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Quality Systems Associate Jobs (NOW HIRING)

VPI Compounding

Quality Associate I

Centennial, CO · On-site

$25 - $30/hr

Quality Systems Associate I Department: Quality Location: Centennial, CO 80112 Employment Type: Full-Time, PRN Compensation: $25-30 DOE Join Our Team as a Quality Systems Associate at VPI Compounding ...

Grifols, S.A

Quality Systems Manager

Rock Hill, SC · On-site

$100 - $125/hr

Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of ...

GRIFOLS, S.A.

Quality Systems Manager

Rock Hill, SC · On-site

... Quality Systems Associate; including direction, assignment of work, hiring, development and ... training, disciplinary actions, termination, maintenance of personnel records, work schedule and ...

Grifols

Quality Systems Manager

Sumter, SC · On-site

... Quality Systems Associate; including direction, assignment of work, hiring, development and ... training, disciplinary actions, termination, maintenance of personnel records, work schedule and ...

Jobtailor

Quality Systems Manager

El Paso, TX · On-site

$80 - $100/hr

... Quality Systems Associate personnel functions, including hiring, training, scheduling, delegation, and performance actions Oversee internal and external audits, including preparation, execution ...

New

Oatey

Quality Systems Engineer

Shakopee, MN · On-site

$85K - $103K/yr

The Quality Systems Engineer provides training to associates on new or revised Quality systems and procedures. The Quality Systems Engineer manages the site level Internal Auditing program and ...

Oatey Es

Quality Systems Engineer

Shakopee, MN · On-site

$85K - $103K/yr

The Quality Systems Engineer provides training to associates on new or revised Quality systems and procedures. The Quality Systems Engineer manages the site level Internal Auditing program and ...

Integer

Associate Quality Systems Engineer

Plymouth, MN · On-site

As an entry level associate, you will ensure that Integer's Quality System Requirements are met or exceededwiththe direction, instruction and guidance from more experienced associates and managers in ...

Oatey

Quality Systems Engineer

Shakopee, MN · On-site

$85K - $103K/yr

The Quality Systems Engineer provides training to associates on new or revised Quality systems and procedures. The Quality Systems Engineer manages the site level Internal Auditing program and ...

Oatey

Quality Systems Engineer

Shakopee, MN · On-site

$85K - $103K/yr

The Quality Systems Engineer provides training to associates on new or revised Quality systems and procedures. The Quality Systems Engineer manages the site level Internal Auditing program and ...

Oatey

Quality Systems Engineer

Shakopee, MN · On-site

$85K - $103K/yr

The Quality Systems Engineer provides training to associates on new or revised Quality systems and procedures. The Quality Systems Engineer manages the site level Internal Auditing program and ...

Boeing

Associate Quality Systems Specialist

Hialeah, FL · On-site

$65K - $92K/yr

Associate Quality Systems Specialist Company: Boeing Distribution, Inc. Boeing Global Services (BGS), Distribution Business , is looking for an Associate Quality Systems Specialist to join our team ...

Boeing

Associate Quality Systems Specialist

Hialeah, FL · On-site

$65K - $92K/yr

Associate Quality Systems Specialist Company: Boeing Distribution, Inc. Boeing Global Services (BGS), Distribution Business , is looking for an Associate Quality Systems Specialist to join our team ...

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Quality Systems Associate information

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$50

How much do quality systems associate jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality systems associate in the United States is $26.93, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $31.49 per hour, depending on experience, location, and employer.

What is the difference between Quality Systems Associate vs Quality Control Technician?

AspectQuality Systems AssociateQuality Control Technician
CertificationsISO auditor, GMP, or quality management certificationsGMP, HACCP, or industry-specific testing certifications
Work EnvironmentDocument control, quality management systems, auditsProduct testing, inspection, sampling
Employer & Industry UsageManufacturing, pharmaceuticals, biotechFood, pharmaceuticals, manufacturing

The Quality Systems Associate focuses on maintaining and improving quality management systems, documentation, and compliance. In contrast, the Quality Control Technician primarily conducts product testing and inspections to ensure quality standards are met. Both roles are essential in quality assurance but differ in their core responsibilities and daily tasks.

Is a Quality Systems Associate an entry level job?

A Quality Systems Associate position is often considered entry level, suitable for candidates with a bachelor's degree in a related field and some familiarity with quality management systems like ISO or GMP. The role typically involves supporting quality processes, documentation, and audits, and may require basic knowledge of tools such as SAP or TrackWise. Experience requirements vary by employer, but many entry-level candidates can qualify with relevant internships or certifications.

What is a quality systems associate?

A quality systems associate is responsible for maintaining and improving a company's quality management system, ensuring compliance with industry standards such as ISO 9001. They often perform audits, document control, and data analysis, and may use tools like quality management software to support continuous improvement efforts.

What cities are hiring for Quality Systems Associate jobs?

Cities with the most Quality Systems Associate job openings:

What are the most commonly searched types of Quality Systems jobs?

The most popular types of Quality Systems jobs are:

What states have the most Quality Systems Associate jobs?

States with the most job openings for Quality Systems Associate jobs include:

What are popular job titles related to Quality Systems Associate jobs?

For Quality Systems Associate jobs, the most frequently searched job titles are:

Infographic showing various Quality Systems Associate job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $56,018 per year, or $26.9 per hour.

Quality Systems Associate (Contract)

San Diego, CA • On-site

ORIC Pharmaceuticals
Biotechnology Research and Development • 1 - 10 employees
Learn more about ORIC Pharmaceuticalsexternal

$25 - $33.50/hr

Contractor

Posted 19 days ago

Job description

Company Description

ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.

Reporting to the Quality Systems Specialist, the Quality Systems Associate will support document control, training, and quality systems activities, providing word processing, archival and electronic system maintenance.  The successful candidate will work closely with Quality Assurance, Technical Operations, Clinical, Regulatory and third-party Contract organizations.   

Job Description
  • Support document processing, review and release of regulated GxP documents .
  • Collaborate closely with document owners to resolve any documentation discrepancies identified during review.
  • Organize review and support activities to ensure timely review and completion of documentation task to meet pre-established timelines.
  • Participate in cross functional program meetings to provide appropriate QA updates.
  • Maintain and update electronic quality systems, documentation files and folders in accordance with written SOPs.
  • Facilitate/coordinate GMP training for internal employees/departments as required.
  • Identify and facilitate continuous improvement of internal Policies, SOPs and Work Instructions, as needed.
  • Provide document support for internal audits and regulatory inspections, as needed.
  • Perform all duties in keeping with ORIC's core values, policies and all applicable regulations.
Qualifications
  • Bachelor's degree or equivalent relevant experience.
  • 0-2 years of relevant experience in Quality Assurance or experience in an academic or regulated environment.
  • Highly polished writing and editing skills.
  • High degree of proficiency in Microsoft Office Suite.
  • Knowledge of GMP regulations and guidance documents is preferred, including but not limited to:
    • 21 CFR Parts 11, 210, 211
    • Applicable ICH Quality Guidelines for Good Manufacturing Practices (GMP)
    • EU EudraLex Volume 4
  • Experience with electronic quality management systems such as Veeva or MasterControl is a plus.
  • Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes external partners. Proven ability to manage multiple priorities and deliver high-quality work.
  • Demonstrated initiative, ownership, problem identification, problem solving, and strategic thinking skills.
  • Demonstrated ability to quickly adapt and find creative solutions to ensure deliverables are met.
  • Excellent verbal and written communication skills
Additional Information

The anticipated hourly rate for candidates who will work on-site at our San Diego location is between $25.00-$33.50 per hour. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship.

ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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