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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Clinical Development & Research – Non-MD Job Category: Scientific/Technology All Job Posting Locations: Irvine, California, United States of America Job Description: Johnson & Johnson MedTech Electrophysiology is recruiting for a Senior Clinical Research Specialist, (Clinical Operations Start-up) to support the Electrophysiology (EP) business unit based in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at . Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at . Summary: The Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization. Duties & Responsibilities: Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: • Serves as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for J&J MedTech Electrophysiology, • Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures, • May serve as the primary contact for clinical trial sites (e.g. site management), • Contributes towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports,….), • Manages/oversees ordering, tracking, and accountability of investigational devices and trial materials, • Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel, • Interfaces, collaborates and oversees Clinical Research Associates (CRAs), • Oversees and supports the development and execution of Investigator agreements and trial payments, • Is responsible for clinical data review to prepare data for statistical analyses and publications, • May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need, • May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects, • May provide on-site procedural protocol compliance and data collection support to the clinical trial sites, • Contributes to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated, • Contributes to delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs), • May assist with the development of e Post-Market Clinical Follow-up (PMCF) Plans and PMCF, • Evaluation Reports (ER) within the defined timelines and review/update at planned intervals, • May assist with maintaining the overview to assure (study) commitments are timely and properly met by coordination of specific documentation and contribution to cross-functional review of associated documents where relevant, • Supports project/study budget activities, • Mentors team members, • May perform other duties assigned as needed, • Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders, • Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures, • Should develop a strong understanding of the pipeline, product portfolio and business needs, • Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or, • Biological Science required., • BS with at least 4 years, MS with at least 3 years, PhD with at least 2 years of relevant, • experience preferred., • Previous experience in clinical research or equivalent is required., • Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO, • 14155, MDR, MEDDEV,…)., • Clinical/medical background is a plus., • Good understanding of clinical research science and processes, clinical trends, and global, • clinical trial regulations, • Proven track record in supporting delivery of clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations, • Good presentation and technical writing skills;, • Good written and oral English communication skills;, • Leadership Competencies:, • Ability to lead small study teams to deliver critical milestones, as may be assigned., • Leadership required in alignment with J&J Leadership Imperatives, • Connect - Develop collaborative relationships with key internal and external stakeholders., • Shape - Make recommendations for and actively participate in departmental process improvement activities., • Lead - Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource. Preferred Skills: Analytical Reasoning, Clinical Data Management, Clinical Evaluations, Clinical Trial Protocols, Coaching, Consulting, Data Savvy, Drug Discovery Development, Good Clinical Practice (GCP), Medicines and Device Development and Regulation, Persistence and Tenacity, Regulatory Affairs Management, Research Documents, Resource Management, Safety-Oriented, Scientific Research, Technologically Savvy The anticipated base pay range for this position is : $92,000.00 - $148,350.00 Additional Description for Pay Transparency: Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: -

About Us We are building the gold-standard data layer that AI drug discovery platforms will run on. Partnered with leading AI labs, global tech companies, and top pharma, we're a fast-growing Palo Alto-based team on a mission to accelerate drug discovery through AI. The Role You don't need an AI background — you need deep scientific expertise. In this role, you'll use your research experience in bioinformatics to help fine-tune large language models (like ChatGPT) built for drug discovery. What You'll Do • Perform bioinformatics analysis and provide drug development expertise for assigned work., • Provide expert scientific feedback to AI researchers from leading labs, helping shape how AI models interpret drug discovery workflows in bioinformatics and computational biology contexts. What We're Looking For • PhD in Bioinformatics, Computational Biology, Systems Biology, or a related life sciences or physical sciences field (postdocs, biopharma scientists, and industry researchers welcome), • 3+ years of bioinformatics research experience Offer Details • Commitment: 15–30 hours/week (with overlap in PST), • Compensation: Highly competitive, top 10% of industry rates, • Engagement: Contractor/freelancer (no medical or paid leave), • Duration: 1 month, with possible extension, • Remote: Fully remote, collaborative environment

Entry-Level Manufacturing Associate (Upstream/Downstream) Location: Irvine, CA Employment Type: Full-Time Compensation: Competitive, DOE (Dependent on Experience) About Us: We are a growing biopharmaceutical company dedicated to developing and manufacturing innovative therapies that improve patient outcomes. Our team is driven by science, quality, and a commitment to excellence in biologics manufacturing. Position Overview: We are seeking motivated and detail-oriented recent graduates to join our Manufacturing team in both Upstream and Downstream operations. This is an excellent opportunity to gain hands-on experience in a GMP-regulated biopharma environment and build a strong foundation in biologics manufacturing. Key Responsibilities: Upstream Manufacturing: • Assist with cell culture processes, including media preparation, bioreactor setup, and monitoring, • Support inoculation, sampling, and harvesting activities, • Perform purification processes such as filtration and chromatography, • Prepare buffers and solutions, • Follow Good Manufacturing Practices (GMP) and standard operating procedures (SOPs), • Document all activities clearly and accurately, • Collaborate with cross-functional teams including Quality and Engineering, • Bachelor’s degree in Biology, Chemistry, Biochemistry, Biopharmaceutical Sciences, or a related field, • Recent graduates are strongly encouraged to apply, • Strong attention to detail and willingness to learn, • Good communication and teamwork skills, • Internship or lab experience in biotech or pharmaceutical settings

Organizational Overview Newport Bay Conservancy (NBC) has a proud history of environmental advocacy having been involved in the protection of Upper Newport Bay for the past 50 years. Our mission is to protect and preserve the Upper Newport Bay through education, restoration, research and advocacy. We are able to do this with the support of over 200 active volunteers contributing over 11,000 hours of service each year. We are excited to work in partnership with the City of Newport Beach and the Newport Dunes Resort to provide FiiN (Fostering Interest In Nature) for 5th grade students. Job Summary The Outdoor Activity Leaders for FiiN are responsible for leading fifth grade students through nature-based science activities. The curriculum includes science/environmental concepts related to the conservation of wetlands/coastal habitats as well as leadership and team building through outdoor recreation. Outdoor Activity Leaders will provide supervision of students in shifts spanning Mondays through Fridays for 9 weeks. Outdoor Activity Leaders will report to the Education Manager or City of Newport Beach Recreation Supervisor. It is requested that all leaders work at least one overnight shift per week in a tent cabin. Principal Responsibilities • Lead groups of fifth grade students through activities around Newport Bay, providing environmental/nature awareness and appreciation., • Provide night programs and group activities such as campfires and cookouts, as well as overnight supervision and care of students in a group tent cabin., • Work with volunteer naturalists to provide activity instruction and education based on fifth grade NGSS (Next Generation Science Standards)., • Work with teachers to respond to student’s health and behavior and make decisions to provide the safest outdoor experience. Job Requirements • Demonstrated ability to lead elementary school children providing a positive and nurturing environment. Minimum of 1 year experience working with youth (ages 10-12)., • College coursework (degree preferred) in child development, recreation, natural/environmental sciences, biology, ecology, or related fields OR equivalent career experience of 2+ years in youth/outdoor education programming (overnight camp experience a plus)., • Behavioral Skills, • Strong work ethic, commitment to the program, and enthusiasm towards leading/teaching youth., • Dedicated to the conservation of wildlife and natural resources., • Exhibits confident communication and leadership skills., • Organized and exhibits excellent time management., • Shows compassion to diversity and sensitivity to all races, ethnicities, class, and sexual orientations., • Computer/Technology, • Checks email regularly and corresponds efficiently through email., • Uses cell phone and communicates efficiently through text messaging and designated communication apps., • Uses Microsoft Office and Google platforms (docs, sheets, drive, etc)., • Physical Requirements, • Will be expected to stand/walk for extended periods of time including light hiking over sandy or unstable terrain (at least two miles)., • Must be able to speak with clarity and at a volume suitable for outdoor presentations, dealing with air traffic noise, children, and other outdoor noises., • Must be able to lift 20 pounds, assist with set up and cleanup of program materials and keep materials organized and clean., • Must be able to work outside in variable weather conditions including heat and sun, rain, wind, or work with exposure to dirt/dust, pollen, various plants, water/mud, insects like bees and spiders, and wildlife., • Ability to spend the night in a tent without access to electricity/electronics or attached restrooms (meaning you will need to walk to a restroom building at night)., • Other, • Punctual and reliable self starter., • Can commit to a set schedule for the 10 week season of FiiN., • Spanish speaking is a plus but fluency is not required., • CPR/First Aid Certification (provided if not currently certified). Additional certifications (lifeguard, EMT, nursing experience a plus)., • Successfully pass a background check., • Requires use of a car to drive safely to get to program locations around the Bay. May use a personal car for transport of program materials and supplies. Location The Outdoor Activity Leader position is based out of the Back Bay Science Center (600 Shellmaker Road, Newport Beach, CA 92660); however, FiiN Camp primarily takes place at a location near Camp James (101 N Bayside Dr, Newport Beach, CA 92660) and occasionally at other sites around Upper Newport Bay. This job cannot be performed from a remote location. Salary Detail and Working Hours $17/hr. Ability to work 5-12 hour shifts Monday through Friday between 8am-8pm, with at least 1 overnight shift (which would pay overtime). A minimum of 12 hours per week is required and a max of 32 is allowed. FiiN runs from September 8 through November 15, 2026. How to Apply We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class. We encourage applications from underrepresented communities to apply. Apply online at newportbay.org/FiiN. Application reviews begin June 2, 2026. More information about NBC can be found at .

Job Description The Manufacturing Associate – Buffer Preparation supports cGMP manufacturing operations by preparing buffers and solutions used in upstream and downstream bioprocessing. This role is critical to ensuring timely, accurate, and compliant production activities within a biotech CDMO environment supporting multiple client programs. The ideal candidate has hands-on buffer preparation experience and a strong understanding of cGMP principles, documentation, and safety requirements. Key Responsibilities • Prepare buffers, media, and process solutions according to batch records, SOPs, and cGMP requirements, • Perform weighing, mixing, pH adjustment, filtration, and transfer of buffers at various scales, • Operate and clean buffer preparation equipment, including tanks, mixers, pumps, and filtration systems, • Execute and document manufacturing activities in batch production records (BPRs) accurately and contemporaneously, • Perform equipment setup, operation, and teardown in classified cleanroom environments, • Adhere to gowning, aseptic techniques, and contamination control procedures, • Perform line clearances, material verification, and inventory transactions as required, • Support buffer hold studies, labeling, storage, and lifecycle management, • Identify and report deviations, discrepancies, or safety concerns promptly, • Participate in continuous improvement initiatives and lean manufacturing efforts Education • Associate’s or Bachelor’s degree in Biotechnology, Biology, Chemistry, or a related scientific field preferred, • Degree in Life Sciences or 1–3 years of experience in cGMP manufacturing within biotech, biopharmaceutical, or CDMO environments, • Hands-on experience with buffer and solution preparation required, • Knowledge of cGMP regulations and documentation practices, • Experience with buffer prep equipment, pH meters, balances, and filtration systems, • Ability to follow complex batch records and SOPs, • Basic understanding of cleanroom operations and aseptic technique Job Title: Manufacturing Associate – Buffer Preparation Location: [Location] Department: Manufacturing / Operations Reports To: Manufacturing Supervisor / Manager Position Summary The Manufacturing Associate – Buffer Preparation supports cGMP manufacturing operations by preparing buffers and solutions used in upstream and downstream bioprocessing. This role is critical to ensuring timely, accurate, and compliant production activities within a biotech CDMO environment supporting multiple client programs. The ideal candidate has hands-on buffer preparation experience and a strong understanding of cGMP principles, documentation, and safety requirements. Key Responsibilities • Prepare buffers, media, and process solutions according to batch records, SOPs, and cGMP requirements, • Perform weighing, mixing, pH adjustment, filtration, and transfer of buffers at various scales, • Operate and clean buffer preparation equipment, including tanks, mixers, pumps, and filtration systems, • Execute and document manufacturing activities in batch production records (BPRs) accurately and contemporaneously, • Perform equipment setup, operation, and teardown in classified cleanroom environments, • Adhere to gowning, aseptic techniques, and contamination control procedures, • Perform line clearances, material verification, and inventory transactions as required, • Support buffer hold studies, labeling, storage, and lifecycle management, • Identify and report deviations, discrepancies, or safety concerns promptly, • Participate in continuous improvement initiatives and lean manufacturing efforts Education • Associate’s or Bachelor’s degree in Biotechnology, Biology, Chemistry, or a related scientific field preferred, • 1–3 years of experience in cGMP manufacturing within biotech, biopharmaceutical, or CDMO environments, • Hands-on experience with buffer and solution preparation required, • Knowledge of cGMP regulations and documentation practices, • Experience with buffer prep equipment, pH meters, balances, and filtration systems, • Ability to follow complex batch records and SOPs, • Basic understanding of cleanroom operations and aseptic technique, • Strong attention to detail and data integrity, • Ability to work effectively in a fast-paced, multi-client environment, • Good communication and teamwork skills, • Strong organizational and time-management abilities, • Willingness to work flexible schedules, including weekends or shifts, as required, • Strong attention to detail and data integrity, • Ability to work effectively in a fast-paced, multi-client environment, • Good communication and teamwork skills, • Strong organizational and time-management abilities, • Willingness to work flexible schedules, including weekends or shifts, as required

Job DescriptionPosition Title: BiologistReports to: Education and Leadership ManagerClassification: Part-time, non-exemptCompensation: $21.00 per hourLocations: Laguna Beach, CA and other locations as necessary, in Orange County, CA Job Summary: The Biologist works within the Laguna Ocean Foundation’s Education and Leadership Manager to educate the public, assist with on-going research projects, and help develop educational programming. The Biologist will educate the public at various tidepool locations in Laguna Beach, community events held within Orange County, and at schools across Orange County. Educational topics include, but are not limited to, tidepool species identification, Marine Protection Area status, how to safely explore tidepools, ocean awareness, climate change, marine debris, and ocean acidification. Research projects and program development will be based on current grants and funding opportunities. Essential Duties: ● Leads onsite education at tidepool locations by informing visitors about the biology of the flora and fauna of these rocky intertidal areas and interpreting the natural surroundings, including the ocean, geology, and surrounding habitats.● Collects data on tidepool visitation, tidepool Marine Protected Area infractions, weather conditions, species sighted and other data as deemed necessary by the Foundation on an online data log.● Participates in various research projects and campaigns ran by the Laguna Ocean Foundation based on current grants and funding● Leads educational activities and lesson plans about tidepools, ocean awareness, marine debris, climate change, ocean acidification, and more, during field trips, community outreach events, and school visits.● Develops educational materials for outreach and education purposes.● Willingness to share knowledge, experience, time and talents with others and work in a team environment.● Attends training sessions and workshops provided by the Laguna Ocean Foundation to improve skillset and grow knowledge base.● Interacts and cooperates with the City of Laguna Beach Marine Safety Department Lifeguards and Protection Officers for their enforcement of State and local laws, as well as patron safety.● Promotes conservation efforts by increasing public awareness of the laws within Marine Protected Areas (MPAs) and the role the public plays in protecting the environment.● Uses a proactive approach to provide interpretive information in a friendly, polite, and professional manner.● Other job duties that may arise and be assigned by the Education and Leadership Manager.● Represent the Laguna Ocean Foundation in public events and forums. Desired Qualifications: ● Interest in the natural world and enthusiasm for the environment.● Enjoys teaching and interacting with the public.● Enjoys being a proactive member of a team, including being dependable and responsible.● Professional knowledge of one of the following: marine biology, oceanography, rocky intertidal habitat, local organisms, and interpretive techniques.Requirements: ● Biologists are representatives of Laguna Ocean Foundation and must maintain a professional appearance and demeanor at all times.● Minimum 18 years of age.● College degree with Marine Biology or other Biology degree with similar science focus preferred, but prior interpretive or research experience will be considered.● Performs job duties according to the Standards of Conduct.● Communicates in a timely manner● Has access to the internet and a Google account for shared Google Drive documents.● Reports directly to the Interim Education and Leadership Manager. Occasional direction may be from Biologist Trainer or Docent Trainer by the guidance of the Education and Leadership Manager.● Ability to work outside in an uneven, rocky, wet, sandy and exposed environment with changing weather conditions.● Performs duties in a safe manner, follows all protocols for safety, and chooses the safest course of action in performing their duties.● Available to work a minimum of six shifts monthly, including weekdays, weekends, and holidays. Hours should total 25-40 hours per month. Skills: The ideal Biologist is motivated, reliable and energetic; interacts well with the public; understands the mission of the Laguna Ocean Foundation; has knowledge of MPA regulations and the rocky intertidal ecosystem; and possesses the following skills:● Problem Solving● Customer Service● Verbal and Written Communication● Professional Judgment● Safety and Security● Adaptability● Initiative Laguna Ocean Foundation will provide approximately ten hours of training covering topics related to the knowledge needed to be an effective interpreter and biologist while engaging with the public. Continuing training and hands-on experience will be available to Biologist through extended education opportunities. Physical Demands: · Ability to be outdoors for shifts of three to six hours long.· Ability to stand and traverse over rocky, wet, and uneven surfaces.· Ability to withstand extreme seasonal weather conditions (e.g., heat, cold, rain, and wind).· Ability to communicate and interact with the public for shifts of two to seven hours long. Work Environment: The Biologist mainly works in an outdoor setting and may be exposed to variable weather and water conditions, including sun, rain, wind, and waves. Tidepool shifts will be during low tides, but other research projects or events may require work outside of low tides. In addition, the Biologist may at times expect to be surrounded by large numbers of people or work events with a high traffic of guests. E04JI800ui414095mbx

Job Description LGM Pharma has an open position for a Senior Regulatory Affairs Specialist based in the Irvine, CA location. RESPONSIBILITIES: Planning: • Oversee ANDA/NDA submission and approval process for regulatory., • Collaborate in company Standard Operating Procedures (SOP’s) development and review., • Reviews documents for regulatory compliance necessary for the acceptability of quality documentation for submission filing., • Develop pre-approval compliance activities during manufacturing submission batches., • Perform label development and reviews for compliance., • Monitor impact of changing regulations on submissions and provides recommendations for implementation., • Maintains annual licenses, registrations, listings and patent information as required., • Prepare annual reports for NDA/ANDAs by scheduling and coordinating receipt of documentation/information, preparing cover pages describing changes made to an application and tracking progress of their preparation., • Review of documents and interacting with multiple departments (QA, Manufacturing, Project Management, Engineering, PD, etc.) which provide information and documentation utilizing the change control database to ensure accurate reporting to FDA., • Maintaining approved NDA/ANDAs current by requesting revisions to technical documentation as part of the annual report preparation process., • Provide a critical detailed review of technical documentation including labeling, distribution reports, analytical procedures, product specifications, manufacturing and packaging batch records, in-process specifications, etc. prior to FDA submission., • Interacts with representatives from the Food and Drug Administration (FDA), Notified Body, Authorized Representative and other regulatory agencies, to resolve issues or questions in the application., • Prepare, revision and approval of labeling., • Participate in the preparation and submission of required post approval reports such as field alert reports, periodic adverse drug experience reports etc. Ensures product safety issues and product-associated events are reported to regulatory agencies., • Ensures compliance with product post-marketing approval requirements, annual reports, drug listings, labeling, pharmacopeia changes (pre and post approval), etc., • Reviews regulatory aspects of contracts with customers., • Provides regulatory support for product recalls and recalls communications., • Other related duties as required. QUALIFICATIONS: • Bachelor's degree in science (biology, chemistry, microbiology, and pharmacy)., • 10+ years’ of experience in a regulatory function within pharmaceuticals (preferred) or medical products; experience in quality assurance and/or compliance may be considered., • Certification such as RAC from the Regulatory Affairs Professionals Society preferred., • Experience with electronic regulatory submissions., • Knowledge of USP, and Code of Federal Regulations 21 CFR 111, 11, 210, and 211. FDA/ICH guidance and the regulatory process pertaining to drug development and approval., • Strong interpersonal skills and ability to handle multiple high priority assignments with discretion, • Strong technical writing skills and acute attention to detail., • Strong knowledge and understanding of CMC., • Ability to read and interpret complex technical documents. Ability to write comprehensive reports., • Strong communication skills, both written and verbal., • Able to build rapport at all levels of the organization as well as with external contacts., • Proficient in MS Office suite of products (Word, Excel, Powerpoint, etc.) At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

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 DescriptionCompany Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Associate Director Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications and supplements/variations. Builds and maintains relationships within the Regulatory Affairs functional areas, Operations and Research & Development (R&D) organizations. Represents CMC on teams such as product development, Global Regulatory Product Teams and Operations brand teams to negotiate, influence, and provide strategic advice. Serves as strategic liaison with the regulatory agencies (e.g., FDA) regarding CMC matters. Responsibilities • Prepares CMC regulatory product strategies. Prepares and manages regulatory submissions, including new applications and amendments, renewals annual reports, supplements and variations and responds to regulatory information., • Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions, • Reviews and revises regulatory submissions to effectively present data and strategy to regulatory agencies, • Develops strategies for CMC agency meetings, manages preparation for agency meetings, and manages content of pre-meeting submissions. Serves as the point of contact for the regulatory agency meetings., • Manages products and change control with an understanding of regulations and company policies and procedures. Analyzes and approves manufacturing change requests., • Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions, • Stays abreast of regulatory procedures and changes in regulatory climate. Analyzes legislation, regulation and guidance, provides analysis to the organization, • Develops, implements, and documents policies and procedures within the regulatory affairs department. Leads initiatives internal to RA CMC., • Represents CMC regulatory affairs on project initiatives with other functional areas to drive efficiencies across the company., • Trains, develops and mentors individuals; may include formal supervisory responsibilitiesQualifications, • Required Education: Bachelor’s Degree in Pharmacy, Chemistry, Biology or Pharmacology, Engineering or related subject., • Preferred Education: Relevant advanced degree preferred. Certification a plus., • Required Experience: 8 years pharmaceutical with at least 3 years of demonstrated leadership, • Preferred Experience: 10 years pharmaceutical experience including 5-plus years in regulatory affairs or 5-plus years in Discovery, R&D, or Manufacturing., • Experience developing and implementing successful global regulatory strategies. Experience working with Health Authority., • Experience working in a complex and matrix environment., • Strong oral and written communication skills., • Note: Higher education may compensate for years of experience 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. 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 Kalon Executive Search is partnering exclusively with a leading contract manufacturer of nutritional supplements to identify a proven R&D Gummy Formulator with strong leadership experience to oversee gummy production operations. The ideal candidate brings 7+ years formulating pectin/gelatin gummies (fruit juice/puree bases preferred), excels in process optimization using Six Sigma/lean tools, and thrives leading cross-functional teams in a fast-paced cGMP environment. *** This role is in person in Irvine CA Key Responsibilities: * Lead gummy formulation/reformulation from concept to scale-up, ensuring regulatory compliance and quality standards * Provide technical expertise for process improvements, cost savings, troubleshooting, and global formula adaptations * Collaborate with Quality, Procurement, PD, and Manufacturing to resolve development/production challenges * Drive continuous improvement via SPC, Six Sigma, rheology analysis, and root cause investigations * Develop/modify formulas; approve PLI, nutrition facts, master formulas, and manufacturing instructions * Monitor KPIs, optimize equipment/resources, and implement new technologies with suppliers/academia * Troubleshoot customer complaints and process losses; communicate project status to leadership Qualifications: * BS Food Science, Nutrition, Chemistry, Biology or related field * 7+ years gummy supplement formulation (pectin/gelatin, variable dosages, juice/puree bases) * Expertise in formulation costing/pricing analysis, potency calculations, and statistical process control * Fluent English (Spanish preferred); strong MS Office skills * Proven leader who multitasks effectively with minimal supervision Compensation: $100,000-130,000 base plus benefits If this sounds like the position you have been waiting for, please apply using the online application or the link below. All inquiries are strictly confidential. Our focus is to assist you in making your best next career move, and we will not use your information for any other purpose. Kalon Search is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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 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 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 DescriptionSalary: $60,048 - $102,536 DOE Job Description: The teachers primary responsibilities and qualifications are listed below. All teachers report to their site administrator (s). The teacher is responsible for the development and performance of the courses they instruct. The teacher will foster a collaborative and stimulating classroom environment for a diverse group of students, as well as foster a strong collaboration between parents, faculty members, board members and community partners. Responsibilities: • Develops lesson plans according to the CA CCSS and CA State Content Standards, • Fosters a safe and nurturing learning environment, • Organizes classroom system/procedures and manages student behavior to ensure all students are fully engaged in learning, • Establishes an environment where students are excited about learning, • Builds strong relationships with students and parents, • Identifies student areas for improvement and is able to work with the student and family and internal resources to suggest options for improvement, • Provides continual assessment of student progress, maintain student records and complete assigned paperwork in provided timeframes, • Collaborates with the Educational specialist and other staff to meet the needs of all students, • Attends and implements professional development training throughout and beyond the school year, • Demonstrates support and knowledge of schools goals and mission, • Participates, attends and plans field trips, • Participates in school events during, before and after school, • Attends and participates in school based meetings and activities Qualifications: • Must possess a current California teaching credential, • Bachelors degree from an accredited college or university, • Masters degree in subject matter field or Education is strongly preferred, • Meet all NCLB requirements, • At times this job may entail lifting, walking, sitting and standing for periods of time No new employee can begin employment until all local mandated trainings are completed and the fingerprints cards are processed by the California Department of Justice and it is determined that there is no criminal conviction that would prohibit the employee from working with students and staff.

Job DescriptionCompany Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Director Regulatory Affairs Therapeutic Area Head, GRS, is responsible for the management of global regulatory leads with product and disease state expertise for specific therapeutic area(s). Provides oversight for the development and implementation of global strategies, ensuring legislation requirements are met. Provides oversight on strategic regulatory decisions and ensures regulatory and cross-functional alignment. Provides oversight of development of impactful strategic messaging in regulatory dossier content. Exercises division and corporate influence, provides expert opinion and leadership to initiatives. When delegated by the TA VP, provides regulatory leadership at the Therapeutic Area Strategy Committee (TASC) to deliver TA strategies, disease state insights, vision and direction to differentiate assets regulatory strategic program risks, regulatory intelligence, and recommendations on portfolio optimization. Has department leadership and budgetary accountabilities • Provides leadership and supervision to a team of global regulatory leads (GRLs) who are responsible for developing and implementing regulatory strategy for development and marketed products. Key internal leader and driver of regulatory policy and strategy; ensures development of creative and impactful global product strategies for each product., • Works to develop and achieve long-range goals and objectives. Determines and pursue courses of action necessary to obtain desired results. Provides guidance to GRL on global regulatory strategies, risk assessments and mitigation strategies. Approves global regulatory product strategies and risk assessments with mitigation plans for products within assigned TAs., • Supervises GRL personnel. Independently manages product and project assignments within TA, and may participate or lead initiatives. Provides direction and guidance to adjacent regulatory personnel; evaluates performance of and assists in career development planning for other regulatory functions, • Works across TAs for assigned products and influences the development of regulations and guidance, • Advises internal personnel on regulatory strategies. Provides expert assessment on disease state insights, vision, and direction to differentiate assets, regulatory intelligence on global regulatory environment, and provides recommendations to TASC and Sr. Management to optimize portfolio., • Follows company policies and procedures for regulatory record keeping and may develop and implement policies and procedures within the RA department and ensures direct reports follow requirements. Ensures regular regulatory management communication of important timely issues and the impact on the global program and across assigned TA., • Develops, communicates, and builds consensus for operating goals that are in alignment with the department. Oversees personnel to achieve department objectives. Ensures creation of immediate to long-range plans to carry out objectives established by executive management. Provides guidance and recommendations to direct reports on work processes and operational plan decision-making., • Advances the organization’s goals by participating in and taking leadership roles in professional associations, industry, and trade groups as appropriate for TA. Represents Regulatory and presents to cross-functional teams as TA Lead. Represents Regulatory on other AbbVie governance and review committees at the request of the TA VP., • Develops and maintains budget for a department or group to meet organizational goals. Forecasts future departmental needs including human and material resources and capital expenditures. Actively participates in leadership meetings, providing regulatory and management expertise and decision-making. Recommend modifications to the structure of organizational units or a centralized functional activity subject to senior management approval.Qualifications, • Required Education: Bachelor's degree (pharmacy, biology, chemistry, pharmacology) related life sciences, • Preferred Education: Relevant graduate degree preferred. Certifications a plus, • Experience working in a complex and matrix environment with multiple stakeholders. Proven success bringing products through development review and approval. Broad experience contributing to enterprise management of a portfolio of products. Strong verbal and written communicator with proven negotiation skills and strategic thinking. Strong business acumen and the ability to work under pressure managing a product portfolio, • Strong experience working with multiple functions (Ad/Promo, Labeling, CMC, devices, Clinical development, etc.) and cross functional teams and executive management., • Proven 10+ years in a strategic leadership role with strong project management skills and demonstrated executive presence., • 3+ years of supervisory/management experience, • 3 years of supervisory/management experience, • Preferred Experience: 12+ years’ experience in pharmaceutical regulatory activities; preferably with experience as lead regulatory product strategist in at least 2 regions in addition to the US (UK, EU, JAPAC, etc.), • NOTE: Higher education may compensate for years of experience 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 thisposting 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 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 anduntil 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 DescriptionThe Center for Inherited Blood Disorders (CIBD) is a mission-driven non-profit organization focused on delivering high-quality, comprehensive, and family-centered care to improve the quality of life for children and adults with blood disorders. The Research Internship Program is designed to provide you real-world experience that challenges you to develop your skills and prepare you to lead at the next level of your career. Working side-by-side with an experienced leader, you will gain hands-on research experience across various stages of the research process. Because each intern's professional development goals are unique, your experience at CIBD will be tailored to advance your career in the areas of most interest to you. Becoming a Research Intern at CIBD means you will gain enriching and diverse experience that will increase your potential for consideration in a variety of future roles and have an impact on the blood disorders community. Department: Research Approximate Assignment Duration: June - September Approximate Shift: M - F, 8:00 - 4:30 (40 hours per week) Location: On-site Paid internship Job Summary This role is ideal for undergraduate or graduate students looking to gain hands on experience in clinical research practices and regulations. Assist in conducting research projects, gathering data, and analyzing information under the guidance of the Research Supervisor and Research Director. Responsible for data collection, analysis, literature reviews, report writing, and administrative tasks as needed. Collaborate with team members, assisting in the laboratory processing specimens, preparing reports, and participating in team meetings. Essential Duties • Conduct literature reviews and synthesize findings to support ongoing projects., • Collect and analyze data using statistical tools and software., • Prepare comprehensive reports and presentations to communicate research findings to stakeholders., • Participate in team meetings and contribute ideas to enhance research strategies and processes., • Support administrative tasks related to project management and documentation.Requirements, • Actively enrolled in either an undergraduate Bachelors degree (or Associates degree for Transfer) or a graduate degree in a health or science-related field (e.g., Biology, Public Health, or Health Sciences) from an accredited institution, • Have reliable transportation to work on-site for the duration of the internship assignment, • Must be legally authorized to work in the United States without Company sponsorship now or in the futureCompensation listed is the expected salary base at time of hire. Actual compensation offered will be determined by factors such as location, level, job-related knowledge, skills, and experience About the Organization The Center for Comprehensive Care & Diagnosis of Inherited Blood Disorders (CIBD), a 501(c)3 non-profit organization, is committed to providing comprehensive care for patients and their families with rare, chronic inherited blood disorders. CIBD is a part of a nationwide network of over 140 Hemophilia Treatment Centers that use multidisciplinary teams of blood disorder specialists to provide expert comprehensive diagnosis, medical care, outreach, education, outcomes monitoring, surveillance, and prevention services to people with hemophilia, Sickle-Cell Anemia, Thalassemia, Von Willebrand Disease, and other related hematology conditions. CIBD is the regional grantee for the Western States Region/Region IX providing regional leadership, fiscal and administrative oversight, grants management, capacity building, clinical education, technical assistance, evaluation, and outreach to public and private health agencies at the local, state, and federal levels. The Center for Inherited Blood Disorders is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the company's non-discrimination policy. We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable and welcoming.

Job Description· Be an Educator at Bionerds biology workshops for kids from K-8th grades.· Teach biology curriculum and assist the kids with hands-on activities. Setting and cleaning up classroom before and after classes. · A bachelor’s degree in Biology or other related science/experience is a must. Teaching experience is preferred, but not required. Other Info and Desired Personality/Skills:· During school session (mid-August to May), required to work IN-PERSON a minimum of 3 days (M-F) between 12pm-6pm and minimum 10 hours per week. During summer session (June to mid-August), required to work IN-PERSON a minimum of 3 days (M-F), 4-8 hours per day between 8am-5pm. Able to work occasionally on weekends for private or marketing events for 2-5 hours. More availability is highly preferred. · 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 29 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 Description Looking for a CLS in Irvine, CA for the following shifts: 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 Description The Department of Natural Sciences at Concordia University Irvine (Irvine, CA) invites applications for a full-time faculty appointment in Biology beginning Fall 2026. The ideal candidate will demonstrate excellence in teaching and scholarship at the university level in one or more subdisciplines of biology; preference will be given to candidates who specialize in molecular biology, cellular biology, microbiology, immunology, or genetics. Candidates must be able to advance the mission and core convictions of Concordia University Irvine and the Natural Sciences Department with a clear commitment to integrating their Christian faith into their teaching, relationships with students and colleagues, and engagement with prospective students and families. This is a full-time, in-person faculty position with rank and salary commensurate with credentials and experience. Qualifications: • Master's degree (Ph.D preferred) in Biology or a closely related field, • At least 2 years of teaching experience preferred, • Teach lower-division courses in General Biology and/or General Chemistry, and upper-division courses in Molecular Biology, Microbiology, Genetics and others as needed by the department, • Teach in Concordia's Enduring Questions and Ideas (Q&I) CORE Curriculum as needed, • Advise and mentor Biology, Biochemistry, and Chemistry majors, including supervision of research capstone projects, • Support departmental initiatives such as peer mentorship programs, supplemental instruction, and prospective student recruitment events Concordia University Irvine does not discriminate in the employment of individuals on the basis of race, color, national or ethnic origin, sex, age, disability or any other protected class in the administration of its employment policies, except to the extent that religious freedom exemptions apply. As a Christian educational institution of The Lutheran Church-Missouri Synod (LCMS), and in compliance with Title VII of the Civil Rights Act of 1964, Concordia employs only those individuals who meet the religious membership requirements established by the University. Certain positions may also require affiliation with the LCMS or status as an ordained or commissioned minister, in accordance with the University's mission and religious beliefs. Application Requirements: Applicants should submit applications via the Concordia University Irvine HR website at the link below. The following materials are required: • 1-2 page cover letter, • Curriculum vitae, • Statement of teaching philosophy, • Transcript showing highest earned degree Review of application materials begins immediately, and will continue until the position is funded and filled. For full consideration, please submit materials within four weeks of the posting date. Concordia University Irvine, California is a Lutheran co-ed, residential liberal arts university serving over 4,300 students, offering undergraduate and graduate degrees in over forty fields of study. Please visit Concordia's website at for additional information. Full Time Faculty, Exempt $66,000-$98,000/yr Benefits: Health, vision, dental, and life insurance. Retirement plans with employer matching. Job Posted by ApplicantPro

