • Instill a culture of customer focus, accountability, professionalism, and performance excellence., • Customer Engagement, • Establish both individually and regionally through the Sales Team strong strategic relationships with customers in the Urgent Care and Primary care markets., • Ensure high standards of professionalism and integrity in all interactions and communications with Customers., • Cross-Functional Collaboration, • Partner with Marketing on executing sales strategy and provide timely feedback for pivots needed to the plan., • Provide market intelligence and feedback from customers to inform product enhancements and strategic direction., • Operational Excellence, • Establish both individually and regionally through the Sales Team strong strategic relationships with customers in the Urgent Care and Primary care markets, • Ensure high standards of professionalism and integrity in all interactions and communications with Customers, • Customer Engagement, • Implement Salesforce CRM and reporting systems to provide visibility into pipeline, forecasting, and sales performance., • As the team is built, provide frequent review and feedback to sales team members on their sales performance versus plan., • Minimum of a high school diploma. A bachelor’s degree preferred., • Experience leading and growing a sales team to launch a new product into a medically regulated market, • Minimum of 3 years of sales leadership experience., • Experience launching products in U.S. markets., • Experience in molecular biology, clinical diagnostics, or life sciences market a plus, • Proven experience in urgent care and CLIA-waived market entry a plus, • Demonstrated ability to build and lead high-performing, geographically dispersed sales teams., • Skilled in fostering collaboration and building productive team relationships, • Exceptional organizational skills, attention to detail, and a methodical approach to sales development., • Clear, articulate communicator—verbally and in writing—with professional presentation and interpersonal skills., • Willingness to travel to support sales in the US and could involve international travel, • Ability to interpret sales data, identify trends, and prepare clear and concise communication to Marketing and AMDI Leadership on solutions., • In-person position that requires working indoors at a computer station., • Based in Santa Ana office. Our commitment to an inclusive workplace: We are an equal opportunity employer and encourage people from all backgrounds to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other protected characteristic under federal, state, or local law. 4XIUlLp7BT

A doctoral degree in a health science, behavioral science, or related field and a minimum of 5 years of experience in health and/or behavioral sciences education, with at least 3 years in a leadership or administrative role, are required. Tailored for workplace relevance, programs include associate,

A minimum of a baccalaureate degree from a program accredited by an agency recognized by the U.

The successful candidate should have an advanced degree and significant, progressive professional experience leading a complex, dynamic, and diverse department.

Seeking an experienced Clinical Lab Scientist for an evening shift position in the Microbiology Department. This role involves performing a wide range of diagnostic testing in microbiology, including culture plating, gram staining, PCR testing, molecular extractions, and rapid test procedures. Condu

General Biology I, Biochemistry I and Biochemistry II (See CUI Catalog for. Candidates should have earned a doctorate or a master's degree in a relevant field. Biology and Biochemistry, and who are eager to explore the connections.

Bachelor's degree and/or equivalent experience required. A law degree (JD) is preferred.

Neuorbiologist Job Duties: Completes neurobiological studies by conducting tests, examinations, and interviews; organizing and analyzing findings; writing results, summaries, and interpretatio

Please be prepared to upload a Statement of Interest; Doctoral Dissertation Plan or Abstract; Curriculum Vitae; Writing Sample; and Confirmation of Degree as a single PDF when prompted to upload your "resume" by the online application system.

Contributes to the development of novel applications in support of government-funded efforts in the areas of microbiology, synthetic biology, and marine biology.

Requirements: Active California CLS license (no temp licenses) 1+ year of recent Microbiology lab experience ASCP certification required/preferred Prior hospital lab experience preferred Must be willing to float if needed.

In close cooperation with our customers, Bruker is enabling innovation, improved productivity, and customer success in life science molecular research, in applied and pharma applications, in microscopy and nano analysis, and in industrial applications, as well as in cell biology, preclinical imaging

Staff Research Associate 2 Non-Exempt - Irvine, CA, Job ID 74113.University of California Agriculture and Natural Resources.The Staff Research Associate II (SRA II) will.Cooperative Extension Advisors (Advisors) with research and education in nurseries and greenhouse production in California, focusi

Master’s degree in Reproductive Biology, Clinical Embryology, or a related field (required). Publication or research experience in reproductive biology.

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. A minimum of a Master's Degree with at least 10 years of clinical, medical affairs or related technical experience. A Life Science, Physic