Quality control analyst jobs in Richmond, VA

CoStar Group (NASDAQ: CSGP) is a leading global provider of commercial and residential real estate information, analytics, and online marketplaces. Included in the S&P 500 Index and the NASDAQ 100, CoStar Group is on a mission to digitize the world's real estate, empowering all people to discover properties, insights and connections that improve their businesses and lives. We have been living and breathing the world of real estate information and online marketplaces for over 35 years, giving us the perspective to create truly unique and valuable offerings to our customers. We've continually refined, transformed and perfected our approach to our business, creating a language that has become standard in our industry, for our customers, and even our competitors. We continue that effort today and are always working to improve and drive innovation. This is how we deliver for our customers, our employees, and investors. By equipping the brightest minds with the best resources available, we provide an invaluable edge in real estate. ABOUT THE ROLE CoStar delivers real-time, verified commercial real estate data that helps clients confidently spot great opportunities and make smart choices ahead of competitors. By combining the power of CoStar's independent research organization - the industry's largest - with global data delivery, software, and application solutions, clients can act on opportunities with confidence. CoStar's research and analytics teams are the heart of CoStar, capturing market-critical information that enables our commercial real estate clients to make informed, high impact business decisions daily. CoStar Group's research contributes to the most important segment of our economy, helping businesses open offices, retail stores, warehouses, and manufacturing facilities. CoStar Group is seeking a Lease Abstraction Auditor to join our Real Estate Manager business unit. This role plays a critical part in maintaining the integrity of CoStar's lease data, ensuring it meets the highest quality standards for our clients. As a Lease Abstraction Quality Control Analyst at CoStar Real Estate Manager, you will be responsible for ensuring the accuracy, completeness, and quality of lease comparables (lease comps) data that have been analyzed and abstracted by our Lease Abstraction Associates. Additionally, this role will assist with training and providing valuable feedback for the development of the Lease Abstraction Analyst Team. This position requires a comprehensive understanding of lease terms and real estate practices, exceptional attention to detail, strong reading comprehension, and a proven ability to teach and guide the ongoing learning and development of team members. This position is in office Monday through Friday. RESPONSIBILITIES Audit lease comps abstracted by the Lease Abstraction Analysts to ensure data accuracy, consistency, and completeness. Cross-reference lease abstract details with original lease documents and other supporting materials to ensure correct interpretation and data entry. Collaborate with stakeholders as needed to determine best practices for capturing data for edge cases and ambiguities in lease language. Provide constructive feedback to analysts to promote continued learning and professional development Collaborate with the Senior Manager, Lease Abstraction Auditor and Lease Abstraction Managers to create and enhance training processes and professional development initiatives. Assist in identifying and refining quality assurance processes, tools, and workflows. Maintain privacy and discretion with all lease data. BASIC QUALIFICATIONS Bachelor's Degree required from an accredited, not-for-profit University or College 2 years of relevant work experience in lease administration, lease abstraction or review of similar legal documents. Comprehensive understanding of commercial lease structures and terminology. Excellent analytical and problem-solving skills, with attention to detail and accuracy. Effective communication skills, both written and verbal. Proven success performing to metrics or key performance indicators (KPIs). A proven track record of commitment to prior employers. Demonstrated success in mentoring or training team members, with a strong commitment to knowledge sharing and contributing to professional development initiatives. Microsoft Excel 365 experience is required. Ability to manage multiple responsibilities, changing priorities, and excel in a fast-paced environment. Natural curiosity, persistence, and ability to conduct thorough investigative research Self-motivated and goal-oriented. Preferred Qualifications and Skills: Bachelor's degree in real estate, finance, economics or accounting. Juris Doctor (J.D.) or equivalent law degree with coursework or experience in commercial real estate, finance, economics, construction or contracts. WHAT'S IN IT FOR YOU? When you join CoStar Group, you'll experience a collaborative and innovative culture working alongside the best and brightest to empower our people and customers to succeed. We offer you generous compensation and performance-based incentives. CoStar Group also invests in your professional and academic growth with internal training and tuition reimbursement. Our benefits package includes (but not limited to): Comprehensive healthcare coverage: Medical / Vision / Dental / Prescription Drug Life, legal, and supplementary insurance Virtual and in person mental health counseling services for individuals and family Commuter and parking benefits 401(K) retirement plan with matching contributions Employee stock purchase plan Paid time off Tuition reimbursement On-site fitness center and/or reimbursed fitness center membership costs (location dependent), with yoga studio, Pelotons, personal training, group exercise classes Access to CoStar Group's Diversity, Equity, & Inclusion Employee Resource Groups We welcome all qualified candidates who are currently eligible to work full-time in the United States to apply. However, please note that CoStar Group is not able to provide visa sponsorship for this position. #LI-AO1 CoStar Group is an Equal Employment Opportunity Employer; we maintain a drug-free workplace and perform pre-employment substance abuse testing

Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our ******************************** is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. Coinbase stores more digital currency than any company in the world, making us a top tier target on the internet. Security is core to our mission and has been a key competitive differentiator for us as we scale worldwide. Essential to scaling is building and running a security compliance program that reflects how we protect the data and assets in our care, to open the doors with customers, regulators, auditors, and other external stakeholders. Coinbase is looking for an Analyst, Tech Controls to support the second line of defense technology compliance initiatives. This role will play a critical part in assisting with the design, implementation, and monitoring of a technology control framework. The Analyst will work closely with cross-functional teams to ensure excellence in control ownership and contribute to the maturity of the Technology Risk and Controls program. *What you'll be doing (ie. job duties):* * Lead IT process and gap assessments against industry standards and technology regulatory requirements to evaluate control design and operating effectiveness * Design, review and validate processes and configurations across technology systems, including cloud environments, operating systems, databases, and network infrastructure, to ensure alignment with established standards, compliance requirements, and best practices * Assist in maintaining and providing oversight over the technology controls inventory to mitigate technology risks and meet regulatory requirements, technology policies, and frameworks * Collaborate with stakeholder teams including Security, Engineering, Technology Governance, IT, and Operational Risk to support technology requirements and ensure control ownership * Developing technology requirements for new products, updating existing controls, and providing subject matter expertise to product teams * Support Security Compliance, Information Security, Platform, and Engineering stakeholders in identifying and executing on continuous control monitoring opportunities * Provide guidance and leverage technical expertise to determine effectiveness of change management processes, i.e. unit testing, CI/CD, etc. * Define, draft and communicate identified issues and technology process improvement opportunities and assist in developing creative solutions to mitigate risks and address regulatory challenges * Provide reporting to stakeholders and management on progress, escalations, and control initiatives * Drive the creation of procedural documentation, including training materials that support first line of defense risk management, in the form of runbooks and narratives * Validate remediation efforts for identified gaps and issues to ensure resolution effectively aligns with regulatory requirements, industry standards, and internal policies * Drive creation of clear and concise technical documentation for control monitoring *What we look for in you (ie. job requirements):* * Minimum of 2+ years of experience in Security Engineering, Technology Compliance, IT audit, or equivalent roles * Strong knowledge and hands-on experience in technology frameworks such as COBIT, NIST, ISO 27001 * Hands on experience in security engineering, implementing security frameworks, or designing and managing technical controls * Proven technical understanding and operation within cloud technologies, AWS preferred * Strong understanding of control monitoring processes * Excellent oral and written communication skills * Ability to effectively and autonomously accomplish outcomes across cross-functional teams in ambiguous situations with limited supervision * Ability to multitask, prioritize work, and meet deadlines in a fast paced environment * Ability to communicate with technical and non-technical stakeholders to align on shared outcomes *Nice to haves:* * BA or BS in a technical field or equivalent experience * Cloud certifications such as AWS Certified Security Specialty, or equivalent certifications * Security certifications e.g. CISA, CISSP, COBIT or other relevant certifications * Technical understanding of fintech services and/or crypto space Position ID: P60079 \#LI-Remote *Pay Transparency Notice:* Depending on your work location, the target annual salary for this position can range as detailed below. Full time offers from Coinbase also include bonus eligibility + equity eligibility**+ benefits (including medical, dental, vision and 401(k)). Pay Range: $135,320-$159,200 USD Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the *********************************************** in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations*********************************** *Global Data Privacy Notice for Job Candidates and Applicants* Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available ********************************************************** By submitting your application, you are agreeing to our use and processing of your data as required. *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. The tool simulates realistic interview scenarios and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of a voice recording and/or transcript, to assess them against the qualifications and characteristics outlined in the job description. For select roles, Coinbase is also piloting an AI interview intelligence platform to transcribe and summarize interview notes, allowing our interviewers to fully focus on you as the candidate. *The above pilots are for testing purposes and Coinbase will not use AI to make decisions impacting employment*. To request a reasonable accommodation due to disability, please contact accommodations[at]coinbase.com

KPMG Advisory practice is currently our fastest growing practice. We are seeing tremendous client demand, and looking forward we do not anticipate that slowing down. In this ever-changing market environment, our professionals must be adaptable and thrive in a collaborative, team-driven culture. At KPMG, our people are our number one priority. With a wealth of learning and career development opportunities, a world-class training facility and leading market tools, we make sure our people continue to grow both professionally and personally. If you're looking for a firm with a strong team connection where you can be your whole self, have an impact, advance your skills, deepen your experiences, and have the flexibility and access to constantly find new areas of inspiration and expand your capabilities, then consider a career in Advisory. KPMG is currently seeking an Associate, Oracle Controls in Technology Risk for our Consulting practice. Responsibilities: * Assist in designing and implementing comprehensive controls and security solutions tailored to client requirements within Oracle Fusion Cloud financial systems. * Assist in the assessment and re-engineering of IT application controls to enhance effectiveness and compliance in client environments. * Develop and oversee the implementation of IT general controls in Oracle Fusion SaaS and Oracle OCI, focusing on access controls, and change management. * Build, test, and manage Oracle Security Roles, ensuring optimized configurations that meet client-specific needs. * Drive enhancements in SoX and other regulatory compliance processes through innovative control solutions within Oracle Fusion Cloud environments. * Guide the deployment of Configuration and Transaction Monitoring Controls using Oracle risk management cloud, ensuring high standards of compliance and oversight. Qualifications: * Minimum of 1 year of demonstrated experience in Oracle Finance Security role configuration, emphasizing controls implementation. * Strong experience in designing, documenting, and testing IT application controls specifically for Oracle Fusion Cloud. * Extensive knowledge and hands-on experience with IT general controls, security role design, and configuration within Oracle Fusion SaaS and OCI. * Proven ability to understand and integrate financial and supply chain business processes with Oracle security configurations. * Expertise in developing strategies to optimize SoX compliance for Oracle Fusion environments. * Skilled in leveraging Oracle Risk Management Cloud for enhancing security measures and control monitoring. * Minimum of bachelors degree from an accredited college/university and Certified Public Accountant (CPA) license is preferred. * Must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future. KPMG LLP will not sponsor applicants for U.S. work visa status for this opportunity (no sponsorship is available for H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT or any other employment-based visa) KPMG complies with all local/state regulations regarding displaying salary ranges. If required, the ranges displayed below or via the URL below are specifically for those potential hires who will work in the location(s) listed. Any offered salary is determined based on relevant factors such as applicant's skills, job responsibilities, prior relevant experience, certain degrees and certifications and market considerations. In addition, the firm is proud to offer a comprehensive, competitive benefits package, with options designed to help you make the best decisions for yourself, your family, and your lifestyle. Available benefits are based on eligibility. Our Total Rewards package includes a variety of medical and dental plans, vision coverage, disability and life insurance, 401(k) plans, and a robust suite of personal well-being benefits to support your mental health. Depending on job classification, standard work hours, and years of service, KPMG provides Personal Time Off per fiscal year. Additionally, each year the firm publishes a calendar of holidays to be observed during the year and provides two firmwide breaks each year where employees will not be required to use Personal Time Off; one is at year end and the other is around the July 4th holiday. Additional details about our benefits can be found towards the bottom of our KPMG US Careers site at Benefits & How We Work. Follow this link to obtain salary ranges by city outside of CA: ********************************************************************** California Salary Range: $72600 - $112200 KPMG LLP (the U.S. member firm of KPMG International) offers a comprehensive compensation and benefits package. KPMG is an equal opportunity employer. KPMG complies with all applicable federal, state and local laws regarding recruitment and hiring. All qualified applicants are considered for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, citizenship status, disability, protected veteran status, or any other category protected by applicable federal, state or local laws. The attached link contains further information regarding the firm's compliance with federal, state and local recruitment and hiring laws. No phone calls or agencies please. KPMG does not currently require partners or employees to be fully vaccinated or test negative for COVID-19 in order to go to KPMG offices, client sites or KPMG events, except when mandated by federal, state or local law. In some circumstances, clients also may require proof of vaccination or testing (e.g., to go to the client site). KPMG recruits on a rolling basis. Candidates are considered as they apply, until the opportunity is filled. Candidates are encouraged to apply expeditiously to any role(s) for which they are qualified that is also of interest to them. Los Angeles County applicants: Material job duties for this position are listed above. Criminal history may have a direct, adverse, and negative relationship with some of the material job duties of this position. These include the duties and responsibilities listed above, as well as the abilities to adhere to company policies, exercise sound judgment, effectively manage stress and work safely and respectfully with others, exhibit trustworthiness, and safeguard business operations and company reputation. Pursuant to the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.