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 AbbVie is dedicated to delivering innovative, safe, and effective medicines and products that address critical health issues and make a remarkable impact on people's lives. As a Global Trade Compliance organization, we are committed to driving and pioneering best-in-class trade compliance practices in a dynamic global environment. The Supervisor, GTC – Tariff Classification, is responsible for ensuring that AbbVie’s cross-border transactions are executed in compliance with import/export regulations worldwide. This Supervisor will play a vital role in the leveraging of technology solutions in the tariff classification area that enables import/export compliance and supports cost savings activities globally. The Supervisor, GTC - Tariff Classification will be assigning import and/or export classifications, documenting the rationale for such determinations, and making updates based on revisions to the classification lists. Responsibilities • Accelerate cross-border business by assigning import/export classifications per the Harmonized Tariff Schedule for each relevant market., • Support the implementation of new technologies (e.g. Agentic AI) that enable a more efficient approach to classification and audit practices., • Serve as a key liaison, collaborating with Purchasing, Supply Chain, Engineering, and other partners to gather critical data and drive informed tariff decisions., • Champion documentation excellence by clearly articulating classification logic and securely managing technical and supporting evidence., • Drive compliance by preparing and reviewing classification requests for government submissions, ensuring accuracy and thoroughness., • Proactively review classifications and implement updates to reflect the evolving tariffs and regulations., • Identify and address potential compliance risks, developing solutions that safeguard our global operations., • Foster a culture of compliance by leading training and monitoring programs, ensuring the highest standards in product classification., • Provide essential support in determining duty preferences under Free Trade Agreements and Special Trade Programs, contributing to global cost efficiencies., • Act as a trusted source for trade compliance insights by proactively tracking, interpreting, and communicating regulatory and legislative updates to GTC stakeholders—ensuring the organization stays ahead of potential impacts with timely and actionable alerts.Qualifications Qualifications • Bachelor's degree in a related field (e.g., international trade, supply chain, engineering)., • 6+ years of experience working in a broker’s agency, multinational company, or consulting firm., • Extensive experience with harmonized tariff codes with particular focus on the United States and the European Union., • Proactive, well-organized and able to simultaneously manage multiple time-sensitive tasks, with little or no direct supervision., • Detail-oriented and possess good research and analytical skills., • Ability to interpret chemical and clinical terminology, process and classifications., • Ability to be inquisitive in many fields, from chemistry to biology to machinery., • Strong planning, analytical, time management, and organizational skills with ability to multitask., • Strong communication, collaboration, and stakeholder management skills, with the ability to effectively engage with stakeholders at all levels of the organization. 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. 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 The Product Development Scientist is involved in planning, conducting and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The scientist works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in decision making that will impact the performance of the final product. • Position is onsite in Irvine, CA., • Master’s degree with a minimum of 3 years’ experience or a Ph.D. with a minimum of 1 year experience., • Knowledgeable, with good technical insight of NGS and PCR-based assay development., • Knowledgeable, with good technical insight of molecular biology, particularly PCR and MSP, DNA extraction and modification., • Knowledge of FDA quality systems regulations (QSR) and ISO standards (ISO 13485 or ISO 9001-2008) a plus., • Excellent mathematical and analytical skills, reasoning ability, critical attitude and communication skills., • Familiarity with data analysis and visualization using R or Python, and experience applying statistical or machine learning methods to experimental datasets, is considered a plus. Mdxhealth is building a world class healthcare company, providing significant career development and financial opportunities. Company Benefits: We offer a comprehensive compensation and benefits package, which includes a competitive salary, company paid medical, dental, vision and life insurance coverage, 401(k) with company match, generous employee discounts, a casual, but driven work environment, and the ability to make a real difference as a key contributor to our growth. Mdxhealth is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Accessibility: If you need an accommodation as part of the employment process, please contact Human Resources at: 866-259-5644.

Job Description Prudential Overall Supply is seeking an experienced Quality Assurance Manager to lead and advance our enterprise Quality Management System (QMS) across all facilities nationwide. This role plays a critical part in supporting our cleanroom and life-science service offerings and will have broad responsibility for ISO compliance, audit readiness, and quality leadership across all laundry plants. Key Responsibilities · Lead the execution, implementation, maintenance, and continuous improvement of the enterprise Quality Management System (QMS) across all ISO-certified facilities. · Ensure compliance with ISO standards, internal quality policies, and customer requirements, with a strong focus on aseptic, sterile, and cleanroom-controlled environments. · Serve as a primary quality representative for internal audits, ISO certification audits, and customer audits, including preparation, participation, and timely closure of findings. · Analyze quality performance data, trends, and risks; develop and implement corrective and preventive actions (CAPA). · Develop, implement, and update quality assurance programs, procedures, and operating practices aligned with business objectives. · Partner cross-functionally with Operations, Engineering, and other teams to standardize quality practices and drive continuous improvement. · Lead, mentor, and support Quality team members and plant-level QA leadership nationwide. · Interface with vendors and suppliers, as needed, to support supply quality and adherence to quality standards. · Travel to plant locations nationwide to provide quality leadership, coaching, training, and audit support. Qualifications · Bachelor’s degree in a Life Science discipline (e.g., Biology, Chemistry, Microbiology, Engineering, or related field) required. · Minimum of 10 years of Quality Assurance experience in one of the following: o Pharmaceutical, biotechnology, or medical device manufacturing in critical aseptic (sterile) environments, or o Quality Assurance leadership within cleanroom laundry operations. · Demonstrated experience supporting and leading ISO-certified quality systems in a multi-site or enterprise environment. · Strong audit-facing experience with customers and certification bodies. · Ability to travel approximately 30% nationwide. Benefits of Working at Prudential Overall Supply · Competitive compensation commensurate with experience. · 401(k) with company match and profit sharing — when the company performs well, our employees share in the success. · Comprehensive medical, dental, and vision insurance coverage for you and your immediate family. · Paid time off, including vacation and sick time. · Paid life insurance. · Tuition reimbursement available after six months of employment. · Monday–Friday work schedule. · Opportunities for career development and advancement within the organization. Company Background Founded in 1932, Prudential Overall Supply provides best-in-class uniform and textile rental solutions to businesses nationwide. Our service offerings include uniform rental, leasing, and purchase programs for industrial and specialized environments, along with related services. As an essential service provider, Prudential is proud of the dedication and tenure of our employees and the long-standing relationships we maintain with our customers. This foundation enables us to consistently deliver high-quality products and dependable service at a fair value — today and into the future. Equal Opportunity Employer Prudential Overall Supply is an equal opportunity employer. We do not discriminate in hiring or employment on the basis of race, color, gender, national origin, ancestry, religion, physical or mental disability, age, veteran status, sexual orientation, gender identity or expression, marital status, pregnancy, citizenship, or any other characteristic protected by applicable law.

Job DescriptionBiologist / Environmental Scientist 🟢 Direct Hire Opportunity with Superior Skilled Trades Superior Skilled Trades is seeking an experienced Biologist / Environmental Scientist to support environmental planning, habitat restoration, biological monitoring, and compliance projects throughout California and surrounding regions. Responsibilities • Conduct biological field surveys for special-status plant and animal species, • Perform habitat assessments, nesting bird surveys, invasive species assessments, and biological monitoring, • Assist with wetland delineations and environmental compliance activities, • Gather and analyze environmental data and prepare technical reports, • Support CEQA/NEPA documentation and permitting efforts, • Deliver environmental compliance training to field staff, • Coordinate with project teams, agencies, and field personnelQualifications, • Bachelor’s degree in Biology, Ecology, Wildlife Biology, Botany, Environmental Science, or related field, • 5+ years of biological field survey and reporting experience, • Strong knowledge of:, • CEQA / NEPA, • Federal & California ESA, • MBTA, • Clean Water Act, • Fish & Game Code, • Section 404 permitting, • Experience identifying special-status species and habitat types, • Strong technical writing and data analysis skills, • Ability to travel and work in field environments throughout CaliforniaPreferred, • Wetland delineation experience, • Construction monitoring experience, • GIS experience ymBKibdTK2

Job DescriptionBenefits: • Flexible schedule, • Free food & snacks The ideal candidate will be able to teach advanced biology concepts clearly, guide problem-solving strategies, and help students develop competitive exam skills. Responsibilities • Teach biology competition classes (group or 1-on-1), • Cover topics including:, • Cell biology, • Genetics, • Evolution, • Physiology, • Ecology, • Develop lesson plans and practice materials, • Train students in problem-solving and exam strategies, • Assign and review homework / practice tests, • Track student progress and provide feedbackQualifications, • Strong background in Biology or related field, • Experience with USABO / Biology Olympiad / Science competitions, • Ability to explain complex concepts clearly, • Strong communication and teaching skills, • Prior teaching or tutoring experience preferredPreferred, • USABO semifinalist/finalist or similar competition experience, • Biology major / pre-med / graduate-level background, • Experience teaching middle school / high school students, • Bilingual (English/Chinese) is a plus

Job DescriptionSalary: $19.00- $20.00/hr Ranch and Life Science Lead Reports to: Program Director Status: Part-time, hourly Benefits: Sick time, flexible schedule Supervises: Ranch assistants Pay Range:$19.00-$20.00/hour GENERAL DESCRIPTION: This position supports the missions and operations of the Orange County Boy Scouts of America and the Irvine Ranch Outdoor Education Center. The mission of the Boy Scouts of America is to prepare young people to make ethical and moral choices over their lifetimes by instilling in them the values of the Scout Oath and Law. The mission of The Irvine Ranch Outdoor Education Center is to serve all youth of Orange County by providing quality outdoor educational programs that instill in them an appreciation of the outdoors and the environment, teach effective teamwork, instruct about the cultural history of Orange County, and provide access to the natural resources of the surrounding areas. REQUIREMENTS • Minimumage requirement is 21, • Four-year degree inhorticulture,botany,agriculture, biology, agronomy,orrelatedfield,or equivalent relevant work experiencehighly preferred, • Knowledgeand experienceinorganic growing practices& soil regeneration, • Able to create and followcrop plans., • Able to workoutdoors formost of the day doing physically demanding tasks., • Maintain certification in Red Cross Adult and Pediatric First Aid, CPR, and AED, • Highly desired: Bilingual JOB DUTIES • Responsible forsupervising,overseeing,andmaintainingfruitorchardandgarden, beehives,chickens,and all associated classes, lessons, activities, training, and curriculum., • Perform regular maintenanceand manual laborincluding planting,thinning,pruning,irrigation/watering, fertilizing, propagating, weeding, soil amending, mulching,Integrated PestManagement,etc. with consideration for wildlife and guests, • Safely use tools and machinery such as trimmers, saws, loppers,etc.as needed, • Lead volunteers and staff to manage fuels and mitigate fire danger, • Must be able to spend most work hours outdoors in the orchard, garden, and other ranchareas doing physically demandingtaskssuch as invasive plant removal., • Teachoutdoorlife science programs toguests, Scouts,and school groups during Outdoor Science Schooland other ranchand life scienceprograms., • Collaborate with developing and implementingnew programsand activities., • Support the overall operations of the Orange County Boy Scouts of America., • Demonstrate proficient knowledge and implementation ofOCBSAsafety standards and regulationsin accordance withAmerican Red Cross,BSANational Camp Accreditation Program (NCAP), American Camp Association (ACA),Orange County Agricultural Services division,Orange County Fire Authority,and best industry practices., • Must be able to maintain physical abilities to uphold certifications and act quickly in emergencies., • Deliverhigh quality programming, personify professionalism, andexhibitexcellent customer service to all staff,guests, and studentsof the IROEC., • Instructordevelopment and in-service training, • Assistinoverall administrationand facilitationof programsas needed., • Complete regularinspectionsand maintenanceof program equipment and facilities., • Maintainand uphold facility standard operating proceduresincluding opening and closing the facility,class tracking, and staff development., • Delivery of timely and professional feedback about inventory, personnel,or other, • Participates in IROEC and OCBSA staff meetings, training, and enhancement activities., • Assist and facilitate programsand property needsin all areas as needed., • Perform other duties as assigned. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Must be able to spend significant time outdoors, • Ability to lift, carry, and balance 50 pounds, • Ability to exert on a regular basis 50 pounds of force, • Constantly able to bend and scoop, sit, and stand, possess hand-eye-foot coordination, and perform good manual dexterity. WORK ENVIRONMENT Working in a camp environment includes providing customer service, solving problems, and cooperation with others, regardless of your title. It also requires a desire to develop and work with youth, which can occasionally lead to challenging interactions. The Orange County Council, Boy Scouts of America is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

About Us We are building the gold-standard data layer that AI drug discovery platforms will run on. Partnered with leading AI labs, global tech companies, and top pharma, we're a fast-growing Palo Alto-based team on a mission to accelerate drug discovery through AI. The Role You don't need an AI background — you need deep scientific expertise. In this role, you'll use your research experience in bioinformatics to help fine-tune large language models (like ChatGPT) built for drug discovery. What You'll Do • Perform bioinformatics analysis and provide drug development expertise for assigned work., • Provide expert scientific feedback to AI researchers from leading labs, helping shape how AI models interpret drug discovery workflows in bioinformatics and computational biology contexts. What We're Looking For • PhD in Bioinformatics, Computational Biology, Systems Biology, or a related life sciences or physical sciences field (postdocs, biopharma scientists, and industry researchers welcome), • 3+ years of bioinformatics research experience Offer Details • Commitment: 15–30 hours/week (with overlap in PST), • Compensation: Highly competitive, top 10% of industry rates, • Engagement: Contractor/freelancer (no medical or paid leave), • Duration: 1 month, with possible extension, • Remote: Fully remote, collaborative environment

Core Qualifications - 3+ years of research, academic, or industry experience in Machine Learning, or Data Science, or Software Engineering, or Computer Science, or Statistics, or Biology, or Electrical/Mechanical/Civil Engineering, or Physics, or Chemistry, or Mathematics, or Materials Science, or o

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 Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Manufacturing Associate Upstream performs multiple aspects of cGMP contract cell culture manufacturing in a multi-product manufacturing facility, including, but not limited to production, documentation, writing reports, requesting, and purchasing materials, and scheduling equipment services and calibrations. The Manufacturing Associate will play an integral role in ensuring the production and on-time release of quality products. The Manufacturing Associate will conduct him/herself in a manner representing the core values (Integrity, Adaptability, Innovation, Teamwork, and Passion) of the company with the common purpose of improving patients’ lives by consistently delivering high-quality biopharmaceutical products. Lead and conduct investigations as they pertain to facilities (or other areas of operations involving equipment or utilities) to determine roots causes and corrective/preventative actions. • Perform daily monitoring of equipment., • Operate and maintain cell culture bioreactors (Wave and 100L – 2000L disposable STR/SUB) in batch, fed-batch, and perfusion modes., • Responsible for cell culture expansions and aseptic techniques (thaw cell banks -1mL vial through cell culture expansion and maintenance - up to 15L spinner flasks performed in a BSC)., • Operate and maintain equipment - NOVA analyzers, pH meters, CO2 analyzers, pH and DO simulators, microscope, pipettors, Vi-Cell cell counter, balance, scale, MFCS, Rees, and Delta V., • Harvest operations - pod filtration, 3M filtration, and TFF system., • Schedule vendor service appointments for equipment., • Purchase necessary equipment and associated materials that are needed or low in supply., • Help create and actively support 5S, Area Improvement, and Safety Team initiatives to ensure a Continuous Improvement culture throughout the department., • Operate Sartocheck filter integrity testers., • Maintain cleanroom facility and equipment., • cGMP Documentation., • Revise and initiate Batch Production Records (BPRs), Standard Operating Procedures (SOPs), and forms., • Collaborate with other departments for raw materials, water, testing requirements, documentation, validation, maintenance, and scheduling., • Identify, escalate, and report deviations (IRs/DRs/CAPAs)., • Set up critical new manufacturing processes and equipment., • Troubleshoot equipment and process issues in collaboration with Facilities (FAC), Manufacturing Sciences and Technology (MSAT), and Validation (VAL) departments., • Ensure that equipment and material are available as required for each production run., • Identify the technical, procedural, and equipment issues that hinder production and compliance. Inform support departments and manager as needed., • Assist in the transfer of technology from PD and MSAT to cGMP Manufacturing., • Assist with periodic technical and compliance investigations, inspections, and audits., • Report all unsafe activities to manager and/or Human Resources., • Participate in proactive team efforts to achieve departmental and company goals., • Communicate with team members, supervisors, and members of other departments, as appropriate, to assure prompt resolution of problems., • Prepare media and buffer., • Perform aseptic filling., • 2+ years of related experience and/or training; or equivalent combination of education and experience. This role is a full-time position operating Monday through Friday on a 5x8 (5 days x 8 hours) schedule, with operating hours from 5:00PM to 2:00AM. Must be available to work overtime, weekends, and/or holidays if needed. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $20.52-$27.35 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way., • Your written and verbal skills are out of this world, and you communicate with clarity and confidence., • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Job Description Job Title: Lab Analyst III FLSA: Non-Exempt Reports to: Lab Department Supervisor, Lab Department Manager Job Summary: The Laboratory Analyst III is a senior-level analyst responsible for independently performing complex analyses, leading laboratory documentation and quality practices, and mentoring junior staff. This role includes designing and validating investigation tests, improving workflows and methods, and ensuring that laboratory operations meet client expectations and industry standards. The Lab Analyst III plays a key role in maintaining high-quality data, supporting continuous improvement, and driving technical excellence across the lab. Looking for experienced GC analyst to step in and work in an environmental laboratory. In addition to analyst duties candidates are expected to mentor junior staff members in the GC area. Analyst III candidates should be capable of independently developing methods and adhering to the laboratories QA program with minimal supervision. Experience in GC/MSD is a mandatory. Additional experience with GC/FID and GC/ECD is preferred. Duties/Responsibilities: • Prepare, analyze, and track sample progress; ensure timely completion and communicate delays appropriately., • Independently set up and load instruments for analysis, train others in proper setup and operation., • Independently manage laboratory documentation and oversee documentation practices for others; identify and implement workflow improvements., • Prepare complex standards and reagents independently; serve as a training resource for junior analysts., • Lead calibration protocols, develop maintenance schedules, and train staff on instrument care and troubleshooting., • Ensure accurate flagging and narrative documentation with minimal corrections, guide others in best practices., • Design, perform, validate, and summarize investigation tests; monitor corrective actions for effectiveness., • Evaluate results against client requirements and industry standards; recommend and implement method improvements to meet performance targets., • Demonstrate advanced knowledge of test codes, SOPs, and the chemistry employed in laboratory methods., • Advanced knowledge of laboratory techniques, instrumentation, and analytical chemistry., • This role requires sufficient experience with GCMS systems (both VOC and SVOC). Additionally, it is preferrable that candidates have experience with other GC systems (e.g., GC-FIF, GC-ECD, GC-TCD), • Strong leadership and mentoring skills., • Proven ability to troubleshoot complex technical issues and improve laboratory processes., • Excellent documentation and communication skills., • High attention to detail and commitment to data integrity and quality. $28-39/hour DOE Education and Experience: • Bachelor’s degree in Chemistry, Biology, Environmental Science, or a related field (Master’s preferred)., • Ability to sit, stand, and walk for extended periods., • Manual dexterity to operate laboratory instruments and computer systems., • Occasional lifting of up to 50 pounds., • Medical, Dental, and Vision Insurance, • Flexible Spending Accounts, • 401(K) Plan with Competitive Match, • Continuing Education and Tuition Assistance, • Employer-Sponsored Disability Benefits, • Life Insurance, • Employee Assistance Program (EAP), • Paid Time Off (PTO), Paid Holidays, & Bonus Floating Holiday (if hired after July 1st), • Profit Sharing or Individual Bonus Programs, • Referral Program, • Per Diem & Paid Travel

Job Description The Clinical Research Associate (CRA) assists the Clinical Affairs Team in the administration of clinical research studies. The CRA will respond to a variety of study account inquiries, issues and requests and act as a liaison between the lab and the study account. The CRA will monitor specimen TAT, set up new study accounts, manage current study accounts, requests, and track specimens, and ensure that all study specimens are adhering to the SOP. The CRA will work independently to monitor your study sites, including evaluation, initiation, routine and close out visits. The CRA will manage multiple aspects of subject’s welfare, including submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. The CRA will monitor clinical study data for completeness and accuracy, perform data cleaning, reconciliation of data queries and generate data reports as needed. When required, the CRA will perform remote or on-site data mining in medical office EMR systems. Provide administrative support as needed to execute clinical study start up and close out duties. Provide assistance to study sites with respect to communication, study supplies, etc. Maintain close communication with the Director, Clinical Affairs, while taking initiative and working independently on assigned tasks. • Location – Irvine, CA. This is a hybrid position – at least 3 days in the office., • Basic knowledge of biology, genomics, or molecular biology., • Minimum of at least 1 year of study experience as a CRA, including at least 1 year of active independent field monitoring experience as a CRA— all types of visits., • Experience with data mining, data review and data management., • Strong problem-solving skills and ability to work independently., • Self-motivated, detail-oriented, organized, and able to prioritize and manage multiple projects requirements simultaneously., • Willingness to travel nationally 50% of the time or as needed., • Hiring range: $64,500 to $75,000 annually. The actual rate will be determined based on experience and other factors permitted by law. MDxHealth is building world class healthcare company, providing significant career development and financial opportunities. Company Benefits: We offer a comprehensive compensation and benefits package, which includes a competitive salary, company paid medical, dental, vision and life insurance coverage, 401(k) with company match, generous employee discounts, a casual, but driven work environment, and the ability to make a real difference as a key contributor to our growth. MDxHealth is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Accessibility: If you need an accommodation as part of the employment process, please contact Human Resources at: 866-259-5644.

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 Director Regulatory Affairs Global Regulatory Lead (GRL I) in Global Regulatory Strategy is responsible for developing and implementing global regulatory strategies to secure and maintain market approval for product(s) in assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Project responsibilities may include Area Lead (US/Canada) role. May lead the Labeling Regulatory Strategy Team (LRST). Ensures strategic messaging in global regulatory dossiers and responses under guidance of management. May serve as the primary regulatory interface with the AST and supporting teams. Ensures compliance with global regulatory requirements. Manages compounds through all phases of development, including post approval and throughout the life cycle of the product. Demonstrates strong understanding of drug development and leadership behaviors consistent with level. Develops and implements acceleration strategies with guidance from supervisor. Responsibilities • Interfaces with the LRST and AST to implement cross-functional company objectives. Under supervision, leads the GRPT to development of creative global strategies in line with applicable regulations to achieve business objectives for development and marketed product. Proactively seeks expert advice and technical support from cross functional stakeholders, supervisor, and TAH level personnel., • Leads cross-functional stakeholders and regulatory professionals to ensure inclusion of appropriate and clear strategic messaging in the content of global regulatory dossiers and responses to regulatory Agency requests., • Accountable for ensuring that corporate goals are met. With support from manager, acts as key internal leader and driver of regulatory policy and strategy for assigned products. Leads preparation and maintenance of global regulatory product strategies for assigned products. Under guidance of supervisor, leads regulatory and cross-functional team in the preparation and maintenance of risk assessment and mitigation strategy development for assigned products and communicates plan to relevant stakeholders, • May participate in regulatory and Company initiatives., • May influence the development of regulations and guidance. Analyzes legislation, regulations and guidance and provides analysis to the organization, with worldwide accountability for assigned products., • Follows company policies and procedures for regulatory record keeping and may develop and implement policies and procedures within the RA department., • Under guidance from supervisor, ensures alignment of global regulatory strategies with Sr. Management Under direction of supervisor, presents meaningful regulatory assessments and regulatory recommendations to executive management with. Proactively informs AST and management of issues, risks and mitigations. Provides assessment of impact on global programs. Provides informed regulatory opinion based on experience and expertise., • Under direction from supervisor, makes decisions regarding work processes or operational plans and schedules to achieve the program objectives established by senior management., • Follows budget allocations and keeps supervisor informed on project resourcing.Qualifications, • Strong communication and proactive negotiation skills. Business acumen and able to work under pressure 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 postingbased 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 paymore 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. 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 untilpaid 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 DescriptionCompany Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Manager, Regulatory Affairs for Chemistry Manufacturing & Controls (CMC) - Biologics Product Lead, works with internal and external partners in order to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new market applications and supplements/variations with limited management supervision. Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life-cycle management teams to negotiate, influence, and provide strategic advice to peers in RA, R&D, and Operations. Responsibilities: • Prepares CMC regulatory product strategies with limited supervision. Prepares regulatory submissions, including new IND/CTA applications and amendments, renewals, annual reports, supplements and variations under limited supervision., • Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions, • Reviews and revises regulatory submission documentation to effectively present data and strategy to regulatory agencies under limited supervision, • Responds to global regulatory information requests under limited supervision., • Develops strategies for CMC-related agency interactions and manages preparation of agency meeting requests and information packages, under limited supervision, • Manages products and change control with an understanding of regulations, agency guidance and company policies and procedures with limited supervision. Analyzes and approves manufacturing change records with limited supervision., • Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations Product Teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions and stays abreast of regulatory procedures and changes in the external regulatory environment., • Analyzes legislation, regulation and guidance and provides analysis to the organization under limited supervision, • Contributes to creation of white papers and policies to illustrate current regulatory thinking under supervision of manager. Participates in initiatives internal to RA CMC, • May act as a formal or informal mentor to others., • Required Education: Bachelor’s degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject., • Preferred Education: Relevant advanced degree preferred. Certification a plus., • Required Experience: 6 years biopharmaceutical or related industry experience., • Preferred Experience: 6 years biopharmaceutical RA, R&D or Operations experience including 3 years in regulatory affairs, • Experience working in a complex and matrix environment, • Strong oral and written communication skills 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 thisposting 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 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 anduntil 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 DescriptionSalary: 18-20 MISSION STATEMENT The mission of the Boys & Girls Clubs of Central Orange Coast is to ensure every child hasmentors and championsin life. ORGANIZATION STRUCTURE AND INTERFACES Position Reports to: General Manager or Unit Director Primary Interfaces: Youth, Parents, Program Staff, General Manager, Operations Team Hours: 23 25 hours/week MUST BE ABLE TO ACCOMMODATE AND PROVIDE AN OPEN/CONSISTENT M-F SCHEDULE unless otherwiseapproved. Daily Hours Include: 1:30 - 6:00PM and WEDNESDAYS/MINIMUM DAYS 12:30PM - 6:00PM POSITION DESCRIPTION The Boys & Girls Clubs of Central Orange Coast is a dynamic, innovative, youth-serving organization that is committed to helping all children build positive, lifelong memories, achieve their greatest potential, and inspire future generations. The Mentor Professionals primary responsibility is toensure thatevery child has a safe, first-classafter-schoolexperience. This is done by acting as a positive, engaging adult role model, teacher, coach, and mentor. Mentor Professionals must have a genuine interest in the growth, development, and provision of a safe and nurturing environment for the students they teach, inspire, encourage, andimpact. Professionals work directly with an assigned group ofapproximately 20-25students. This is a part-time, non-exempt position. KEY ROLES: • Commitment to Safety, • Contribute to the environment of safety through the learning and implementation and monitoring of all safety-related best practices, policies, and procedures., • Promote accountability to safety through consistent observation, adherence to all safety rules and practices and proactive communication among members, parents, peers, and leadership., • Obtain and maintain Mandated Reporter training and complete annual Child Abuse Prevention training., • Complete training and participate in all Emergency Preparedness protocols including drills and communication practices. DISCLAIMER:The Boys & Girls Clubs of Central Orange Coast requires a 4-point background check for all employees before hire and during employment that includessocial security verification, local comprehensive criminal history search, national comprehensive criminal history search, and sex offender registry search. Per the organizations Screening & Onboarding Policy, a person is ineligible to obtain employment with the Boys & Girls Clubs of Central Orange Coast if such person has been convicted of any misdemeanor against children or any felony consisting of murder, child abuse,domestic violence, abduction or human trafficking, rape or sexual assault, arson, weapons, physical assault or battery, or drug possession (use or distribution) in the last five years. This position may require the ability to sit, stand, walk, bend, or reach as needed, and to lift, carry, push, or pull objects up to 50 lbs. Employees must have the dexterity, coordination, vision, and hearing necessary toperform job tasks safely and accurately. • Support Boys & Girls Clubs of Central Orange Coasts mission, To ensure every child has mentors and champions in life., • Work as a tutor/mentor in an After-School Enrichment Program providing homework assistance, academic enrichment and fitness using curriculum and materials provided by Boys & Girls Club of Central Orange Coast. This also includes making sure the classroom is clean upon your shift departure,which could include sweeping and wiping down tables., • Serve as a positive adult role model for children in the program through reliability, punctuality,appropriate dress, speech, and attitude., • Demonstrateprogram leadership skills through group expectations management and effective practices of the Clubs Guiding Principles: respect each other, respect the Club, try yourbestand have fun., • Approach behavior as communication by practicing positive reinforcement and implementing strategies that help members identify and correct challenging behaviors., • Plan, organize, and prioritize programmatic deliverables including safety practices, curriculum, and individualized member engagement., • Develop program delivery skills in a way that fosters engagement and learning while building upon the mentor-mentee relationship., • Participatein staff development and training activities when needed after hours or on weekends. 11. Operate a 9-passenger van to transport youth from school sites to Boys & Girls Clubs locations,as needed., 12. Conduct pre-trip vehicle inspections; promptly report mechanical issues or safety concerns; and maintain vehicles in a clean, safe, and orderly condition (including fueling and routine upkeep)., 13. Accurately complete and maintain transportation records, including mileage logs, vehicle inspection reports, and incident documentation., 14. Inspect and ensure availability of emergency equipment, including fire extinguishers and first aid kits., 15. Ensure the safety and well-being of all youth during transportation by maintaining appropriate supervision, applying positive behavior management techniques, and following established emergency procedures. Job Skills & Requirements: • High School Diploma and a minimum of 24-48 college units (provide proof upon interview)., • Have a drive to work with a diverse group of students from different socio-economic backgrounds and levels of educational preparedness. Exhibit the characteristics of strong leadership, patience, effective communication, and a consistent desire to learn and executenew programs. • Ability to teach Math and English skills (K5th) or (6th 8th) & additional subject such as science, biology, chemistry, history, as well as intervention/prevention topics (Preferred but not required)., • Time management, planning, and organization skills., • Ability to speak and write Standard English appropriate in apublic-schoolsetting., • Must pass Live Scan Fingerprinting and CRA background check., • CPR & Basic First Aid certified preferred (provide proof upon interview)., • Proof of negative TB Test valid within the past 3 years from hire date., • Must have transportation to and from work DISCLAIMER: The information presented indicates the general nature and level of work expected of employees in this classification. It is not designed to contain, or to be interpreted as, a comprehensive inventory of all duties, responsibilities, qualifications, and objectives required of employees assigned to this job.

Job Description We are currently seeking resumes from qualified, responsible, self-sufficient, energetic Wildlife Biologist’s currently holding an International Society of Arboriculture (ISA) Arborist Certification 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 and company. We offer a friendly, professional atmosphere with excellent benefits and a salary commensurate with experience. Job Description: The position entails a mid-level biologist possessing general knowledge and experience with the assessment of impacts from various development projects on flora, fauna, and the natural environments in the Southwest US (California and Arizona). The ideal candidate can lead a small project team of biologists to conduct field assessments independently. This role will be a key link between entry level biologists and senior biologists. Essential qualifications for this position include beyond basic understanding of the natural systems of Southern California, including various habitat types, and vegetation communities. Desirable qualification includes a sound knowledge of California and Arizona regulatory agencies and their regulatory oversight of natural resources. Key Responsibilities: • Lead and execute field surveys, data collection, and ecological assessments for diverse projects., • Conduct (pre-construction) wildlife/plant habitat assessments and surveys (including jurisdictional waters and wetlands)., • Monitor construction activities and ensure compliance with applicable permit conditions, • Review health and inventory plant material on construction sites, • Assist with the development of plant salvage plans and documentation, • Record and identify flora and flora., • Independently collect, compile, and analyze biological data collected in the field and/or from desktop research., • Prepare survey reports, habitat suitability assessments, and technical memorandums related to biological resources., • Under the guidance of a Senior Biologist, prepare biological assessment/evaluation reports, and various plans such as mitigation plans, habitat restoration plans, and habitat conservation plans., • Under the guidance of a Senior Biologist, prepare biological sections of various technical documents (such as CEQA and NEPA documents)., • Prepare application packages for Clean Water Act Section 404 permits, Section 401 water quality certifications, and Section 1602 Lake and Streambed Alterations., • Develop appropriate and feasible mitigation measures., • Collect, compile, and analyze geospatial data using GPS equipment and GIS software., • Other duties as assigned. Job Qualifications (Education, Experience, and Skills): • Minimum of a bachelor’s degree in wildlife biology, botany, conservation biology, ecology, natural resources, or a closely related field, • Minimum of three (3) years of experience in the fields of wildlife or fisheries biology, • ISA Certified Arborist, • Field experience in the Southwest US with native threatened/endangered wildlife or plant species, • References regarding experience will be required., • Knowledge of Southwest US (including California and Arizona) flora and fauna and natural communities., • Knowledge of Southwest US (including California and Arizona) regulatory agencies with oversight of natural resources., • Proficient understanding of the federal Endangered Species Act, Clean Water Act and National Environmental Policy Act., • Proficient understanding of the California Endangered Species Act, California Department of Fish and Game Section 1602, and California Environmental Quality Act., • Strong written and oral communication skills., • Proficiency in Microsoft Office Suite, as well as computer hardware and software skills., • Ability to collaborate closely with fellow employees and clients., • Ability to work independently on one’s own initiative as well as a member of a diverse team., • Ability to foster a positive work environment and organize and progress multiple assignments., • Ability to pass a background check., • Valid driver's license, with the ability to maintain insurability under the company's insurance carrier Preferred Qualifications: • Experience with GPS equipment and GIS software or other spatial analysis tools., • Additional arborist certifications such as American Society of Certified Arborists (ASCA), ISA Certified Arborist Specialties (Municipal, Utilities, and Tree Risk Assessor), and ISA Tree Risk Assessment Qualified (TRAQ)., • Experience preparing environmental regulatory compliance documents such as biological assessments/evaluations., • Experience with Clean Water Action Sections 404 and 401 compliance and permitting., • Experience with the California Department of Fish and Game Section 1602 Lake and Streambed Alteration agreements., • California linear project experience (utility line, transmission line, roadway, railway, etc.), is preferred, • Survey and/or monitoring experience with the following species: Western burrowing owl, blunt nose leopard lizard, San Joaquin kit fox, Tipton kangaroo rat, giant kangaroo rat, and Swainson’s hawk., • Experience with and ability to lead nesting migratory bird surveys, • Experience with and ability to lead native plant surveys, • Attended an agency-led training for and experience surveying for protected species including but not limited to federally-listed, state-listed species, Bureau of Land Management sensitive species, and US Forest Service sensitive species. Other Requirements: • Ability to work in harsh outdoor conditions (heat, cold, dust, wind, and rough terrain)., • Ability to travel with overnight stays for extended periods., • Ability to climb stairs without assistance., • Ability to lift 30 pounds and carry a 30-pound backpack for at least 1 hour., • Ability to use a computer while sitting for extended periods, daily. 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. TYPSA, Inc. Culture: • Thinking toward future company and personal growth, • Yielding equity, inclusion, and diversity, • Passionate supporter of clients and teammates, • Shared comradery, • Action oriented and flexible TYPSA, Inc. Benefits: TYPSA, Inc. 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. TYPSA, Inc. Overview: TYPSA in the United States is a multi-discipline engineering and environmental consulting firm assisting public and private clients in planning, developing, designing, constructing, and maintaining critical infrastructure projects across the United States. With offices in Arizona and California, TYPSA provides local expertise with the backing of a global network. Originally established in 1992 as AZTEC Engineering Group, Inc., the company began as a two-person DBE firm and grew into a trusted corporation serving clients nationwide. In 2006, AZTEC joined TYPSA Group, an international leader in engineering, architecture, and environmental consulting headquartered in Spain with more than 60 offices worldwide. Today, as TYPSA in the United States, we proudly carry forward the AZTEC legacy while connecting our clients to the resources, innovation, and international experience of the TYPSA Group. This integration allows us to deliver tailored local solutions with the depth and reach of a global firm. TYPSA, Inc. 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 DescriptionJob description: Position Overview: We are seeking a dedicated and knowledgeable KoreanEnglish bilingual High School Tutor to join our team on a part-time basis. The ideal candidate will be able to teach one or more high school-level subjects (such as English, Math, Science, History, or elective courses) and communicate effectively with students and parents in both Korean and English. This role involves delivering personalized academic support, reinforcing classroom learning, and helping students build strong study and problem-solving skills. Key Responsibilities: • Provide one-on-one or small-group tutoring in various high school subjects based on your expertise., • Communicate clearly with students and parents in both Korean and English regarding progress, goals, and expectations., • Adapt instruction to meet diverse learning styles and academic levels., • Support students with homework, test preparation, concept mastery, and skill-building., • Track student progress and provide constructive, actionable feedback., • Create a supportive, motivating, and respectful learning environment.Qualifications:, • Fluency in Korean and English (required)., • Ability to teach high schoollevel subjects (e.g., English, Math, Biology, Chemistry, History, etc.)., • Previous tutoring or teaching experience preferred, especially with high school students., • Strong communication, patience, and instructional skills., • Ability to explain complex concepts clearly and effectively., • Reliable, professional, and comfortable working part-time with flexible scheduling.

