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Associate Quality Compliance Jobs (NOW HIRING)

Compliance Coordinator Location :Clarkston, WA Reports to: Operations Manager Pay Range: $43,200 ... Associates or bachelor's degree in Engineering (Manufacturing, Mechanical, Electrical, or Quality ...

What You Will Achieve The primary function of the Quality Compliance Specialist is to provide ... OR an associate's degree with 4 years of experience; OR a high schooldiploma (or equivalent) and 6 ...

What You Will Achieve The primary function of the Quality Compliance Specialist is to provide ... OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 ...

Job Title Associate Quality Engineer About Abbott Abbott is a global healthcare leader, creating ... Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Job Title Associate Quality Engineer About Abbott Abbott is a global healthcare leader, creating ... Administrative Shift What You'll Do Responsible for compliance with applicable Corporate and ...

Job Title Associate Quality Engineer About Abbott Abbott is a global healthcare leader, creating ... Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

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Associate Quality Compliance information

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How much do associate quality compliance jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for associate quality compliance 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 jobs pay 70k a year with an associate's degree?

Associate Quality Compliance roles can pay around $70,000 annually, especially in industries like manufacturing, healthcare, and pharmaceuticals. These positions often require knowledge of quality standards, regulatory compliance, and sometimes certifications such as Six Sigma or ISO. Other jobs that may pay similar wages with an associate's degree include dental hygienist, radiologic technologist, and certain technical roles in engineering or IT support.

How does an Associate Quality Compliance professional typically collaborate with other departments to ensure regulatory standards are met?

As an Associate Quality Compliance professional, you’ll regularly interact with teams such as manufacturing, research and development, and quality assurance to ensure all products and processes meet regulatory requirements. This collaboration often involves reviewing documentation, coordinating audits, and providing compliance training to other departments. You'll also help resolve non-conformities and support continuous improvement initiatives, making strong communication and teamwork skills essential for success in this role.

What is the difference between Associate Quality Compliance vs Quality Assurance Specialist?

AspectAssociate Quality ComplianceQuality Assurance Specialist
CertificationsISO, GMP, HACCPISO, GMP, HACCP
Work EnvironmentManufacturing, Healthcare, PharmaceuticalsManufacturing, Software, Healthcare
Employer & Industry UsageRegulated industries requiring complianceQuality process improvement across industries

Both roles focus on quality but differ in scope. Associate Quality Compliance primarily ensures adherence to regulations and standards, often supporting compliance documentation and audits. Quality Assurance Specialists focus on testing, process validation, and improving quality systems. While overlapping in certifications and industry settings, compliance roles emphasize regulatory adherence, whereas QA specialists concentrate on product quality and process improvements.

What jobs pay 500,000 a year in the US?

High-paying roles such as senior executives, specialized surgeons, and successful entrepreneurs can earn $500,000 or more annually. In the context of associate quality compliance, senior compliance managers or directors in large corporations with extensive experience and certifications may approach or exceed this income level, especially with bonuses and stock options.

What are the key skills and qualifications needed to thrive as an Associate Quality Compliance, and why are they important?

To thrive as an Associate Quality Compliance, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO or GMP), and a relevant bachelor’s degree, often in life sciences or engineering. Familiarity with compliance management systems, audit tools, and documentation software is typically required, along with knowledge of industry-specific certifications. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for this role. These skills ensure accurate compliance processes, mitigate risks, and support organizational adherence to regulatory requirements.

What is an Associate Quality Compliance?

An Associate Quality Compliance is a professional who helps ensure that a company’s products, processes, and operations meet regulatory and quality standards. They assist in monitoring compliance with industry regulations, conducting audits, reviewing documentation, and supporting the implementation of quality management systems. This role is often found in industries such as pharmaceuticals, medical devices, food production, and manufacturing, where maintaining high standards is critical. Associate Quality Compliance professionals work closely with other departments to identify areas of improvement and help resolve quality issues.

Is QC a high paying job?

Quality Control (QC) roles, including Associate Quality Compliance positions, typically offer salaries that are average or slightly above average compared to other entry-level manufacturing or compliance jobs. Salary levels depend on industry, location, experience, and certifications such as ISO or GMP standards. While some QC positions can be well-paying, they are generally not considered high-paying compared to specialized or managerial roles.

What does a compliance associate do?

A compliance associate ensures that a company's operations adhere to industry regulations, standards, and internal policies. They conduct audits, review documentation, and implement procedures to maintain compliance, often using tools like compliance management software. Strong attention to detail and knowledge of relevant regulations are essential for this role.
What cities are hiring for Associate Quality Compliance jobs? Cities with the most Associate Quality Compliance job openings:
What are the most commonly searched types of Quality Compliance jobs? The most popular types of Quality Compliance jobs are:
What states have the most Associate Quality Compliance jobs? States with the most job openings for Associate Quality Compliance jobs include:
Quality Compliance Analyst

Quality Compliance Analyst

Johnson and Johnson

New Brunswick, NJ • On-site

Full-time

Retirement, PTO

Posted 8 days ago


Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Customer Management
Job Sub Function:
Customer Service Operations
Job Category:
Professional
All Job Posting Locations:
New Brunswick, New Jersey, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
DePuy Synthes is recruiting for a Quality/Compliance Analyst - Customer Service, located in New Brunswick, NJ, West Chester, Pennsylvania, and Raynham Ma. Remote locations may be considered.
This role is responsible for executing and supporting regional operations in the areas of Document Management, Quality, Compliance, and SOX Reporting and for providing superior advisory and analytical support to internal and external customers enabling the compliant execution of critical customer focused operations.
Key Responsibilities:
Day-to-Day Activities: 70%
  • Support and continually work within the parameters established by a risk-based Quality Management System framework.

  • Serve as the Customer Service (CS) Subject Matter Expert (SME) regarding SOX financial reporting, Quality and Compliance.

  • Benchmark internally and externally, regionally and globally, to gather, share, and implement standard methodologies accordingly.

  • Assist CS Senior Leaders with development and implementation of organizational and strategic plans designed to improve efficiency of department processes, using technology and other platforms to standardize, leverage and/or eliminate manual interactions wherever possible.

  • Lead and manage projects related to broader Supply Chain initiatives, as required.

  • Your Key Performance Indicators for this role include on-time completion/compliance with SOX reporting.

  • Support change management strategies by applying change management principles and tools

  • Support the development and maintenance of internal resources to provide accurate SOX financial, Quality and Compliance information.

Day-to-Day Activities: 10%
  • Provide CS Quality & Compliance expertise on applicable projects.

  • Lead and/or support key departmental/cross-functional/cross-sector projects, as assigned, by developing and utilizing in-depth knowledge of business processes and systems, as well as project management skills.

  • Use continuous improvement tools and methodology, including Process Excellence, LEAN, and project management, to identify, evaluate, challenge, develop solutions, and optimize business processes that drive measurable improvement.

  • Regularly communicate in all directions to keep associates, peers, and Management informed of project status, process changes, and opportunities.

  • Drives / supports regional and global CS projects for the US region using FPX methodology, tools and best practices. Conducts lessons learned post-implementation and identifies opportunities to continuously improve.

Dat-to-Day Activities: 10%
  • Support documentation management, Quality, and Job Function Curriculum (JFC).

  • Support with managing departmental/Regional Change Control documentation and deliverables to ensure the on-time completion.

  • Support with the on-time completion of Annual Training Record Review (ATRR) and lead on-time completion of controlled document periodic review.

  • Support with Key Performance Indicators for On-Time Periodic Review.

  • Support with development, implementation, and evaluation of metrics with meaningful insights for customer service in the areas of Document Management.

Day-to-Day Activities: 10%
  • Complete required compliance/assigned training by required due date.

  • All duties as assigned by manager and/or supervisor.

Qualifications
Education
  • Required: Bachelor's degree in Quality, Engineering, Supply Chain, Life Sciences, Business, or a related field.

  • Preferred: Coursework or concentration in Quality Management, Regulatory Affairs, or Operations.

Experience and Skills
Required:
  • 2 to 4 years work experience in relevant Quality, Compliance, or Supply Chain position within a regulated, fast-paced business environment required

  • Work experience in Quality, Compliance, Document Management/Control, Technical Writing, or Supply Chain

  • Ability to analyze basic data and identify trends to support continuous improvement.

  • Proficiency with standard office and data tools (e.g., Microsoft Office).

  • Demonstrated time management skills with consistent track record to handle multiple competing priorities/deadlines, ability to act with a sense of urgency, and deliver expected/exceeding results

Preferred:
  • Experience in a medical device, pharmaceutical, or other regulated industry.

  • Exposure to audits, CAPA, change management, or supplier quality activities.

  • Familiarity with Lean, Six Sigma, or continuous improvement methodologies.

  • Experience supporting global or multi-site operations.

  • Ability to work effectively in cross-functional teams.

  • Effective written and verbal communication skills.

  • Strong attention to detail and ability to manage documentation accurately.

Other:
  • Language: English (required).

  • Travel: Up to 10% domestic and/or international, as needed.

  • Certifications: Quality-related certifications (e.g., ASQ) preferred, not required.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
#DePuySynthesCareers
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Behavior, Customer Centricity, Customer Intelligence, Customer Service Philosophy, Customer Support Operations, Customer Support Platforms, Customer Support Policies and Procedures, Customer Support Trends, Data Analysis, Execution Focus, Issue Escalation, Mentorship, Order Processing, Service Excellence, Service Request Management
The anticipated base pay range for this position is :
117,000 - 65,000 USD
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: • Vacation -120 hours per calendar year • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year • Holiday pay, including Floating Holidays -13 days per calendar year • Work, Personal and Family Time - up to 40 hours per calendar year • Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child • Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year • Caregiver Leave - 80 hours in a 52-week rolling period10 days • Volunteer Leave - 32 hours per calendar year • Military Spouse Time-Off - 80 hours per calendar year For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits