The Director, Global Product Quality, GMP Processes is a strategic leadership role responsible for **benchmarking, standardizing, and optimizing global quality processes** across the organization. This role ensures that product quality systems are aligned with **Good Manufacturing Practices (GMP)** and regulatory requirements while driving **efficiency, consistency, and continuous improvement** across all regions and product lines.
The Director will lead global initiatives to harmonize and enhance processes related to **product quality complaints, deviations, CAPA, and management reporting** , ensuring timely and effective resolution and robust compliance.
**Key Responsibilities**
+ Global Process Ownership: Lead the design, implementation, and continuous improvement of global quality processes for:
+ Product Quality Complaints
+ Corrective and Preventive Actions (CAPA)
+ Deviations
+ Management Reporting and Trending
+ Benchmarking & Best Practices: Evaluate internal and external quality practices to identify and implement best-in-class solutions that enhance compliance and operational efficiency.
+ GMP Compliance: Ensure all quality processes meet global regulatory requirements (e.g., FDA, EMA, PMDA) and align with current GMP standards.
+ Governance & Standardization: Develop and enforce global standards, SOPs, templates, and tools to ensure consistency across all manufacturing sites and affiliates.
+ Quality Systems Leadership: Oversee the global deployment and optimization of electronic quality systems (e.g., TrackWise), including configuration, training, and validation.
+ Cross-Functional Collaboration: Partner with regional quality leaders, manufacturing, regulatory affairs, and technical operations to ensure alignment and effective execution of quality strategies.
+ Data-Driven Insights: In collaboration with Quality Operations, lead the development of global quality metrics and dashboards to monitor performance, identify trends, and support decision-making.
+ Team Leadership: Build and lead a high-performing global team of quality professionals, fostering a culture of accountability, innovation, and excellence.
**Qualifications**
Required
**Required Qualifications:**
+ Bachelor's degree in a scientific discipline (e.g., Chemistry, Biology, Pharmaceutical Sciences); advanced degree preferred.
+ Minimum 12 years of experience in pharmaceutical quality assurance or quality systems, with at least 5 years in a global leadership role.
+ Deep understanding of GMP regulations and global regulatory requirements (e.g., 21 CFR Parts 210, 211, 820).
+ Proven experience in managing global quality systems and optimizing complaint, CAPA, and deviation processes.
+ Strong analytical and problem-solving skills with a data-driven mindset.
+ Excellent communication, leadership, and stakeholder management skills.
+ Proficiency in quality management systems (e.g., TrackWise) and Microsoft Office tools.
+ Ability to travel internationally as needed.
Preferred
+ Basic understanding of artificial intelligence and advanced analytics
+ Experience supporting risk management programs or frameworks.
+ Familiarity with quality management systems and digital tools.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $183,335.00 - Maximum $274,160.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
$183.3k yearly 43d ago
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Quality Manager
SKF Inc. 4.6
Quality manager job in Sumter, SC
Salary Range: $123,000.00 to $146,000.00 About SKF: SKF, reducing friction since 1907, re-imagining rotation for a better tomorrow! SKF is an industry-leading manufacturer that has been a cornerstone in industrial life. Wherever there are machines or products in motion, SKF bearings are there to reduce friction. SKF drives the industries that support our way of life, powers the machines that put food on the table, and even helps explore the cosmos.
Sustainability is at the heart of everything we do. SKF is on pace to decarbonize all its production facilities by 2030.
We're guided by our SKF values. Collaboration is critical to the success of our colleagues, partners, and customers. Curiosity and Courage provide a foundation for innovation and advancement. And we do this work out of Care for our people, customers, communities, and the planet.
We're a company committed to a culture of belonging, where all our people are encouraged to be themselves and grow their careers in an equitable environment.
Learn about SKF at ************
Summary:
This position is responsible for developing, coordinating, administering and supervising the plant's Quality Assurance program, ensuring that quality control procedures and policies are coordinated throughout the organization. Assures that all products manufactured meet customer specifications and achieve the quality and reliability requirements in support of company objectives.
Job Duties and Responsibilities (including but not limited to):
* Directs and coordinates the overall quality specifications, standards, inspection and testing procedures for raw materials for processes and finished products
* Develops quality control plans or process control procedures that will ensure production of finished products, which meet quality specifications and standards
* Responsible for establishing testing policies and procedures for maintaining a program that will meet the quality control needs of the organization
* Conducts and/or reviews all complaints received from customers to determine where quality control emphasis should be placed at the plants to eliminate problems
* Reviews research on product defects and recommends modifications in products or quality standard where warranted
* Directs the ISO certification and associated programs, ensuring that all requirements are established and meant. Ensures the Plants annual ISO certification
* Assists research and development and other departments as necessary in formulating new products or in establishing standards for these products prior to initial production
* Provides technical assistance to the Purchasing Department in connection with the purchase of raw materials, supplies and equipment
* Contacts and/or visits customers and suppliers when necessary to confer on specific quality problems
* May police subcontractors' quality control programs
* Assists vendors in establishing inspection standards to meet the Company's quality requirements
* Supplies technical assistance to the sales and/or marketing functions in developing suitable products for customers or overcoming difficulties in the use of company products
* Directs the continuing review of the quality control program and the formulation of new or revised procedures to effect improvements, reduce costs and enhance efficiency
* Ensures compliance with government regulations
* Formulates department objectives: directs staff activities to meet Company objectives; ensures that all department personnel are trained to perform their jobs effectively
* Administers Quality Assurance Department budget preparation; assure compliance and other administrative functions to effect a well-integrated, efficient operation
* Responsible for procuring state of the art gauging keeping the Plant current with technology changes
* Responsible for coordinating gauging procedures between Kaydon Plants and customers.
Job Education, Experience and Requirements:
* Must have a Bachelor's degree in Engineering
* Quality Management, or related technical field or the equivalent in practical experience and specialized training
* Five to seven (5-7) years including at least three (3) years in a supervisory capacity of applicable experience in Quality Assurance
* Must have broad and in-depth knowledge of manufacturing processes and techniques, quality control, technology and exposure to data processing
* Ability to relate and interact effectively with various levels and organizations within the operation required
What You'll Love About SKF: Rest and Relaxation. Enjoy a generous PTO policy and 13 paid holidays.
Work/Life Integration. SKF supports work/life integration, home, family, community, personal well-being and health.
Diversity in the Workplace. ?At SKF, we strive to embed Diversity, Equity and Inclusion in everything we do. By developing a culture of belonging, our people can flourish; leading to an inclusive, equitable environment that promotes leadership, engagement and innovation.
Best in Class Benefits. SKF cares about the wellbeing of our employees. Comprehensive healthcare options to fit your needs and opt out payment. Added benefits include company paid life insurance, STD, LTD. Supplemental benefits include critical illness coverage, tuition reimbursement, employee discount programs, and much more!
Bonus. SKF offers STVS (Short Term Variable Salary) or Sales Incentive based on company performance and at the discretion of management.
Invest in your Future. Participate in our 401K program that boasts a 10% employer contribution: 100% match up to 5% of your elected contribution (100% Vested) plus an additional 5% company contribution.
Reports to: Regional Quality Director
Location: Sumter, Sc
Job ID: 23735
SKF provides equal employment [and affirmative action] opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
By applying to this job you acknowledge how SKF treats candidate data. Click HERE to review the SKF Data Privacy Consent Statement.
$123k-146k yearly 36d ago
Director, Quality - Life Sciences
Datavant
Quality manager job in Columbia, SC
Datavant is a data platform company and the world's leader in health data exchange. Our vision is that every healthcare decision is powered by the right data, at the right time, in the right format. Our platform is powered by the largest, most diverse health data network in the U.S., enabling data to be secure, accessible and usable to inform better health decisions. Datavant is trusted by the world's leading life sciences companies, government agencies, and those who deliver and pay for care.
By joining Datavant today, you're stepping onto a high-performing, values-driven team. Together, we're rising to the challenge of tackling some of healthcare's most complex problems with technology-forward solutions. Datavanters bring a diversity of professional, educational and life experiences to realize our bold vision for healthcare.
Datavant is seeking a strategic and hands-on **Director of Quality** to lead product and supplier quality assurance efforts within our **Life Sciences business unit** , which includes the **Datavant Connect** and **Aetion Evidence Platform** . These platforms deliver regulatory-grade real-world data (RWD) solutions through tokenization, data linkage, and privacy-preserving analytics.
As Director of Quality, you will own the implementation and evolution of GxP-aligned quality practices that support regulated data services and software. This includes oversight of software validation, privacy compliance, supplier qualification, and audit readiness. You will also lead a team of quality specialists and partner cross-functionally with Product, Engineering, Security, Privacy, and Customer Assurance to ensure that we meet or exceed regulatory expectations and customer trust standards.
This role is essential to operationalizing Datavant's **Quality Management System (QMS)** across internal and external stakeholders and enabling continued growth in regulated RWD and evidence generation environments.
**What You Will Do**
+ Lead the development and continuous improvement of Datavant's QMS across Life Sciences products and supplier relationships, ensuring GxP and privacy compliance.
+ Manage and mentor a team of quality specialists responsible for core functions such as CAPA, internal audits, validation, and supplier monitoring.
+ Serve as the primary quality liaison to product development teams (Connect and Aetion), providing guidance on SDLC quality controls, validation strategies (GAMP 5, Part 11), and regulatory risk mitigation.
+ Oversee supplier qualification and re-evaluation processes, including risk-based assessments, audit coordination, and performance monitoring.
+ Establish and maintain quality metrics (e.g., CAPA closure, audit readiness scores, supplier performance) and drive continuous improvement initiatives.
+ Support readiness for and participation in customer audits and external assessments (e.g., pharma clients, CROs, regulatory partners).
+ Partner with Security and Privacy teams to align product and supplier practices with frameworks like HIPAA, GDPR, and FedRAMP.
+ Lead or support periodic management reviews of the QMS and contribute to strategic quality planning and resource allocation.
+ Ensure clear documentation and traceability across all quality activities, systems, and changes in compliance with FDA 21 CFR Part 11 and ICH E6(R3).
+ Represent Datavant's quality program in external communications, including client onboarding, RFIs, and quality-related escalations.
**What You Need to Succeed**
+ 8+ years of experience in quality, compliance, or regulatory roles within life sciences, digital health, or regulated software organizations.
+ Strong working knowledge of relevant regulations and frameworks, including **FDA 21 CFR Part 11, GAMP 5, ISO 9001, ICH E6(R3), HIPAA** , and **GDPR** .
+ Proven leadership in scaling and operationalizing a **QMS in a SaaS, RWD, or GxP context** .
+ Experience managing and mentoring cross-functional teams.
+ Demonstrated success overseeing **validation, supplier oversight, internal audits, and CAPA management** .
+ Deep understanding of **data governance, privacy, and security** best practices.
+ Experience interacting with external auditors, customer compliance teams, or regulatory agencies.
+ Strong communication skills-capable of explaining complex quality topics to product, legal, technical, and customer-facing stakeholders.
**What Helps You Stand Out**
+ Prior experience supporting real-world data (RWD) platforms or evidence generation technologies used in regulatory submissions.
+ Background working in or with tokenization, health data linkage, or privacy-enhancing technologies.
+ Experience interfacing directly with pharmaceutical, biotech, or CRO quality teams.
+ Training or certification in Six Sigma, ISO Auditing, or software validation methodologies.
+ Familiarity with supplier portals, quality dashboards, or eQMS platforms (e.g., Veeva, MasterControl).
+ Experience contributing to industry working groups on quality, data integrity, or health data compliance.
\#LI-BC1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. This role is eligible for additional variable compensation.
The estimated base salary range (not including variable pay) for this role is:
$165,000-$230,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (************************************************** . Know Your Rights (*********************************************************************** , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (************************************************************** Id=**********48790029&layout Id=**********48795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (******************************************************************************************************* . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (**************************************** .
$165k-230k yearly 50d ago
Director of Quality Assurance and Evaluation
Sisters of Charity Health System 4.0
Quality manager job in Columbia, SC
Director of Quality Assurance and Evaluation Job Description Who Are We? The SC Center for Fathers and Families (Center) is a faith-based nonprofit organization dedicated to ending father absence through educational programming, wraparound services, research, and advocacy. For over 20 years, we have helped create stronger, safer, and more prosperous families and communities by re-engaging fathers with their children, aiming to improve overall childhood well-being and reduce poverty. We are the voice for fathers in South Carolina and lead one of the nation's largest and most experienced networks of community-based organizations providing men with the tools and resources they need to be great dads. Our Center office is in Columbia, SC, and we have a network of five fatherhood organizations across the state.
Responsibilities: Evaluation Leadership & Strategy
Design and implement evaluation frameworks across partner fatherhood organizations
Guide performance monitoring and continuous quality improvement efforts
Translate complex data into actionable insights for program refinement and strategic planning
Collaborate with leadership to align evaluation with organizational goals and values
Data Systems & Reporting
Oversee data systems, reporting protocols, and performance dashboards
Ensure compliance with grant requirements and contribute to funder reporting
Supervise the Data and Quality Manager, providing strategic direction and support
Promote data literacy and documentation best practices across teams
Capacity Building & Collaboration
Build staff capacity in evaluation, storytelling, and evidence-based decision-making
Foster a culture of learning and accountability across the organization
Serve as a thought partner to program and leadership teams in using data to drive impact
Preferred Qualifications
Master's degree in public administration, social sciences, evaluation, or related field-or equivalent experience
5+ years in program evaluation, nonprofit leadership, or quality assurance
Strong command of data systems, reporting platforms, and performance metrics
Proficiency with Apricot, nForm, or similar case management and evaluation databases
Experience working with community-based programs and underserved populations
Excellent communication skills-able to translate data into compelling stories
Commitment to equity, learning, and mission-driven service
Ability to travel statewide and work flexible hours as needed
This is a full-time grant-funded position. Salary $75K - $95K. Qualified candidates should submit a cover letter and resume with the online application.
$75k-95k yearly 60d+ ago
Quality Assurance Manager
Maximus 4.3
Quality manager job in Columbia, SC
Description & Requirements Maximus is currently hiring for a Quality Assurance Manager to support our Missouri Enrollment Broker project. This is a full time remote opportunity. The Quality Manager is responsible for overseeing the daily operations for the Quality Assurance team, and for creating efficient business partnerships to meet business goals. The project will be a multi-channel contact center that will support multiple clients throughout the state of Missouri.
*This job is contingent upon contract award.*
At Maximus we offer a wide range of benefits to include:
- • Competitive Compensation - Quarterly bonuses based on performance included!
- • Comprehensive Insurance Coverage - Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance.
- • Future Planning - Prepare for retirement with our 401K Retirement Savings plan and Company Matching.
- • Unlimited Time Off Package - Enjoy UTO, Holidays, and sick leave,
- • Holistic Wellness Support - Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP).
- • Recognition Platform - Acknowledge and appreciate outstanding employee contributions.
- • Tuition Reimbursement - Invest in your ongoing education and development.
- • Employee Perks and Discounts - Additional benefits and discounts exclusively for employees.
- • Maximus Wellness Program and Resources - Access a range of wellness programs and resources tailored to your needs.
- • Professional Development Opportunities- Participate in training programs, workshops, and conferences.
Essential Duties and Responsibilities:
- Oversee the day-to-day functions of the Quality Assurance (QA) department.
- Manage an effective quality assurance program that monitors and resolves issues before they become problems.
- Supervise the development and regular update of policies and procedures.
- Evaluate the need for and ensure the provision of necessary training for project personnel, providing up-to-date information on relevant programs, community resources, and options for consumers.
- Arrange staff training on a regular and ongoing basis. Ensure project training program meets all corporate requirements.
- Provide project leadership with updates on all issues regarding quality, operations, training, and policy and procedures.
- Provide leadership to all staff in the areas of quality improvement as it relates to process improvement, customer service and conflict resolution.
- Prepare reports and briefings for project leadership and review monthly and quarterly project status reports provided to the Department.
Minimum Requirements
- Bachelor's degree in relevant field of study and 5+ years of relevant professional experience required, or equivalent combination of education and experience.
- Must be willing and able to travel up to 25% of the time as business need dictates.
- Lean Six Sigma experience with a minimum of Yellow Belt Certification required.
- Experience managing direct reports remotely required.
- Experience with designing, implementing and reporting customer satisfaction surveys required.
- Experience with standardized quality tools required.
- Experience with call and voice monitoring platforms required.
- Experience with a large-scale telephony system required.
- Experience with Client Relationship Management (CRM) platforms required.
- Experience with contract compliance and quality platforms required.
- Experience with statistical processes required.
- Premium contact center billing experience required.
- Financial experience with Oracle preferred.
Home Office Requirements:
- Internet speed of 20mbps or higher required (you can test this by going to *******************
- Connectivity to the internet via either Wi-Fi or Category 5 or 6 ethernet patch cable to the home router.
- Must currently and permanently reside in the Continental US.
#max Priority #LI-Remote
EEO Statement
Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics.
Pay Transparency
Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances.
Accommodations
Maximus provides reasonable accommodations to individuals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at **************************.
Minimum Salary
$
80,000.00
Maximum Salary
$
95,000.00
$59k-84k yearly est. Easy Apply 2d ago
Quality Control Manager
United Infrastructure Group, Inc.
Quality manager job in Columbia, SC
JOB DESCRIPTION: QUALITY CONTROL MANAGER General Expectations: The Quality Control Manager (QCM) is a senior, proactive leadership role responsible for protecting the Carolina Crossroads Phase 3C Project from quality-driven cost, schedule, and reputational risk. This position is not a compliance-only or box-checking role. The QCM is expected to actively engage with construction operations, identify quality risks early, and prevent non-conforming work before it occurs, rather than reacting after deficiencies are identified by Quality Assurance (QA) or Owner Verification (OV).
This role is designed to prevent quality failures-not document them after the fact.
The QCM will serve as the Contractor's primary quality authority, embedding quality planning into daily operations through rigorous pre-planning, activity planning, and consistent field presence. The successful candidate will anticipate quality challenges, intervene early, and drive corrective action before issues escalate into Deficiency Notices (DNs), Non-Conformance Reports (NCRs), rework, or schedule impacts.
This role requires full-time, on-site leadership. The QCM must be physically present in the field and/or project office daily and is not eligible for remote or hybrid work arrangements. Relocation to the Columbia, South Carolina area is required.
The QCM is empowered to stop work, manage and release hold points, and reject non-conforming materials or workmanship without additional approval. The QCM reports directly to the UBJV Executive Management Team and operates independently from construction production management to preserve objectivity and authority.
Quality Control Program Leadership
* Manage, implement, and continuously improve the Contractor's Quality Control Program in accordance with the approved CQMP.
* Update QC components of the CQMP as required to address changing work activities or identified deficiencies.
* Promote awareness of SCDOT requirements and stakeholder expectations throughout UBJV staff and subcontractors.
* Report to the UBJV Management Team on QC performance, trends, and improvement opportunities.
Pre-Planning & Activity Planning
* Manage and implement the Pre-Planning and Activity Planning process for all major construction activities.
* Schedule, lead, and document Pre-Activity Meetings prior to commencement of work.
* Verify readiness of work activities before release to production.
Hold Points & Inspection Authority
* Schedule, manage, and document all CQMP and Appendix A hold points.
* Verify all prerequisites are satisfied prior to releasing hold points.
* Exercise authority to stop work and reject non-conforming materials or workmanship.
Coordination with QA and Owner Verification
* Coordinate with the Independent Quality Firm (IQF) to ensure proper staffing, coverage, and compliance with the CQMP.
* Provide oversight of QA activities from a Contractor QC perspective without interfering with acceptance functions.
* Serve as the primary QC liaison with SCDOT and the Owner Verification Firm.
Non-Conformance & Corrective Action
* Manage Deficiency Notices (DNs) and Non-Conformance Reports (NCRs) through closure.
* Lead root cause analysis and corrective action development.
* Ensure timely documentation, tracking, and resolution of quality issues.
Field QC Inspections & Reporting
* Perform or oversee QC inspections for self-performed and subcontracted work.
* Ensure inspections and testing are performed by properly certified personnel.
* Review daily QC inspection reports and weekly QC submissions.
Environmental & Traffic Control Compliance
* Oversee environmental compliance inspections including SWPPP and erosion control.
* Oversee Maintenance of Traffic and Traffic Control Plan compliance.
Documentation & Records Management
* Manage QC document control systems including inspection reports, test results, and material certifications.
* Ensure records are complete, accurate, and immediately available for audit or review.
Materials & Laboratory Coordination
* Coordinate QC laboratory scheduling and testing activities.
* Ensure sampling and testing are performed using AASHTO-accredited laboratories.
* Coordinate QC responsibilities with subcontractors, including paving subcontractor-provided HMA QC.
Reporting & Authority
* The QCM reports directly to the UBJV Executive Management Team and does not report to the Construction Manager. The QCM has independent authority to stop work, manage and release hold points, reject non-conforming work, and direct corrective actions as required.
Position Requirements: (Must have or be able to get required certifications)
* 10-15 years of progressive experience in heavy civil highway and bridge construction QC.
* Experience managing QC programs on large DOT projects.
* Demonstrated coordination with QA/IQF and Owner Verification teams.
* SCDOT Earthwork and Base Course Technician
* Nuclear Gauge HazMat Certification
* ACI Concrete Field Testing Technician - Level I (Level II preferred)
* Foundations Technician
* Certified Erosion Prevention & Sediment Control Inspector (CEPSCI)
* Work Zone Traffic Control Certification
* NACE Coating Inspector Level I or SSPC Bridge Coating Inspector Level I (as applicable)
* IMSA Traffic Signals Level II and IMSA Fiber Optic Technician Level II (as applicable)
* Strong interpersonal and organizational skills.
* Self-starter and ability to work unsupervised.
* Team player and self-motivated to be successful.
* Legally able to work in the US.
Equal Opportunity Employer, including disabled and veterans.
View Company Information
$68k-106k yearly est. 3d ago
Director, Quality
Stratus Unlimited
Quality manager job in Lexington, SC
There's never been a better time to join Stratus! As the market leader in brand implementation and maintenance, we transform how national brands connect with their customers. From exterior signage & interior branding to site refresh & remodel, from energy & lighting to repair & maintenance solutions, we deliver ideal solutions to meet all our client's branding needs.
From our locations across the country, to our corporate headquarters in Mentor, Ohio, every employee is a stakeholder in Stratus' success. This environment offers endless career opportunities for individuals with a commitment to customer service, focus on execution and bias for action.
Summary
Stratus is seeking a strategic and enterprise-minded Director, Quality to lead all quality assurance and control initiatives for our brand implementation business, with a strong focus on exterior signage and interior branding and the manufacturing and installation for each service line. This role ensures that products meet the highest standards of craftsmanship, durability, and compliance while driving continuous improvement across design, fabrication, and field operations. The Director will champion a culture of quality excellence and customer satisfaction throughout the organization.
Location Preference: We have a strong preference for candidates based in San Antonio, TX, Lexington, SC, Greater Chicago, or Greater Cleveland. However, we are open to highly qualified remote candidates who can commit to regular travel as needed.
Responsibilities
Quality Strategy & Leadership
* Develop and implement a comprehensive quality strategy aligned with business goals and client expectations.
* Lead and mentor the Quality team, fostering accountability and continuous improvement.
* Collaborate cross-functionally with Project Management, Engineering, Design, and Supply Chain teams to align quality objectives and support new product introductions and process changes.
Manufacturing & Fabrication Quality
* Develop and implement quality standards across three internal plants and multiple external manufacturing partners to ensure compliance with company specifications and regulatory requirements.
* Monitor and audit production processes at internal and external facilities, identifying deviations and driving corrective actions to maintain consistent product quality.
* Ensure compliance with structural integrity standards.
Process & Compliance
* Maintain and improve Quality Management Systems (QMS) in line with ISO standards and industry best practices.
* Ensure adherence to local building codes, electrical standards, and environmental regulations.
Supplier & Vendor Quality
* In partnership with Field Partner Management (FPMG) and Supply Chain, establish and maintain supplier/vendor quality programs, including qualification, performance reviews, and continuous improvement initiatives for field partners and external manufacturing partners.
* Collaborate with procurement to ensure material consistency and reliability.
Field Installation & Customer Experience
* Implement quality checks for installation teams to ensure flawless execution and brand consistency.
* Drive initiatives to reduce rework, improve timelines, and enhance client satisfaction.
Continuous Improvement
* Utilize Lean, Six Sigma, or similar methodologies to optimize processes and reduce defects.
* Lead root cause analysis and corrective/preventive action processes for quality issues, ensuring timely resolution and documentation.
Metrics & Reporting
* Define and monitor KPIs such as defect rates, on-time delivery, and customer satisfaction scores with action plans to strengthen underperforming areas.
* Provide regular quality performance reports to senior leadership.
Qualifications
* Bachelor's degree in Engineering, Operations, Quality Management, or equivalent work experience preferred; Master's degree or MBA a plus.
* 10+ years of experience in quality management, with at least 5 years in a leadership role within a manufacturing environment.
* Strong knowledge of ISO standards, QMS, and regulatory compliance.
* Experience with Exterior Signage, Architectural elements, and Interior Branding projects preferred.
* Lean Six Sigma certification or equivalent strongly desired.
* Ability to manage quality across design, production, and installation phases.
Travel
This role will travel due to the need for in-person interaction with employees, customers, field partners, and/or business stakeholders. Travel may include local, regional, or national destinations and may be conducted via automobile, air, or other modes of transportation. All travel must be pre-approved in accordance with company policy and conducted in compliance with applicable safety and expense guidelines.
Why Work With Us
* Supportive & Friendly Culture
* Manage national accounts for Fortune 500 companies
* Medical, Dental, Vision insurance coverage options
* Flexible Spending & Health Savings Accounts (HSA) with company contribution to HSA
* Company paid Life Insurance
* 401k with competitive Employer Contribution
* Company paid Short/Long Term Disability Insurance
* Generous Paid Time Off program + Holidays
* Career Growth Opportunities and Career Mapping
* Additional perks including Pet Insurance, Employee Assistance Program, Educational Assistance Program, Identity Theft Protection, Critical Illness Plans, Commuter Benefits and various employee discount offerings from our Vendors
Pay Range
$130,000- $155,000 annually - Pay range listed reflects the potential pay for this role. The pay will depend on various factors, such as responsibilities of the position, job duties/requirements, and relevant experience and skills. Not all positions posted will have a pay range listed.
eeo/mfdv
#LI-REMOTE
$130k-155k yearly Auto-Apply 4d ago
Director, Quality
Working With Us Become A Part of The Team
Quality manager job in Lexington, SC
There's never been a better time to join Stratus! As the market leader in brand implementation and maintenance, we transform how national brands connect with their customers. From exterior signage & interior branding to site refresh & remodel, from energy & lighting to repair & maintenance solutions, we deliver ideal solutions to meet all our client's branding needs.
From our locations across the country, to our corporate headquarters in Mentor, Ohio, every employee is a stakeholder in Stratus' success. This environment offers endless career opportunities for individuals with a commitment to customer service, focus on execution and bias for action.
Summary
Stratus is seeking a strategic and enterprise-minded Director, Quality to lead all quality assurance and control initiatives for our brand implementation business, with a strong focus on exterior signage and interior branding and the manufacturing and installation for each service line. This role ensures that products meet the highest standards of craftsmanship, durability, and compliance while driving continuous improvement across design, fabrication, and field operations. The Director will champion a culture of quality excellence and customer satisfaction throughout the organization.
Location Preference: We have a strong preference for candidates based in San Antonio, TX, Lexington, SC, Greater Chicago, or Greater Cleveland. However, we are open to highly qualified remote candidates who can commit to regular travel as needed.
Responsibilities
Quality Strategy & Leadership
Develop and implement a comprehensive quality strategy aligned with business goals and client expectations.
Lead and mentor the Quality team, fostering accountability and continuous improvement.
Collaborate cross-functionally with Project Management, Engineering, Design, and Supply Chain teams to align quality objectives and support new product introductions and process changes.
Manufacturing & Fabrication Quality
Develop and implement quality standards across three internal plants and multiple external manufacturing partners to ensure compliance with company specifications and regulatory requirements.
Monitor and audit production processes at internal and external facilities, identifying deviations and driving corrective actions to maintain consistent product quality.
Ensure compliance with structural integrity standards.
Process & Compliance
Maintain and improve Quality Management Systems (QMS) in line with ISO standards and industry best practices.
Ensure adherence to local building codes, electrical standards, and environmental regulations.
Supplier & Vendor Quality
In partnership with Field Partner Management (FPMG) and Supply Chain, establish and maintain supplier/vendor quality programs, including qualification, performance reviews, and continuous improvement initiatives for field partners and external manufacturing partners.
Collaborate with procurement to ensure material consistency and reliability.
Field Installation & Customer Experience
Implement quality checks for installation teams to ensure flawless execution and brand consistency.
Drive initiatives to reduce rework, improve timelines, and enhance client satisfaction.
Continuous Improvement
Utilize Lean, Six Sigma, or similar methodologies to optimize processes and reduce defects.
Lead root cause analysis and corrective/preventive action processes for quality issues, ensuring timely resolution and documentation.
Metrics & Reporting
Define and monitor KPIs such as defect rates, on-time delivery, and customer satisfaction scores with action plans to strengthen underperforming areas.
Provide regular quality performance reports to senior leadership.
Qualifications
Bachelor's degree in Engineering, Operations, Quality Management, or equivalent work experience preferred; Master's degree or MBA a plus.
10+ years of experience in quality management, with at least 5 years in a leadership role within a manufacturing environment.
Strong knowledge of ISO standards, QMS, and regulatory compliance.
Experience with Exterior Signage, Architectural elements, and Interior Branding projects preferred.
Lean Six Sigma certification or equivalent strongly desired.
Ability to manage quality across design, production, and installation phases.
Travel
This role will travel due to the need for in-person interaction with employees, customers, field partners, and/or business stakeholders. Travel may include local, regional, or national destinations and may be conducted via automobile, air, or other modes of transportation. All travel must be pre-approved in accordance with company policy and conducted in compliance with applicable safety and expense guidelines.
Why Work With Us
Supportive & Friendly Culture
Manage national accounts for Fortune 500 companies
Medical, Dental, Vision insurance coverage options
Flexible Spending & Health Savings Accounts (HSA) with company contribution to HSA
Company paid Life Insurance
401k with competitive Employer Contribution
Company paid Short/Long Term Disability Insurance
Generous Paid Time Off program + Holidays
Career Growth Opportunities and Career Mapping
Additional perks including Pet Insurance, Employee Assistance Program, Educational Assistance Program, Identity Theft Protection, Critical Illness Plans, Commuter Benefits and various employee discount offerings from our Vendors
Pay Range
$130,000- $155,000 annually - Pay range listed reflects the potential pay for this role. The pay will depend on various factors, such as responsibilities of the position, job duties/requirements, and relevant experience and skills. Not all positions posted will have a pay range listed.
eeo/mfdv
#LI-REMOTE
$130k-155k yearly Auto-Apply 5d ago
Supplier Quality Engineer
Solectron Corp 4.8
Quality manager job in Columbia, SC
Job Posting Start Date 12-18-2025 Job Posting End Date 02-16-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary
To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Supplier Quality Engineer located in Columbia, SC.
The Supplier Quality Engineer will be responsible for supplier development in a manufacturing or service process; works with suppliers to continuously improve performance, implement process controls and develop quality assurance plans
What a typical day looks like:
Supplier Selection---Select the suitable supplier with jointed-effort of sourcing on aspects of quality, capability, pricing, delivery, environment, society regulation, etc. against customer requirements.
Supplier Qualification---Implement the new supplier qualification thru the process of capability matching, supplier risk assessment, supplier self-assessment, onsite qualification audit, qualification database management.
VEA (Value-Added Engineering Activity) ---Understand customer drawing, specification to feedback value-added engineering proposal to customer and supplier for optimization of supplier manufacturing process or products.
Material (Component) Qualification---Implement PPAP (FAI). PPAP include FAI, Material Certificates, Quality/Process Control Plan, FMEA, MSA, Process Parameter Sheet, RoHS compliance, Reliability Test, COC, etc.
Pilot Run Tracking---Track the new qualified parts quality performance to ensure meet the customer quality requirements in pilot run phase. Drive supplier corrective action from supplier in Pilot Runs (1-3 lots) and smoothly transfer the pilot run to mass production.
Hot Issue Solution and Trouble Shooting--- Working as SME (Subject Matter Expert) to help on supplier quality hot issue and trouble shooting.
Holds up Maintenance Audit---helps on the annual maintenance audit for existing suppliers with SQE.
Holds up Supplier CIP (Continuous Improvement Program) --- Helps supplier to use the quality tools to improve manufacturing process and product quality.
ECO/ECN/SCR implementation---Handle with ECO/ECN/SCR from customer, follow up the status in case that PPAP/FAI is required prior to production.
Has knowledge of a company's manufacturing process, applications and process development in order to intently work with suppliers in improving quality components of goods and services.
Performs quality audits on suppliers to assure products and services meet International Organization for Standards (ISO) and regulatory standards.
Forms a good relationship with the purchasing engineer and the supplier system in order to maintain a strong system and supplier relationships for the organization in which they work.
Provides cross functional help to select, approve and develop suppliers to meet customer and business needs
Ensures supplier selection, development, approval and rejection according to SJM vendor guidelines and requirements
Drives full assessment for effectiveness of supplier process control plans, measures and activities
Uses statistical techniques and professional judgment to research data for process improvement
Develops and guides execution of process validations and tests; explores resulting data and document results (protocols/reports)
Guides supplier process capability studies
Constructs Design of Experiments to characterize supplier processes and/or sets on root cause
Develops and implements procedures for new and/or improved supplier processes
Provides engineering help to Receiving Inspection including statistical research, measurement systems exploring, Gage R&R studies and inspection procedures
Participates in Material Review Board resolutions on supplier provided parts and services
Participates in supplier Quality System Improvement Plans
Guides the Supplier Requests for Change process
Performs supplier Quality System audits
Performs corrective and preventive actions with suppliers
Performs researches of non-conformances and supplier performance for key performance indicators
Performs dock-to-stock monitoring and part selection activities
Provides guidance to project teams for supplied component and supplier qualifications
Guides teams in identification of risks/hazards relative to new product designs, processes, suppliers and applications
Skillful and safe operation of job-related equipment
Rate and track supplier's performance and drive supplier continuous improvement
Establish and maintain supplier management processes and tools
The experience we're looking to add to our team:
6 years of supplier quality experince
Previous manufacturing experience
Corrective actions and audit experince
ISO9001
Audit certification( prefer)
What you'll receive for the great work you provide:
Full range of medical, dental, and vision plans
Life Insurance
Short-term and Long-term Disability
Matching 401(k) Contributions
Vacation and Paid Sick Time
Tuition Reimbursement
Job CategoryQuality
Is Sponsorship Available?
NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).
$71k-90k yearly est. Auto-Apply 41d ago
BMS Quality Manager (BQM) - Data Center Design, Engineering and Construction
Meta 4.8
Quality manager job in Columbia, SC
Meta is seeking an experienced Building Management System (BMS) Quality Manager to join our Data Center Engineering & Construction (DEC) Quality team. Our team's mission is to optimize the delivery of our Building Management Systems to ensure it is completed on time, is safe, robust, reliable, and conforms to our design and quality requirements. Role will be supporting internal cross-functional teams, lead installation and commissioning efforts, oversee quality, and quickly adapt in an evolving space.Our data centers are the foundation upon which our rapidly growing infrastructure efficiently operates, and our innovative services are delivered. Building and operating data centers the "right" way is synonymous with ensuring high uptime, capacity availability and capital conservation. The data center engineering team thinks from chip to chiller (or electrical substation), determining configurations and ensuring maximum efficiency of our compute infrastructure.
**Required Skills:**
BMS Quality Manager (BQM) - Data Center Design, Engineering and Construction Responsibilities:
1. Manage, onboard, and lead the General Contractor BMS Lead(s), the Control Systems Integrator (CSI) and Electrical and Installation (E&I) controls contractor s throughout all phases of the project, while developing efficiency improvements and incorporating lessons learned to ensure a safe, robust, reliable and functional controls system that adheres to Meta's design and quality requirements
2. Establish a clear vision and foster cross-functional collaboration, coordination, and support among on-site project teams, including the Meta BMS team, general contractors, Control System Integrators, and installation contractors
3. Drive consistency and standardization across all buildings and Control System Integrators and installation contractors
4. Review, understand and ensure project level adherence to the issued revision of the BMS PLC Playbook
5. Perform BMS inspections (wiring, installation, and commissioning) and validate the status/progress of the projects including supporting the project teams, both internal and external, starting from the early stages of Mechanical, Electrical and Plumbing (MEP) construction by working with project level Construction Managers (both internal and external) to check the health of the project (including schedule), working with the project teams and supporting Regional Quality Managers (RQMs). Align internally on program/project related communications to ensure a clear, consistent message to trade partners
6. Assess team performance, build relationships and to support the project benchmark and mock-up process of the BMS installations to assure consistency across the project while coordinating these efforts across multiple cross-functional partners, in a timely manner, to minimize re-work
7. Work with Construction Managers, Regional Quality Managers and General Contractors to ensure creation, accuracy and maintenance of logical schedule(s) for construction, commissioning, and packaged equipment BMS activities while leveraging this data to identify early finish dates for detailed design delivery
8. Coordinate and manage both packaged equipment factory installed controls audits and BMS commissioning audits to ensure specification/requirement adherence and track identified deficiencies through completion
9. Coordinate and lead large multi-stakeholder meetings on a regular basis and communicate discussions to all key stakeholders
10. Support custom tooling and their integration into the construction processes as well as supporting other cross-functional program/project initiatives that directly impact the delivery of the BMS while simultaneously working to identify and mitigate risk associated with these efforts
11. Travel domestically as needed (anticipated 40-50% travel)
**Minimum Qualifications:**
Minimum Qualifications:
12. Bachelor's degree (Engineering, Construction Management, or equivalent degree) or relevant work experience
13. 10+ years of experience with a combination of Instrumentation and Controls programming/installation, general contractor MEP coordination/project management, commissioning (both mechanical and electrical) of data centers, or other large scale mission critical buildings
14. Experience with Industrial Automation and Building Management Control Systems (i.e. PLC/DDC)
15. 3+ years of experience with programming/designing of HVAC control systems & Electrical Power Monitoring
**Preferred Qualifications:**
Preferred Qualifications:
16. Experience with PLC, SCADA and OPC UA systems
17. Experience with Schneider Electric Unity Pro, AVEVA, and Ignition platforms
18. Experience with Schneider Modicon and Rockwell Allen-Bradley PLC Platforms
19. Experience with Autodesk ACC Build and Procore Platforms
20. Certified in the following: cGMP, CAP (Certified Automation Professional), and/or PMP (Project Management Professional)
**Public Compensation:**
$150,000/year to $209,000/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@meta.com.
$150k-209k yearly 39d ago
Supervisor Quality
Zeus Industrial Products 4.7
Quality manager job in Orangeburg, SC
The Manufacturing Supervisor-Quality supervises all shift employees as assigned and complies with all safety, quality, productivity, and housekeeping standards.
• Two or more years of experience in a quality preferred
• High School Diploma required
• ASQ, CQT and/or CQE certification is preferred
• Attendance and punctuality are essential functions of this position. Any unscheduled absence or tardy will have a negative impact on our ability to meet our production objectives.
• Physical aspects of the job are defined on the Physical Demands Analysis located in HR.
• Maintains area quality system in compliance with ISO 9001:2000, UL/CSA, and specific customer requirements.
• Monitors effectiveness of inspection function and implements changes as needed.
• Initiates corrective and preventive action including investigation and resolution of customer complaints related to area of responsibility.
• Conducts system audits, process audits, and audits related to specific corrective and preventive actions. Evaluates and performs failure analysis on rejected material and communicates findings.
• Analyses quality data to identify improvement opportunities and initiates actions for improvement in area of responsibility.
• Provides training as needed to quality personnel and operators.
• Supervises inspection personnel.
• Reviews inspection records for accuracy and completeness.
• Reviews and approves test reports and shipping documentation.
• Monitors inspection data to ensure that daily goals are being met.
$58k-80k yearly est. Auto-Apply 6d ago
Quality Control Manager
Blythe Construction Inc. 3.9
Quality manager job in West Columbia, SC
Blythe Construction has lead development in North and South Carolina for over 90 years since our company's founding in 1921. In that time, our many generations of employees have completed thousands of contracts, from large highways to small commercial site development. Our company's history is one of continued evolution and growth. Beginning as a small independent asphalt development company, Blythe expanded its resources and influence through significant mergers throughout many years, eventually becoming part of the Vinci USA network extending from as far north as Maine to as far west as Texas.
General Description
The Quality Control Manager will help manage and lead efforts of the Asphalt Quality Control Department which includes managing the field and asphalt plant QC technicians.
Responsibilities
* Monitoring contractor's on-site construction activities and inspecting materials produced.
* Ensure compliance with plans, specifications and special provisions for the construction contract.
* Maintain detailed records of the contractor's daily quality operations and events that affect the worksite.
* Perform sampling and testing of component materials and completed work in accordance with the construction contract.
Key Duties
* Ability to lift materials weighing up to 60 lbs.
* Basic Math skills are used to compute test results
* Performs duties at multiple job sites
* Ability to read plans, specifications and MDOT design standards
* Prepare written reports
* Clean and maintain testing equipment
* Clean and maintain truck
* Perform other duties as assigned
* Performing jobsite testing as required by specifications and contract documents
* Performing product tests
* Enter QC Plans, addendums, test results, and checking sample data
* Must possess strong written and verbal communication skills and have the ability to interact with individuals at any level of the organization (i.e. plant production personnel, area managers, contractors, and agency representatives)
* Ability to problem-solve and work independently
* Prepare various QC reports and formulate specific recommendations to resolve or correct quality issues; and work with outside venders, agencies, and customers on a variety of quality related issues
Qualification Requirements
* General. To perform this job successfully, an individual must be able to perform each Key Duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* Education and Experience. This position typically is not an entry-level job, as it requires demonstrable previous experience as a Quality Control Manager. SCDOT Certified HMA Level 3 Quality Control Manager certification is required. A high school diploma or general education degree (GED) is preferred. One (1) or two (2) years of college or equivalent (e.g. trade school, specialized training)or more of industry related experience is required for this position, with an emphasis on roads, highways, and bridges. Must be able to understand work directions and communicate effectively with job site supervisors and fellow employees.
* Physical Demands. The following physical demands are representative of those that must be met by a Quality Control Manager to successfully perform the essential functions of this job.
* Constant physical effort, including standing, is required during a regular work shift of at least eight hours per day. Employee must be able to stand for extended periods of time, and to stoop, bend, and crouch as required to perform Key Duties.
* Ability to lift and carry, on a frequent basis, at least 30 pounds and, at times, as much as 50 pounds, as may be assigned.
* Physical dexterity involving stretching, proper placement of legs, and use of arms and hands in repetitive motions.
* Maintain constant alertness to the multiple concurrent activities including the activities of other employees and contractors, the operation of stationary equipment, and the movement of mobile equipment.
* Frequently walk on uneven surfaces, including natural ground in varying weather conditions.
* Work Environment. The work environment characteristics described below are representative of those that a Quality Control Manager encounters while performing the essential functions of this job.
* Work is performed outdoors in all weather conditions.
* Work environment periodically exposes the employees to high levels of noise, grease, and dust that is typically associated with a construction site.
* Employee regularly works near heavy equipment and moving machinery.
* Work may involve a variety of substances commonly found on a construction site such as form oil, grease, curing compounds, gasoline, diesel fuel and asphalt.
Company Benefits
* Top tier medical, dental, and vision coverage with HSA option
* Healthcare FSA and Dependent Care FSA
* Company-paid Life Insurance
* Company-paid Accidental Death and Dismemberment (AD&D) Insurance Plan
* Paid Vacation
* Paid Holidays
* Paid Parental Leave
* 401k Retirement Plan with employer match - up to 6%
* Annual Company Stock Purchasing Offering w/company match
* Fitness Plan Incentive
* Wellness Programs, Wellness coaching and Employee Assistance Program
We promote a Drug-Free Workplace.
EOE AA M/F/Vet/Disability are encouraged to apply
Equal Opportunity Employer, including disabled and veterans.
$71k-97k yearly est. 49d ago
Quality Assurance (QA) Technician- UT Level II
American Spiralweld Pipe Company, LLC
Quality manager job in Columbia, SC
Job Description
Tests, inspects, and approves products and samples at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. Assists in training new personnel as required.
Interprets engineering drawings, specifications, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards.
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, or mechanical characteristics.
Records test data, applying standard operating procedures.
Evaluates data and writes reports to validate or indicate deviations from existing standards.
Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics.
Enters data into computer for analysis.
Observes in-process operations to ensure compliance with customer specifications for manufacturing, such as pre-heating pipe, hydro testing, roundness.
Performs visual inspection of finished goods to ensure compliance with customer specifications.
May be required to calibrate lab equipment to conform to legal and manufacturing requirements.
Coordinates calibrations of production equipment, QA tests, and NDE equipment as needed.
Assist in training new personnel in QA functions.
Performs other duties as instructed by supervision.
MINIMUM QUALIFICATIONS
Must be able to work 2nd Shift schedule.
Must be physically able to perform the essential functions of the job, with or without reasonable accommodations.
Must be able to read and comprehend simple instructions, short correspondence, and memos.
Must be able to write simple correspondence.
Must be able to effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization.
Must be able to compute basic arithmetic problems and accurately operate a calculator.
Must be able to perform these operations using units of American money and weight measurement, volume, and distance.
Must be able to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.
Must be able to deal with problems involving a few concrete variables in standardized situations.
Must be able to read, write and effectively communicate in English.
PREFERRED QUALIFICATIONS
Knowledge of welding processes; experience as a welder.
UT Level II Certified.
ESSENTIAL PHYSICAL FUNCTIONS
The employee is regularly required to use hands to finger, handle, or feel and talk or hear.
The employee is frequently required to stand; walk and stoop, kneel, crouch, or crawl.
The employee is occasionally required to sit; reach with hands and arms and climb or balance.
The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and ability to adjust focus.
$63k-100k yearly est. 2d ago
Quality Supervisor
Vac Magnetics LLC
Quality manager job in Sumter, SC
The Quality Supervisor supports the overall quality function by managing quality technicians, overseeing inspection processes, and ensuring product conformance to specifications. This role is not customer-facing but plays a critical part in supporting the Quality Engineer through hands-on problem-solving, data collection, and the enforcement of quality standards across production processes.
ESSENTIAL DUTIES:
Responsible for supervising daily quality inspection activities to ensure timely and accurate execution of quality checks on incoming, in-process, and finished goods.
Lead and mentor the quality technician team to ensure proper understanding and execution of quality protocols, documentation, and inspection methods.
Support the Quality Engineer in implementing corrective actions, process audits, and root cause investigations related to internal non-conformances.
Ensure calibration and proper use of metrology tools and equipment (micrometers, calipers, CMM, optical devices, etc.).
Manage quality documentation, including inspection records, non-conformance reports, rework logs, and internal audit findings.
Conduct layered process audits, Gemba walks, and product checks to confirm adherence to standard work and quality control plans.
Monitor and report key performance indicators (KPIs) such as scrap, rework, and defect rates; assist in driving continuous improvement initiatives.
Support training programs related to quality standards, measurement tools, and inspection methods.
Assist in preparation for audits by internal teams, regulatory bodies, or certifying agencies.
Ensure workplace safety practices are upheld within the quality area.
Maintain quality area housekeeping and 5S standards.
Escalate quality concerns or abnormal conditions promptly to the Quality Engineer or Quality Manager.
QUALIFICATIONS:
Solid understanding of quality inspection tools and techniques; working knowledge of ISO 9001 or IATF 16949 standards preferred.
Demonstrated experience with inspection documentation, control plans, and non-conformance handling.
Detail-oriented with strong communication, documentation, and organizational skills.
Experience using Microsoft Office (Word, Excel, Outlook); familiarity with ERP or quality management systems is a plus.
Ability to read and interpret blueprints, technical drawings, and quality standards.
Familiarity with basic statistical tools and root cause analysis methods (e.g., 5 Whys, Fishbone).
Education and/or Experience:
Associate degree in a technical or manufacturing-related field required; Bachelor's degree preferred.
3+ years of quality experience in a manufacturing environment, preferably with 1+ year in a leadership or supervisory role.
PHYSICAL DEMANDS AND WORK ENVIRONMENT:
The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Physical demands: While performing the duties of this job, the associate may occasionally be required to stand, sit, use hands to handle or feel, reach with hands and arms, climb stairs, balance, stoop, kneel, crouch, or crawl. The associate must occasionally lift and/or move up to 25 pounds. Vision requirements include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to focus.
Work Environment: The role requires exposure to both office and manufacturing environments. The associate may work in supplier facilities during audits or problem resolution. PPE may be required in certain environments.
EMPLOYMENT AT WILL
This job description is intended as an outline of the duties of the position at VAC Magnetics LLC and is subject to change by VAC from time to time. It is NOT a contract of employment. Employment at VAC is voluntarily entered into and is subject to termination by you or VAC AT WILL, with or without cause at any time either party believes such action to be appropriate.
$45k-72k yearly est. 23d ago
Quality Coordinator (Certification Auditor)
Atimetals
Quality manager job in Richburg, SC
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us.
Primary Purpose of this Job
The primary purpose of this job is to execute internal audit policies and procedures to ensure compliance of material for release through certification or recertification to required standards, specifications, established organizational systems, policies and procedures, technical and additional customer requirements.
Essential Functions
(other duties may be assigned)
Access and analyze data/information from a wide variety of applications and sources to prepare the package for audit.
Prepare Certificate of Test in compliance with all purchase orders, specification, organizational policies, and procedures
Identify, locate, read, understand, and interpret product-specific industry and customer specifications, process outlines, customer documentation, end-user documents, etc.
Consult and interact with intersecting departments (sales, product engineering, lab, document control, and central quality) during the audit process (i.e. obtain needed information, specifications, clarifications, and customer acceptance)
Perform heat file audits, and compile audit check sheets when applicable
Identify missing and/or incorrect testing or processing
Recertification of depot material as well as issue amended and corrected certifications.
Able to work independently and as part of a larger team
$42k-67k yearly est. 7h ago
Quality Coordinator (Certification Auditor)
Atimaterials
Quality manager job in Richburg, SC
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us.
Primary Purpose of this Job
The primary purpose of this job is to execute internal audit policies and procedures to ensure compliance of material for release through certification or recertification to required standards, specifications, established organizational systems, policies and procedures, technical and additional customer requirements.
Essential Functions
(other duties may be assigned)
Access and analyze data/information from a wide variety of applications and sources to prepare the package for audit.
Prepare Certificate of Test in compliance with all purchase orders, specification, organizational policies, and procedures
Identify, locate, read, understand, and interpret product-specific industry and customer specifications, process outlines, customer documentation, end-user documents, etc.
Consult and interact with intersecting departments (sales, product engineering, lab, document control, and central quality) during the audit process (i.e. obtain needed information, specifications, clarifications, and customer acceptance)
Perform heat file audits, and compile audit check sheets when applicable
Identify missing and/or incorrect testing or processing
Recertification of depot material as well as issue amended and corrected certifications.
Able to work independently and as part of a larger team
$42k-67k yearly est. 7h ago
Director, Quality & Compliance Training (Princeton, Hybrid)
Otsuka America Pharmaceutical Inc. 4.9
Quality manager job in Columbia, SC
The Director, Quality & Compliance Training, is a senior leader within the Learning Center of Excellence under Global Quality. This role is responsible for developing and executing global training strategies for various functions (e.g., Commercial, Finance, HR, Legal, and other General & Administrative areas). The position ensures that learning programs drive business performance, compliance with corporate standards, and foster a culture of continuous development across the organization.
**Key Responsibilities:**
**Strategic Leadership & Governance**
+ Define and lead the global training strategy aligned with corporate objectives and quality principles.
+ Establish governance frameworks for training compliance and operational excellence, including policies and SOPs.
+ Serve as a key advisor to senior leadership on learning trends, capability-building strategies, and risk mitigation.
**Program Development & Delivery**
+ Design and oversee training programs for Commercial and G&A functions, ensuring relevance and scalability.
+ Implement innovative learning solutions leveraging adult learning principles, digital platforms, and blended learning approaches.
+ Ensure training content aligns with corporate standards and supports organizational priorities.
**Stakeholder Engagement & Collaboration**
+ Partner with functional leaders, HR, and Quality to identify learning needs and align initiatives with business goals.
+ Act as a trusted advisor to senior leadership on training effectiveness and workforce capability development.
**Continuous Improvement & Analytics**
+ Define KPIs and leverage data analytics to measure training impact and drive enhancements.
+ Stay current with industry best practices, emerging technologies, and evolving business needs to continuously improve learning programs.
**Operational Oversight**
+ Collaborate with training operations teams to ensure efficient delivery and compliance tracking.
+ Oversee vendor relationships for training services and technology solutions
**Qualifications:**
+ Bachelor's degree required; advanced degree in Life Sciences, Education, Organizational Development, or related field preferred.
+ 10+ years in pharmaceutical or life sciences industry with significant experience designing and implementing global training programs.
+ Proven track record in designing and implementing global training programs and managing cross-functional teams.
+ Strong understanding of R&D functions and the regulatory landscape (GxP, ICH, FDA, EMA, etc.).
+ Proven ability to design and deliver impactful learning programs using adult learning principles.
+ Experience with learning technologies (e.g., LMS, virtual learning platforms) and data-driven training strategies.
+ Excellent communication, collaboration, and stakeholder engagement skills.
**Preferred Attributes:**
+ Strategic thinker with a passion for scientific learning and development.
+ Agile and adaptable in a fast-paced, matrixed environment.
+ Strong project management and organizational skills.
+ Committed to fostering innovation, compliance, and continuous improvement through learning.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $164,530.00 - Maximum $245,985.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
$164.5k yearly 53d ago
Supervisor Quality
Zeus 4.7
Quality manager job in Orangeburg, SC
The Manufacturing Supervisor-Quality supervises all shift employees as assigned and complies with all safety, quality, productivity, and housekeeping standards.
$58k-80k yearly est. Auto-Apply 6d ago
Quality Assurance (QA) Technician- UT Level II
American Spiralweld Pipe Company
Quality manager job in Columbia, SC
Tests, inspects, and approves products and samples at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. Assists in training new personnel as required.
Interprets engineering drawings, specifications, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards.
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, or mechanical characteristics.
Records test data, applying standard operating procedures.
Evaluates data and writes reports to validate or indicate deviations from existing standards.
Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics.
Enters data into computer for analysis.
Observes in-process operations to ensure compliance with customer specifications for manufacturing, such as pre-heating pipe, hydro testing, roundness.
Performs visual inspection of finished goods to ensure compliance with customer specifications.
May be required to calibrate lab equipment to conform to legal and manufacturing requirements.
Coordinates calibrations of production equipment, QA tests, and NDE equipment as needed.
Assist in training new personnel in QA functions.
Performs other duties as instructed by supervision.
MINIMUM QUALIFICATIONS
Must be able to work 2nd Shift schedule.
Must be physically able to perform the essential functions of the job, with or without reasonable accommodations.
Must be able to read and comprehend simple instructions, short correspondence, and memos.
Must be able to write simple correspondence.
Must be able to effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization.
Must be able to compute basic arithmetic problems and accurately operate a calculator.
Must be able to perform these operations using units of American money and weight measurement, volume, and distance.
Must be able to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.
Must be able to deal with problems involving a few concrete variables in standardized situations.
Must be able to read, write and effectively communicate in English.
PREFERRED QUALIFICATIONS
Knowledge of welding processes; experience as a welder.
UT Level II Certified.
ESSENTIAL PHYSICAL FUNCTIONS
The employee is regularly required to use hands to finger, handle, or feel and talk or hear.
The employee is frequently required to stand; walk and stoop, kneel, crouch, or crawl.
The employee is occasionally required to sit; reach with hands and arms and climb or balance.
The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and ability to adjust focus.
$63k-100k yearly est. 30d ago
Pend Management Coordinator
Datavant
Quality manager job in Columbia, SC
Datavant is a data platform company and the world's leader in health data exchange. Our vision is that every healthcare decision is powered by the right data, at the right time, in the right format. Our platform is powered by the largest, most diverse health data network in the U.S., enabling data to be secure, accessible and usable to inform better health decisions. Datavant is trusted by the world's leading life sciences companies, government agencies, and those who deliver and pay for care.
By joining Datavant today, you're stepping onto a high-performing, values-driven team. Together, we're rising to the challenge of tackling some of healthcare's most complex problems with technology-forward solutions. Datavanters bring a diversity of professional, educational and life experiences to realize our bold vision for healthcare.
As Datavant's PEND Management Coordinator, you will be responsible for managing PEND inventory, coordinating closely with Client, Provider, and Datavant Operations Teams to coordinate the release of medical records requests.
**You will:**
+ Participate in outbound and inbound calling campaigns
+ Retrieves charts from electronic medical record systems and compile medical records to send to other parties for coding
+ Log all call transactions into the designated computer software system(s)
+ Requests medical records by making outbound phone calls to provider groups and resolve schedule issues as required
+ Completes supplemental medical records requests using Excel files
+ Assist with providing updated member and provider information to operations teams as required, including researching bad data as necessary
+ Directs medical record requests to the responsible party
+ Resolves outstanding vendor pending request within a timely manner
+ Assist with resolving technical issues related to data reporting issues
+ Assist with ad hoc requests
+ Responsible to meet company set performance goals (KPIs)
+ Adhere to the Company's code of Conduct and policies and maintain HIPPA compliance
**What you will bring to the table:**
+ High school diploma or equivalent
+ 2+ year of experience in medical records, medical record coding or a related field, preferred
+ Prior outbound/sales/collections/call center experience preferred
+ Understanding of medical terminology and HIPAA medical privacy regulations, preferred
+ Proficient time management, problem solving and analytical skills
+ Self-motivated and dependable - must excel in a minimally supervised role
+ Schedule flexibility; schedule may include hours outside of normal shift and weekends
+ Ability to receive coaching from Supervisor in a constructive/positive manner
+ Exceptional attention to detail with high level of accuracy
+ Experience meeting changing requirements/priorities, and meeting deadlines
+ Ability to deal with personnel at all levels, exercise discretion of all confidential health information, and ensure compliance with HIPAA standards
+ Ability to multi-task with high degree of organization and time management skills
+ Proficient in entire MS Suite with heavy emphasis on Excel skills and Email Appreciation and understanding of the medical record retrieval industry
+ Clear and concise verbal and written communication skills
+ Ability to work autonomously in a fast-paced environment
+ Track, report and prioritize scheduled retrieval locations
+ Make independent decisions regarding the hoc documentation to Provider Group that contains Protected Healthcare Information (PHI) and Personally Identifiable Information (PII)
+ Ability to work on multiple long-term projects concurrently to include balancing resources and priorities to different projects along their life cycle
+ Excellent Time Management skills
+ Must be extremely detail oriented
+ Ability to Research and ungroup orgs, detailed understanding and competency in the use of Chart Finder
+ Exceptional Verbal and Written Communication skills
+ Assist with additional work duties or responsibilities as evident or required
+ Understand and analyze project data to identify trends related to project goals and act accordingly within the organization
+ Work within client project management to create frameworks to ensure projects are completed on time
+ Comprehensive understanding of Datavant and Client processes to include intake methods/processes; the workflows between Outreach and
+ Onsite/Remote teams; Onsite/Remote workflows; Offsite Scheduling
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
Our compensation philosophy is to be externally competitive, internally fair, and not win or lose on compensation. Salary ranges for this position are developed with the support of benchmarks and industry best practices.
_At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your responses will be_ _anonymous and_ _used to help us identify areas of improvement in our recruitment process._ _(_ _We can only see aggregate responses, not individual responses. In fact, we aren't even able to see if you've responded or not_ _.)_ _Responding is your choice and it will not be used in any way in our hiring process_ _._
Pay ranges for this job title may differ based on location, responsibilities, skills, experience, and other requirements of the role.
The estimated base pay range per hour for this role is:
$16.29-$19.69 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (************************************************** . Know Your Rights (*********************************************************************** , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (************************************************************** Id=**********48790029&layout Id=**********48795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (******************************************************************************************************* . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (**************************************** .
How much does a quality manager earn in Columbia, SC?
The average quality manager in Columbia, SC earns between $53,000 and $125,000 annually. This compares to the national average quality manager range of $64,000 to $128,000.
Average quality manager salary in Columbia, SC
$82,000
What are the biggest employers of Quality Managers in Columbia, SC?
The biggest employers of Quality Managers in Columbia, SC are: