Quality assurance tester jobs in Allentown, PA - 52 jobs

Christian Brothers Automotive Our mission is simple: To create an uncommonly great experience for customers in need of auto service and repair. Christian Brothers Automotive was founded in 1982 on the principles of honesty and integrity. These principles have taken our organization to over 300+ locations all across the country. We strive for excellence in service as the #1 Automotive Repair Franchise in the country. We have a great culture, a great mission, and a great time. We hope you'll consider joining us! The job description will be dependent upon the position that you are interested in. This is an opportunity to apply for general consideration. Qualifications The qualifications will be dependent upon the position that you are interested in. This is an opportunity to apply for general consideration. Additional Information All of your information will be kept confidential according to EEO guidelines. Christian Brothers Automotive is an Equal Opportunity Employer.

Cleveland Steel Container, an Employee Owned and World Class Steel Pail Manufacturing company, is seeking an enthusiastic, responsible, and customer-oriented individual that has a positive attitude and shares the values of our company culture, which is built around teamwork, family, honest communication and producing desirable results for our Quakertown, PA manufacturing facility. INDUSTRY LEADING BENEFIT PROGRAM THAT INCLUDES LOW EMPLOYEE PREMIUMS FOR MEDICAL INSURANCE, UNMATCHED RETIREMENT PROGRAMS AS AN EMPLOYEE OWNER. DENTAL, VISION, LIFE AND DISABILITY INSURANCES. NEW EMPLOYEES ARE ELIGIBLE FOR 15 DAYS OF PAID VACATION PER CALENDAR YEAR AND 11 PAID COMPANY HOLIDAYS. SIGN ON BONUS OF $2,000 PAID OUT IN FIVE INSTALLMENTS OVER THE COURSE OF ONE YEAR. $1,000 REFERRAL BONUS FOR ANYONE THAT IS REFERRED THAT GETS HIRED BY THE COMPANY This Quality Assurance Technician position is responsible to ensure company and customer quality standards are being achieved. Duties and Responsibilities: Test and conduct routine and non-routine in-process inspection of production output, measure samples of finished product and check production quality verifications for completeness, timeliness and tolerances as well as complete product testing of finished goods Assist with incoming inspections for internal / external suppliers as directed. Confirm discrete job special instructions are being followed or met Member of daily audit team for various product and process audits per checklist Participant in the revision and update of standard operating procedures. Conduct and complete Internal Quality audits and may be involved in the development of testing methods Ensure employees adhere to safety and quality standards Skills and qualifications: 1-3 years manufacturing experience: required (metal, paint/finishing industries: a plus) High School Diploma or GED: required ISO 9000 and 5S Program knowledge and experience Customer focused mindset Proven hands-on shop floor experience; forklift experience Working knowledge Microsoft Office (Word, Excel, PowerPoint) Good work record; Strong work ethic Strong communication and interpersonal skills Good teamwork and time management skills Experience in a high volume fast paced environment Cleveland Steel Container was founded in 1963 to provide customers with a dependable steel pail. Currently, we have four pail plants located strategically throughout the United States to support our customers. At our Streetsboro facility, we have a metal stamping plant to provide component parts for our pails. Our goal is to continuously provide our customers with quality pails through excellent service at an outstanding value. Finally, we make good pails and deliver them on time! Cleveland Steel Container offers a competitive salary based on commensurate experience and a comprehensive benefits program that includes medical, dental, and vision insurance, flexible spending accounts, 401k with company contribution, profit sharing, paid holidays and vacations, life insurance and short & long-term disability coverages along with an Employee Stock Ownership Plan (ESOP).

Business: Critical Care Department: Quality Assurance Provides continuous oversight of all daily Quality activities to assure compliance with internal procedures and regulatory requirements. Provide proper control, review, and management of site documentation to ensure GMP and regulatory compliance. Key Stakeholders: Internal Quality Assurance Team, Site Management, All Departments Key Stakeholders: External FDA or other health organizations Reporting Structure Directly reports to Quality Assurance Supervisor Essential Duties and Responsibilities Responsible for the review, approval, and disposition of finished product for the site and final CoA signature Facilitates client project management as required ensuring “quality on time and in full” Coordinates the investigation and closure of non-conformances ensuring appropriate corrective and preventive actions (CAPA) and change controls are initiated and deviations are closed Leads or participates in focused deviation cross-functional investigations, improvement projects Reviews and approves laboratory investigations in a timely manner and ensures appropriate root cause is identified Provides assistance to other QA associates and assist with department trainings Provides support to QA management during regulatory audits Reviews BOMs, inspection plans, pallet patterns, calibration records and SOPs Performs internal audits and assist in writing reports for audits Maintains and revises procedures related to the quality assurance activities. Supports Annual Product Review (APR) reports by collecting batch record data, creating and maintaining data bases Maintain the vendor complaint process Maintain, monitor and provide trend analysis of DIs, LIs, CAPAs, customer complaints and change controls Performs special projects and/or assignments as indicated by Quality Management Oversee and review of Obsolete material destruction Perform Quality inspections on packaging line as needed Maintain supplier approval program Support/Maintain site Document Control System Review, approve and close out Document Change Requests Tracking of changes using DCC spreadsheet and supporting actions through closure Maintain original documentation archive and Archival of documents offsite Printing of new and revised documents, Issuance of forms, logbooks Review documentation submitted for routing in eDMS for proper formatting and accuracy. Load documents into an electronic Documentation Management System (eDMS) Route documents for approval in the eDMS Recall documentation for audits in a timely manner Performs external audits and assist in writing reports for audits Responsible for maintenance and revision procedures related to document control May require up to 25% travel. Key Competencies (knowledge, skills, and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Energetic, enthusiastic, and motivated disposition Attention to detail with strong organizational skills Ability to explain problems, solutions and make recommendations, and the ability to manage various urgent requests in a professional manner Ability to analyze data/trends to make sound regulatory interpretation while preparing metrics and reports The ability to drive projects in relation to implementation of new workflows and updates to new systems Education / Experience Bachelor's degree in relevant scientific quality assurance / technical field 5+ years of experience Strong understanding of pharmaceutical cGMP, industry standards, and regulations Strong verbal and written communication skills with the ability to interact across functions, departments, and seniority levels Expert level user for Quality computer systems Knowledge of and ability to use Microsoft Outlook, Excel, and Word, as well as other web-based systems Thorough understanding of computer system validation and GAMP requirements

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role Overview The QA Investigations Lead is responsible for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality and complaint product supply. Key Responsibilities Support compliance activities for site Quality Operations in accordance with Legend standards, procedures and cGMPs. Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues. Ensure accurate and timely maintenance and review of manufacturing investigations, CAPAs, change controls and complaints. Review and approve manufacturing procedures. Support regulatory inspections and audits by ensuring inspection readiness within facility. Perform internal housekeeping audits. Perform analysis on quality indicating data and identifying trends. Provide oversight for trending of quality compliance metrics. Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals. Works in a collaborative team setting with quality counterparts that include Manufacturing Operations, Operations Technical Support, Maintenance, Supply Chain and Planning. Requirements A minimum of a Bachelor's Degree in Science, Engineering or equivalent technical discipline is required. A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices. Great attention to detail and ability to follow the procedures. The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision. Good written and verbal communication skills are required. Ability to summarize and present results, and experience with team-based collaborations is a must. Must be able to interpret problems and effectively determine appropriate resolutions that ensure compliance and minimize risk. Must exhibit strong leadership skills and effectively develop others. Ability to collaborate well with stakeholders, customers and peers. Must exhibit strong decision-making ability and think creatively while maintaining compliance and quality. Must be able to discern the criticality of issues and to communicate to management regarding complex issues. Ability to manage conflict and issues that arise with internal or external customers. #Li-BG1 #Li-Onsite The anticipated base pay range is$81,273-$106,669 USD Benefits We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles. We offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes vacation days, personal days, sick time, 11 company holidays, and 3 floating holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs - demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. Please note: These benefits are offered exclusively to permanent employees. Contract employees are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.

Requirements Desired Qualifications Education: Mechanical Engineering Degree CMM Experience: While not strictly required, experience as a CMM Operator/Programmer is preferred, and training will be provided for the right candidate. Machinist Background: A background as a machinist is also preferred but not mandatory. HYDAC offers employees a comprehensive medical/dental/vision plan, paid holidays, PTO, 401k with company matching, FSA account, short term disability and life insurance, and pet insurance. Click the “apply” button to be considered for this opening! HYDAC is committed to providing equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. 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. #IND123

Job DescriptionDIRECT HIRE: A great opportunity for a Quality Assurance Assistant to join a dynamic team in the Allentown, PA. area. Hourly Rate: $19hr - $23hr Benefits: Medical, dental, vision, PTO, 401K, short-term disability, employee life Schedule: M-F, 40hrs +OT Roles & Responsibilities: Test and conduct routine and non-routine in-process inspection of production output, measure samples of finished product and check production quality verifications for completeness, timeliness and tolerances as well as complete product testing of finished goods Assist with incoming inspections for internal / external suppliers as directed Confirm discrete job special instructions are being followed or met Member of daily audit team for various product and process audits per checklist Participant in the revision and update of standard operating procedures Conduct and complete Internal Quality audits and may be involved in the development of testing method Ensure employees adhere to safety and quality standards Skills and qualifications: 1-3 years manufacturing experience: required (metal, paint/finishing industries: a plus) High School Diploma or GED: required ISO 9000 and 5S Program knowledge and experience Measuring tools knowledge and experience Customer focused mindset Proven hands-on shop floor experience; forklift experience Working knowledge Microsoft Office (Word, Excel, PowerPoint) Good work record; Strong work ethic Strong communication and interpersonal skills Good teamwork and time management skills Experience in a high volume fast paced environment Once you apply, please text "QAA" to ************ for a faster reply. INDH Powered by JazzHR za964VIUsY

Software Quality Engineer. Understand requirements for all new features and design, develop, and maintain automated test scripts. Perform manual testing for functional, regression, integration, system and user acceptance testing. Perform smoke and sanity testing. Perform functional, integration and cross browser testing on web and mobile apps. Perform Database testing using SQL Server to ensure backend functionality and data integrity. Collaborate with cross functional teams including developers, Manager, Business Analyst to define quality standards and ensure compliance with requirements. Identify, document and track software issues/defects using bug-tracking tools and follow up with the development team. Conduct root cause analysis of defects and recommend process improvements to prevent recurrence. Review and analyze technical specifications, requirements and system designs to identify potential risks or areas for improvement. Work with Manual (Web and Mobile) and Automation testing, C#, JavaScript, POSTMAN, SQL server, Selenium Web Driver, TestNG, Oracle, TFS, Figma, BrowserStack, DevOps. JIRA, IVR system testing, Agile methodology. 40 hrs/wk. Must have Bachelor's degree or equivalent in Computer Science, Computer Engineering, or a related field and 2 years experience (or 2 years experience as QA Analyst or related occupation). Must have 2 years experience performing manual testing for functional, regression, integration, system and user acceptance testing; Designing, developing, and maintaining automated test scripts; Working with C#, Selenium WebDriver, TestNG, POSTMAN, JavaScript, SQL server, Oracle, JIRA, TFS. Telecommuting permitted. Email or mail resume with ID#347 to [email protected] or Corporate Recruiting, Ideal Concepts, Inc., 842 Hamilton St, Suite 800, Allentown, PA 18101.

Title: ICQA Associate Hours/Shift: 1st Shift Mon - Fri 8:00 am - 4:30 pm at $20.25hr or 2nd Shift Sat - Wed 3:00pm to 11:30pm at $21.25hr If you're looking to be at the forefront of disrupting the ecommerce industry, wanting to make your mark and be continuously challenged to grow, your time has come. ShipBob is recognized as #1 on Crain's 2020 “Fast 50” list of the fastest-growing companies in Chicago & Inc.5000 top 500 companies with the most proven track records. With this growth, we are looking for top talent to help us reach the next level. Role Description: This is an incredibly important position that helps to monitor inventory activities of all clients at each fulfillment center while allowing all existing operations team members to remain focused on their day-to-day responsibilities. As ShipBob continues to grow, it is imperative to provide a great experience in serving our clients' needs while maintaining sustainable growth and scalability from an operations perspective. About Us: ShipBob is a cloud based logistics platform that partners with over 5,200+ e-commerce businesses to help them be more successful online. We offer a full suite of fulfillment solutions for our merchants, including the ability to improve their transit times, shipping costs and deliver best in class experience to their customers. With almost 100% accuracy rate in fulfilling orders and orders shipped on time, our merchants can count on us to deliver excellent service. As one of the fastest growing tech companies in Chicago with over $330M+ raised from blue-chip investors like Menlo Ventures, Bain Capital Ventures, Hyde Park Venture Partners and SoftBank Vision Fund 2, our goal is to continue to be the #1 best fulfillment technology in the industry. To help us meet this standard, we are scaling our entire team and looking for people who share our core values and have an entrepreneurial mindset About You: At ShipBob, we're looking for individuals who embody our core values: Be Mission-Driven. We want team members that are passionate about helping entrepreneurs improve their business, and bring that passion every day. Be Humble. We have ambitious goals, and our team members understand that success or failure depends on us working together and leaving egos at the door. Be Resilient. Logistics is a complicated business. So is software. We value team members that never give up and keep iterating until a problem is solved. Be a Creative Problem Solver. As a startup, we value smart, innovative solutions to complex problems. We fall in love with the problem, not our “favorite” solution. Be Safety Minded. It's not just talk; it's the way you work. What You'll Do: Investigate inventory discrepancies reported by the Operations team. Perform physical inventory cycle counts, and reconcile inventory variances. Communicate updates and relay important operational information about clients directly to ICQA Lead. Play a pivotal role in understanding the root cause of inventory adjustments and participate in efforts to correct. Vocalize concerns around inventory practices to ICQA Lead, helping to identify areas of opportunity in day to day processes. Expectations: Proficient in cycle counting and inventory control processes according to written SOP's. Perform Root Cause Analysis around inventory discrepancies and review findings with ICQA Lead. Ensure inventory variances are researched and resolved in a timely manner, allowing fulfillment of outbound orders. Ensure timely communications to MC team for any orders not able to be fulfilled due inventory discrepancies. What You'll Bring To The Table: Demonstrates the ability to quickly adapt to changing conditions and solve problems immediately. Ability to determine inventory discrepancies, perform physical inventory cycle counts, and reconcile inventory variances. Possesses effective written and verbal communication skills; displays reading comprehension skills. Displays the ability to multitask and handle multiple issues at the same time without stress. Displays attention to details. Ability to lift 40lbs without any health limitations. Able to stand and walk continuously during and up to an 8-10hr shift. Able to bend, stoop, reach above, and push/pull frequently. May be required to flex into other departments for support as needed. We recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and excellence; therefore, we encourage people from all backgrounds to apply to our positions. Perks and Benefits: Medical, Dental, Vision & Basic Life Insurance 401K Match Variety of voluntary benefits, such as: short term disability Weekly paychecks & Wage Progression Program KinderBob Daycare Stipend program Paid Time Off & Sick Time Off Referral Bonus Program Fun Culture >>> Check us out on Instagram Reports to: ICQA Area Manager Classification: Hourly/Non-Exempt ShipBob provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 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. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Quality Assurance Manufacturing Engineer, Lehigh Valley, PA The Quality Engineer leads the quality assurance program for the manufacturing plant. This individual collaborates with manufacturing and technical groups to build and monitor quality systems. This role assures all products produced in the plant perform as intended and deliver the desired customer and consumer experience. PRINCIPAL DUTIES & RESPONSIBILITIES: * Determine and lead improvement plans for product quality levels and cost of poor quality. Use consumer data, internal audits and manufacturing records to support continuous improvement. * Partner with manufacturing and engineering teams to improve and maintain quality systems which provide safe, high quality products. * Empower manufacturing areas to meet quality goals through problem solving and root cause investigation; specifically coach manufacturing staff and quality coordinators. * Lead the implementation of statistical process control techniques. Use the techniques to standardize quality control methods and escalate problems. Recommend and lead data bases corrective actions. * Delight customers through partnerships with the product development teams which assure newly launched products perform as intended. JOB SPECIFICATIONS: (Knowledge, skills and abilities normally required for competent performance in the job.) * B.S. degree required in an engineering discipline required. * Three to five years experience in quality assurance/manufacturing environment. * Ability to interpret product specifications and drawings. * Proficiency in the use of laboratory and metrology equipment. * Proficient in use of statistical analysis tools. * Ability to interpret testing procedures and develop test reports based on findings. * Good written, oral and problem-solving abilities required. PHYSICAL CONDITIONS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to sit, talk and hear. The employee is frequentl required to walk; use hands and fingers to operate, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, the ability to adjust focus, and the ability to perceive differences in color. DISCLAIMER: The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. WHY CRAYOLA? * Kid Inspired Culture * Free Admission to Crayola Experience for Employees * Community Volunteerism Opportunities * Annual Bonus Potential for all Full-Time Employees * Company Matched 401k & Employee Value Sharing Plan * Comprehensive Healthcare Benefits for Eligible Employees * Education Assistance Program * Wellness Programs * Employee Resource Groups * Generous Product Discounts Onsite & Online * Company Sponsored Employee Events * Discounts on a wide variety of products and services - automotive, electronics, fitness, travel and entertainment Green is our favorite color! Crayola cares about the environment and responsibly makes the products you love. Learn more about Crayola's creative solutions for greener tomorrows: ***************************************************************** We offer competitive salary, outstanding benefits and the potential for advancement through the use of creative abilities. No phone calls please. Search Firm Representatives - Please Read Carefully: Crayola LLC is not seeking assistance or accepting unsolicited resumes from search firms for this employment opportunity. Regardless of past practice, all resumes submitted by search firms to any employee at Crayola LLC via e-mail, the Internet, or directly to hiring managers at Crayola LLC in any form without valid written search agreement in place for that position will be deemed the sole property of Crayola LLC, and no fee will be paid in the event the candidate is hired by Crayola LLC as a result of the referral or through other means. Search firms are essential to the recruitment and staffing efforts at Crayola LLC, and we value the partnerships we have built with our vendors. For this reason, Crayola LLC has established and regularly maintains a preferred vendor list. Please note that even preferred vendors need to have a written search agreement signed by Human Resources at Crayola LLC in place for the specific position in order for a fee to be paid for any candidate referrals.

Do you have a knack for technology, automation, and smart grid systems? Do you have experience programming smart grid devices and troubleshooting communication networks? If so, we'd love to have you on our team! About the Role We are seeking an Automation Engineer to support the programming, troubleshooting, and operation of remote devices on the distribution line, including reclosers and capacitor banks. This role is critical in ensuring the efficient operation of the grid by managing new installations, equipment failures, and protection setting updates. You will also be responsible for programming applicable systems to support automation initiatives. Key Responsibilities Remotely program distribution devices such as reclosers and capacitor banks Troubleshoot device communications and operational issues Support new installations by programming applicable systems Work collaboratively with internal teams to ensure system reliability Basic Requirements Must be local to Allentown, PA or willing to be in-office three days per week (Tues-Thurs) Advanced computer skills with the ability to quickly learn new systems Bachelor's degree in Computer Science, Engineering, Mathematics, or a related field 2-5 years of utility experience Experience programming SEL relays or similar smart grid devices Knowledge of distribution/transmission protection and controls and/or relay testing experience Why Join Us? Work in an innovative and dynamic environment supporting the future of the energy grid Hybrid work model with a balance of in-office collaboration and remote flexibility Competitive compensation and benefits package Opportunities for career growth and professional development This is a contract position expected to last AT LEAST 6 months - possibly longer. Salary will be based on experience. This position is with a utility company based in Allentown. If you're ready to make an impact in the field of automation and smart grid technology, apply today through the HTSS website OR email resume to ********************!

Do you have a knack for technology, automation, and smart grid systems? Do you have experience programming smart grid devices and troubleshooting communication networks? If so, we'd love to have you on our team! About the Role We are seeking an Automation Engineer to support the programming, troubleshooting, and operation of remote devices on the distribution line, including reclosers and capacitor banks. This role is critical in ensuring the efficient operation of the grid by managing new installations, equipment failures, and protection setting updates. You will also be responsible for programming applicable systems to support automation initiatives. Key Responsibilities Remotely program distribution devices such as reclosers and capacitor banks Troubleshoot device communications and operational issues Support new installations by programming applicable systems Work collaboratively with internal teams to ensure system reliability Basic Requirements Must be local to Allentown, PA or willing to be in-office three days per week (Tues-Thurs) Advanced computer skills with the ability to quickly learn new systems Bachelor's degree in Computer Science, Engineering, Mathematics, or a related field 2-5 years of utility experience Experience programming SEL relays or similar smart grid devices Knowledge of distribution/transmission protection and controls and/or relay testing experience Why Join Us? Work in an innovative and dynamic environment supporting the future of the energy grid Hybrid work model with a balance of in-office collaboration and remote flexibility Competitive compensation and benefits package Opportunities for career growth and professional development This is a contract position expected to last AT LEAST 6 months - possibly longer. Salary will be based on experience. This position is with a utility company based in Allentown. If you're ready to make an impact in the field of automation and smart grid technology, apply today through the HTSS website OR email resume to ********************!

One of our large Biopharmaceutical clients is seeking an Automation Engineer to join their growing team. This person will be responsible for owning a project list of scripts that have to be written for the automation of liquid handlers. We are looking for a skilled automation engineer who has experience in a biopharmaceutical setting and can fully own the script writing automation process without leadership oversight. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Automation Engineering Experience Tecan Fluent Software Experience Script/Method Generation In Vitro DMPK Assay and Sample Management Experience Tecan Fluent Training

Join Our Team Lenape Valley Foundation is seeking individuals to support quality care assurance, documentation compliance, and audit readiness within our Community Based and Outpatient Programs. These positions will collaborate with Department Managers and the Compliance Committee to strengthen and monitor Quality Assurance policies and workflows specific to outpatient services. What We Offer NEW!! DailyPay- gives you the flexibility to access your earnings immediately- on your own schedule! Paid training and supervision 403(b) Retirement Plan FULL TIME Benefits Package Includes: Generous PTO Policy 15 PTO Days, 10 Paid Sick Days, 4 Paid Personal Days, 7 Paid Holidays, 5 Paid Conference Days Medical, Dental, and Vision Insurance Credit available for medical opt-out Flexible Spending Account (FSA) Long-Term Disability and Basic Life Insurance Employee Assistance Program (EAP) Continuing Education Assistance Program Access to student loan management and repayment support What You Bring Bachelor's Degree with major coursework in Psychology, Sociology, Social Work, Counseling, or related fields. Minimum of 1-year related work experience Strong attention to detail Excellent organization and communication skills High data-entry accuracy Analytical thinking and problem-solving ability Ability to work under pressure and meet deadlines Strong proficiency in MS Office, including Excel, and database management Ability to meet the physical demands of the role, with or without accommodation Your Role Review clinical charts, treatment plans, and documentation to ensure compliance with payer coding requirements, best practices, state/federal regulations, and accreditation standards. Implement and support Quality Assurance Policies and Procedures across assigned programs. Monitor and track compliance-related needs, including but not limited to: Encounter Form signatures submitted via the client portal; follow up with clients who have not completed them prior to their next appointment. Review Zoom session durations against encounter and service documentation; follow up with providers when times do not match. Track Release of Information (ROI) forms sent through the portal and ensure completion/signatures. Outpatient Only: Track timely completion of all required service documentation, including but not limited to: Compiling Encounter Forms for Outpatient Prescribers following telehealth services Monitoring treatment plan completion and required signatures Supporting compliance with G-Codes documentation, including Depression Screeners Safety Plans Tobacco-related documentation Social Detriments of Health Ensuring appropriate documentation and billing for family sessions Ensuring rational is clearly documented for telephone-based services About Lenape Valley Foundation Since 1958, Lenape Valley Foundation (LVF) has been a trusted non-profit provider of essential human services in Bucks and Montgomery Counties. Our mission is to partner with individuals facing mental health, substance use, or developmental challenges as they pursue personal goals and improved quality of life. With over 30 programs and a commitment to evidence-based care, LVF continues to evolve to meet community needs. Our Commitment To Diversity and Inclusion LVF is an Equal Opportunity Employer. We are committed to fostering a workplace that respects and celebrates diversity. We welcome applicants of all backgrounds and ensure a discrimination and harassment free environment where everyone is treated with dignity.

Our Automation Engineer supports, develops, and maintains automated systems used in pharmaceutical manufacturing. This role ensures that production equipment, control systems, and digital infrastructure operate reliably, efficiently, and in compliance with cGMP and regulatory standards. The engineer collaborates with cross‑functional teams to troubleshoot issues, implement improvements, and support new system installations or upgrades. Operates within legal and regulatory compliance, ensuring systems are maintained and operational within site and regulatory requirements. Capable of following procedures, documenting work as/when performed and maintaining a clean/organized workplace supporting site compliance and quality standards. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is an onsite role in Bloomsbury, New Jersey; Monday - Friday 6 AM - 2:30 PM. What the Automation Engineer Does Each Day: Provides technical skills and expertise to support operations, ensuring automated manufacturing equipment operates efficiently, including network configuration and integration principles, and the ability to work effectively with IT Supports constant operations by trouble shooting machines, monitoring PLC issues, performing root cause analysis on complex issues, and executing improvements Investigates automation incidents and problems to prevent recurrence including the development and implementation of corrective actions Design and implementation of equipment and facilities related controls including PLC coding (Allen-Bradley/Siemens), HMI and SCADA systems Evaluates automated and information technology systems, and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade Efficient use of different software tools and computer applications including but not limited to Microsoft Office, PLC programming software, electrical schematic design software, HMI programming software, SCADA systems and industrial networks (Allen-Bradley/Siemens) Effectively and accurately handles most technical questions and objections for assigned products Maintains appropriate documentation for equipment and processes including change control, drawings, manuals, and validation Streamlines workflows and develop automated laboratory processes and instrumentation systems, including collecting and documenting requirements, developing concepts, design, testing/validation, implementation, and training Recognizes priorities and takes action; makes productive use of time Understands and adheres to policies and procedures Software validation, data integrity, GAMP 5 and 21 CFR part 11 experience Operating and troubleshooting of Fanuc Robotics Our Most Successful Automation Engineer Has: Experience in aseptic processing preferred Experience with FDA, GMP, and ISO standards preferred Must possess the ability to work effectively with all levels of organization Demonstrated ability to build and maintain strong business and collaborative relationships, internally and externally Must possess excellent interpersonal, communication, and writing skills, ability to analyze technical issues, define/solve problems, establish project plans, and draw valid conclusions Ability to think analytically and systematically Aseptic Operator Qualification and Process Simulation Proficient in technical writing and current computer usage (Word, Excel, PowerPoint, etc.) Good working knowledge of regulatory guidance as it pertains to APIs and injectable drug products Minimum Requirements for this Role: Bachelor's degree in electrical engineering, Mechanical Engineering, or another related field, with 5+ years' experience in a manufacturing environment Experience working with PLCs, HMIs, Robotics (Fanuc, Staubli), and SCADA systems, preferably Rockwell or Siemens platforms Equipment/Instrument Calibration principles Proven ability to adapt and manage effectively in fast paced, changing environment 18+ years of age Able to successfully complete a drug and background check Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions Range: $85,993 - $134,364 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Retlif Testing Laboratories is looking to hire a full-time Test Engineer to join our Harleysville, PA laboratory. Do you have a background in electrical engineering and want a career, not just a job? This position earns competitive pay, depending on experience. We also offer excellent benefits, including medical, dental, vision, a 401(k) plan, paid holidays, paid time off (PTO), and a tuition reimbursement program. If this sounds like the right opportunity for you in electrical engineering, consider applying today! ABOUT RETLIF TESTING LABORATORIES An industry leader for over 45 years, we are an independent testing laboratory that provides compliance testing and engineering services to customers in such industries as aerospace, rail, maritime, military, defense, and medical. Retlif provides electromagnetic compatibility, radio approval, product safety, and environmental simulation testing to national and international standards. We pride ourselves on providing exceptional customer service. We have a loyal and long-standing customer base that appreciates our commitment to the highest quality in testing and engineering services. Our mission is to fully address the testing and compliance needs of our clients. As a team member at one of the USA's leading independent testing laboratories, you can expect excellent personal growth opportunities, a professional atmosphere, and comprehensive employee benefits. We are an equal opportunity employer that values each member of our team. A DAY IN THE LIFE OF A TEST ENGINEER As a Test Engineer, you are a critical member of our team. You oversee and mentor other technical staff members who are the technical interface with our customers, serving as a technical resource during the performance of contracted testing as well as during our initial sales efforts. You are involved with the pre-test engineering reviews, test sample preparation, setup, execution of the tests, and the documentation of test results. You regularly interact directly with customers. In order to apply appropriate test standards and provide time and cost estimates, you provide support to the sales team. You also get to support Engineering in the development of new service offerings. You get great satisfaction out of helping our clients succeed by fully addressing their compliance needs! QUALIFICATIONS FOR A TEST ENGINEER * Bachelor's degree in a relevant field OR equivalent training * 2 years of work experience in the electrical engineering field * Excellent knowledge about measurement equipment, such as digital multimeters (DMMs), Oscilloscopes, and Spectrum Analyzers * Excellent computer skills * Ability to lift 50 pounds, bend, lift, and twist * Background that would permit the U.S. Dept. of Defense (DoD) to issue a Secret Clearance, which requires U.S. Citizenship Are you organized and attentive to detail? Do you have excellent interpersonal skills? Can you effectively prioritize multiple tasks in order to meet strict deadlines? Do you have strong communication skills, both written and verbal? Can you work well independently? Do you thrive in a fast-paced environment? If so, you might just be perfect for this Test Engineer position! WORK SCHEDULE This full-time Test Engineer job is Monday - Friday, 8:00 AM - 4:30 PM. Additional hours may be necessary at times, depending on customer needs. READY TO JOIN OUR TEAM? We understand your time is valuable, and that is why we have a very quick and easy application process. If you feel that you would be right for this Test Engineer job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you! Location: 19438