Job Description Ready to take your HPTLC expertise to the next level and make a measurable impact in a growing lab environment? Tentamus California is searching for an HPTLC Chemist to support advanced analytical testing of botanical materials, dietary supplements, and natural health products. This role requires strong expertise in high-performance thin-layer chromatography (HPTLC) and complementary analytical techniques, with a focus on method development, validation, and regulatory compliance. Experience in botanical analysis and manufacturing environments is strongly preferred. WHAT YOU'LL DO As the HPTLC Chemist, reporting to the Lab Manager, your responsibilities include (but are not limited to): • Perform qualitative and quantitative analysis of botanical and related products using HPTLC and other analytical techniques, • Develop, validate, and optimize analytical methods in accordance with regulatory and internal standards, • Operate, maintain, and troubleshoot laboratory instrumentation (HPTLC, HPLC, LC-MS, GC-MS, GC), • Conduct botanical identification using established methods and reference standard libraries, • Analyze and interpret complex data sets, ensuring accuracy, integrity, and compliance, • Prepare technical reports, validation protocols, and documentation for regulatory and client requirements, • Support testing of dietary supplements, natural health products, and, where applicable, pharmaceutical products, • Collaborate cross-functionally with quality, production, and R&D teams, • Ensure adherence to applicable regulatory standards (e.g., FDA, ICH, ISO 17025) and internal quality systems This is a full-time, onsite role located at Tentamus California 133 Technology Dr #150, Irvine, CA 92618. The schedule is M-F 9AM – 5PM with the occasional weekends required. WHAT'S IN IT FOR YOU? Tentamus offers an annual salary between $65,000 - $78,000, plus a comprehensive, low-cost, benefits package, including medical, dental, vision, disability, and life insurance. Employees also enjoy paid time off (PTO), 40 hours of sick time per California State Law, a matching 401k plan, and access to our free Employee Assistance Program! QUALIFICATIONS The ideal candidate will be authorized to work in the United States indefinitely and without restrictions or sponsorship, hold a Bachelor's Degree in Chemistry, Microbiology, or related life science and/or with experience in analytical laboratory testing will be considered; and who meets the following qualifications: • BS degree in Chemistry, Biology, or related field., • Minimum of 3 – 5 years of hands-on analytical laboratory experience, preferably in pharmaceutical, biotechnology, or related industry., • Minimum 1 - 2 years of hands-on HPTLC experience highly preferred., • Experience with analytical method development and/or validation preferred, • Expertise in a wide range of analytical techniques and instrumentation, with proficiency in method optimization and troubleshooting., • Familiarity with regulatory standard requirements (e.g., FDA, ICH guidelines, ISO 17025) and experience with regulatory submissions., • Excellent data analysis skills, including proficiency in statistical analysis software, • Leadership or mentorship experience is a plus., • Effective communication skills, both verbal and written, can convey complex technical information to diverse audiences., • Detail-oriented approach with a commitment to quality, safety, and compliance. This job operates in an analytical laboratory environment with exposure to chemicals and analytical instrumentation. This role routinely uses standard lab equipment such as beakers, test tubes, flasks, thermometers, and computers, among other instruments. While performing the essential duties of this job, the employee is regularly required to use hands and fingers to hold or feel, reach with hands and arms, talk, and hear. The employee is occasionally required to sit, stand; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. ABOUT TENTAMUS: Labs for Life®. We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Visit us at Tentamus.com|Follow Tentamus on LinkedIn|Follow Tentamus CA on LinkedIn Job Posted by ApplicantPro

Job Description Immerse yourself in the vibrant, innovative environment of Tentamus California in Irvine! We're seeking an Analytical Chemist to join our growing Tentamus Team! We're looking for someone who not only embodies boundless enthusiasm for scientific discovery but also thrives on collaboration, creativity, and problem-solving. If you're ready to make a meaningful real-world impact, we can't wait to welcome you aboard! How you will excel as part of our team: The Analytical Chemist will be responsible for conducting qualitative and quantitative chemical analyses on various substances to support research, development, and quality control activities under the direction of the Laboratory General Manager. Main duties include: • Executing established laboratory chemistry procedures to provide accurate and prompt chemistry data to clients., • Perform analytical chemistry testing using various instrumentation such as: GCFID, HPLC, ICPMS, GCMSMS, • Assist, oversee, and mentor Lab Techs to help them advance in their chemistry career., • Reviewing and approving QC data within parameters of precision and accuracy., • Maintaining complete and accurate chemistry documentation of activities in compliance with the Quality System., • Preparing stock standards and reagents as needed, performing dilutions of samples and solutions, weighing stock compounds, preparing standard and fortification solutions, and calibrating preparation of primary analytical methods., • Perform routine maintenance and follow preventative maintenance schedules on various instrumentation., • Notifying chemistry supervisor and taking appropriate actions for non-conformances. Participate in corrective action process., • Ensure the safe and efficient use of laboratory equipment and chemicals. Position Type & Expected Schedule Full-Time | M - F 7AM-4PM / 8AM-5PM | Some weekend/holiday hours required To flourish as an Analytical Chemist, you'll need: Our ideal candidate will be authorized to work in the United States indefinitely without restriction or sponsorship, possess a combination of technical skills, attention to detail, and a strong work ethic. Other qualifications include: • Bachelor's degree in chemistry, biology, or related science field, • 3 –5 years of experience in a commercial lab setting. Experience in testing supplements and nutraceticals is a plus!, • Hands-on experience with analytical techniques such as chromatography, spectroscopy, and wet chemistry methods., • GC and GCMSMS experience highly preferred., • Comfortability with applying tests from USP and FCC monographs, • Proficiency in data analysis software (e.g., ChemStation, Empower) and Microsoft Office Suite., • Strong attention to detail and ability to follow standard operating procedures., • Excellent communication skills, both written and verbal., • Ability to work independently and collaborate effectively in a team environment., • Knowledge of Good Laboratory Practices (GLP) and regulatory requirements is desirable. What's in it for you? Annual Salary between $65,000 - $85,000, comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance) Ample PTO and 40 hours of sick time per CA state law, and a matching 401k. Work Environment & Physical Requirements This job operates in an analytical laboratory environment with exposure to chemicals and analytical instrumentation. This role routinely uses standard lab equipment such as beakers, test tubes, flasks, thermometers, and computers, among other instruments. While performing the essential duties of this job, the employee is regularly required to use hands and fingers to hold or feel, reach with hands and arms, talk, and hear. The employee is occasionally required to sit, stand; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. About Tentamus: Labs for Life®. We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Visit us at Tentamus.com|Follow Tentamus on LinkedIn|Follow Tentamus CA on LinkedIn Job Posted by ApplicantPro

Job DescriptionBenefits: • Flexible schedule, • Free food & snacks A+1 Academy is looking for an experienced AP Biology Instructor to join our teaching team. The ideal candidate should be familiar with the AP Biology curriculum and able to help high school students build a strong understanding of biological concepts, lab-based reasoning, data analysis, and AP-style free-response questions. Responsibilities • Teach AP Biology small-group or 1-on-1 classes, • Prepare students for the AP Biology exam, including MCQ and FRQ practice, • Explain key biology concepts clearly, such as cell biology, genetics, evolution, ecology, and physiology, • Help students improve scientific reasoning, graph/data interpretation, and experimental design skills, • Provide class feedback and communicate student progress when needed, • Prepare lesson materials or adapt existing curriculum based on student needsQualifications, • Strong background in Biology, Life Sciences, Biomedical Science, or a related field, • Prior AP Biology teaching or tutoring experience preferred, • Familiarity with AP Biology exam format and College Board expectations, • Able to teach in person in Irvine, CA preferred, • Responsible, patient, and good at working with high school students, • Experience with Biology Olympiad or other biology competitions is a plus

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 About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace, technology and business knowledge; collects and analyzes issues and trends that affect the business. The Associate Director identifies and acts upon cross-organization or cross-business opportunities & possesses and leverages broad industry knowledge. Responsibilities: • Make decisions and plans for operations (work flow, assignments, staff development) within area of responsibility with minimal direction. Sets strategy and leads cross-functional/multidisciplinary therapeutic teams and multidivisional initiatives., • Maintains and evaluates productivity metrics to project current and future business needs, • Aligns and maintains effective communication channels with key Medical, Marketing, Regulatory, Legal and Public Affairs counterparts. Identifies areas of improvement in process/policy, develops recommendations/plan, and leads initiatives., • Assists in the management of the departmental budget, identifies and communicates budgetary needs to Operations and Finance, and identifies and projects current and future expenditures and business needs., • Collects and analyzes issues/trends that affect business to identify and act on cross-organization or cross business opportunities. Effective use of knowledge of global marketplace, technology and business levels., • Operates independently, with recognition of when to consult departmental senior concerning risks. In absence of Director, is responsible for day-to-day operations. Responsible for departmental initiatives, which have significant impact on both internal and external customers., • Encourages innovation and holds employees accountable for delivering on their goals; recognizes, mentors, rewards and recommends promotion for staff members based on their performance, results, and development., • Exhibits solid understanding of regulations, and guidance of regulatory authorities, political and legal climate and industry practices related to advertising and promotions to assist in meeting organizational goals. Possesses and leverages broad industry knowledge, • Develops and implements complex processes and projects and develops and delivers strategic presentations for senior management, • Identifies areas of improvement in process, policy, develops recommendations/plan and leads initiatives, • Minimum: Bachelor’s degree in science (biology, chemistry, microbiology immunology, medical technology, pharmacy, pharmacology, nursing, pharmacy) + 8 years of relevant industry experience (e.g. regulatory affairs fellowship, Health Authority, ad promo, etc.), • Preferred PharmD degree plus 6 years of relevant industry experience (e.g. regulatory affairs fellowship, Health Authority, ad promo, etc.), • Experience working in a complex and matrix environment, • Strong communication skills, both oral and written, • The candidate must have a solid understanding of regulatory advertising and promotion regulations, having had direct responsibility in this area ., • Experience developing and implementing successful global strategies 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 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 POSITION SUMMARY: The Associate Director of Manufacturing is responsible for training and supervising manufacturing personnel while leading GMP-compliant fill/finish operations. This role oversees the execution of manufacturing activities, ensuring proper documentation, reporting, and record management. Provides leadership support for equipment monitoring, troubleshooting, maintenance, and validation to ensure efficient and compliant manufacturing processes PRINCIPAL DUTIES: • Execute and/or monitor the Manufacturing processes and procedural activities as required for a GMP compliant Fill/Finish operation., • Serve as Subject Matter Expert (SME) in aseptic operations, including filling and preparation activities such as washing, autoclaving, formulation and associated support processes,, • Manage, initiate and oversee the set-up of manufacturing equipment including activities required for validation activities. Assist in designing and executing validation protocols and or machinability studies., • Support the preparation and execution of validation related qualification documents and the resourcing of associated tasks (engineering batches, aseptic process simulation, validation activities)., • Develop and implement operator training strategies, including qualification plans, technical training, aseptic behavior training, and knowledge transfer for new products., • Skilled in troubleshooting various equipment as required for the manufacturing process., • Perform technical evaluation of manufacturing related information and provide management with status reports including information required for decision-making purposes., • Writing and/or review of Process Support operational documentation (Master Batch Records, SOPs, Work Instructions, Deviations, CAPAs Change Controls, Complaints)., • Directly accountable for production schedule adherence., • Train, mentor and supervise employees within manufacturing areas., • Ensure that manufacturing systems and processes are effective and compliant and can be defended to regulatory agencies., • Initiate problem solving, trouble-shooting and technical decision-making commensurate with level of experience., • Strong knowledge of GMP procedures and requirements, as related to the position., • Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation., • Ensure batch records and logbooks are completed and reviewed in a timely manner to support batch release., • Train and supervise employees within manufacturing areas, as applicable. Ensure all training is thorough and documented., • Perform various manufacturing duties according to the GMP guidelines and initiate appropriate documentation as required including all forms, logs, batch records, etc., according to the applicable SOPs., • Ensure staff maintains and tracks manufacturing supplies and product specific materials within the manufacturing areas. Manage and ensure that all activities within the ERP system are completed real time to ensure accurate inventory levels and usage., • A minimum of BS is Chemical Engineering, Biology, or life science, with and advanced degree (MS) preferred, or equivalent relevant experience., • 10 – 12 years of relevant experience in the pharmaceutical industry, with at least 5 years in a leadership role., • Strong knowledge of Drug Product manufacturing technologies and processes to include:, • Vial Lines (stoppering and capping), • Syringe Lines within RABS, • Cartridge lines, • Manual filling equipment, • Knowledge of cGMP, FDA, DEA, and related international regulations.

Job Description Research Scientist - Simply Biotech OVERVIEW 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 Research Scientist in Irvine, CA who possess: • Experience developing immunoassays for Phadia or IMMULITE systems, • Bachelors, Masters, or Ph. D in biochemistry, life science, biology, chemistry or a related field FULL DESCRIPTION: We are seeking a highly motivated Research Scientist with expertise in immunoassay development and optimization, particularly on automated diagnostic platforms such as Phadia System and/or IMMULITE. The ideal candidate will have hands-on experience creating QC systems for, developing, validating, and troubleshooting immunoassays for clinical or research applications, with a strong understanding of assay performance characteristics, reagent development, and analytical methods. The selected candidate will be responsible for: • Design, develop, optimize, and validate immunoassays for automated platforms including Phadia and/or IMMULITE systems., • Perform assay feasibility studies, analytical validation, and troubleshooting activities., • Develop and optimize assay components including antibodies, antigens, calibrators, controls, and buffers., • Analyze experimental data and prepare technical reports, protocols, and validation documentation., • Collaborate cross-functionally with R&D, Quality, Regulatory, Manufacturing, and Clinical teams., • Support technology transfer and scale-up activities for assay commercialization., • Ensure compliance with applicable regulatory and quality standards (e.g., GLP, GMP, CLIA, ISO 13485, FDA guidance)., • Direct hands-on experience with Phadia and/or IMMULITE assay platforms., • Strong knowledge of immunoassay techniques including ELISA, chemiluminescence, fluorescence, or multiplex assays., • Experience with assay validation parameters including sensitivity, specificity, precision, linearity, and reproducibility., • Proficiency in experimental design, statistical analysis, and scientific documentation., • Excellent problem-solving, communication, and collaboration skills. For immediate and confidential consideration, please email your resume to and call 858.258.6501. 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 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech 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 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.

Job DescriptionCompany Description Eurofins Scientific is a network of independent companies 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 to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more. Job Description Eurofins Built Environment Testing is searching for an experienced Asbestos Analyst in Tustin, CA and possibly other CA locations. Relocation assistance may be available. The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. Asbestos Analyst responsibilities include, but are not limited to, the following: * Prepare and analyze aerobiological and environmental samples for asbestos. * Accurately enters and reports analytical data using the LIMS * Performs independent data reviews for other analysts’ work * Performs analysis of reference materials, proficiency samples and other quality control samples as needed * Maintains client service and provides technical support as needed * Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests * Performs confirmation of lab results as needed by client services personnel * Performs and completes all analytical testing and Quality Assurance related tasks as needed * Assists in pursuing, receiving and maintaining necessary laboratory accreditations * Maintains and updates all necessary Training and QA documents onsite as necessary * Coordinates and manages projects according to their rush status and due time for timely delivery * Assists co-workers on analytical questions, as necessary * Participates in Lean initiatives as needed * Follows company policies and procedures and ensures that coworkers are doing the same * Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed * Manages and disposes analyzed samples as needed * Provides training support for relevant analytical services (i.e. mycology, bacteriology, asbestos, ect) as needed * Recommends and coordinates sample transfer as necessary * Establishes and maintains laboratory stock culture and reference samples * Performs root cause analysis and implements corrective actions for errors and issues as necessary * Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed * Routinely communicates available capacity to Regional Manager * Supports other departments within the lab (mycology, asbestos, bacteriology, and other) when appropriate and as needed * Other responsibilities as deemed necessary by the Supervisor/Manager Qualifications Basic Minimum Qualifications: * 1+ years of experience performing asbestos microscopy using Polarizing Light Microscope (PLM) * Bachelor’s degree in microbiology, biology, geology or a closely related science * Authorization to work in the United States indefinitely without restriction or sponsorship * Professional working proficiency in English is a requirement, including the ability to read, write and speak in English The ideal candidate would also possess: * 8 units of Geology courses preferred * General regulatory requirements knowledge * Knowledge of computers, spreadsheets, and databases * Strong computer, scientific, and organizational skills Additional Information Compensation Range: $25-$28 per hour depending on level of experience and qualifications. Position is full-time, with possible weekends and overtime as needed. Candidates must be available to work Monday - Friday, 8:00am to 5:00pm. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler. Find out more in our career page: Company 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 discovery pharmacology, forensics, advanced material sciences and agroscience contract research 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job Title: Chemistry Data Reviewer Job Description The Chemistry Data Reviewer plays a key role in ensuring the accuracy, integrity, and compliance of analytical chemistry data generated by quality control laboratories. This position focuses on reviewing and validating laboratory data, including high-volume and complex HPLC and wet chemistry testing, to support the release of finished products, stability studies, and raw materials. The role requires strong hands-on analytical chemistry experience, deep familiarity with HPLC and related software systems, method development and validation and a solid understanding of GxP and FDA regulations. Responsibilities • Review and validate chemistry data in laboratory notebooks, data printouts, lab test requests, assessments, reports, investigations, controlled data sheets, and associated electronic records and audit trails generated by QC Chemistry laboratories., • Work within the Quality Assurance Oversight team to perform detailed technical review of laboratory documents and records., • Review and approve data in accordance with laboratory notebook entries and LIMS documentation, ensuring proper execution of tests, including preparations, instrument setup, and data and result generation., • Perform electronic review of chromatography data using Empower software to verify accuracy, completeness, and compliance., • Track data review requirements to support the timely release of finished products, stability samples, and raw material lots., • Participate in cross-functional teams to support the closure of chemistry-related investigations and ensure appropriate documentation., • Review and draft investigations and risk assessments related to chemistry quality compliance, ensuring alignment with internal procedures and regulatory expectations., • Support investigations, CAPAs, and effectiveness checks related to product testing and laboratory data., • Compile, review, interpret, and present statistical data and metrics related to laboratory performance and data review activities., • Perform administrative duties to support chemistry-related assessments, investigations, and documentation control., • Benchmark and apply industry best practices in laboratory data review, quality oversight, and documentation., • Review, compare, and update documentation for processes and equipment functionality and design to ensure compliance with FDA 21 CFR Parts 210 and 211., • Progress from reviewing high-volume, simpler tests to more complex testing as training advances, including wet chemistry tests such as titrations, limit testing, and pH testing, as well as HPLC analyses., • Collaborate closely with QC laboratory staff and other stakeholders to resolve data discrepancies, clarify test results, and maintain high standards of data quality., • Bachelor’s degree in a scientific discipline, preferably Chemistry; Biochemistry or Biology may also be considered., • 3–5 years of hands-on analytical chemistry experience using HPLC or UPLC in a pharmaceutical, biotechnology, or medical device environment., • Experience with method transfer and development using HPLC/UPLC., • Practical experience performing analytical chemistry testing, including HPLC and wet chemistry techniques., • Experience working with Empower software for chromatography data review., • Experience working with LIMS, preferably LabWare LIMS, for sample and data management., • Working knowledge of GxP requirements and quality control laboratory practices., • Strong accuracy and attention to detail when reviewing technical data and documentation., • Well-developed analytical and problem-solving skills, with the ability to use reasoning to resolve issues., • Strong oral and written communication skills, with the ability to compose clear, concise messages and interact effectively with cross-functional teams., • Ability to make sound decisions and determine appropriate courses of action when addressing data and quality issues., • Organizational skills with the ability to follow systematic methods and manage multiple review tasks., • Ability to interpret and apply FDA regulations, particularly 21 CFR Parts 210 and 211, to laboratory documentation and processes., • Customer-oriented mindset with the ability to support internal stakeholders while adhering to procedures., • Hands-on chemistry laboratory experience beyond data review, including wet chemistry techniques such as titrations, limit testing, and pH testing., • Familiarity with FTIR, UV-Vis, IR, and other analytical instrumentation used in QC laboratories., • Experience reviewing method development and validation protocols., • Experience in biochemistry or related analytical techniques is beneficial., • Prior exposure to quality investigations, CAPAs, risk assessments, and effectiveness checks., • Experience compiling and presenting metrics and statistical data related to laboratory performance., • Conceptual thinking skills with the ability to understand abstract concepts and complex testing strategies., • Ability to benchmark and incorporate industry best practices into existing processes. This role is based within a controlled laboratory and manufacturing facility, with the primary work performed at a desk in an office setting dedicated to data review. The Chemistry Data Reviewer works closely and collaboratively with QC staff and the Quality Assurance Oversight team, typically within a group of approximately eight colleagues. While the majority of the work involves reviewing data at a computer, there may be occasional need to enter QC testing areas, where appropriate laboratory attire such as a lab coat, safety shoes, and safety glasses is required. The environment follows GxP and FDA-compliant procedures, with access to technologies such as HPLC/UPLC systems, Empower chromatography software, LabWare LIMS, FTIR, UV-Vis, and other analytical instruments. New team members receive structured training during the first few weeks, including SOP readings, partnering with a GMP trainer, and a phased approach from simple wet chemistry tests to more complex, high-volume testing. The setting supports a collaborative, team-oriented culture focused on quality, compliance, and continuous improvement. Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay range for this position is $40.00 - $48.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionBenefits: • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off Position Overview Concord Preparatory School is seeking a dedicated and experienced High School Science Teacher to join our growing academic team. This role involves teaching Biology, Chemistry, and/or Physics courses, ranging from regular to AP level, while supporting students academic growth and college readiness in a small, student-centered learning environment. Key Responsibilities • Teach high school science courses including Biology, Chemistry, and/or Physics (regular and AP levels), • Develop and deliver engaging, standards-aligned lesson plans, • Prepare students for AP exams and support strong academic outcomes, • Assess student performance and provide timely, constructive feedback, • Differentiate instruction to meet diverse student needs, including international students, • Maintain accurate records of grades, assignments, and student progress, • Collaborate with academic leadership on curriculum development and instructional improvement, • Participate in faculty meetings, professional development, and school events, • Support a positive, structured, and inclusive classroom environmentQualifications, • Bachelors degree or higher in Science or related field (Biology, Chemistry, Physics, or similar), • Minimum 3 years of teaching experience at the high school level, • Experience teaching AP-level courses strongly preferred, • Familiarity with College Board AP curriculum and exam requirements, • Strong classroom management and communication skills, • Ability to work with students from diverse academic and cultural backgrounds, • Passion for teaching and supporting student successPreferred Qualifications, • Experience teaching international or ESL/ELL students, • Experience with curriculum development or AP program design, • Familiarity with LMS platforms and student information systems(e.g., Blackbaud)Benefits:, • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off, • Retirement plan, • Vision insurance

Job DescriptionDescription: Chemistry Instructor FLEX College Prep is seeking dynamic individuals with strong communication skills to join our pool of instructors and teach both Biology (Highly preferred) 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 Chemistry 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 Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description AbbVie's Local Delivery and Translational Science group seeks a Senior Scientist II/Principal Research Scientist I to lead translational science activities across the eyecare therapeutic portfolio. The successful candidate will drive program execution from preclinical development through early clinical translation in close collaboration with internal teams and external research partners. Responsibilities • Serve as translational science lead and primary scientific representative across a diverse, multi-program eyecare development portfolio spanning preclinical through early clinical stages, • Apply computational and data science approaches to synthesize and interpret biological datasets, generating evidence-based insights to support portfolio evaluation and program decision-making, • Oversee preclinical study design, data review, and interpretation in collaboration with internal study teams, ensuring scientific rigor and alignment with program objectives, • Develop translational plans that map preclinical evidence to early clinical decision points, ensuring continuity across development stages, • Coordinate external research partnerships with CROs, academic collaborators, and biotech partners, including data management and scientific communication, • Serve as scientific author for regulatory briefing documents and cross-functional program summaries, • Synthesize input from drug delivery, clinical pharmacology, regulatory affairs, and business development to inform integrated program plans, • Present scientific findings and program-level summaries to internal leadership and at external scientific meetings, • Apply scientific judgment and analytical rigor to evaluate eyecare therapeutic candidates and inform portfolio prioritization and asset advancement decisionsQualifications Qualifications • Senior Scientist II Qualifications: PhD with 4+ years, Master's with 10+ years, or Bachelor's with 12+ years of relevant experience in a biological, biomedical, computational biology, or related life science discipline, • Principal Research Scientist I Qualifications: PhD with 6+ years, Master's with 12+ years, or Bachelor's with 14+ years of relevant experience in a biological, biomedical, computational biology, or related life science discipline, • Therapeutic area experience in ophthalmology, including familiarity with retinal disease biology and multiple treatment modalities, • Proficiency in scientific programming (Python, R, or equivalent) for analysis and visualization of complex biological datasets, • Experience with in vivo preclinical studies, including disease model development, study oversight, and interpretation of pharmacodynamic and efficacy endpoints, • Track record of effective cross-functional collaboration in a matrixed pharmaceutical or biotechnology environment, • Experience presenting scientific findings to external advisory boards, regulatory bodies, or equivalent forums, • Familiarity with the translational development considerations for novel or emerging ophthalmic therapeutic approaches, • Experience developing or applying translational biomarker strategies in preclinical or early clinical settings 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 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: