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Performs nuclear medicine and PET exams maintaining maximal patient safety and comfort. Exams include all parts of the vasculature structures and organ systems. SPECIFIC SKILLS NEEDED • Technical skills in nuclear medicine technology, • Technical skills in computed tomography, • Knowledge of all vasculature and organ systems, • Skilled in the use of radioisotopes, • Basic patient care and assessment techniques, • Knowledgeable in ALARA, radiation physics, radiation biology, radiation protection and medical terminology., • High degree of accuracy in radioisotope exposure techniques Required: • State of California DHS License (N) (R), • ARRT certification in CT and/or NMTCB certification in PET, • Two (2) years training in an AMA approved school for Nuclear Medicine Technology, • CPR/BLS

Job DescriptionCompany Description At Western Digital, our vision is to power global innovation and push the boundaries of technology to make what you thought was once impossible, possible. At our core, Western Digital is a company of problem solvers. People achieve extraordinary things given the right technology. For decades, we’ve been doing just that—our technology helped people put a man on the moon and capture the first-ever picture of a black hole. We offer an expansive portfolio of technologies, HDDs, and platforms for business, creative professionals, and consumers alike under our Western Digital®, WD®, WD_BLACK™, and SanDisk® Professional brands. We are a key partner to some of the largest and highest-growth organizations in the world. From enabling systems to make cities safer and more connected, to powering the data centers behind many of the world’s biggest companies and hyperscale cloud providers, to meeting the massive and ever-growing data storage needs of the AI era, Western Digital is fueling a brighter, smarter future. Today’s exceptional challenges require your unique skills. Together, we can build the future of data storage. Job Description As a Chemical Support Operator, you will monitor, prepare, and distribute a wide variety of materials needed to sustain wafer production. You will mix/maintain plating baths and conduct bath calculations, preparations, and adjustments. Candidate will use wet chemistry techniques and perform daily/weekly/monthly titrations, extractions, surface tension, XRF, and pH measurements of chemicals and bath solutions. Will work with laboratory equipment daily and will be expected to troubleshoot and repair minor equipment issues. Shift available: Sunday-Tuesday, alternating Saturday ESSENTIAL DUTIES AND RESPONSIBILITIES: • Monitor chemical consumption of assigned tooling/areas and replenish as needed., • Remove chemical waste and empty containers from equipment for proper disposal., • Following documented procedures, will be required to select, measure, dispense, mix and deliver materials to the manufacturing line., • Set up laboratory equipment and instrumentation for tests, research, and process control., • Test and analyze products to determine strength, stability, purity, chemical content, and other characteristics., • Document results of tests, analyses, and displays in SPC charts., • Once trained, will be expected to work independently with little oversight or direction. Qualifications REQUIRED: • Candidate must be flexible to work a 12-hour AWS Shift and overtime, as required by the team., • Significant amount of standing, walking, carrying, and lifting., • Ability to lift 10 pounds often and up to 50 pounds occasionally., • Use of personal protective equipment, such as gloves, aprons and eye protection when executing certain tasks is required, as well as working in a cleanroom environment where production tools are located., • When in the cleanroom, full gown including hood, mask, booties, bunny suit, etc must be worn., • This position requires exceptional attention to detail, careful precision, and the ability to handle a variety of sensitive/hazardous materials safely., • Must have strong written/oral communication skills and be technically competent., • Willingness to commit to a substantial training process., • Must be a self-starter, hands-on worker that can learn technical details quickly., • Basic knowledge of laboratory chemicals and chemical handling procedures., • Ability to follow documented procedures and make accurate chemical solutions., • Must possess good computer skills and be familiar with Microsoft Excel., • Proven ability to work on complex assignments, manage several projects at once, and keep good written documentation of activities., • Fundamental knowledge in the area of Titrations, Extractions, Surface Tension, XRF, pH Readings, and general chemical mixing procedures is preferred., • Familiarity with use of common laboratory equipment such as: Spectro Titan XRF