Quality assurance specialist jobs in Saint Charles, MO

Job Description Rx Systems, Inc. is currently seeking a Quality Assurance Specialist. Rx Systems, Inc. is a climate-controlled facility, which is located in the Point West Industrial Park in St. Charles, MO. Our company has been specializing in pharmacy packaging and supplies since 1979. Employees at Rx Systems, Inc. have ample opportunity to grow within our company. We are seeking a positive, team-oriented applicant that is interested in becoming part of our growing company. Job Summary Ensure that all products produced meet Rx Systems, and customer standards. ESSENTIAL DUTIES Review previous shift sign-offs and samples. Perform Quality Control inspections throughout each run, on each press in Flexo, Board, and Bags. Record any in-process non-conformances and report to supervisor when necessary. Ensure products produced meet Rx Systems standards and customer standards. Check and confirm all documentation is being filled out and is accurate. Perform Lot Acceptance testing, when applicable. Record and keep records of all job sign-offs for First Pass Yield analysis. Prepare weekly reports for management. Reports any non-conformance to supervision. Have the ability to differentiate between various colors and shades as part of quality control and product inspection duties. Any other duties as determined by management. Attendance on-site required Candidate Requirements Qualifications: High School Diploma (or GED), working knowledge of products produced, good customer focus, sharp attention to detail, problem-solving skills, team player, ability to work with minimal supervision once trained, able to distinguish between colors and hues, able to communicate with shop floor and able to stand and walk for long periods. Education and Experience: Prefer high school education or a GED. Knowledge of current products and processes desired but not essential. Language skills: Must be able to read, speak and comprehend English. Certificates and Registrations: TBD Other: Must be able to use measurement instruments, computer skills (Microsoft products at a minimum, other programs will be trained). Required training documents: Physical demands Must be able to push, pull, kneel, reach, sit, hear, walk and see. Must be able to stand for up to 8 hours at the time. Must be able to see fine detailing in finish product. Must be able to lift up to 50 lbs on a random basis. WORK ENVIRONMENT Employees may feel vibration from machinery. Noise levels are required PPE levels on machinery, ear plugs or earmuffs required. No other negatives noted.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Quality Assurance Document Control Specialist is responsible for supporting the documentation system for the St. Louis Cell Marque group, ensuring accuracy, consistency and compliance with regulatory requirements. This role involves managing document creation, revision, distribution, and archiving as well as providing training and support to employees on document control procedures. This position is based in 3050 Spruce Street, St. Louis, MO. Key Responsibilities: * Maintain a comprehensive document control system * Control the issuance, distribution, and retrieval of documents * Ensure documents are accurately indexed, filed, and archived * Manage electronic and physical document repositories * Maintain accurate records of document changes and approvals * Collaborate with various departments to ensure document accuracy and availability * Provide training and support to employees on document control procedures * Respond to document requests and inquiries promptly Who You Are: Minimum Qualifications: * Bachelor's Degree in Biology, Chemistry, Microbiology or other scientific discipline Preferred Qualifications: * Experience in quality documentation and/or learning management systems * Highly developed interpersonal, written, and verbal communication skills * Ability to establish collaborative relationships with various departments to deliver on quality commitments * Ability to work autonomously, effectively manage time and deliver results on time * Strong problem-solving skills * Strong computer skills, including Microsoft Office and quality systems software * Understanding or experience with ISO & FDA regulations RSREMD Pay Range for this position: $66,800- $109,300 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

The Quality Assurance (QA) Manager is responsible for ensuring that all airfield construction and rehabilitation activities meet the highest standards of quality, safety, and regulatory compliance. This position oversees the implementation and monitoring of the project's Construction Management Program, verifying that materials, workmanship, and processes conform to design documents, FAA standards, and contract specifications. The QA Manager plays a critical role in maintaining the integrity, safety, and longevity of airfield infrastructure, serving as a key liaison between engineering, construction, and airport operations. KEY RESPONSIBILITIES Quality Assurance Oversight Develop, implement, and maintain the project-specific Construction Management Program (CMP) in accordance with FAA Advisory Circular 150/5370-12 and applicable standards. Conduct independent inspections, audits, and material verification tests to confirm compliance with contract requirements. Monitor contractor quality control (QC) activities, ensuring their processes are effective and properly documented. Review and approve material certifications, test results, and QC reports. Ensure corrective actions are implemented for any non-conforming work or materials. Coordination & Communication Serve as the primary point of contact for quality assurance between the airport authority, construction management team, contractors, and regulatory agencies. Coordinate with resident engineers, inspectors, and laboratories to maintain consistent quality practices. Facilitate regular QA/QC coordination meetings to review findings, trends, and lessons learned. Provide technical guidance on testing procedures, materials acceptance, and construction best practices. Documentation & Reporting Maintain thorough and accurate QA records, including inspection reports, test data, and deficiency logs. Track quality metrics and prepare weekly and monthly QA status reports. Review contractor submittals, change orders, and material sources for quality impacts. Support FAA documentation requirements for grant-funded projects. Compliance & Safety Ensure all QA activities are conducted in compliance with FAA, ASTM, AASHTO, and airport authority standards. Verify environmental, safety, and security compliance related to testing and field inspections. Support safety audits and hazard identification on airfield projects. Training & Continuous Improvement Train project staff and field inspectors on QA procedures and documentation requirements. Promote a culture of quality and continuous improvement within the construction team. Identify opportunities to enhance testing protocols, inspection techniques, and data reporting. QUALIFICATIONS Education & Experience Bachelor's degree in Civil Engineering, Construction Management, or related field. Minimum 4 years of experience in airfield, heavy civil, or transportation construction quality management. Demonstrated experience with FAA-funded airport projects and compliance with FAA Advisory Circulars. Certification as an ACI Concrete Field Testing Technician - Grade I is recommended. Technical Skills Deep understanding of FAA AC 150/5370-10, FAA 150/5300 series, ASTM, and AASHTO testing standards. Knowledge of geotechnical material properties and soil classifications. Proficient with construction quality software and data management tools (e.g., Appia, Procore, e-Builder, Primavera, GIS systems). Strong knowledge of materials testing (asphalt, concrete, base course, lighting systems). Ability to interpret engineering drawings, technical specifications, and geotechnical reports. Other Requirements Excellent leadership, analytical, and communication skills. Ability to work flexible hours, including nights and weekends, as required by airfield operations. Valid driver's license and ability to obtain airport security clearance (SIDA badge). WORKING CONDITIONS Primarily field-based at active airfield construction sites. Exposure to varying weather, construction noise, and aircraft operations. Must comply with all safety, security, and environmental regulations in an airport environment.

Before we opened Strive Pharmacy we were unsatisfied with the current state of the pharmaceutical industry. Most of the current pharmaceuticals only offer a one size fits all approach and often come with unwanted and potentially dangerous side effects. We found that through compounding we can offer a much more personalized solution to medicine. Through this we have been able to help patients get the results they are seeking for their personal needs. After years of working for corporate chains we took the risk and opened Strive Pharmacy. We are dedicated to providing a better experience for each customer and clinic that we work with. Come see the Strive difference. Our Mission We're flipping the script with personal medicine. We strive to interrupt an industry that has been closed to personalized care, accessibility, and nuance for too long. We strive to shift a reactive view of self-care and ignite a proactive baseline-shifting approach to health for all. 'The human element' is our crux and catalyst, driving all that we do, whether we're interacting with patients, providers, or practices. We're here to partner with those ready for a change. More than a compounding pharmacy, we're on a mission to positively disrupt healthcare as we know it. Strive is about more than medicine. Strive is about striving for the personal side of healthcare. Position Schedule: Monday - Friday, 8:00am - 4:30pm Location: Fenton, MO Salary: $80,000 - $90,000 Position Overview: The Quality Assurance (QA) Manager provides site-specific quality oversight and ensures full compliance with Strive Pharmacy's Standard Operating Procedures (SOPs), specifications, and applicable state and federal regulatory standards. This position leads and manages the QA function at the assigned pharmacy location, with responsibility for documentation review, label control, investigations, change control, audits, and product release. The QA Manager supports continuous improvement initiatives and serves as the primary on-site liaison between pharmacy operations, compounding, and corporate Quality leadership. Key Responsibilities: Leadership & Team Oversight Supervise the site Quality Assurance team, including task assignment, workload prioritization, timecard management, performance reviews, coaching, and discipline as needed. Lead QA candidate interviews and oversee onboarding, training, and competency development. Conduct routine QA team meetings and cross-department quality huddles. Train QA personnel to ensure proficiency in documentation, review, and compliance expectations. Documentation & Quality Review Conduct regular reviews of compounding, production, and cleaning documentation (batch records, cleaning logs, inventory sheets) for accuracy and completeness. Verify and reconcile all labeling to ensure control and accountability. Review temperature monitoring and Building Management System (BMS) alarms to verify timely investigation and resolution. Confirm that product test results meet specifications prior to release. Review documentation for media fill and process validation activities. Approve equipment calibration, preventive maintenance, and certification records to ensure adherence to schedules and standards. Ensure that all documentation follows Good Documentation Practices (GDP) and complies with USP ///. Quality Systems & Compliance Management Triage and escalate customer complaints into formal quality events when applicable. Review and approve deviation, non-conformance, and CAPA documentation for completeness and adequacy of root-cause analysis. Oversee change control activities, ensuring that proposed changes are properly assessed for quality impact. Collaborate with QA Specialists to document non-compliance events and coordinate third-party testing for particulate or microbial identification when necessary. Review supplier qualification records and verify materials are sourced from compliant, approved vendors. Maintain control of printed and electronic labels and other controlled documents. Ensure proper retention and retrieval of all quality records per Strive retention policy. Auditing & Reporting Lead external audits (regulatory, partner, or client) in partnership with the Pharmacist-in-Charge (PIC). Conduct internal audits to verify compliance with SOPs, USP standards, and regulatory requirements. Report weekly site quality metrics and trend data to the Director of Quality. Review all documentation submitted to third-party agencies or partners for accuracy and completeness. Report product complaints and adverse drug events to appropriate regulatory agencies in collaboration with corporate QA. Authority Authorized to approve or reject compounded products, raw materials, and components based on quality review and testing results. Authorized to pause or halt operations pending investigation when quality, safety, or compliance risks are identified. Qualifications: Required High School Diploma or GED Minimum of five (5) years experience in a quality or manufacturing department within a pharmaceutical, medical device, or allied health science environment Proven experience in aseptic operations and working in regulated environments Strong knowledge of pharmaceutical quality assurance practices, including deviation management, CAPA, change control, and documentation review Ability to analyze and interpret data, identify trends, and recommend preventive actions Strong organizational, communication, and problem-solving skills Proficiency with Microsoft Office Suite and quality management systems (QMS) Preferred: Associate's or higher degree in Biology, Microbiology, Chemistry, or Pharmacy Prior experience leading a QA team in a compounding or manufacturing environment Familiarity with 503A or 503B compounding regulations, USP //, and FDA 21 CFR 210/211 Experience participating in or leading regulatory or partner audits Annual Salary$80,000-$90,000 USDBenefits/ Perks Strive Pharmacy provides a comprehensive benefits package that encompasses various perks such as employer paid healthcare coverage available after 30 days of employment, the choice of an FSA/HSA, a voucher for new hire scrubs (if applicable), parental leave, a 401(k) plan with matching contributions, and the benefit of weekends and holidays off. FREE COMPOUNDED MEDS to employees and immediate family members. Culture At Strive, culture plays a fundamental role in shaping our workplace atmosphere. Beyond our exceptional benefits package, we foster a sense of community. Throughout the year, we arrange various holiday potlucks and festive celebrations. Strive is committed to promoting both personal and professional development, striving for our employees to excel and grow in every aspect of their lives, both within and outside of the workplace. EEO Strive Pharmacy is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristics as outlined by federal, state or local laws. Disclaimer*** Please do not call the pharmacy location with questions about your application or interview. A talent acquisition partner will reach out to you.

The QA Specialist will support various Quality department duties involved with the release of pharmaceutical products. This role requires a meticulous individual to review completed records, logbooks, and some laboratory and manufacturing notebooks. The specialist will assist in managing the quality documentation system, including routing for signatures, editing, uploading, and filing. Additionally, the QA Specialist will author Standard Operating Procedures (SOPs) and manage stability studies. Responsibilities * Conduct quality assurance reviews of completed records, logbooks, and laboratory and manufacturing notebooks. * Assist in managing the quality documentation system, including routing for signatures, editing, uploading, and filing. * Author and update Standard Operating Procedures (SOPs). * Manage stability studies and participate in quarterly QA audits. * Assist in investigations for Out of Specification (OOS), Deviations, and Corrective and Preventive Actions (CAPAs). * Contribute to the writing of annual product reports and help with trending analytical and manufacturing data, proposing improvements. * Review and release raw materials based on specifications. * Support customer and regulatory audits. Essential Skills * Experience in quality assurance and record review. * High integrity and transparent communication skills. * Ability to collaborate effectively and educate on corrective measures. * Experience with CAPA, audit processes, FDA regulations, and document control. Additional Skills & Qualifications * Bachelor's degree preferred but not required. * 3-5 years of GMP quality experience, preferably in a pharmaceutical manufacturing environment. * Direct experience with record review and release. Work Environment The role is based in a brand-new manufacturing and lab space within an existing building. The QA Specialist will primarily work at a desk but may have exposure to manufacturing suites and lab environments. The position operates on a Monday to Friday day shift. The company fosters a growing team with a growth mindset, ideal for those willing to take on additional responsibilities or learn new skills. Job Type & Location This is a Contract to Hire position based out of Ballwin, MO. Pay and Benefits The pay range for this position is $30.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Ballwin,MO. Application Deadline This position is anticipated to close on Dec 8, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

BETTER MOBILITY FOR LIFE Savaria is a global leader in accessibility and patient care products, designing and building wheelchair lifts, stairlifts, elevators for home and commercial applications, medical beds, therapeutic surfaces, ceiling track lifts and patient slings. Savaria employs 2,450 valued associates globally and has 11+ manufacturing facilities to reach markets in North America, Europe, Australia, and Asia. SAVARIA PATIENT CARE Built from a heritage of brands including Span, Handicare and Silvalea, Savaria Patient Care provides products designed for safe patient handling and positive outcomes. Our research and clinically based product portfolio include therapeutic surfaces for pressure management and positioning, a complete range of innovative ceiling and floor lifts and slings. Savaria Patient Care is a division of Savaria Corporation, a global leader in accessibility. OVERVIEW: The Quality Assurance Specialist is responsible for overseeing the nonconforming product and vendor evaluation processes, as well as assisting with customer returns and conducting audits of internal processes. This role will work closely with other departments including Procurement, Engineering, and Production to ensure product and process requirements are being met and optimized. Exceptional communication skills and the ability to work well with others will be critical to success within this role. ESSENTIAL DUTIES AND RESPONSIBILITIES: Working with Operations to identify process failures and/or potential improvements Conducting regular Production audits to confirm quality checks are being performed as specified Reviewing work instructions to ensure they are accurate and being followed Assessing processes to identify potential improvements to quality and efficiency Overseeing Preventative Maintenance audits to ensure all required checks are being conducted and documented per our procedures Managing nonconforming product process Coordinating and documenting vendor returns and product reworks Ensuring product is dispositioned and nonconformance reports are closed in a timely manner Overseeing vendor approval, evaluation, and monitoring to ensure product conformity Reviewing qualifications of new vendors and maintaining vendor log and documentation Conducting vendor evaluations including, as needed, vendor audits and corrective actions Assisting with investigating and dispositioning customer returns Receiving and sorting customer returned product Inspecting returned product to confirm it meets requirements for return to inventory Documenting and executing the disposition of returned product Releasing product and acting as work coverage for Incoming and Final Inspectors as needed Supporting various Quality processes such as corrective/preventive actions and internal audits Conducting process and software validations as required Working with Engineering on ad-hoc projects such as documentation and drawing reviews, product testing, temporary deviations, and implementing change orders Facilitating continuous improvement projects and acting as support to meeting various company goals Additional duties as requested or required SUPERVISORY RESPONSIBILITIES: This position has no supervisory responsibilities. COMPETENCIES: Exceptional communication skills and the ability to both write and speak clearly and effectively Comfortable with and capable of communicating successfully with internal and external customers Excellent time management skills and the ability to balance multiple responsibilities High level of initiative to complete tasks accurately, thoroughly, and in a timely manner Mechanically inclined, preferably with experience using electronic and pneumatic equipment Knowledge of quality system requirements, such as ISO, FDA, etc. Experience in the operation of inspections equipment (micrometers, calipers, etc.) Ability and desire to work closely with others as an effective team player Follows instructions and responds positively to management direction Looks for ways to improve and promote quality across multiple departments and functions Observes quality, safety, and security policies and procedures Takes responsibility for own actions and edits work for accuracy Commits to communicating and coordinating scheduling needs to ensure work is covered LANGUAGE SKILLS: Ability to read, analyze and interpret documents such as safety rules, operating and maintenance instructions, dimensional drawings/specifications and procedural manuals. Ability to write reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization. EDUCATION, EXPERIENCE & TRAINING: High School Diploma or general education degree (GED) Educational or professional background in quality, science, or engineering: Bachelor of Science degree (B.S.) from a four-year college or university OR Associate or Technical degree and 1 to 3 years of professional Quality Assurance experience CERTIFICATES, LICENSES OR REGISTRATIONS: Already obtained or willing to pursue the following certifications is preferred: ISO 13485 Lead Auditor certification Forklift operator certification COMPUTER SKILLS: Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook is required. Proficiency in ERP system such as Microsoft Dynamics AX12 and electronic Quality Management System such as Qualio is preferred. PHYSICAL DEMANDS: The employee may occasionally stand, walk, stoop, kneel or crouch during shift. Employee will be required to regularly sit, use hand to finger, handle, feel and reach with hands and arms. Employee must be able to occasionally lift and or move up to 50 lbs. WORK ENVIRONMENT: This position works in an environment with moderate noise levels. TRAVEL: Infrequent (less than 5% of the time). Valid passport and willingness to travel to other company sites or supplier locations as needed to acquire product knowledge or conduct onsite audits is preferred. Note: Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Critical features of this job are described under various headings above. They may change at any time due to reasonable accommodations or other reasons. The above statements are strictly intended to describe the general nature and level of the work being performed. They are to not be construed as a complete list of all responsibilities, duties and skills requires of employees in this position. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential duties of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Savaria provides equal employment opportunities and consideration to all qualified employees and applicants, including disabled individuals and veterans. # SAVARIAPATIENTCARE

DIVE IN TO A NEW CAREER WITH A LESLIE'S COMPANY: In September 2022, Stellar Manufacturing was acquired by Leslie's as an affiliate. Stellar Manufacturing is a contract manufacturer of solid particle products and specializes in chemical processing services such as specialty tableting, compaction granulation, and granular filling. We support the manufacturing of a variety of consumer and industrial products including water treatment chemicals, janitorial and sanitation products, agrochemicals, raw materials, and more. With over 30 years of providing best-in-class products and solutions to our customers, there is nothing that we value more than the development and growth of our team. Both Leslie's and Stellar strive to create a positive and fun atmosphere where our Team Members feel valued and are enthusiastic about the contributions they make to the success of Stellar. Summary: The QA Specialist - Positive Release is primarily responsible for ensuring that all manufactured products have been verified against their quality acceptance criteria and are authorized for shipment according to the organization's quality management system which meets the requirements of ISO 9001:2015 standard. Responsibilities: Core duties and responsibilities include the following. Other duties may be assigned. * Review and approve production batch records with the requirements of current GMPs. * Review and approve inbound and outbound shipping paperwork * Review and approve quality data which supports the generation of product COAs. * Review and approve incoming raw material COAs. * Follow good documentation practices when creating, reviewing, revising, obsoleting, and archiving controlled documents per the QMS. * Support change management processes, deviations, and CAPAs as required. * Monthly reporting to management on all outstanding NCAPs. * Partake in internal and external auditing processes to provide supporting documentation as required. * Support site risk management and continuous improvement efforts according to the site QMS. * Data entry and review in Excel * Performs other duties and special projects as assigned. Qualifications: * Bachelor's Degree or equivalent work experience * Technical Writer (1 year preferred) * Ability to read, write and speak English to properly communicate information related to job functions, test methods, procedures, training requirements and specifications, etc. * Must be well-organized with a high attention to detail skillset. * Must have great oral and written communication skills as this position works closely with site management. * Self-directed and motivated * Must be able to work in environments that have minimum supervision as well as cross-functional teams * Proficient with Microsoft Word, Excel, and Office. PHYSICAL DEMANDS: * Employee must be able to sit, stand, type for extended periods of time. * Employee may be exposed to various chemicals. Pay $28 - $30/Hour #FieldHiring

Blink Health is the fastest growing healthcare technology company that builds products to make prescriptions accessible and affordable to everybody. Our two primary products - BlinkRx and Quick Save - remove traditional roadblocks within the current prescription supply chain, resulting in better access to critical medications and improved health outcomes for patients. BlinkRx is the world's first pharma-to-patient cloud that offers a digital concierge service for patients who are prescribed branded medications. Patients benefit from transparent low prices, free home delivery, and world-class support on this first-of-its-kind centralized platform. With BlinkRx, never again will a patient show up at the pharmacy only to discover that they can't afford their medication, their doctor needs to fill out a form for them, or the pharmacy doesn't have the medication in stock. We are a highly collaborative team of builders and operators who invent new ways of working in an industry that historically has resisted innovation. Join us! This is a hybrid position based out of our Chesterfield, MO location. What You'll Do: Perform daily Quality Assurance evaluations on all lines of business, meeting or exceeding the assigned productivity targets Conduct patient interaction evaluations for Patient Services phone, chat and emails Conduct pharmacy workflow audits, such as Prior Authorization process adherence and data entry for the Hub Identify trends and opportunities to improve quality in patient interactions and workflow adherence. Communicate these opportunities to QA leadership or other pertinent stakeholders. Collaborate with agents, leaders, and other QA analysts to identify best practices, knowledge gaps and opportunities to enhance protocols, scripting, training and Knowledge Base articles. Remain current on our products, protocols, scripting, new clients, features and departmental processes Participate in calibration sessions to ensure consistency in grading and auditing practices. Serve as a subject matter expert for assigned business segment(s), and function as the expert scoring interactions that others will be calibrated against. Facilitate discussions to explain rationale for scoring, actively listen and make recommendations as necessary to the appropriate scorecards to drive improvement in calibration scores Cross train to be able to evaluate quality on other business segments as needed Complete other duties as assigned What You'll Need: A minimum of 2 years of QA experience in a contact center or hub pharmacy environment Experience with healthcare, insurance, or other highly regulated industry preferred Track record of strong performance and QA scores Attention to detail with a knack for precision Analytical and process oriented Comfortable in a fast-paced environment Ability to work independently and as a member a team Confident, patient, respectful, and a clear communicator Passion for problem solving and troubleshooting Why Join Us: It is rare to have a company that both deeply impacts its customers and is able to provide its services across a massive population. At Blink, we have a huge impact on people when they are most vulnerable: at the intersection of their healthcare and finances. We are also the fastest growing healthcare company in the country and are driving that impact across millions of new patients every year. Our business model not only helps people, but drives economics that allow us to build a generational company. We are a relentlessly learning, constantly curious, and aggressively collaborative cross-functional team dedicated to inventing new ways to improve the lives of our customers. We are an equal opportunity employer and value diversity of all kinds. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

The Assurance Associate will be responsible for preparing financial statements with disclosures, applying basic areas of GAAP as necessary and documenting, validating, testing, and assessing various control systems. This position may also be involved in reviews and agreed-upon procedure engagements. The Assurance Associate will be expected to travel, as needed, to meet firm and client needs. Job Duties Control Environment: Applies knowledge and understanding of the collective effect of various factors on establishing or enhancing effectiveness, or mitigating the risks, of specific policies and procedures by: Identifying and considering all applicable policies, laws, rules, and regulations of the firm, regulators, or other authoritative bodies as part of engagement team; Making constructive suggestions to improve client internal controls and accounting procedures; Documenting and validating the operating effectiveness of the clients' internal control system. GAAP: Applies knowledge and understanding of governing principles; applying these principles to client transactions; and documenting and communicating an understanding and application of these principles by: Providing support of conclusions with authoritative literature; Drafting basic sets of financial statements with disclosures; Researching intermediate areas of accounting and forming an initial opinion on the correct treatment independently GAAS: Applies knowledge and understanding of professional standards; application of the principles contained in professional standards; and the ability to document and communicate an understanding and application of professional standards on an engagement by: Developing and applying an intermediate knowledge of auditing theory, a sense of audit skepticism, and the use of BDO audit manuals Applying auditing theory to various client situations Documenting in line with BDO policy, identifying deviations and notifying more senior team members in order to obtain appropriate approvals Applying knowledge to identify instances where testing may be reduced or expanded and notifying more senior team members of the occurrence Contributing ideas/opinions to the engagement teams Methodology: Applies knowledge and application of BDO standards to guide effective and efficient delivery of quality services and products by: Completing all appropriate documentation of BDO work papers Ensuring assigned work is performed in accordance with BDO methodology and requirements Research: Applies methodology used to seek or maintain information from authoritative sources and to draw conclusions regarding a target issue based on the information by: Researching basic and intermediate accounting topics and forming an initial opinion on the treatment independently Other duties as required Qualifications, Knowledge, Skills and Abilities: Education: Bachelor's degree in Accounting, Finance, Economics or Statistics, required OR Bachelor's degree in other focus area and CPA certification, required Master's in Accountancy, preferred Experience: Leadership experience, preferred Accounting based internship, preferred License/Certifications: Eligible to sit for the CPA exams upon starting employment, required Actively pursuing completion of CPA exams, preferred Software: Proficient with the Microsoft Office Suite, required Other Preferred Knowledge, Skills & Abilities: Strong written and verbal communication skills Ability to follow instructions as directed Ability to work effectively in a team setting Ability and willingness to travel, as needed, required Takes appropriate actions without being asked Basic understanding and experience planning and coordinating the stages to perform an audit of a basic public and/or private company Individual salaries that are offered to a candidate are determined after consideration of numerous factors including but not limited to the candidate's qualifications, experience, skills, and geography. California Range: $85,000 - $90,000 Colorado Range: $73,000 - $77,000 Illinois Range: $78,000 - $82,000 Maryland Range: $83,000 - $87,000 Massachusetts Range: $83,000 - $87,000 Minnesota Range: $70,000 - $74,000 New Jersey Range: $74,000 - $82,000 NYC/Long Island/Westchester Range: $83,000 - $87,000 Washington Range: $78,000 - $80,000 Washington DC Range: $83,000 - $87,000

_________________________________________________________________________________________________ Masego is an award-winning small business that specializes in GEOINT services. As a Service-Disabled Veteran-Owned Small Business (SDVOSB), we recognize and award your hard work. Description We are looking for an L3 TS/SCI-cleared Office/Staff Supporter to join our team. Responsibilities: Oversee the activity of the quality assurance deliverables. Develop, implement and maintain a system of quality and reliability testing. Provides development of project Software Quality Assurance Plan and the implementation of procedures that conforms to the requirements of the contract. Provides an independent assessment of how the project's software development process is being implemented relative to the defined process and recommends methods to optimize the organization's process. May be responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. Conducts Quality Assurance audits and reviews/analyzes data and documentation. Develops and implements procedures and test plans for assuring quality in a system development environment which supports large databases and applications. Required Skills and Experience: 7-10 years of relevant experience Demonstrated experience with methods and processes used to monitor the production of a product or service in order to maintain a desired level of quality. Demonstrated knowledge of quality management system standards established by the International Organization for Standardization (ISO) 9001 standard published by the ISO. Demonstrated experience with methods and processes used to ensure that materials, components, or products meet expected standards or compliance requirements. Bachelor's degree or equivalent experience within a related field Security Clearance Requirement: Active TS/SCI, must be willing to take and pass a CI Polygraph Salary Range: $86,760+ based on ability to meet or exceed stated requirements Job Number: TO1_SFA-QAM-001-015 About Masego Masego Inc. provides expert Geospatial Intelligence Solutions in addition to Activity Based Intelligence (ABI) and GEOINT instructional services. Masego provides expert-level Geospatial Collection Management, Full Motion Video; Human Geography; Information Technology and Cyber; Technical Writing; and ABI, Agile, and other professional training. Masego is a Service-Disabled Veteran-Owned Small Business headquartered in Fredericksburg, Virginia. With high-level expertise and decades of experience, coupled with proven project management systems and top-notch client support, Masego enhances the performance capabilities of the Department of Defense and the intelligence community. Pay and Benefits We seek to provide and take care of our team members. We currently offer Medical, Dental, Vision, 401k, Generous PTO, Referral bonuses, and more! Diversity Masego, Inc. is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all applicable Federal and Virginia State laws, regulations, and executive orders regarding nondiscrimination and affirmative action in its programs and activities. Masego, Inc. does not discriminate on the basis of race, color, religion, ethnic or national origin, gender, genetic information, age, disability, sexual orientation, gender identity, gender expression, and veteran's status.

Full-time Description Sev-Rend Corporation is a printing and manufacturing company leading the industry in tag and label application, flexible packaging, and product identification. We are looking for hardworking and driven individuals interested in helping us uphold our longstanding commitment to our customers through quick lead times and superior quality. Our Culture At Sev-Rend Corporation we exist to make people's lives better. We encourage our people to reach for their full potential professionally and personally. We drive the success of our company through employee involvement. We value: Compassion - To empathize with others who are needing assistance and feel compelled to help. Humility - Thinking about oneself less and having a focus on others. Inspiration - Something that moves someone to act, create, or feel an emotion. Overview The person in this role will monitor and maintain all food safety and quality assurance initiatives, including, but not limited to, GMP, GFSI auditing schemes (SQF), and FDA regulatory requirements and will be responsible for food safety continuous improvement initiatives with the responsibility of maintaining GFSI standards. Job Duties Understand the SQF Food Safety Code for Manufacture of Food Packaging and the requirements to maintain SQF System. Oversite of the SQF program including but not limited to adherence to SQF code requirements, document and record management, monthly leadership meetings, verification, and validation activities. Maintains compliance with FDA and other governing bodies (city/ state/ health department) where applicable. Serves as SQF practitioner, HACCP coordinator for the facility; leads a cross-functional Food Safety Team. Preparing for and leading a team through third party food safety/ GMP audit. Ensure compliance to all SOP's and GMP. Fully monitor, record and validate all food safety checks, including HACCP, Verification and Validation processes, and all quality and food safety programs Execute or coordinate outside 3rd party microbiology tests in accordance with QA requirements. Fully manage Document Control program ensuring all SOP, Policies, Vendor COA, Letter of Guarantees, MSDS, and other regulatory documents are updated. Train company personnel on their relevant SQF components to ensure the effective implementation of the SQF System. Audit procedures, programs, and verifications, post and pre-production, implementing necessary corrective action. Monitor and update Customer Complaint log and assist with root cause analysis and corrective actions. Supports plant management in resolving non-conforming product or compliance issues. Responsible for internal lab testing methods and lab equipment data. Reviews quality and food safety data and responds appropriately to out of specification results or trends where applicable. Works closely with facility leadership to foster a positive quality and food safety culture and support personnel safety and continuous improvement efforts. Escalates food safety and quality issues to Sev-Rend leadership as needed. Performs other duties as assigned that will impact and support the overall outcome of the company and department objectives. Requirements Bachelor's degree or equivalent experience Two or more years' experience in food safety or quality assurance in a food packaging manufacturing environment; experience with production equipment is preferred but not required. Must demonstrate a working understanding of all GMP, HACCP, SQF, and other food safety auditing schemes and regulations and auditing in a GFSI environment. Internal Auditing and HACCP certifications required. Experience with ERP and QMS, or other Inventory management systems with lot traceability needed. Experience with SafetyChain and Alcehmy a plus. Previous experience as a food safety practitioner highly preferred. Self-starter with superb initiative. Must have excellent verbal and written communication skills. Must have the ability to lead teams and conduct employee training. Able to work well independently or as an active team member. Possesses time management and organization skills. Advanced computer skills in Microsoft Suite, and proficiency with electronic devices. Strong critical thinking skills. Able to attend training programs and participate in company-sponsored educational opportunities. Sev-Rend Corporation is an Equal Opportunity Employer. Employees and applicants for employment will not be discriminated against on the basis of age, race, creed, color, religion, national origin, ancestry, gender, sex, pregnancy, physical or mental disability, sexual orientation, marital status, citizenship status, military or veteran status, or any other characteristic protected by applicable law in any employment decisions. Salary Description $55,000 - $75,000 annually

Wouldn't it be great to build your career at a growing company recognized 6 years in a row from 2019 to 2025 as the winner of Best Places to Work in collections and the 2025 winner of Best Places to Work for Women. At Credit Control, we know without a doubt that our driven, dedicated team members are the foundation of our success. Employees are rewarded with excellent benefits, competitive compensation, and opportunities for growth. Position Overview We are looking for detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure they meet regulatory requirements (FDCPA, HIPAA, state laws) and client/company quality standards. You'll play a crucial role in helping our agents maintain compliance and deliver a positive experience, as outlined in the Position Overview. We are seeking detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure compliance with regulatory standards (FDCPA, HIPAA, state laws) and meet client/company quality standards. You will play a vital role in helping our agents maintain compliance and deliver a positive experience for consumers. Job Duties: Listen to and evaluate inbound and outbound collection calls based on a predetermined scorecard Score calls are based on set criteria such as professionalism, accuracy, compliance, and overall effectiveness. Provide clear, documented feedback to leadership for training and improvement based on observations while monitoring calls Ensures day-to-day operations are conducted in compliance with regulatory and legal requirements, including FDCPA, state regulations, HIPAA, and the company's policies and procedures, by performing ongoing testing of the business's operations and procedures. Review other quality-related documentation or reports assigned by management Skills/Qualifications: Strong listening skills and attention to detail Comfortable working with evaluation forms, checklists, and scoring criteria. Basic proficiency with Microsoft Word and Excel. Good written communication skills. Knowledge of FDCPA and HIPAA is a plus (training provided). High school diploma or equivalent required Job Type: Full-time. This is an in-office position. Salary: $16.00 - $18.00 per hour Benefits: Flexible Schedule Medical/Dental/Vision Life Insurance Paid Time Off Paid Vacation Time Paid Holidays Paid Bereavement Paid Training 401k with company match Annual Retention Bonus Professional Development Grant Program Employee Assistance Program Ongoing Contests & Prizes Annual Company Events Company Referral Program ADP Lifemart Employee Discounts Schedule: 8-hour shift Day shift Holidays Monday to Friday No nights Overtime Education: High school or equivalent (Preferred) Experience: Computer skills: 1 year (Preferred) Data entry: 1 year (Preferred) Microsoft Office: 1 year (Preferred) Work Location: In-office position 3300 Riders Trail South Suite 500 Earth City, Missouri 63045

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Quality Assurance Product Release Specialist plays a critical role in ensuring the timely and compliant release of purchased and produced goods at MilliporeSigma. This position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications and regulatory requirements. The Quality Product Release Specialist will collaborate with various internal stakeholders and will be a subject matter expert in QA product release processes. Key Responsibilities: * Ensure that raw materials and finished goods meet analytical, performance, packaging, and labeling specifications in accordance with established acceptance criteria and regulatory requirements. * Review vendor documentation, including certificates of origin, certificates of analysis and customer and regulatory questionnaires. * Create customer-facing documents, including supply chain declarations/affidavits, certificates of analysis and certificates of origin. * Evaluate raw materials and final products to determine acceptability and compliance with import/export requirements derived from animal by-product (ABP) regulations. * Perform thorough review of production and packaging batches and determine usage decisions regarding the acceptability of materials and products. Who You Are: Minimum Qualifications: * Bachelor's Degree in a Scientific (Biology, Chemistry, etc.) or Engineering discipline (Chemical, Mechanical, etc.) Preferred Qualifications: * 1+ year quality experience * Strong computer skills, including knowledge of SAP systems * Experience in quality management systems * Highly developed interpersonal, written, and verbal communication skills * Ability to establish collaborative relationships with various departments * Ability to work autonomously, effectively manage time and deliver results on time * Strong problem-solving skills RSREMD * Pay Range for this position: $64,400.00- $104,900.00. * The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job DescriptionSalary: DOE The Quality Assurance (QA) Manager is responsible for ensuring that all airfield construction and rehabilitation activities meet the highest standards of quality, safety, and regulatory compliance. This position oversees the implementation and monitoring of the projects Construction Management Program, verifying that materials, workmanship, and processes conform to design documents, FAA standards, and contract specifications. The QA Manager plays a critical role in maintaining the integrity, safety, and longevity of airfield infrastructure, serving as a key liaison between engineering, construction, and airport operations. KEY RESPONSIBILITIES Quality Assurance Oversight Develop, implement, and maintain the project-specific Construction Management Program (CMP) in accordance with FAA Advisory Circular 150/5370-12 and applicable standards. Conduct independent inspections, audits, and material verification tests to confirm compliance with contract requirements. Monitor contractor quality control (QC) activities, ensuring their processes are effective and properly documented. Review and approve material certifications, test results, and QC reports. Ensure corrective actions are implemented for any non-conforming work or materials. Coordination & Communication Serve as the primary point of contact for quality assurance between the airport authority, construction management team, contractors, and regulatory agencies. Coordinate with resident engineers, inspectors, and laboratories to maintain consistent quality practices. Facilitate regular QA/QC coordination meetings to review findings, trends, and lessons learned. Provide technical guidance on testing procedures, materials acceptance, and construction best practices. Documentation & Reporting Maintain thorough and accurate QA records, including inspection reports, test data, and deficiency logs. Track quality metrics and prepare weekly and monthly QA status reports. Review contractor submittals, change orders, and material sources for quality impacts. Support FAA documentation requirements for grant-funded projects. Compliance & Safety Ensure all QA activities are conducted in compliance with FAA, ASTM, AASHTO, and airport authority standards. Verify environmental, safety, and security compliance related to testing and field inspections. Support safety audits and hazard identification on airfield projects. Training & Continuous Improvement Train project staff and field inspectors on QA procedures and documentation requirements. Promote a culture of quality and continuous improvement within the construction team. Identify opportunities to enhance testing protocols, inspection techniques, and data reporting. QUALIFICATIONS Education & Experience Bachelors degree in Civil Engineering, Construction Management, or related field. Minimum 4 years of experience in airfield, heavy civil, or transportation construction quality management. Demonstrated experience with FAA-funded airport projects and compliance with FAA Advisory Circulars. Certification as an ACI Concrete Field Testing Technician Grade I is recommended. Technical Skills Deep understanding of FAA AC 150/5370-10, FAA 150/5300 series, ASTM, and AASHTO testing standards. Knowledge of geotechnical material properties and soil classifications. Proficient with construction quality software and data management tools (e.g., Appia, Procore, e-Builder, Primavera, GIS systems). Strong knowledge of materials testing (asphalt, concrete, base course, lighting systems). Ability to interpret engineering drawings, technical specifications, and geotechnical reports. Other Requirements Excellent leadership, analytical, and communication skills. Ability to work flexible hours, including nights and weekends, as required by airfield operations. Valid drivers license and ability to obtain airport security clearance (SIDA badge). WORKING CONDITIONS Primarily field-based at active airfield construction sites. Exposure to varying weather, construction noise, and aircraft operations. Must comply with all safety, security, and environmental regulations in an airport environment.

The QA Specialist will support various Quality department duties involved with the release of pharmaceutical products. This role requires a meticulous individual to review completed records, logbooks, and some laboratory and manufacturing notebooks. The specialist will assist in managing the quality documentation system, including routing for signatures, editing, uploading, and filing. Additionally, the QA Specialist will author Standard Operating Procedures (SOPs) and manage stability studies. Responsibilities + Conduct quality assurance reviews of completed records, logbooks, and laboratory and manufacturing notebooks. + Assist in managing the quality documentation system, including routing for signatures, editing, uploading, and filing. + Author and update Standard Operating Procedures (SOPs). + Manage stability studies and participate in quarterly QA audits. + Assist in investigations for Out of Specification (OOS), Deviations, and Corrective and Preventive Actions (CAPAs). + Contribute to the writing of annual product reports and help with trending analytical and manufacturing data, proposing improvements. + Review and release raw materials based on specifications. + Support customer and regulatory audits. Essential Skills + Experience in quality assurance and record review. + High integrity and transparent communication skills. + Ability to collaborate effectively and educate on corrective measures. + Experience with CAPA, audit processes, FDA regulations, and document control. Additional Skills & Qualifications + Bachelor's degree preferred but not required. + 3-5 years of GMP quality experience, preferably in a pharmaceutical manufacturing environment. + Direct experience with record review and release. Work Environment The role is based in a brand-new manufacturing and lab space within an existing building. The QA Specialist will primarily work at a desk but may have exposure to manufacturing suites and lab environments. The position operates on a Monday to Friday day shift. The company fosters a growing team with a growth mindset, ideal for those willing to take on additional responsibilities or learn new skills. Job Type & Location This is a Contract to Hire position based out of Ballwin, MO. Pay and Benefits The pay range for this position is $30.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Ballwin,MO. Application Deadline This position is anticipated to close on Dec 9, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Blink Health is the fastest growing healthcare technology company that builds products to make prescriptions accessible and affordable to everybody. Our two primary products - BlinkRx and Quick Save - remove traditional roadblocks within the current prescription supply chain, resulting in better access to critical medications and improved health outcomes for patients. BlinkRx is the world's first pharma-to-patient cloud that offers a digital concierge service for patients who are prescribed branded medications. Patients benefit from transparent low prices, free home delivery, and world-class support on this first-of-its-kind centralized platform. With BlinkRx, never again will a patient show up at the pharmacy only to discover that they can't afford their medication, their doctor needs to fill out a form for them, or the pharmacy doesn't have the medication in stock. We are a highly collaborative team of builders and operators who invent new ways of working in an industry that historically has resisted innovation. Join us! This is a hybrid position based out of our Chesterfield, MO location. What You'll Do: Perform daily Quality Assurance evaluations on all lines of business, meeting or exceeding the assigned productivity targets Conduct patient interaction evaluations for Patient Services phone, chat and emails Conduct pharmacy workflow audits, such as Prior Authorization process adherence and data entry for the Hub Identify trends and opportunities to improve quality in patient interactions and workflow adherence. Communicate these opportunities to QA leadership or other pertinent stakeholders. Collaborate with agents, leaders, and other QA analysts to identify best practices, knowledge gaps and opportunities to enhance protocols, scripting, training, and Knowledge Base articles. Remain current on our products, protocols, scripting, new clients, features and departmental processes Participate in calibration sessions to ensure consistency in grading and auditing practices. Serve as a subject matter expert for assigned business segment(s), and function as the expert scoring interactions against which others will be calibrated. Facilitate discussions to explain rationale for scoring, actively listen and make recommendations as necessary to the appropriate scorecards to drive improvement in calibration scores Cross-train to be able to evaluate quality on other business segments as needed Complete other duties as assigned What You'll Need: A minimum of 2 years of QA experience in a contact center or hub pharmacy environment Spanish language proficiency, both written and spoken. Experience with healthcare, insurance, or other highly regulated industry preferred Track record of strong performance and QA scores Attention to detail with a knack for precision Analytical and process-oriented Comfortable in a fast-paced environment Ability to work independently and as a member a team Confident, patient, respectful, and a clear communicator Passion for problem solving and troubleshooting #blinkindeed Why Join Us: It is rare to have a company that both deeply impacts its customers and is able to provide its services across a massive population. At Blink, we have a huge impact on people when they are most vulnerable: at the intersection of their healthcare and finances. We are also the fastest growing healthcare company in the country and are driving that impact across millions of new patients every year. Our business model not only helps people, but drives economics that allow us to build a generational company. We are a relentlessly learning, constantly curious, and aggressively collaborative cross-functional team dedicated to inventing new ways to improve the lives of our customers. We are an equal opportunity employer and value diversity of all kinds. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Job Description _________________________________________________________________________________________________ Masego is an award-winning small business that specializes in GEOINT services. As a Service-Disabled Veteran-Owned Small Business (SDVOSB), we recognize and award your hard work. Description We are looking for an L3 TS/SCI-cleared Office/Staff Supporter to join our team. Responsibilities: Oversee the activity of the quality assurance deliverables. Develop, implement and maintain a system of quality and reliability testing. Provides development of project Software Quality Assurance Plan and the implementation of procedures that conforms to the requirements of the contract. Provides an independent assessment of how the project's software development process is being implemented relative to the defined process and recommends methods to optimize the organization's process. May be responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. Conducts Quality Assurance audits and reviews/analyzes data and documentation. Develops and implements procedures and test plans for assuring quality in a system development environment which supports large databases and applications. Required Skills and Experience: 7-10 years of relevant experience Demonstrated experience with methods and processes used to monitor the production of a product or service in order to maintain a desired level of quality. Demonstrated knowledge of quality management system standards established by the International Organization for Standardization (ISO) 9001 standard published by the ISO. Demonstrated experience with methods and processes used to ensure that materials, components, or products meet expected standards or compliance requirements. Bachelor's degree or equivalent experience within a related field Security Clearance Requirement: Active TS/SCI, must be willing to take and pass a CI Polygraph Salary Range: $86,760+ based on ability to meet or exceed stated requirements Job Number: TO1_SFA-QAM-001-015 About Masego Masego Inc. provides expert Geospatial Intelligence Solutions in addition to Activity Based Intelligence (ABI) and GEOINT instructional services. Masego provides expert-level Geospatial Collection Management, Full Motion Video; Human Geography; Information Technology and Cyber; Technical Writing; and ABI, Agile, and other professional training. Masego is a Service-Disabled Veteran-Owned Small Business headquartered in Fredericksburg, Virginia. With high-level expertise and decades of experience, coupled with proven project management systems and top-notch client support, Masego enhances the performance capabilities of the Department of Defense and the intelligence community. Pay and Benefits We seek to provide and take care of our team members. We currently offer Medical, Dental, Vision, 401k, Generous PTO, Referral bonuses, and more! Diversity Masego, Inc. is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all applicable Federal and Virginia State laws, regulations, and executive orders regarding nondiscrimination and affirmative action in its programs and activities. Masego, Inc. does not discriminate on the basis of race, color, religion, ethnic or national origin, gender, genetic information, age, disability, sexual orientation, gender identity, gender expression, and veteran's status. Powered by JazzHR LDl4B333op

Job DescriptionDescription: Sev-Rend Corporation is a printing and manufacturing company leading the industry in tag and label application, flexible packaging, and product identification. We are looking for hardworking and driven individuals interested in helping us uphold our longstanding commitment to our customers through quick lead times and superior quality. Our Culture At Sev-Rend Corporation we exist to make people's lives better. We encourage our people to reach for their full potential professionally and personally. We drive the success of our company through employee involvement. We value: Compassion - To empathize with others who are needing assistance and feel compelled to help. Humility - Thinking about oneself less and having a focus on others. Inspiration - Something that moves someone to act, create, or feel an emotion. Overview The person in this role will monitor and maintain all food safety and quality assurance initiatives, including, but not limited to, GMP, GFSI auditing schemes (SQF), and FDA regulatory requirements and will be responsible for food safety continuous improvement initiatives with the responsibility of maintaining GFSI standards. Job Duties Understand the SQF Food Safety Code for Manufacture of Food Packaging and the requirements to maintain SQF System. Oversite of the SQF program including but not limited to adherence to SQF code requirements, document and record management, monthly leadership meetings, verification, and validation activities. Maintains compliance with FDA and other governing bodies (city/ state/ health department) where applicable. Serves as SQF practitioner, HACCP coordinator for the facility; leads a cross-functional Food Safety Team. Preparing for and leading a team through third party food safety/ GMP audit. Ensure compliance to all SOP's and GMP. Fully monitor, record and validate all food safety checks, including HACCP, Verification and Validation processes, and all quality and food safety programs Execute or coordinate outside 3rd party microbiology tests in accordance with QA requirements. Fully manage Document Control program ensuring all SOP, Policies, Vendor COA, Letter of Guarantees, MSDS, and other regulatory documents are updated. Train company personnel on their relevant SQF components to ensure the effective implementation of the SQF System. Audit procedures, programs, and verifications, post and pre-production, implementing necessary corrective action. Monitor and update Customer Complaint log and assist with root cause analysis and corrective actions. Supports plant management in resolving non-conforming product or compliance issues. Responsible for internal lab testing methods and lab equipment data. Reviews quality and food safety data and responds appropriately to out of specification results or trends where applicable. Works closely with facility leadership to foster a positive quality and food safety culture and support personnel safety and continuous improvement efforts. Escalates food safety and quality issues to Sev-Rend leadership as needed. Performs other duties as assigned that will impact and support the overall outcome of the company and department objectives. Requirements: Bachelor's degree or equivalent experience Two or more years' experience in food safety or quality assurance in a food packaging manufacturing environment; experience with production equipment is preferred but not required. Must demonstrate a working understanding of all GMP, HACCP, SQF, and other food safety auditing schemes and regulations and auditing in a GFSI environment. Internal Auditing and HACCP certifications required. Experience with ERP and QMS, or other Inventory management systems with lot traceability needed. Experience with SafetyChain and Alcehmy a plus. Previous experience as a food safety practitioner highly preferred. Self-starter with superb initiative. Must have excellent verbal and written communication skills. Must have the ability to lead teams and conduct employee training. Able to work well independently or as an active team member. Possesses time management and organization skills. Advanced computer skills in Microsoft Suite, and proficiency with electronic devices. Strong critical thinking skills. Able to attend training programs and participate in company-sponsored educational opportunities. Sev-Rend Corporation is an Equal Opportunity Employer. Employees and applicants for employment will not be discriminated against on the basis of age, race, creed, color, religion, national origin, ancestry, gender, sex, pregnancy, physical or mental disability, sexual orientation, marital status, citizenship status, military or veteran status, or any other characteristic protected by applicable law in any employment decisions.

Job DescriptionSalary: $16.00 - $18.00 per hour Wouldnt it be great to build your career at a growing company recognized 6 years in a row from 2019 to 2025 as the winner of Best Places to Work in collections and the 2025 winner of Best Places to Work for Women. At Credit Control, we know without a doubt that our driven, dedicated team members are the foundation of our success. Employees are rewarded with excellent benefits, competitive compensation, and opportunities for growth. Position Overview We are looking for detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure they meet regulatory requirements (FDCPA, HIPAA, state laws) and client/company quality standards. Youll play a crucial role in helping our agents maintain compliance and deliver a positive experience, as outlined in the Position Overview. We are seeking detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure compliance with regulatory standards (FDCPA, HIPAA, state laws) and meet client/company quality standards. You will play a vital role in helping our agents maintain compliance and deliver a positive experience for consumers. Job Duties: Listen to and evaluate inbound and outbound collection calls based on a predetermined scorecard Score calls are based on set criteria such as professionalism, accuracy, compliance, and overall effectiveness. Provide clear, documented feedback to leadership for training and improvement based on observations while monitoring calls Ensures day-to-day operations are conducted in compliance with regulatory and legal requirements, including FDCPA, state regulations, HIPAA, and the companys policies and procedures, by performing ongoing testing of the businesss operations and procedures. Review other quality-related documentation or reports assigned by management Skills/Qualifications: Strong listening skills and attention to detail Comfortable working with evaluation forms, checklists, and scoring criteria. Basic proficiency with Microsoft Word and Excel. Good written communication skills. Knowledge of FDCPA and HIPAA is a plus (training provided). High school diploma or equivalent required Job Type: Full-time.This is an in-office position. Salary: $16.00 - $18.00 per hour Benefits: Flexible Schedule Medical/Dental/Vision Life Insurance Paid Time Off Paid Vacation Time Paid Holidays Paid Bereavement Paid Training 401k with company match Annual Retention Bonus Professional Development Grant Program Employee Assistance Program Ongoing Contests & Prizes Annual Company Events Company Referral Program ADP Lifemart Employee Discounts Schedule: 8-hour shift Day shift Holidays Monday to Friday No nights Overtime Education: High school or equivalent (Preferred) Experience: Computer skills: 1 year (Preferred) Data entry: 1 year (Preferred) Microsoft Office: 1 year (Preferred) Work Location: In-office position 3300 Riders Trail South Suite 500 Earth City, Missouri 63045