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Qms Manager Jobs in Kentucky (NOW HIRING)

Pinnaql, Inc.

$70 - $100/hr

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Digital Validation / QMS Specialist What you will do: * Facilitate and lead structured working ...

New

UpDoc, Inc.

$110 - $170/hr

Lead internal audits, gap assessments, and action item closure for periodic QMS reviews * Manage and Maintain Design and Development Files for FDA regulated products. * Manage Quality Training: Guide ...

New

Axion Recruitment

Be Seen First

Quality Engineer

Shepherdsville, KY · On-site

$80K - $90K/yr

Support the Quality Management System (QMS) * Manage non-conforming material and quality issues * Perform layout inspections and support product testing * Work directly with customers and suppliers ...

New

Real Alloy

Quality Manager

Morgantown, KY · On-site

The Quality Manager will be responsible for leading, developing, and sustaining effective Quality Management Systems (QMS). The Quality Manager role will need to ensure we are ISO 9001 compliant ...

Real Alloy

Quality Manager

Morgantown, KY

The Quality Manager will be responsible for leading, developing, and sustaining effective Quality Management Systems (QMS). The Quality Manager role will need to ensure we are ISO 9001 compliant ...

Real Alloy

Quality Manager

Morgantown, KY · On-site

The Quality Manager will be responsible for leading, developing, and sustaining effective Quality Management Systems (QMS). The Quality Manager role will need to ensure we are ISO 9001 compliant ...

International Erosion Control Association

$110 - $130/hr

The Lead Project Manager ensures the application of PMI-based project management principles, Lean Six-Sigma practices, and the AEH Quality Management System (QMS) across the full project portfolio ...

Posted today

Bisco Inc.

$112 - $168/hr

You will work with senior management to share ideas and improve operation, recommending, supporting, and implementing continuous improvement activities for the QMS. Responsibilities will be: * Lead ...

Posted today

MX Holdings

$160 - $210/hr

MES & QMS Product Management: Own the licensing management, vendor management, and coordination of application updates/patches for the MES and QMS packages used in the plants. * Requirements ...

Verily Life Sciences LLC

$113 - $170/hr

Leads ongoing implementation and continuous improvement of the Software Quality Management System (QMS) across consumer, research, and SaMD product domains - in conformance with FDA QMSR, ISO 13485 ...

Posted today

Gray Construction

Site Manager, MEP

Lexington, KY · On-site +1

Will insure the company QMS program is used and maintained in accordance to company standards ... Strong people management skills. * Must possess basic computer skills including the ability to ...

Gray, Inc.

Site Manager, MEP

Lexington, KY · On-site

$90 - $130/hr

Will insure the company QMS program is used and maintained in accordance to company standards ... Strong people management skills. * Must possess basic computer skills including the ability to ...

Stryker Corporation

$90 - $130/hr

Support computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc.), ERP ...

New

PLP Group

$130 - $190/hr

The Senior Product Manager will define, build, launch, and grow the next generation of Quality ... QMS. · Comply with all internal CQ Quality and Information Security requirements. · All other ...

Akima

KY · On-site

The Quality Assurance Manager is responsible for developing, implementing, and maintaining a Quality Management System (QMS) that ensures compliance with ISO 9001:2015 standards and all applicable U.

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All JobsQms JobsQms Manager JobsQms Manager Jobs in Kentucky

Qms Manager information

See Kentucky salary details

$20.8K

$74.8K

$137.2K

How much do qms manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for qms manager in Kentucky is $74,832.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,200.00 and $118,100.00 per year, depending on experience, location, and employer.

What is a QMS manager?

QMS Managers, or Quality Management System Managers, are professionals responsible for developing, implementing, and overseeing an organization's quality management system. They ensure that processes and products meet established quality standards and comply with relevant regulations. Their duties often include conducting audits, managing documentation, training staff on quality procedures, and driving continuous improvement initiatives. QMS Managers play a crucial role in maintaining customer satisfaction and supporting organizational efficiency.

How does a QMS manager typically collaborate with other departments to ensure compliance and continuous improvement?

A QMS Manager regularly works cross-functionally with departments such as production, engineering, and procurement to implement and maintain quality standards. This involves coordinating audits, facilitating training sessions, and gathering feedback to identify areas for process improvement. Effective communication and negotiation skills are essential, as the QMS Manager must align diverse teams toward compliance goals and foster a culture of continuous improvement. Regular meetings and collaborative problem-solving are part of ensuring that quality objectives are met across the organization.

What are the key skills and qualifications needed to thrive as a QMS manager, and why are they important?

To thrive as a QMS Manager, you need expertise in quality management systems, regulatory compliance, and process improvement, typically supported by a relevant degree and experience in quality assurance. Familiarity with ISO standards (such as ISO 9001), audit management tools, and quality software platforms is essential. Strong leadership, problem-solving skills, and effective communication help drive a culture of continuous improvement and team alignment. These competencies ensure that organizational processes meet regulatory requirements and consistently deliver high-quality outcomes.

What is the difference between Qms Manager vs Quality Assurance Supervisor?

AspectQms ManagerQuality Assurance Supervisor
CertificationsISO 9001 Lead Auditor, CQEISO 9001 Lead Auditor, CQE
Work EnvironmentOversees quality management systems across departmentsSupervises quality assurance team and daily testing activities
Industry UsageUsed in manufacturing, aerospace, automotiveCommon in manufacturing, pharmaceuticals, food industry
Primary FocusDeveloping, maintaining, and improving QMSMonitoring product quality and compliance

The Qms Manager and Quality Assurance Supervisor roles share similar certifications and industry usage, but the Qms Manager focuses on managing the entire quality management system, while the Supervisor concentrates on daily quality assurance activities. Both positions are vital for ensuring product quality and compliance within manufacturing and related industries.

What are the most commonly searched types of Qms jobs in Kentucky?

The most popular types of Qms jobs in Kentucky are:

What are popular job titles related to Qms Manager jobs in Kentucky?

For Qms Manager jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching Qms Manager jobs in Kentucky look for?

The top searched job categories for Qms Manager jobs in Kentucky are:

What cities in Kentucky are hiring for Qms Manager jobs?

Cities in Kentucky with the most Qms Manager job openings:

Qms Manager jobs near you
Infographic showing various Qms Manager job openings in Kentucky as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $74,832 per year, or $36 per hour.

Digital Validation / QMS Specialist

Pinnaql, Inc.

On-site

$70 - $100/hr

Other

Posted 3 days ago

New

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Digital Validation / QMS Specialist
What you will do:
  • Facilitate and lead structured working sessions with cross-functional stakeholders (Validation, QC, Manufacturing, MSAT, Engineering) to define ~350 entities across Phase 1 and Phase 2.
  • Complete and route GVLMS worksheets within the Veeva Validation Management module, operating with Validation Lead role access within the Veeva Vault environment.
  • Pre-populate entity definition templates with available source data prior to each working session to maximize efficiency and minimize stakeholder time.
  • Ensure all GVLMS worksheets are completed, routed, and progressed through the approval workflow in compliance with 21 CFR Part 11 electronic record requirements.
  • Execute the scanning and Veeva upload of approximately 150 executed IOQ binders (estimated 50-200 pages each).
  • Follow the Document Control Room retrieval SOP for all binder access and chain-of-custody handling.
  • Build and maintain the Master Validation Data Repository — a traceability index covering 2-5 validation documents per system across ~350 qualified systems — drawing from documents already available in Veeva and the RMC Doc Control Room.
  • Verify upload accuracy against source binder index and elevate discrepancies within 1 business day.
Qualifications:
  • 3-5+ years of validation experience in a regulated pharmaceutical, biotech, or CDMO environment.
  • Direct hands‑on experience authoring and revising GxP validation documents — VMPs, SOPs, Guidance Documents, and validation templates.
  • Experience with Validation Lifecycle Management Systems (VLMS) — Veeva Validation Management, Kneat, ValGenesis, or equivalent platform.
  • Familiarity with the Veeva Vault ecosystem, including document routing, approval workflows, and 21 CFR Part 11 electronic record management.
  • Experience executing IOQ binder documentation, scanning, and electronic document management in a GMP environment.
  • Demonstrated ability to facilitate cross‑functional working sessions with quality, engineering, and manufacturing stakeholders.
Preferred Qualifications
  • Experience in a cell therapy, gene therapy, or advanced biologics GMP manufacturing environment.
  • Prior experience supporting a GVLMS implementation or digital validation platform rollout.
  • Direct experience with Veeva Validation Management — entity definition, worksheet creation, routing, and approval workflows.
  • Familiarity with SAP PM (Plant Maintenance) for calibration or requalification scheduling.
  • Experience supporting multiple concurrent document types under a single change control record.
  • Prior experience working on a Pinnaql or similar consulting/managed service engagement — you understand the accountability model.
  • Bachelor's degree in Life Sciences, Engineering, Chemistry, or a related field.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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