Post job

Quality assurance manager jobs in Lexington, KY - 39 jobs

All
Quality Assurance Manager
Director Of Quality
Quality Engineer
Quality Assurance
Senior Quality Manager
Microbiology Laboratory Manager
Quality Manager
Quality Assurance Specialist
Quality Assurance Engineering Manager
Quality Lead
Manager, Quality Engineer
Assistant Manager Quality Management
Quality Specialist
Quality Control Engineer
  • Director, Global Quality GMP Processes

    Otsuka America Pharmaceutical Inc. 4.9company rating

    Quality assurance manager job in Frankfort, KY

    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 30d ago
  • Job icon imageJob icon image 2

    Looking for a job?

    Let Zippia find it for you.

  • Director, Quality - Life Sciences

    Datavant

    Quality assurance manager job in Frankfort, KY

    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 37d ago
  • Director of Quality- SOF GLSS 2 Program

    Vectrus (V2X

    Quality assurance manager job in Lexington, KY

    This position is contingent upon contract award. Key Responsibilities * Develop and implement the SOF GLSS quality management strategy in alignment with contract requirements and USSOCOM objectives. * Lead Quality Assurance and Quality Control teams across multiple CONUS and OCONUS sites. * Ensure compliance with applicable standards and regulations, including ISO 9001, AS9100, DCMA, DoD, and USSOCOM directives. * Oversee internal and external audits, government surveillance activities, and corrective action processes. * Establish and monitor key performance indicators (KPIs) tied to contract deliverables and readiness metrics. * Collaborate with engineering, logistics, supply chain, and program management teams to resolve quality issues and enhance system reliability. * Manage document control, training programs, and quality certifications across the SOF GLSS enterprise. * Serve as the primary interface with USSOCOM quality representatives, DCMA, and other oversight entities. * Lead root cause analysis and continuous improvement initiatives focused on lifecycle sustainment and field support. * Promote a culture of quality and compliance through proactive leadership, communication, and training. Qualifications * Bachelor's degree in Engineering, Quality Management, or related field (Master's preferred). * 10+ years of progressive experience in quality assurance/control, with at least 5 years in a leadership role supporting DoD or federal contracts. * Strong knowledge of DoD acquisition regulations, FAR/DFARS, and government quality oversight practices. * Proven experience with CAPA, Six Sigma, Lean, and performance-based logistics (PBL) environments. * Excellent leadership, communication, and stakeholder engagement skills. * Experience with ERP systems and quality management platforms (e.g., AS9100-compliant systems). Preferred Certifications * Certified Quality Auditor (CQA) * Certified Manager of Quality/Organizational Excellence (CMQ/OE) * Six Sigma Black Belt or Lean Certification * ASQ or equivalent professional membership * Familiarity with DCMA surveillance protocols and government audit readiness Employee benefits include the following: * Healthcare coverage * Life insurance, AD&D, and disability benefits * Retirement plan * Wellness programs * Paid time off, including holidays and leave of absences * Eligible Tuition Reimbursement * Learning and Development resources * Employee assistance resources Pay and benefits are subject to change at any time and may be modified at the discretion of the company, consistent with the terms of any applicable compensation or benefit plans.
    $96k-132k yearly est. 60d+ ago
  • Director of Quality- SOF GLSS 2 Program

    V2X Current Openings

    Quality assurance manager job in Lexington, KY

    is contingent upon contract award. Key Responsibilities Develop and implement the SOF GLSS quality management strategy in alignment with contract requirements and USSOCOM objectives. Lead Quality Assurance and Quality Control teams across multiple CONUS and OCONUS sites. Ensure compliance with applicable standards and regulations, including ISO 9001, AS9100, DCMA, DoD, and USSOCOM directives. Oversee internal and external audits, government surveillance activities, and corrective action processes. Establish and monitor key performance indicators (KPIs) tied to contract deliverables and readiness metrics. Collaborate with engineering, logistics, supply chain, and program management teams to resolve quality issues and enhance system reliability. Manage document control, training programs, and quality certifications across the SOF GLSS enterprise. Serve as the primary interface with USSOCOM quality representatives, DCMA, and other oversight entities. Lead root cause analysis and continuous improvement initiatives focused on lifecycle sustainment and field support. Promote a culture of quality and compliance through proactive leadership, communication, and training. 🔹 Qualifications Bachelor's degree in Engineering, Quality Management, or related field (Master's preferred). 10+ years of progressive experience in quality assurance/control, with at least 5 years in a leadership role supporting DoD or federal contracts. Strong knowledge of DoD acquisition regulations, FAR/DFARS, and government quality oversight practices. Proven experience with CAPA, Six Sigma, Lean, and performance-based logistics (PBL) environments. Excellent leadership, communication, and stakeholder engagement skills. Experience with ERP systems and quality management platforms (e.g., AS9100-compliant systems). 🔹 Preferred Certifications Certified Quality Auditor (CQA) Certified Manager of Quality/Organizational Excellence (CMQ/OE) Six Sigma Black Belt or Lean Certification ASQ or equivalent professional membership Familiarity with DCMA surveillance protocols and government audit readiness Employee benefits include the following: Healthcare coverage Life insurance, AD&D, and disability benefits Retirement plan Wellness programs Paid time off, including holidays and leave of absences Eligible Tuition Reimbursement Learning and Development resources Employee assistance resources Pay and benefits are subject to change at any time and may be modified at the discretion of the company, consistent with the terms of any applicable compensation or benefit plans.
    $96k-132k yearly est. 60d+ ago
  • Director of Quality- SOF GLSS 2 Program

    V2X

    Quality assurance manager job in Lexington, KY

    is contingent upon contract award.** **Key Responsibilities** + Develop and implement the SOF GLSS quality management strategy in alignment with contract requirements and USSOCOM objectives. + Lead Quality Assurance and Quality Control teams across multiple CONUS and OCONUS sites. + Ensure compliance with applicable standards and regulations, including ISO 9001, AS9100, DCMA, DoD, and USSOCOM directives. + Oversee internal and external audits, government surveillance activities, and corrective action processes. + Establish and monitor key performance indicators (KPIs) tied to contract deliverables and readiness metrics. + Collaborate with engineering, logistics, supply chain, and program management teams to resolve quality issues and enhance system reliability. + Manage document control, training programs, and quality certifications across the SOF GLSS enterprise. + Serve as the primary interface with USSOCOM quality representatives, DCMA, and other oversight entities. + Lead root cause analysis and continuous improvement initiatives focused on lifecycle sustainment and field support. + Promote a culture of quality and compliance through proactive leadership, communication, and training. **** **Qualifications** + Bachelor's degree in Engineering, Quality Management, or related field (Master's preferred). + 10+ years of progressive experience in quality assurance/control, with at least 5 years in a leadership role supporting DoD or federal contracts. + Strong knowledge of DoD acquisition regulations, FAR/DFARS, and government quality oversight practices. + Proven experience with CAPA, Six Sigma, Lean, and performance-based logistics (PBL) environments. + Excellent leadership, communication, and stakeholder engagement skills. + Experience with ERP systems and quality management platforms (e.g., AS9100-compliant systems). **** **Preferred Certifications** + Certified Quality Auditor (CQA) + Certified Manager of Quality/Organizational Excellence (CMQ/OE) + Six Sigma Black Belt or Lean Certification + ASQ or equivalent professional membership + Familiarity with DCMA surveillance protocols and government audit readiness **Employee benefits include the following:** + Healthcare coverage + Life insurance, AD&D, and disability benefits + Retirement plan + Wellness programs + Paid time off, including holidays and leave of absences + Eligible Tuition Reimbursement + Learning and Development resources + Employee assistance resources _Pay and benefits are subject to change at any time and may be modified at the discretion of the company, consistent with the terms of any applicable compensation or benefit plans._ Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (**************************** notice from the Department of Labor.
    $96k-132k yearly est. 60d+ ago
  • Manager Quality Assurance

    Hilton 4.5company rating

    Quality assurance manager job in Frankfort, KY

    _\*\*\*This position will be Remote, but with a preference for candidates in Ohio, Missouri, Texas or Louisiana\*\*\*_ This is your chance to be part of an in\-house Brands team of industry experts in the domains of hospitality, brand management, innovation, food and beverage, wellness, owner relations, and more, for all of Hilton's unique brands\! As Manager, QA Auditor, you will support the team that leads our brands with the steadfast goal of strengthening and growing the Hilton portfolio\. On the Brands team reporting to Area Manager Quality Assurance, you will perform numerous QA audits and have responsibility for 100 hotels in your territory\. Your main duty is to protect the integrity of the brands inspected in terms of cleanliness, condition, guest safety, and brand standards\. **HOW WE WILL SUPPORT YOU** Hilton is proud to support the mental and physical wellbeing of all Team Members so they can Thrive personally and professionally in a diverse and inclusive environment, thanks to programs and benefits such as: + Go Hilton travel program: 110 nights of discounted travel with room rates as low as $40/night + Hilton Shares: Our employee stock purchase program \(ESPP\) \- you can purchase Hilton shares at a 15 percent discount + Paid parental leave for eligible Team Members, including partners and adoptive parents + Mental health resources including free counseling through our Employee Assistance Program + Paid Time Off \(PTO\) + Learn more about the rest of our benefits \(****************************************** At Hilton, we believe every Team Member is a leader\. We are committed to offering leadership development opportunities and programs through every step of a Team Member's career journey and at every level, both in our hotels and across corporate\. \*\*Available benefits may vary depending upon terms and conditions of employment and are subject to the terms and conditions of the plans\. **HOW YOU WILL MAKE AN IMPACT** Your role is important and below are some of the fundamental job duties that make your work unique\. **What your day\-to\-day will be like:** + Perform routine Quality Assurance evaluations\. + Address inquiries and communications made internally, both verbally and in written communications\. + Monitor expenses incurred from travel completed/scheduled, both based upon monthly and yearly goals\. + Participate in Consistency exercises\. + Participate in activities outside of QA to gain a better knowledge of other departments\. **How you will collaborate with others:** + Communicate with Quality Auditors, Area Managers in QA, Directors, Vice President of QA, Brand teams, Design and Construction, and Human Resources to answer inquiries about brand standard compliance, QA, brand protocol, procedures, and Improvement Plans\. **What projects you will take ownership of:** + Coordinate upcoming activities such as travel plans and hotel scheduling, ensuring downtime work is completed and submitted by established deadlines\. **WHY YOU'LL BE A GREAT FIT** **You have these minimum qualifications:** + Five \(5\) years of management experience \- Hotel Operations + Three \(3\) years of experience as a General Manager, Executive Committee Member, or Director + Valid Driver's license + Travel 90% of the time **It would be useful if you have:** + BA/BS Bachelor's Degree + Fluency in a foreign language + Food Safety certification + Project management skills + Working knowledge of product replacement cycles, renovations and physical upgrades + Problem resolution and consulting skills to mitigate potential conflicts/issues with general managers, owners, and/or internal customers while upholding the integrity of the brand + Current resident in the states of Ohio, Missouri, Texas, or Louisiana **WHAT IT IS LIKE WORKING FOR HILTON** Hilton, the \#1 World's Best Workplace, is a leading global hospitality company with a diverse portfolio of world\-class brands \(**************************************** \. Dedicated to filling the earth with the light and warmth of hospitality, we have welcomed more than 3 billion guests in our more\-than 100\-year history\. Hilton is proud to have an award\-winning workplace culture and we are consistently named among one of the World's Best Workplaces\. Check out the Hilton Careers blog \(************************************** and Instagram \(******************************************** to learn more about what it's like to be on Team Hilton\! We provide reasonable accommodations to qualified persons with disabilities to perform the essential functions of the position and provide other benefits and privileges of employment in accordance with applicable law\. Please contact us \(https://cdn\.phenompeople\.com/CareerConnectResources/prod/HILTGLOBAL/documents/Applicant\_Accommodation\_and\_Accessibility\_Assistance\-English\-20************253430519\.pdf\) if you require an accommodation during the application process\. Hilton offers its eligible team members a comprehensive benefits package including medical and prescription drug coverage, dental coverage, vision coverage, life insurance, short\-and long\-term disability insurance, access to our employee stock purchase plan \(ESPP\) where you can purchase Hilton shares at a 15 percent discount, a 401\(k\) savings plan, 20 days of paid time off accruing over your first year of employment and increasing up to 25 days after completing one year of full employment, up to 12 weeks of paid leave for birth parents and 4 weeks for non\-birth parents, 10 paid holidays and 2 floating holidays throughout the year, up to 5 bereavement days, flexible spending accounts, a health savings account, an employee assistance program, access to a care coordination program \("Wellthy"\), a legal services program, an educational assistance program, adoption assistance, a backup childcare program, pre\-tax commuter benefit and our travel discount\. The annual salary range for this role is $75,000 \- $100,000 and is determined based on applicable and specialized experience and location\. Subject to plan terms and conditions, you will be eligible to participate in the Hilton Annual Incentive \(Bonus\) Plan, consistent with other team members at the same level and/or position within the Company\.\#LI\-REMOTE **Job:** _Brands_ **Title:** _Manager Quality Assurance_ **Location:** _null_ **Requisition ID:** _COR015IF_ **EOE/AA/Disabled/Veterans**
    $75k-100k yearly 29d ago
  • Manager, Data Quality

    Dodge Construction Network

    Quality assurance manager job in Frankfort, KY

    The Manager, Data Quality, is responsible for overseeing the full data management lifecycle and operational workflow of Company Entity Management (CEM) for company and contact data within Dodge Construction Network's (Dodge) master data ecosystem. This role leads both onshore and offshore teams to ensure the accuracy, completeness, and standardization of company entities that power Dodge's products, customer experiences, and analytics. The Manager will define and execute the end-to-end operating model for CEM including the development of Standard Operating Procedures (SOPs), establishing KPIs, designing quality and governance frameworks, and defining requirements for automation and human-in-the-loop workflows. This role drives continuous improvement by refining processes, enhancing data sourcing and enrichment, evaluating automation outputs, and collaborating closely with cross-functional partners across Product, Engineering, and Operations. This leader must bring strong people management and project management skills, an analytical mindset, and have experience working in scalable data operations environments. This is a full-time position and reports directly to the Director of Data Acquisition. **_Preferred Location_** + This is a remote, home-office-based role, and candidates located in the continental United States will be considered. + For this position, there is a preference to hire in the Central and Eastern Time Zone; however, candidates in other areas/time zones would be considered as well. **_Travel Requirements_** Expected travel is minor for this role. **_Essential Functions_** + Design, maintain, and improve company and contact entity workflows, SOPs, SLAs, and quality standards + Define and track KPIs for team efficiency, business impact, financial stewardship, and client satisfaction + Oversee entity creation, updates, merges, conflict resolution, and exception handling + Partner with automation, engineering, and data science to integrate and optimize human-in-the-loop and machine-assisted processes + Analyze performance patterns to identify automation gaps, reduce manual interventions, and continuously improve processes + Lead, mentor, and develop CEM team members + Establish performance expectations, work allocation, and capacity planning + Manage relationships with third party data providers and offshore vendors + Collaborate closely with Engineering, Product, Sourcing, and Sales to align CEM standards with business and platform needs + Participate in roadmap discussions, attribute model design, and classification/taxonomy updates **_Education Requirement_** Bachelor's degree in Information Systems, Data Analytics, Supply Chain Management, Computer Science, Engineering, Operational Management, or related technical fields or equivalent education and work experience. **_Required Experience, Knowledge and Skills_** + 7+ years of experience in data operations, master data management, digital operations, or business transformation + 2+ years managing teams + Proven experience managing both onshore and offshore teams + Experience with SQL and/or Python programming + Advanced problem solving and data driven decision making capabilities + Proven record of managing external vendor relationships + Ability to translate technical concepts into actional business insights for non-technical stakeholders + Experience with automation tools, scraping frameworks, and data pipelines + Exposure to data operations utilizing machine learning and data enrichment techniques + Proficiency in data governance, KPI management, and quality assurance + Strong project management skills, including planning, prioritization, and execution of change management + Excellent written and verbal communication skills for presenting strategies, reporting performance metrics, and building relationships with stakeholders **_Preferred Experience, Knowledge and Skills_** + Data Visualization tools such as AWS Quicksight, PowerBI, Tableau + Knowledge of construction industry or content workflows a plus + Experience with salesforce a plus + Familiarity with cloud-based data environments + Familiarity with Jira/Confluence **_About Dodge Construction Network_** Dodge Construction Network exists to deliver the comprehensive data and connections the construction industry needs to build thriving communities. Our legacy is deeply rooted in empowering our customers with transformative insights, igniting their journey towards unparalleled business expansion and success. We serve decision-makers who seek reliable growth and who value relationships built on trust and quality. By combining our proprietary data with cutting-edge software, we deliver to our customers the essential intelligence needed to excel within their respective landscapes. We propel the construction industry forward by transforming data into tangible guidance, driving unparalleled advancement. Dodge is the catalyst for modern construction. **_Salary Disclosure_** Dodge Construction Network's compensation and rewards package for full time roles includes a market competitive salary, comprehensive benefits, and, for applicable roles, uncapped commissions plans or an annual discretionary performance bonus. **_For this role, we are only considering candidates who are legally authorized to work in the United States and who do not now or in the future require sponsorship for employment visa status._** **_A background check is required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job and consistent with all federal state and local ordinances._** **_Reasonable Accommodation_** **_Dodge Construction Network is committed to recruiting, hiring, and promoting people with disabilities. If you need an accommodation or assistance completing the online application, please email_** **_***************************_** **_._** **_Equal Employment Opportunity Statement_** **_Dodge Construction Network is an Equal Opportunity Employer. We are committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All employment decisions shall be based on merit, qualifications, and business needs without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, pregnancy, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law._** \#LI-Remote \#LI-CS1 \#DE-Remote \#DE-2026-22
    $68k-107k yearly est. 6d ago
  • CypJob: Future Assurance Orchestrator_Bplb5Bv9

    B6001Test

    Quality assurance manager job in Brodhead, KY

    Full-time Description Directives International Director Requirements Vis spectaculum vulgaris patria cras pauper theatrum vehemens. Optio vacuus tardus acidus amoveo umerus. Damno cattus sed armarium. Voluptate casus cornu conservo quidem concido calcar.
    $88k-129k yearly est. 60d+ ago
  • BMS Quality Manager (BQM) - Data Center Design, Engineering and Construction

    Meta 4.8company rating

    Quality assurance manager job in Frankfort, KY

    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@fb.com.
    $150k-209k yearly 26d ago
  • Manufacturing Quality Assurance Specialist

    Piramal Enterprises Ltd.

    Quality assurance manager job in Lexington, KY

    Business: Pharma Solutions Department: Quality Assurance Job Overview The primary purpose of the role is to perform In-process Process QA activities, the environmental monitoring of facilities and Utility systems, Audits and QMS support according to Good Manufacturing Practices (GMP) and site specific Standard Operating Procedures (SOP). Reporting Structure This position reports to the Quality Assurance Supervisors Shift Night Shift Key Responsibilities: Acquire an understanding of aseptic technique, continuously exhibit proper clean room behaviour, and adhere to cGMPs. Perform all In-process QA activities, inspection, labeling and packaging Line clearances following as per company SOP's. Review executed batch records and executed protocols and meet the batch disposition timelines as per business requirement. Perform environmental monitoring of classified cleanroom areas (Viable Surface/air, Non-Viable air) Sampling and lab testing of the utilities including water, steam, and compressed gases. Perform plate enumeration and documentation of the results. Assist in the performance and documentation for cleaning verification sample collection and analysis. Participates in audits and involve in onsite client interactions as needed by management. Maintain laboratory instrumentation required for testing including calibrations. Aide in the maintenance of environmental monitoring trend data to drive continuous improvements and identify trends. Participate in Microbiology material inventory control for EM media plates. Prepare and summarize data associate with site metrics, write, read, and revise SOP's QA and EM, technical reports. Conduct GMP investigations; specifically root cause analyses, risk assessments, and impact evaluations per PPS QMS systems. Adhere to all applicable regulations, policies, and procedure for health, safety, environmental compliance and support the Quality management as needed basis. QUALIFICATIONS: Bachelor's Degree in physical or biological sciences or related scientific field preferred 1 years of Quality assurance or Environmental monitoring experience performing quality related activities within a pharmaceutical manufacturing environment Must have previous experience working within QA Plant support (IPQA /EM), strict regulatory guidelines, cGMP or FDA Prior knowledge and/or ability to understand and follow job related regulatory requirements (cGMP, OSHA, FDA) Proficiency in the Microsoft Office applications (Word, Excel, Outlook and Access) Demonstrated ability to effectively communicate both verbally and in writing Ability to read and follow written instructions Detail oriented Understanding of sterile manufacturing preferred Technical writing skills preferred
    $39k-65k yearly est. Auto-Apply 47d ago
  • LAB-QUALITY & ASSURANCE-SPRINGFIELD

    Bluegrass Ingredients Inc.

    Quality assurance manager job in Springfield, KY

    DEPARTMENT: Lab Lab Technician REPORT TO: QA Manager CLASSIFICATION: Special Skilled/Non-Exempt WORKING HOURS: Full Time, 12-hour shifts Nights (7P - 7A), Overtime as needed DUTIES AND RESPONSIBILITIES: Including, but not limited to, the following: Perform daily analytical and microbiological testing on incoming “raw” products, on-line samples, and finished products following established guidelines and procedures. Complete data entry in the Food Safety System as well as the internal ERP System. Accurately report and document test results and complete appropriate forms, reports. Be able to recognize abnormal results and lab equipment malfunctions, be able to make appropriate decisions in relation to quality issues. Communicate out of spec results to QA manager. Organize work to obtain maximum efficiency. Do general routine maintenance and QC of equipment and cleaning in area. Perform weekly environmental swabbing. Present a positive attitude toward job, co-workers, and other departments. Use appropriate resource materials. Complies with plant regulations concerning GMP's (Good Manufacturing Practices), safety requirements and work rules, and loss control procedures. Responsible for identifying and addressing any food safety hazards. In the event that a food safety hazard is identified, the employee is to notify their supervisor, a member of Quality, or a member of the Leadership Team. Employees are empowered to immediately address a food safety hazard if they have the ability. Responsible for attending all required safety and food safety training. Perform any and all duties as assigned by supervisor. Must exhibit accuracy and repeatability in all areas of testing. ACCOUNTABILITY: In the absence of the Lab Technician, the QA Manager will be responsible for assigning another trained operator to do this job. REQUIREMENTS: Must be neat and clean. Must be punctual. Must have good computer skills. Microsoft Office, ERP Systems, etc. Must have good manual dexterity. Must present a positive attitude toward co-workers and job. Must do other work as assigned. Must obtain certification for testing of raw milk, UK Regulatory Services. Must obtain certification for antibiotics, micro testing, Kentucky Dept for Public Health. OTHER PHYSICAL REQUIRMENTS: Physical Demands: Standing, walking, sitting, bending, stooping, pushing, pulling, kneeling, reaching, twisting, lifting, climbing ladders and stairs, and carrying up to 85 pounds. Environmental Demands: Noise levels above 85 DBA. Hot and cold working conditions. Job Hazards: Caustics, acids, chlorine, ammonia, high pressure steam and water, hot equipment, trucks fork lifts, conveyers, mechanical hazards, slick or wet floors, confined space entry, elevated work areas on platforms, and equipment above 10 feet. Other Job Requirements: This job description in no way states or implies that these are the only duties to be performed by this employee. He/she will be required to follow any other instructions and to perform any other duties requested by management. Excellent Benefits: medical, dental, vision and life; air evac coverage, PTO, sick days, holiday pay, matching 401K
    $29k-56k yearly est. Auto-Apply 13d ago
  • Supplier Quality Specialist I

    Hitachi Astemo Ohio Manufacturing

    Quality assurance manager job in Berea, KY

    Skills: Professional communication skills Internal/external networking and relationship-building Microsoft Office Tools (Outlook, Excel, Word, Teams, etc.) Aptitude for learning computer-based systems (System 21, AS400, etc.) Measurement/quality inspection experience Quality core tool knowledge Fork truck license (can be obtained after hire) Core Responsibilities: Support 2nd shift production operations for all purchased component-related issues Ensure appropriate measurement techniques are used Prioritization of activities based on plant needs if necessary Report investigation results to responsible dayshift SQE Initiate containment activities and write sort instructions per the process Find and route internal nonconforming/suspect material to SQA hold Support SQE/SQM for plans that need to be executed or read across Touchpoints at different areas of the plant to monitor component issues Coordinate 3rd party supplier quality sorting activities on 2nd shift Ensure correct quantities are released to prevent impact to production lines Confirm and communicate the PPMH (parts per man hour) to 3rd party supervisor Monitor Receiving for Suspect material in transit (ensure routing to inspection) Monitor receiving for critical receipts of clean points, certified materials or materials that need urgent sort/inspection arriving on 2nd shift Monitor Shipping for outgoing returns to vendors Supplier Quality inventory management Disposition and paperwork for Scrap/Return to Vendor; this includes coordinating inventory movement and disposal with Warehouse and PCL Maintain certified/decertified list status as directed by SQEs Equal Opportunity Employer (EOE) - Qualified applicants will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender, identity, disability, protected veteran status and national origin. At Astemo, we're challenging the status quo with the power of diversity, inclusion, and collaboration. Our goal is to build an inclusive work environment that celebrates the differences of our employees. We want to ensure that every employee feels valued, respected and empowered. We don't just accept difference-we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. Astemo is proud to be an equal opportunity employer. If you need a reasonable accommodation to apply for a job at Astemo, please send the nature of the request and contact information to ************************* when applying for the position.
    $44k-70k yearly est. Auto-Apply 60d+ ago
  • Quality Assurance

    United Talent Staffing 3.8company rating

    Quality assurance manager job in Shelbyville, KY

    Job description United Talent is immediately hiring Quality Assurance Associates in Louisville, KYJob Responsibilities: Conducting quality inspection of parts for a major company Stacking the good parts on pallets Placing the defected parts in a bin Pay and Shift: 7 am - 3:30 pm Monday-Friday, $14 per hour Requirements: Pass a background check and drug screen Ability to stand entire shift Steel toed shoes Long pants Lift up to 30 pounds Perks and Benefits: Referral Bonus(each referral you send that works 40 hours you will receive $80. When they work 100 hours, you will receive $200) Weekly pay via direct deposit or pay card Medical benefits available How to apply: give us a call at (502) 390-2131 or text at (502) 206-4815 or apply directly at utalent.com. You can always come see us in person as well! Office hours are Monday - Friday 8am-5pm. Our address is 10013 Forest Green Blvd, Louisville KY 40223EEO
    $21k-27k yearly est. 18d ago
  • Lead, Food Safety & Quality

    CTI Foods 4.2company rating

    Quality assurance manager job in Owingsville, KY

    Welcome to CTI Foods, where quality, service, and people are at the heart of everything we do. We are a leading food manufacturing company, dedicated to providing our customers with the best possible products and our employees with a rewarding career. At CTI, we passionately believe that people are our #1 ingredient. We provide a positive and supportive work environment, opportunities for growth and advancement, and a competitive compensation package. We value our employees' contributions and strive to create a culture of respect, teamwork, and excellence. Whether you're interested in a career in production, quality control, or management, we have a variety of opportunities available. We believe that our success is a result of our focus on quality, service, and people, and we look forward to continuing to serve our customers and employees with excellence. If you're looking for a rewarding career in the food manufacturing industry, look no further than CTI Foods! Join our team and become a part of a company that values quality, service, and people. Job Overview Job Summary: This position will assist in leading the FSQ Team alongside the shift supervisor. This may include, but not limited to, assisting Techs in trouble shooting daily problems and training as needed. This role is expected to be familiar with all line processes and procedures. Several key functions alongside leading the team include providing detailed daily shift recap reports to management, assisting with internal audits, understanding customer specifications to ensure in-process and finished product testing meet all quality parameters. Responsibilities Duties and Essential Job Functions: Responsible for ensuring all non-conforming products are placed on hold until disposition has been determined. Releasing of items on “pending pre-shipment” hold once the appropriate documentation, specification compliance, and micro results have been verified as accurate and in specification and pre-shipment review is completed. Revise and present data in weekly hold/rework meeting. Perform documentation review, HACCP verification activities (Pre-shipment review, cook system verifications, direct observations) and SSOP monitoring activities (pre-op and operational) as necessary. Competent in all FSQ functions, activities, and practices (including all duties performed by the FSQ Tech). Train and lead other FSQ techs. Cover FSQ line responsibilities during employee absences and vacations. Follow and enforce all food safety (GMP, HACCP) and general safety guidelines. Assist with the execution of internal audits, product traceability and mock recall exercises, and 3 rd party and customer audits. Provide technical assistance to operations with process deviation reports and product specifications. Coordinate and adhere to crew scheduling and changes in production schedule. Provide accurate and detailed shift recaps including deficiencies and opportunities to Management (operations and FSQ) Must be able to perform all duties of the FSQ Tech 12. While performing the duties of this Job, the employee is regularly required to stand; walk; reach with hands and arms; stoop, communicate. 13. Continuous walking during shift on cement floor 14. The employee will frequently lift and/or move up to 30 pounds repetitively. 15. Shifts are 10 hours long and must be able to stand on concrete floors and walk back and forth as needed to workstations. Any other duties as assigned. 17. Ability to identify visual defects and make correction as needed and identify and distinguish between colors. 18. Must be able to work in areas of varying temperatures. 19. Relieve other associates as necessary. 20. Maintain good housekeeping. 21. Regular attendance 22. Promotes, adheres, and is responsible for Food Safety and Quality 23. Contributes to team effort by accomplishing related results as needed. 24. Perform all job duties and responsibilities in a compliant and ethical manner and in accordance with applicable Federal, State, and local laws as well as company policies and procedures. 25. Follow all company Safety Rules and Good Manufacturing Practices (GMP's) and adhere to JSA guidelines. 26. Responsible for Food Safety and Quality Culture. 27. Follow daily set up and/or shutdown procedures. 28. Maintain accurate records. 29. Must be able to work any shift, overtime, weekends and/or holidays. 30. Ability to follow written and verbal instructions. Qualifications Qualifications, Knowledge, Skills, & Abilities: · High School Diploma/GED or equivalent experience. · Read, write, and communicate as needed. · Experience in a food manufacturing environment preferred. Excellent customer service skills Strong communication/training skills. Preferred HACCP and PCQI certified Deep understanding of GFSI standard Knowledge of necessary administrative duties to maintain and organize records, reports, or other information Computer literate in Office programs Self-Starter, able to work independently Ability to multi-task Problem solving skills Time management skills Skilled in presenting information or ideas concisely, accurately, and clearly verbally and in writing. Skilled in analyzing and documenting simple and complex business processes. Skilled in communication with a focus on listening and influencing skills. Ability to exercise appropriate judgment in decision-making and problem solving; seeks help promptly as necessary. · Ability to read, write and interpret documents such as box markings, labels, schedules, safety rules, GMP's and general instructions. · Good verbal and written communication skills · Knowledge of process and equipment · Ability to work in a high paced environment. · Reliable attendance is an essential function of the job. · All other duties as assigned. Physical Requirements: While performing the duties of this job, the employee is required to stand; walk; use hands, fingers, handle, or feel; and talk and hear. The employee frequently is required to reach with hands and arms. The employee will be required to climb or balance and stoop, kneel, and crouch on ladders or mechanical equipment/ The employee must occasionally lift and/or move up to 30 pounds. Walk between a cold, warm and hot environment. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job; While performing the duties of this Job, the employee is regularly required to stand; walk; reach with hands and arms; stoop, talk or hear. The employee is occasionally required to sit and taste/smell; and frequently required to climb and must be able to reach all levels in the bay. The employee will frequently lift and/or move up to 30 pounds and regularly lifts to 50 pounds. Work Environment: While performing the duties of this Job, the employee is exposed to wet, cold and or humid conditions and moving mechanical parts. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to high, precarious places; toxic or caustic chemicals; extreme cold; extreme heat and vibration. The noise level in the work environment is usually loud and requires that hearing protection be always worn in production areas; While performing the duties of this Job, the employee is regularly exposed to wet and/or humid conditions and moving mechanical parts. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to high, precarious places; toxic or caustic chemicals; extreme cold; extreme heat and vibration. The noise level in the work environment is usually loud and requires that hearing protection be always worn in production areas at all times.
    $69k-87k yearly est. Auto-Apply 9d ago
  • Quality Control Engineer - Manufacturing / Fabrication

    Qualdoc

    Quality assurance manager job in Winchester, KY

    Quality Control Engineer - Manufacturing / FabricationWinchester, KYDirect HireSalary: Up to $70,000.00 per year (Depending on Experience) We are seeking a Quality Control Engineer to support and maintain our quality standards and processes. This role will interface with customers regarding quality issues, lead scrap reduction activities, manage gauge control systems, and provide training and support across departments. The ideal candidate promotes teamwork, safety, and a strong quality culture.Essential Functions Support the development and maintenance of the Quality System. Serve as the primary contact for customer quality issues, including claims. Analyze customer reject product (warranty, field, or plant-level) and prepare detailed reports. Investigate quality defects in the manufacturing process and lead corrective actions to prevent recurrence. Lead countermeasure meetings and support implementation of corrective, preventive, and continuous improvement actions. Manage gauge calibration and recall systems according to AIAG Measurement System Analysis (MSA), including: Repairing or reworking precision gauges Determining appropriate gauges for specific measurement applications Coordinating with external vendors for gauge/fixture quotes Supporting gauge design with internal/external teams Conduct internal process audits to reduce quality risks. Prepare and maintain reports for internal and external quality status and process performance. Follow applicable quality standards including PPAP, MSA, APQP, and other industry guidelines. Travel as needed to customer sites to perform reject product analysis. Train quality technicians and inspectors as required. Develop inspection standards for receiving, in-process, shipping, and layout inspections. Qualifications Bachelor's degree in Quality Engineering and 3 years of experience in the quality field; OR Master's degree in Quality Engineering and 2 years of experience; OR 8 years of exempt-level experience in the quality field. Knowledge of machining, heat treatment, metallurgy, gauge development, and gauge control. Understanding of non-destructive testing related to raw materials, heat treatment, and welding. ASQ Certified Quality Technician preferred. Ability to read and interpret blueprints. Proficiency with SPC data and collection. Experience with CMM. Knowledge of gauge calibration and tracking systems. Strong verbal and written communication skills. Proficiency with MS Office (Word, Excel, Access). We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
    $70k yearly Auto-Apply 1d ago
  • Quality Engineer

    Ledvance

    Quality assurance manager job in Versailles, KY

    This position will work to fully resolve our customers' claims while remaining fiscally responsible and applying resolution within our written warranty terms as quickly and efficiently as possible to meet our customers' needs. This position manages customer claim resolution including testing of failed products and communicating resolution to customers and sales representatives for those accounts. This position contacts relevant manufacturing teams and works with them to improve future products. Claims include technical claims of failed product, installation issues, product safety loss claims with our product, and retail claims returned by general consumers to our lab. Escalating technical and product issues to product management, manufacturing plant and suppliers for corrective actions. ESSENTIAL DUTIES * Working under general management and with a high level of technical creativity, develops comprehensive approaches to meeting the technical Quality objectives of customer technical system analysis, interaction with Customers, Sales, Product Management, Marketing, R&D, Supplier Quality and Manufacturing to effectively resolve customer claims and reduce cycle time. * Evaluate failed product to identify root cause. Propose and/or evaluate design and process quality measures and systems to ensure product quality during design and manufacturing phases, often identified as a result of 8D Methodology for resolving the problem. * Design and install quality control process sampling systems, procedures and statistical techniques for claim management. * Designs or specifies inspection and testing mechanisms and equipment necessary to troubleshoot customer claims. Recommends revision of specifications when needed and collaborates with manufacturing plants to validate effectiveness. * Provide first level technical support to customers for troubleshooting technical issues as well as responding to product safety and liability claims involving our product. * Conduct customer site visits and report on results. Travel time can be up to 25%. * Ensure that all claims handled are appropriately reported within Customer Quality Management so they become part of the feedback to the Business Unit Product, Quality and Supplier Managers COMPETENCIES * Solid understanding of troubleshooting and typical failure modes of circuit boards and their components with minimal access to schematics. Position requires an individual who will help identify root causes and implement solutions. * Experience with instruments such as oscilloscopes, multimeters, color measuring and temperature measuring equipment. * Demonstrated ability to work within a team structure with cross-functional relationships. * In-depth working knowledge of SAP and Microsoft Office Suite * Statistical methods training and experience are desired (8D Methodology, FMEA and Six Sigma, Lean Manufacturing) * Must have excellent written and verbal communication since this position will be in contact with customers as well as internal key function heads. Communications must be in English * with concise verbiage that leaves no ambiguity and requires no review / editing prior to submittal directly to customers. * Ability to negotiate resolutions with customers is key REQUIREMENTS AND QUALIFICATIONS * Bachelor's degree in Electrical Engineering (or relevant field) Preference for 1 year of experience or more. OTHER: * Position will be located in Versailles, KY with regular on-site office hours Monday-Friday. * Relocation and/or work sponsorship are not available with this position. * Position is eligible for the LEDVANCE employee referral program.
    $57k-73k yearly est. 7d ago
  • Quality Engineer

    Precision Resource 4.4company rating

    Quality assurance manager job in Mount Sterling, KY

    Precision Resource is a leading global supplier of precision metal components and assemblies using fineblank technology. Our eight North American divisions serve a global customer base with a commitment to continuous improvement. For over 50 years we have provided solutions to quality, cost and production challenges for market-leading customers in the automotive, heavy duty and off-highway vehicles, tools and hardware, electronics and cutlery. Job Description Responsibilities Include Quality system audits and maintenance of ISO/TS 16949 quality systems Process auditing and data analysis for continual improvement Capability and measuring systems analysis and corrective action activities Auditing and tracking of suppliers Position reports directly to Quality Manager and assists in training of quality and production team members Qualifications 5 years quality experience in an automotive metal stamping/metal fabrication environment 4 year degrees in applied sciences Working knowledge of SPC, blue print reading, measuring tools and measuring system analysis Hands on experience in Kaizen/Six Sigma continual improvement applications Development or maintenance of ISO/TS 16949 quality system Employment history must show progressive advancement responsibilities in the quality field CQE, CQA, Six Sigma certification will be a plus Additional Information
    $56k-75k yearly est. 3d ago
  • Director, Quality & Compliance Training (Princeton, Hybrid)

    Otsuka America Pharmaceutical Inc. 4.9company rating

    Quality assurance manager job in Frankfort, KY

    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 40d ago
  • Microbiology Manager

    Piramal Enterprises Ltd.

    Quality assurance manager job in Lexington, KY

    Business: Pharma Solutions Department: Microbiology (MQC) The Microbiology Manager provides oversight of activities related to microbiological testing of bulk and finished products, packaging materials, scale-up samples, process validation samples, marketed stability samples, development and investigational samples Reporting Structure Directly reports to Director, Quality Key Responsibilities * Effectively mentor and manage the Microbiology analysts in the laboratory * Provide and/or manages cGMP and safety training to the Micro staff * Provides information regarding Quality Control systems and data to internal or external regulatory personnel during inspections or inquiries * Develop/implement procedural guidelines within the Microbiology lab in conjunction with Quality Assurance * Conduct or manage the performance of method and equipment validation/qualification exercises * Write necessary protocols, analyze data, and compile final reports for methods and equipment protocols * Establish, implement, and manage Lab Programs and/or Policies, SOPs, and good record keeping practices * Ensure that all equipment in the microbiology laboratory is functional and in a calibrated state * Troubleshoot equipment and methods and communicate with vendors and outside contract laboratories. * Train analysts in laboratory practices and standard microbiological procedures * Manage and ensure that smooth function of the laboratory daily activities, including organizing the frequency of testing and prioritizing workload on a daily basis * Analyze and trend sample results and perform statistical studies and evaluations of key performance indicators. * Regularly monitor applicable internet and written information published by US FDA, pharmaceutical manufacturing and laboratory technology organizations for the purpose of review/incorporation of latest requirements and guidelines into routine PPS laboratory operations * Establish short and long-range plans for the timely and efficient execution of the microbiological testing activities within scope of the business priorities and applicable regulatory requirements (FDA, OSHA, etc.) * Ensure Lab Sustain Permanent Inspection Readiness (PIR) Education Requirements * Bachelor of Science in Microbiology, Biology, Life Sciences, or related scientific discipline. Work Experience * 4+ years of experience managing high throughput Microbiology Laboratories * 5 years of applied Microbiology experience in a commercial pharmaceutical, GMP manufacturing environment (preferably parenteral and in a CMO/CDMO/Clinical Environment) * Prior management/supervisory experience in a laboratory environment Functional Or Technical Skills * Possess excellent technical writing and oral communication skills. * SME as it relates to Micro Lab Operations, EM, SAL and the following pharmaceutical Industry guidelines, standards, and statutes: ISPE (International Society of Professional Engineers) guidelines ,FDA and PDA Parenteral Drug Association guidelines, cGMP pharmaceutical industry standards for cleaning, sterilization, and environmental monitoring and control, US Code of Federal Regulations, Titles 210 and 211, US Pharmacopoeia methods and general information chapters related to sterility assurance. * Knowledge and understanding of cGMPs; Knowledge of cGMP validation requirements and techniques * Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques * Experience managing direct reports * Proficiency using Microsoft Office applications
    $61k-93k yearly est. Auto-Apply 55d ago
  • Quality Engineer

    Precision Resource 4.4company rating

    Quality assurance manager job in Mount Sterling, KY

    Precision Resource is a leading global supplier of precision metal components and assemblies using fineblank technology. Our eight North American divisions serve a global customer base with a commitment to continuous improvement. For over 50 years we have provided solutions to quality, cost and production challenges for market-leading customers in the automotive, heavy duty and off-highway vehicles, tools and hardware, electronics and cutlery. Job Description Responsibilities Include Quality system audits and maintenance of ISO/TS 16949 quality systems Process auditing and data analysis for continual improvement Capability and measuring systems analysis and corrective action activities Auditing and tracking of suppliers Position reports directly to Quality Manager and assists in training of quality and production team members Qualifications 5 years quality experience in an automotive metal stamping/metal fabrication environment 4 year degrees in applied sciences Working knowledge of SPC, blue print reading, measuring tools and measuring system analysis Hands on experience in Kaizen/Six Sigma continual improvement applications Development or maintenance of ISO/TS 16949 quality system Employment history must show progressive advancement responsibilities in the quality field CQE, CQA, Six Sigma certification will be a plus Additional Information
    $56k-75k yearly est. 60d+ ago

Learn more about quality assurance manager jobs

How much does a quality assurance manager earn in Lexington, KY?

The average quality assurance manager in Lexington, KY earns between $56,000 and $120,000 annually. This compares to the national average quality assurance manager range of $70,000 to $140,000.

Average quality assurance manager salary in Lexington, KY

$82,000
Job type you want
Full Time
Part Time
Internship
Temporary