Performance Test Engineer QAD has an opening for a Performance Test Engineer based in Ireland. QAD is looking for an energetic candidate who wants to grow their career through experience and taking ownership of new challenges. The team is friendly, supportive and responsible for performance benchmarking and scalability of QAD products. We are based in Limerick and we are responsible for the architecture, design and execution of performance tests. The work is varied and often includes researching new methods and approaches along with working alongside both global teams and customers. What we Offer: Competitive compensation packages based on experience and desired skill set Benefits, health insurance & vision and optical and other great benefits Collaborative culture of smart and hard-working people who support one another to get the job done An atmosphere of growth and opportunity, where idea-sharing is always prioritized over level or hierarchy Flexible working options (remote, hybrid or office based) What You will Do: Benchmark QAD Products in both single and multiple users in a dedicated performance lab primarily on Linux against agreed SLAs Holistic analysis of server side resources and key product areas Create performance scripts using JMeter Create Linux scripts to extract meaningful data when required Root cause analysis and problem solving of performance issues Collaborate with various QAD teams Contribute in team meetings Essential Knowledge and Skills: Bachelor's degree in Software Engineering, Science, Engineering, or Mathematics or equivalent work experience At least 2 years experience in a performance engineering role Fluent English and excellent communication skills Experience working with Linux or UNIX including scripting Excellent problem solving, troubleshooting, research and analysis skills Proven ability to work off own initiative, think laterally, problem-solve, communicate and collaborate Experience working in a medium to large organization Ability to efficiently debug complex problems Analytical approach to problem solving Valued Skills and Knowledge Experience with Progress OpenEdge Experience with Performance testing tools such as JMeter or Selenium Experience with Databases; ideally familiar with basic database operations and management. Experience with Enterprise Level Operating Systems; e.g. Linux Experience with scripting in python, awk etc. Experience working in an agile environment Experience with Atlassian tools (JIRA and Confluence) Experience with Excel or similar spreadsheet tools About QAD: QAD Inc. is a leading provider of adaptive, cloud-based enterprise software and services for global manufacturing companies. Global manufacturers face ever-increasing disruption caused by technology-driven innovation and changing consumer preferences. In order to survive and thrive, manufacturers must be able to innovate and change business models at unprecedented rates of speed. QAD calls these companies Adaptive Manufacturing Enterprises. QAD solutions help customers in the automotive, life sciences, packaging, consumer products, food and beverage, high tech and industrial manufacturing industries rapidly adapt to change and innovate for competitive advantage. QAD is committed to ensuring that every employee feels they work in an environment that values their contributions, respects their unique perspectives and provides opportunities for growth regardless of background. QAD's DEI program is driving higher levels of diversity, equity and inclusion so that employees can bring their whole self to work.

DIRECT HIRE: A great opportunity for a Quality Assurance Assistant to join a dynamic team in the Allentown, PA. area. Hourly Rate: $19hr - $23hr Benefits: Medical, dental, vision, PTO, 401K, short-term disability, employee life Schedule: M-F, 40hrs +OT Roles & Responsibilities: Test and conduct routine and non-routine in-process inspection of production output, measure samples of finished product and check production quality verifications for completeness, timeliness and tolerances as well as complete product testing of finished goods Assist with incoming inspections for internal / external suppliers as directed Confirm discrete job special instructions are being followed or met Member of daily audit team for various product and process audits per checklist Participant in the revision and update of standard operating procedures Conduct and complete Internal Quality audits and may be involved in the development of testing method Ensure employees adhere to safety and quality standards Skills and qualifications: 1-3 years manufacturing experience: required (metal, paint/finishing industries: a plus) High School Diploma or GED: required ISO 9000 and 5S Program knowledge and experience Measuring tools knowledge and experience Customer focused mindset Proven hands-on shop floor experience; forklift experience Working knowledge Microsoft Office (Word, Excel, PowerPoint) Good work record; Strong work ethic Strong communication and interpersonal skills Good teamwork and time management skills Experience in a high volume fast paced environment Once you apply, please text "QAA" to ************ for a faster reply. INDH