Job Description Sr. SOX Controls Analyst Status: Full-Time/ Salaried Exempt Our Company Universal is headquartered in Richmond, Virginia, and is the leading global leaf tobacco supplier. Tobacco sourcing and processing has been the Company's principal focus since its founding in 1918. The largest portion of the Company's business involves procuring and processing flue-cured, burley, and dark air-cured leaf tobacco for manufacturers of consumer tobacco products. Over the past few years, Universal has expanded its business through a series of acquisitions to develop a plant-based ingredients business segment to support the food and beverage markets which will provide future growth opportunities for Universal. We are now a global business-to-business agri-products supplier to consumer product manufacturers, that sources and processes leaf tobacco and plant-based ingredients. Through our plant-based ingredients platform, we provide a variety of value-added manufacturing processes to produce high-quality, specialty vegetable- and fruit-based ingredients as well as botanical extracts and flavorings for human and pet food end markets. Universal conducts business in over 30 countries on five continents and employs over 25,000 permanent and seasonal workers. Domestically, Universal employs over 1,000 permanent and seasonal workers, and its revenues ending March 31, 2024, were $2.75 billion. For more information on Universal, visit our website at ********************* Summary As a Sr. SOX Controls Analyst at Universal, you will be responsible for leading the annual SOX risk-based scoping process and ensuring alignment with corporate risk priorities. This role involves evaluating internal controls, performing process reviews, and assessing the impact of regulatory and organizational changes on the control environment. This position collaborates with cross-functional teams and leadership to standardize controls, conduct controls testing, and provides mentorship to junior staff. What You'll Be Doing (Essential Duties) Lead the annual SOX risk-based scoping process at both the account and process levels, ensuring alignment with corporate risk priorities. Perform process reviews to evaluate current business practices, internal control structures, and existing SOX documentation. Assess the SOX implications of changes in the control environment due to updates in accounting regulations, company policies, system enhancements or implementations, or organizational restructuring. Determine if adjustments to existing controls or the establishment of new controls are required. Partner with cross-functional teams and subsidiary leadership to evaluate, identify, and develop standard controls by process for use across all subsidiaries. Conduct system walkthroughs, assess the adequacy of internal controls, and perform detailed control testing. Provide oversight and mentorship to junior team members, including reviewing control testing and providing guidance on best practices. Monitor the progress of process owners' testing activities to ensure timely completion, research risks and impacts of control findings, recommend remediation plans to management, develop re-testing timelines, and maintain compliance with SOX documentation requirements. Communicate effectively with all levels of business management. Collaborate with internal and external auditors to coordinate audit timing, address control finding remediation and re-testing, and manage SOX reporting. Develop SOX training materials for process owners. Communicate SOX compliance status, risks, and remediation plans to management. Minimum Requirements Bachelor's degree in accounting, Finance, or Business or equivalent work experience Minimum four years of audit/accounting experience Certified Public Accountant (CPA); Certified Internal Auditor (CIA); or Certified Information Systems Auditor (CISA) certification or active pursuit of certification(s) Proficiency in SOX 404 requirements: identifying controls, control gap analysis, and evaluating testing effectiveness Comprehensive understanding of GAAP, PCAOB standards, SOX Compliance, COSO Framework, and/or SEC regulations Excellent written and verbal communication skills Motivated to work independently and complete responsibilities with little supervision yet work well and promote a collaborative culture Strong organizational abilities, attention to detail, time management, and interpersonal skills Preferred Skills Experience in a manufacturing environment Experience with SOX compliance software i.e., Workiva Wdesk Project management experience: proven ability to continuously move forward multiple projects in various states Multi-lingual skills Benefits We offer a wide range of market-competitive total rewards that include 401(k) match, pension, merit increases, paid holidays, medical, dental, life, vision, short and long-term disability benefits, and tuition assistance to name a few. EOE M/F/Disabled/Vet Employer All applicants must be authorized to work in the United States.

Oldcastle APG, a CRH Company, is North America's leading provider of innovative outdoor living solutions that enable customers to Live Well Outside. The manufacturer's portfolio of premier building products inspires endless possibilities while providing enduring outdoor spaces where people can connect, reflect and recharge. Award-winning brands include Belgard hardscape, Echelon Masonry, MoistureShield composite decking, RDI railing, Catalyst Fence Solutions, Sakrete packaged concrete, Amerimix mortar, Pebble Technology International pool finishes, Lawn & Garden mulches and landscape features, and Techniseal sands and sealant technologies. Job Summary We are currently looking for a Quality Control Associate with experience in a manufacturing environment. This person will be responsible for the material handling and preparation for routine testing and maintenance of assigned laboratory equipment as well as testing finished products and quality testing both raw and finished materials. Job Responsibilities * Preparation of materials and products for testing * Sampling and reduction of samples * Routine tests of raw materials, calculation of results and preparation of tests reports * Support manufacturing team in producing the highest quality products * Test all products and raw materials and record results * Calculate adjustments needed to correct the product if necessary * Obtain product samples and communicate what will be produced * Perform production material test throughout shift * Perform product reject analysis * Visit manufacturing sites to test machinery and report proposed process improvements * Inspect all finished goods * Know all ASTM standards that apply and ensure all products meet these standards * Maintenance and housekeeping of assigned areas and equipment * Other duties and responsibilities related to the nature of the job may be assigned on a temporary or permanent basis as needed Job Requirements * High school diploma/equivalent or equivalent Vocational Training/Certification, other related experience or combination of education and experience * Familiar with lab equipment * Production experience in a block plant * Knowledge of ASTM standards for manufactured concrete products * Knowledge of parts and basic assembly of molds * Knowledge of concrete product sizes, shapes, and colors * Strong numerical skills * Ability to read and understand equipment manuals and directions * Knowledge of electronics and programmable controllers * Must communicate effectively both verbally and in writing with superiors, colleagues, and individuals inside and outside the company * Computer literate experienced with Microsoft Office software * This position may require a standing position for an extensive amount of time * Ability to lift up to 50 lbs * Flexible work schedule * Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties of the job What CRH Offers You * Highly competitive base pay * Comprehensive medical, dental and disability benefits programs * Group retirement savings program * Health and wellness programs * An inclusive culture that values opportunity for growth, development, and internal promotion About CRH CRH has a long and proud heritage. We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of a large international organization. If you're up for a rewarding challenge, we invite you to take the first step and apply today! Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day. Thank you for your interest! Oldcastle APG, a CRH Company, is an Affirmative Action and Equal Opportunity Employer. EOE/Vet/Disability CRH is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or any other characteristic protected under applicable federal, state, or local law. Date: Oct 7, 2025

QC Weld InspectorLocation: Richmond, VAPay rate: $28-30/hr | Contract-to-HireSchedule: Monday-Friday, 6:00 AM - 4:30 PM Job SummaryWe are seeking a detail-oriented QC Weld Inspector to join a structural steel fabrication team. In this role, you will ensure all welds and fabricated components meet company and industry standards through inspections, documentation, and collaboration with production teams.Key Responsibilities: Perform visual weld inspections to verify compliance with AWS D1.1 structural welding code and project specifications. Use precision measuring instruments (calipers, micrometers, weld gauges, etc.) to confirm weld size, fit-up, alignment, and overall dimensional accuracy. Review and interpret welding symbols, fabrication drawings, and blueprints to ensure correct application in production. Monitor welding processes to verify welders are following approved Welding Procedure Specifications (WPS). Identify and document weld defects, discontinuities, or deviations from required tolerances. Collaborate with welders, fitters, and supervisors to address and correct nonconformities in a timely manner. Verify proper base materials, filler metals, and consumables are used in accordance with job specifications. Maintain accurate records of inspections, test results, and quality control documentation for compliance and traceability. Assist with welder qualification testing and requalification as required. Ensure all inspection activities meet OSHA safety standards and company quality policies. Support continuous improvement by identifying recurring issues and working with production teams on corrective and preventive measures. Qualifications: Previous experience as a QC Inspector or Weld Inspector in a structural steel fabrication environment required. Strong knowledge of AWS D1.1 Structural Steel Welding Code and related standards. CWI (Certified Welding Inspector) certification preferred but not always required. Ability to read and interpret blueprints, welding symbols, and fabrication drawings. Proficiency with weld inspection tools and measuring equipment. Strong attention to detail, accuracy, and problem-solving skills. Ability to communicate effectively with production teams and management. Familiarity with material traceability, shop documentation, and quality management systems. Basic computer skills for documentation and reporting.

About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, nearly 60 health systems have joined Civica, representing over 1,400 hospitals and approximately one-third of all U.S. hospital beds. Civica has also supplied the U.S. Department of Veteran's Affairs, the U.S. Department of Defense and the U.S. Strategic National Stockpile with essential medicines. Civica currently supplies medicines to health system members in 49 states. Civica's mission has expanded beyond the hospital setting to reach consumers directly through CivicaScript, which is dedicated to making quality outpatient generic medicines affordable and available. CivicaScript works with trusted manufacturing partners to develop quality generic medicines and has forged partnerships with like-minded payors, pharmacy benefit managers and pharmacies to enable significant cost savings to be passed along to their customers. Civica's new 140,000 square foot state-of-the-art manufacturing facility in Virginia will soon produce a steady supply of more than three dozen sterile injectables, all drugs that are currently in or near shortage. The plant will also produce affordable biosimilar insulins, ensuring all Americans have access to lower cost, quality insulins, regardless of their insurance status. The Civica Foundation is a 501(c)(3) organization that fosters philanthropic support for Civica's work to manufacture and distribute affordable medications. The Foundation's first commitment is to support Civica's efforts to bring affordable insulin to all Americans. Leaders from nearly every corner of the diabetes ecosystem are partners in this initiative. Civica is leading a movement for patients, not profits. Because eliminating shortages and stabilizing high prices are in the best interest of patients. Join us. Learn more at **************** Job Description: The QC Specialist II Insulin will join the Civica, Inc. organization and its newly forming team at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance. The Petersburg site serves as Civica's new fill-finish facility dedicated to the manufacture and supply of essential generic, insulin, and biosimilar sterile injectable medications. Responsibilities of the position include performing analytical testing on sterile injectable products. Responsibilities also include maintenance of analytical equipment and executing method verification, validations, and transfers. The role is essential to ensure the intended materials are utilized for manufacturing and meet the required standards to ensure the finished product meets the applicable standards of identity, strength, quality, and purity. You will help Civica achieve its mission of delivering quality medicines that are available and affordable to everyone by complying with applicable regulatory standards (e.g., Current Good Manufacturing Practices, and FDA Guidance documents) and expectations for the development and reliable supply of quality medicines. Essential Duties and Responsibilities: This position will focus on the needs of the Insulin project and all activities required to support this product. Perform analytical testing and interpret and document actions and results using proper documentation practices. Participate in analytical method transfers and perform method verifications/validations. Notify management of OOS, OOT or atypical results on the day of discovery with the appropriate level of urgency. Lead and/or participate in laboratory investigations. Ability to complete HPLC analysis with minimal supervision. Experience with Empower software, and diode array and single quad detection experience is a plus. Maintain LIMS data. Contribute to and promote a safety culture by adhering to established safety procedures, engineering controls and appropriate PPE. Maintain a clean and organized work environment in accordance with 6S lean principles. Inform management of continuous improvement and opportunities Lead and/or participate in 6S and OPEX initiatives Ability to work independently or in a team setting effectively. Complete chemical inventory and order supplies as required. Conduct other duties as required by management. Basic Qualifications and Capabilities: Bachelor's degree in a scientific discipline with at least 8+ years' experience working in the pharmaceutical industry. Proficiency with LIMS software, analytical data acquisition software, and Microsoft Office applications, including Excel, Word, and PowerPoint. Ability to multi-task and change priorities in a fast-paced environment. Self-motivated and willingness to learn and help others. Working knowledge of relevant FDA and ICH guidelines and USP requirements. Wet chemistry testing by USP methods, pH, conductivity, atomic absorption, and loss on drying. Proficient in HPLC analyses. Prepare and/or review technical documents such as protocols, reports, SOPs, and testing procedures. Analytical method transfers, method verifications, and validations.

Job DescriptionAt Mercedes-Benz of Richmond, part of the Murgado Automotive Group, we are dedicated to providing top-tier luxury vehicles and an unparalleled customer experience. We are passionate about delivering excellence in everything we do, and we are looking for a dedicated and detail-oriented Quality Control Associate to ensure the highest standards of quality in our service department. Job Overview:As a Quality Control Associate, you will play a vital role in maintaining the reputation of Mercedes-Benz vehicles by inspecting, testing, and verifying that all service work meets the brand's rigorous standards. This role is critical to ensuring customer satisfaction, safety, and the performance of every vehicle serviced at our dealership. If you are meticulous, committed to quality, and have an eye for detail, we want you on our team! Key Responsibilities:Inspect vehicles after service or repair to ensure all work is completed to manufacturer standards.Conduct road tests to evaluate vehicle performance post-repair.Ensure vehicles are clean and properly prepared for customer delivery.Work closely with service technicians and advisors to address any issues or discrepancies found during inspections.Verify that all paperwork, including repair orders, is complete and accurate.Maintain a clean and organized work area, adhering to safety guidelines.Assist in maintaining service department quality by identifying trends and suggesting improvements.Communicate clearly and professionally with service staff and management to ensure smooth operations. Qualifications:High school diploma or equivalent required; technical or automotive training preferred.Previous automotive service experience is highly desirable.Strong attention to detail with the ability to identify issues and inconsistencies.Basic understanding of automotive systems and repairs.Excellent organizational and time management skills.Valid driver's license with a clean driving record.Ability to work in a fast-paced environment and meet deadlines.Strong communication skills and a team-oriented mindset. What We Offer:Competitive pay based on experience.Comprehensive benefits package including medical, dental, and vision insurance.401K retirement plan with company match.Paid time off and holidays.Ongoing training and professional development opportunities.Employee discounts on vehicles, services, and parts.A supportive and positive work environment with opportunities for career advancement. Why Join Mercedes-Benz of Richmond?At Mercedes-Benz of Richmond, we are committed to providing not only luxury vehicles but also an exceptional customer experience. As a Quality Control Associate, you will play a crucial role in ensuring the satisfaction of our customers and the quality of our service department. Join a dealership where attention to detail and dedication to excellence come together. How to Apply:If you're passionate about quality and automotive excellence, we want to hear from you! Apply today by submitting your resume. Murgado Automotive Group is an equal opportunity employer. Murgado Automotive Group does not discriminate in employment on account of race/ethnicity, color, religion, national origin, gender, sexual orientation/transgender status, age disability, martial/parental status, citizenship status, military status, political affiliation and/or beliefs, pregnancy, order of protection status or other non-merit status. We are an employer who participates in the E-verify program with the Department of Homeland and Security. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

The Anti-Money Laundering (AML) Quality Associate is an integral part of the Financial Intelligence Unit (FIU) Investigations Support Team, providing support to FIU teams by performing quality assurance (QA) tasks related to suspicious activity decisions. This role is part of a highly collaborative, mission-oriented team that ensures potentially unusual or suspicious transactions are appropriately identified, documented, and filed with the appropriate authorities. Additionally, the AML Quality Associate will escalate to leadership any suspicious activity investigation that has not been decisioned appropriately within the Bank Secrecy Act (BSA)/AML framework and company policies and procedures. Responsibilities: * Work with FIU Supervisors and Investigators to uphold the high bar of their teams' investigation quality * Assist Investigations team in process improvements, change management and QA * Work with supervisors to escalate potential gaps and deliver suggestions for training and improvement based on data, for both investigation and quality processes * Partner with Quality leadership, supervisors and investigators to develop a deep understanding of investigation process * Review Suspicious Activity Reporting decisions to ensure that decision framework is appropriate and thorough * Assess if supporting documentation from investigations is accurately captured and aligned with Suspicious Activity Reporting decisions * Review Suspicious Activity Reports to ensure that all appropriate fields in the SAR form are filled out correctly, SAR narrative is thorough, and appropriate levels of supporting documentation were obtained and maintained within Actimize * Document activity that is out of compliance with BSA regulatory guidance and/or AML Policies and Procedures * As needed, assist Quality Management with developing reporting and metrics * As needed, assist Quality Management with maintaining AML Quality Policies and Procedures Basic Qualifications: * High School Diploma, GED or equivalent certification * At least 1 year of Microsoft Office or Google Suite experience * At least 2 years of Anti-Money Laundering experience Preferred Qualifications: * Bachelor's Degree or Military experience * 1 year of Quality Assurance experience or 1 year of Quality Control Audit experience * 2 years of Bank Secrecy Act (BSA) investigative experience * Association of Certified Anti-Money Laundering Specialists (ACAMS) certification Are you looking for a challenging role that includes the convenience of working virtually at home? Then a Capital One Anti-Money Laundering Quality Associate role may be the role for you! You must be within 50 miles driving distance from our Capital One hub in Chicago, IL / Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / McLean, VA Work From Home Technology Requirements: * A secure home office environment that is free from background noise and distractions * A reliable private internet connection that is not supplied by use cellular data (hot spot) * Cable or fiber connections are preferred * Internet service download speeds must be at least 5 mbps, with 10+ mbps preferred - check your download speed using a speed test. A sample one can be found here. To test your home internet from your personal computer at home, type ***************** into the web browser of your personal computer. * Sustained ability to maintain latency less than 250 ms in voice calls is required * Hard wired connectivity is preferred, any use of wireless connectivity must be Private (non-public) and password protected through WPA2-PSK (AES) encryption. If you have any questions about your encryption, please consult with your internet provider * A private network is password protected where you have ownership or line of site to every device on the network * Capital One reserves the right to request proof of internet provider, speed and service package from the associate * Requirements are subject to change, as new systems and technology is delivered. Capital One reserves the right to modify internet service requirements with sixty (60) days notice. Work from Home Living Requirements: * Candidates must live within 50 miles driving distance of one of the hub locations based in Chicago, IL / Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / McLean, VA and be comfortable coming in person whenever required with no less than 24 hours notice. At this time, Capital One will not sponsor a new applicant for employment authorization for this position. The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked. Chicago, IL: $72,800 - $83,100 for AML Sr. Investigator I Jericho, NY: $87,400 - $99,700 for AML Sr. Investigator I McLean, VA: $80,100 - $91,400 for AML Sr. Investigator I New Orleans, LA: $72,800 - $83,100 for AML Sr. Investigator I Plano, TX: $72,800 - $83,100 for AML Sr. Investigator I Richmond, VA: $72,800 - $83,100 for AML Sr. Investigator I Wilmington, DE: $72,800 - $83,100 for AML Sr. Investigator I Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate's offer letter. This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan. Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level. This role is expected to accept applications for a minimum of 5 business days. No agencies please. Capital One is an equal opportunity employer (EOE, including disability/vet) committed to non-discrimination in compliance with applicable federal, state, and local laws. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City's Fair Chance Act; Philadelphia's Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at ************** or via email at RecruitingAccommodation@capitalone.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations. For technical support or questions about Capital One's recruiting process, please send an email to ********************** Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site. Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).

Are you passionate about ensuring quality and precision? Do you thrive in an environment where attention to detail is of utmost importance? If so, then our Full-Time Quality Control Inspector position at Kinsley Steel, Inc. is the perfect opportunity for you. As a Quality Control Inspector, you will play a vital role in maintaining the highest standards of quality for our products. You will be responsible for thoroughly inspecting materials, components, and finished products to ensure compliance with specifications and industry standards. Your meticulous eye for detail will help us deliver products that meet and exceed customer expectations. Additionally, you will have the opportunity to collaborate with cross-functional teams, identify process improvements, and contribute to a culture of continuous improvement. This is an on-site position, allowing you to be hands-on with our products and processes. You will have benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Competitive Salary, and Paid Time Off. To recognize and reward your expertise and commitment to quality. Join our team today and be a part of our commitment to excellence in everything we do. ABOUT Kinsley Steel, Inc. Since 1985, Kinsley Steel has been delivering unmatched quality steel on time and on budget. Our certified and highly-skilled teams specialize in structural steel design, engineering, detailing, fabrication, erection and retrofit to existing structural members. RESPONSIBILITIES as a Quality Control Inspector As a Quality Control Inspector at Kinsley Steel, Inc., you will have the opportunity to perform daily inspections of fabricated steel in our AISC certified facility. Your expertise in fabricating Structural Steel (D1.1/D1.5) will be crucial as you address and document any non-conformances that may arise during the inspection process. Your attention to detail will also be put to use as you inspect fabricated material to ensure it meets the specifications outlined in the shop drawings. In addition to these responsibilities, you will play a key role in both in-process and final inspections, ensuring the dimensional layout and placement of parts meet our rigorous standards. You will have the chance to showcase your commitment to quality as you participate in our annual AISC QC Audits and develop goals to improve and promote quality throughout the organization. Your ability to work well with production to solve any issues that arise will be crucial in maintaining our high standards. Requirements & QUALIFICATIONS To be successful as a Quality Control Inspector at Kinsley Steel, Inc., you will need to possess a range of skills and qualifications. A minimum of 3-5 years of experience in laying out and fabricating steel is required for this position. Your ability to accurately read and interpret fabrication and construction drawings will be essential in ensuring the quality of our products. While not mandatory, a Welding Certification in D1.1 and/or D1.5 is preferred. Equal Opportunity Employer: All qualified applicants are encouraged to apply. Kinsley Steel, Inc. is a Drug Free Workplace where post-offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies. Kinsley Steel, Inc. is a participant in the Federal E-Verify Program.

Job DescriptionOverview:Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan. Job Summary: Inspects electronic systems, assemblies, subassemblies, components and parts for conformance to specifications. Job Duties: Performs visual inspection of electronic card and sub-assemblies, and systems or units to ensure that all product meets the established specifications for reliability and workmanship. Utilizes gages, templates, microscopes and other manufacturing aids to ensure that all product meets the established specifications for reliability and workmanship. Ensures that all required process operations have been performed on the product that is being inspected. Enters all quality data into the appropriate electronic or manual systems. Notifies the appropriate personnel if unusual product defects are identified or if process falls below acceptable levels. Provides timely feedback to manufacturing if non-conforming product is identified. Accurately completes all administrative activities associated with quality inspection. Performs process audits and assists manufacturing with the interpretation of the quality and workmanship standards. Assists with the disposition of all non-conforming materials/product Qualifications: Ability to read electrical schematics Experience with measurement tools, calipers, and good computer skills (Microsoft Office) Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information. #pro1

City : Morristown State : Indiana (US-IN) Country : United States (US) Requisition Number : 41720 A Day in the Life: This internship role will be focused on Quality & Food Safety.If you have a career interest in food science and quality assurance and the desire to gain hands on experience in a manufacturing facility, you should become our next Quality & Food Safety Intern. This position will offer students the opportunity to build upon the knowledge acquired in the classroom to a food business and manufacturing environment. The Bunge Quality and Food Safety internship program is designed to offer students the opportunity to learn and work with Bunge business units to provide solutions to internal and external stakeholders. Interns will have the opportunity to impact several quality and food safety initiatives and gain exposure to a wide array of QFS programs, including but not limited to, HACCP & Food Safety Plans, laboratory & instrumentation programs, equipment performance & maintenance, food manufacturing & prerequisite programs, product inspection and disposition, and additional project work in related areas. Location to be determined based on current business needs. Ability and willingness to relocate for the duration of the internship is required. Positions Details: Summer Work Term - Approximately 12 weeks What You'll Be Doing: A project with the Quality & Food Safety organization will include one or multiple of the following activities, depending on the business unit and manufacturing location: * Validation of microbial sampling/testing techniques and procedures * Thermal inactivation validation studies * Development and review of laboratory and sampling Standard Operating Procedures * Customer complaint reduction initiatives and use of Root Cause Analysis and Corrective & Preventive Action techniques * Analysis of changes to processing conditions (temperatures, pressures, pump speeds, etc.) on finished product characteristics * Training of the Operations and Mechanics on the impact to finished product quality and optimization of production parameters * Validation of analytical methods used for measurement of oils and corn milling streams * Participation in internal audits and updates to Food Safety Plans * Engagement with Bunge's Quality & Food Safety Management System Qualifications: * Currently enrolled in a Bachelor's or Master's degree in Food Science, Biology/Microbiology, Chemistry/Biochemistry, Chemical Engineering, or applicable field with an interest in Quality & Food Safety as a career * Strong computer skills and knowledge of Microsoft applications (Word, Excel, PowerPoint) * Ability to analyze data to summarize and present in clear and concise reports * Ability to execute tasks and follow-through to completion with appropriate documentation * Strong attention to detail, problem solving, prioritization and organizational skills * Ability to work in a team environment and possess strong interpersonal communication skills * Effective verbal and written communication skills Our 12 weeks long Bunge Summer Internship program provides: * A developmental experience through structured learning goals, combining soft skills training, hands-on projects, and Bunge knowledge. * Comprehensive understanding of our business through assignments with specific goals and deliverables. * Networking opportunities with our leaders through Lunch and Learn Series. At Bunge, people don't just come here to work, they come here to grow - solving challenges that directly impact the world with a diverse and talented team working to make us the most innovative and dynamic company in our industry. Bunge offers a strong compensation and benefits package and most importantly, in all we do we live our values: * We Are One Team by fostering collaboration, respect, and inclusion * We Lead the Way by being agile, empowered, and innovative * We Do What's Right by acting safely, sustainably, and with integrity At Bunge (NYSE: BG), our purpose is to connect farmers to consumers to deliver essential food, feed and fuel to the world. As a premier agribusiness solutions provider, our team of ~37,000 dedicated employees partner with farmers across the globe to move agricultural commodities from where they're grown to where they're needed-in faster, smarter, and more efficient ways. We are a world leader in grain origination, storage, distribution, oilseed processing and refining, offering a broad portfolio of plant-based oils, fats, and proteins. We work alongside our customers at both ends of the value chain to deliver quality products and develop tailored, innovative solutions that address evolving consumer needs. With 200+ years of experience and presence in over 50 countries, we are committed to strengthening global food security, advancing sustainability, and helping communities prosper where we operate. Bunge has its registered office in Geneva, Switzerland and its corporate headquarters in St. Louis, Missouri. Learn more at Bunge.com. Every day our people exemplify these values, which represent Bunge at its core: * We Are One Team - Collaborative, Respectful, Inclusive * We Lead The Way - Agile, Empowered, Innovative * We Do What's Right - Safety, Sustainability, With Integrity If this sounds like you, join us! We value and invest in people who believe in our purpose and are excited to live it every day - people who are #ProudtoBeBunge Nearest Major Market: Richmond Job Segment: Chemical Research, Agronomy, Biochemistry, Agricultural, Microbiology, Engineering, Agriculture, Science

ITAC serves Process & Industrial clients with integrated engineering and construction services for complex capital projects. We also offer specialty services including power systems services and products, custom machine fabrication, and fall protection services and equipment. Founded in 1988 on a dream and a $5K loan, ITAC is a true success story. From humble beginnings to an ENR-Ranked Top Design Firm with a nationwide footprint and over 500 employees operating from 6 offices in Virginia, North Carolina and South Carolina, we provide Fortune 500 companies with innovative design-build solutions. We specialize in power generation & utilities, chemicals, food & beverage, forest products, advanced manufacturing, and minerals & metals. ITAC's purpose is to make life better. For our employees, this means providing them with the resources and flexibility they need to have both a rewarding career and a fulfilling family life. ITAC is 100% employee-owned. Through our Employee Stock Ownership Plan (ESOP) and Direct Stock Ownership, every team member has the unique opportunity to be an owner who shares in the company's growth and earnings. We offer our team a comprehensive benefits package and numerous employee incentives. Rooted in love, we serve and care for our employees like family. We hire passionate and motivated people with an innovative mindset and the desire to grow. If the thought of challenging, fast-paced projects excites you, then you've come to the right place. At ITAC, you'll be part of a collaborative team that works hard to make life better. For more information, visit itac.us.com. Responsibilities: On-Site Quality Installation Oversight: Monitor and inspect all electrical work on-site, including conduit and cable installations, MV/LV switchgear, panels, lighting, lighting controls, and grounding systems. Ensure all works align with project specifications, electrical codes (NEC), and client requirements. Conduct daily walkdowns and quality checks during active construction phases. Conduct in-process inspections during critical milestones (slab pours, wall closures, panel energization, etc.). Testing & Commissioning: Supervise and document pre-commissioning and final testing of electrical systems (IR, continuity, phase sequence, loop checks, VLF, ground resistance, etc.). Witness and document pre-commissioning and commissioning activities in coordination with testing vendors and commissioning agents. Ensure all test equipment is calibrated, and procedures are followed precisely. Documentation & Reporting: Maintain up-to-date site daily inspection QA/QC logs, test records, inspection reports, NCRs, and punch lists. Maintain and track submittal and RFI log Verify that as-built drawings and redline markups reflect field conditions accurately. Issue Resolution & Coordination Identify workmanship issues, non-conformances, or code violations on-site and drive resolution through corrective actions. Interface with project engineers, electrical foremen, subcontractors, and the client's QA/QC representatives to ensure quality expectations are met. Participate in daily toolbox talks, safety walks, and progress meetings, acting as the quality voice on site. Team Collaboration & Compliance: Work closely with site engineers, foremen, and subcontractors to resolve quality issues. Report to the QA/QC Manager and attend site coordination and progress meetings. Ensure adherence to site safety standards, permitting requirements, and company policies. Requirements High school diploma or GED required, field personnel encouraged to apply Journeyman/Master's License Minimum [2] years of hands-on QA/QC experience in commercial or industrial electrical construction. (A plus) Strong working knowledge of national electrical codes (NEC), testing methods, and installation best practices. Comfortable working full-time on-site in active construction zones. Familiarity with QA documentation, Microsoft Office, and tools like Procore or BIM 360 is a plus. OSHA 30, NFPA 70E, or other safety certifications are highly desirable. Ability to work independently and as part of a team. Benefits Salary: $40 - $45 hourly Benefits: From internships to seasoned professionals, our growing company provides career opportunities for all levels of experience. We offer our team a comprehensive benefits package and numerous employee incentives. For life's challenges, we also provide our employees and their immediate families with certified chaplains for around-the-clock encouragement and support. Rooted in love, we serve and care for our employees like family. ITAC provides benefits such as Health, Vision, and Dental Insurance 401k & ESOP Life Insurance Short & Long-Term Disability Sick Time Off Paid Time Off Paid Holidays Employee Assistance Program Tuition Reimbursement Professional Development Wellness Program Mentorship Program - Note: this may not be applicable to onsite roles Safety Incentive Program 24/7 Chaplain Care

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: Perform QC Biochemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished biological products (monoclonal antibodies) under FDA/EU regulations, applicable International Regulations, and BeOne Medicines' processes and procedures. Essential Functions of the job: * Perform routine and non-routine testing using capillary electrophoresis techniques (e.g., CE-SDS, CZE, ic IEF) in the QC biochemistry laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of manufacturing operations. * Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. * Lead troubleshooting efforts for analytical methods and instrumentation related to CE. * Conduct laboratory investigations, including OOS, Out of Trend, deviations, and invalid assays. * Implement corrective actions and preventive actions (CAPAs). * Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. * Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc. * Maintain equipment in a qualified and calibrated state, coordinating with metrology or vendors as needed. * Manage inventory of reagents and supplies for the laboratory. * Participate in internal and external GMP audits, as needed. * Train other junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis. * Serving as subject matter expert in one or more areas of required testing. * Undertake other duties as required. Core Competencies, Knowledge, and Skill Requirements * Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline. * Minimum of 5-7 years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required. * Working knowledge and experience with biochemistry analytical methods such as residual DNA by qPCR, host cell protein ELISA, Residual Protein A ELISA, binding activity ELISA, Capillary Electrophoresis (CE), capillary isoelectric focusing (cIEF), etc. * Familiar with Waters Empower Chromatography Data System. * Working knowledge with USP/EP and cGMP/EU GMP regulations. * Familiar with instrument and equipment validation. * Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. * Strong leadership/team management skills and experience. * Credible and confident communicator (written and verbal) at all levels. * Strong analytical and problem-solving ability. * Hands-on approach, with a 'can do' attitude. * Ability to prioritize, demonstrating good time management skills. * Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. * Self-motivated, with the ability to work proactively using own initiative. * Committed to learning and development. Significant Contacts * Interacts with all levels of BeOne employees. Supervisory Responsibilities: * N/A Computer Skills: * Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint). Travel: * Must be willing to travel approximately 10%. * Ability to work on a computer for extended periods of time. Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. * Fosters Teamwork * Provides and Solicits Honest and Actionable Feedback * Self-Awareness * Acts Inclusively * Demonstrates Initiative * Entrepreneurial Mindset * Continuous Learning * Embraces Change * Results-Oriented * Analytical Thinking/Data Analysis * Financial Excellence * Communicates with Clarity Salary Range: $89,100.00 - $124,100.00 annually BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.

Title: Temp QC Lab Tech I Shift: 1st shift, 9am-5:30pm Pay: $21/hour Overview: In the Temp QC Lab Tech position your responsibilities will be to perform tests on materials and products to ensure they meet quality standards and regulatory requirements. Minimum Qualifications: Acknowledge and process all quality documentation regarding production. Minimize errors through document proofing/review. Label and retain production material to provide traceability. Coordinate with leadership to ensure product meets specifications. Performs standardized quality control tests. Make effective material additions that ensure product design. Approve completed batches against prescribed specifications. Support calibration and equipment verification systems. Maintain quality control records in accordance with ISO standards. Maintain lab and equipment with high standards in a clean working environment. Actively support quality investigations, problem solving. Independently adjust products, fix/use Work-off. Support other technicians through coaching, training, and troubleshooting. Directs and coordinates all quality control department staff. Schedules and assigns work based on priorities of group leader or supervisor. Required Skills: High School Diploma or GED (Mandatory) Approve completed batches against prescribed specifications. Physical Requirements: Standing and walking. Drug screen, background check, Education and Employment verification are mandatory if you are offered this position.

Are you passionate about ensuring quality and precision? Do you thrive in an environment where attention to detail is of utmost importance? If so, then our Full-Time Quality Control Inspector position at Kinsley Steel, Inc. is the perfect opportunity for you. As a Quality Control Inspector, you will play a vital role in maintaining the highest standards of quality for our products. You will be responsible for thoroughly inspecting materials, components, and finished products to ensure compliance with specifications and industry standards. Your meticulous eye for detail will help us deliver products that meet and exceed customer expectations. Additionally, you will have the opportunity to collaborate with cross-functional teams, identify process improvements, and contribute to a culture of continuous improvement. This is an on-site position, allowing you to be hands-on with our products and processes. You will have benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Competitive Salary, and Paid Time Off. To recognize and reward your expertise and commitment to quality. Join our team today and be a part of our commitment to excellence in everything we do. ABOUT Kinsley Steel, Inc. Since 1985, Kinsley Steel has been delivering unmatched quality steel on time and on budget. Our certified and highly-skilled teams specialize in structural steel design, engineering, detailing, fabrication, erection and retrofit to existing structural members. RESPONSIBILITIES as a Quality Control Inspector As a Quality Control Inspector at Kinsley Steel, Inc., you will have the opportunity to perform daily inspections of fabricated steel in our AISC certified facility. Your expertise in fabricating Structural Steel (D1.1/D1.5) will be crucial as you address and document any non-conformances that may arise during the inspection process. Your attention to detail will also be put to use as you inspect fabricated material to ensure it meets the specifications outlined in the shop drawings. In addition to these responsibilities, you will play a key role in both in-process and final inspections, ensuring the dimensional layout and placement of parts meet our rigorous standards. You will have the chance to showcase your commitment to quality as you participate in our annual AISC QC Audits and develop goals to improve and promote quality throughout the organization. Your ability to work well with production to solve any issues that arise will be crucial in maintaining our high standards. Requirements & QUALIFICATIONS To be successful as a Quality Control Inspector at Kinsley Steel, Inc., you will need to possess a range of skills and qualifications. A minimum of 3-5 years of experience in laying out and fabricating steel is required for this position. Your ability to accurately read and interpret fabrication and construction drawings will be essential in ensuring the quality of our products. While not mandatory, a Welding Certification in D1.1 and/or D1.5 is preferred. Equal Opportunity Employer: All qualified applicants are encouraged to apply. Kinsley Steel, Inc. is a Drug Free Workplace where post-offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies. Kinsley Steel, Inc. is a participant in the Federal E-Verify Program.

About Civica Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. Today, more than 55 health systems have joined Civica. They represent over 1,500 hospitals and one-third of all U.S. hospital beds. Civica has also begun to supply the U.S. Department of Veteran's Affairs, the U.S. Department of Defense and the U.S. Strategic National Stockpile of essential medicines. Civica recently announced plans to expand its mission, via a unit called CivicaScript, to into the outpatient pharmacy space and to manufacture and distribute insulins that, once approved, will be available to people with diabetes at significantly lower prices than insulins currently on the market. The availability of Civica's affordable insulins, beginning in 2024, will benefit people with diabetes who have been forced to choose between life sustaining medicines and living expenses, particularly those uninsured or underinsured who often pay the most out of pocket for their medications. Civica's mission is to ensure that quality generic medications are accessible and affordable to everyone. Since established, the #1 Policy for the Civica team has been “Do What Is in the Best Interest of Patients.” Civica's manufacturing facility in Petersburg, Virginia, is the future home of affordable insulin and essential sterile injectable medicines. The facility is currently in late-stage construction and hiring for the site is well-underway. To find out more about how Civica's innovative model is directly impacting patient care, click here to read a summary from the New England Journal of Medicine. (******************************************************* To learn more about Civica's plans to bring affordable insulin to Americans living with diabetes, click here to read an article in BioSpace. (************************************************************************************************* Job Description: The Quality Systems Associate will join the Civica, Inc. (“Civica”) organization and its team at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance. The Petersburg site serves as Civica's fill finish facility dedicated to the manufacture and supply of essential generic sterile injectable medications. The role supports aspects of quality to ensure compliance with applicable regulatory standards (e.g., Current Good Manufacturing Practices, Good Distribution Practices), internal standards, and expectations for the development and reliable supply of quality medicines. Responsibilities include supporting activities related to change control, investigations and CAPA, complaints, Quality Risk Management, inspection readiness, metrics and other quality systems activities as needed. Essential Duties and Responsibilities: Work cross functionally to participate in the implementation and maintenance of the site's quality system framework including quality systems and processes necessary to enable the development and reliable supply of Civica generic medications to patients. Support, track, and trend quality processes and systems across the product lifecycle including, but not limited to, change control, CAPA, deviations and investigations, product quality complaints, Annual Product Quality Review (APQR), and management notification. Support cGMP compliance and inspection readiness within the organization. Participate in internal self-assessment audits. Participate in root cause analysis investigations as either investigator or Quality Assurance. Proactively identify and work collaboratively to resolve problems taking risk-based and compliant approaches to solutions. Working across functions to ensure compliant document control and training programs. Contribute to Quality Risk Management and Data Governance Processes as needed. Participate in activities to support regulatory agency inspections. Support site objectives with a minimal amount of supervision. Includes simple project management that may involve other functional areas. Promote a quality mindset and quality excellence approach to all activities. Maintain written procedures for personnel qualification and training and support the delivery of compliance training sessions. Basic Qualifications and Capabilities: 4+ years' experience working directly with manufacturing in the pharmaceutical or medical device industries. Appropriate combinations of experience and bachelor-level or higher education. Participating in activities that support regulatory agency inspections is required. Excellent interpersonal and written communication skills and experience using various software/electronic applications required. Self-motivated, flexible, and able to work in a small, fast-paced, dynamic, environment. Project management, organization, and execution skills are desired. Ability to apply technical expertise to solve problems and issues. Ability to work autonomously and within established guidelines, procedures, and practices. Committed to delivering high-quality results, working with others to overcome challenges, and focusing on what matters. Continuously looking for opportunities to learn, build skills, and share knowledge with others. Physical Demands and Work Environment: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate.

Overview:Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan. Job Summary: Inspects electronic systems, assemblies, subassemblies, components and parts for conformance to specifications. Job Duties: Performs visual inspection of electronic card and sub-assemblies, and systems or units to ensure that all product meets the established specifications for reliability and workmanship. Utilizes gages, templates, microscopes and other manufacturing aids to ensure that all product meets the established specifications for reliability and workmanship. Ensures that all required process operations have been performed on the product that is being inspected. Enters all quality data into the appropriate electronic or manual systems. Notifies the appropriate personnel if unusual product defects are identified or if process falls below acceptable levels. Provides timely feedback to manufacturing if non-conforming product is identified. Accurately completes all administrative activities associated with quality inspection. Performs process audits and assists manufacturing with the interpretation of the quality and workmanship standards. Assists with the disposition of all non-conforming materials/product Qualifications: Ability to read electrical schematics Experience with measurement tools, calipers, and good computer skills (Microsoft Office) Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information. #pro1

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: Perform QC Biochemistry laboratory activities to support GMP manufacturing, testing and release of material, intermediates and finished biological products (monoclonal antibodies) under FDA/EU regulations, applicable International Regulations, BeiGene processes and procedures. Essential Functions of the job: * Perform QC biochemistry laboratory testing (e.g., DS, DP release and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations. * Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, testing record keeping, etc. * Manage inventory of reagents and supplies for the laboratory. * Conduct laboratory investigations, including OOS, Out of Trend, deviations, and invalid assays. * Implement corrective actions and preventive actions (CAPAs). * Participate in internal and external GMP audits, as needed. * Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. * Train other junior level analysts and new hires. * Subject matter expert in one or more areas of required testing. * Undertake any other duties as required. Core Competencies, Knowledge, and Skill Requirements: * Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline. * Minimum of 2 years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required. * 5+ years of related experience preferred with no higher education * Working knowledge and experience with biochemistry analytical methods such as residual DNA by qPCR, host cell protein ELISA, Residual Protein A ELISA, binding activity ELISA, Capillary Electrophoresis (CE), capillary isoelectric focusing (cIEF), etc. * Expertise in sterile cell culture and aseptic techniques with advanced troubleshooting skills are required. * Deep understanding and practical experience with various potency assay technologies including cell-based reporter gene assay and immune binding assays. * Working knowledge with USP/EP and cGMP/EU GMP regulations. * Familiar with instrument and equipment validation. * Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. * Strong leadership/team management skills and experience. * Credible and confident communicator (written and verbal) at all levels. * Strong analytical and problem-solving ability. * Hands-on approach, with a 'can do' attitude. * Ability to prioritize, demonstrating good time management skills. * Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. * Self-motivated, with the ability to work proactively using own initiative. * Committed to learning and development. Education Required: Bachelor's Degree required in Chemistry, Biochemistry, or Biotechnology related scientific discipline and 5+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required. Master's degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline and 2+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are preferred. Computer Skills: * Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint). * Ability to work on a computer for extended periods of time. Other Qualifications: Interacts with all levels of BeOne employees Travel: * Must be willing to travel approximately 10%. Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. * Fosters Teamwork * Provides and Solicits Honest and Actionable Feedback * Self-Awareness * Acts Inclusively * Demonstrates Initiative * Entrepreneurial Mindset * Continuous Learning * Embraces Change * Results-Oriented * Analytical Thinking/Data Analysis * Financial Excellence * Communicates with Clarity Salary Range: $89,100.00 - $124,100.00 annually BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.