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Quality Operation Jobs (NOW HIRING)

LGM Pharma, LLC

SUPERVISOR, QUALITY ASSURANCE

Irvine, CA · On-site

$90K - $105K/yr

Provide periodic KPI trend reports to senior management as required. • Review and approve Manufacturing, Packaging, and Quality Operation Processes, and GMP documentation. • Approve Master Labels ...

Alcon

Manager, Quality Operations

Huntington, WV · On-site

The Manager, Quality Operations (Management Path), is primarily responsible for leading a team to manage quality operations in manufacturing and distribution. You will ensure product quality, resolve ...

Air Liquide

Quality Operations Supervisor

Fremont, CA · On-site

$105K - $130K/yr

R10095135 Quality Operations Supervisor (Open) Location: Fremont, CA - 46401 Landing Pkwy - Advanced materials The science of electronics is transforming exponentially through innovation and ...

Air Liquide

Quality Operations Supervisor

Fremont, CA · On-site

$105K - $130K/yr

R10095135 Quality Operations Supervisor (Open) Location: Fremont, CA - 46401 Landing Pkwy - Advanced materials The science of electronics is transforming exponentially through innovation and ...

Sealed Air Corporation

Quality Auditor

Rogers, AR · On-site

Maintains quality documentation related to operations * Supports and assists the manufacturing areas with quality issues, working closely with department personnel to support the production of ...

Danaher

Quality Operations Engineer

Lodi, CA

$70K - $85K/yr

The Quality Operations Engineer supports day-to-day Manufacturing Quality activities by completing structured assignments using established procedures and under the guidance of senior Quality ...

Danaher

Quality Operations Engineer

Lodi, CA · On-site

$70K - $85K/yr

The Quality Operations Engineer supports day-to-day Manufacturing Quality activities by completing structured assignments using established procedures and under the guidance of senior Quality ...

PTI Quality Containment Solutions

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Quality Manager

Jeffersonville, IN · On-site

$75K - $90K/yr

Excellent customer service * 7 years minimum experience related to Quality Operations * Automotive background a must, paint line experience a plus * Experience with OEM Containment Standards ...

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Quality Operation information

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$38.5K

$91K

$138.5K

How much do quality operation jobs pay per year?

As of Jul 7, 2026, the average yearly pay for quality operation in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.

What is the difference between Quality Operation vs Quality Assurance?

AspectQuality OperationQuality Assurance
Primary FocusImplementing and maintaining quality processes in daily operationsDeveloping and verifying quality standards and procedures
Work EnvironmentManufacturing plants, production lines, or service delivery settingsOffice settings, labs, or quality departments within organizations
Required CredentialsOften requires technical certifications or experience in operationsTypically requires quality management certifications like CQE or ISO training
Common UsageUsed by companies to ensure operational quality controlUsed to establish and audit quality systems and standards

While both roles focus on quality, Quality Operations centers on executing quality processes in daily work, whereas Quality Assurance emphasizes creating and maintaining quality standards and systems. Understanding these differences helps in selecting the right career path or job focus within quality management.

What states have the most Quality Operation jobs? States with the most job openings for Quality Operation jobs include:
SUPERVISOR, QUALITY ASSURANCE

SUPERVISOR, QUALITY ASSURANCE

LGM Pharma, LLC

Irvine, CA • On-site

$90K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 14 days ago

Job description

RESPONSIBILITIES:


• Assist in supervision of various quality programs such as but limited to labeling, GMP training, compliance, document control, information tracking, and equipment calibration.

• Manages or assists in the compliance profile of the site and drives continuous improvements, QRB and metrics.

• Review and approve protocol/reports for various qualifications and validations.

• Uses statistical process control to evaluate trends. Provide periodic KPI trend reports to senior management as required.

• Review and approve Manufacturing, Packaging, and Quality Operation Processes, and GMP documentation.

• Approve Master Labels and Finished Product C of A’s. Assist with creation, revision and approval of SOP’s. Review and approve change controls.

• Improves and/or develops comprehensive quality sub-systems (e.g., corrective/preventative action, MRB, customer complaints, vendor management programs, etc.).

• Assist Senior Management during inspections by FDA, DEA, and other regulatory agencies and customers.

• Helps in establishing raw material and finished product specifications based on regulatory requirements and customer needs.

• Lead investigation activities, perform root-cause analyses, and develop corrective and preventative action plans.

• Assist in preparations for Annual Product Review.

• Comply with cGMP regulations and follow all standard operating procedures.

• Other related duties as required.


QUALIFICATIONS:

• Bachelor’s Degree, preferable in a scientific discipline.

• 6+ years of experience in Quality Assurance in a GMP facility, including people management and/or equivalent combination of education and experience.

• Strong commitment to quality standards with leadership and management skills.

• Ability to read and interpret technical procedures, SOP’s, GMP’s and governmental regulations: 21 CFR 111, 11, 210, and 211.

• Strong communication skills, both written and verbal.

• Possess positive qualities of effective leadership, staff motivation and conflict resolution.

• ASQC quality certifications, ISO 9000 or other Audit training preferred.

• Strong knowledge of validation, investigations, application of audit principles, concepts and practices related to a regulated quality system is required.

• Strong solid dose manufacturing quality compliance experience is preferred.


At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.