Tool, Mettler DL70ES Titrator, Orion pH meters, Agilent 8453, or equivalent is preferred. Additional Information Western Digital is committed to providing equal opportunities to all applicants and employees and will not discriminate against any applicant or employee based on their race, color, ancestry, religion (including religious dress and grooming standards), sex (including pregnancy, childbirth or related medical conditions, breastfeeding or related medical conditions), gender (including a person’s gender identity, gender expression, and gender-related appearance and behavior, whether or not stereotypically associated with the person’s assigned sex at birth), age, national origin, sexual orientation, medical condition, marital status (including domestic partnership status), physical disability, mental disability, medical condition, genetic information, protected medical and family care leave, Civil Air Patrol status, military and veteran status, or other legally protected characteristics. We also prohibit harassment of any individual on any of the characteristics listed above. Our non-discrimination policy applies to all aspects of employment. We comply with the laws and regulations set forth in the "Know Your Rights: Workplace Discrimination is Illegal” poster. Our pay transparency policy is available here. Western Digital thrives on the power and potential of diversity. As a global company, we believe the most effective way to embrace the diversity of our customers and communities is to mirror it from within. We believe the fusion of various perspectives results in the best outcomes for our employees, our company, our customers, and the world around us. We are committed to an inclusive environment where every individual can thrive through a sense of belonging, respect and contribution. Western Digital is committed to offering opportunities to applicants with disabilities and ensuring all candidates can successfully navigate our careers website and our hiring process. Please contact us at to advise us of your accommodation request. In your email, please include a description of the specific accommodation you are requesting as well as the job title and requisition number of the position for which you are applying. Based on our experience, we anticipate that the application deadline will be 10-14-2025 (3 months from posting), although we reserve the right to close the application process sooner if we hire an applicant for this position before the application deadline. If we are not able to hire someone from this role before the application deadline, we will update #LI-BL1 Compensation & Benefits Details • An employee’s pay position within the salary range may be based on several factors including but not limited to (1) relevant education; qualifications; certifications; and experience; (2) skills, ability, knowledge of the job; (3) performance, contribution and results; (4) geographic location; (5) shift; (6) internal and external equity; and (7) business and organizational needs., • The salary range is what we believe to be the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range and this range is only applicable for jobs to be performed in California, Colorado, New York or remote jobs that can be performed in California, Colorado and New York. This range may be modified in the future., • If your position is non-exempt, you are eligible for overtime pay pursuant to company policy and applicable laws. You may also be eligible for shift differential pay, depending on the shift to which you are assigned. You will be eligible to be considered for bonuses under either Western Digital’s Short Term Incentive Plan (“STI Plan”) or the Sales Incentive Plan (“SIP”) which provides incentive awards based on Company and individual performance, depending on your role and your performance. You may be eligible to participate in our annual Long-Term Incentive (LTI) program, which consists of restricted stock units (RSUs) or cash equivalents, pursuant to the terms of the LTI plan. Please note that not all roles are eligible to participate in the LTI program, and not all roles are eligible for equity under the LTI plan. RSU awards are also available to eligible new hires, subject to Western Digital’s Standard Terms and Conditions for Restricted Stock Unit Awards. • We offer a comprehensive package of benefits including paid vacation time; paid sick leave; medical/dental/vision insurance; life, accident and disability insurance; tax-advantaged flexible spending and health savings accounts; employee assistance program; other voluntary benefit programs such as supplemental life and AD&D, legal plan, pet insurance, critical illness, accident and hospital indemnity; tuition reimbursement; transit; the Applause Program; employee stock purchase plan; and the Western Digital Savings 401(k) Plan.

Job DescriptionDirect Counsel is representing an Am Law 100 firm in its search for an IP Litigation Associate to join its thriving Intellectual Property Litigation Practice. Positions are available in the following offices: Austin, Boston, Chicago, New York, San Francisco, Silicon Valley, and Washington D.C. Position: Associate – IP Litigation Location: Austin, Boston, Chicago, New York, San Francisco, Silicon Valley, Washington D.C. Practice: IP Litigation Experience Level: Minimum of 3 years Compensation: Cravath Scale About the Role: The firm’s Litigation & Trial Department is seeking a skilled and highly qualified associate with at least 3 years of patent litigation experience to support its rapidly growing Intellectual Property Litigation practice. The team handles high-profile, cutting-edge disputes for some of the world’s most innovative companies. Key Qualifications: • J.D. from a top law school, • Minimum 3 years of experience in patent litigation, • Undergraduate and/or advanced degree in a technical field such as engineering, computer science, chemistry, biology, or physics, • Strong legal research, writing, and communication skills, • Admission to practice in the jurisdiction of the office, or ability to become admitted

Job DescriptionCompany Description CDL Sign-on Bonus: $3,000 Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace ®. We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: • Health benefits available Day 1, • 401k available Day 1, • 10+ paid holidays/year, • Free HAZWOPER training and certification, • Overtime opportunities, • Ability to be cross-trained into different roles Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations., • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract., • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle, • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures., • May require obtaining and maintaining a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations., • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies. Basic Requirements: • An associate’s degree in general science (BS preferred) is required for the Lab Pack Chemist., • Driver’s License with clear record, • Moderate to extensive travel with 20% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Enviri Clean Earth’s website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free (833) 209-2659 and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response. Military veterans encouraged to apply

Job DescriptionBenefits: • Academic Support, • Competitive salary Position Overview: We are seeking enthusiastic and experienced High School Science Instructors to join our dynamic faculty team. The ideal candidate will have a strong academic background in science and the ability to teach a variety of courses, including: • Physics (Physics, Honors Physics, AP Physics 1 & 2, AP Physics C: Mechanics, and Electricity & Magnetism), • Biology (General Biology, AP Biology), • Chemistry (General Chemistry, AP Chemistry), • Environmental Science (Environmental Studies, AP Environmental Science)We are looking for educators who are passionate about science education and committed to fostering an inclusive, engaging, and academically rigorous classroom environment that nurtures critical thinking, inquiry, and scientific literacy. Key Responsibilities: • Design and deliver high-quality, standards-aligned lessons that promote scientific inquiry and deep conceptual understanding., • Foster a positive, inclusive classroom environment that encourages collaboration, respect for diverse perspectives, and active participation., • Differentiate instruction to meet the needs of diverse learners, including students with special needs and English language learners., • Evaluate student progress through formative and summative assessments, and provide timely, constructive feedback to support their academic development., • Maintain an organized and supportive classroom through effective classroom management strategies., • Stay current with developments in science education and integrate relevant technologies and instructional practices into the curriculum.Qualifications:, • Bachelors degree in Science, Education, or a closely related field required; Masters degree strongly preferred., • Valid secondary-level teaching credential or certification in science (preferred but not required)., • Minimum of two years of high school teaching or tutoring experience with demonstrated success in science instruction., • Proven ability to engage students, support diverse learning needs, and cultivate a growth-oriented academic environment., • Passion for science and teaching, with a genuine desire to inspire students to explore, question, and think critically.Job Type: Part-time Pay: $40.00 - $45.00 per hour Benefits: • Flexible schedulePhysical Setting:, • Private school

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with a high employer contribution, • Tuition reimbursement, the ___ student debt program, and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity We currently have several opportunities for the Medical Device Regulatory Affairs Development (RAD) Program to be located in Alameda, Pleasanton, and Santa Clara, CA, Minneapolis, MN or Plano, TX. This position performs three 1-year rotations that include specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory registration, ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for product market entry. Additionally, during certain rotational periods the position may be responsible for regulatory operations activities such as logistics management of global product release, and maintaining tools needed for managing global regulatory business such as the regulatory database and global regulatory SharePoint sites. What You’ll Work On • Assists in the preparation of regulatory applications (including annual reports) to achieve departmental and organizational objectives., • Creates, reviews and approves engineering changes., • Acts as a regulatory representative responsible for review and analysis of applicable regulatory guidelines., • Reviews and evaluates communications to ensure communications convey all necessary detail and adhere to applicable regulatory standards including those set by the FDA or other worldwide regulatory agencies to various international affiliates., • Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are current, up-to-date and are entered into regulatory submission data base and file systems. Ensures that information of such regulations and requirements, especially those that are new or modified, are distributed to appropriate personnel, if requested., • Supports the product release process by creating GTS licenses or reviewing and approving requests for product release., • May interface directly with FDA and other regulatory agencies if so directed., • Reviews protocols and reports to support regulatory submissions., • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements., • Complies with U.S. Food and Drug Administration (FDA) regulations, international regulations and other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors., • Performs other related duties and responsibilities, on occasion, as assigned. Required Qualifications • Ability to work in a highly matrixed and geographically diverse business environment., • Ability to work within a team and as an individual contributor in a fast-paced, changing environment., • Ability to leverage and/or engage others to accomplish projects., • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization., • Multitasks, prioritizes and meets deadlines in timely manner., • Strong organizational and follow-up skills, as well as attention to detail., • Ability to maintain regular and predictable attendance., • Ability to move to various US locations based on rotational assignment Preferred Qualifications • BA or BS degree in life sciences (i.e., chemistry, biology, etc.) or engineering (i.e., biomedical, mechanical, chemical, etc.)., • Some experience with medical device industry., • Experience working in a broader enterprise/cross-division business unit model. This position is not available for sponsorship. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___, and on Twitter @AbbottNews. The base pay for this position is $72,100.00 – $114,700.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of, • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree, • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune, • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. This Regulatory Affairs Manager position is an onsite opportunity working out of our Santa Clara, CA location in the Abbott Vascular Division. As an individual contributor, the candidate will combine knowledge of scientific, regulatory, and business issues to enable products, including combination products, that are developed, manufactured or distributed to meet required legislation. This new team member has department/group/site level influence and is generally recognized as an expert resource and mentor within the department. WHAT YOU’LL DO • Provide regulatory input to product lifecycle planning. Provide strategic input and technical guidance on regulatory requirements to development and manufacturing teams, • Prepare robust regulatory applications (FDA and international regulatory agencies) to achieve departmental and organizational objectives, • Assist in the development of multi-country regulatory strategy and update strategy based upon regulatory changes, • Support pre and post approval clinical strategy and submission activities, • Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions with other members of regulatory and related teams, • Assess the acceptability of development, quality, preclinical and clinical documentation for submission filing. Compile, prepare, review and submit regulatory submissions to authorities, • Negotiate and interact with regulatory authorities during the development and review process to ensure submission approval, • Ensure compliance with US and global product post marketing approval requirements, • Evaluate proposed clinical and manufacturing changes for regulatory filing strategies, • Execute and manage technical and scientific regulatory activities. Must function independently as a decisionmaker on regulatory issues and must assure that deadlines are met, • Effectively communicate, prepare, and negotiate both internally and externally with various regulatory agencies. Properly interpret and apply regulatory requirements., • Interface with a variety of management levels on significant matters, often requiring the coordination of activity across organizational units, • Provide leadership and guidance towards achieving department objectives and act as a mentor to less-experienced staff, • May lead a cross-functional or cross-divisional project team, • Responsible for compliance with applicable Corporate and Divisional Policies and procedures Required Qualifications • Bachelor's Degree in a related field OR an equivalent combination of education and work experience, • Minimum 4 years’ experience in a regulated industry (e.g., medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area., • Ability to effectively communicate verbally and in writing, prepare, and negotiate both internally and externally with diverse audiences., • Domestic and international regulatory guidelines, policies and regulations., • Lead functional groups in the development of relevant data to complete a regulatory submission. Preferred Qualifications • Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields., • Master’s or Ph.D. in a technical area, • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.), • Previous experience with PMA / IDE and international submissions, • Experience with combination product and/or Class III medical devices, • Experience with IDE trial strategy and post market clinical activities, • Ability to define regulatory strategy. Able to follow scientific arguments, identify regulatory scientific data needs and solve regulatory issues., • Experience with post-approval manufacturing and design changes, • Ability to work effectively on cross-functional teams, • Strong attention to detail, • Experience with organizing and tracking complex information. Able to juggle multiple and competing priorities, • Uses in-depth knowledge of business functions and cross group dependencies/ relationships Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews.Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $112,000.00 – $224,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. In Abbott’s Global Regulatory Services (GRS) division, we’re helping people to have access our life-changing technologies and products by providing strategic and predictable Regulatory Services in collaboration with the medical device business units that Leveraged Services team supports. The Opportunity The Senior Manager Regulatory Affairs will work for our Global Regulatory Services division within Leveraged Services. As a Senior Manager, the individual is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. This new team member will support key digital health technology activities (i.e., software, cybersecurity, telehealth, digital solutions, etc.) and be recognized as an expert and resource within the division. The individual should have a strong understanding of the software lifecycle management and software development, including design, validation, and maintenance in the device regulatory environment. Demonstrates ability to interpret and apply regulatory requirements to software systems, including documentation, risk management, and compliance strategies. Assists management and leadership on regulatory activities and works with the medical device business units that Leverage Services team supports, including the execution of strategic regulatory initiatives, regulatory submissions, agency relationship and evaluation of regulatory policies. The individual will apply strong communication skills, strategic thinking, and leadership experience to support the medical device business units with their regulatory submissions. Collaborates closely with internal regulatory colleagues to ensure project strategies and regulatory submissions meet global requirements, drawing on sound knowledge of medical device regulations and experience such as from the Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH). This Senior Manager Regulatory Affairs may analyze broad scope implications of changing regulations, guidance, or regulatory shifts. Additionally, may identify data needed, obtain this data, and ensure that the information is effectively shared across the medical device businesses. What You’ll Work On • Review regulatory submissions involving software components (e.g., 510(k), PMAs, CE marking, technical files)., • Collaborate closely with internal regulatory colleagues to ensure project strategies and regulatory submissions meet global requirements, • Develops regulatory strategies with the medical device business units for new products or changing existing products especially with FDA, • Supports and provide critical review of key documents necessary for regulatory submissions for new products or changes to existing products., • Ensure that regulatory submissions that contain digital health technologies (i.e., software, cybersecurity, telehealth, etc.) have targeted mitigations to align with FDA expectations, ensuring high-quality submissions and predictability for approval, • Assists BU RA at team meetings and applies influence and negotiation skills to resolve issues, • Works with BU RA to resolve deficiencies that may have received for submissions, • Maintains awareness of regulatory legislation, regulations, and guidances, • Communicates with internal groups to share updates on regulatory changes as it pertains to the FDA, • Utilizes technical regulatory skills to proposed strategies on complex issues, • Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and update leadership, • Monitor impact of changing regulations on submission strategies and update internal stakeholders, • Provide strategic input and technical guidance on regulatory requirements to development teams as requested, • Identify and present option for risk mitigation to decision makers, • Support regulatory trackers for submissions to identify areas for new or continued training in order to implement appropriate regulatory strategies to mitigate risks, • Provide summary of key issues related to submissions at a high level to leadership, • Utilize technical regulatory skills to propose strategies on complex issues. Determine submission and approval requirements. Identify emerging issues., • Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions with other members of regulatory and related teams., • Evaluate risk of and regulatory solutions to product and clinical safety issues during clinical phases and recommend solutions., • Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies. Required Qualifications • Bachelor's degree or an equivalent combination of education and experience, • Minimum 8 years’ experience in R&D or related area; ideally includes 4 years in Regulatory Affairs., • Effectively communicate verbally and in writing, prepare, and negotiate both internally and externally with various regulatory agencies. Preferred Qualifications • Bachelor's degree in science (biology; chemistry; microbiology; immunology; medical technology; pharmacy; pharmacology); math; engineering; or medical fields., • M.S. in a technical area or MBA. A Ph.D. in a technical area or law is helpful., • At least 5 years’ experience in regulatory affairs; highly preferred with medical devices., • At least 5 years working directly with the FDA on medical devices, • Knowledge on PMAs, IDEs, 510(k)s: Past experience in strategic thinking, planning, preparing or reviewing and demonstrated experience with US submissions and a solid knowledge of FDA regulations, • Strong understanding of software lifecycle management, including design, validation, and maintenance in regulated environments., • In-depth knowledge of regulatory frameworks (e.g., FDA, EMA, ISO 13485, GDPR) relevant to software products, especially in healthcare and medical devices., • Ability to interpret and apply regulatory requirements to software systems, including documentation, risk management, and compliance strategies., • Familiarity with cybersecurity and data privacy regulations as they pertain to software products, • Experience managing projects, planning and conducting meetings and leading teams to ensure completion of project tasks, • Previous experience with 510k / PMA /IDEs / Q-submissions., • Must be able to juggle multiple and competing priorities., • Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions., • Ability to problem solve while being detailed oriented is critical, • Has a sound knowledge of a variety of alternatives and their impact on the business., • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews.Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $128,000.00 – $256,000.00. In specific locations, the pay range may vary from the range posted.

Metric Bio backed with a private equity backed Clinical Site Network who are growing rapidly! They are seeking a Clinical Research Coordinator (CRC) responsible for coordinating and managing clinical trials and research studies in accordance with regulatory requirements, study protocols, and institutional policies. The CRC will work closely with investigators, sponsors, and study participants to ensure the ethical and accurate collection of data and the integrity of the research process. Key Responsibilities: • Coordinate day-to-day clinical trial activities and ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines., • Recruit, screen, and enroll study participants; obtain informed consent., • Schedule and conduct study visits, collect and enter data accurately into electronic databases or case report forms., • Manage study documentation including regulatory binders, source documentation, and adverse event logs., • Act as liaison between study sponsors, monitors, investigators, and participants., • Prepare for and participate in monitoring visits, audits, and inspections., • Ensure proper handling, storage, and accountability of investigational products., • Maintain IRB submissions and updates (initial submissions, amendments, continuing reviews)., • Educate participants on study procedures, risks, and benefits., • Track study progress, enrollment, and data collection milestones. Required: • Bachelor’s degree in a health or science-related field (Nursing, Public Health, Biology, etc.)., • 1–2 years of experience in clinical research or a related healthcare setting., • Knowledge of clinical research regulations and GCP., • Strong organizational and communication skills., • Certification through ACRP (CCRC) or SOCRA (CCRP)., • Experience with IRB submissions and sponsor communications., • Office and clinical environment., • May require occasional evening or weekend hours depending on study needs., • Occasional travel for meetings or training.

Our client develops, manufactures and supplies a wide array of innovative medical diagnostic products, services, tests, platforms and technologies. Summary: Seeking a qualified and highly motivated individual for the role of Scientist II in BioSpecimen Acquisition and Management to support Culture Collection and Panel production activities. The BioSpecimen Acquisition and Management function is a centralized service function which supports the acquisition, characterization, and management of biological materials, as well as build of select panels for clinical research and cultivation and characterization of various Microorganisms and Mammalian cell lines. The Scientist II position will facilitate the daily operations associated with fulfilling service requests for Culture Collection and panel activities, while providing best-in-class simple biological solutions to our customers to drive innovation. Specific Responsibilities: • Under minimal supervision, executes assigned project activities using established procedures and applying scientific knowledge and accumulated experience to complete projects involving manipulating human cell lines, microorganism and/or other biological material., • Perform standard recombinant DNA techniques including cloning, restriction digestion, ligation, and transformation of bacteria., • Grow bacterial cultures under sterile conditions to ensure successful transformation and plasmid propagation., • Analyze plasmid DNA and RNA transcripts for purity, concentration, and quality., • Makes recommendations to resolve problems encountered while performing procedures., • Receives general direction; plans and executes own work. May act as a project lead., • Maintains an effective scientific knowledge base and effectively uses broad scientific concepts to resolve problems of moderate scope and complexity., • Analyzes alternative approaches to solve problems or develop new perspectives on existing solutions., • Responsible for the accuracy, quality, and timeliness of all assigned projects, tasks and related activities. Summarizes experimental results, and reviews conclusions with supervisor/project leader. May communicate the results of experiments in the form of reports and presentations., • Accountable for electronic records management and use of validated systems ensuring information is recorded in a timely manner, accurately and consistently., • Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA)., • Participates in routine lab maintenance, lab safety, ISO, and QSR implementation. Position Requirements & Experience: • Bachelors degree in Molecular Biology, Cellular Biology, or Microbiology or related field and 4+ years of relevant experience., • Masters Degree in Molecular Biology, Cellular Biology, or Microbiology or related field and 2+ years of relevant experience., • Experience with aseptic techniques and bacterial culture or cell culture., • Must be able to manually manipulate samples (plating, pipetting, labeling and vialing) on a routine basis., • Experience with cloning techniques including plasmid design and preparation, restriction enzyme digestion, ligation and bacterial transformation and processing., • Experience in performing nucleic acid extractions (DNA/RNA), quantification, amplification and characterization using Qubit, Nanodrop, Gel electrophoresis, PCR machines etc., • Must be able to work in a laboratory environment on a daily basis under BSL-2 laboratory conditions. May work a variety of infectious human material (HxV, pathogenic bacteria, or engineered material, etc) and sample types (blood, serum, urine, stool etc)., • Must be able to work in a dynamic and collaborative team environment with multiple stakeholders across the organization., • Understanding of good laboratory, data and documentation practices., • Ability to plan work and determine next steps within the context of an overall project., • Competent with Microsoft Office and Google applications, • Experience with LIMS software, eLN and JMP (Preferred)., • Client facing experience is a plus. Personal Characteristics & Cultural Fit: • Must be well organized and meticulous., • Flexibility with respect to projects, unique biological material handling requirements, and meeting client/organizational goals and expectations., • Good written and verbal communication skills. Able to follow written and verbal instructions., • Truly passionate about the importance of biorepository management, as well as the ability to work in a global, matrix environment., • Demonstrated aptitude in cross-functional collaboration., • Results and goals oriented.

Our client, a global law firm, is seeking a Patent Agent or Patent Attorney with expertise in biophysics, bioinformatics, or AI/ML. Schedule: Hybrid 2/3. Billable Hours: The firm has a billable hour target of 1,600-1,800 hours. Salary: Patent Agent: $150k- $250k Patent Attorney: $180k-$300k Location: This role is open in their Los Angeles or San Francisco office. Responsibilities: • Draft patent applications and documents for all stages of the patent prosecution process., • Coordinate and correspond with inventors and clients regarding invention disclosures., • Conduct and analyze prior art searches to support patent applications., • Maintain up-to-date knowledge of patent laws to assist clients effectively. Patent Agent Qualifications: • Minimum of 3 years of experience as a registered Patent Agent, with 5+ years preferred., • Strong background in biophysics, biomedical engineering, computational biology, bioinformatics, data science, or AI/ML., • Proficiency in drafting patent applications and managing client portfolios., • A degree and/or experience in biophysics, biomedical engineering, computational biology, bioinformatics, data science, or AI/ML (Advanced degree is preferred)., • Registered to practice with the USPTO. Patent Attorney Qualifications: • Registered to practice with the USPTO., • A degree and/or experience in biophysics, biomedical engineering, computational biology, bioinformatics, data science, or AI/ML (Advanced degree is preferred)., • Minimum of 3 years of experience as a registered Patent attorney, with 5+ years preferred., • Active member in good standing of the California State Bar., • Juris Doctor (JD) degree from an accredited law school.

Senior Regulatory Science Technician - Onsite Pay Rate Range: $28.00/hr. - $30.66/hr. Description/Comment: Assists in developing and validating testing methodology used to control raw materials, production intermediates and final products. Helps establish, validate and document new or existing compound identification methods. May conduct testing of analytical samples for the laboratory area, the separation and characterization of protein drug candidates, formulation development, peptide mapping and other analytical methods of development. Conducts work in compliance with cGMP, safety and regulatory requirements. May provide analysis and evaluation of material and products at all stages of development process. This position requires knowledge that is acquired through experience, specialized education, or training. The role has clearly defined procedures and tasks as well as defined guidelines to aid in decision making. The job should possess a good knowledge and comprehensive understanding of the range of processes, procedures and systems to be used in carrying out assigned tasks and a basic understanding of the underlying concepts & principles upon which the job is based. The knowledge can be acquired through a combination of job-related training and considerable on-the-job experience. The job works within well-defined procedures that may involve a variety of work routines. This job typically requires a minimum of 3 or more years experience. Additional Job Details: The majority of this role involves the understanding and operation of FTIR spectroscopy, Inductively coupled plasma mass spectrometry (ICP-MS), X-ray fluorescence (XRF), and UV-Vis spectroscopy and will also employ gravimetric analysis. Additional analytical chemistry tests may be conducted based on the needs of the business. 1. Fully onsite (Mon-Friday), 2. Degree highly preferred (biology, chemistry, biochemistry, life sciences, etc), 3. Top 3 skills: a) Lab experience, preferred chemistry lab, preferred FTIR experience b) Good written & verbal communication c) Can act independently and have good time management 4. Virtual screening, then on-site with 2 or 3 individuals., 5. This is a contract only., 6. Overview of position and day to day responsibilities: The Lab Technician will be primarily responsible for the timely chemical testing, analysis, and reporting of materials and products. The technician will ensure that the lab is well stocked, clean, and compliant to lab WIs and SOPs. The majority of this role involves the understanding and operation of FTIR spectroscopy, Inductively coupled plasma mass spectrometry (ICP-MS), X-ray fluorescence (XRF), and UV-Vis spectroscopy and will also employ gravimetric analysis. Additional analytical chemistry tests may be conducted based on the needs of the business. The Lab technician will be responsible for the following (not an exclusive list): • Intake of test requests (understanding and alignment of preparation and testing requested)., • Provide feedback on required samples, testing preparations, testing method and results., • Management of testing timelines, including communication of delays., • Preparation of samples for analysis., • Perform chemical analysis (FTIR, ICP-MS, XRF, UV Vis, Gravimetric analysis)., • Cross functional partnerships with R&D, Regulatory, Biosafety, and Operations teams in relation to testing., • Interpreting data and reporting data., • Communication of any delays., • Maintenance of lab supplies, • Cleaning the lab, • Ensuring lab EH&S compliance, • Maintain lab metrics All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Sr. Regulatory Affairs Specialist Location: SF Bay Area - East Bay - 5 days onsite Compensation: $120,000 – $160,000 + 8% bonus Type: Full-time, Direct Hire Overview We are seeking a Senior Regulatory Affairs Specialist to support U.S. and international submissions for medical devices. This role focuses on compiling, preparing, and submitting regulatory documentation, with emphasis on products involving software, wireless, cybersecurity, or sterilization. Key Responsibilities • Prepare, review, and submit regulatory submissions (510(k), technical files, amendments, annual reports) in the U.S. and international markets, • Maintain regulatory databases, product licenses, and documentation in compliance with FDA QSR (21 CFR Part 820) and ISO standards, • Support regulatory strategy, policies, and SOPs to ensure adherence to global requirements, • Interface with FDA, international authorities, and internal teams to resolve regulatory questions, • Collaborate cross-functionally to support product development, risk management, and compliance activities, • Bachelor’s degree in Engineering, Biology, Chemistry, or related technical discipline, • 8–10 years in Regulatory Affairs, including at least 2+ years in medical devices, • Must have direct experience in at least one: software, wireless, cybersecurity, or sterilization, • Proven experience with international registrations and post-market submissions, • Strong knowledge of 21 CFR, FDA guidelines, GMPs, and ISO standards, • Excellent writing, communication, and project management skills, • Proficiency in Microsoft Office (Word, Excel, PowerPoint)

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

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 Job Function: Supply Chain Engineering Job Sub Function: Manufacturing Engineering Job Category: People Leader All Job Posting Locations: Santa Clara, California, United States of America Job Description: Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at Johnson & Johnson MedTech is recruiting for a Senior Manager, NPI Manufacturing Engineering to be located on site in Santa Clara, CA. The Senior Manager, NPI Manufacturing Engineering is a critical leadership position overseeing the day to day manufacturing engineering operations. The position responsibilities will ensure the manufacturing line operates effectively, efficiently and with a quality mindset. This exciting opportunity will be instrumental in the continued development of processes and ability for multiple DFX efforts and further automation. Driving the internal processes with a continued improvement mindset will be another critical aspect of this role. Key Duties & Responsibilities: \n • Lead the direct line support Manufacturing Engineering team to provide strategic and technical guidance\n, • Oversee multiple groups executing multiple product lines simultaneously\n, • Establish KPIs for group and team members to meet programmatic and organizational goals\n, • Maintain compliance with quality system including overseeing corrective actions, material disposition and change orders\n, • Assess and collaborate on the manufacturing strategy for commercialization optimization including DFX, scalable processes and automation opportunities\n, • Long term vision to incorporate digital framework aspects to manufacturing operations\n, • Assess team and skill capability to ensure team member development\n, • Review, evaluate & manage process risk in the manufacturing environment (PFMEA) and associated mitigations\n, • Oversee the validation and qualification of manufacturing equipment and processes\n, • Work with Quality Engineering group to ensure that the team follows appropriate GMP, design history file (DHF), and device history record (DHR) guidelines per FDA requirements, and support design reviews in accordance with product development procedures.\n\n Qualifications: Requirements: \n • A Bachelor's Degree is required (preferably in Engineering or a technical discipline)\n, • A minimum of 10 years of relevant professional experience \n, • A minimum of 4 years of people management with an organization \n\n\n, • Proven manufacturing operations experience\n, • Experience in the development and introduction of new products including quality and regulatory implications for the supply chain design\n, • Knowledge of multiple manufacturing processes, such as machining, plastics, electromechanical\n, • Excellent quantitative process development skills\n, • Understanding of design for manufacturing, design to value, design for lean sigma\n, • Experience in organizational design and accelerating talent through people development\n, • Comfortable navigating to deliver results in a global matrix organization\n, • This position may require 15% travel (domestic and international)\n\n Preferred: \n • Advanced degree in an Engineering or a Business-related discipline\n, • MedTech, Product or Process Engineering or Manufacturing Operations experience for complex electro-mechanical products\n\n Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and 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 email the Employee Health Support Center ([email protected]) or contact AskGS to be directed to your accommodation resource. The anticipated base pay range for this position is : $138,000 - $238,050 Additional Description for Pay Transparency: