Quality control analyst jobs in Tuckahoe, VA

This individual will perform bench tests in a chemical lab to support ATF, Gear, Off-Road, and MTF formulators. They would work relatively autonomous after the training period on a team of 8-10 other Technicians. Responsibilities: Accurately weighing chemical components and blending fluids associated with ATF, GEAR, OFF-ROAD and MTF chemistries. Conducting and scheduling Analytical/Bench Testing. Maintaining Critical Lab Equipment. Adhering to corporate safety and ISO 9001 guidelines. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Bachelor's degree in a science-related field. At least one year of lab experience. It is preferred that they have someone who will be around for two years. If this individual's goal is to go back to graduate school, they would invest in training someone and lose that investment.

Job DescriptionIndustrial Cybersecurity Consultant (Virginia) Type: Full-time W2 | Duration: 1-year contract (likely multi-year) Travel: Daily to multiple sites across Virginia | Work Authorization: U.S. only Third-Party Firms: Not accepted Role OverviewWe're seeking a mid-level Industrial Cybersecurity Consultant (3+ years) to support patching, controls, and cybersecurity work across power generation and industrial facilities in Virginia. This is a hands-on, onsite-heavy role with regular travel. When not at client sites, you'll work remotely on documentation and compliance tasks.What You'll Do Validate and remediate patch levels, firmware, and control system configurations. Perform hands-on updates to OT/ICS equipment and verify vendor work. Support vulnerability assessments, system hardening, and NIST-aligned security. Follow structured checklists and collaborate with senior engineers. Document work performed and produce clear validation reports. What We're Looking For 3+ years real-world experience in IT/OT cybersecurity (internships don't count). Strong knowledge of firewalls, access control, patching, and logging. Familiarity with industrial control systems (utilities or similar). Ability to work safely in industrial settings and follow strict processes. Excellent communication and attention to detail. Preferred: Allen Bradley PLC experience, Siemens systems, Modbus familiarity, CISA certification.Travel Daily travel to sites across Virginia (mostly within 2.5 hours of Richmond). Occasional overnight stays; mileage reimbursed; hotels provided for long drives. Additional Info Must pass background + MVR and client BI clearance (up to 6 weeks). No per diem or relocation; must be local to Virginia. Must have car and mileage reimbursement is provided. Ideal for candidates finishing a current assignment.

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

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.

At 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.

Job Description The Quality Control Technician inspects work performed by client employees, internal employees, or client subcontractors. Work is inspected for process and specification compliance against company/client guidelines. (This purpose is meant to be a guide. Duties may vary dependent upon client.) Essential Position Functions: Inspect assigned work locations for compliance with client or company specifications and guidelines. Inspections may include but are not limited to work safety, installation, and troubleshooting compliance. Use appropriate testing equipment based upon client specifications. Assist in preparing and developing inspection instructions and procedures. Develop and create project specific checklists and standards. Record and document inspection results and findings in applicable data sheets and forms. Complete and submit inspection documentation to the appropriate supervisory personnel. Ensure completion of inspections in a timely manner and track/report activities and metrics. Drive safely to work sites and comply with all company/client safety standards. Follow company/client standards by using related technical documentation. Deliver feedback and supplemental training to employees/contractors as required. Other duties assigned. Education and/or Experience: High School diploma or GED preferred. 2 or more years of relevant inspection experience from the telecommunications, construction, or utilities industries. Equivalent, applicable experience in lower level role may be substituted. Must be proficient with a Windows and Android operating systems (proficiency with a tablet is preferred). Must be proficient with Microsoft office applications (emphasis on Excel). Must be able to read blueprints and other technical documentation. Must be able to operate testing equipment relevant to the inspections such as an OTDR. Experience with a major MSO or Telecom Operator is preferred. Strong analytical and problem-solving ability required. Ability to prioritize and complete assignments accurately and in a timely manner. Able to effectively handle multiple priorities with a strong attention to detail in a fast-paced environment. Strong interpersonal, organizational, oral and written communications skills. Must be able to work alone, and with a team. Must be able to pass a drug screen and criminal background check. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential duties of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent walking, standing, sitting within the work area. Lifting of up to 50 pounds less than one-third of the time. Ability to sit/stand/walk for extended periods of time. Ability to effectively communicate with employees, management, peers, et al. Ability to work in extreme hot/cold environments for lengthy periods of time. Work Environment: The work environment characteristics described here are representative of those of a standard office environment. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Travel up to 100% required. Ability to work in all temperatures, climates and weather conditions. The work environment is that of being in the field. The position requires working independently, as well as part of a team. This position requires verbal and face-to-face contact with others daily. Frequent use of a computer is necessary. This position requires use of all general office equipment. Powered by JazzHR IMKYuUqsez

Job Description 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 4+ 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 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.

JobID: 8801 JobSchedule: Full time JobShift: Day : As a 100% employee-owned contractor, when you work at Sundt, you're not just hiring on at a company, you're joining a culture. Because everyone at Sundt is part owner, you'll join a team of people who are deeply invested in their work. From apprentices to managers, we're passionate about the details and deliberate in everything we do. At Sundt we focus on building long-term prosperity for our clients, communities and employee-owners. We offer competitive pay, industry-leading benefits including a 401k and employee stock ownership plan, incentive programs for craft and administrative employees as well as training that focuses on your personal and professional growth. We're driven by skill, grit and purpose. Join us as we strive to be the most skilled builder in America Job Summary Basic Job FunctionsPosition is required to assist in the inspection, acceptance, and/or rejection of work performed in a particular discipline in compliance with applicable codes and/or specifications as dictated by quality programs and/or contract documents and specifications.Structural Inspection:Experience level must fall within the erection of structural steel. Must be able to work in elevated areas. Must have knowledge of AISC, AWS D1.1, and AWS D1.6 Codes. Must have knowledge of bolt?up inspection including bolt lot verifications using Skidmore?Wilhelm. Additionally, must have knowledge of architectural, insulation and lagging, grout and concrete placement, Epoxy anchor installation inspection. Must have CWI (Certified Welding Inspector) certification.Electrical and Instrumentation Inspection:Experience must fall in the installation of electrical and instrumentation components, including interconnecting wiring, cables, and tubing. Must be knowledgeable of ICEA, IEEE, ISA, NEC, NEMA, NESC, and NFPA Codes and standards.Mechanical Inspection:Experience level must fall in the setting and alignment of static and rotating equipment, equipment skids, coolers, tanks, and interconnecting process piping fabrication and installation. Must be able to use measuring tools such as micrometers, calipers, transits, etc. and be able to set up dial indicators and laser alignment devices.Piping Inspection:Experience level must fall in pipe installation inspection, including welding, supports, instrumentation, etc. Must have CWI (Certified Welding Inspector) certification. Key Responsibilities 1. Assists material handling personnel with required material storage and PM requirements as needed. 2. Communicates with others regarding inspections results and recommends corrective procedures. 3. Participates in activities to support the company's strategic planning efforts. 4. Participates in the preparation of Quality control ITP. 5. Performs control measuring and tests equipment. 6. Verifies the installation of the systems, components and equipment in accordance with the assigned discipline. Minimum Job Requirements 1. 1+ year construction practices 2. 1+ year in quality control inspection discipline 3. HS Degree Required 4. Proficient use of all Microsoft Office Suite programs Note: Job Description is subject to change at any time and may include other duties as assigned. Physical Requirements 1. Ability to wear personal protective equipment is required (including but not limited to; steel toed shoes, gloves, safety glasses, hearing protection, hardhat, vest, etc.) 2. May reach above shoulder heights and below the waist on a frequent basis 3. May stoop, kneel, or bend, on an occasional basis 4. May use telephone, computer system, email, or other electronic devices on a limited basis to communicate with internal and external customers or vendors 5. Must be able to comply with all safety standards and procedures 6. Occasionally will climb stairs, ladders, etc. 7. Required to use hands to grasp, lift, handle, carry or feel objects on a frequent basis 8. Will interact with people frequently during a shift/work day 9. Will lift, push or pull objects on an occasional basis 10. Will sit, stand or walk short distances for up to the entire duration of a shift/work day. Safety Level Safety-Sensitive Note: Jobs with the Safety-Sensitive designation are those that include tasks or duties that the employer reasonably believes could affect the safety and health of the employee performing the task or others such as operating a vehicle, operating equipment, operating machinery or power tools, repairing/maintaining the operation of any vehicle/equipment, the handling/disposal/transport of hazardous materials, or the handling/treatment/disposal of potentially flammable/combustible materials. Equal Opportunity Employer Statement: Sundt is committed to the equal treatment of all employees, and/or applicants for employment, and prohibits discrimination based on race, religion, sex (including pregnancy), sexual orientation, gender identity, color, age, disability, national origin, covered veteran status, genetic information; or any other classification protected by applicable Federal, state, or local laws. Benefit list: Market Competitive Salary (paid weekly) Bonus Eligibility based on company, group, and individual performance Employee Stock Ownership Plan & 401K Industry Leading Health Coverage Starting Your First Day Flexible Time Off (FTO) Medical, Health Savings, and Wellness credits Flexible Spending Accounts Employee Assistance Program Workplace Wellness Programs Mental Health Program Life and Disability Insurance Employee-Owner Perks Educational Assistance Sundt Foundation - Charitable Employee-Owner's program #LI-KW1

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.

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 DescriptionDescription: As a Quality Control (QC) Techniacian, you will be responsible for testing or inspecting all of our products after production or in association with customer items returned for repair. You will execute Factory Acceptance Tests and other tests or inspections as required to ensure that our customers only receive defect-free products. In addition, in support of special projects you may also be expected to help assemble passthrough items as part of the final test sequence. You will use electronics equipment such as oscilloscopes, spectrum analyzers, multimeters, and others during testing. You will be expected to operate a variety of software tools to access test plans and document test results and defects. You will need to be familiar with testing electronic products, be able to read circuit diagrams, follow detailed test steps, and troubleshoot faults or defects. You will test system functionality on developed platforms that support a variety of RF or cellular survey and signals analysis applications. Essential Job Functions: Inspect, test and certify all manufactured equipment and accessories shipping to customers. Assemble, Dress and Pack passthrough items to assure no out of box failures for the customer. Execute Factory Acceptance Test plans and procedures with repeatable precision. Document test results in formal test reports and present findings to management weekly. Document and track all identified defects and present findings to company leadership. Requirements: Basic Qualifications: Candidate should have knowledge of electronics and electronics repair with experience and aptitude to mechanical assembly Candidate must have the ability follow both detailed and summarized Test Plans. Candidate must have 2 to 5 years of experience as a QA Technician, Electronics Technician or Mechanical Assembler or equivalent Military Experience. Extremely Strong attention to detail. Solid written and verbal communication skills. Preference will be given to candidates that can demonstrate basic soldering skills and/or have current IPC J-STD-001, IPC/WHMA-A-620 and IPC-A-610 certifications. Preference will be given to those with experience trouble shooting systems to board level circuit or component level root cause. The candidate must be able to obtain a clearance when sponsored by QRC EDUCATION/CERTIFICATIONS High School Diploma or Equivalent is required. Electronic Training Certificate, and Military Electronics Training or applicable AA degree is preferred. ABOUT QRC QRC LLC (QRC), a Parsons Company, specializes in development and manufacture of RF Test and Measurement products. QRC develops and produces survey tools for cellular communication systems, phone-based measurement, stimulation tools, forensic tools, and integrated RF recording and playback equipment. QRC was founded in 1987 and has been serving as a systems integrator since its inception, and in the last decade has expanded with a portfolio of RF Test and Measurement products. The company has over 50 employees in multiple locations, including the world headquarters located in Fredericksburg, VA. QRC Technologies is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status.

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.

Description Job Description: Is Kymanox the right fit for you? You want to make a difference and have an impact… You enjoy having an influence in your day-to-day work… You are motivated by working alongside a team filled with subject matter experts who will help you learn and grow… You wake up every day and do what you do … because patients deserve better. If this sounds like you, you've come to the right place. We are looking for a meticulous (Contract) QC Inspector to support one of our projects for 1 year based in Petersburg, VA. Responsibilities: Verify engineering drawings and inspection plans against manufacturing facility inventory, maintain inventory control, and ensure compliance using NIST measuring devices Follow written procedures for testing and legibly and accurately document all test data. Maintaining compliance to appropriate US FDA regulations and ISO 13485 Quality Management System standards by following written procedures. Lead and manage the inspection process (incoming, in-process and final) for medical devices, including developing and maintaining inspection procedures, and ensuring compliance with regulatory and company requirements. Review and approve inspection results and related documentation, including NCRs and corrective actions. Performing investigations for: NCR's, Preventive and Corrective Actions, Deviations and Complaints Reviewing Device History Records (DHR) and providing test/inspection support to all new process developments. Reviewing lab results and approve product release. Maintain accurate and up-to-date records of inspection results and related documentation. The ability to use manual dexterity to measure, using rulers, calipers, micrometers, and other instruments. Educational Background: The ideal candidate will have a bachelor's degree in a science-related field such as Biomedical Engineering, Mechanical Engineering, or Chemical Engineering. Experience: 3-5 years of experience working in manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required. Demonstrated level of experience in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required. Experience with pre-filled syringes, autoinjectors, co-packaged kits, other drug delivery platforms, and/or other combination product platforms is desired. Familiarity with risk management tools and applications as well as data analysis tools and applications. Strong knowledge of medical device regulations and standards, including FDA regulations and ISO 13485 and GMP. Knowledgeable in applications of caliper use, calibration and verification of tools, basic math skills and blueprints/drawings comprehension, SPC, IQ/OQ/PQ and quality principles. Proficiency in using a wide range of measuring tools and equipment. Detail-oriented with excellent organizational and communication skills. Attention to Detail in a fast-paced environment Ability to work independently and as part of a team, and to lead and mentor others. Proficient in Microsoft Office applications, including Word and Excel. Desired Aptitude and Skill Set: Detail-oriented Strong organizational skills and verbal/written communication skills Highly motivated self-starter with a sense of ownership and willingness to learn Thrive in a fast-paced, growing, and dynamic work environment Ability to form partnerships with internal stakeholders Seasoned soft skills (i.e., high EQ) Technology savvy Travel: Up to 10% travel is possible. Compensation: Pay rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions. About Kymanox:Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole. Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC. To learn more about our company, please visit our website: Life Science Solutions | Kymanox Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

We are Engineered to Serve. Tindall Corporation is a leading Precast Concrete Manufacturer, with locations throughout the Southeastern U.S. Our mission is to support our customers, create remarkable structures, and deliver never-before-seen solutions every step of the way. Our employees enjoy benefits including: Low Cost Employee Health plan, Dental, Vision, STD/LTD, Fully-paid Basic Life, Voluntary Life, Whole Life, Accident, Hospitalization, Critical Illness, EAP and a 401k Plan with Company Match & Profit Sharing. Summary of Primary Functions: Conducts pre-pour and post-pour inspections to ensure that concrete members achieve tolerances as required by shop cards and PCI. Performs concrete testing, witnesses stressing, and establishes adequate curing controls. Essential Duties and Responsibilities: All employees are required to follow all Safety and Quality rules and processes to ensure a safe working environment, and the production of high-quality products. * Inspect bed set-up according to shop drawings for proper size and placement of all reinforcement, including strands, plate location, all structural connections. * Note any nonconforming items and notify proper personnel to bring product into conformance. * Perform concrete testing: slumps, unit weights, air content, release cylinders, 28 day cylinders. * Set-up steam clocks to insure proper curing temperature. * Monitor finishing procedures in finishing shed. * Inspect final products, note any nonconformance's and notify the Engineering Department for approval or repair work order. All conforming products receive a green tag, all nonconforming products requiring engineering approval receive a red tag. * Check red tagged members after they are repaired to insure that they conform to Engineering's requirements. * All non-conformances for engineering approval are to be drawn up and submitted in writing. Job Specifications or Qualifications: Education and/or Experience: High School Diploma or general education degree (GED) is required. * All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

ABOUT US: Afton Chemical Corporation is part of the NewMarket Corporation (NYSE: NEU) family of companies, and is one of the largest global suppliers of lubricant additives and offers a broad line of fuel additives worldwide. SUMMARY: Afton Chemical Corporation is seeking a detail-oriented Chemical Technician to support analytical testing within our petroleum additives laboratory. The ideal candidate will be responsible for performing elemental analysis using ICP-OES and ensuring the accuracy, reliability, and timely delivery of analytical results. Responsibilities Conduct elemental analysis using ICP-OES (Inductively Coupled Plasma-Optical Emission Spectroscopy) following established methods and quality standards. Prepare samples, standards, and reagents in accordance with laboratory protocols. Operate, calibrate, and maintain ICP-OES instrumentation and related equipment. Review, interpret, and document analytical data with high attention to accuracy and compliance. Troubleshoot instrumentation issues and assist in method optimization when needed. Adhere to all safety, environmental, and quality management procedures. Collaborate with fellow laboratory personnel and communicate findings to technical staff. Qualifications Qualifications Associate or bachelor's degree in chemistry or a related scientific field, or a minimum of two years of directly relevant professional experience. Experience with ICP-OES or other elemental analysis techniques strongly preferred. Familiarity with laboratory information systems (LIMS), analytical instrumentation, and good laboratory practices. Strong attention to detail, organizational skills, and data integrity. Ability to work independently and as part of a team in a fast-paced laboratory environment. Willing to work in a temp to hire capacity. This role would be a contract position for the first 3-6 months. Preferred Skills Experience in petroleum additives, petrochemicals, or related industries. Understanding of sample digestion techniques and quality control practices. Basic troubleshooting and maintenance of analytical instrumentation. Working at Afton Who We Are - We're a diverse, global family of individuals, who share a passion for developing innovative solutions. We build our professional relationships on respect, integrity and a commitment to safety and quality. Just as these values apply to our professional relationships, they also apply to the way we feel about our neighbors and communities. Our Work - At Afton, our innovative R&D programs lead to global growth. Our lubricant and fuel additives are among the most highly developed and widely used in the petroleum industry. Afton is a recognized and trusted supplier of driveline lubricant additives, engine oil additives, fuel additives and industrial lubricant additives. Benefits / Compensation - We offer competitive compensation and benefit packages that reflect our commitment to our employees. Our employees are our most treasured asset and we have dedicated resources that allow us to reward our employees for their commitment on an ongoing basis - ensuring our compensation packages are competitive in the industry An Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to the individual's race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), political affiliation, military service, or other non-merit based factors.

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.