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Quality Validation Manager Jobs in Fountain Inn, SC

Bausch + Lomb

Validation Technician IV

Greenville, SC · On-site

Perform applicable department responsibilities as defined by Validation Manager / Validation ... or QC lab experience. * Preferred Skills: Self-Driven, Strong Verbal and Written Communication ...

Pinnaql

Senior Packaging CQV Engineer

Greenville, SC · On-site

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... and quality. While the primary focus will be packaging systems, this role may also support ...

jadex

Alltrista - Manager, Quality

Greer, SC

The Quality Manager - Injection Molding is responsible for leading site quality activities in a ... Support process validation, change control, risk assessments, control plans, root cause ...

Jadex

Alltrista - Manager, Quality

Greer, SC · On-site

The Quality Manager - Injection Molding is responsible for leading site quality activities in a ... Support process validation, change control, risk assessments, control plans, root cause ...

Smurfit Westrock

Mgr I, Quality

Anderson, SC · On-site

... validation processes. • Oversee document control processes including SOPs, work instructions, specifications and record retention. • Monitor and report Quality KPIs to the General Manager and ...

Westrock

Mgr I, Quality

Anderson, SC · On-site

... validation processes. • Oversee document control processes including SOPs, work instructions, specifications and record retention. • Monitor and report Quality KPIs to the General Manager and ...

Eaton

Supplier Quality Engineer

Hodges, SC · On-site

$97K - $143K/yr

You will drive quality planning and execution, including audits, inspections, and control processes ... validation. * Manage warranty issues, DMRs, and customer complaints in coordination with JV ...

Eaton

Supplier Quality Engineer

Hodges, SC · On-site

$97K - $143K/yr

You will drive quality planning and execution, including audits, inspections, and control processes ... validation. Manage warranty issues, DMRs, and customer complaints in coordination with JV partners.

Fluor

Project Manager II - Life Sciences

Greenville, SC · On-site

... quality, validation, and regulatory teams Identify and manage project risks, issues, and changes in a controlled and compliant manner Support the PD in delivering the project in accordance with ...

VAYAN GROUP, LLC

Be Seen First

Quality Site Manager

Spartanburg, SC · On-site

$60K - $65K/yr

Quality Site Manager Location: Spartanburg Employment Type: Full-Time Reports To: Operations ... Conduct and document Layered Process Audits (LPAs) , process validations, and corrective actions.

TRIGO

QDL (Quality Delivery Liaison)

Greer, SC · On-site

May Report to Site Manager/Quality Delivery Manager Responsibilities Client relationship & Business ... Responsible for validating operational output via audits, and acknowledging Work Order/Mission ...

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Quality Validation Manager information

See Fountain Inn, SC salary details

$42.4K

$94.1K

$143.3K

How much do quality validation manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for quality validation manager in Fountain Inn, SC is $94,093.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $117,800.00 per year, depending on experience, location, and employer.

What is the difference between Quality Validation Manager vs Quality Assurance Specialist?

AspectQuality Validation ManagerQuality Assurance Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, pharmaceuticals, tech companiesManufacturing, healthcare, software development
ResponsibilitiesOversees validation processes, ensures compliance, manages validation teamsPerforms audits, develops QA procedures, monitors quality metrics

The main difference is that a Quality Validation Manager focuses on validating processes and systems to ensure compliance, often managing validation teams, while a Quality Assurance Specialist concentrates on implementing QA procedures, conducting audits, and maintaining quality standards. Both roles require similar certifications and are vital in industries like manufacturing and healthcare, but their core responsibilities differ in scope and focus.

What job categories do people searching Quality Validation Manager jobs in Fountain Inn, SC look for?

The top searched job categories for Quality Validation Manager jobs in Fountain Inn, SC are:

What cities near Fountain Inn, SC are hiring for Quality Validation Manager jobs?

Cities near Fountain Inn, SC with the most Quality Validation Manager job openings:

Quality Validation Manager jobs near you
Infographic showing various Quality Validation Manager job openings in Fountain Inn, SC as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $94,093 per year, or $45.2 per hour.

Validation Technician IV

Greenville, SC • On-site

Bausch + Lomb
Medical Equipment and Supplies Manufacturing • 10K+ employees

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

22nd of 545 rated manufacturers

People enjoy working here

Good employer

Recommended by parents

Learn more about Bausch + Lombexternal

Full-time

Posted 6 days ago

Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Objectives/Purpose of Job:
Validation Technician will be responsible for supporting tasks outlined in the Site Validation Master Plan (SVMP).
Key Activities/Responsibilities:
Job Functions:
  • Lead and coordinate validations for routine re-qualifications of steam sterilizers, line sterilization, heat sterilization, aseptic simulations (Media Fills), sterility isolators that support the SVMP, among others.
  • Re-qualifications require entry to aseptic areas, tank entry and use of Ellab Datalogger or equivalent.
  • Author validation strategies, protocols, execute validations, analyze data and write final reports for projects that support equipment, steam sterilization, process or cleaning validations, among others.
  • Conduct periodic reviews of validated equipment and systems as outlined in SVMP.
  • Conduct peer reviews of validation packages for fellow team members and provide feedback.
  • Perform applicable department responsibilities as defined by Validation Manager / Validation Supervisor and needs of the department.

SCOPE/RESPONSIBILITIES:
Validation Technician will be responsible for supporting tasks outlined in the Site Validation Master Plan (SVMP). These tasks include re-qualifications, periodic reviews and projects supporting capital equipment or process changes. The Validation Technician interacts with various facets of the organization including but not limited to operations, microbiology, chemistry, metrology and maintenance.
Qualifications/Training:
  • Education: Associate Degree in Science preferred, BS desirable.
  • Desired use of a Ellab (or equivalent data logger).
  • Experience: 0-3 years of validation experience, 5 years in Pharma/Medical device industries with manufacturing or QC lab experience.
  • Preferred Skills: Self-Driven, Strong Verbal and Written Communication, Strong GMP and Data Integrity knowledge, Strong Interpersonal skills, Results Oriented, quality mindset.

This position may be available in the following location: Greenville, SC
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Our US Benefit Programs: Employee Benefits: Bausch + Lomb
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853

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