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Dea Auditor Jobs (NOW HIRING)

Sharp Services

QA Auditor

Allentown, PA · On-site

The Auditor responsibilities encompass Sharp Packaging Services, LLC commercial US facilities ... Knowledge of DEA regulations, ISO 9001 and ISO 15378 desired. * Above average written and oral ...

Sharp Services

QA Auditor

Allentown, PA · On-site

The Auditor responsibilities encompass Sharp Packaging Services, LLC commercial US facilities ... Knowledge of DEA regulations, ISO 9001 and ISO 15378 desired. * Above average written and oral ...

Sharpservices

QA Auditor

Allentown, PA · On-site

The Auditor responsibilities encompass Sharp Packaging Services, LLC commercial US facilities ... Knowledge of DEA regulations, ISO 9001 and ISO 15378 desired. * Above average written and oral ...

Sharp Services, LLC

Knowledge of DEA regulations, ISO 9001 and ISO 15378 desired. * Above average written and oral ... auditing and comparator sourcing. #J-18808-Ljbffr

Drug Enforcement Administration

Accountant

Arlington, VA · On-site +1

$57K - $91K/yr

Summary This position is located in the DEA, Financial Management Division (FC), Office of Finance ... Twenty-four semester hours in accounting or auditing courses of appropriate type and quality. This ...

Department of Justice

Accountant

Arlington, VA · On-site

$57K/yr

DEA Employment Eligibility Applicants must meet the required qualification requirements described ... Twenty-four semester hours in accounting or auditing courses of appropriate type and quality. This ...

AbbVie

PR · On-site

Auditing experience. Requires direct experience with FDA, DEA, and European regulations and experience in government inspection and audit techniques at least two (2) years. * Total combined minimum ...

Allergan

Officer, Compliance II

Barceloneta, PR · On-site

Auditing experience. Requires direct experience with FDA, DEA, and European regulations and experience in government inspection and audit techniques at least two (2) years. * Total combined minimum ...

TekWissen LLC

Laboratory Technician 1

Walpole, MA · On-site

$43/hr

The scope of this role includes auditing of chromatography batch records. This role will provide ... This position includes the handling of all types of materials, including hazardous and DEA (Drug ...

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Dea Auditor information

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How much do dea auditor jobs pay per year?

As of Sep 10, 2026, the average yearly pay for dea auditor in the United States is $72,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What states have the most Dea Auditor jobs?

States with the most job openings for Dea Auditor jobs include:

What are popular job titles related to Dea Auditor jobs?

For Dea Auditor jobs, the most frequently searched job titles are:

Infographic showing various Dea Auditor job openings in the United States as of August 2026, with employment types broken down into 2% Locum Tenens, 3% As Needed, 78% Full Time, 14% Part Time, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $72,633 per year, or $34.9 per hour.

Director, Quality Compliance (DEA)

Greenville, SC • On-site

Kelly Services
See more jobs at Kelly Servicesexternal

$180K - $220K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 9 days ago

Key responsibilities

  • Develop and implement enterprise quality compliance strategies, programs, and policies.

  • Lead inspection readiness programs and provide on-site support during regulatory inspections.

  • Manage internal and external audit programs, review audit observations, and drive CAPA implementation.

Job description

Sr. Director of Quality Compliance (DEA)

Full-Time | Senior Leadership

Location: Greenville, SC (Onsite Role)

Compensation: Approximately $180,000-$220,000 base salary + bonus potential

Position Summary

A growing pharmaceutical manufacturing organization is seeking a Sr. Director of Quality Compliance to lead enterprise-wide compliance strategy, governance, audit readiness, inspection management, escalation processes, and quality risk management activities. This individual will serve as a key member of the Quality Leadership team and will drive continuous improvement initiatives to ensure sustained compliance with cGMP, FDA, DEA, DSCSA, and international regulatory requirements.

This role will oversee quality compliance systems and inspection readiness programs while partnering cross-functionally with Quality, Manufacturing, Regulatory, Supply Chain, and Executive Leadership teams. The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory inspections, auditing, and enterprise compliance strategy within GMP-regulated manufacturing environments.

Key Responsibilities

Quality Compliance & Regulatory Oversight

  • Develop and implement enterprise quality compliance strategies, programs, and policies
  • Ensure compliance with FDA, DEA, cGMP, ICH, DSCSA, and global regulatory requirements
  • Lead inspection readiness programs and provide on-site support during regulatory inspections
  • Serve as the primary escalation point for significant quality and compliance risks
  • Manage quality notification-to-management and escalation programs
  • Interpret evolving regulatory requirements and implement systemic compliance improvements

Audit & Inspection Management

  • Direct internal audit programs across manufacturing and quality operations
  • Lead and manage external audits conducted by FDA, DEA, notified bodies, clients, and global health authorities
  • Review audit observations and drive effective CAPA implementation
  • Maintain audit-ready quality systems and documentation practices
  • Track and trend quality indicators and compliance metrics

Quality Systems & Risk Management

  • Oversee core Quality Management System (QMS) processes including:
  • Change control
  • Deviations
  • CAPAs
  • Document management
  • Supplier quality
  • Escalation management
  • Analyze quality data and trends to identify systemic risks and improvement opportunities
  • Ensure effective statistical monitoring and reporting of quality compliance metrics
  • Support post-market surveillance and ongoing product quality monitoring activities

Leadership & Cross-Functional Collaboration

  • Lead and develop Quality Compliance teams and associated quality personnel
  • Partner with Manufacturing, Quality Control, Regulatory Affairs, and Executive Leadership to drive strategic quality initiatives
  • Foster a culture of compliance, accountability, and continuous improvement
  • Support implementation of quality-focused operational efficiencies and business improvements
  • Present quality compliance updates and risk assessments to senior leadership

Continuous Improvement & Strategy

  • Drive initiatives focused on improving inspection outcomes, audit performance, and overall quality culture
  • Lead implementation of systemic process improvements across manufacturing and quality operations
  • Evaluate and enhance quality systems effectiveness through analytics and risk management principles
  • Support modernization initiatives involving predictive analytics, technology platforms, and quality data visibility

Qualifications

Required Education & Experience

  • Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or related scientific discipline
  • 15+ years of progressive pharmaceutical quality experience within GMP-regulated manufacturing environments
  • Prior senior leadership experience in Quality Compliance, Quality Assurance, or Regulatory Compliance
  • Strong experience interacting directly with FDA and global regulatory agencies

Technical Expertise

  • Deep knowledge of:
  • cGMP regulations
  • FDA and global regulatory requirements
  • DEA compliance
  • Quality systems and auditing
  • Risk management principles
  • Pharmaceutical manufacturing operations
  • Experience supporting API, aseptic, sterile, or OTC manufacturing environments preferred
  • Strong understanding of:
  • Deviations
  • CAPAs
  • Change controls
  • Inspection readiness
  • Supplier quality management
  • Data integrity

Additional Information

  • Travel up to approximately 40% may be required
  • Relocation assistance may be available
  • Experience within pharmaceutical manufacturing, CDMO, or highly regulated GMP environments strongly preferred

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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