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Associate Quality Compliance Jobs (NOW HIRING)

Boeing

Associate Quality Engineer

Hialeah, FL · On-site

$69K - $98K/yr

Associate Quality Engineer Company: Boeing Distribution, Inc. Boeing Global Services (BGS ... To meet export control compliance requirements, a "U.S. Person" as defined by 22 C.F.R. 120.15 is ...

Legend Biotech USA, Inc.

Legend Biotech is seeking an Associate Director, Site Quality Compliance Lead as part of the Quality team based in Raritan, NJ.Role OverviewThe Site Quality Compliance Lead (Raritan-CARVYKTI) role is ...

Airboss

Associate Quality Engineer

Scotland Neck, NC · On-site

Role: Reporting to the Quality Engineer, the Associate Quality Engineer is to assist the ... Oversee plant ISO 9001, 14001 & 17025 compliance including: serve as internal lead auditor; promote ...

Mesa Labs

Associate Quality Auditor

Bozeman, MT · On-site

$33.77/hr

The Associate Quality Auditor plans, conducts, and reports on customer audits, internal quality ... This role ensures compliance with internal quality systems and applicable external regulations and ...

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Associate Quality Compliance information

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How much do associate quality compliance jobs pay per hour?

As of Aug 10, 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.

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 are the key skills and qualifications needed to thrive as an associate quality compliance?

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 compliance a stressful job?

Associate Quality Compliance roles can be stressful due to the responsibility of ensuring adherence to strict regulations and standards. The job often involves detailed audits, documentation, and deadlines, requiring strong attention to detail and organizational skills. However, workload and stress levels vary depending on the organization and specific responsibilities.
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:
Associate Quality Compliance jobs near you

Sr. Associate, QA Compliance

Jubilant HollisterStier Spokane

Spokane, WA • On-site

Full-time

Medical, Dental, Vision, Life

Posted 5 days ago

Job description

Join a Leader in Pharmaceutical Manufacturing - And Build What's Next
As Spokane's Largest Manufacturing Company, Jubilant HollisterStier LLC is a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world.
We are nationally recognized for our expertise in producing sterile injectable vials and lyophilized products, and our Allergy business is a global leader in allergenic extracts that support treatments for allergies and asthma. Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world.
For the Builders, Innovators, and Doers - This Is Your Place
If you are someone who thrives on solving complex problems, improving systems, and building real solutions, you'll feel at home here. At Jubilant HollisterStier, your ideas matter - and your impact is felt globally.
Why builders choose us:
  • Immediate impact: Your work directly supports essential medicines and allergenic therapies used worldwide.
  • Benefits start on day one: Medical, Dental, Vision, FSA/HSA, Life, AD&D, and Disability benefits begin immediately because your well-being shouldn't have a waiting period.
  • A career you can grow: We provide opportunities for growth, promotion, and annual raises, with midpoint compensation reserved for high performance and longevity.
  • A culture of improvement: We value people who thrive on continuous improvement, innovation, and hands on contribution.
  • A stable industry leader: Backed by Jubilant Pharma, we pair long term stability with forward looking innovation.

If you want to build something meaningful with a team that values your drive, skills, and ideas - you belong here.
Job Description:
The QA Compliance Associate provides support to the company Deviation, Corrective and Preventive Action (CAPA) program through a complete assessment of Root Cause Analysis (RCA) of Deviations and vendor complaints/issues. Assure product compliance and product safety. Ensure accurate and timely data entry and oversight of the company Quality Systems related to Deviation, CAPA and vendor complaint activities.
1. Lead, facilitate, and conduct deviations, non-conformances investigations.
2. Author/draft investigation reports with minimal guidance.
3. Ensure timely completion of investigations with accuracy, consistency and compliance with applicable
SOPs/Policies, Specifications and related guidelines/regulations.
4. Interview Subject Matter Experts (SMEs) and involved employee(s) across multiple shifts to investigate
reported problems and assess the quality impact.
5. Conduct investigational meetings with required team member(s) and Verify Investigational findings
against documented process per SOP.
6. Coordinate immediate actions in conjunction with QA and department management upon identification of
a non-conformance.
7. Utilize problem solving techniques and appropriate tools to determine root cause and appropriate causal
factors.
8. Facilitate root cause analysis meetings with key stakeholders to identify solutions for quality
improvements based on identified trends.
9. Work with cross functional team member(s) to develop appropriate CAPA actions.
10. Ensure investigations, corrections and CAPA are generated and approved in a timely manner.
11. Act as liaison as it relates to specific investigations during client calls and audits.
12. Support and/or coordinate data collection required for management reviews, KPI reports, client trend
review meetings, and all other established regular quality reporting and review mechanisms.
13. Communicate/Escalate to management any issues or delays identified during the investigation process.
14. Provide investigation training as needed to the Quality Unit and other departments to ensure that
investigations are handled consistently throughout the company.
15. Speak to assigned deviations during regulatory and client audits. 16. Act as the QAC Lead Associate when requested by the QAC SUPERVISOR (in the absence of the QAC Lead Associate)
Required:
- Associate's degree in biology, Chemistry or related field required.
- Bachelor's degree in a science field desired.
- Minimum of 5 years related experience required with an Associate's Degree.
- Minimum of 2 years related experience required with a Bachelor's degree.
- Pharmaceutical and FDA Regulated Experience required.
- Experience with technical writing, investigations, CAPA system, building and manufacturing processes/systems, QA operations systems, and QC analysis is required.
- Microsoft Word & Excel required.
- Knowledge of cGMPs required.
Preferred:
- Sologic Certificate
- Direct or supporting aseptic manufacturing experience in bio/pharma industry desired.
Working Environment:
  • Vision Requirements: 14/14 Corrected Near-Point
  • Pass Color Deficiency Test
  • Ability to lift 30 pounds unassisted.
  • Prolonged sitting required.

Location: Spokane, WA - On Site, Full- -Time
Shift: Weekday Days, 8 hour shifts
Compensation & Benefits That Start on Day One - Because Your Well Being Matters
Hiring Wage: $81,800.00-$130,900, with opportunities for growth, promotion, and annual raises.
At Jubilant HollisterStier, we don't believe in waiting periods. From the moment you join us, you and your family have access to a full suite of benefits designed to support your health, stability, and long-term success.
Starting on your first day, you receive:
  • Medical, Dental & Vision coverage
  • Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
  • Life & AD&D Insurance
  • Short-Term & Long-Term Disability Insurance
  • Employee Assistance Program

Unlock Your Potential
If you're seeking a dynamic and rewarding career, we welcome your application today. Apply online:
Careers - Jubilant HollisterStier
Jubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
If you require assistance applying for a position, contact:
JHS-TalentAcquisition@jubl.com
Our Promise: Caring, Sharing, Growing
We are committed to enhancing value for customers and stakeholders by delivering innovative and economically efficient solutions, always with care for the environment and society.

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