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The Position Genentech's Hillsboro Oregon campus-Hillsboro Innovative Therapies (HIT)-serves as a critical hub for emerging cell & gene therapy manufacturing. Housed within a modern 75-acre facility just outside Portland, HIT is at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech's mission to bring transformative therapies to patients. This role is a valuable part of our Manufacturing Sciences and Technology (MSAT) team, which is committed to achieving our mission of delivering innovative cell and gene therapies to patients. As a member of this team, you will have the opportunity to collaborate closely with key stakeholders in Process Development, Analytical Development, Manufacturing, and Quality. The Opportunity: As an Automation/Senior Automation Engineer, you will play a key role in developing, implementing, and optimizing automation solutions to support emerging cell and gene therapy manufacturing. You will collaborate with cross-functional teams to streamline processes, improve efficiency, and ensure alignment with regulatory and quality standards to advance our mission of delivering transformative therapies to patients. Additionally, you will: • Lead the design, development, and implementation of automated control systems to support cell and gene therapy manufacturing processes., • Partner with stakeholders, including Process Development, Analytical Development, Manufacturing, and Quality teams, to identify and address automation needs., • Support the integration, testing, and validation of new automation technologies and systems to ensure scalability and reliability., • Troubleshoot and resolve automation system issues to minimize downtime and maintain operational excellence., • Develop and maintain technical documentation, including functional specifications, system designs, and validation protocols., • Monitor, analyze, and improve automated systems to enhance process control, safety, and compliance with quality standards., • Serve as a subject matter expert in automation, providing technical guidance and training to cross-functional teams on system functionality and best practices. Who you are: Note that this position can be hired as either Automation or Senior Automation Engineer, depending on candidate qualifications. • You possess a Bachelor's degree in engineering, computer science, or related field, with 2-4 years of experience in automation engineering within the pharmaceutical or biotechnology manufacturing industry., • You have demonstrated experience managing diverse stakeholders and building strong partnerships across Process Development, Analytical Development, Manufacturing, and Quality functions., • You have experience working in a matrixed environment, coordinating cross-functional projects, and managing competing priorities effectively., • You possess experience working with automation platforms and systems, such as SCADA, DCS, and PLCs, with a focus on supporting complex manufacturing processes., • You have an understanding of FDA regulations, cGMP standards, and compliance requirements for pharmaceutical or biotechnology production., • You are able to serve as a member of the 24/7 Rotational On Call Support Team. Preferred Experience: • Cell/gene therapy industry experience., • Experience working in an environment utilizing change control and good documentation practices., • Experience with Rockwell and Emerson Automation technologies., • Experience developing automation solutions., • Experience interpreting electrical schematics and P&ID drawings. The expected salary range for this position based on the primary location of Oregon is $80,500 - $149,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this___. Relocation benefits are approved for this posting. This is an on-site position; no remote options are offered at this time. #LI-CA1 #ptcareers #cellandgenetherapycareers# Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form ___.

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing y

Job Title: L3 AVT Tech Duration: 8 months (Temp to perm) Location: Hillsboro OR 97124 Schedule: Monday - Friday (8 am - 5 pm) Overview: You will work in a corporate environment located onsite with one of our largest and most well-known customers. Your duties will include but will not be limited to: PC SERVICES • Preparing old equipment for re-dispositioning and e-waste handling., • Managing inventory counts and updating the peripheral tool regularly., • Load balancing equipment to different Intel and non-Intel sites., • Loading/unloading assets into lockers., • Updating and closing tasks in ServiceNow with all required fields correctly filled out or attached., • Closing tasks within their SLA (service level agreement) timeline, if not there is an exception/explanation for the breach recorded in the task., • Processing assets returned from clients leaving the company; cleaning and testing used systems for redeployment., • Ensuring all client inventory assets are stored and distributed in a clean and professional manner., • Sending emails to clients for asset collection., • Opportunities to train to move into a more technical role., • Performing inter department deliveries using company van (site specific)., • Picking up surplus equipment from users., • Pulling new orders that come in on ServiceNow (ticketing system)., • Scrapping e-waste., • Testing and cleaning laptops., • Taking out trash/metal bins., • Diagnosis and categorize the assets in non-available state in Service-Now (no assets are to be in not available status more than 10 days)., • Basic to moderate Hardware repairs and must be comfortable with replacing PC components and PC peripherals., • Basic to moderate software troubleshooting and OS imaging required., • Adjustment/troubleshooting of Monitors and docking stations in Hybrid Cube offices., • Imaging of drives to a server location for Intel's legal department., • Must be comfortable with working with clients directly in person, via phone, E-mail, and instant message., • Assisting with locating systems physically or by remote means of investigation during audits., • You will be required to cross train for other positions within the team to provide backfill coverage. Your duties will include but are not limited to: • Quickly troubleshooting AV systems with minimal use of BKMs., • Engage external vendors for RMA replacement and out of scope maintenance., • Improvise and use creative troubleshooting to work around rooms that are ?hard down"., • Building and maintaining IPL GC3 Files (removing and adding drivers)., • Updating Extron and AMX firmware for preventative maintenance., • Requires an in-depth knowledge of the functionality of monitors, projectors and video conferencing systems., • Managing and completing Quarterly Preventative Maintenance project., • Creating/Resolving break/fix tickets by monitoring client ticketing system., • Engaging customers' requests for meeting support., • Escalating large break/fix issues and workarounds to VC Lead Technician., • Manage site inventory and spares with use of database., • Acting as point of contact for Level 2 technicians., • Engaging VC Lead on site for large project deployments and floor renovations and escalations. You will have frequent interaction with clients in person and via phone, email and IM. You will be working in a dynamic team and cross training to backfill for peer team members. We will challenge you with additional responsibilities, assigned periodically aimed to help meet our client's needs and provide you with continuous hands-on training and experience. Requirements: • 3+ years audio/visual experience desired., • Complete knowledge of live sound signal flow and must be able to troubleshoot integrated audio systems (Clearone), track and update wireless microphone frequencies, group and channel spreadsheet., • Must understand AMX/Extron Control System Functionality (Master Controllers, RS-232, Touch Panels, GC3 Configuration, pull control code and touch panel files from AMX/Extron devices)., • Must understand Extron components and integrated AV signal paths (Scalers, Switchers, DAs, Extenders) for high level troubleshooting., • May be required to travel between sites using personal vehicle/company van., • Must be able to lift up to 35 lbs. solo., • May be required to walk/sit/stand/crawl/kneel for extended periods., • Must have excellent customer service skills and excellent written/verbal communication skills., • Requires knowledge of Microsoft suite (Outlook, Excel and Word primarily) and Windows.

The Position This position is part of a consolidated Analytical Development and Quality Control (ADQC) team within Genentech's cutting edge Pharma Technical Cell and Gene Therapy (PTC) organization. PTC is dedicated to advancing cell and gene therapies aimed at treating or curing various diseases. In this position, you'll support development and conduct quality control (QC) activities to support the clinical progress of cell and gene therapies. This role is a key part of our Analytical Sciences team, dedicated to ensuring the highest quality standards for raw materials, in-process samples, and finished products. Our team conducts both routine and complex chemical and biochemical analyses, supports stability programs, and plays a critical role in maintaining and calibrating laboratory and analytical equipment. By collaborating with cross-functional teams and contributing to method development, equipment qualification, and reagent management, this team ensures the integrity of our products, directly supporting our mission of delivering safe and effective solutions to our patients. The Opportunity: As a QC Associate (Molecular Biology), you will play a vital role in implementing and performing analytical methods that support Cell and Gene Therapy manufacturing. You will ensure product quality and production consistency while collaborating with cross-functional teams to meet clinical and commercial milestones. Key responsibilities include: • Conducting analytical testing, qualifying and validating methods, and implementing new molecular biology procedures to support GMP production., • Drafting and reviewing documentation for method implementation, equipment qualification, and procedural updates., • Collaborating with Technical Development Teams (TDTs), Pharma Technical Cell Therapies (PTCC), Pharma Technical Development (PTD), and global teams to enable clinical proof of concept and readiness for commercial manufacturing., • Calibrating, maintaining, and troubleshooting laboratory and analytical equipment to ensure operational accuracy., • Developing and improving molecular and potency testing assays for routine and non-routine analyses., • Technically reviewing data for compliance with acceptance criteria, addressing technical issues, deviations, and discrepancies., • Supporting regulatory inspections, internal audits, and compliance initiatives to maintain quality standards. Who You Are: • You possess a Bachelor's degree in Biology, Chemistry, Biochemistry, Molecular Biology, or a relevant scientific discipline with at least 2 years of laboratory experience in the pharma or biopharmaceutical industry., • You have demonstrated experience in executing, qualifying, and validating molecular biology-based methods such as PCR, qPCR, ddPCR, Sanger Sequencing, and Next-Generation Sequencing (NGS)., • You possess the ability to apply scientific theories and techniques to analytical or biological testing in a Quality Control or GMP-regulated environment., • You have a proven ability to interpret and implement Quality standards while ensuring regulatory compliance., • You possess proficiency in molecular biology techniques, analytical test method development, equipment qualification, and quality system documentation., • You have strong stakeholder management skills with experience collaborating effectively across matrixed, cross-functional global teams., • You possess excellent communication, organizational, and problem-solving skills, with the ability to prioritize tasks and meet deadlines in a dynamic environment., • You are able to work in both office and laboratory settings, with extended periods working at benches and frequent lifting (up to 25 lbs), bending, reaching, and twisting Preferred: • Cell therapy QC experience, • Understanding of cGMPs or similar regulations, • Experience in immunoassays such as ELISA The expected salary range for this position based on the primary location of Oregon is $64,800 (min) - $92,500 (mid) - $120,300 (max). Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this ___. Relocation is approved for this position. This is an on-site position; no remote options are offered at this time. #LI-CA1 #ptcareers #cellandgenetherapycareers# Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form ___.

The Position Genentech's Hillsboro Oregon campus-Hillsboro Innovative Therapies (HIT)-serves as a critical hub for emerging cell & gene therapy manufacturing. Housed within a modern 75-acre facility just outside Portland, HIT is at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech's mission to bring transformative therapies to patients. This role is a critical part of our Quality Assurance (QA) team, which plays an essential role in ensuring the delivery of high-quality commercial and clinical (IMP) products in compliance with global regulations and Roche's internal standards. As a leader within QA, you will oversee end-to-end quality processes, including batch release, deviation management, and regulatory compliance, while collaborating closely with Manufacturing, Regulatory Affairs, Global Quality, and site functions. This position offers the opportunity to drive strategic goals, foster a culture of continuous improvement, and contribute to a state of operational excellence in alignment with Good Manufacturing Practices (GMP). The Opportunity: As the Head of Quality Assurance Operations(Senior Director), you will ensure that commercial and clinical (IMP) products meet quality and compliance requirements while driving operational excellence and maintaining a state of readiness for regulatory inspections. You will be responsible for overseeing Quality Assurance activities, managing robust quality systems, and fostering a culture of continuous improvement and collaboration across a highly matrixed organization. Key strategic responsibilities include: • Leading the implementation and monitoring of manufacturing and analytical processes in compliance with GMP, ensuring a state of operational control., • Overseeing deviation and CAPA management systems, ensuring comprehensive investigations, effective corrective actions, and timely resolution., • Managing the efficient review of GMP documentation and timely lot disposition to support compliant product release for both commercial and clinical products., • Providing leadership for QA decision-making and serving as the primary escalation point for significant quality issues across the organization., • Establishing and monitoring Quality key performance indicators, driving continuous improvement and maintaining readiness for regulatory inspections., • Building strong partnerships with key stakeholders, including Site Leadership, Regulatory Affairs, and Global Quality teams, to achieve strategic quality objectives., • Championing a positive safety culture and promoting adherence to Safety, Health, and Environment (SHE) requirements aligned with corporate and local regulations. Who You Are: You are a quality and compliance expert with a strong ability to lead cross-functional teams in a highly regulated, matrixed environment. Your expertise in stakeholder management and leadership has enabled you to deliver sustainable results while fostering a culture of collaboration and continuous improvement. • You possess a Bachelor's degree in a scientific discipline (a graduate or higher-level degree strongly preferred)., • You bring 15+ years of progressive leadership experience in the pharmaceutical or life sciences industry, including at least 8 years of people leadership experience in highly regulated environments., • You have substantial expertise in Quality Assurance leadership, demonstrated by your successful oversight of critical quality systems, including deviation management, complaint handling, CAPA, and product release processes. You excel at embedding operational excellence in complex, large-scale manufacturing environments., • You have advanced knowledge of GMP requirements and quality regulations within the pharmaceutical industry, backed by extensive experience in preparing for and successfully navigating inspections conducted by global regulatory agencies, including the FDA and EMA. Your expertise includes translating these regulations into lean, scalable operational strategies across the organization., • Beyond traditional pharmaceuticals, you bring deep knowledge and extensive experience with Advanced Therapy Medicinal Products (ATMP), specifically Cell Therapy manufacturing or Individualized Medicine, demonstrating your ability to navigate evolving regulatory landscapes and support groundbreaking therapies., • You are a strategic leader with a proven track record of influencing and collaborating across highly matrixed, global organizations. You have successfully aligned cross-functional teams from R&D, Quality, Manufacturing, Regulatory Affairs, and IT to drive shared goals and organizational success., • You possess exceptional communication skills with an executive presence to engage and guide senior leadership, the technical expertise to address inquiries from regulatory authorities, and the interpersonal skills to foster high-impact relationships across internal teams and external stakeholders., • You are a proactive and visible leader with a strong commitment to continuous improvement, operational readiness, safety culture, and business resilience. You inspire innovation, adaptability, and collaboration across teams while fostering a culture of agility and excellence. Physical Requirements: • Work in office and laboratory environment, • Lift up to 25 lbs may be required, • Ability to sit, stand and move within work space for extended periods, • May be required to sit at a computer terminal for extended periods, • Ability to travel up to 30% to other sites as required The expected salary range for this position based on the primary location of Oregon is $171,000 - $317,600. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this ___. Relocation benefits are approved for this posting. This is an on-site position; no remote options are offered at this time. #LI-CA1 #ptcareers #cellandgenetherapycareers# Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form ___.

Side Hustles Flexible Work to Earn Extra Cash Looking to make extra money on the side? You dont need to leave your full-time job to do it. With flexible side hustles, you can earn on your own schedule nights, weekends, whenever it works for you. Freelancing (writing, design, tech, etc.) Delivery driving or rideshare Online tutoring or teaching Selling products or crafts online Virtual assistant and remote admin roles Social media or content creation * Set your own hours * Work from anywhere * No experience required for many gigs * Turn hobbies and skills into income Whether youre saving for something big or just want more breathing room in your budget, a side hustle can help you get there.

Remote Jobs are now available in your area. Great pay and flexible hours. Easy apply online. This position is a work from home position. You will not need to come into the office. No Experience Needed. Benefits: Health Insurance, 401K, Vacation& PTO. Apply now! Work from home roles are a critical part of our mission to deliver timely, accurate and professional customer service to all customers. This vital position requires an action-oriented, flexible problem-solver who will assist customers in expediting orders and correcting post-sales problems. Employees communicate with customers primarily through phone and email and utilize a variety of software tools to navigate customer accounts, research and review policies and communicate effective solutions in a fun and fast-paced environment.

The hours are flexible and no previous experience is needed. No prior study experience is required. Due to demand, we are now accepting applications for personnel to participate in our local in-person and nationwide remote research studies.

The hours are flexible and no previous experience is needed. No prior study experience is required. Due to demand, we are now accepting applications for personnel to participate in our local in-person and nationwide remote research studies.

The Position Genentech's Hillsboro Oregon campus-Hillsboro Innovative Therapies (HIT)-serves as a critical hub for emerging cell & gene therapy manufacturing. Housed within a modern 75-acre facility just outside Portland, HIT is at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech's mission to bring transformative therapies to patients. This role is a valuable part of our Manufacturing Sciences and Technology (MSAT) team, which is committed to achieving our mission of delivering innovative cell and gene therapies to patients. As a member of this team, you will have the opportunity to collaborate closely with key stakeholders in Process Development, Analytical Development, Manufacturing, and Quality. The Opportunity: As a Principal Automation Engineer, you will play a key role in developing, implementing, and optimizing automation solutions to support emerging cell and gene therapy manufacturing. You will collaborate with cross-functional teams to streamline processes, improve efficiency, and ensure alignment with regulatory and quality standards to advance our mission of delivering transformative therapies to patients. Additionally, you will: • Perform automation tasks for commissioning and qualification of new systems while ensuring compliance with regulatory and operational standards., • Collaborate with cross-functional engineering teams to enhance the performance and reliability of automation and production equipment., • Monitor, troubleshoot, and maintain running automation systems to ensure uninterrupted plant operations and resolve system issues., • Develop solutions for recurring issues, create necessary change records, and provide proactive strategies for process and system improvement., • Conduct investigations into cross-site issues with potential enterprise-level impact, implementing effective resolutions., • Support the development of user requirements, design reviews, and planning for new equipment integrations., • Mentor and support junior Automation Engineers while providing guidance on troubleshooting, technical best practices, and continuous improvement opportunities. Who You Are: • You possess a Bachelor's degree in engineering, computer science, or related field, with 5 or more years of experience in automation engineering within the pharmaceutical or biotechnology manufacturing industry., • You possess extensive hands-on experience with automation platforms and systems such as SCADA, DCS, PLCs, Human Machine Interfaces (HMIs), and thin clients to support complex manufacturing processes., • You possess advanced expertise in troubleshooting and resolving complex automation issues, performing root cause analysis, and implementing robust technical solutions., • You have proven experience integrating automation controls with factory manufacturing processes, including the successful integration of electrical and mechanical systems., • You have a demonstrated ability to manage and influence diverse stakeholders while building effective partnerships across Process Development, Analytical Development, Manufacturing, and Quality functions., • You possess significant experience navigating matrixed environments, managing multiple cross-functional projects, and balancing competing priorities in a fast-paced setting., • You possess in-depth knowledge of FDA regulations, cGMP standards, and compliance requirements specific to pharmaceutical and biotechnology production., • You are able to serve as a member of the 24/7 Rotational On Call Support Team. Preferred: • Cell/gene therapy industry experience., • Experience working in an environment utilizing change control and good documentation practices., • Experience with Rockwell and Emerson Automation technologies., • Experience developing automation solutions., • Experience interpreting electrical schematics and P&ID drawings. The expected salary range for this position based on the primary location of Oregon is $95,200 - $176,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this ___. Relocation benefits are approved for this posting. This is an on-site position; no remote options are offered at this time. #LI-CA1 #ptcareers #cellandgenetherapycareers# Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form ___.

Job Title : Bomb Technician (EOD) Category / Component : Enlisted • Active Overview Explosive Ordnance Disposal Technicians locate, identify, render safe, and dispose of explosive threats on land, at sea, and underwater, using advanced robotics, diving, and explosives skills to protect forces and civilians and support fleet and joint operations worldwide. Key Responsibilities Detonate and demolish hazardous munitions, pyrotechnics, and outdated explosives; neutralize ordnance including sea mines, torpedoes, depth charges, and improvised explosive devices; remotely disable unsafe ordnance using robotic and diagnostic technology; conduct parachute and helicopter insertion operations; clear waterways of mines in support of ships and submarines; provide explosive ordnance support to law enforcement agencies and organizations such as the United States Secret Service and Department of State. What to Expect Global missions in every environment, from parachuting into remote terrain to arriving by small boat on foreign shores; majority of time spent in the field conducting high risk, time critical tasks with strict safety and risk management; regular integration with Special Operations, fleet units, and interagency partners; intense physical and mental demands with a culture that values precision, calm decision making, and discipline. Work Environment Operate worldwide on land, at sea, and underwater from EOD Mobile Units and detachments; insert via parachute, helicopter, and small boats; work from ships, shore commands, and forward locations; serve in small team based units that balance training, readiness, and operational tasking with limited administrative overhead compared to field work. Pathways, Training & Advancement Recruit Training followed by an EOD preparatory course at Great Lakes, Illinois, that builds swimming, conditioning, small boat skills, and risk management fundamentals; EOD Assessment and Selection Course that evaluates aquatic adaptability, running, swimming, academics, professionalism, and teamwork; Navy diver training at the Naval Diving and Salvage Training Center; Naval School Explosive Ordnance Disposal, which covers demolition, conventional ordnance, underwater mines, missiles, landmines, and chemical, biological, radiological, and nuclear threats; Basic Parachute Training and ongoing advanced training and qualifications throughout a career. Apply for the Navy Warrior Challenge contract for EOD during initial enlistment, then pass the EOD Physical Screening Test and diver medical screening; complete required assessments and receive recommendation and screening from an EOD officer or senior enlisted EOD technician; additional in service accession requirements may include minimum time on board, performance standards, and command endorsement. Qualifications All Navy jobs require meeting general enlistment or commissioning standards, which typically include: Eligibility to serve in the United States Navy, which may involve United States citizenship or other legal residency and work status, depending on the program and current law and policy A high school diploma or equivalent for enlisted positions, and a bachelor's or qualifying professional degree for officer positions Meeting age limits that vary by program and are set in law and Navy policy. Some communities have more restrictive age ranges Meeting medical, vision, and dental standards, including body composition and physical fitness requirements, with some jobs requiring more demanding standards Meeting character and conduct standards, including background screening Achieving required test scores for your program, such as the Armed Services Vocational Aptitude Battery for enlisted roles or officer qualification tests for officer programs Eligibility for a security clearance when required for your rating or designator Additional qualifications can include specific skills, education, licensure, or experience that are unique to a job or community and will be reviewed with you by a recruiter. Additional qualifications for this job may include: Eyesight correctable within EOD diving standards, with no color blindness; qualifying ASVAB scores using combinations such as arithmetic reasoning and verbal expression or general science, mechanical comprehension, and electronics information; age typically 30 or younger at accession; United States citizenship and eligibility for a security clearance; excellent physical condition and swimming ability, with the capacity to perform detailed technical tasks under stress and in hazardous environments. Education Education benefits are available through standard Navy programs such as Tuition Assistance, the Post-9/11 GI Bill, ACE-recommended college credit for Navy training, Navy COOL-funded certifications, USMAP apprenticeships, and other Navy College Program opportunities. Specific options depend on the Sailor's status, training, and current Navy policy. Pay, Benefits & Service Pay, benefits, and service commitments follow standard Navy Active and/or Reserve policies for this type of role, including basic pay, allowances when eligible, health coverage, and retirement options. Exact entitlements, special pays, and service obligations depend on program, component, years of service, and current law and Navy guidance. Incentives Incentives such as bonuses, special pays, and loan repayment may be available at times for specific ratings or communities, but they change frequently and cannot be guaranteed. Applicants must confirm current incentives and eligibility with an official Navy recruiter or authoritative Navy source. Notes and Disclaimers This description is a general overview of typical duties, training, and opportunities in this community. It does not replace official Navy instructions, policies, or contracts and does not guarantee specific assignments, training, incentives, or outcomes. Actual opportunities depend on Navy needs, individual performance, screening results, and current law and policy.

Job DescriptionDescription: Nurse Practitioner or Physician Assistant – Addiction Medicine - Full-Time (W2) Ideal Option PLLC Location: Hillsboro, OR Compensation: $66-$76/hr Schedule: 4x10-hour shifts (7:30 AM – 6:00 PM, Monday–Thursday) Employment Type: Full-Time, 40 hours per week (W-2) Please note: We are not currently hiring for part-time, 1099/contract, or remote/hybrid positions. About Ideal Option Ideal Option is a national leader in outpatient addiction medicine, dedicated to helping individuals overcome substance use disorders with evidence-based, compassionate care. Since 2012, we’ve grown to 80+ clinics across 9 states, empowering thousands of patients each week to reclaim their lives, reunite with family, and rebuild their futures. Position Overview We’re seeking a passionate full-time, on-site Nurse Practitioner or Physician Assistant to join the Hillsboro clinic team. In this role, you’ll provide life-changing care to patients throughout the continuum of recovery - from initial stabilization to long-term maintenance. Responsibilities include: • Conduct new and established patient assessments, and develop individualized treatment plans for patients with substance use disorders, including opioids, alcohol, stimulants, and sedatives, • Initiate and manage patients on buprenorphine and other maintenance medications for substance use disorders, • Administer long-acting injectable medications (buprenorphine, naltrexone), • Monitor response to treatment, adjust medications, and review lab results, • Collaborate with behavioral health and care coordination teams, • Document appropriately in our EMR (eCW), • Deliver care both in-person and via telemedicine What We Offer • Competitive pay and full benefits, • Medical, dental, and vision insurance, • Short- and long-term disability, life insurance, and Employee Assistance Program, • Paid time off and holidays, • 401(k) retirement plan, • Malpractice coverage, • ASAM membership, • UpToDate license, • Active, unrestricted Nurse Practitioner or Physician Assistant license, • Active DEA license, • Strong and efficient communication and documentation skills, • Commitment to compassionate, patient-centered addiction care, • No prior addiction medicine experience required!

Administrative Assistant - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Administrative Assistant experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • $75-$150 (per 1 hour session) If you are a data entry clerk, administrative assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call centre employee or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

Call Center Representative Agent - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Call Center Representative Agent experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • $75-$150 (per 1 hour session) If you are a data entry clerk, administrative assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call center representative, call center agent or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

Data Entry Clerk - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Data Entry Clerk experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • High school diploma or it’s equivalent, • $75-$150 (per 1 hour session) If you are a data entry clerk, admin assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call centre employee or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

Data Entry Clerk - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Data Entry Clerk experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • High school diploma or it’s equivalent, • $75-$150 (per 1 hour session) If you are a data entry clerk, admin assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call centre employee or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

Data Entry Clerk - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Data Entry Clerk experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • High school diploma or it’s equivalent, • $75-$150 (per 1 hour session) If you are a data entry clerk, admin assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call centre employee or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

Data Entry Clerk - Remote Work From Home Focus Group Panelist - Full Time / Part Time Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Data Entry Clerk experience is not necessary but helpful, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • High school diploma or it’s equivalent, • $75-$150 (per 1 hour session) If you are a data entry clerk, admin assistant, receptionist, warehouse or factory worker, driver, medical assistant, nurse, call centre employee or anyone who is looking for a flexible part time remote work from home job, this is a great position to supplement your income.

No admin virtual assistant experience required. We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies. Most research studies are conducted remotely from home, though some may be in-p

Location: Remote (USA) Company: ProductReviewJobs Thank you for your interest in becoming a Paid Product Tester. Notes on Product Testing: - Each product test is conducted by a third party, independent company. There is no cost to use our service.