Title: ICQA Associate Hours/Shift: 1st Shift Mon - Fri 8:00 am - 4:30 pm at $20.25hr or 2nd Shift Sat - Wed 3:00pm to 11:30pm at $21.25hr If you're looking to be at the forefront of disrupting the ecommerce industry, wanting to make your mark and be continuously challenged to grow, your time has come. ShipBob is recognized as #1 on Crain's 2020 "Fast 50" list of the fastest-growing companies in Chicago & Inc.5000 top 500 companies with the most proven track records. With this growth, we are looking for top talent to help us reach the next level. Role Description: This is an incredibly important position that helps to monitor inventory activities of all clients at each fulfillment center while allowing all existing operations team members to remain focused on their day-to-day responsibilities. As ShipBob continues to grow, it is imperative to provide a great experience in serving our clients' needs while maintaining sustainable growth and scalability from an operations perspective. About Us: ShipBob is a cloud based logistics platform that partners with over 5,200+ e-commerce businesses to help them be more successful online. We offer a full suite of fulfillment solutions for our merchants, including the ability to improve their transit times, shipping costs and deliver best in class experience to their customers. With almost 100% accuracy rate in fulfilling orders and orders shipped on time, our merchants can count on us to deliver excellent service. ShipBob's growing fulfillment network is powered by our proprietary technology and acts as a back office for logistics, providing merchants with full visibility into orders, inventory levels in real time, and access to advanced analytics, over 27 integrations and data reporting. As one of the fastest growing tech companies in Chicago with over $330M+ raised from blue-chip investors like Menlo Ventures, Bain Capital Ventures, Hyde Park Venture Partners and SoftBank Vision Fund 2, our goal is to continue to be the #1 best fulfillment technology in the industry. To help us meet this standard, we are scaling our entire team and looking for people who share our core values and have an entrepreneurial mindset About You: At ShipBob, we're looking for individuals who embody our core values: * Be Mission-Driven. We want team members that are passionate about helping entrepreneurs improve their business, and bring that passion every day. * Be Humble. We have ambitious goals, and our team members understand that success or failure depends on us working together and leaving egos at the door. * Be Resilient. Logistics is a complicated business. So is software. We value team members that never give up and keep iterating until a problem is solved. * Be a Creative Problem Solver. As a startup, we value smart, innovative solutions to complex problems. We fall in love with the problem, not our "favorite" solution. * Be Safety Minded. It's not just talk; it's the way you work. What You'll Do: * Investigate inventory discrepancies reported by the Operations team. * Perform physical inventory cycle counts, and reconcile inventory variances. * Communicate updates and relay important operational information about clients directly to ICQA Lead. * Play a pivotal role in understanding the root cause of inventory adjustments and participate in efforts to correct. * Vocalize concerns around inventory practices to ICQA Lead, helping to identify areas of opportunity in day to day processes. Expectations: * Proficient in cycle counting and inventory control processes according to written SOP's. * Perform Root Cause Analysis around inventory discrepancies and review findings with ICQA Lead. * Ensure inventory variances are researched and resolved in a timely manner, allowing fulfillment of outbound orders. * Ensure timely communications to MC team for any orders not able to be fulfilled due inventory discrepancies. What You'll Bring To The Table: * Demonstrates the ability to quickly adapt to changing conditions and solve problems immediately. * Ability to determine inventory discrepancies, perform physical inventory cycle counts, and reconcile inventory variances. * Possesses effective written and verbal communication skills; displays reading comprehension skills. * Displays the ability to multitask and handle multiple issues at the same time without stress. * Displays attention to details. * Ability to lift 40lbs without any health limitations. * Able to stand and walk continuously during and up to an 8-10hr shift. * Able to bend, stoop, reach above, and push/pull frequently. * May be required to flex into other departments for support as needed. We recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and excellence; therefore, we encourage people from all backgrounds to apply to our positions. Perks and Benefits: * Medical, Dental, Vision & Basic Life Insurance * 401K Match * Variety of voluntary benefits, such as: short term disability * Weekly paychecks & Wage Progression Program * KinderBob Daycare Stipend program * Paid Time Off & Sick Time Off * Referral Bonus Program * Fun Culture >>> Check us out on Instagram Reports to: ICQA Area Manager Classification: Hourly/Non-Exempt ShipBob provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 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. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Quality Assurance Validation Intern as part of the Quality team based in Raritan, NJ. Role Overview The QA Validation Intern will support validation activities by organizing and tracking documentation, assisting with QA release processes, and maintaining compliance records. This role provides exposure to GMP documentation practices and quality assurance workflows. Key Responsibilities * Organize and track document spreadsheets for validation activities. * Print QA release labels and file release copies to Cartna. * Pick up and deliver documents between departments and buildings. * Compose a list of site SOPs sorted by topic. * Support QA team with administrative and compliance tasks. Requirements * Enrolled in an undergraduate program (Desired Academic Grade Level: Junior/ Senior) * Strong working knowledge of Excel. * Ability to work collaboratively in a team environment. * Strong organizational and presentation skills. Skills You'll Gain * Hands-on experience with QA validation processes. * Exposure to GMP documentation and compliance standards. * Development of organizational and communication skills. #Li-RP1 #Li-Contract Benefits We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles. We offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes vacation days, personal days, sick time, 11 company holidays, and 3 floating holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs - demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. Please note: These benefits are offered exclusively to permanent employees. Contract employees are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.